{"Case.ID":4227848,"Initial.FDA.Received.Date":"10/01/1969","Event.Date":"02/16/1969","Latest.FDA.Received.Date":"01-OCT-1969","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Colchicine;Allopurinol","Reason.for.Use":"-","Reactions":"Myopathy;Stevens-Johnson Syndrome;Hepatocellular Injury","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"58 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4227553,"Initial.FDA.Received.Date":"10/01/1969","days.since.last.fda":0,"Event.Date":"07/10/1969","Latest.FDA.Received.Date":"01-OCT-1969","Suspect.Product.Names":"Mintezol","Suspect.Product.Active.Ingredients":"Thiabendazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"2 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"Temaril"}
{"Case.ID":4237449,"Initial.FDA.Received.Date":"11/01/1969","days.since.last.fda":31,"Event.Date":"","Latest.FDA.Received.Date":"01-NOV-1969","Suspect.Product.Names":"Butazolidin Alka","Suspect.Product.Active.Ingredients":"Aluminum Hydroxide\\Magnesium Trisilicate\\Phenylbutazone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4226120,"Initial.FDA.Received.Date":"11/01/1969","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"01-NOV-1969","Suspect.Product.Names":"Butazolidin Alka","Suspect.Product.Active.Ingredients":"Aluminum Hydroxide\\Magnesium Trisilicate\\Phenylbutazone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4234859,"Initial.FDA.Received.Date":"02/01/1970","days.since.last.fda":92,"Event.Date":"","Latest.FDA.Received.Date":"01-FEB-1970","Suspect.Product.Names":"Keflin","Suspect.Product.Active.Ingredients":"Cephalothin Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"38 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"-"}
{"Case.ID":4236714,"Initial.FDA.Received.Date":"03/01/1970","days.since.last.fda":28,"Event.Date":"10/15/1969","Latest.FDA.Received.Date":"01-MAR-1970","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Penicillin G Procaine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"39 YR","Sender":"-","Concomitant.Product.Names":"Tolbutamide;Penicillin V Potassium"}
{"Case.ID":4232811,"Initial.FDA.Received.Date":"03/01/1970","days.since.last.fda":0,"Event.Date":"10/15/1969","Latest.FDA.Received.Date":"01-MAR-1970","Suspect.Product.Names":"Hypaque","Suspect.Product.Active.Ingredients":"Diatrizoate Meglumine\\Diatrizoate Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Sterling","Concomitant.Product.Names":"-"}
{"Case.ID":4234415,"Initial.FDA.Received.Date":"05/01/1970","days.since.last.fda":61,"Event.Date":"","Latest.FDA.Received.Date":"01-MAY-1970","Suspect.Product.Names":"Butazolidin","Suspect.Product.Active.Ingredients":"Phenylbutazone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"46 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4251992,"Initial.FDA.Received.Date":"06/01/1970","days.since.last.fda":31,"Event.Date":"12/04/1968","Latest.FDA.Received.Date":"01-JUN-1970","Suspect.Product.Names":"Tandearil","Suspect.Product.Active.Ingredients":"Oxyphenbutazone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"48 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4256468,"Initial.FDA.Received.Date":"11/01/1970","days.since.last.fda":153,"Event.Date":"","Latest.FDA.Received.Date":"01-NOV-1970","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cortisone Acetate","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"50 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4266043,"Initial.FDA.Received.Date":"09/01/1971","days.since.last.fda":304,"Event.Date":"06/16/1971","Latest.FDA.Received.Date":"01-SEP-1971","Suspect.Product.Names":"Mintezol","Suspect.Product.Active.Ingredients":"Thiabendazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"2 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4259684,"Initial.FDA.Received.Date":"09/01/1971","days.since.last.fda":0,"Event.Date":"06/16/1971","Latest.FDA.Received.Date":"01-SEP-1971","Suspect.Product.Names":"Mintezol","Suspect.Product.Active.Ingredients":"Thiabendazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"2 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4259555,"Initial.FDA.Received.Date":"09/01/1971","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"01-SEP-1971","Suspect.Product.Names":"Mintezol","Suspect.Product.Active.Ingredients":"Thiabendazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"1 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4262294,"Initial.FDA.Received.Date":"02/01/1972","days.since.last.fda":153,"Event.Date":"","Latest.FDA.Received.Date":"01-FEB-1972","Suspect.Product.Names":"Cytoxan","Suspect.Product.Active.Ingredients":"Cyclophosphamide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Mead Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":4264741,"Initial.FDA.Received.Date":"05/01/1972","days.since.last.fda":90,"Event.Date":"11/17/1971","Latest.FDA.Received.Date":"01-MAY-1972","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Skin Necrosis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4267472,"Initial.FDA.Received.Date":"07/01/1972","days.since.last.fda":61,"Event.Date":"","Latest.FDA.Received.Date":"01-JUL-1972","Suspect.Product.Names":"Cytoxan","Suspect.Product.Active.Ingredients":"Cyclophosphamide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Mead Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":4276624,"Initial.FDA.Received.Date":"05/01/1973","days.since.last.fda":304,"Event.Date":"04/04/1973","Latest.FDA.Received.Date":"01-MAY-1973","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Erythromycin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"Penicillin;Dilantin;Phenergan"}
{"Case.ID":4280988,"Initial.FDA.Received.Date":"10/01/1973","days.since.last.fda":153,"Event.Date":"06/04/1973","Latest.FDA.Received.Date":"01-OCT-1973","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"56 YR","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":4283552,"Initial.FDA.Received.Date":"01/01/1974","days.since.last.fda":92,"Event.Date":"10/12/1908","Latest.FDA.Received.Date":"01-JAN-1974","Suspect.Product.Names":"Sulla","Suspect.Product.Active.Ingredients":"Sulfameter","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Ah Robins","Concomitant.Product.Names":"-"}
{"Case.ID":4283040,"Initial.FDA.Received.Date":"01/01/1974","days.since.last.fda":0,"Event.Date":"06/21/1973","Latest.FDA.Received.Date":"01-JAN-1974","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampicillin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4289347,"Initial.FDA.Received.Date":"09/01/1974","days.since.last.fda":243,"Event.Date":"","Latest.FDA.Received.Date":"01-SEP-1974","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Aldactone;Lasix;Tylenol"}
{"Case.ID":4291432,"Initial.FDA.Received.Date":"02/01/1975","days.since.last.fda":153,"Event.Date":"","Latest.FDA.Received.Date":"01-FEB-1975","Suspect.Product.Names":"Butazolidin","Suspect.Product.Active.Ingredients":"Phenylbutazone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4307323,"Initial.FDA.Received.Date":"07/01/1975","days.since.last.fda":150,"Event.Date":"11/09/1973","Latest.FDA.Received.Date":"01-JUL-1975","Suspect.Product.Names":"Sulla","Suspect.Product.Active.Ingredients":"Sulfameter","Reason.for.Use":"-","Reactions":"Hepatitis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"65 YR","Sender":"Ah Robins","Concomitant.Product.Names":"Keflex"}
{"Case.ID":4313338,"Initial.FDA.Received.Date":"02/01/1977","days.since.last.fda":581,"Event.Date":"11/16/1976","Latest.FDA.Received.Date":"01-FEB-1977","Suspect.Product.Names":"Septra Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Renal Failure;Haemorrhage;Stevens-Johnson Syndrome;Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"61 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Quinine"}
{"Case.ID":4314406,"Initial.FDA.Received.Date":"04/01/1977","days.since.last.fda":59,"Event.Date":"","Latest.FDA.Received.Date":"01-APR-1977","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4317101,"Initial.FDA.Received.Date":"06/01/1977","days.since.last.fda":61,"Event.Date":"01/21/1977","Latest.FDA.Received.Date":"01-JUN-1977","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"-","Concomitant.Product.Names":"Dyazide"}
{"Case.ID":4317590,"Initial.FDA.Received.Date":"07/01/1977","days.since.last.fda":30,"Event.Date":"04/05/1977","Latest.FDA.Received.Date":"01-JUL-1977","Suspect.Product.Names":"Macrodantin","Suspect.Product.Active.Ingredients":"Nitrofurantoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"22 YR","Sender":"-","Concomitant.Product.Names":"Methenamine Mandelate"}
{"Case.ID":4319803,"Initial.FDA.Received.Date":"09/01/1977","days.since.last.fda":62,"Event.Date":"06/04/1977","Latest.FDA.Received.Date":"01-SEP-1977","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"55 YR","Sender":"-","Concomitant.Product.Names":"Digoxin;Hydrochlorothiazide;Lasix"}
{"Case.ID":4320201,"Initial.FDA.Received.Date":"10/01/1977","days.since.last.fda":30,"Event.Date":"","Latest.FDA.Received.Date":"01-OCT-1977","Suspect.Product.Names":"Motrin","Suspect.Product.Active.Ingredients":"Ibuprofen","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Upjohn","Concomitant.Product.Names":"-"}
{"Case.ID":4322379,"Initial.FDA.Received.Date":"11/01/1977","days.since.last.fda":31,"Event.Date":"03/01/1977","Latest.FDA.Received.Date":"01-NOV-1977","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Scopolamine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"35 YR","Sender":"Ah Robins","Concomitant.Product.Names":"Sultrin;Compazine;Ampicillin;Periactin"}
{"Case.ID":4320910,"Initial.FDA.Received.Date":"11/01/1977","days.since.last.fda":0,"Event.Date":"03/01/1977","Latest.FDA.Received.Date":"01-NOV-1977","Suspect.Product.Names":"Sultrin","Suspect.Product.Active.Ingredients":"Sulfabenzamide\\Sulfacetamide\\Sulfathiazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"35 YR","Sender":"Ortho","Concomitant.Product.Names":"Ampicillin"}
{"Case.ID":4320554,"Initial.FDA.Received.Date":"11/01/1977","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"01-NOV-1977","Suspect.Product.Names":"Nalfon","Suspect.Product.Active.Ingredients":"Fenoprofen Calcium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"-"}
{"Case.ID":4323039,"Initial.FDA.Received.Date":"03/01/1978","days.since.last.fda":120,"Event.Date":"09/26/1977","Latest.FDA.Received.Date":"01-MAR-1978","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":4326782,"Initial.FDA.Received.Date":"09/01/1978","days.since.last.fda":184,"Event.Date":"11/01/1977","Latest.FDA.Received.Date":"01-SEP-1978","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"74 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4329620,"Initial.FDA.Received.Date":"08/01/1979","days.since.last.fda":334,"Event.Date":"04/13/1979","Latest.FDA.Received.Date":"01-AUG-1979","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Pneumonia;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4363537,"Initial.FDA.Received.Date":"05/21/1980","days.since.last.fda":294,"Event.Date":"","Latest.FDA.Received.Date":"21-MAY-1980","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Myocardial Infarction;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"81 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"Dichloralphenazone;Acth;Prednisone;Moduretic 5-50"}
{"Case.ID":4336328,"Initial.FDA.Received.Date":"06/01/1980","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"01-JUN-1980","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":4338865,"Initial.FDA.Received.Date":"08/01/1980","days.since.last.fda":61,"Event.Date":"01/25/1980","Latest.FDA.Received.Date":"01-AUG-1980","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Pneumonia;Stevens-Johnson Syndrome;Gastrointestinal Haemorrhage;Jaundice Cholestatic","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"Calcium Pantothenate;Aspirin;Niacin"}
{"Case.ID":4352215,"Initial.FDA.Received.Date":"06/02/1981","days.since.last.fda":305,"Event.Date":"","Latest.FDA.Received.Date":"02-JUN-1981","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4342929,"Initial.FDA.Received.Date":"07/01/1981","days.since.last.fda":29,"Event.Date":"","Latest.FDA.Received.Date":"01-JUL-1981","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4345662,"Initial.FDA.Received.Date":"10/01/1981","days.since.last.fda":92,"Event.Date":"09/01/1979","Latest.FDA.Received.Date":"01-OCT-1981","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":4363393,"Initial.FDA.Received.Date":"10/22/1981","days.since.last.fda":21,"Event.Date":"","Latest.FDA.Received.Date":"22-OCT-1981","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Jaundice Cholestatic;Stevens-Johnson Syndrome;Pneumonia;Hepatic Function Abnormal","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"74 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"E-Mycin;Enduron;Dalmane;Tetracycline"}
{"Case.ID":4362927,"Initial.FDA.Received.Date":"10/22/1981","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"22-OCT-1981","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"Aspirin;Dyazide;Unspecified Ingredient;Keflex"}
{"Case.ID":4362532,"Initial.FDA.Received.Date":"10/22/1981","days.since.last.fda":0,"Event.Date":"06/01/1981","Latest.FDA.Received.Date":"22-OCT-1981","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"61 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4347262,"Initial.FDA.Received.Date":"11/01/1981","days.since.last.fda":10,"Event.Date":"01/11/1981","Latest.FDA.Received.Date":"01-NOV-1981","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"5 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4347960,"Initial.FDA.Received.Date":"12/01/1981","days.since.last.fda":30,"Event.Date":"01/27/1981","Latest.FDA.Received.Date":"01-DEC-1981","Suspect.Product.Names":"Septra Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4354010,"Initial.FDA.Received.Date":"04/01/1982","days.since.last.fda":121,"Event.Date":"01/01/1981","Latest.FDA.Received.Date":"01-APR-1982","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"60 YR","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":4358219,"Initial.FDA.Received.Date":"05/12/1982","days.since.last.fda":41,"Event.Date":"12/14/1981","Latest.FDA.Received.Date":"12-MAY-1982","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"83 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"Hydropres 25;Vitamin B Complex"}
{"Case.ID":4367210,"Initial.FDA.Received.Date":"06/23/1982","days.since.last.fda":42,"Event.Date":"02/01/1982","Latest.FDA.Received.Date":"23-JUN-1982","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenacetin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"-","Concomitant.Product.Names":"Clinoril"}
{"Case.ID":4365981,"Initial.FDA.Received.Date":"07/01/1982","days.since.last.fda":8,"Event.Date":"02/01/1982","Latest.FDA.Received.Date":"01-JUL-1982","Suspect.Product.Names":"Bactrim Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Hepatic Function Abnormal;Jaundice Cholestatic","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"Roche","Concomitant.Product.Names":"Allopurinol;Cytoxan;Lasix;Vincristine Sulfate"}
{"Case.ID":4359613,"Initial.FDA.Received.Date":"07/21/1982","days.since.last.fda":20,"Event.Date":"","Latest.FDA.Received.Date":"21-JUL-1982","Suspect.Product.Names":"Oraflex","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Pneumonia;Stevens-Johnson Syndrome;Pancytopenia;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Chloroquine;Mechlorethamine Hydrochloride;Lasix;Folic Acid"}
{"Case.ID":4360449,"Initial.FDA.Received.Date":"08/16/1982","days.since.last.fda":26,"Event.Date":"","Latest.FDA.Received.Date":"16-AUG-1982","Suspect.Product.Names":"Oraflex","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Agranulocytosis;Pneumonia;Pancytopenia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Methotrexate;Lasix;Folic Acid;Asendin"}
{"Case.ID":4368728,"Initial.FDA.Received.Date":"08/26/1982","days.since.last.fda":10,"Event.Date":"06/21/1982","Latest.FDA.Received.Date":"26-AUG-1982","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Agranulocytosis;Dermatitis;Dermatitis Bullous;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"-","Concomitant.Product.Names":"Methotrexate;Asendin;Lasix"}
{"Case.ID":4361936,"Initial.FDA.Received.Date":"09/08/1982","days.since.last.fda":13,"Event.Date":"06/28/1982","Latest.FDA.Received.Date":"08-SEP-1982","Suspect.Product.Names":"Oraflex","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Pancytopenia;Stevens-Johnson Syndrome;Pneumonia;Dermatitis Bullous","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Methotrexate;Asendin;Folic Acid;Lasix"}
{"Case.ID":4364417,"Initial.FDA.Received.Date":"10/07/1982","days.since.last.fda":29,"Event.Date":"04/21/1981","Latest.FDA.Received.Date":"07-OCT-1982","Suspect.Product.Names":"Oraflex","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"82 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"-"}
{"Case.ID":4364416,"Initial.FDA.Received.Date":"10/07/1982","days.since.last.fda":0,"Event.Date":"02/13/1981","Latest.FDA.Received.Date":"07-OCT-1982","Suspect.Product.Names":"Oraflex","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Fenoprofen Calcium"}
{"Case.ID":4379795,"Initial.FDA.Received.Date":"10/21/1982","days.since.last.fda":14,"Event.Date":"02/01/1982","Latest.FDA.Received.Date":"21-OCT-1982","Suspect.Product.Names":"Oraflex","Suspect.Product.Active.Ingredients":"Benoxaprofen","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"74 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"-"}
{"Case.ID":4374415,"Initial.FDA.Received.Date":"10/29/1982","days.since.last.fda":8,"Event.Date":"","Latest.FDA.Received.Date":"29-OCT-1982","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Chlorothiazide"}
{"Case.ID":4381547,"Initial.FDA.Received.Date":"03/30/1983","days.since.last.fda":152,"Event.Date":"","Latest.FDA.Received.Date":"30-MAR-1983","Suspect.Product.Names":"Indocin","Suspect.Product.Active.Ingredients":"Indomethacin","Reason.for.Use":"-","Reactions":"Death;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4378544,"Initial.FDA.Received.Date":"04/15/1983","days.since.last.fda":16,"Event.Date":"","Latest.FDA.Received.Date":"15-APR-1983","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"4 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4392462,"Initial.FDA.Received.Date":"06/21/1983","days.since.last.fda":67,"Event.Date":"","Latest.FDA.Received.Date":"21-JUN-1983","Suspect.Product.Names":"Butazolidin","Suspect.Product.Active.Ingredients":"Phenylbutazone","Reason.for.Use":"-","Reactions":"Infection;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"79 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4383397,"Initial.FDA.Received.Date":"06/22/1983","days.since.last.fda":1,"Event.Date":"04/01/1983","Latest.FDA.Received.Date":"22-JUN-1983","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Pulmonary Embolism;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"5 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4383398,"Initial.FDA.Received.Date":"06/30/1983","days.since.last.fda":8,"Event.Date":"04/05/1983","Latest.FDA.Received.Date":"30-JUN-1983","Suspect.Product.Names":"Bactrim Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"27 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":4391493,"Initial.FDA.Received.Date":"09/23/1983","days.since.last.fda":85,"Event.Date":"","Latest.FDA.Received.Date":"23-SEP-1983","Suspect.Product.Names":"Pipracil","Suspect.Product.Active.Ingredients":"Piperacillin Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Lederle","Concomitant.Product.Names":"-"}
{"Case.ID":4404197,"Initial.FDA.Received.Date":"06/01/1984","days.since.last.fda":252,"Event.Date":"","Latest.FDA.Received.Date":"01-JUN-1984","Suspect.Product.Names":"Zinacef","Suspect.Product.Active.Ingredients":"Cefuroxime Sodium","Reason.for.Use":"-","Reactions":"Coombs Positive Haemolytic Anaemia;Stevens-Johnson Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Metronidazole"}
{"Case.ID":4403763,"Initial.FDA.Received.Date":"06/01/1984","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"01-JUN-1984","Suspect.Product.Names":"Zinacef","Suspect.Product.Active.Ingredients":"Cefuroxime Sodium","Reason.for.Use":"-","Reactions":"Acute Kidney Injury;Stevens-Johnson Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"68 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Furosemide;Gentamicin"}
{"Case.ID":4413527,"Initial.FDA.Received.Date":"07/06/1984","days.since.last.fda":35,"Event.Date":"","Latest.FDA.Received.Date":"06-JUL-1984","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Acute Kidney Injury;Death;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4405938,"Initial.FDA.Received.Date":"07/23/1984","days.since.last.fda":17,"Event.Date":"08/06/1983","Latest.FDA.Received.Date":"23-JUL-1984","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Hepatic Necrosis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"6 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4416649,"Initial.FDA.Received.Date":"10/23/1984","days.since.last.fda":92,"Event.Date":"","Latest.FDA.Received.Date":"23-OCT-1984","Suspect.Product.Names":"Clinoril","Suspect.Product.Active.Ingredients":"Sulindac","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4415538,"Initial.FDA.Received.Date":"11/30/1984","days.since.last.fda":38,"Event.Date":"10/07/1984","Latest.FDA.Received.Date":"30-NOV-1984","Suspect.Product.Names":"Feldene","Suspect.Product.Active.Ingredients":"Piroxicam","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"47 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":4438128,"Initial.FDA.Received.Date":"02/26/1985","days.since.last.fda":88,"Event.Date":"","Latest.FDA.Received.Date":"26-FEB-1985","Suspect.Product.Names":"Feldene","Suspect.Product.Active.Ingredients":"Piroxicam","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":4449207,"Initial.FDA.Received.Date":"05/30/1985","days.since.last.fda":93,"Event.Date":"","Latest.FDA.Received.Date":"30-MAY-1985","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Hypersensitivity;Erythema Multiforme","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4496273,"Initial.FDA.Received.Date":"07/09/1986","days.since.last.fda":405,"Event.Date":"","Latest.FDA.Received.Date":"09-JUL-1986","Suspect.Product.Names":"Keflin","Suspect.Product.Active.Ingredients":"Cephalothin Sodium","Reason.for.Use":"-","Reactions":"Dermatitis Exfoliative;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"4 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"-"}
{"Case.ID":4505869,"Initial.FDA.Received.Date":"09/15/1986","days.since.last.fda":68,"Event.Date":"10/23/1979","Latest.FDA.Received.Date":"15-SEP-1986","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cefuroxime","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Coagulopathy;Hepatorenal Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"53 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":4507935,"Initial.FDA.Received.Date":"09/23/1986","days.since.last.fda":8,"Event.Date":"","Latest.FDA.Received.Date":"23-SEP-1986","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Fluorouracil","Reason.for.Use":"-","Reactions":"Colitis;Stevens-Johnson Syndrome;Sepsis;Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"Cisplatin;Methotrexate"}
{"Case.ID":4521143,"Initial.FDA.Received.Date":"12/10/1986","days.since.last.fda":78,"Event.Date":"","Latest.FDA.Received.Date":"10-DEC-1986","Suspect.Product.Names":"Omnipaque","Suspect.Product.Active.Ingredients":"Iohexol","Reason.for.Use":"-","Reactions":"Renal Vasculitis;Pulmonary Oedema;Vasculitis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Sterling","Concomitant.Product.Names":"Hydralazine;Atenolol"}
{"Case.ID":4528717,"Initial.FDA.Received.Date":"01/29/1987","days.since.last.fda":50,"Event.Date":"","Latest.FDA.Received.Date":"29-JAN-1987","Suspect.Product.Names":"Zyloprim;Capoten","Suspect.Product.Active.Ingredients":"Captopril;Allopurinol","Reason.for.Use":"-","Reactions":"Infection;Renal Failure;Stevens-Johnson Syndrome;Leukopenia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Er Squibb","Concomitant.Product.Names":"Mellaril"}
{"Case.ID":4529448,"Initial.FDA.Received.Date":"02/03/1987","days.since.last.fda":5,"Event.Date":"12/12/1986","Latest.FDA.Received.Date":"03-FEB-1987","Suspect.Product.Names":"Platinol","Suspect.Product.Active.Ingredients":"Cisplatin;Fluorouracil","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"47 YR","Sender":"Bristol Myers","Concomitant.Product.Names":"Reglan;Compazine;Ativan"}
{"Case.ID":4546906,"Initial.FDA.Received.Date":"05/26/1987","days.since.last.fda":112,"Event.Date":"10/01/1983","Latest.FDA.Received.Date":"26-MAY-1987","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4554332,"Initial.FDA.Received.Date":"07/07/1987","days.since.last.fda":42,"Event.Date":"","Latest.FDA.Received.Date":"07-JUL-1987","Suspect.Product.Names":"Macrodantin","Suspect.Product.Active.Ingredients":"Nitrofurantoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4574907,"Initial.FDA.Received.Date":"11/04/1987","days.since.last.fda":120,"Event.Date":"11/19/1984","Latest.FDA.Received.Date":"04-NOV-1987","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"16 YR","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":4576780,"Initial.FDA.Received.Date":"11/09/1987","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"09-NOV-1987","Suspect.Product.Names":"Ilosone","Suspect.Product.Active.Ingredients":"Erythromycin Estolate","Reason.for.Use":"-","Reactions":"Eye Disorder;Lung Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Dista","Concomitant.Product.Names":"-"}
{"Case.ID":4586263,"Initial.FDA.Received.Date":"02/02/1988","days.since.last.fda":85,"Event.Date":"11/08/1987","Latest.FDA.Received.Date":"02-FEB-1988","Suspect.Product.Names":"Cipro","Suspect.Product.Active.Ingredients":"Ciprofloxacin Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"36 YR","Sender":"Miles","Concomitant.Product.Names":"Ampicillin;Oxacillin;Chloramphenicol;Vancomycin"}
{"Case.ID":4586947,"Initial.FDA.Received.Date":"02/16/1988","days.since.last.fda":14,"Event.Date":"01/01/1985","Latest.FDA.Received.Date":"16-FEB-1988","Suspect.Product.Names":"Lopid","Suspect.Product.Active.Ingredients":"Gemfibrozil","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Parke Davis","Concomitant.Product.Names":"Bactrim;Naprosyn;Zyloprim"}
{"Case.ID":4589853,"Initial.FDA.Received.Date":"03/09/1988","days.since.last.fda":22,"Event.Date":"02/01/1988","Latest.FDA.Received.Date":"09-MAR-1988","Suspect.Product.Names":"Vasotec","Suspect.Product.Active.Ingredients":"Enalapril Maleate","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Skin Ulcer","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4594624,"Initial.FDA.Received.Date":"04/25/1988","days.since.last.fda":47,"Event.Date":"","Latest.FDA.Received.Date":"25-APR-1988","Suspect.Product.Names":"Inderal La","Suspect.Product.Active.Ingredients":"Propranolol Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"74 YR","Sender":"Ayerst","Concomitant.Product.Names":"Allopurinol;Nitroglycerin"}
{"Case.ID":4612927,"Initial.FDA.Received.Date":"08/29/1988","days.since.last.fda":126,"Event.Date":"07/24/1988","Latest.FDA.Received.Date":"29-AUG-1988","Suspect.Product.Names":"Retrovir","Suspect.Product.Active.Ingredients":"Zidovudine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"36 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Pyrimethamine;Clindamycin;Phenytoin"}
{"Case.ID":4652216,"Initial.FDA.Received.Date":"05/05/1989","days.since.last.fda":249,"Event.Date":"","Latest.FDA.Received.Date":"05-MAY-1989","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4660461,"Initial.FDA.Received.Date":"06/22/1989","days.since.last.fda":48,"Event.Date":"01/24/1989","Latest.FDA.Received.Date":"22-JUN-1989","Suspect.Product.Names":"Cipro","Suspect.Product.Active.Ingredients":"Ciprofloxacin Hydrochloride","Reason.for.Use":"-","Reactions":"Acute Kidney Injury;Respiratory Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Miles","Concomitant.Product.Names":"Glipizide"}
{"Case.ID":4673485,"Initial.FDA.Received.Date":"09/11/1989","days.since.last.fda":81,"Event.Date":"","Latest.FDA.Received.Date":"11-SEP-1989","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"50 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4673437,"Initial.FDA.Received.Date":"09/11/1989","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"11-SEP-1989","Suspect.Product.Names":"Keflex","Suspect.Product.Active.Ingredients":"Cephalexin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"50 YR","Sender":"Dista","Concomitant.Product.Names":"-"}
{"Case.ID":4673894,"Initial.FDA.Received.Date":"09/26/1989","days.since.last.fda":15,"Event.Date":"01/01/1989","Latest.FDA.Received.Date":"26-SEP-1989","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":4678081,"Initial.FDA.Received.Date":"10/12/1989","days.since.last.fda":16,"Event.Date":"06/01/1989","Latest.FDA.Received.Date":"12-OCT-1989","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Chlorthalidone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"35 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4681316,"Initial.FDA.Received.Date":"10/27/1989","days.since.last.fda":15,"Event.Date":"04/15/1988","Latest.FDA.Received.Date":"27-OCT-1989","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital","Reason.for.Use":"-","Reactions":"Hepatic Failure;Hepatic Necrosis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"2 YR","Sender":"-","Concomitant.Product.Names":"Amoxicillin"}
{"Case.ID":4685456,"Initial.FDA.Received.Date":"11/20/1989","days.since.last.fda":24,"Event.Date":"10/05/1987","Latest.FDA.Received.Date":"20-NOV-1989","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Pyrexia;Sepsis;Rash Maculo-Papular;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"32 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Ketoconazole;Nystatin;Pentamidine"}
{"Case.ID":4731827,"Initial.FDA.Received.Date":"07/12/1990","days.since.last.fda":234,"Event.Date":"08/01/1989","Latest.FDA.Received.Date":"12-JUL-1990","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":4748889,"Initial.FDA.Received.Date":"08/28/1990","days.since.last.fda":47,"Event.Date":"04/24/1989","Latest.FDA.Received.Date":"28-AUG-1990","Suspect.Product.Names":"Cotrimoxazole","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Hepatic Necrosis;Stevens-Johnson Syndrome;Renal Failure;Aplastic Anaemia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"72 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4744276,"Initial.FDA.Received.Date":"09/26/1990","days.since.last.fda":29,"Event.Date":"08/25/1989","Latest.FDA.Received.Date":"26-SEP-1990","Suspect.Product.Names":"Zovirax","Suspect.Product.Active.Ingredients":"Acyclovir","Reason.for.Use":"-","Reactions":"Shock;Pneumonia;Dermatitis Bullous;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"54 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Chlorpheniramine;Phenytoin;Vidarabine"}
{"Case.ID":4755121,"Initial.FDA.Received.Date":"11/06/1990","days.since.last.fda":41,"Event.Date":"","Latest.FDA.Received.Date":"06-NOV-1990","Suspect.Product.Names":"Capoten","Suspect.Product.Active.Ingredients":"Captopril","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Dermatitis;Condition Aggravated","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Er Squibb","Concomitant.Product.Names":"-"}
{"Case.ID":4775719,"Initial.FDA.Received.Date":"02/21/1991","days.since.last.fda":107,"Event.Date":"","Latest.FDA.Received.Date":"21-FEB-1991","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"4 YR","Sender":"Barre","Concomitant.Product.Names":"-"}
{"Case.ID":4777109,"Initial.FDA.Received.Date":"02/26/1991","days.since.last.fda":5,"Event.Date":"01/07/1991","Latest.FDA.Received.Date":"26-FEB-1991","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vincristine Sulfate;Dactinomycin","Reason.for.Use":"-","Reactions":"Mucosal Disorder;Stevens-Johnson Syndrome;Tongue Oedema;Haemorrhage","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":4787049,"Initial.FDA.Received.Date":"03/11/1991","days.since.last.fda":13,"Event.Date":"10/29/1990","Latest.FDA.Received.Date":"11-MAR-1991","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Skin Necrosis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"-","Concomitant.Product.Names":"Methylprednisolone;Theophylline Anhydrous;Triamcinolone;Metaproterenol"}
{"Case.ID":4813631,"Initial.FDA.Received.Date":"08/05/1991","days.since.last.fda":147,"Event.Date":"03/15/1991","Latest.FDA.Received.Date":"05-AUG-1991","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Parke Davis","Concomitant.Product.Names":"Aldomet;Timentin;Zantac"}
{"Case.ID":4812005,"Initial.FDA.Received.Date":"08/09/1991","days.since.last.fda":4,"Event.Date":"06/28/1991","Latest.FDA.Received.Date":"09-AUG-1991","Suspect.Product.Names":"Retrovir","Suspect.Product.Active.Ingredients":"Zidovudine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"31 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Epogen;Ceftazidime;Folate Sodium;Phenytoin"}
{"Case.ID":4832624,"Initial.FDA.Received.Date":"10/21/1991","days.since.last.fda":73,"Event.Date":"05/02/1991","Latest.FDA.Received.Date":"21-OCT-1991","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Visual Impairment;Leukopenia;Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"32 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":4834641,"Initial.FDA.Received.Date":"10/22/1991","days.since.last.fda":1,"Event.Date":"07/17/1990","Latest.FDA.Received.Date":"22-OCT-1991","Suspect.Product.Names":"Eryped","Suspect.Product.Active.Ingredients":"Erythromycin Ethylsuccinate","Reason.for.Use":"-","Reactions":"Infection;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"9 YR","Sender":"Abbott","Concomitant.Product.Names":"-"}
{"Case.ID":4832863,"Initial.FDA.Received.Date":"10/31/1991","days.since.last.fda":9,"Event.Date":"06/06/1990","Latest.FDA.Received.Date":"31-OCT-1991","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Renal Failure;Coagulopathy;Stevens-Johnson Syndrome;Respiratory Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Metoclopramide;Misoprostol;Diltiazem;Lorazepam"}
{"Case.ID":4835156,"Initial.FDA.Received.Date":"11/25/1991","days.since.last.fda":25,"Event.Date":"","Latest.FDA.Received.Date":"25-NOV-1991","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4842360,"Initial.FDA.Received.Date":"12/26/1991","days.since.last.fda":31,"Event.Date":"11/16/1991","Latest.FDA.Received.Date":"26-DEC-1991","Suspect.Product.Names":"Septra Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Rash Maculo-Papular;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"66 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Ancef;Dilantin;Azt"}
{"Case.ID":4852127,"Initial.FDA.Received.Date":"02/20/1992","days.since.last.fda":56,"Event.Date":"10/27/1991","Latest.FDA.Received.Date":"20-FEB-1992","Suspect.Product.Names":"Zovirax","Suspect.Product.Active.Ingredients":"Acyclovir","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":4864714,"Initial.FDA.Received.Date":"03/13/1992","days.since.last.fda":22,"Event.Date":"10/29/1990","Latest.FDA.Received.Date":"13-MAR-1992","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Skin Discolouration;Stevens-Johnson Syndrome;Skin Necrosis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Elkins Sinn","Concomitant.Product.Names":"Methylprednisolone;Gentamicin;Theophylline Anhydrous;Terbutaline Sulfate"}
{"Case.ID":4861445,"Initial.FDA.Received.Date":"03/13/1992","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"13-MAR-1992","Suspect.Product.Names":"Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"31 YR","Sender":"Beecham","Concomitant.Product.Names":"-"}
{"Case.ID":4879578,"Initial.FDA.Received.Date":"05/06/1992","days.since.last.fda":54,"Event.Date":"06/13/1991","Latest.FDA.Received.Date":"06-MAY-1992","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"-","Reactions":"Pneumonia;Stevens-Johnson Syndrome;Hyperbilirubinaemia;Bone Marrow Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"16 YR","Sender":"Lederle","Concomitant.Product.Names":"Ticarcillin;Clindamycin;Tylenol;Tobramycin"}
{"Case.ID":4885269,"Initial.FDA.Received.Date":"06/11/1992","days.since.last.fda":36,"Event.Date":"","Latest.FDA.Received.Date":"11-JUN-1992","Suspect.Product.Names":"Ceclor","Suspect.Product.Active.Ingredients":"Cefaclor","Reason.for.Use":"-","Reactions":"Renal Failure;Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Insulin Nos"}
{"Case.ID":4894198,"Initial.FDA.Received.Date":"06/28/1992","days.since.last.fda":17,"Event.Date":"06/17/1991","Latest.FDA.Received.Date":"28-JUN-1992","Suspect.Product.Names":"Retrovir","Suspect.Product.Active.Ingredients":"Zidovudine;Phenytoin","Reason.for.Use":"-","Reactions":"Hypertension;Acute Kidney Injury;Pyrexia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"31 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Percocet"}
{"Case.ID":4896496,"Initial.FDA.Received.Date":"07/15/1992","days.since.last.fda":17,"Event.Date":"","Latest.FDA.Received.Date":"15-JUL-1992","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampicillin;Furosemide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Sepsis;Thrombocytopenia;Leukopenia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"6 MTH","Sender":"Hoechst","Concomitant.Product.Names":"Vancomycin;Digoxin"}
{"Case.ID":4892830,"Initial.FDA.Received.Date":"08/05/1992","days.since.last.fda":21,"Event.Date":"","Latest.FDA.Received.Date":"05-AUG-1992","Suspect.Product.Names":"Maxitrol","Suspect.Product.Active.Ingredients":"Dexamethasone\\Neomycin Sulfate\\Polymyxin B Sulfate","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Alcon","Concomitant.Product.Names":"-"}
{"Case.ID":4910595,"Initial.FDA.Received.Date":"09/22/1992","days.since.last.fda":48,"Event.Date":"07/01/1989","Latest.FDA.Received.Date":"22-SEP-1992","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":4915827,"Initial.FDA.Received.Date":"09/25/1992","days.since.last.fda":3,"Event.Date":"10/24/1990","Latest.FDA.Received.Date":"25-SEP-1992","Suspect.Product.Names":"Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium;Furosemide;Allopurinol;Insulin Beef/Pork;Glyburide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Hoechst","Concomitant.Product.Names":"-"}
{"Case.ID":4916742,"Initial.FDA.Received.Date":"10/13/1992","days.since.last.fda":18,"Event.Date":"","Latest.FDA.Received.Date":"13-OCT-1992","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Rifampin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"Isoniazid;Streptomycin"}
{"Case.ID":5723987,"Initial.FDA.Received.Date":"10/14/1992","days.since.last.fda":1,"Event.Date":"10/12/1990","Latest.FDA.Received.Date":"14-OCT-1992","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Furosemide\\Spironolactone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"Hoechst","Concomitant.Product.Names":"-"}
{"Case.ID":4922552,"Initial.FDA.Received.Date":"10/30/1992","days.since.last.fda":16,"Event.Date":"","Latest.FDA.Received.Date":"30-OCT-1992","Suspect.Product.Names":"Ceftin","Suspect.Product.Active.Ingredients":"Cefuroxime Axetil","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"52 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":4929459,"Initial.FDA.Received.Date":"11/04/1992","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"04-NOV-1992","Suspect.Product.Names":"Lodine","Suspect.Product.Active.Ingredients":"Etodolac","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Wyeth","Concomitant.Product.Names":"-"}
{"Case.ID":4930657,"Initial.FDA.Received.Date":"11/13/1992","days.since.last.fda":9,"Event.Date":"11/26/1991","Latest.FDA.Received.Date":"13-NOV-1992","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ofloxacin","Reason.for.Use":"-","Reactions":"Renal Failure;Stevens-Johnson Syndrome;Condition Aggravated;Pulmonary Embolism","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"59 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Clofibrate;Aminophylline;Enalapril"}
{"Case.ID":4931303,"Initial.FDA.Received.Date":"12/04/1992","days.since.last.fda":21,"Event.Date":"10/24/1990","Latest.FDA.Received.Date":"04-DEC-1992","Suspect.Product.Names":"Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Beecham","Concomitant.Product.Names":"Ciprofloxacin Hydrochloride;Aldactone;Digitoxin;Acetylcysteine"}
{"Case.ID":4952669,"Initial.FDA.Received.Date":"12/24/1992","days.since.last.fda":20,"Event.Date":"10/24/1990","Latest.FDA.Received.Date":"24-DEC-1992","Suspect.Product.Names":"Imodium","Suspect.Product.Active.Ingredients":"Loperamide Hydrochloride;Allopurinol;Furosemide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Janssen","Concomitant.Product.Names":"Amoxicillin;Diazepam"}
{"Case.ID":4945298,"Initial.FDA.Received.Date":"01/13/1993","days.since.last.fda":20,"Event.Date":"10/25/1992","Latest.FDA.Received.Date":"13-JAN-1993","Suspect.Product.Names":"Ergamisol","Suspect.Product.Active.Ingredients":"Levamisole Hydrochloride;Fluorouracil","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Bone Marrow Failure;Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"28 YR","Sender":"Janssen","Concomitant.Product.Names":"-"}
{"Case.ID":4945382,"Initial.FDA.Received.Date":"01/15/1993","days.since.last.fda":2,"Event.Date":"02/06/1991","Latest.FDA.Received.Date":"15-JAN-1993","Suspect.Product.Names":"Dulcolax (Bisacodyl)","Suspect.Product.Active.Ingredients":"Bisacodyl","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Cardiac Arrest;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Aldactone;Lactulose;Lasix;Acetaminophen"}
{"Case.ID":4950802,"Initial.FDA.Received.Date":"02/01/1993","days.since.last.fda":17,"Event.Date":"10/05/1992","Latest.FDA.Received.Date":"01-FEB-1993","Suspect.Product.Names":"Dulcolax (Bisacodyl)","Suspect.Product.Active.Ingredients":"Bisacodyl","Reason.for.Use":"-","Reactions":"Cardiac Failure;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Lasix;Flunitrazepam;Allopurinol;Ciprofloxacin Hydrochloride"}
{"Case.ID":4962297,"Initial.FDA.Received.Date":"02/16/1993","days.since.last.fda":15,"Event.Date":"02/15/1993","Latest.FDA.Received.Date":"16-FEB-1993","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin","Reason.for.Use":"-","Reactions":"Oedema;Stevens-Johnson Syndrome;Vasodilatation;Pruritus","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"16 YR","Sender":"-","Concomitant.Product.Names":"Sodium Chloride;Heparin;Benadryl"}
{"Case.ID":5724008,"Initial.FDA.Received.Date":"03/02/1993","days.since.last.fda":14,"Event.Date":"07/15/1991","Latest.FDA.Received.Date":"02-MAR-1993","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Furosemide;Spironolactone;Allopurinol;Aspirin;Furosemide\\Spironolactone","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Hoechst","Concomitant.Product.Names":"-"}
{"Case.ID":4984797,"Initial.FDA.Received.Date":"04/30/1993","days.since.last.fda":59,"Event.Date":"06/04/1991","Latest.FDA.Received.Date":"30-APR-1993","Suspect.Product.Names":"Primaxin Im","Suspect.Product.Active.Ingredients":"Cilastatin Sodium\\Imipenem;Furosemide;Ciprofloxacin;Ranitidine;Diazepam","Reason.for.Use":"-","Reactions":"Cardiac Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"52 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":5000288,"Initial.FDA.Received.Date":"05/11/1993","days.since.last.fda":11,"Event.Date":"02/24/1993","Latest.FDA.Received.Date":"11-MAY-1993","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Leukopenia;Jaundice Cholestatic","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"87 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Neupogen;Clindamycin;Cardizem;Biaxin"}
{"Case.ID":5009718,"Initial.FDA.Received.Date":"05/27/1993","days.since.last.fda":16,"Event.Date":"","Latest.FDA.Received.Date":"27-MAY-1993","Suspect.Product.Names":"Maxitrol","Suspect.Product.Active.Ingredients":"Dexamethasone\\Neomycin Sulfate\\Polymyxin B Sulfate;Sulfacetamide Sodium","Reason.for.Use":"-","Reactions":"Pyrexia;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Hypersensitivity","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4996722,"Initial.FDA.Received.Date":"06/03/1993","days.since.last.fda":7,"Event.Date":"06/11/1991","Latest.FDA.Received.Date":"03-JUN-1993","Suspect.Product.Names":"Capoten","Suspect.Product.Active.Ingredients":"Captopril;Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Er Squibb","Concomitant.Product.Names":"Furosemide;Spironolactone;Digoxin"}
{"Case.ID":5004104,"Initial.FDA.Received.Date":"06/08/1993","days.since.last.fda":5,"Event.Date":"07/31/1992","Latest.FDA.Received.Date":"08-JUN-1993","Suspect.Product.Names":"Voltarol","Suspect.Product.Active.Ingredients":"Diclofenac Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Novartis","Concomitant.Product.Names":"Allopurinol;Indomethacin;Zovirax"}
{"Case.ID":5016611,"Initial.FDA.Received.Date":"07/21/1993","days.since.last.fda":43,"Event.Date":"03/04/1993","Latest.FDA.Received.Date":"21-JUL-1993","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Penicillin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Pancytopenia;Sepsis;Acute Kidney Injury","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"44 YR","Sender":"-","Concomitant.Product.Names":"Primaxin Im;Fluconazole;Nafcillin;Timentin"}
{"Case.ID":5028896,"Initial.FDA.Received.Date":"08/31/1993","days.since.last.fda":41,"Event.Date":"07/31/1992","Latest.FDA.Received.Date":"31-AUG-1993","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol;Indomethacin;Diclofenac Sodium","Reason.for.Use":"-","Reactions":"Shock;Cardiac Failure;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Metoclopramide;Calcitonin Salmon"}
{"Case.ID":5032971,"Initial.FDA.Received.Date":"09/15/1993","days.since.last.fda":15,"Event.Date":"08/19/1993","Latest.FDA.Received.Date":"15-SEP-1993","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Hepatic Failure;Dermatitis;Ecchymosis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"5 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":5033207,"Initial.FDA.Received.Date":"09/17/1993","days.since.last.fda":2,"Event.Date":"05/01/1993","Latest.FDA.Received.Date":"17-SEP-1993","Suspect.Product.Names":"Cefoxitin","Suspect.Product.Active.Ingredients":"Cefoxitin Sodium","Reason.for.Use":"-","Reactions":"Dermatitis Bullous;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"39 YR","Sender":"-","Concomitant.Product.Names":"Zantac"}
{"Case.ID":5039105,"Initial.FDA.Received.Date":"10/07/1993","days.since.last.fda":20,"Event.Date":"09/04/1993","Latest.FDA.Received.Date":"07-OCT-1993","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Pyrexia;Stevens-Johnson Syndrome;Mouth Ulceration;Hypotension","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"Novartis","Concomitant.Product.Names":"Nitrazepam"}
{"Case.ID":5061000,"Initial.FDA.Received.Date":"11/17/1993","days.since.last.fda":41,"Event.Date":"08/30/1992","Latest.FDA.Received.Date":"17-NOV-1993","Suspect.Product.Names":"Cardizem","Suspect.Product.Active.Ingredients":"Diltiazem Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Urinary Tract Infection","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"94 YR","Sender":"-","Concomitant.Product.Names":"Cefuroxime;Fenoterol Hydrobromide;Glyburide;Theophylline Anhydrous"}
{"Case.ID":5197905,"Initial.FDA.Received.Date":"01/24/1994","days.since.last.fda":68,"Event.Date":"11/26/1994","Latest.FDA.Received.Date":"24-JAN-1994","Suspect.Product.Names":"Cefobid","Suspect.Product.Active.Ingredients":"Cefoperazone;Carbamazepine;Fluconazole","Reason.for.Use":"-","Reactions":"Shock;Stevens-Johnson Syndrome;Dermatitis Bullous","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"29 YR","Sender":"Pfizer","Concomitant.Product.Names":"Prednisolone;Cephalexin"}
{"Case.ID":5070068,"Initial.FDA.Received.Date":"01/25/1994","days.since.last.fda":1,"Event.Date":"01/01/1990","Latest.FDA.Received.Date":"25-JAN-1994","Suspect.Product.Names":"Hydergine;Amantadine.;Adalat","Suspect.Product.Active.Ingredients":"Nifedipine;Allopurinol;Lactulose;Amantadine Hydrochloride;Ergoloid Mesylates","Reason.for.Use":"-","Reactions":"Cardiac Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Solvay","Concomitant.Product.Names":"-"}
{"Case.ID":5080012,"Initial.FDA.Received.Date":"01/28/1994","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"28-JAN-1994","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Jaundice Cholestatic;Leukopenia;Dermatitis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"87 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Cardizem;Isordil"}
{"Case.ID":5091697,"Initial.FDA.Received.Date":"02/01/1994","days.since.last.fda":4,"Event.Date":"08/17/1993","Latest.FDA.Received.Date":"01-FEB-1994","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Apnoea;Pneumonia;Superinfection","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"49 YR","Sender":"Biocraft","Concomitant.Product.Names":"Haloperidol;Nifedipine;Vancomycin;Timentin"}
{"Case.ID":5080778,"Initial.FDA.Received.Date":"02/09/1994","days.since.last.fda":8,"Event.Date":"05/14/1992","Latest.FDA.Received.Date":"09-FEB-1994","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Captopril;Clavulanate Potassium","Reason.for.Use":"-","Reactions":"Blood Creatinine Increased;Cor Pulmonale;Leukocytosis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"Bristol Myers","Concomitant.Product.Names":"Furosemide;Nystatin;Allopurinol"}
{"Case.ID":5104629,"Initial.FDA.Received.Date":"04/15/1994","days.since.last.fda":65,"Event.Date":"02/03/1994","Latest.FDA.Received.Date":"15-APR-1994","Suspect.Product.Names":"Adalat","Suspect.Product.Active.Ingredients":"Nifedipine","Reason.for.Use":"-","Reactions":"Blood Lactate Dehydrogenase Increased;Stevens-Johnson Syndrome;Eosinophilia;Hepatic Function Abnormal","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"76 YR","Sender":"Miles","Concomitant.Product.Names":"Nicardipine Hydrochloride;Hydralazine Hydrochloride"}
{"Case.ID":5128367,"Initial.FDA.Received.Date":"06/01/1994","days.since.last.fda":47,"Event.Date":"10/05/1993","Latest.FDA.Received.Date":"01-JUN-1994","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Eosinophilia;Stevens-Johnson Syndrome;Pruritus;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"-","Concomitant.Product.Names":"Amitriptyline;Amlodipine;Enalapril;Metoprolol"}
{"Case.ID":5133700,"Initial.FDA.Received.Date":"06/02/1994","days.since.last.fda":1,"Event.Date":"01/01/1993","Latest.FDA.Received.Date":"02-JUN-1994","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampicillin;Cefuroxime","Reason.for.Use":"-","Reactions":"Nephritis;Hypersensitivity;Renal Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"-","Concomitant.Product.Names":"Dilantin;Aztreonam;Vancomycin"}
{"Case.ID":5156852,"Initial.FDA.Received.Date":"08/29/1994","days.since.last.fda":88,"Event.Date":"12/29/1992","Latest.FDA.Received.Date":"29-AUG-1994","Suspect.Product.Names":"Lodine","Suspect.Product.Active.Ingredients":"Etodolac","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"Wyeth","Concomitant.Product.Names":"Prothiaden;Buspar;Amiloride;Naprosyn"}
{"Case.ID":5163395,"Initial.FDA.Received.Date":"10/03/1994","days.since.last.fda":35,"Event.Date":"06/15/1990","Latest.FDA.Received.Date":"03-OCT-1994","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Haemorrhagic Stroke;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"67 YR","Sender":"Parke Davis","Concomitant.Product.Names":"Dexamethasone;Cardizem"}
{"Case.ID":5171376,"Initial.FDA.Received.Date":"10/18/1994","days.since.last.fda":15,"Event.Date":"06/24/1994","Latest.FDA.Received.Date":"18-OCT-1994","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin;Gentamicin","Reason.for.Use":"-","Reactions":"Pyrexia;Stevens-Johnson Syndrome;Eosinophilia;Dermatitis Bullous","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"39 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5187266,"Initial.FDA.Received.Date":"12/13/1994","days.since.last.fda":56,"Event.Date":"06/15/1994","Latest.FDA.Received.Date":"13-DEC-1994","Suspect.Product.Names":"Mexitil","Suspect.Product.Active.Ingredients":"Mexiletine Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Diarrhoea;Erythema Multiforme;Coagulopathy","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"79 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Gaster;Warfarin Sodium;Bufferin;Isosorbide Dinitrate"}
{"Case.ID":5210278,"Initial.FDA.Received.Date":"02/09/1995","days.since.last.fda":58,"Event.Date":"08/29/1994","Latest.FDA.Received.Date":"09-FEB-1995","Suspect.Product.Names":"Nizoral","Suspect.Product.Active.Ingredients":"Ketoconazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"37 YR","Sender":"Janssen","Concomitant.Product.Names":"-"}
{"Case.ID":5222397,"Initial.FDA.Received.Date":"03/07/1995","days.since.last.fda":26,"Event.Date":"11/18/1994","Latest.FDA.Received.Date":"07-MAR-1995","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Benazepril Hydrochloride","Reason.for.Use":"-","Reactions":"Dermatitis Bullous;Pancytopenia;Acute Kidney Injury;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"58 YR","Sender":"Novartis","Concomitant.Product.Names":"Valproic Acid;Piperacillin Sodium;Phenobarbital"}
{"Case.ID":5221400,"Initial.FDA.Received.Date":"03/14/1995","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"14-MAR-1995","Suspect.Product.Names":"Ceclor","Suspect.Product.Active.Ingredients":"Cefaclor","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"-"}
{"Case.ID":5239099,"Initial.FDA.Received.Date":"04/27/1995","days.since.last.fda":44,"Event.Date":"09/30/1992","Latest.FDA.Received.Date":"27-APR-1995","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Furosemide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Respiratory Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"Hoechst","Concomitant.Product.Names":"Flucloxacillin;Dexamethasone;Fentanyl;Piperacillin Sodium"}
{"Case.ID":5276260,"Initial.FDA.Received.Date":"07/20/1995","days.since.last.fda":84,"Event.Date":"10/03/1992","Latest.FDA.Received.Date":"20-JUL-1995","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Alfentanil Hydrochloride;Etomidate;Fentanyl","Reason.for.Use":"-","Reactions":"Eye Disorder;Dermatitis Bullous;Respiratory Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Janssen","Concomitant.Product.Names":"Gentamicin;Piperacillin."}
{"Case.ID":5284545,"Initial.FDA.Received.Date":"07/26/1995","days.since.last.fda":6,"Event.Date":"06/14/1995","Latest.FDA.Received.Date":"26-JUL-1995","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Chlorambucil","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"67 YR","Sender":"-","Concomitant.Product.Names":"Cyanocobalamin;Synthroid"}
{"Case.ID":5722792,"Initial.FDA.Received.Date":"08/03/1995","days.since.last.fda":8,"Event.Date":"05/30/1995","Latest.FDA.Received.Date":"03-AUG-1995","Suspect.Product.Names":"Timentin","Suspect.Product.Active.Ingredients":"Clavulanate Potassium\\Ticarcillin Disodium","Reason.for.Use":"-","Reactions":"Jaundice Cholestatic;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Shock","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"Smithkline Beecham","Concomitant.Product.Names":"Augmentin;Neupogen;Ciprofloxacin;Amikacin"}
{"Case.ID":5295396,"Initial.FDA.Received.Date":"08/29/1995","days.since.last.fda":26,"Event.Date":"","Latest.FDA.Received.Date":"29-AUG-1995","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":5321426,"Initial.FDA.Received.Date":"11/07/1995","days.since.last.fda":70,"Event.Date":"","Latest.FDA.Received.Date":"07-NOV-1995","Suspect.Product.Names":"Cefotaxime","Suspect.Product.Active.Ingredients":"Cefotaxime Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"34 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5326744,"Initial.FDA.Received.Date":"11/20/1995","days.since.last.fda":13,"Event.Date":"10/07/1995","Latest.FDA.Received.Date":"20-NOV-1995","Suspect.Product.Names":"Piperacillin.","Suspect.Product.Active.Ingredients":"Piperacillin Sodium;Ciprofloxacin;Verapamil Hydrochloride;Felodipine;Fluconazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"71 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5341350,"Initial.FDA.Received.Date":"12/21/1995","days.since.last.fda":31,"Event.Date":"09/08/1995","Latest.FDA.Received.Date":"21-DEC-1995","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Drug Level Above Therapeutic;Dermatitis;Hepatic Function Abnormal;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"61 YR","Sender":"Parke Davis","Concomitant.Product.Names":"Relafen;Lasix;Depakote;Procardia Xl"}
{"Case.ID":5363929,"Initial.FDA.Received.Date":"02/05/1996","days.since.last.fda":46,"Event.Date":"","Latest.FDA.Received.Date":"05-FEB-1996","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Vasculitis;Nephritis;Erythema Multiforme;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"Burrough Wellcome","Concomitant.Product.Names":"Atenolol;Ibuprofen"}
{"Case.ID":5392387,"Initial.FDA.Received.Date":"04/10/1996","days.since.last.fda":65,"Event.Date":"09/17/1998","Latest.FDA.Received.Date":"04-NOV-1998","Suspect.Product.Names":"Cotrimoxazole","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Prophylaxis","Reactions":"Vasculitis;Stevens-Johnson Syndrome;Dermatitis;Toxic Epidermal Necrolysis;Sepsis;Dehydration","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"53 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5391055,"Initial.FDA.Received.Date":"04/15/1996","days.since.last.fda":5,"Event.Date":"05/19/1995","Latest.FDA.Received.Date":"15-APR-1996","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Tramadol Hydrochloride","Reason.for.Use":"-","Reactions":"Thrombocytopenia;Stevens-Johnson Syndrome;Cardiac Failure;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Lactulose;Calciparine;Benzthiazide;Omeprazole"}
{"Case.ID":5389996,"Initial.FDA.Received.Date":"04/18/1996","days.since.last.fda":3,"Event.Date":"05/19/1995","Latest.FDA.Received.Date":"18-APR-1996","Suspect.Product.Names":"Calciparine","Suspect.Product.Active.Ingredients":"Heparin Calcium;Omeprazole;Benzthiazide;Tramadol Hydrochloride;Lactulose","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Solvay","Concomitant.Product.Names":"-"}
{"Case.ID":5398485,"Initial.FDA.Received.Date":"04/23/1996","days.since.last.fda":5,"Event.Date":"05/19/1995","Latest.FDA.Received.Date":"23-APR-1996","Suspect.Product.Names":"Xylocaine","Suspect.Product.Active.Ingredients":"Lidocaine Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Astra","Concomitant.Product.Names":"Ciprofloxacin;Ascorbic Acid;Heparin;Lactulose"}
{"Case.ID":5414939,"Initial.FDA.Received.Date":"06/03/1996","days.since.last.fda":41,"Event.Date":"02/23/1996","Latest.FDA.Received.Date":"03-JUN-1996","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin;Indomethacin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"Abbott","Concomitant.Product.Names":"-"}
{"Case.ID":5424480,"Initial.FDA.Received.Date":"07/12/1996","days.since.last.fda":39,"Event.Date":"05/25/1996","Latest.FDA.Received.Date":"12-JUL-1996","Suspect.Product.Names":"Vasotec","Suspect.Product.Active.Ingredients":"Enalapril Maleate;Metolazone","Reason.for.Use":"-","Reactions":"Dermatitis;Disseminated Intravascular Coagulation;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"87 YR","Sender":"Merck Sharp And Dohme","Concomitant.Product.Names":"-"}
{"Case.ID":5446546,"Initial.FDA.Received.Date":"08/27/1996","days.since.last.fda":46,"Event.Date":"05/05/1996","Latest.FDA.Received.Date":"27-AUG-1996","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Metolazone;Enalapril","Reason.for.Use":"-","Reactions":"Disseminated Intravascular Coagulation;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"87 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5498149,"Initial.FDA.Received.Date":"12/18/1996","days.since.last.fda":113,"Event.Date":"09/27/1996","Latest.FDA.Received.Date":"18-DEC-1996","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Dermatitis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"22 YR","Sender":"Novartis","Concomitant.Product.Names":"Ludiomil"}
{"Case.ID":5531158,"Initial.FDA.Received.Date":"01/24/1997","days.since.last.fda":37,"Event.Date":"12/27/1994","Latest.FDA.Received.Date":"24-JAN-1997","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Glyburide","Reason.for.Use":"-","Reactions":"Mouth Ulceration;Stevens-Johnson Syndrome;Cardiac Failure;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Roche","Concomitant.Product.Names":"Acetaminophen"}
{"Case.ID":5553324,"Initial.FDA.Received.Date":"03/07/1997","days.since.last.fda":42,"Event.Date":"12/10/1996","Latest.FDA.Received.Date":"07-MAR-1997","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5563923,"Initial.FDA.Received.Date":"03/20/1997","days.since.last.fda":13,"Event.Date":"12/04/1996","Latest.FDA.Received.Date":"20-MAR-1997","Suspect.Product.Names":"Mexitil","Suspect.Product.Active.Ingredients":"Mexiletine Hydrochloride","Reason.for.Use":"-","Reactions":"Malaise;Stevens-Johnson Syndrome;Conjunctivitis;Dermatitis Bullous","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"66 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Quinapril Hydrochloride;Lasix;Slow-K"}
{"Case.ID":5543772,"Initial.FDA.Received.Date":"03/21/1997","days.since.last.fda":1,"Event.Date":"01/10/1996","Latest.FDA.Received.Date":"21-MAR-1997","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Leucovorin Calcium","Reason.for.Use":"-","Reactions":"Conjunctivitis;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"45 YR","Sender":"Immunex","Concomitant.Product.Names":"Allopurinol;Amphotericin B;Acyclovir;Cyclophosphamide"}
{"Case.ID":5558656,"Initial.FDA.Received.Date":"04/25/1997","days.since.last.fda":35,"Event.Date":"03/08/1995","Latest.FDA.Received.Date":"25-APR-1997","Suspect.Product.Names":"Ludiomil","Suspect.Product.Active.Ingredients":"Maprotiline Hydrochloride;Alprazolam","Reason.for.Use":"-","Reactions":"Rash Maculo-Papular;Mouth Ulceration;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":5580269,"Initial.FDA.Received.Date":"04/29/1997","days.since.last.fda":4,"Event.Date":"08/02/1996","Latest.FDA.Received.Date":"29-APR-1997","Suspect.Product.Names":"Cytotec;Sandimmune","Suspect.Product.Active.Ingredients":"Cyclosporine;Misoprostol;Tobramycin Sulfate;Midazolam Hydrochloride;Imipenem","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"54 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":5579278,"Initial.FDA.Received.Date":"05/22/1997","days.since.last.fda":23,"Event.Date":"","Latest.FDA.Received.Date":"22-MAY-1997","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Leuprolide Acetate","Reason.for.Use":"-","Reactions":"Pathological Fracture;Pneumonia;Pyrexia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"Takeda","Concomitant.Product.Names":"Dimenhydrinate;Cinnarizine"}
{"Case.ID":3047303,"Initial.FDA.Received.Date":"05/28/1997","days.since.last.fda":6,"Event.Date":"10/22/1996","Latest.FDA.Received.Date":"28-MAY-1997","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol Sodium","Reason.for.Use":"-","Reactions":"Anaemia;Pyrexia;Pneumonia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"57 YR","Sender":"-","Concomitant.Product.Names":"Cytoxan;Prednisone;Adriamycin;Vincristine Sulfate"}
{"Case.ID":5568716,"Initial.FDA.Received.Date":"06/02/1997","days.since.last.fda":5,"Event.Date":"06/12/1996","Latest.FDA.Received.Date":"02-JUN-1997","Suspect.Product.Names":"Bactrim;Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Sulfamethoxazole\\Trimethoprim;Vancomycin;Phenytoin","Reason.for.Use":"-","Reactions":"Cardiac Arrest;Shock;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"32 YR","Sender":"Pfizer","Concomitant.Product.Names":"Zovirax"}
{"Case.ID":3052452,"Initial.FDA.Received.Date":"06/02/1997","days.since.last.fda":0,"Event.Date":"05/11/1997","Latest.FDA.Received.Date":"02-JUN-1997","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin;Valproate Sodium;Gabapentin","Reason.for.Use":"-","Reactions":"Drug Level Below Therapeutic;Dermatitis;Hypoproteinaemia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Parke Davis","Concomitant.Product.Names":"Ceftin;Floxin"}
{"Case.ID":5595110,"Initial.FDA.Received.Date":"07/02/1997","days.since.last.fda":30,"Event.Date":"05/23/1997","Latest.FDA.Received.Date":"02-JUL-1997","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Levofloxacin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":3072145,"Initial.FDA.Received.Date":"09/26/1997","days.since.last.fda":86,"Event.Date":"03/14/1997","Latest.FDA.Received.Date":"26-SEP-1997","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Mucosal Disorder;Stevens-Johnson Syndrome;Dermatitis Exfoliative","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"75 YR","Sender":"Parke Davis","Concomitant.Product.Names":"Decadron;Methadone Hydrochloride;Diflucan"}
{"Case.ID":3023927,"Initial.FDA.Received.Date":"11/10/1997","days.since.last.fda":45,"Event.Date":"05/23/1997","Latest.FDA.Received.Date":"10-NOV-1997","Suspect.Product.Names":"Levaquin","Suspect.Product.Active.Ingredients":"Levofloxacin","Reason.for.Use":"Urinary Tract Infection","Reactions":"Respiratory Failure;Oedema;Hypoaesthesia Oral;Stevens-Johnson Syndrome;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Nitrendipine;Piroxicam;Unspecified Ingredient;Sennosides;Simvastatin;Famotidine;Isosorbide Mononitrate"}
{"Case.ID":3001336,"Initial.FDA.Received.Date":"11/17/1997","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"17-NOV-1997","Suspect.Product.Names":"Zoloft","Suspect.Product.Active.Ingredients":"Sertraline Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Erythema Multiforme;Skin Disorder;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":3043689,"Initial.FDA.Received.Date":"12/01/1997","days.since.last.fda":14,"Event.Date":"08/01/1997","Latest.FDA.Received.Date":"01-DEC-1997","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome;Mental Impairment;Dermatitis;Skin Exfoliation","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"-","Concomitant.Product.Names":"Aspirin;Albuterol;Diltiazem;Potassium Chloride;Famotidine;Lactulose"}
{"Case.ID":3003823,"Initial.FDA.Received.Date":"12/12/1997","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"12-DEC-1997","Suspect.Product.Names":"Zaroxolyn","Suspect.Product.Active.Ingredients":"Metolazone;Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"Medeva","Concomitant.Product.Names":"-"}
{"Case.ID":3116897,"Initial.FDA.Received.Date":"01/08/1998","days.since.last.fda":27,"Event.Date":"","Latest.FDA.Received.Date":"08-JAN-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol;Metolazone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":3008130,"Initial.FDA.Received.Date":"01/09/1998","days.since.last.fda":1,"Event.Date":"10/17/1997","Latest.FDA.Received.Date":"09-JAN-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cefdinir","Reason.for.Use":"Urinary Tract Infection","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":3028370,"Initial.FDA.Received.Date":"01/14/1998","days.since.last.fda":5,"Event.Date":"03/31/1997","Latest.FDA.Received.Date":"14-JAN-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Neoplasm Malignant","Reactions":"Dermatitis Exfoliative;Superinfection;Respiratory Arrest;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"56 YR","Sender":"-","Concomitant.Product.Names":"Diflucan;Pepcid"}
{"Case.ID":3031718,"Initial.FDA.Received.Date":"01/20/1998","days.since.last.fda":6,"Event.Date":"09/30/1997","Latest.FDA.Received.Date":"20-JAN-1998","Suspect.Product.Names":"Keflex;Ancef;Bactrim;Zosyn","Suspect.Product.Active.Ingredients":"Piperacillin Sodium\\Tazobactam Sodium;Sulfamethoxazole\\Trimethoprim;Cefazolin Sodium;Cephalexin;Vancomycin;Rifampin","Reason.for.Use":"-","Reactions":"Hypersensitivity;Pyrexia;Eye Discharge;Toxic Epidermal Necrolysis;Cardio-Respiratory Arrest;Dermatitis Exfoliative;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"57 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3008533,"Initial.FDA.Received.Date":"01/20/1998","days.since.last.fda":0,"Event.Date":"10/19/1997","Latest.FDA.Received.Date":"20-JAN-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lorazepam;Allopurinol","Reason.for.Use":"-","Reactions":"Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"91 YR","Sender":"Wyeth Ayerst","Concomitant.Product.Names":"Tianeptine;Celectol;Lasix;Allopurinol;Enalapril Maleate"}
{"Case.ID":3117312,"Initial.FDA.Received.Date":"02/03/1998","days.since.last.fda":14,"Event.Date":"10/17/1997","Latest.FDA.Received.Date":"03-FEB-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cefdinir","Reason.for.Use":"Pyrexia","Reactions":"Pyrexia;Toxic Epidermal Necrolysis;Rash Erythematous;Stevens-Johnson Syndrome;Renal Disorder;Blood Creatinine Increased;Rash;Vulval Ulceration;Stomatitis;White Blood Cell Count Decreased;Protein Total Decreased;Blood Lactate Dehydrogenase Increased;Renal Failure;Platelet Count Decreased;Blood Urea Increased;Nephritis;Pemphigoid;Red Blood Cell Count Decreased;Renal Impairment;Blood Glucose Increased;Metabolic Acidosis;Anaemia;Blood Bilirubin Increased;Aspartate Aminotransferase Increased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Parke Davis","Concomitant.Product.Names":"Dipyridamole;Insulin Nos;Allopurinol;Amlodipine Besylate;Senna Leaf;Furosemide"}
{"Case.ID":3016123,"Initial.FDA.Received.Date":"02/17/1998","days.since.last.fda":14,"Event.Date":"10/19/1997","Latest.FDA.Received.Date":"17-FEB-1998","Suspect.Product.Names":"Zyloprim","Suspect.Product.Active.Ingredients":"Allopurinol;Celiprolol Hydrochloride;Furosemide;Enalapril;Tianeptine;Lorazepam","Reason.for.Use":"-","Reactions":"Eye Disorder;Stevens-Johnson Syndrome;Skin Lesion;Multiple Organ Dysfunction Syndrome;Mouth Ulceration","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"91 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"-"}
{"Case.ID":3041216,"Initial.FDA.Received.Date":"05/13/1998","days.since.last.fda":85,"Event.Date":"02/17/1998","Latest.FDA.Received.Date":"13-MAY-1998","Suspect.Product.Names":"Zithromax","Suspect.Product.Active.Ingredients":"Azithromycin Dihydrate;Allopurinol","Reason.for.Use":"Gout;Upper Respiratory Tract Infection","Reactions":"Stevens-Johnson Syndrome;Skin Necrosis;Oral Mucosal Exfoliation;Stomatitis;Haemorrhagic Disorder;Skin Exfoliation","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3120412,"Initial.FDA.Received.Date":"06/04/1998","days.since.last.fda":22,"Event.Date":"07/03/1995","Latest.FDA.Received.Date":"02-JUL-1998","Suspect.Product.Names":"Valium;Haldol;Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Caffeine;Furosemide;Heparin Sodium;Levomepromazine;Haloperidol;Diazepam;Dimenhydrinate;Oxazepam;Metoclopramide;Nisoldipine","Reason.for.Use":"Agitation;Nausea;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Mental Disorder;White Blood Cell Count Increased;Urinary Tract Infection;Dermatitis Bullous;Acute Kidney Injury;Pruritus;Dermatitis;Toxic Epidermal Necrolysis;Blood Urea Increased;Blood Creatinine Increased;Leukocytosis;Pyrexia;Blood Lactate Dehydrogenase Increased;Cardiac Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"91 YR","Sender":"Roche","Concomitant.Product.Names":"Methylprednisolone;Adalat Cc;Nitrendipine;Ismo;Insulin Nos"}
{"Case.ID":3135821,"Initial.FDA.Received.Date":"07/13/1998","days.since.last.fda":39,"Event.Date":"05/31/1996","Latest.FDA.Received.Date":"13-JUL-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Tramadol Hydrochloride","Reason.for.Use":"Pain","Reactions":"Staphylococcal Infection;Stevens-Johnson Syndrome;Pneumonia;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Ranitidine;Glyburide;Unspecified Ingredient;Oxazepam;Heparin;Acarbose"}
{"Case.ID":3134765,"Initial.FDA.Received.Date":"08/12/1998","days.since.last.fda":30,"Event.Date":"","Latest.FDA.Received.Date":"12-AUG-1998","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"Hiv Infection Cdc Group I","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":5830230,"Initial.FDA.Received.Date":"08/27/1998","days.since.last.fda":15,"Event.Date":"11/22/1997","Latest.FDA.Received.Date":"27-AUG-1998","Suspect.Product.Names":"Zovirax;Fortaz;Septra;Zantac","Suspect.Product.Active.Ingredients":"Ranitidine Hydrochloride;Dipyrone;Sulfamethoxazole\\Trimethoprim;Fluconazole;Gentamicin Sulfate;Ceftazidime Sodium;Acyclovir;Piperacillin Sodium\\Tazobactam Sodium;Diazepam","Reason.for.Use":"Pneumonia;Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"8 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Ondansetron Hydrochloride;Thiotepa;Acyclovir;Amphotericin B;Unspecified Ingredient"}
{"Case.ID":5830228,"Initial.FDA.Received.Date":"08/27/1998","days.since.last.fda":0,"Event.Date":"11/22/1997","Latest.FDA.Received.Date":"27-AUG-1998","Suspect.Product.Names":"Zantac;Fortaz;Zovirax;Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Acyclovir;Ceftazidime Sodium;Ranitidine Hydrochloride;Piperacillin Sodium\\Tazobactam Sodium;Gentamicin Sulfate;Fluconazole;Dipyrone;Diazepam","Reason.for.Use":"Pneumonia;Prophylaxis","Reactions":"Toxic Epidermal Necrolysis;Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"8 YR","Sender":"Monarch","Concomitant.Product.Names":"Amphotericin B;Ondansetron;Unspecified Ingredient;Thiotepa;Acyclovir"}
{"Case.ID":3147405,"Initial.FDA.Received.Date":"09/04/1998","days.since.last.fda":8,"Event.Date":"","Latest.FDA.Received.Date":"04-SEP-1998","Suspect.Product.Names":"Duphalac","Suspect.Product.Active.Ingredients":"Lactulose;Omeprazole;Sucralfate;Prednisone;Pyridoxine Hydrochloride\\Thiamine Hydrochloride;Niacinamide;Potassium Chloride;Octreotide","Reason.for.Use":"Gastritis;Hepatic Encephalopathy;Hepatitis Alcoholic;Hypokalaemia;Hypovitaminosis","Reactions":"Blister;Stevens-Johnson Syndrome;Shock;Pemphigoid;Tachypnoea;Dermatitis;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"36 YR","Sender":"Solvay","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":3154136,"Initial.FDA.Received.Date":"09/11/1998","days.since.last.fda":7,"Event.Date":"07/21/1998","Latest.FDA.Received.Date":"11-SEP-1998","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Pyrexia;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Mental Impairment;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"72 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3160689,"Initial.FDA.Received.Date":"09/22/1998","days.since.last.fda":11,"Event.Date":"07/21/1998","Latest.FDA.Received.Date":"22-SEP-1998","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Neoplasm;Seizure","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Toxic Epidermal Necrolysis;Mental Impairment","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"72 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7072916,"Initial.FDA.Received.Date":"09/30/1998","days.since.last.fda":8,"Event.Date":"11/22/1997","Latest.FDA.Received.Date":"04-NOV-1998","Suspect.Product.Names":"Ambisome;Neupogen","Suspect.Product.Active.Ingredients":"Filgrastim;Amphotericin B;Piperacillin Sodium\\Tazobactam Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Dermatitis;Rash Maculo-Papular;Epidermolysis Bullosa;Conjunctivitis;Blister;Toxic Epidermal Necrolysis;Multiple Organ Dysfunction Syndrome;Pneumonia;Pruritus;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"8 YR","Sender":"Fujisawa","Concomitant.Product.Names":"Dimethindene Maleate;Intralipid;Fluconazole;Diazepam;Phenobarbital;Clemastine;Dobutamine Hydrochloride;Glucose, Liquid;Heparin Sodium;Thiotepa;Myleran;Metamizole Sodium;Digoxin;Piperacillin.;Busulfan;Zofran;Konakion;Vancomycin;Vitamins;Octagam Immune Globulin (Human);Sandoglobulin;Furosemide;Sulfamethoxazole\\Trimethoprim;Povidone;Acetaminophen;Human Immunoglobulin G;Unspecified Ingredient;Magaldrate;Calcium Gluconate;Potassium Chloride;Epinephrine;Aminophylline;Levomepromazine;Ceftazidime;Dopamine;Acyclovir;Gentamicin"}
{"Case.ID":3157925,"Initial.FDA.Received.Date":"10/21/1998","days.since.last.fda":21,"Event.Date":"11/23/1997","Latest.FDA.Received.Date":"21-OCT-1998","Suspect.Product.Names":"Eprex","Suspect.Product.Active.Ingredients":"Erythropoietin","Reason.for.Use":"Anaemia","Reactions":"Blister;Dermatitis;Mucosal Erosion;Sepsis;Toxic Epidermal Necrolysis;Shock;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Allopurinol;Spironolactone;Cefaclor;Vancomycin Hydrochloride;Temazepam;Fluvastatin Sodium;Fluconazole;Furosemide;Potassium Chloride;Ampicillin Sodium"}
{"Case.ID":3157420,"Initial.FDA.Received.Date":"10/28/1998","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"28-OCT-1998","Suspect.Product.Names":"Tavist Allergy","Suspect.Product.Active.Ingredients":"Clemastine Fumarate","Reason.for.Use":"Pruritus","Reactions":"Stevens-Johnson Syndrome;Cardiac Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"88 YR","Sender":"Novartis","Concomitant.Product.Names":"Digitoxin;Unspecified Ingredient;Zyrtec;Heparin Sodium;Furosemide;Levomepromazine;Ginkgo;Ciprofloxacin Hydrochloride;Dexpanthenol;Dexpanthenol Hydrochloride;Acetaminophen;Allopurinol"}
{"Case.ID":3159906,"Initial.FDA.Received.Date":"11/02/1998","days.since.last.fda":5,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"02-NOV-1998","Suspect.Product.Names":"Novolin R","Suspect.Product.Active.Ingredients":"Insulin Human","Reason.for.Use":"Diabetes Mellitus","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Sepsis;Pneumonia Fungal;Gastroenteritis;Blister;Leukopenia;Diarrhoea;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Novo Nordisk","Concomitant.Product.Names":"Allopurinol;Diflucan;Methotrexate;Lasix;Novalgin (Metamizole Sodium)"}
{"Case.ID":3162244,"Initial.FDA.Received.Date":"11/10/1998","days.since.last.fda":8,"Event.Date":"05/07/1997","Latest.FDA.Received.Date":"19-NOV-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Aspirin;Metoprolol Succinate","Reason.for.Use":"Myocardial Infarction","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"Astra","Concomitant.Product.Names":"Adenosine;Unspecified Ingredient;Ciprofloxacin Hydrochloride;Calcium;Optiray;Actrapid;Human Red Blood Cell;Molsidomine"}
{"Case.ID":3163042,"Initial.FDA.Received.Date":"11/12/1998","days.since.last.fda":2,"Event.Date":"06/16/1998","Latest.FDA.Received.Date":"12-NOV-1998","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Sciatica","Reactions":"Stevens-Johnson Syndrome;Disseminated Intravascular Coagulation;Liver Function Test Abnormal;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"45 YR","Sender":"Novartis","Concomitant.Product.Names":"Voglibose;Glyburide;Harnal"}
{"Case.ID":6749090,"Initial.FDA.Received.Date":"11/16/1998","days.since.last.fda":4,"Event.Date":"03/17/1998","Latest.FDA.Received.Date":"16-NOV-1998","Suspect.Product.Names":"Excedrin Extra Strength","Suspect.Product.Active.Ingredients":"Acetaminophen\\Aspirin\\Caffeine","Reason.for.Use":"-","Reactions":"Syncope;Cardio-Respiratory Arrest;Immunodeficiency;Asthenia;Vomiting;Abdominal Pain;Cardiac Arrest;Viral Infection;Faeces Discoloured;Blood Pressure Decreased;Hypotension;Upper Gastrointestinal Haemorrhage;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"45 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3166553,"Initial.FDA.Received.Date":"11/16/1998","days.since.last.fda":0,"Event.Date":"08/06/1997","Latest.FDA.Received.Date":"16-NOV-1998","Suspect.Product.Names":"Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Phenytoin;Trimipramine;Dipyrone","Reason.for.Use":"Pain;Seizure;Sleep Disorder;Urinary Tract Infection","Reactions":"Red Blood Cell Count Decreased;Toxic Epidermal Necrolysis;Haematocrit Decreased;Face Oedema;Respiratory Failure;Blister;Dysphagia;Cardio-Respiratory Arrest;Haemoglobin Decreased;Stomatitis;Mucosal Erosion;Pyrexia;Rash Maculo-Papular;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Pfizer","Concomitant.Product.Names":"Digitoxin;Ferrous Gluconate;Acetaminophen;Metoprolol;Amitriptyline;Naloxone Hydrochloride;Enoxaparin Sodium;Clemastine Fumarate;Famotidine;Calcium;Tramadol Hydrochloride;Phytonadione"}
{"Case.ID":3165630,"Initial.FDA.Received.Date":"11/16/1998","days.since.last.fda":0,"Event.Date":"12/06/1997","Latest.FDA.Received.Date":"16-NOV-1998","Suspect.Product.Names":"Unasyn","Suspect.Product.Active.Ingredients":"Ampicillin Sodium\\Sulbactam Sodium;Ramipril;Sulfamethoxazole\\Trimethoprim;Aspirin","Reason.for.Use":"Cardiac Failure;Prophylaxis;Sepsis","Reactions":"Genital Ulceration;Dermatitis Bullous;Conjunctival Hyperaemia;Multiple Organ Dysfunction Syndrome;Pyrexia;Mucosal Erosion;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Pfizer","Concomitant.Product.Names":"Metoprolol;Dexpanthenol Hydrochloride;Sodium Chloride;Amaryl;Iopentol;Digoxin"}
{"Case.ID":3170449,"Initial.FDA.Received.Date":"11/23/1998","days.since.last.fda":7,"Event.Date":"06/20/1998","Latest.FDA.Received.Date":"23-NOV-1998","Suspect.Product.Names":"Voltaren","Suspect.Product.Active.Ingredients":"Diclofenac Sodium","Reason.for.Use":"Pyrexia","Reactions":"Stevens-Johnson Syndrome;Hepatic Function Abnormal;Jaundice;Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"43 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":6245006,"Initial.FDA.Received.Date":"11/27/1998","days.since.last.fda":4,"Event.Date":"07/03/1997","Latest.FDA.Received.Date":"27-NOV-1998","Suspect.Product.Names":"Zantac","Suspect.Product.Active.Ingredients":"Ranitidine Hydrochloride;Dipyrone;Ciprofloxacin;Sulfamerazine Sodium\\Trimethoprim;Phenytoin","Reason.for.Use":"Infection;Pain;Seizure","Reactions":"Cardio-Respiratory Arrest;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"17 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":3171824,"Initial.FDA.Received.Date":"12/04/1998","days.since.last.fda":7,"Event.Date":"07/04/1996","Latest.FDA.Received.Date":"04-DEC-1998","Suspect.Product.Names":"Tavist Allergy","Suspect.Product.Active.Ingredients":"Clemastine Fumarate","Reason.for.Use":"Pruritus","Reactions":"Dermatitis Bullous;Corneal Erosion;Stevens-Johnson Syndrome;Sepsis;Toxic Epidermal Necrolysis;Multiple Organ Dysfunction Syndrome;Mucosal Erosion;Rash Maculo-Papular;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"17 YR","Sender":"Novartis","Concomitant.Product.Names":"Lactulose;Acetaminophen;Folic Acid;Metoclopramide Hydrochloride;Targocid;Metronidazole;Lasix;Amphotericin B;Vancomycin;Meperidine;Ciprofloxacin Hydrochloride;Diflucan;Zovirax;Promethazine Hydrochloride;Potassium Chloride;Piperacillin Sodium;Cotrim;Octagam Immune Globulin (Human);Prednisone;Levomepromazine;Neupogen;Ganciclovir;Dipyrone;Zantac;Omeprazole;Diazepam;Ceftazidime;Doxycycline;Imipenem;Midazolam Hydrochloride;Liquaemin Sodium"}
{"Case.ID":3179227,"Initial.FDA.Received.Date":"12/08/1998","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"08-DEC-1998","Suspect.Product.Names":"Adalat","Suspect.Product.Active.Ingredients":"Nifedipine","Reason.for.Use":"Hypertension","Reactions":"Toxic Epidermal Necrolysis;Lip Ulceration;Infection;Stevens-Johnson Syndrome;Nasopharyngitis;Haemorrhage;Epidermolysis Bullosa;Atrial Fibrillation;Rash Macular;Mucosal Erosion;Cardiac Failure;Bronchitis Chronic;Blepharitis;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"75 YR","Sender":"Bayer","Concomitant.Product.Names":"Omeprazole;Heparin Sodium;Mcp"}
{"Case.ID":3171953,"Initial.FDA.Received.Date":"12/08/1998","days.since.last.fda":0,"Event.Date":"07/04/1996","Latest.FDA.Received.Date":"08-DEC-1998","Suspect.Product.Names":"Neupogen;Diflucan;Targocid;Liquaemin Sodium;Cotrim;Octagam Immune Globulin (Human);Zantac;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Levomepromazine;Vancomycin;Dipyrone;Piperacillin Sodium\\Promethazine Hydrobromide;Midazolam Hydrochloride;Ceftazidime;Imipenem;Ciprofloxacin;Human Immunoglobulin G;Ranitidine Hydrochloride;Metoclopramide Hydrochloride;Prednisolone Hemisuccinate;Sulfamethoxazole\\Trimethoprim;Heparin Sodium;Lactulose;Teicoplanin;Fluconazole;Filgrastim;Meropenem;Amphotericin B;Acetaminophen;Ganciclovir;Promethazine Hydrochloride;Clemastine;Tobramycin Sulfate;Potassium Chloride;Omeprazole;Diazepam;Meperidine","Reason.for.Use":"Antibiotic Therapy;Anxiety;Blood Immunoglobulin A;Constipation;Hypokalaemia;Immunosuppression;Nausea;Neutropenia;Oedema;Pain;Prophylaxis;Pruritus;Restlessness;Sedation","Reactions":"Pyrexia;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"16 YR","Sender":"Roche","Concomitant.Product.Names":"Doxycycline;Metronidazole;Lynestrenol;Folic Acid;Prednisone;Zovirax"}
{"Case.ID":3178860,"Initial.FDA.Received.Date":"12/11/1998","days.since.last.fda":3,"Event.Date":"01/15/1997","Latest.FDA.Received.Date":"11-DEC-1998","Suspect.Product.Names":"Serevent Diskus","Suspect.Product.Active.Ingredients":"Salmeterol Xinafoate;Oxazepam;Unspecified Ingredient;Amoxicillin","Reason.for.Use":"Chronic Obstructive Pulmonary Disease;Sleep Disorder","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":3178846,"Initial.FDA.Received.Date":"12/11/1998","days.since.last.fda":0,"Event.Date":"08/19/1996","Latest.FDA.Received.Date":"11-DEC-1998","Suspect.Product.Names":"Zyloprim;Zofran;Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium;Allopurinol;Ondansetron Hydrochloride;Dipyrone;Unspecified Ingredient","Reason.for.Use":"Hyperuricaemia;Nausea;Pain","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"34 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":4130928,"Initial.FDA.Received.Date":"01/06/1999","days.since.last.fda":26,"Event.Date":"09/13/1996","Latest.FDA.Received.Date":"06-JAN-1999","Suspect.Product.Names":"Zyloprim;Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Allopurinol;Dipyrone;Allopurinol;Furosemide","Reason.for.Use":"Hyperuricaemia;Pain","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"61 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":7751278,"Initial.FDA.Received.Date":"01/11/1999","days.since.last.fda":5,"Event.Date":"09/13/1996","Latest.FDA.Received.Date":"11-JAN-1999","Suspect.Product.Names":"Lasix;Rocephin","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium;Sulfamethoxazole\\Trimethoprim;Magaldrate;Vitamins;Cytarabine;Methotrexate;Furosemide;Acetaminophen;Meropenem;Dipyrone;Tramadol Hydrochloride;Amitriptyline Hydrochloride;Vancomycin;Natamycin;Daunorubicin;Dexamethasone\\Dexamethasone Sodium Phosphate;Calcium Carbonate;Gentamicin Sulfate;Allopurinol;Morphine Sulfate","Reason.for.Use":"Blood Calcium;Depression;Gastrointestinal Disorder;Hyperuricaemia;Oedema;Pain;Restlessness;Stomatitis","Reactions":"Mucosal Disorder;Epidermolysis Bullosa;Renal Impairment;Genital Rash;Stevens-Johnson Syndrome;Dermatitis;Blister;Oropharyngeal Blistering","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"61 YR","Sender":"Hoechst","Concomitant.Product.Names":"Egg Phospholipids\\Glycerin\\Soybean Oil;Potassium Chloride;Liquaemin Sodium;Zofran;Famotidine;Ambroxol Hydrochloride;Promethazine Hydrochloride"}
{"Case.ID":3189354,"Initial.FDA.Received.Date":"01/12/1999","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"12-JAN-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Infection","Reactions":"Rash Maculo-Papular;Mucosal Erosion;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome;Pyrexia;Corneal Erosion;Blister;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"17 YR","Sender":"-","Concomitant.Product.Names":"Cotrim;Prednisone;Promethazine Hydrochloride;Piperacillin Sodium;Lasix;Acetaminophen;Diazepam;Midazolam Hydrochloride;Levomepromazine;Folic Acid;Dipyrone"}
{"Case.ID":3196562,"Initial.FDA.Received.Date":"01/22/1999","days.since.last.fda":10,"Event.Date":"07/11/1997","Latest.FDA.Received.Date":"22-JAN-1999","Suspect.Product.Names":"Heparin;Norvasc","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Heparin Sodium;Sultamicillin Hydrochloride;Isosorbide Mononitrate","Reason.for.Use":"Coronary Artery Disease;Hypertension;Pneumonia;Thrombosis Prophylaxis","Reactions":"Blister;Mouth Ulceration;Multiple Organ Dysfunction Syndrome;Dermatitis;Lip Ulceration;Conjunctivitis;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"75 YR","Sender":"Pfizer","Concomitant.Product.Names":"Isosorbide Mononitrate;Prednisone;Aspirin;Acetylcysteine;Aminophylline;Xipamide;Omeprazole;Fenoterol Hydrobromide\\Ipratropium Bromide;Glimepiride"}
{"Case.ID":3196728,"Initial.FDA.Received.Date":"01/25/1999","days.since.last.fda":3,"Event.Date":"08/13/1995","Latest.FDA.Received.Date":"25-JAN-1999","Suspect.Product.Names":"Septra","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Urinary Tract Infection","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"Monarch","Concomitant.Product.Names":"-"}
{"Case.ID":3200780,"Initial.FDA.Received.Date":"01/29/1999","days.since.last.fda":4,"Event.Date":"07/04/1996","Latest.FDA.Received.Date":"11-FEB-1999","Suspect.Product.Names":"Diflucan;Lasix;Neupogen;Zovirax;Cotrim;Targocid;Zantac","Suspect.Product.Active.Ingredients":"Ranitidine Hydrochloride;Hydrocortisone;Midazolam Hydrochloride;Teicoplanin;Calcium;Heparin Sodium;Ceftazidime Sodium;Ascorbic Acid\\Cholecalciferol\\Dexpanthenol\\Niacinamide\\Pyridoxine Hydrochloride\\Riboflavin 5'-Phosphate Sodium\\Thiamine Hydrochloride;Cilastatin Sodium;Prednisolone;Dipyrone;Tobramycin;Sulfamethoxazole\\Trimethoprim;Promethazine Hydrochloride;Amphotericin B;Folic Acid;Acyclovir;Ciprofloxacin Hydrochloride;Omeprazole;Potassium Chloride;Piperacillin Sodium;Lynestrenol;Ganciclovir;Meropenem;Filgrastim;Acetaminophen;Prednisone;Furosemide;Diazepam;Human Immunoglobulin G;Vancomycin Hydrochloride;Fluconazole;Metoclopramide Hydrochloride;Levomepromazine;Lactulose;Meperidine;Clemastine","Reason.for.Use":"Bone Marrow Transplant","Reactions":"Oropharyngeal Blistering;Sepsis;Stevens-Johnson Syndrome;Neutropenia;Multiple Organ Dysfunction Syndrome;Genital Ulceration;Pyrexia;Corneal Erosion;Rash Maculo-Papular","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"17 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":3202415,"Initial.FDA.Received.Date":"02/02/1999","days.since.last.fda":4,"Event.Date":"12/02/1998","Latest.FDA.Received.Date":"02-FEB-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Bone Sarcoma","Reactions":"Oral Pain;Oedema;Stevens-Johnson Syndrome;Seizure;Condition Aggravated;Fungal Infection;Mouth Ulceration;Stomatitis;Oliguria;Respiratory Arrest;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"13 YR","Sender":"Lederle","Concomitant.Product.Names":"-"}
{"Case.ID":3204678,"Initial.FDA.Received.Date":"02/04/1999","days.since.last.fda":2,"Event.Date":"08/19/1996","Latest.FDA.Received.Date":"04-FEB-1999","Suspect.Product.Names":"Novalgin (Metamizole Sodium);Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium;Gentamicin Sulfate;Metamizole Sodium;Sargramostim;Clemastine Fumarate","Reason.for.Use":"Infection;Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Lip Ulceration;Shock;Epidermolysis Bullosa;Toxic Epidermal Necrolysis;Blister;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"34 YR","Sender":"Schering Plough","Concomitant.Product.Names":"-"}
{"Case.ID":3207897,"Initial.FDA.Received.Date":"02/10/1999","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"29-MAR-1999","Suspect.Product.Names":"Levaquin","Suspect.Product.Active.Ingredients":"Levofloxacin;Vancomycin;Diltiazem;Gentamicin","Reason.for.Use":"Atrial Fibrillation;Pyrexia","Reactions":"Liver Function Test Abnormal;Stevens-Johnson Syndrome;Dermatitis;Blood Creatinine Increased;Blood Urea Increased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Ortho","Concomitant.Product.Names":"-"}
{"Case.ID":3210559,"Initial.FDA.Received.Date":"02/16/1999","days.since.last.fda":6,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"22-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Dopamine Hydrochloride","Reason.for.Use":"-","Reactions":"Leukopenia;Toxic Epidermal Necrolysis;Systemic Mycosis;Skin Ulcer;Stevens-Johnson Syndrome;Brain Oedema;Blister;Thrombocytopenia;Bone Marrow Failure;Sepsis;Pneumonia Fungal;Pneumonia Bacterial","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Midazolam Hydrochloride;Amphotericin B;Cernevit;Neupogen;Acetaminophen;Digitoxin;Dobutrex;Fluconazole;Dexamethasone;Cytarabine"}
{"Case.ID":3210189,"Initial.FDA.Received.Date":"02/16/1999","days.since.last.fda":0,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"16-FEB-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Heparin Sodium","Reason.for.Use":"-","Reactions":"Brain Oedema;Haemorrhagic Stroke;Skin Ulcer;Leukopenia;Paresis;Pyrexia;Cutaneous T-Cell Lymphoma;Coma;Pneumonia Bacterial;Thrombocytopenia;Bone Marrow Failure;Sepsis;Meningoencephalitis Herpetic;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Blister;Pneumonia Fungal;Pancreatitis;Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Fluconazole;Cernevit;Dexamethasone;Dobutrex;Midazolam Hydrochloride;Acetaminophen;Digitoxin;Neupogen;Amphotericin B"}
{"Case.ID":3210288,"Initial.FDA.Received.Date":"02/17/1999","days.since.last.fda":1,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"23-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin Hydrochloride","Reason.for.Use":"-","Reactions":"Systemic Mycosis;Pneumonia Bacterial;Pneumonia Fungal;Blister;Sepsis;Stevens-Johnson Syndrome;Leukopenia;Toxic Epidermal Necrolysis;Skin Ulcer;Bone Marrow Failure;Brain Oedema","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Midazolam Hydrochloride;Digitoxin;Cernevit;Cytarabine;Acetaminophen;Amphotericin B;Dobutrex;Neupogen;Dexamethasone;Fluconazole"}
{"Case.ID":3210822,"Initial.FDA.Received.Date":"02/17/1999","days.since.last.fda":0,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"17-FEB-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Etomidate","Reason.for.Use":"-","Reactions":"Bone Marrow Failure;Thrombocytopenia;Blister;Leukopenia;Skin Ulcer;Brain Oedema;Pneumonia Fungal;Pneumonia Bacterial;Sepsis;Stevens-Johnson Syndrome;Systemic Mycosis;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Neupogen;Acetaminophen;Cytarabine;Dobutrex;Digitoxin;Cernevit;Fluconazole;Midazolam Hydrochloride;Amphotericin B;Dexamethasone"}
{"Case.ID":3210815,"Initial.FDA.Received.Date":"02/17/1999","days.since.last.fda":0,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"17-FEB-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Fentanyl","Reason.for.Use":"-","Reactions":"Pneumonia Fungal;Thrombocytopenia;Pneumonia Bacterial;Skin Ulcer;Bone Marrow Failure;Leukopenia;Sepsis;Toxic Epidermal Necrolysis;Brain Oedema;Systemic Mycosis;Coma;Stevens-Johnson Syndrome;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Acetaminophen;Cernevit;Digitoxin;Neupogen;Dobutrex;Fluconazole;Dexamethasone;Midazolam Hydrochloride;Cytarabine"}
{"Case.ID":3230499,"Initial.FDA.Received.Date":"03/18/1999","days.since.last.fda":29,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"18-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Dopamine Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Bone Marrow Failure;Blister;Toxic Epidermal Necrolysis;Skin Ulcer","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Dexamethasone;Midazolam Hydrochloride;Acetaminophen;Amphotericin B;Digitoxin;Dobutrex;Cytarabine;Neupogen;Fluconazole;Cernevit"}
{"Case.ID":3232807,"Initial.FDA.Received.Date":"03/23/1999","days.since.last.fda":5,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"23-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin Hydrochloride","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Bone Marrow Failure;Pneumonia Fungal;Blister;Skin Ulcer;Sepsis;Toxic Epidermal Necrolysis;Leukopenia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Cytarabine;Cernevit;Midazolam Hydrochloride;Dexamethasone;Digitoxin;Fluconazole;Amphotericin B;Acetaminophen;Neupogen;Dobutrex"}
{"Case.ID":3231212,"Initial.FDA.Received.Date":"03/23/1999","days.since.last.fda":0,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"23-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Fentanyl","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Skin Ulcer;Brain Oedema;Toxic Epidermal Necrolysis;Leukopenia;Pneumonia Fungal;Blister;Sepsis;Pneumonia Bacterial;Systemic Mycosis;Thrombocytopenia;Bone Marrow Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Cytarabine;Fluconazole;Cernevit;Midazolam Hydrochloride;Acetaminophen;Amphotericin B;Dobutrex;Digitoxin;Neupogen;Dexamethasone"}
{"Case.ID":3231211,"Initial.FDA.Received.Date":"03/23/1999","days.since.last.fda":0,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"23-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Heparin Sodium","Reason.for.Use":"-","Reactions":"Skin Ulcer;Bone Marrow Failure;Toxic Epidermal Necrolysis;Rash;Stevens-Johnson Syndrome;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Amphotericin B;Digitoxin;Dexamethasone;Acetaminophen;Neupogen;Fluconazole;Dobutrex;Cytarabine;Cernevit;Midazolam Hydrochloride"}
{"Case.ID":3231209,"Initial.FDA.Received.Date":"03/23/1999","days.since.last.fda":0,"Event.Date":"05/10/1997","Latest.FDA.Received.Date":"23-MAR-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Etomidate","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Skin Ulcer;Stevens-Johnson Syndrome;Blister;Bone Marrow Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Abbott","Concomitant.Product.Names":"Dobutrex;Dexamethasone;Midazolam Hydrochloride;Cytarabine;Amphotericin B;Fluconazole;Cernevit;Neupogen;Digitoxin;Acetaminophen"}
{"Case.ID":5741299,"Initial.FDA.Received.Date":"03/30/1999","days.since.last.fda":7,"Event.Date":"07/04/1996","Latest.FDA.Received.Date":"30-MAR-1999","Suspect.Product.Names":"Liquaemin Sodium;Lasix;Neupogen;Zantac;Ciprofloxacin Extended-Release;Targocid;Diflucan;Cotrim;Octagam Immune Globulin (Human)","Suspect.Product.Active.Ingredients":"Human Immunoglobulin G;Vancomycin;Midazolam Hydrochloride;Sulfamethoxazole\\Trimethoprim;Clemastine;Metoclopramide Hydrochloride;Piperacillin Sodium;Diazepam;Fluconazole;Meropenem;Ganciclovir;Levomepromazine;Promethazine Hydrochloride;Omeprazole;Dipyrone;Teicoplanin;Tobramycin Sulfate;Ciprofloxacin\\Ciprofloxacin Hydrochloride;Ranitidine Hydrochloride;Amphotericin B;Filgrastim;Acetaminophen;Furosemide;Potassium Chloride;Meperidine;Heparin Sodium;Imipenem;Prednisolone;Ceftazidime;Lactulose","Reason.for.Use":"Antibiotic Therapy;Oedema;Pain;Postoperative Analgesia","Reactions":"Blister;Shock;Mucosal Erosion;Corneal Erosion;Stevens-Johnson Syndrome;Female Reproductive Tract Disorder;Skin Disorder;Toxic Epidermal Necrolysis;Multiple Organ Dysfunction Syndrome;Dermatitis;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"17 YR","Sender":"Hoechst","Concomitant.Product.Names":"Metronidazole;Lynestrenol;Folic Acid;Doxycycline;Calcium;Zovirax;Prednisone"}
{"Case.ID":6564596,"Initial.FDA.Received.Date":"04/08/1999","days.since.last.fda":9,"Event.Date":"03/11/1999","Latest.FDA.Received.Date":"08-APR-1999","Suspect.Product.Names":"Neurontin","Suspect.Product.Active.Ingredients":"Gabapentin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome;Pain;Enterococcal Bacteraemia;Staphylococcal Infection;Systemic Candida;Dermatitis;Sepsis;Condition Aggravated;Erythema;Escherichia Infection;Mouth Ulceration;Blister;Rash Pruritic","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"6 YR","Sender":"-","Concomitant.Product.Names":"Morphine;Codeine;Ceftazidime Sodium;Diphenhydramine;Prednisolone;Methylphenidate Hydrochloride;Nafcillin Sodium;Fluoxetine;Acetaminophen;Dopamine;Ranitidine;Silvadene;Amphotericin B"}
{"Case.ID":3247852,"Initial.FDA.Received.Date":"04/09/1999","days.since.last.fda":1,"Event.Date":"12/25/1997","Latest.FDA.Received.Date":"14-APR-1999","Suspect.Product.Names":"Dulcolax (Bisacodyl);Heparin;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Bupivacaine Hydrochloride;Allopurinol;Unspecified Ingredient;Heparin Sodium;Oxazepam;Midazolam Hydrochloride;Bisacodyl;Amezinium Metilsulfate;Ciprofloxacin;Citric Acid Monohydrate\\Potassium Bicarbonate\\Potassium Citrate;Sodium Picosulfate","Reason.for.Use":"Anaesthesia;Constipation;Gastrointestinal Infection;Hyperuricaemia;Hypokalaemia;Oedema;Prophylaxis;Sedation;Sleep Disorder;Thrombosis Prophylaxis","Reactions":"Blood Lactate Dehydrogenase Increased;Blood Creatinine Increased;Cardiac Failure;Conjunctivitis;Right Ventricular Failure;Emphysema;Stevens-Johnson Syndrome;Inguinal Hernia;Dermatitis;Oropharyngeal Blistering","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Roche","Concomitant.Product.Names":"Lactated Ringers Solution;Methylprednisolone;Gentamicin Sulfate;Verapamil Hydrochloride;Dopamine Hydrochloride;Heparin;Lactulose;Insulin Nos"}
{"Case.ID":3246237,"Initial.FDA.Received.Date":"04/12/1999","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"12-APR-1999","Suspect.Product.Names":"Levaquin","Suspect.Product.Active.Ingredients":"Levofloxacin;Vancomycin;Diltiazem;Gentamicin","Reason.for.Use":"Atrial Fibrillation;Pyrexia","Reactions":"Dermatitis;Blood Urea Increased;Stevens-Johnson Syndrome;Liver Function Test Abnormal;Blood Creatinine Increased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Hoechst","Concomitant.Product.Names":"-"}
{"Case.ID":3256278,"Initial.FDA.Received.Date":"04/27/1999","days.since.last.fda":15,"Event.Date":"07/15/1997","Latest.FDA.Received.Date":"11-MAY-1999","Suspect.Product.Names":"Mysoline","Suspect.Product.Active.Ingredients":"Primidone;Carbamazepine","Reason.for.Use":"Epilepsy","Reactions":"Stomatitis;Pyrexia;Rash Erythematous;Stevens-Johnson Syndrome;Oculomucocutaneous Syndrome;Hepatomegaly;Respiratory Failure;Hypersensitivity;Erythema Multiforme;Liver Disorder;Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"24 MTH","Sender":"Elan","Concomitant.Product.Names":"Valproate Sodium"}
{"Case.ID":3264403,"Initial.FDA.Received.Date":"05/03/1999","days.since.last.fda":6,"Event.Date":"04/01/1999","Latest.FDA.Received.Date":"03-MAY-1999","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin","Reason.for.Use":"Peritonitis;Sepsis","Reactions":"Oxygen Saturation Decreased;Dermatitis Exfoliative Generalised;Stevens-Johnson Syndrome;Hypotension;Syncope;Pain;Abscess Oral;Differential White Blood Cell Count Abnormal;Mouth Ulceration;Rash Erythematous;Rash Maculo-Papular;Sepsis;Infection;Neutrophil Toxic Granulation Present","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"-","Concomitant.Product.Names":"Axid;Albuterol;Calcium Carbonate;Epogen"}
{"Case.ID":3272240,"Initial.FDA.Received.Date":"05/19/1999","days.since.last.fda":16,"Event.Date":"12/25/1997","Latest.FDA.Received.Date":"03-JUN-1999","Suspect.Product.Names":"Sensorcaine","Suspect.Product.Active.Ingredients":"Bupivacaine Hydrochloride","Reason.for.Use":"-","Reactions":"Blister;Blood Lactate Dehydrogenase Increased;Stevens-Johnson Syndrome;Blood Creatinine Increased;Conjunctivitis;Dermatitis;Oropharyngeal Blistering;Emphysema;Right Ventricular Failure;White Blood Cell Disorder;Inguinal Hernia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Astra","Concomitant.Product.Names":"Heparin;Ciprofloxacin Hydrochloride;Unspecified Ingredient;Allopurinol;Verapamil Hydrochloride"}
{"Case.ID":3278434,"Initial.FDA.Received.Date":"05/24/1999","days.since.last.fda":5,"Event.Date":"04/18/1998","Latest.FDA.Received.Date":"24-MAY-1999","Suspect.Product.Names":"Zyrtec;Novalgin (Metamizole Sodium);Claforan;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Codeine\\Diclofenac Sodium;Nitrazepam;Myrrh;Ofloxacin;Oxazepam;Dexpanthenol;Cefotaxime Sodium;Triflupromazine;Metamizole Sodium;Cetirizine Hydrochloride;Flucloxacillin;Allopurinol;Metoclopramide Hydrochloride;Clemastine;Acetaminophen;Nizatidine;Sulfamethoxazole\\Trimethoprim;Tramadol Hydrochloride;Gentamicin Sulfate;Ampicillin;Methylprednisolone;Sodium Picosulfate Monohydrate","Reason.for.Use":"Balanoposthitis;Constipation;Hyperuricaemia;Nausea;Oliguria;Oropharyngeal Pain;Pain;Urethritis","Reactions":"Blister;Stevens-Johnson Syndrome;Peritonitis;Balanoposthitis;Dermatitis;Condition Aggravated;Epidermolysis Bullosa","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Methionine;Pantozol;Lactulose;Tpn;Sitosterols;Serevent Diskus;Glucose, Liquid;Potassium Bicarbonate\\Potassium Citrate;Sodium Chloride;Heparin;Diazepam;Potassium Chloride;Povidone-Iodine;Trospium Chloride;Urea;Unspecified Ingredient"}
{"Case.ID":3286598,"Initial.FDA.Received.Date":"06/08/1999","days.since.last.fda":15,"Event.Date":"04/21/1999","Latest.FDA.Received.Date":"11-APR-2000","Suspect.Product.Names":"Norvasc","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Clonazepam;Ketoprofen;Teprenone;Zopiclone;Nitroglycerin","Reason.for.Use":"Epilepsy;Gastritis;Hypertension;Insomnia;Pulmonary Congestion;Pyrexia","Reactions":"Mean Cell Volume Abnormal;Haemoglobin Decreased;Duodenal Ulcer;Lymphocyte Count Decreased;Blood Alkaline Phosphatase Increased;Thrombocytopenia;Gastrointestinal Haemorrhage;Hepatic Function Abnormal;Blood Lactate Dehydrogenase Increased;Blood Glucose Increased;Abnormal Behaviour;Protein Total Decreased;Pulmonary Congestion;Oedema Peripheral;Red Blood Cell Count Decreased;Stevens-Johnson Syndrome;Liver Function Test Abnormal;Mucosal Disorder;Leukopenia;Shock;Erosive Duodenitis;Cardiac Failure Congestive;Blood Creatine Phosphokinase Increased;Blood Creatinine Increased;Dermatitis;Basophil Count Increased;Hallucination;Neutrophil Count Increased;Pyrexia;Monocyte Count Increased;Skin Ulcer;Nasopharyngitis;Haematocrit Decreased;Drug Eruption;C-Reactive Protein Increased;Small Intestinal Haemorrhage;Blood Urea Increased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"Roche","Concomitant.Product.Names":"Beraprost Sodium;Halcion"}
{"Case.ID":3285366,"Initial.FDA.Received.Date":"06/09/1999","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"09-JUN-1999","Suspect.Product.Names":"Tavist Allergy","Suspect.Product.Active.Ingredients":"Clemastine Fumarate","Reason.for.Use":"Dermatitis","Reactions":"Oral Mucosal Eruption;Oropharyngeal Blistering;Epidermolysis Bullosa;Stevens-Johnson Syndrome;Peritonitis Bacterial","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Novartis","Concomitant.Product.Names":"Lasix;Nitrazepam;Unspecified Ingredient;Zyrtec;Oxazepam;Allopurinol;Claforan;Ampicillin;Novalgin (Metamizole Sodium)"}
{"Case.ID":5941301,"Initial.FDA.Received.Date":"06/30/1999","days.since.last.fda":21,"Event.Date":"04/26/1995","Latest.FDA.Received.Date":"30-JUN-1999","Suspect.Product.Names":"Propulsid;Cytotec;Dulcolax (Bisacodyl);Gastrografin;Lasix;Embolex","Suspect.Product.Active.Ingredients":"Dihydroergotamine Mesylate\\Heparin Sodium\\Lidocaine Hydrochloride;Furosemide;Ferrous Sulfate;Diatrizoate Meglumine\\Diatrizoate Sodium;Ofloxacin;Allopurinol;Theophylline Anhydrous;Bisacodyl;Clonidine Hydrochloride;Misoprostol;Cisapride;Acetaminophen","Reason.for.Use":"Dyspnoea;Gastrointestinal Disorder;Hyperuricaemia;Infection;Iron Metabolism Disorder;Oedema;Pyrexia;Thrombosis Prophylaxis","Reactions":"Dermatitis;Blister;Skin Ulcer;Conjunctivitis;Pain;Mouth Ulceration;Pruritus;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Hoechst","Concomitant.Product.Names":"Potassium Chloride;Ambroxol Hydrochloride;Sodium Picosulfate;Dopamine Hydrochloride;Acetaminophen;Meperidine"}
{"Case.ID":3298280,"Initial.FDA.Received.Date":"06/30/1999","days.since.last.fda":0,"Event.Date":"06/11/1999","Latest.FDA.Received.Date":"30-JUN-1999","Suspect.Product.Names":"Pepcid;Adalat","Suspect.Product.Active.Ingredients":"Nifedipine;Famotidine","Reason.for.Use":"-","Reactions":"Renal Failure;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Merck","Concomitant.Product.Names":"Prednisolone;Betamethasone"}
{"Case.ID":5769723,"Initial.FDA.Received.Date":"07/01/1999","days.since.last.fda":1,"Event.Date":"04/18/1998","Latest.FDA.Received.Date":"01-MAR-2000","Suspect.Product.Names":"Zyrtec;Serevent Diskus;Claforan;Lasix;Ringers Solution;Pantozol;Heparin","Suspect.Product.Active.Ingredients":"Heparin Sodium;Triamcinolone Acetonide\\Zinc Oxide;Tramadol Hydrochloride;Methylprednisolone;Sitosterols;Metoclopramide;Dexpanthenol;Clemastine Fumarate;Pantoprazole Sodium;Unspecified Ingredient;Acetaminophen;Theophylline Anhydrous;Dipyrone;Ampicillin;Sodium Picosulfate;Nizatidine;Methionine;Trospium Chloride;Sodium Chloride;Oxazepam;Nitrazepam;Calcium Chloride\\Potassium Chloride\\Sodium Chloride;Myrrh;Furosemide;Ofloxacin;Potassium Chloride;Cefotaxime Sodium;Gentamicin Sulfate;Fluticasone Propionate;Codeine\\Diclofenac;Dextrose;Salmeterol Xinafoate;Lactulose;Povidone-Iodine;Cetirizine Hydrochloride;Mineral Oil;Urea;Allopurinol;Triflupromazine Hydrochloride;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Asthma;Automatic Bladder;Balanoposthitis;Constipation;Dehydration;Dermatitis;Dry Skin;Hyperuricaemia;Hypokalaemia;Incontinence;Infection;Insomnia;Liver Disorder;Micturition Urgency;Nausea;Neck Pain;Pain;Parenteral Nutrition;Polyuria;Prophylaxis;Pyrexia;Sleep Disorder;Thrombosis Prophylaxis;Urethritis;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Peritonitis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Solvay","Concomitant.Product.Names":"Diazepam;Unspecified Ingredient;Fosfomycin;Lasix;Potassium Chloride"}
{"Case.ID":3302913,"Initial.FDA.Received.Date":"07/01/1999","days.since.last.fda":0,"Event.Date":"01/05/1995","Latest.FDA.Received.Date":"01-JUL-1999","Suspect.Product.Names":"Esidrix;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Allopurinol;Dimethindene Maleate;Ofloxacin;Neomycin;Hydrochlorothiazide","Reason.for.Use":"Hepatic Cirrhosis;Hyperuricaemia;Infection;Oedema;Pruritus","Reactions":"Mouth Ulceration;Skin Ulcer;Dermatitis;Conjunctivitis;Gamma-Glutamyltransferase Increased;Genital Ulceration;Stevens-Johnson Syndrome;Blood Creatinine Increased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"32 YR","Sender":"Hoechst","Concomitant.Product.Names":"Sucralfate;Lactulose"}
{"Case.ID":6252157,"Initial.FDA.Received.Date":"07/02/1999","days.since.last.fda":1,"Event.Date":"11/01/1994","Latest.FDA.Received.Date":"02-JUL-1999","Suspect.Product.Names":"Voltaren;Humatin;Rocephin;Konakion;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Furosemide;Cholestyramine;Phytonadione;Dopamine Hydrochloride;Ceftriaxone Sodium;Lactulose;Promethazine Hydrochloride;Paromomycin Sulfate;Diclofenac Sodium;Amoxicillin\\Clavulanate Potassium;Acetaminophen;Dipyrone","Reason.for.Use":"Gastrointestinal Disorder;Hepatic Cirrhosis;Hepatic Encephalopathy;Infection;Oedema;Pain;Pyrexia;Renal Failure;Vitamin K Deficiency","Reactions":"Sepsis;Dermatitis;Oedema;Coma;Hepatic Cirrhosis;Infection;Liver Function Test Abnormal;Hepatic Encephalopathy;Renal Impairment;Hepatitis B;Blood Creatinine Increased;Anal Ulcer;Stevens-Johnson Syndrome;Pain;Pyrexia;Hepatic Failure;Jaundice;Mouth Ulceration;Blood Urea Increased;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"26 YR","Sender":"Roche","Concomitant.Product.Names":"Levomethadone;Valium;Tramadol Hydrochloride;Butylscopolamine Bromide;Maalox Antacid"}
{"Case.ID":3476194,"Initial.FDA.Received.Date":"07/06/1999","days.since.last.fda":4,"Event.Date":"04/25/1995","Latest.FDA.Received.Date":"22-MAY-2000","Suspect.Product.Names":"Embolex;Dulcolax (Bisacodyl);Lasix;Cytotec;Propulsid;Gastrografin","Suspect.Product.Active.Ingredients":"Diatrizoate Meglumine\\Diatrizoate Sodium;Cisapride;Clonidine Hydrochloride;Ofloxacin;Misoprostol;Allopurinol;Furosemide;Bisacodyl;Dihydroergotamine Mesylate\\Heparin Sodium\\Lidocaine Hydrochloride;Ferrous Sulfate;Acetaminophen;Aminophylline","Reason.for.Use":"Anaemia;Anticoagulant Therapy;Bacterial Infection;Constipation;Dyspnoea;Glaucoma;Hyperuricaemia;Oedema;Post Procedural Complication;Relapsing Fever","Reactions":"Skin Ulcer;Pyrexia;Oropharyngeal Blistering;Duodenal Ulcer Haemorrhage;Toxic Epidermal Necrolysis;Blister;Conjunctivitis;Stevens-Johnson Syndrome;Pain","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Janssen","Concomitant.Product.Names":"Glycerin\\Lecithin\\Soybean Oil;Calcium Carbonate;Meperidine;Ambroxol Hydrochloride;Multi Vitamin Infusion;Dopamine Hydrochloride;Clemastine Fumarate;Ferrlecit;Tramadol;Lactulose;Sodium Picosulfate;Gastrozepin;Potassium Chloride;Magaldrate"}
{"Case.ID":3303029,"Initial.FDA.Received.Date":"07/06/1999","days.since.last.fda":0,"Event.Date":"04/20/1999","Latest.FDA.Received.Date":"06-JUL-1999","Suspect.Product.Names":"Furadantin","Suspect.Product.Active.Ingredients":"Nitrofurantoin","Reason.for.Use":"Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"88 YR","Sender":"Procter And Gamble","Concomitant.Product.Names":"Digoxin;Phenytoin;Amlodipine;Furosemide"}
{"Case.ID":3303220,"Initial.FDA.Received.Date":"07/07/1999","days.since.last.fda":1,"Event.Date":"01/05/1995","Latest.FDA.Received.Date":"07-JUL-1999","Suspect.Product.Names":"Lasix;Esidrix","Suspect.Product.Active.Ingredients":"Hydrochlorothiazide;Furosemide;Neomycin;Ofloxacin;Dimethindene Maleate","Reason.for.Use":"Hyperuricaemia;Oedema;Pruritus","Reactions":"Skin Ulcer;Stevens-Johnson Syndrome;Gamma-Glutamyltransferase Increased;Dermatitis;Blood Creatine Increased;Female Reproductive Tract Disorder;Mucosal Erosion;Conjunctivitis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"32 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Spironolactone;Lactulose;Sucralfate"}
{"Case.ID":3305192,"Initial.FDA.Received.Date":"07/13/1999","days.since.last.fda":6,"Event.Date":"04/18/1998","Latest.FDA.Received.Date":"13-JUL-1999","Suspect.Product.Names":"Zyrtec","Suspect.Product.Active.Ingredients":"Cetirizine Hydrochloride","Reason.for.Use":"Drug Eruption","Reactions":"Hypokalaemia;Peritonitis;Sleep Disorder;Dermatitis;Skin Disorder;Pyrexia;Stevens-Johnson Syndrome;Infection;Epidermolysis Bullosa;Skin Hyperpigmentation;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Pfizer","Concomitant.Product.Names":"Acetaminophen;Clemastine Fumarate;Pantoprazole Sodium;Triamcinolone;Fluticasone;Potassium Chloride;Unspecified Ingredient;Sodium Chloride;Cefotaxime;Metamizole Sodium;Ampicillin;Gentamicin;Oxazepam;Sulfamethoxazole\\Trimethoprim;Flucloxacillin;Theophylline Anhydrous;Nizatidine;Bisacodyl;Lactulose;Nitrazepam;Povidone-Iodine;Heparin;Metoclopramide;Salmeterol;Methylprednisolone;Furosemide;Glucose, Liquid;Allopurinol"}
{"Case.ID":3315251,"Initial.FDA.Received.Date":"07/26/1999","days.since.last.fda":13,"Event.Date":"06/13/1999","Latest.FDA.Received.Date":"10-SEP-1999","Suspect.Product.Names":"Cardizem Cd;Cerezyme","Suspect.Product.Active.Ingredients":"Imiglucerase;Diltiazem Hydrochloride","Reason.for.Use":"Gaucher'S Disease","Reactions":"Stevens-Johnson Syndrome;Splenic Artery Aneurysm;Haemorrhage;Myopathy;Calcinosis;Renal Tubular Disorder;Intra-Abdominal Haemorrhage;Arterial Rupture;Kidney Fibrosis;Tubulointerstitial Nephritis;Shock;Haemoglobin Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Genzyme","Concomitant.Product.Names":"-"}
{"Case.ID":3322125,"Initial.FDA.Received.Date":"08/03/1999","days.since.last.fda":8,"Event.Date":"08/19/1996","Latest.FDA.Received.Date":"03-AUG-1999","Suspect.Product.Names":"Actrapid","Suspect.Product.Active.Ingredients":"Insulin Human","Reason.for.Use":"Diabetes Mellitus","Reactions":"Mucosal Erosion;Blister;Toxic Epidermal Necrolysis;Dermatitis;Stevens-Johnson Syndrome;Shock;Epidermolysis Bullosa","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"36 YR","Sender":"Novo Nordisk","Concomitant.Product.Names":"Novalgin (Metamizole Sodium);Lasix;Acetaminophen;Diflucan;Gentamicin Sulfate;Amoxicillin\\Clavulanate Potassium;Allopurinol"}
{"Case.ID":3323783,"Initial.FDA.Received.Date":"08/05/1999","days.since.last.fda":2,"Event.Date":"04/16/1998","Latest.FDA.Received.Date":"05-AUG-1999","Suspect.Product.Names":"Taxotere","Suspect.Product.Active.Ingredients":"Docetaxel","Reason.for.Use":"Breast Cancer Female","Reactions":"Sedation;Ascites;Apathy;Capillary Leak Syndrome;Acute Respiratory Distress Syndrome;Stevens-Johnson Syndrome;Sinus Arrhythmia;Epidermolysis Bullosa;Hypertension;Lung Infiltration;Abdominal Distension;Dyspnoea;Erythema Multiforme","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"53 YR","Sender":"Rhone Poulenc Rorer","Concomitant.Product.Names":"-"}
{"Case.ID":3324208,"Initial.FDA.Received.Date":"08/06/1999","days.since.last.fda":1,"Event.Date":"11/01/1994","Latest.FDA.Received.Date":"06-AUG-1999","Suspect.Product.Names":"Voltaren;Humatin;Rocephin;Lasix;Maalox Antacid;Konakion","Suspect.Product.Active.Ingredients":"Phytonadione;Aluminum Hydroxide\\Dimethicone\\Magnesium Hydroxide;Lactulose;Promethazine Hydrochloride;Furosemide;Amoxicillin\\Clavulanate Potassium;Furosemide;Dopamine Hydrochloride;Ceftriaxone Sodium;Acetaminophen;Cholestyramine;Paromomycin Sulfate;Diclofenac Sodium;Dipyrone;Levomethadone","Reason.for.Use":"Drug Abuser;Gastrointestinal Disorder;Hepatic Cirrhosis;Hepatic Encephalopathy;Infection;Oedema;Pain;Polyuria;Pyrexia;Vitamin K Deficiency","Reactions":"Anal Ulcer;Stevens-Johnson Syndrome;Blister;Hepatic Encephalopathy;Jaundice","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"26 YR","Sender":"Solvay","Concomitant.Product.Names":"Butylscopolamine Bromide;Tramadol;Valium"}
{"Case.ID":3348465,"Initial.FDA.Received.Date":"09/14/1999","days.since.last.fda":39,"Event.Date":"05/06/1999","Latest.FDA.Received.Date":"14-SEP-1999","Suspect.Product.Names":"Lozol","Suspect.Product.Active.Ingredients":"Indapamide","Reason.for.Use":"Cardiac Failure","Reactions":"White Blood Cell Count Increased;Stevens-Johnson Syndrome;Laryngeal Oedema;Oropharyngeal Pain;Platelet Count Decreased;Dermatitis Bullous;Neutrophil Count Increased;Mouth Ulceration;Lung Infiltration;Respiratory Failure;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Rhone Poulenc Rorer","Concomitant.Product.Names":"Theophylline Anhydrous;Losartan Potassium"}
{"Case.ID":3347900,"Initial.FDA.Received.Date":"09/16/1999","days.since.last.fda":2,"Event.Date":"03/10/1998","Latest.FDA.Received.Date":"28-OCT-1999","Suspect.Product.Names":"Cleocin Phosphate;Cleocin Hydrochloride","Suspect.Product.Active.Ingredients":"Clindamycin Hydrochloride;Acetylpheneturide;Clonazepam;Arbekacin Sulfate;Cefdinir;Valproate Sodium;Clindamycin Phosphate;Carbamazepine;Caffeine\\Phenobarbital\\Phenytoin;Minocycline Hydrochloride;Sparfloxacin","Reason.for.Use":"Abdominal Pain;Cough;Epilepsy;Pneumonia;Seizure;Upper Respiratory Tract Infection","Reactions":"Drug Hypersensitivity;Toxic Epidermal Necrolysis;Gingival Hypertrophy;Dyspnoea;Gamma-Glutamyltransferase Increased;Stevens-Johnson Syndrome;Flushing;Condition Aggravated;Pyrexia;Acute Respiratory Distress Syndrome;Seizure;Hepatocellular Injury;Skin Ulcer;Dermatitis;Genital Ulceration;Disseminated Intravascular Coagulation;Pneumonia;Mucosal Ulceration;Sepsis;Abdominal Pain","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"31 YR","Sender":"Pharmacia And Upjohn","Concomitant.Product.Names":"Diazepam"}
{"Case.ID":3361630,"Initial.FDA.Received.Date":"09/29/1999","days.since.last.fda":13,"Event.Date":"05/25/1999","Latest.FDA.Received.Date":"29-SEP-1999","Suspect.Product.Names":"Doxazosin;Amlodipine;Prilosec","Suspect.Product.Active.Ingredients":"Omeprazole Magnesium;Amlodipine Besylate;Doxazosin Mesylate","Reason.for.Use":"Duodenal Ulcer","Reactions":"Dermatitis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"Astra","Concomitant.Product.Names":"-"}
{"Case.ID":3375087,"Initial.FDA.Received.Date":"10/21/1999","days.since.last.fda":22,"Event.Date":"06/10/1999","Latest.FDA.Received.Date":"20-DEC-1999","Suspect.Product.Names":"Ziagen","Suspect.Product.Active.Ingredients":"Abacavir Sulfate","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome;Lethargy;Pyrexia;Malaise;Dermatitis Exfoliative;Mouth Ulceration;Rash Macular;Drug Hypersensitivity;Rash Erythematous;Insomnia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"35 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Nelfinavir Mesylate;Zidovudine;Lamivudine;Nevirapine;Saquinavir"}
{"Case.ID":3406598,"Initial.FDA.Received.Date":"12/17/1999","days.since.last.fda":57,"Event.Date":"07/24/1999","Latest.FDA.Received.Date":"17-DEC-1999","Suspect.Product.Names":"Levaquin;Synercid","Suspect.Product.Active.Ingredients":"Dalfopristin\\Quinupristin;Levofloxacin","Reason.for.Use":"Infection","Reactions":"Renal Failure;Pseudomonas Infection;Dermatitis;Stevens-Johnson Syndrome;Rash;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"68 YR","Sender":"Rhone Poulenc Rorer","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":3416889,"Initial.FDA.Received.Date":"01/05/2000","days.since.last.fda":19,"Event.Date":"","Latest.FDA.Received.Date":"31-MAR-2000","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Blister;Stevens-Johnson Syndrome;Renal Failure;Dermatitis;Hypersensitivity;Hepatic Failure;Hepatic Necrosis;Pyrexia;Liver Function Test Abnormal;Blood Pressure Decreased;Jaundice","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"29 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":3435535,"Initial.FDA.Received.Date":"02/16/2000","days.since.last.fda":42,"Event.Date":"01/09/2000","Latest.FDA.Received.Date":"10-MAR-2000","Suspect.Product.Names":"Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole","Reason.for.Use":"Candida Infection","Reactions":"Staphylococcal Infection;Stevens-Johnson Syndrome;Rash Erythematous;Hepatic Function Abnormal;Clostridium Colitis;Hepatic Enzyme Increased;Condition Aggravated;Pulmonary Oedema;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"66 YR","Sender":"Pfizer","Concomitant.Product.Names":"Vancomycin Hydrochloride"}
{"Case.ID":3452262,"Initial.FDA.Received.Date":"03/28/2000","days.since.last.fda":41,"Event.Date":"04/29/1999","Latest.FDA.Received.Date":"28-MAR-2000","Suspect.Product.Names":"Daraprim","Suspect.Product.Active.Ingredients":"Pyrimethamine;Phenytoin;Sulfadiazine;Fluconazole","Reason.for.Use":"Epilepsy;Oesophageal Candidiasis;Toxoplasmosis","Reactions":"Conjunctivitis;Eye Pain;Toxic Epidermal Necrolysis;Rash Erythematous;Stevens-Johnson Syndrome;Rash Maculo-Papular;Pyrexia;Genital Ulceration;Vision Blurred","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"33 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Ceftriaxone;Flucloxacillin;Leucovorin;Acetaminophen;Lactulose;Metronidazole;Metoclopramide;Mometasone Furoate;Dexamethasone"}
{"Case.ID":3453809,"Initial.FDA.Received.Date":"03/30/2000","days.since.last.fda":2,"Event.Date":"04/29/1999","Latest.FDA.Received.Date":"30-MAR-2000","Suspect.Product.Names":"Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Pyrimethamine;Sulfadiazine;Phenytoin","Reason.for.Use":"Epilepsy;Oesophageal Candidiasis;Toxoplasmosis","Reactions":"Toxic Epidermal Necrolysis;Genital Ulceration;Vision Blurred;Rash Maculo-Papular;Stevens-Johnson Syndrome;Pyrexia;Mucosal Disorder;Lacrimation Increased;Conjunctivitis;Rash Erythematous","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"33 YR","Sender":"Pfizer","Concomitant.Product.Names":"Metoclopramide;Ceftriaxone;Dexamethasone;Acetaminophen"}
{"Case.ID":6689427,"Initial.FDA.Received.Date":"04/12/2000","days.since.last.fda":13,"Event.Date":"02/03/2000","Latest.FDA.Received.Date":"12-APR-2000","Suspect.Product.Names":"Plavix","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Deflazacort;Pentoxifylline;Cyanocobalamin\\Pyridoxine\\Thiamine;Felodipine","Reason.for.Use":"Hypertension;Neuritis;Optic Neuritis;Retinitis","Reactions":"Dermatitis Bullous;Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Pruritus","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"81 YR","Sender":"Sanofi","Concomitant.Product.Names":"-"}
{"Case.ID":3465551,"Initial.FDA.Received.Date":"04/25/2000","days.since.last.fda":13,"Event.Date":"04/10/2000","Latest.FDA.Received.Date":"17-MAY-2000","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin;Teicoplanin;Linezolid;Rifampin","Reason.for.Use":"Staphylococcal Infection","Reactions":"Conjunctival Disorder;Myocardial Infarction;Left Ventricular Failure;Empyema;Blood Albumin Decreased;Chest X-Ray Abnormal;Cardiomyopathy;Insomnia;Dermatitis Exfoliative;Fluid Overload;Pulmonary Oedema;Pneumonia;Stevens-Johnson Syndrome;Cardiac Failure;Blood Culture Positive;Dermatitis Atopic;Dyspnoea;Infection;Eosinophil Count Increased;Constipation;Renal Impairment;Dermatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"74 YR","Sender":"Pharmacia And Upjohn","Concomitant.Product.Names":"Diltiazem;Eurax;Simvastatin;Cetirizine Hydrochloride;Temazepam;Metoclopramide;Doxazosin;Aspirin;Furosemide;Nitroglycerin;Acetaminophen;Isosorbide Mononitrate"}
{"Case.ID":3474329,"Initial.FDA.Received.Date":"05/08/2000","days.since.last.fda":13,"Event.Date":"05/21/1999","Latest.FDA.Received.Date":"08-MAY-2000","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Dexpanthenol;Ganciclovir Sodium","Reason.for.Use":"Bronchospasm;Prophylaxis","Reactions":"Toxic Epidermal Necrolysis;Erythema;Blister;Neutropenia;Bronchospasm;Stevens-Johnson Syndrome;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"55 YR","Sender":"Roche","Concomitant.Product.Names":"Busulfan"}
{"Case.ID":3471748,"Initial.FDA.Received.Date":"05/08/2000","days.since.last.fda":0,"Event.Date":"05/07/1999","Latest.FDA.Received.Date":"08-MAY-2000","Suspect.Product.Names":"Fortaz;Ventolin","Suspect.Product.Active.Ingredients":"Albuterol Sulfate;Ceftazidime Sodium;Dipyrone","Reason.for.Use":"Pain;Pneumonia","Reactions":"Graft Versus Host Disease;Sepsis;Rash Erythematous;Gastroenteritis;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Pyrexia;Pneumonia;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"55 YR","Sender":"Glaxo Wellcome","Concomitant.Product.Names":"Acyclovir;Unspecified Ingredient"}
{"Case.ID":3474166,"Initial.FDA.Received.Date":"05/10/2000","days.since.last.fda":2,"Event.Date":"05/04/1999","Latest.FDA.Received.Date":"10-MAY-2000","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Quinidine Sulfate;Midazolam Hydrochloride;Articaine Hydrochloride;Penicillin;Ketoprofen","Reason.for.Use":"Anaesthesia;Arrhythmia;Pain;Prophylaxis;Sedation","Reactions":"Conjunctivitis;Tongue Coated;Multiple Organ Dysfunction Syndrome;Pyrexia;Stevens-Johnson Syndrome;Dermatitis;Face Oedema;Blister;Toxic Epidermal Necrolysis;Mucosal Erosion","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"58 YR","Sender":"Roche","Concomitant.Product.Names":"Novodigal (.Beta.-Acetyldigoxin);Acetaminophen;Marcumar;Verapamil Hydrochloride"}
{"Case.ID":3473451,"Initial.FDA.Received.Date":"05/15/2000","days.since.last.fda":5,"Event.Date":"03/22/2000","Latest.FDA.Received.Date":"15-MAY-2000","Suspect.Product.Names":"Levaquin","Suspect.Product.Active.Ingredients":"Levofloxacin","Reason.for.Use":"Pneumonia","Reactions":"Stevens-Johnson Syndrome;Dermatitis;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3477535,"Initial.FDA.Received.Date":"05/24/2000","days.since.last.fda":9,"Event.Date":"","Latest.FDA.Received.Date":"24-MAY-2000","Suspect.Product.Names":"Zaroxolyn","Suspect.Product.Active.Ingredients":"Metolazone;Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"77 YR","Sender":"Medeva","Concomitant.Product.Names":"-"}
{"Case.ID":3485038,"Initial.FDA.Received.Date":"06/07/2000","days.since.last.fda":14,"Event.Date":"01/02/2000","Latest.FDA.Received.Date":"07-JUN-2000","Suspect.Product.Names":"Levaquin;Dilantin;Zithromax","Suspect.Product.Active.Ingredients":"Azithromycin Dihydrate;Phenytoin;Levofloxacin;Erythromycin","Reason.for.Use":"Decubitus Ulcer","Reactions":"Stevens-Johnson Syndrome;Pseudomonas Infection;Dermatitis Exfoliative;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5938737,"Initial.FDA.Received.Date":"06/22/2000","days.since.last.fda":15,"Event.Date":"08/04/1999","Latest.FDA.Received.Date":"22-JUN-2000","Suspect.Product.Names":"Toprol Xl","Suspect.Product.Active.Ingredients":"Metoprolol Succinate;Allopurinol","Reason.for.Use":"Hypertension","Reactions":"Dermatitis;Blister;Cardiac Failure;Stevens-Johnson Syndrome;Conjunctival Hyperaemia;Shock;Pyrexia;Toxic Epidermal Necrolysis;C-Reactive Protein Increased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"61 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"Euthyrox;Xenical;Risperdal;Mellaril"}
{"Case.ID":3521447,"Initial.FDA.Received.Date":"08/21/2000","days.since.last.fda":60,"Event.Date":"","Latest.FDA.Received.Date":"21-AUG-2000","Suspect.Product.Names":"Viagra","Suspect.Product.Active.Ingredients":"Sildenafil Citrate;Levofloxacin;Sulindac","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Skin Disorder;Dermatitis Exfoliative;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":3561140,"Initial.FDA.Received.Date":"10/26/2000","days.since.last.fda":66,"Event.Date":"09/13/2000","Latest.FDA.Received.Date":"26-OCT-2000","Suspect.Product.Names":"Celebrex","Suspect.Product.Active.Ingredients":"Celecoxib","Reason.for.Use":"Arthritis","Reactions":"Myocardial Infarction;Liver Function Test Abnormal;Oedema Peripheral;Vomiting;Cardiac Disorder;Renal Failure;Ejection Fraction Abnormal;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"-","Concomitant.Product.Names":"Insulin Nos;Hyzaar"}
{"Case.ID":3591415,"Initial.FDA.Received.Date":"01/16/2001","days.since.last.fda":82,"Event.Date":"","Latest.FDA.Received.Date":"28-MAR-2001","Suspect.Product.Names":"Roferon-A","Suspect.Product.Active.Ingredients":"Interferon Alfa-2a","Reason.for.Use":"Chronic Myeloid Leukaemia","Reactions":"Gastritis Erosive;Upper Gastrointestinal Haemorrhage;Stress Ulcer;Right Ventricular Failure;Pericarditis;Sepsis;Oedema Peripheral;Extramedullary Haemopoiesis;Ejection Fraction Abnormal;Splenomegaly;Malnutrition;Gastric Ulcer;Pneumonia;Stevens-Johnson Syndrome;Oesophageal Disorder;Hypotension;Lung Disorder;Protein Total Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":4187701,"Initial.FDA.Received.Date":"01/29/2001","days.since.last.fda":13,"Event.Date":"12/28/1998","Latest.FDA.Received.Date":"29-JAN-2001","Suspect.Product.Names":"Diflucan;Albumin (Human);Rocephin;Zosyn;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Vancomycin;Digitoxin;Furosemide;Nafronyl Oxalate;Diltiazem;Piperacillin Sodium\\Tazobactam Sodium;Ceftriaxone Sodium;Benazepril Hydrochloride;Erythromycin;Roxithromycin;Albumin Human;Sodium Polystyrene Sulfonate;Hops\\Melissa Officinalis\\Valerian;Heparin Sodium;Fluconazole;Trimipramine Maleate;Omeprazole;Cilastatin Sodium\\Imipenem;Midazolam Maleate;Hydrochlorothiazide;Citric Acid Monohydrate\\Potassium Bicarbonate\\Potassium Citrate","Reason.for.Use":"Aortic Valve Incompetence;Cardiac Failure;Hyperkalaemia;Hypertension;Hypokalaemia;Prophylaxis;Sepsis;Tremor;Ulcer","Reactions":"Stevens-Johnson Syndrome;Sepsis;Toxic Epidermal Necrolysis;Cheilitis;Stomatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Wyeth Ayerst","Concomitant.Product.Names":"-"}
{"Case.ID":3608296,"Initial.FDA.Received.Date":"01/31/2001","days.since.last.fda":2,"Event.Date":"04/26/2000","Latest.FDA.Received.Date":"31-JAN-2001","Suspect.Product.Names":"Vioxx","Suspect.Product.Active.Ingredients":"Rofecoxib;Sulfasalazine;Allopurinol","Reason.for.Use":"Colitis;Gout","Reactions":"Renal Failure;Stevens-Johnson Syndrome;Faecaloma;Toxic Epidermal Necrolysis;Dehydration;Metabolic Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"-","Concomitant.Product.Names":"Prednisone;Zyprexa;Metoprolol;Olanzapine;Aspirin"}
{"Case.ID":5830239,"Initial.FDA.Received.Date":"02/01/2001","days.since.last.fda":1,"Event.Date":"12/28/1998","Latest.FDA.Received.Date":"20-JUN-2005","Suspect.Product.Names":"Crataegus Extract\\Valerian Extract\\Viscum Album Fruit;Rocephin;Konakion;Benazepril Hydrochloride And Hydrochlorothiazide;Heparin;Albumin (Human);Primaxin Im","Suspect.Product.Active.Ingredients":"Furosemide;Cilastatin Sodium\\Imipenem;Omeprazole;Fluconazole;Erythromycin;Digitoxin;Nafronyl Oxalate;Midazolam Hydrochloride;Albumin Human;Heparin Sodium;Phytonadione;Benazepril Hydrochloride\\Hydrochlorothiazide;Potassium Chloride;Ceftriaxone Sodium;Diltiazem Hydrochloride;Hawthorn Leaf With Flower\\Valerian Extract\\Viscum Album Fruit;Piperacillin Sodium\\Tazobactam Sodium;Vancomycin;Sodium Polystyrene Sulfonate;Trimipramine Maleate","Reason.for.Use":"Aortic Valve Incompetence;Cardiac Failure;Hyperkalaemia;Hypertension;Hypokalaemia;Ill-Defined Disorder;Restlessness;Sepsis;Stoma Care;Thrombosis Prophylaxis","Reactions":"Cardiac Failure;Sepsis;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Restlessness;Haemorrhage","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Pfizer","Concomitant.Product.Names":"Heparin;Human Red Blood Cell;Phytonadione;Lansoprazole;Acetaminophen;Lactulose;Spironolactone"}
{"Case.ID":3612520,"Initial.FDA.Received.Date":"02/16/2001","days.since.last.fda":15,"Event.Date":"","Latest.FDA.Received.Date":"16-FEB-2001","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin Hydrochloride","Reason.for.Use":"Skin Ulcer;Staphylococcal Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3611801,"Initial.FDA.Received.Date":"02/20/2001","days.since.last.fda":4,"Event.Date":"01/10/2001","Latest.FDA.Received.Date":"08-MAR-2001","Suspect.Product.Names":"Uft;Taxotere","Suspect.Product.Active.Ingredients":"Docetaxel;Tegafur\\Uracil","Reason.for.Use":"Breast Cancer Female","Reactions":"Metastases To Skin;Metastases To Bone;Purpura;Metastases To Liver;Nail Disorder;Hepatic Function Abnormal;Multiple Organ Dysfunction Syndrome;Pulmonary Function Test Decreased;Condition Aggravated;Stevens-Johnson Syndrome;Haemodialysis;Stomatitis;Metastases To Lymph Nodes;Leukopenia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"44 YR","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":3614260,"Initial.FDA.Received.Date":"02/21/2001","days.since.last.fda":1,"Event.Date":"11/15/2000","Latest.FDA.Received.Date":"21-FEB-2001","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Fluconazole","Reason.for.Use":"Pneumonia Streptococcal","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"53 YR","Sender":"-","Concomitant.Product.Names":"Nystatin;Liposyn;Cipro;Tpn;Colace;Acyclovir;Granulocyte Colony-Stimulating Factor Nos;Solu-Medrol;Procrit"}
{"Case.ID":3618609,"Initial.FDA.Received.Date":"03/06/2001","days.since.last.fda":13,"Event.Date":"02/01/2001","Latest.FDA.Received.Date":"31-MAY-2001","Suspect.Product.Names":"Actos","Suspect.Product.Active.Ingredients":"Pioglitazone Hydrochloride","Reason.for.Use":"Diabetes Mellitus","Reactions":"Cardiac Failure;Toxic Skin Eruption;Platelet Count Decreased;Stevens-Johnson Syndrome;Liver Disorder;Haemodialysis;Pleural Effusion;Renal Failure;Disseminated Intravascular Coagulation;Asthma;Herpes Simplex;Mouth Ulceration;Cardio-Respiratory Arrest","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"76 YR","Sender":"Takeda","Concomitant.Product.Names":"Allopurinol;Calcium Polystyrene Sulfonate;Nifedipine;Glyburide;Furosemide"}
{"Case.ID":3620287,"Initial.FDA.Received.Date":"03/09/2001","days.since.last.fda":3,"Event.Date":"02/20/2001","Latest.FDA.Received.Date":"03-APR-2001","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine;Stavudine","Reason.for.Use":"Hiv Infection","Reactions":"Multiple Organ Dysfunction Syndrome;Hepatic Encephalopathy;Neoplasm Malignant;Pancreatitis Haemorrhagic;Conjunctivitis;Hepatic Failure;Metabolic Acidosis;Hepatic Necrosis;Sepsis;Toxic Epidermal Necrolysis;Hepatorenal Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"33 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Didanosine"}
{"Case.ID":3641400,"Initial.FDA.Received.Date":"04/13/2001","days.since.last.fda":35,"Event.Date":"","Latest.FDA.Received.Date":"13-APR-2001","Suspect.Product.Names":"Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"Pneumonia","Reactions":"Sepsis;Pruritus;Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome;Injury;Hepatocellular Injury;Dermatitis;Jaundice Cholestatic","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"37 YR","Sender":"Smithkline Beecham","Concomitant.Product.Names":"-"}
{"Case.ID":3648915,"Initial.FDA.Received.Date":"05/03/2001","days.since.last.fda":20,"Event.Date":"","Latest.FDA.Received.Date":"03-MAY-2001","Suspect.Product.Names":"Neurontin","Suspect.Product.Active.Ingredients":"Gabapentin","Reason.for.Use":"Pain;Polyneuropathy","Reactions":"Angioedema;Renal Failure;Dyspnoea;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"75 YR","Sender":"Parke Davis","Concomitant.Product.Names":"-"}
{"Case.ID":3661884,"Initial.FDA.Received.Date":"06/01/2001","days.since.last.fda":29,"Event.Date":"02/06/2001","Latest.FDA.Received.Date":"01-JUN-2001","Suspect.Product.Names":"Cipro","Suspect.Product.Active.Ingredients":"Ciprofloxacin Hydrochloride;Ciprofloxacin","Reason.for.Use":"Coronary Artery Bypass;Upper Respiratory Tract Infection","Reactions":"Toxic Epidermal Necrolysis;Blood Pressure Decreased;Cellulitis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Bayer","Concomitant.Product.Names":"Aspirin;Amiodarone;Albuterol Sulfate;Propofol;Epinephrine;Dalteparin;Acetaminophen;Milrinone;Flucloxacillin;Nystatin;Ranitidine;Lisinopril"}
{"Case.ID":3666972,"Initial.FDA.Received.Date":"06/13/2001","days.since.last.fda":12,"Event.Date":"","Latest.FDA.Received.Date":"13-JUN-2001","Suspect.Product.Names":"Celebrex","Suspect.Product.Active.Ingredients":"Celecoxib","Reason.for.Use":"Back Pain","Reactions":"Dermatitis;Infection;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Gd Searle","Concomitant.Product.Names":"-"}
{"Case.ID":3669211,"Initial.FDA.Received.Date":"06/19/2001","days.since.last.fda":6,"Event.Date":"03/09/2001","Latest.FDA.Received.Date":"19-JUN-2001","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Levofloxacin","Reason.for.Use":"Cough;Upper Respiratory Tract Infection","Reactions":"Atrial Fibrillation;Hepatic Failure;Oropharyngeal Pain;Dysphagia;Sepsis;Disseminated Intravascular Coagulation;Eye Irritation;Respiratory Failure;Pyrexia;Lip Dry;Stevens-Johnson Syndrome;Pancreatitis;Confusional State;Hallucination;Supraventricular Tachycardia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"54 YR","Sender":"-","Concomitant.Product.Names":"Cefuroxime"}
{"Case.ID":3685310,"Initial.FDA.Received.Date":"07/20/2001","days.since.last.fda":31,"Event.Date":"","Latest.FDA.Received.Date":"20-JUL-2001","Suspect.Product.Names":"Cefobid","Suspect.Product.Active.Ingredients":"Cefoperazone","Reason.for.Use":"Post Procedural Complication;Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"60 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":3696376,"Initial.FDA.Received.Date":"08/06/2001","days.since.last.fda":17,"Event.Date":"01/04/2001","Latest.FDA.Received.Date":"06-AUG-2001","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Acute Kidney Injury;Hyperkalaemia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3710431,"Initial.FDA.Received.Date":"09/17/2001","days.since.last.fda":42,"Event.Date":"04/03/2000","Latest.FDA.Received.Date":"07-NOV-2001","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin;Allopurinol","Reason.for.Use":"Gout;Urinary Tract Infection","Reactions":"Sepsis;Drug Hypersensitivity;Sedation;Asthenia;Stevens-Johnson Syndrome;Hepatic Failure;Duodenal Ulcer Perforation;Hepatocellular Injury","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"63 YR","Sender":"Bayer","Concomitant.Product.Names":"Metoprolol"}
{"Case.ID":3710743,"Initial.FDA.Received.Date":"09/18/2001","days.since.last.fda":1,"Event.Date":"07/28/2001","Latest.FDA.Received.Date":"18-SEP-2001","Suspect.Product.Names":"Herbesser","Suspect.Product.Active.Ingredients":"Diltiazem Hydrochloride","Reason.for.Use":"Angina Pectoris","Reactions":"Stevens-Johnson Syndrome;Chest Discomfort;Ventricular Tachycardia;Renal Failure;Face Oedema;Blood Creatine Phosphokinase Increased;Cardio-Respiratory Arrest;Haemorrhage;Blood Lactate Dehydrogenase Increased;Decreased Appetite","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"88 YR","Sender":"Biovail","Concomitant.Product.Names":"-"}
{"Case.ID":3710680,"Initial.FDA.Received.Date":"09/18/2001","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"18-SEP-2001","Suspect.Product.Names":"Ciprofloxacin Extended-Release","Suspect.Product.Active.Ingredients":"Ciprofloxacin\\Ciprofloxacin Hydrochloride","Reason.for.Use":"-","Reactions":"Blood Urea Increased;Stevens-Johnson Syndrome;Renal Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"55 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":3714280,"Initial.FDA.Received.Date":"09/20/2001","days.since.last.fda":2,"Event.Date":"08/11/2001","Latest.FDA.Received.Date":"20-SEP-2001","Suspect.Product.Names":"Zaroxolyn;Ceftin","Suspect.Product.Active.Ingredients":"Cefuroxime Axetil;Metolazone;Allopurinol","Reason.for.Use":"Cardiac Failure Congestive;Gout;Pyrexia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"-","Concomitant.Product.Names":"Reglan;Maalox Antacid;Prevacid;Aspirin;Levothyroxine;Lotrisone;Humulin 70/30;Celexa;Lasix;Metoprolol;Morphine Sulfate;Cardura;Magnesium Hydroxide;Quinine Sulfate;Phenergan;Epogen;Zocor"}
{"Case.ID":3715882,"Initial.FDA.Received.Date":"09/24/2001","days.since.last.fda":4,"Event.Date":"08/26/2001","Latest.FDA.Received.Date":"20-DEC-2001","Suspect.Product.Names":"Voltaren;Kerlone","Suspect.Product.Active.Ingredients":"Betaxolol Hydrochloride;Trapidil;Cefotiam Hydrochloride;Diclofenac Sodium;Imidapril Hydrochloride","Reason.for.Use":"Angina Pectoris;Hypertension;Pyrexia","Reactions":"Malaise;Rash;Dyspnoea Exertional;Drug Eruption;Oedema Peripheral;Erythema;Multiple Organ Dysfunction Syndrome;Renal Failure;Pruritus;Wheezing;Dizziness;Anal Incontinence;Liver Disorder;Heart Rate Increased;Hepatic Function Abnormal;Face Oedema;Blood Pressure Increased;Abdominal Distension;Dermatitis;Pyrexia;Cardiac Failure;Respiratory Failure;Drug Hypersensitivity;Somnolence;Coma;Stevens-Johnson Syndrome;Cardio-Respiratory Arrest;Gastrointestinal Sounds Abnormal;Anuria;Vertigo;Eyelid Oedema;Cyanosis;Productive Cough","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"Novartis","Concomitant.Product.Names":"Teprenone;Unspecified Ingredient"}
{"Case.ID":3715044,"Initial.FDA.Received.Date":"09/24/2001","days.since.last.fda":0,"Event.Date":"08/11/2001","Latest.FDA.Received.Date":"24-SEP-2001","Suspect.Product.Names":"Ceftin;Zaroxolyn","Suspect.Product.Active.Ingredients":"Metolazone;Cefuroxime Axetil;Allopurinol","Reason.for.Use":"Cardiac Failure Congestive;Gout;Pyrexia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"-","Concomitant.Product.Names":"Quinine Sulfate;Lotrisone;Magnesium Hydroxide;Levothyroxine;Clonidine;Metoprolol;Prevacid;Isosorbide Mononitrate;Aspirin;Phenergan;Cardura;Celexa;Maalox Antacid;Zocor;Lasix;Humulin 70/30;Epogen;Allopurinol"}
{"Case.ID":3728421,"Initial.FDA.Received.Date":"11/13/2001","days.since.last.fda":50,"Event.Date":"10/07/2000","Latest.FDA.Received.Date":"13-NOV-2001","Suspect.Product.Names":"Embolex;Novalgin (Metamizole Sodium);Aldactone;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Potassium Chloride;Omeprazole;Gentamicin Sulfate;Torsemide;Meropenem;Fentanyl;Acetylcysteine;Propofol;Spironolactone;Metamizole Sodium;Cefotiam Hydrochloride;Ceftazidime;Dihydroergotamine Mesylate\\Heparin Sodium\\Lidocaine Hydrochloride;Ketamine Hydrochloride;Clonidine Hydrochloride;Erythromycin;Enoxaparin Sodium;Ceruletide Diethylamine;Insulin Nos;Amphotericin B;Theophylline Anhydrous;Sodium Selenite;Lactulose;Vancomycin;Ofloxacin;Midazolam Hydrochloride;Hydrocortisone","Reason.for.Use":"Ascites;Bronchitis Chronic;Constipation;Dyspepsia;Gastrointestinal Disorder;Hyperglycaemia;Nutritional Supplementation;Oedema;Pain;Prophylaxis;Pyrexia;Sedation;Sepsis;Thrombosis Prophylaxis;Unevaluable Event","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"51 YR","Sender":"Roche","Concomitant.Product.Names":"Dulcolax (Bisacodyl)"}
{"Case.ID":6375961,"Initial.FDA.Received.Date":"11/20/2001","days.since.last.fda":7,"Event.Date":"10/16/2001","Latest.FDA.Received.Date":"20-NOV-2001","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampiroxicam;Levofloxacin","Reason.for.Use":"Rheumatoid Arthritis;Urinary Tract Infection","Reactions":"Thrombocytopenia;Stevens-Johnson Syndrome;Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"76 YR","Sender":"Rw Johnson","Concomitant.Product.Names":"Lansoprazole"}
{"Case.ID":3739416,"Initial.FDA.Received.Date":"11/28/2001","days.since.last.fda":8,"Event.Date":"10/07/2000","Latest.FDA.Received.Date":"28-NOV-2001","Suspect.Product.Names":"Duragesic;Lasix;Novalgin (Metamizole Sodium)","Suspect.Product.Active.Ingredients":"Metamizole Sodium;Furosemide;Insulin Nos;Ofloxacin;Fentanyl;Enoxaparin Sodium;Acetylcysteine;Midazolam Maleate;Meropenem;Gentamicin Sulfate;Erythromycin;Hydrocortisone;Propofol;Cefotiam Hydrochloride","Reason.for.Use":"Bronchitis Chronic;Hyperglycaemia;Infection;Injection;Oedema;Pain;Prophylaxis;Pyrexia;Skin Disorder","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"51 YR","Sender":"Janssen","Concomitant.Product.Names":"Amphotericin B;Aldactone;Omeprazole;Embolex;Lactulose;Fentanyl;Dulcolax (Bisacodyl);Vancomycin"}
{"Case.ID":6629275,"Initial.FDA.Received.Date":"12/04/2001","days.since.last.fda":6,"Event.Date":"09/13/2000","Latest.FDA.Received.Date":"04-DEC-2001","Suspect.Product.Names":"Advil;Piperacillin And Tazobactam;Diflucan;Fragmin;Lasix;Aredia;Novalgin (Metamizole Sodium)","Suspect.Product.Active.Ingredients":"Amphotericin B;Metoprolol Succinate;Metamizole Sodium;Piperacillin Sodium;Pamidronate Disodium;Human Immunoglobulin G;Dexamethasone;Furosemide;Heparin Sodium;Acetaminophen;Sulbactam Sodium;Oxazepam;Dalteparin Sodium;Fluconazole;Meropenem;Piperacillin Sodium\\Tazobactam Sodium;Fentanyl;Allopurinol;Ibuprofen;Norepinephrine Hydrochloride-C 11;Citric Acid Monohydrate\\Potassium Bicarbonate\\Potassium Citrate;Methotrexate;Cytarabine;Valerian Extract;Lormetazepam","Reason.for.Use":"Arrhythmia;Coagulopathy;Diarrhoea;Fungal Infection;Hypercalcaemia;Hyperuricaemia;Hypokalaemia;Lymphoma;Oedema;Pain;Pneumonia;Prophylaxis;Pyrexia;Sedation;Sepsis;Sleep Disorder;Ulcer","Reactions":"Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"45 YR","Sender":"Lederle","Concomitant.Product.Names":"Omeprazole;Voltaren"}
{"Case.ID":3739018,"Initial.FDA.Received.Date":"12/10/2001","days.since.last.fda":6,"Event.Date":"09/13/2000","Latest.FDA.Received.Date":"10-DEC-2001","Suspect.Product.Names":"Heparin;Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Sulbactam;Heparin Sodium;Cytarabine","Reason.for.Use":"Pneumonia;Systemic Mycosis","Reactions":"Diarrhoea;Stevens-Johnson Syndrome;Oedema;Renal Failure;Genital Ulceration;Sepsis;Epidermolysis;Salmonellosis;Gastroenteritis;Arrhythmia;Multiple Organ Dysfunction Syndrome;Hyperuricaemia;Sedation;Systemic Mycosis;Hypercalcaemia;Pneumonia;Rash;Pyrexia;Sleep Disorder;Pain;Conjunctivitis;Hypokalaemia;Erythema","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"44 YR","Sender":"Pfizer","Concomitant.Product.Names":"Aredia;Allopurinol;Metoprolol Succinate;Levofloxacin;Loperamide;Voltaren;Fragmin;Lasix;Dexamethasone;Omeprazole;Unspecified Ingredient;Heparin;Fentanyl;Novalgin (Metamizole Sodium);Ibuprofen"}
{"Case.ID":3746314,"Initial.FDA.Received.Date":"12/27/2001","days.since.last.fda":17,"Event.Date":"05/12/2001","Latest.FDA.Received.Date":"27-DEC-2001","Suspect.Product.Names":"Pantozol;Heparin;Mcp","Suspect.Product.Active.Ingredients":"Metoclopramide Hydrochloride;Dimethindene Maleate;Heparin Sodium;Prednisolone Sodium Succinate;Dimenhydrinate;Ciprofloxacin Hydrochloride;Pantoprazole Sodium;Mezlocillin Sodium;Loperamide Hydrochloride;Pentazocine;Omeprazole;Hymecromone;Etilefrine Hydrochloride;Metronidazole","Reason.for.Use":"Cholangitis","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Cardiac Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":3747972,"Initial.FDA.Received.Date":"12/31/2001","days.since.last.fda":4,"Event.Date":"08/01/2000","Latest.FDA.Received.Date":"02-JUL-2003","Suspect.Product.Names":"Pepcid","Suspect.Product.Active.Ingredients":"Famotidine","Reason.for.Use":"-","Reactions":"Arteriosclerosis;Urinary Tract Infection;Gastrointestinal Candidiasis;Cardiomegaly;Nephrosclerosis;Pneumonia;Disseminated Intravascular Coagulation;Haemorrhagic Diathesis;Stevens-Johnson Syndrome;Ulcer Haemorrhage;Jaundice;Alveolitis;Lung Abscess;Haemophagocytic Lymphohistiocytosis;Hepatic Necrosis;Pancytopenia;Bone Marrow Failure;Sepsis;Biopsy Bone Marrow Abnormal;Immune System Disorder;Prostatitis;Myocarditis;Adrenal Insufficiency","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Merck","Concomitant.Product.Names":"Bufferin;Carbocysteine;Cefcapene Pivoxil Hydrochloride;Voltaren"}
{"Case.ID":3744674,"Initial.FDA.Received.Date":"01/02/2002","days.since.last.fda":2,"Event.Date":"08/20/2001","Latest.FDA.Received.Date":"02-JAN-2002","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome;Liver Function Test Abnormal","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"50 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3747010,"Initial.FDA.Received.Date":"01/04/2002","days.since.last.fda":2,"Event.Date":"11/07/2001","Latest.FDA.Received.Date":"04-JAN-2002","Suspect.Product.Names":"Promethazine","Suspect.Product.Active.Ingredients":"Promethazine Hydrochloride;Morphine","Reason.for.Use":"Procedural Pain;Pruritus","Reactions":"Acute Respiratory Distress Syndrome;Seizure;Stevens-Johnson Syndrome;Sepsis;Purpura;Pulmonary Embolism;Hepatomegaly;Acute Kidney Injury;Pulmonary Congestion;Pneumonia;Hypoxia;Blister;Pulmonary Oedema;Pruritus;Electroencephalogram Abnormal;Disseminated Intravascular Coagulation;Respiratory Distress","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"31 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4055212,"Initial.FDA.Received.Date":"01/15/2002","days.since.last.fda":11,"Event.Date":"09/06/2001","Latest.FDA.Received.Date":"15-JAN-2002","Suspect.Product.Names":"Bactrim Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Mouth Haemorrhage","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7653106,"Initial.FDA.Received.Date":"01/18/2002","days.since.last.fda":3,"Event.Date":"08/01/2000","Latest.FDA.Received.Date":"25-JAN-2002","Suspect.Product.Names":"Gaster;Voltaren;Bufferin","Suspect.Product.Active.Ingredients":"Aspirin;Diclofenac Sodium;Carbocysteine;Famotidine;Cefcapene Pivoxil Hydrochloride","Reason.for.Use":"Cerebral Infarction;Pyrexia;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Mucosal Erosion;Disseminated Intravascular Coagulation;Haemophagocytic Lymphohistiocytosis;Erythema Multiforme;Asthenia;Malaise;Pancytopenia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Novartis","Concomitant.Product.Names":"Arbekacin Sulfate;Vancomycin Hydrochloride;Minocycline Hydrochloride"}
{"Case.ID":3750872,"Initial.FDA.Received.Date":"01/23/2002","days.since.last.fda":5,"Event.Date":"05/08/2001","Latest.FDA.Received.Date":"25-JAN-2002","Suspect.Product.Names":"Haldol;Aldactone;Pantozol;Albumin (Human);Placebo","Suspect.Product.Active.Ingredients":"Unspecified Ingredient;Albumin Human;Magnesium Aspartate\\Potassium Aspartate;Midazolam Maleate;Cholestyramine;Sodium;Pantoprazole Sodium;Spironolactone;Haloperidol;Ornithine;Melperone;Biotin\\Vitamin B Complex;Glucose, Liquid\\Magnesium Chloride\\Potassium Phosphate, Monobasic\\Sodium Acetate\\Sodium Chloride;Lactulose;Torsemide;Temazepam","Reason.for.Use":"Constipation;Dehydration;Hepatic Cirrhosis;Hyperlipidaemia;Hypertension;Hypokalaemia;Parenteral Nutrition;Prophylaxis;Restlessness;Sedation;Sleep Disorder;Vitamin B Complex Deficiency","Reactions":"Pneumonia;Toxic Epidermal Necrolysis;Infection;Acute Respiratory Distress Syndrome;Respiratory Failure;Stevens-Johnson Syndrome;Enanthema","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"53 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":3759716,"Initial.FDA.Received.Date":"01/31/2002","days.since.last.fda":8,"Event.Date":"10/25/2001","Latest.FDA.Received.Date":"31-JAN-2002","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Seizure","Reactions":"Thrombocytopenia;Asthenia;Vomiting;Dehydration;Hallucination;Neutropenia;Renal Failure;Coagulopathy;Bronchitis;Seizure;Mental Status Changes;Stevens-Johnson Syndrome;Rhabdomyolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"44 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3785092,"Initial.FDA.Received.Date":"02/05/2002","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"05-FEB-2002","Suspect.Product.Names":"Toradol","Suspect.Product.Active.Ingredients":"Ketorolac Tromethamine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"Coumadin"}
{"Case.ID":3770501,"Initial.FDA.Received.Date":"02/28/2002","days.since.last.fda":23,"Event.Date":"","Latest.FDA.Received.Date":"28-FEB-2002","Suspect.Product.Names":"Omnipaque","Suspect.Product.Active.Ingredients":"Iohexol","Reason.for.Use":"Renal Impairment","Reactions":"Renal Impairment;Eye Disorder;Skin Necrosis;Ulcer;Stevens-Johnson Syndrome;Klebsiella Infection;Vasculitis;Periorbital Oedema;Sepsis;Peritoneal Dialysis;Haemorrhage;Pulmonary Oedema;Condition Aggravated","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"-","Concomitant.Product.Names":"Hydralazine;Atenolol"}
{"Case.ID":3778575,"Initial.FDA.Received.Date":"03/29/2002","days.since.last.fda":29,"Event.Date":"12/08/2001","Latest.FDA.Received.Date":"29-MAR-2002","Suspect.Product.Names":"Geodon","Suspect.Product.Active.Ingredients":"Ziprasidone Hydrochloride\\Ziprasidone Mesylate","Reason.for.Use":"-","Reactions":"Hepatic Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"29 YR","Sender":"-","Concomitant.Product.Names":"Paxil;Coumadin"}
{"Case.ID":6115171,"Initial.FDA.Received.Date":"04/22/2002","days.since.last.fda":24,"Event.Date":"03/06/2002","Latest.FDA.Received.Date":"22-APR-2002","Suspect.Product.Names":"Lendorm","Suspect.Product.Active.Ingredients":"Brotizolam;Zonisamide","Reason.for.Use":"Epilepsy","Reactions":"Stevens-Johnson Syndrome;Acute Respiratory Distress Syndrome;Staphylococcal Sepsis;Pulmonary Oedema;Hypophagia;Dialysis;Cardiac Failure Congestive;Renal Impairment","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"Elan","Concomitant.Product.Names":"Aldactone;Loxoprofen Sodium;Depakene;Isosorbide Dinitrate;Enalapril Maleate;Lasix;Allopurinol;Digoxin"}
{"Case.ID":3792393,"Initial.FDA.Received.Date":"05/07/2002","days.since.last.fda":15,"Event.Date":"12/06/2000","Latest.FDA.Received.Date":"07-MAY-2002","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Aspirin;Furosemide;Ciprofloxacin Hydrochloride;Acetaminophen","Reason.for.Use":"Cardiac Failure;Pyrexia;Respiratory Tract Infection","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Renal Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Bayer","Concomitant.Product.Names":"Dulcolax (Bisacodyl);Lactulose;Benserazide Hydrochloride\\Levodopa"}
{"Case.ID":3792847,"Initial.FDA.Received.Date":"05/08/2002","days.since.last.fda":1,"Event.Date":"11/08/2000","Latest.FDA.Received.Date":"08-MAY-2002","Suspect.Product.Names":"Glucobay;Lasix;Amaryl","Suspect.Product.Active.Ingredients":"Glimepiride;Furosemide;Sulfamethoxazole\\Trimethoprim;Dimenhydrinate;Allopurinol;Sucralfate;Amoxicillin\\Clavulanate Potassium;Acarbose;Etilefrine Hydrochloride;Ciprofloxacin Hydrochloride","Reason.for.Use":"Cardiac Failure;Diabetes Mellitus;Hyperuricaemia;Hypotonia;Prophylaxis;Ulcer;Urinary Tract Infection;Vomiting","Reactions":"Multiple Organ Dysfunction Syndrome;Vomiting;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Bayer","Concomitant.Product.Names":"Captopril;Marcumar;Omeprazole;Novodigal (.Beta.-Acetyldigoxin);Isoptin"}
{"Case.ID":3796424,"Initial.FDA.Received.Date":"05/22/2002","days.since.last.fda":14,"Event.Date":"04/08/2002","Latest.FDA.Received.Date":"22-MAY-2002","Suspect.Product.Names":"Procrit","Suspect.Product.Active.Ingredients":"Erythropoietin","Reason.for.Use":"-","Reactions":"Hypersensitivity;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"75 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3801544,"Initial.FDA.Received.Date":"06/06/2002","days.since.last.fda":15,"Event.Date":"04/28/2002","Latest.FDA.Received.Date":"06-JUN-2002","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital;Meropenem;Levofloxacin","Reason.for.Use":"Pyrexia;Seizure","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"Omeprazole;Atorvastatin;Plavix;Rivotril"}
{"Case.ID":3813172,"Initial.FDA.Received.Date":"06/28/2002","days.since.last.fda":22,"Event.Date":"06/15/2000","Latest.FDA.Received.Date":"01-JUL-2002","Suspect.Product.Names":"Tavor (Lorazepam)","Suspect.Product.Active.Ingredients":"Lorazepam;Phenytoin","Reason.for.Use":"Affective Disorder;Epilepsy","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"65 YR","Sender":"Wyeth","Concomitant.Product.Names":"Pantozol;Captopril;Dexamethasone"}
{"Case.ID":6689156,"Initial.FDA.Received.Date":"07/09/2002","days.since.last.fda":11,"Event.Date":"04/21/2002","Latest.FDA.Received.Date":"09-JUL-2002","Suspect.Product.Names":"Tegretol;Inderal;Antabuse;Aldactone","Suspect.Product.Active.Ingredients":"Spironolactone;Disulfiram;Propranolol Hydrochloride;Carbamazepine;Chlorprothixene Hydrochloride;Lansoprazole","Reason.for.Use":"-","Reactions":"Epidermolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"61 YR","Sender":"Pharmacia","Concomitant.Product.Names":"-"}
{"Case.ID":3834359,"Initial.FDA.Received.Date":"08/27/2002","days.since.last.fda":49,"Event.Date":"05/13/2002","Latest.FDA.Received.Date":"27-AUG-2002","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3837032,"Initial.FDA.Received.Date":"08/28/2002","days.since.last.fda":1,"Event.Date":"06/10/2002","Latest.FDA.Received.Date":"27-SEP-2002","Suspect.Product.Names":"Rifadin","Suspect.Product.Active.Ingredients":"Rifampin;Acetaminophen;Isoniazid","Reason.for.Use":"Pleural Infection;Tuberculosis","Reactions":"Stevens-Johnson Syndrome;Platelet Count Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Aventis","Concomitant.Product.Names":"Nystatin;Pancreatin"}
{"Case.ID":3838308,"Initial.FDA.Received.Date":"09/05/2002","days.since.last.fda":8,"Event.Date":"12/17/1999","Latest.FDA.Received.Date":"05-SEP-2002","Suspect.Product.Names":"Dolobid","Suspect.Product.Active.Ingredients":"Diflunisal","Reason.for.Use":"-","Reactions":"Night Sweats;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3850021,"Initial.FDA.Received.Date":"10/07/2002","days.since.last.fda":32,"Event.Date":"","Latest.FDA.Received.Date":"07-OCT-2002","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Hypersensitivity;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":3856748,"Initial.FDA.Received.Date":"10/18/2002","days.since.last.fda":11,"Event.Date":"12/25/2001","Latest.FDA.Received.Date":"18-OCT-2002","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"27 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":3859571,"Initial.FDA.Received.Date":"10/29/2002","days.since.last.fda":11,"Event.Date":"08/23/2002","Latest.FDA.Received.Date":"07-NOV-2002","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Breast Cancer Female","Reactions":"Oxygen Saturation Decreased;Stomatitis;Leukopenia;Stevens-Johnson Syndrome;Pneumonia Aspiration;Seizure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"59 YR","Sender":"Lederle","Concomitant.Product.Names":"Fluorouracil;Cyclophosphamide"}
{"Case.ID":3860782,"Initial.FDA.Received.Date":"11/05/2002","days.since.last.fda":7,"Event.Date":"11/07/2000","Latest.FDA.Received.Date":"05-NOV-2002","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Cerebrovascular Accident","Reactions":"Candida Infection;Stevens-Johnson Syndrome;Pneumonia;Renal Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"51 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3873112,"Initial.FDA.Received.Date":"11/29/2002","days.since.last.fda":24,"Event.Date":"05/01/2002","Latest.FDA.Received.Date":"29-NOV-2002","Suspect.Product.Names":"Zonegran","Suspect.Product.Active.Ingredients":"Zonisamide","Reason.for.Use":"Neuropathy Peripheral","Reactions":"Dizziness;Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome;Balance Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"58 YR","Sender":"Elan","Concomitant.Product.Names":"Ambien;Vioxx;Estradiol"}
{"Case.ID":3873056,"Initial.FDA.Received.Date":"12/04/2002","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"04-DEC-2002","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin;Phenobarbital","Reason.for.Use":"-","Reactions":"Infection;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"52 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3870209,"Initial.FDA.Received.Date":"12/09/2002","days.since.last.fda":5,"Event.Date":"01/01/2002","Latest.FDA.Received.Date":"03-APR-2003","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Bipolar Disorder","Reactions":"Stevens-Johnson Syndrome;Overdose;Medication Error","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"8 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Celexa;Depakote;Risperdal"}
{"Case.ID":3904513,"Initial.FDA.Received.Date":"02/07/2003","days.since.last.fda":60,"Event.Date":"","Latest.FDA.Received.Date":"07-FEB-2003","Suspect.Product.Names":"Celebrex","Suspect.Product.Active.Ingredients":"Celecoxib","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Pharmacia And Upjohn","Concomitant.Product.Names":"-"}
{"Case.ID":3906066,"Initial.FDA.Received.Date":"02/13/2003","days.since.last.fda":6,"Event.Date":"07/03/2002","Latest.FDA.Received.Date":"06-MAR-2003","Suspect.Product.Names":"Fludara","Suspect.Product.Active.Ingredients":"Fludarabine Phosphate;Levofloxacin","Reason.for.Use":"Lymphoma;Pneumonia","Reactions":"Stevens-Johnson Syndrome;Pneumonia;Sepsis;Therapeutic Product Effect Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"Berlex","Concomitant.Product.Names":"-"}
{"Case.ID":3916329,"Initial.FDA.Received.Date":"03/07/2003","days.since.last.fda":22,"Event.Date":"02/08/2003","Latest.FDA.Received.Date":"07-MAR-2003","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Depression","Reactions":"Nausea;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"55 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3918992,"Initial.FDA.Received.Date":"03/11/2003","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"11-MAR-2003","Suspect.Product.Names":"Bextra","Suspect.Product.Active.Ingredients":"Valdecoxib","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"100 YR","Sender":"Pharmacia","Concomitant.Product.Names":"-"}
{"Case.ID":6637769,"Initial.FDA.Received.Date":"04/28/2003","days.since.last.fda":48,"Event.Date":"04/24/2003","Latest.FDA.Received.Date":"28-APR-2003","Suspect.Product.Names":"Rocephin","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium","Reason.for.Use":"Cellulitis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"-","Concomitant.Product.Names":"Aspirin;Prednisone;Lasix"}
{"Case.ID":3959537,"Initial.FDA.Received.Date":"06/12/2003","days.since.last.fda":45,"Event.Date":"","Latest.FDA.Received.Date":"12-JUN-2003","Suspect.Product.Names":"Avelox","Suspect.Product.Active.Ingredients":"Moxifloxacin Hydrochloride","Reason.for.Use":"Bronchitis","Reactions":"Stevens-Johnson Syndrome;Liver Transplant;Dialysis;Pyrexia;Hepatic Failure;Abdominal Pain;Rash;Liver Function Test Abnormal;Toxic Epidermal Necrolysis;Cardiac Failure;Jaundice","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"23 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3973962,"Initial.FDA.Received.Date":"07/16/2003","days.since.last.fda":34,"Event.Date":"01/01/2003","Latest.FDA.Received.Date":"16-JUL-2003","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Diverticulitis","Reactions":"Hepatic Failure;Sepsis;Stevens-Johnson Syndrome;Gastrointestinal Perforation;Jaundice;Renal Failure;Drug Ineffective","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"44 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":3985990,"Initial.FDA.Received.Date":"08/06/2003","days.since.last.fda":21,"Event.Date":"08/03/2003","Latest.FDA.Received.Date":"06-AUG-2003","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Non-Small Cell Lung Cancer;Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"63 YR","Sender":"-","Concomitant.Product.Names":"Septra Ds"}
{"Case.ID":3986030,"Initial.FDA.Received.Date":"08/18/2003","days.since.last.fda":12,"Event.Date":"","Latest.FDA.Received.Date":"18-AUG-2003","Suspect.Product.Names":"Rocephin","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"85 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":3991736,"Initial.FDA.Received.Date":"08/25/2003","days.since.last.fda":7,"Event.Date":"03/16/2003","Latest.FDA.Received.Date":"25-AUG-2003","Suspect.Product.Names":"Cotrimoxazole","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Urinary Tract Infection","Reactions":"Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"66 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4009925,"Initial.FDA.Received.Date":"09/22/2003","days.since.last.fda":28,"Event.Date":"","Latest.FDA.Received.Date":"22-SEP-2003","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Nevirapine;Unspecified Ingredient","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":4014639,"Initial.FDA.Received.Date":"09/23/2003","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"01-OCT-2003","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Citalopram Hydrobromide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Dermatitis Allergic;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"Forest","Concomitant.Product.Names":"-"}
{"Case.ID":4014695,"Initial.FDA.Received.Date":"10/01/2003","days.since.last.fda":8,"Event.Date":"09/10/2003","Latest.FDA.Received.Date":"23-OCT-2003","Suspect.Product.Names":"Rifadin","Suspect.Product.Active.Ingredients":"Rifampin;Isoniazid","Reason.for.Use":"Tuberculosis","Reactions":"Oculomucocutaneous Syndrome;Stevens-Johnson Syndrome;Blood Alkaline Phosphatase Increased;Circulatory Collapse;Encephalopathy;Visual Impairment;Pyrexia;Cardio-Respiratory Arrest;Cor Pulmonale Acute;Blood Bicarbonate;Blood Pressure Measurement","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"38 YR","Sender":"Aventis","Concomitant.Product.Names":"Aspirin;Pyrazinamide;Ethambutol Hydrochloride"}
{"Case.ID":4017168,"Initial.FDA.Received.Date":"10/07/2003","days.since.last.fda":6,"Event.Date":"08/01/2003","Latest.FDA.Received.Date":"26-DEC-2003","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lansoprazole","Reason.for.Use":"Gastritis;Post Procedural Complication","Reactions":"Medication Error;Multiple Organ Dysfunction Syndrome;Hypersensitivity;Stevens-Johnson Syndrome;Cardiac Arrest","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"Wyeth","Concomitant.Product.Names":"-"}
{"Case.ID":4018832,"Initial.FDA.Received.Date":"10/29/2003","days.since.last.fda":22,"Event.Date":"","Latest.FDA.Received.Date":"24-NOV-2003","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":4021700,"Initial.FDA.Received.Date":"11/04/2003","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"04-NOV-2003","Suspect.Product.Names":"Lamisil","Suspect.Product.Active.Ingredients":"Terbinafine Hydrochloride","Reason.for.Use":"Onychomycosis","Reactions":"Rash;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":4029994,"Initial.FDA.Received.Date":"11/07/2003","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"07-NOV-2003","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4047988,"Initial.FDA.Received.Date":"12/18/2003","days.since.last.fda":41,"Event.Date":"10/04/2003","Latest.FDA.Received.Date":"18-DEC-2003","Suspect.Product.Names":"Levaquin","Suspect.Product.Active.Ingredients":"Levofloxacin","Reason.for.Use":"Asthma;Bronchitis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"57 YR","Sender":"-","Concomitant.Product.Names":"Baclofen;Hydrochlorothiazide;Diltiazem;Allopurinol Sodium;Metoclopramide;Kcl;Warfarin Sodium;Carbamazepine"}
{"Case.ID":4082979,"Initial.FDA.Received.Date":"01/29/2004","days.since.last.fda":42,"Event.Date":"","Latest.FDA.Received.Date":"29-JAN-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4092314,"Initial.FDA.Received.Date":"02/11/2004","days.since.last.fda":13,"Event.Date":"10/20/2003","Latest.FDA.Received.Date":"30-MAR-2004","Suspect.Product.Names":"Neupogen;Imodium;Fludara","Suspect.Product.Active.Ingredients":"Fludarabine Phosphate;Loperamide Hydrochloride;Cyclophosphamide;Filgrastim;Allopurinol","Reason.for.Use":"Lymphoma","Reactions":"Rash Papular;Dermatitis Exfoliative;Feeling Cold;Pancytopenia;Rash Erythematous;Stevens-Johnson Syndrome;Neoplasm Malignant;General Physical Health Deterioration;Pneumocystis Jirovecii Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"Berlex","Concomitant.Product.Names":"-"}
{"Case.ID":4090141,"Initial.FDA.Received.Date":"02/18/2004","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"27-APR-2006","Suspect.Product.Names":"Lamisil;Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine;Terbinafine Hydrochloride","Reason.for.Use":"Fungal Infection;Product Used For Unknown Indication","Reactions":"Medication Error;Stevens-Johnson Syndrome;Product Dispensing Error","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":4104953,"Initial.FDA.Received.Date":"03/08/2004","days.since.last.fda":19,"Event.Date":"02/12/2004","Latest.FDA.Received.Date":"08-MAR-2004","Suspect.Product.Names":"Ciprofloxacin Extended-Release;Zosyn","Suspect.Product.Active.Ingredients":"Ciprofloxacin\\Ciprofloxacin Hydrochloride;Piperacillin Sodium\\Tazobactam Sodium","Reason.for.Use":"Pneumonia Pseudomonal","Reactions":"Sepsis;Therapy Non-Responder;Organ Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"-","Concomitant.Product.Names":"Digoxin;Cordarone;Vitamins;Procrit;Altace;Zetia;Rifampin;Zithromax;Vancomycin;Megace;Dopamine;Flomax;Cardizem;Claforan;Ferrous Sulfate;Protonix;Plavix;Lovenox;Combivent;Gentamicin"}
{"Case.ID":4117157,"Initial.FDA.Received.Date":"03/25/2004","days.since.last.fda":17,"Event.Date":"01/30/2004","Latest.FDA.Received.Date":"25-MAR-2004","Suspect.Product.Names":"Amoxicillin And Clavulanate Potassium","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium;Dapsone","Reason.for.Use":"Infection Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"45 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4121365,"Initial.FDA.Received.Date":"03/30/2004","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"19-APR-2004","Suspect.Product.Names":"Amoxil","Suspect.Product.Active.Ingredients":"Amoxicillin","Reason.for.Use":"Pneumonia Pneumococcal","Reactions":"Drug Hypersensitivity;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Erythromycin;Prednisone"}
{"Case.ID":4146934,"Initial.FDA.Received.Date":"05/20/2004","days.since.last.fda":51,"Event.Date":"04/26/2004","Latest.FDA.Received.Date":"20-MAY-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Lung Disorder;Stevens-Johnson Syndrome;Infection;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":4168609,"Initial.FDA.Received.Date":"06/30/2004","days.since.last.fda":41,"Event.Date":"","Latest.FDA.Received.Date":"30-JUN-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Leucovorin;Fluorouracil","Reason.for.Use":"Colon Cancer","Reactions":"Diarrhoea;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Mayne","Concomitant.Product.Names":"-"}
{"Case.ID":4187090,"Initial.FDA.Received.Date":"08/09/2004","days.since.last.fda":40,"Event.Date":"07/29/2004","Latest.FDA.Received.Date":"01-DEC-2004","Suspect.Product.Names":"Lasix;Diovan;Rocaltrol;Atarax","Suspect.Product.Active.Ingredients":"Fursultiamine;Hydroxyzine Hydrochloride;Calcitriol;Mosapride;Valsartan;Dietary Supplement\\Probiotics;Furosemide;Norucholic Acid;Ammonium Glycyrrhizate;Brotizolam","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Haematocrit Decreased;White Blood Cell Count Increased;Skin Abrasion;Blood Urea Increased;General Physical Health Deterioration;Hypophagia;Sepsis;Pruritus;Blood Albumin Decreased;Platelet Count Decreased;Erythema","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Aventis","Concomitant.Product.Names":"Unspecified Ingredient;Albumin Human"}
{"Case.ID":4199467,"Initial.FDA.Received.Date":"08/13/2004","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"27-AUG-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Acute Lymphocytic Leukaemia","Reactions":"Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"37 YR","Sender":"Mayne","Concomitant.Product.Names":"-"}
{"Case.ID":4202148,"Initial.FDA.Received.Date":"08/24/2004","days.since.last.fda":11,"Event.Date":"11/23/2002","Latest.FDA.Received.Date":"24-AUG-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital;Minocycline Hydrochloride","Reason.for.Use":"Pneumonia;Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Lederle","Concomitant.Product.Names":"Depakene;Diovan"}
{"Case.ID":4197849,"Initial.FDA.Received.Date":"08/27/2004","days.since.last.fda":3,"Event.Date":"01/01/2004","Latest.FDA.Received.Date":"27-AUG-2004","Suspect.Product.Names":"Zyban","Suspect.Product.Active.Ingredients":"Bupropion Hydrochloride","Reason.for.Use":"Ex-Tobacco User","Reactions":"Death;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":5665339,"Initial.FDA.Received.Date":"10/01/2004","days.since.last.fda":35,"Event.Date":"08/12/2004","Latest.FDA.Received.Date":"16-DEC-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Rituximab","Reason.for.Use":"Non-Hodgkin'S Lymphoma","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"77 YR","Sender":"Genentech","Concomitant.Product.Names":"Allopurinol;Fluconazole;Vincristine Sulfate;Unspecified Ingredient;Prednisolone;Cyclophosphamide"}
{"Case.ID":5651253,"Initial.FDA.Received.Date":"10/25/2004","days.since.last.fda":24,"Event.Date":"","Latest.FDA.Received.Date":"25-OCT-2004","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":5679361,"Initial.FDA.Received.Date":"11/16/2004","days.since.last.fda":22,"Event.Date":"07/23/2004","Latest.FDA.Received.Date":"16-NOV-2004","Suspect.Product.Names":"Avelox","Suspect.Product.Active.Ingredients":"Moxifloxacin Hydrochloride","Reason.for.Use":"Clostridial Infection;Pneumonia;Sepsis;Urinary Tract Infection","Reactions":"Fluid Intake Reduced;Dementia;Sepsis;General Physical Health Deterioration;Pain;Stevens-Johnson Syndrome;Hypophagia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"92 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5688511,"Initial.FDA.Received.Date":"11/24/2004","days.since.last.fda":8,"Event.Date":"10/29/2004","Latest.FDA.Received.Date":"24-NOV-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Dermatitis Bullous;Hypotension;Acute Kidney Injury;Gastrointestinal Necrosis;Drug Level Below Therapeutic;Intestinal Infarction;Stevens-Johnson Syndrome;Cardio-Respiratory Arrest","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"58 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5695389,"Initial.FDA.Received.Date":"12/07/2004","days.since.last.fda":13,"Event.Date":"02/04/2003","Latest.FDA.Received.Date":"08-DEC-2004","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital;Phenytoin;Zonisamide","Reason.for.Use":"Epilepsy","Reactions":"Depressed Level Of Consciousness;Dialysis;Erythema;Pyrexia;Acidosis;Therapy Non-Responder;Rash;Acute Respiratory Distress Syndrome;Respiratory Disorder;Gastroenteritis Pseudomonas;Drug Hypersensitivity;Gastroenteritis Staphylococcal;Nasopharyngitis;Hepatic Failure;Acute Kidney Injury;Disseminated Intravascular Coagulation;Leukopenia;Liver Disorder;Condition Aggravated;Enterococcal Infection;Cardiac Arrest;Hypothermia;Seizure;Rectal Haemorrhage;Enteritis;Inflammation;Hyperammonaemia;Stevens-Johnson Syndrome;Septic Shock;Pneumonia Staphylococcal;Pneumonia;Pharyngeal Oedema;Delirium","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"33 YR","Sender":"Eisai","Concomitant.Product.Names":"Cefditoren Pivoxil;Methylcobalamin;Lansoprazole"}
{"Case.ID":5698417,"Initial.FDA.Received.Date":"12/08/2004","days.since.last.fda":1,"Event.Date":"11/22/2004","Latest.FDA.Received.Date":"23-MAY-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Levocarnitine;Lansoprazole","Reason.for.Use":"Gastric Haemorrhage","Reactions":"Pain;Gastric Ulcer Haemorrhage;Anuria;Platelet Aggregation Increased;Confusional State;Transaminases Increased;Blood Pressure Increased;Stevens-Johnson Syndrome;Antithrombin Iii Decreased;Toxic Epidermal Necrolysis;Band Neutrophil Count Increased;Renal Failure;Multi-Organ Disorder;Cardiac Arrest;Pleural Effusion;Asthenia;Anaemia;Blood Cholinesterase Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"42 YR","Sender":"Sigma Tau","Concomitant.Product.Names":"Calcijex;Eprex;Renagel"}
{"Case.ID":5717413,"Initial.FDA.Received.Date":"12/14/2004","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"14-DEC-2004","Suspect.Product.Names":"Bextra","Suspect.Product.Active.Ingredients":"Valdecoxib","Reason.for.Use":"Ill-Defined Disorder","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":5717411,"Initial.FDA.Received.Date":"12/14/2004","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"14-DEC-2004","Suspect.Product.Names":"Bextra","Suspect.Product.Active.Ingredients":"Valdecoxib","Reason.for.Use":"Ill-Defined Disorder","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":5695728,"Initial.FDA.Received.Date":"12/15/2004","days.since.last.fda":1,"Event.Date":"08/31/2004","Latest.FDA.Received.Date":"15-DEC-2004","Suspect.Product.Names":"Rocephin","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium;Allopurinol;Amoxicillin\\Clavulanic Acid","Reason.for.Use":"Pharyngitis;Product Used For Unknown Indication","Reactions":"Nephritis;Pneumonitis;Hypersensitivity;Stevens-Johnson Syndrome;Toxic Skin Eruption;Oedema Peripheral","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"72 YR","Sender":"Roche","Concomitant.Product.Names":"Pravastatin;Sectral;Hydrochlorothiazide\\Valsartan"}
{"Case.ID":5703051,"Initial.FDA.Received.Date":"12/16/2004","days.since.last.fda":1,"Event.Date":"08/21/2002","Latest.FDA.Received.Date":"12-JAN-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin","Reason.for.Use":"Wound Infection Staphylococcal","Reactions":"Lymphocyte Stimulation Test Positive;Pancytopenia;Infection;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"26 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Sulfamethoxazole\\Trimethoprim;Cefcapene Pivoxil Hydrochloride"}
{"Case.ID":5706345,"Initial.FDA.Received.Date":"12/28/2004","days.since.last.fda":12,"Event.Date":"12/25/2004","Latest.FDA.Received.Date":"28-DEC-2004","Suspect.Product.Names":"Levaquin","Suspect.Product.Active.Ingredients":"Levofloxacin;Fluconazole","Reason.for.Use":"Candida Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"75 YR","Sender":"-","Concomitant.Product.Names":"Neulasta"}
{"Case.ID":5710308,"Initial.FDA.Received.Date":"01/07/2005","days.since.last.fda":10,"Event.Date":"06/22/2003","Latest.FDA.Received.Date":"07-JAN-2005","Suspect.Product.Names":"Claritin;Mucomyst;Vastarel","Suspect.Product.Active.Ingredients":"Trimetazidine Dihydrochloride;Potassium Chloride;Acetylcysteine;Furosemide;Loratadine","Reason.for.Use":"Angina Pectoris;Gastritis;Respiratory Disorder;Rhinitis Allergic","Reactions":"Pneumonia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Aventis","Concomitant.Product.Names":"Rabeprazole Sodium"}
{"Case.ID":5720067,"Initial.FDA.Received.Date":"01/10/2005","days.since.last.fda":3,"Event.Date":"11/13/2003","Latest.FDA.Received.Date":"10-JAN-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Enalapril Maleate;Tramadol Hydrochloride;Spironolactone;Furosemide;Pantoprazole Sodium","Reason.for.Use":"Ascites;Gastritis Haemorrhagic;Hypertension;Ill-Defined Disorder","Reactions":"Cardiovascular Disorder;Pulmonary Function Test Decreased;Toxic Epidermal Necrolysis;Renal Failure;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"57 YR","Sender":"Pfizer","Concomitant.Product.Names":"Phytonadione;Lactulose"}
{"Case.ID":5711877,"Initial.FDA.Received.Date":"01/11/2005","days.since.last.fda":1,"Event.Date":"06/10/2001","Latest.FDA.Received.Date":"23-FEB-2005","Suspect.Product.Names":"Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Allopurinol","Reason.for.Use":"Diuretic Therapy;Hypertension;Hyperuricaemia","Reactions":"Urinary Retention;Cardiac Failure;Hyperuricaemia;Renal Failure;Hypertension;Stomatitis;Oculomucocutaneous Syndrome;Blood Ph Decreased;Stevens-Johnson Syndrome;Diarrhoea","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"79 YR","Sender":"Aventis","Concomitant.Product.Names":"Norvasc;Nu-Lotan;Bisoprolol Fumarate"}
{"Case.ID":5768065,"Initial.FDA.Received.Date":"03/18/2005","days.since.last.fda":66,"Event.Date":"03/29/2004","Latest.FDA.Received.Date":"18-MAR-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5763926,"Initial.FDA.Received.Date":"03/23/2005","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"23-MAR-2005","Suspect.Product.Names":"Claforan","Suspect.Product.Active.Ingredients":"Cefotaxime Sodium","Reason.for.Use":"Pneumonia;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Aventis","Concomitant.Product.Names":"Nafronyl Oxalate;Trental;Aspirin;Lormetazepam;Isosorbide Dinitrate;Pantoprazole Sodium;Alfacalcidol;Epoetin Beta;Cardura Xl"}
{"Case.ID":5776674,"Initial.FDA.Received.Date":"04/05/2005","days.since.last.fda":13,"Event.Date":"03/11/2005","Latest.FDA.Received.Date":"26-MAY-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mosapride Citrate;Lansoprazole","Reason.for.Use":"Gastric Ulcer;Vomiting","Reactions":"Stevens-Johnson Syndrome;Gastric Ulcer;Blood Cholesterol Increased;Nephrotic Syndrome;Cardiac Massage","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Takeda","Concomitant.Product.Names":"Lasix;Lisinopril;Novorapid;Primperan"}
{"Case.ID":5776104,"Initial.FDA.Received.Date":"04/14/2005","days.since.last.fda":9,"Event.Date":"01/01/2001","Latest.FDA.Received.Date":"28-APR-2005","Suspect.Product.Names":"Keppra","Suspect.Product.Active.Ingredients":"Levetiracetam;Lamotrigine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":5794816,"Initial.FDA.Received.Date":"05/03/2005","days.since.last.fda":19,"Event.Date":"03/01/2000","Latest.FDA.Received.Date":"03-MAY-2005","Suspect.Product.Names":"Cordarone","Suspect.Product.Active.Ingredients":"Amiodarone Hydrochloride","Reason.for.Use":"Atrial Tachycardia","Reactions":"Sepsis;Toxic Epidermal Necrolysis;Pneumonia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Wyeth","Concomitant.Product.Names":"Diltiazem;Aspirin;Unspecified Ingredient;Sulindac"}
{"Case.ID":5803371,"Initial.FDA.Received.Date":"05/17/2005","days.since.last.fda":14,"Event.Date":"04/01/2005","Latest.FDA.Received.Date":"31-AUG-2005","Suspect.Product.Names":"Avelox","Suspect.Product.Active.Ingredients":"Moxifloxacin Hydrochloride","Reason.for.Use":"-","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"82 YR","Sender":"Bayer","Concomitant.Product.Names":"Cordarone"}
{"Case.ID":5813734,"Initial.FDA.Received.Date":"05/27/2005","days.since.last.fda":10,"Event.Date":"03/14/2005","Latest.FDA.Received.Date":"27-MAY-2005","Suspect.Product.Names":"Prozac;Ritalin;Provigil;Strattera;Effexor Xr","Suspect.Product.Active.Ingredients":"Venlafaxine Hydrochloride;Atomoxetine Hydrochloride;Alprazolam;Modafinil;Methylphenidate Hydrochloride;Fluoxetine Hydrochloride","Reason.for.Use":"-","Reactions":"Sepsis;Diarrhoea;Subarachnoid Haemorrhage;Stevens-Johnson Syndrome;Post Procedural Complication;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"54 YR","Sender":"-","Concomitant.Product.Names":"Caspofungin;Zosyn;Flagyl;Dilaudid;Vancomycin;Dilantin"}
{"Case.ID":5824950,"Initial.FDA.Received.Date":"06/20/2005","days.since.last.fda":24,"Event.Date":"06/14/2005","Latest.FDA.Received.Date":"20-JUN-2005","Suspect.Product.Names":"Nafcillin","Suspect.Product.Active.Ingredients":"Nafcillin Sodium","Reason.for.Use":"Endocarditis Staphylococcal","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"-","Concomitant.Product.Names":"Epogen;Prevacid;Rifampin;Ms Contin;Coumadin;Amitriptyline;Phoslo"}
{"Case.ID":5832099,"Initial.FDA.Received.Date":"06/30/2005","days.since.last.fda":10,"Event.Date":"05/19/2005","Latest.FDA.Received.Date":"30-JUN-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amiodarone","Reason.for.Use":"Atrial Fibrillation","Reactions":"Dermatitis Exfoliative;Stevens-Johnson Syndrome;Pyrexia;Chills;Influenza Like Illness;Pharyngitis;Oropharyngeal Pain;Leukopenia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"66 YR","Sender":"-","Concomitant.Product.Names":"Warfarin Sodium;Hydrocodone;Ramipril;Furosemide;Spironolactone;Carvedilol;Atorvastatin"}
{"Case.ID":5831533,"Initial.FDA.Received.Date":"07/06/2005","days.since.last.fda":6,"Event.Date":"03/15/2005","Latest.FDA.Received.Date":"12-JUL-2005","Suspect.Product.Names":"Colchicine\\Dicyclomine\\Opium","Suspect.Product.Active.Ingredients":"Colchicine\\Dicyclomine Hydrochloride\\Opium;Allopurinol;Fexofenadine Hydrochloride","Reason.for.Use":"-","Reactions":"Lymphadenopathy;Tubulointerstitial Nephritis;Pyrexia;Drug Reaction With Eosinophilia And Systemic Symptoms;Eosinophilia;Stevens-Johnson Syndrome;Hepatomegaly","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"58 YR","Sender":"Aventis","Concomitant.Product.Names":"Indapamide;Valsartan;Amlodipine Besylate"}
{"Case.ID":5846267,"Initial.FDA.Received.Date":"07/15/2005","days.since.last.fda":9,"Event.Date":"06/20/2005","Latest.FDA.Received.Date":"15-JUL-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ceftriaxone;Ceftazidime Sodium","Reason.for.Use":"Osteomyelitis","Reactions":"Stevens-Johnson Syndrome;Clostridium Colitis;Pulse Absent;Cardio-Respiratory Arrest;Neutropenia;Unresponsive To Stimuli;Hypotension;Toxic Epidermal Necrolysis;Pupillary Reflex Impaired;Oculocephalogyric Reflex Absent;Blood Culture Positive;Infection;Pyrexia;Liver Function Test Abnormal","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"-","Concomitant.Product.Names":"Metronidazole;Acetaminophen;Metoprolol;Heparin;Loperamide;Gabapentin;Oxycodone;Nystatin"}
{"Case.ID":5849247,"Initial.FDA.Received.Date":"07/20/2005","days.since.last.fda":5,"Event.Date":"06/07/2005","Latest.FDA.Received.Date":"19-SEP-2005","Suspect.Product.Names":"Avelox","Suspect.Product.Active.Ingredients":"Moxifloxacin Hydrochloride","Reason.for.Use":"Upper Respiratory Tract Infection","Reactions":"Stevens-Johnson Syndrome;Erythema;Skin Laceration;Petechiae;Red Blood Cell Sedimentation Rate Increased;Skin Warm","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"88 YR","Sender":"Bayer","Concomitant.Product.Names":"Magnesium Hydroxide;Alphagan P;Prevacid;Gabapentin;Zoloft;Propoxyphene Hydrochloride And Acetaminophen;Atenolol;Aricept;Aspirin;Depakote;Synthroid"}
{"Case.ID":5852293,"Initial.FDA.Received.Date":"07/27/2005","days.since.last.fda":7,"Event.Date":"07/01/2003","Latest.FDA.Received.Date":"27-JUL-2005","Suspect.Product.Names":"Prograf","Suspect.Product.Active.Ingredients":"Tacrolimus","Reason.for.Use":"Stem Cell Transplant","Reactions":"General Physical Health Deterioration;Stevens-Johnson Syndrome;Cholestasis;Gastrointestinal Haemorrhage;Drug Eruption;Pyrexia;Therapy Non-Responder;Erythema;Graft Versus Host Disease;Erythema Multiforme;Biliary Tract Disorder;Eye Discharge;Aspergillus Infection","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"8 YR","Sender":"Astellas","Concomitant.Product.Names":"Sulfamethoxazole\\Trimethoprim"}
{"Case.ID":5853928,"Initial.FDA.Received.Date":"08/03/2005","days.since.last.fda":7,"Event.Date":"06/10/2005","Latest.FDA.Received.Date":"03-AUG-2005","Suspect.Product.Names":"Zyvox","Suspect.Product.Active.Ingredients":"Linezolid","Reason.for.Use":"Bacteraemia;Pathogen Resistance","Reactions":"Bacteraemia;Urinary Tract Candidiasis;Escherichia Infection;Eosinophil Count Increased;Urinary Tract Infection;Acute Kidney Injury;Device Related Infection;Stevens-Johnson Syndrome;Candida Infection;Thrombocytopenia;Drug Eruption","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5875125,"Initial.FDA.Received.Date":"09/09/2005","days.since.last.fda":37,"Event.Date":"","Latest.FDA.Received.Date":"09-SEP-2005","Suspect.Product.Names":"Vioxx","Suspect.Product.Active.Ingredients":"Rofecoxib","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Merck","Concomitant.Product.Names":"Celebrex"}
{"Case.ID":5887793,"Initial.FDA.Received.Date":"09/29/2005","days.since.last.fda":20,"Event.Date":"06/26/2005","Latest.FDA.Received.Date":"30-SEP-2005","Suspect.Product.Names":"Diovan","Suspect.Product.Active.Ingredients":"Valsartan","Reason.for.Use":"Hypertension","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"61 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":5903479,"Initial.FDA.Received.Date":"10/11/2005","days.since.last.fda":12,"Event.Date":"05/23/2005","Latest.FDA.Received.Date":"11-OCT-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Staphylococcal Infection","Reactions":"Hypotension;Abscess Limb;Stevens-Johnson Syndrome;Cholelithiasis;Multiple Organ Dysfunction Syndrome;Heart Rate Increased;Diarrhoea;Extravasation;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"45 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":5907026,"Initial.FDA.Received.Date":"10/14/2005","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"14-OCT-2005","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"43 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Phenytoin Sodium"}
{"Case.ID":5907025,"Initial.FDA.Received.Date":"10/14/2005","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"14-OCT-2005","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Dermatitis Exfoliative;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"21 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Carbamazepine"}
{"Case.ID":5915064,"Initial.FDA.Received.Date":"10/19/2005","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"19-OCT-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Furuncle","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":5925825,"Initial.FDA.Received.Date":"11/09/2005","days.since.last.fda":21,"Event.Date":"","Latest.FDA.Received.Date":"09-NOV-2005","Suspect.Product.Names":"Levaquin;Zosyn","Suspect.Product.Active.Ingredients":"Piperacillin Sodium\\Tazobactam Sodium;Levofloxacin;Allopurinol;Ciprofloxacin;Cephalexin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Wyeth","Concomitant.Product.Names":"-"}
{"Case.ID":5935372,"Initial.FDA.Received.Date":"11/23/2005","days.since.last.fda":14,"Event.Date":"10/30/2005","Latest.FDA.Received.Date":"23-NOV-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cephalexin;Allopurinol","Reason.for.Use":"Gout","Reactions":"Blood Sodium Decreased;Stevens-Johnson Syndrome;Alanine Aminotransferase Increased;Blood Bilirubin Increased;Blood Creatine Phosphokinase Mb Increased;Haemoglobin Decreased;Blood Creatine Phosphokinase Increased;Blood Creatinine Increased;Platelet Count Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"Advancis","Concomitant.Product.Names":"Simvastatin;Aspirin;Lansoprazole;Bisoprolol;Spironolactone;Furosemide;Ferrous Sulfate;Colchicine;Thiamine"}
{"Case.ID":5939241,"Initial.FDA.Received.Date":"12/12/2005","days.since.last.fda":19,"Event.Date":"","Latest.FDA.Received.Date":"12-DEC-2005","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Zidovudine;Lamivudine"}
{"Case.ID":5963887,"Initial.FDA.Received.Date":"01/10/2006","days.since.last.fda":29,"Event.Date":"","Latest.FDA.Received.Date":"10-JAN-2006","Suspect.Product.Names":"Bextra","Suspect.Product.Active.Ingredients":"Valdecoxib","Reason.for.Use":"Pain","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":5981025,"Initial.FDA.Received.Date":"02/09/2006","days.since.last.fda":30,"Event.Date":"","Latest.FDA.Received.Date":"24-FEB-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Unspecified Ingredient;Torsemide","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"83 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":5981748,"Initial.FDA.Received.Date":"02/10/2006","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"10-FEB-2006","Suspect.Product.Names":"Risperdal","Suspect.Product.Active.Ingredients":"Risperidone","Reason.for.Use":"Delirium","Reactions":"Liver Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Johnson And Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":6004913,"Initial.FDA.Received.Date":"03/01/2006","days.since.last.fda":19,"Event.Date":"","Latest.FDA.Received.Date":"01-MAR-2006","Suspect.Product.Names":"Levaquin;Ciprofloxacin Extended-Release;Zosyn","Suspect.Product.Active.Ingredients":"Piperacillin Sodium\\Tazobactam Sodium;Ciprofloxacin\\Ciprofloxacin Hydrochloride;Cephalexin;Allopurinol;Levofloxacin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Ranbaxy","Concomitant.Product.Names":"-"}
{"Case.ID":6001389,"Initial.FDA.Received.Date":"03/02/2006","days.since.last.fda":1,"Event.Date":"11/18/2005","Latest.FDA.Received.Date":"02-MAR-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Metronidazole;Levofloxacin","Reason.for.Use":"Drug Therapy","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"24 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6008350,"Initial.FDA.Received.Date":"03/06/2006","days.since.last.fda":4,"Event.Date":"02/01/2006","Latest.FDA.Received.Date":"07-MAR-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ibuprofen","Reason.for.Use":"Oropharyngeal Pain","Reactions":"Hypersensitivity;Multi-Organ Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"24 YR","Sender":"Wyeth","Concomitant.Product.Names":"-"}
{"Case.ID":6009163,"Initial.FDA.Received.Date":"03/13/2006","days.since.last.fda":7,"Event.Date":"11/27/2005","Latest.FDA.Received.Date":"13-MAR-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Torsemide","Reason.for.Use":"Fluid Retention","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Post Procedural Complication;Erythema;Fluid Retention","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"90 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6007990,"Initial.FDA.Received.Date":"03/20/2006","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"20-MAR-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Iopamidol","Reason.for.Use":"-","Reactions":"Normochromic Normocytic Anaemia;Jaundice;Oliguria;Nephritis;Lymphopenia;Pericarditis;Stevens-Johnson Syndrome;Bile Duct Necrosis;Peritoneal Dialysis;Pulmonary Haemorrhage;Cyanosis;Cardio-Respiratory Arrest;Toxicity To Various Agents;Blood Creatinine Increased;Diffuse Alveolar Damage","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"46 YR","Sender":"Bracco","Concomitant.Product.Names":"-"}
{"Case.ID":6023441,"Initial.FDA.Received.Date":"04/03/2006","days.since.last.fda":14,"Event.Date":"07/06/2004","Latest.FDA.Received.Date":"03-APR-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Gout","Reactions":"Drug Ineffective;Thrombosis;Alopecia;Drug Level Increased;Peritonitis;Pancreatitis;Leg Amputation;Peritoneal Dialysis;Stevens-Johnson Syndrome;Infection;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"29 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6030609,"Initial.FDA.Received.Date":"04/07/2006","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"07-APR-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lansoprazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"65 YR","Sender":"Takeda","Concomitant.Product.Names":"-"}
{"Case.ID":6048508,"Initial.FDA.Received.Date":"05/10/2006","days.since.last.fda":33,"Event.Date":"04/28/2006","Latest.FDA.Received.Date":"10-MAY-2006","Suspect.Product.Names":"Bactrim Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"-","Concomitant.Product.Names":"Lasix;Prilosec;Synthroid;Hydralazine;Prednisone;Coreg"}
{"Case.ID":6067872,"Initial.FDA.Received.Date":"06/07/2006","days.since.last.fda":28,"Event.Date":"05/07/2004","Latest.FDA.Received.Date":"07-JUN-2006","Suspect.Product.Names":"Flagyl;Childrens Motrin","Suspect.Product.Active.Ingredients":"Ibuprofen;Metronidazole\\Metronidazole Hydrochloride","Reason.for.Use":"Ill-Defined Disorder;Pain","Reactions":"Stevens-Johnson Syndrome;Renal Failure;Toxic Epidermal Necrolysis;Multiple Organ Dysfunction Syndrome;Cardiac Failure;Blood Urine Present;Diabetes Mellitus;Respiratory Failure;Wound Secretion;Septic Shock;Peripheral Ischaemia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"10 YR","Sender":"Pfizer","Concomitant.Product.Names":"Tylenol;Morphine;Codeine;Colace;Pepcid;Decadron;Cefepime"}
{"Case.ID":6066721,"Initial.FDA.Received.Date":"06/16/2006","days.since.last.fda":9,"Event.Date":"","Latest.FDA.Received.Date":"16-JUN-2006","Suspect.Product.Names":"Pepcid","Suspect.Product.Active.Ingredients":"Famotidine;Unspecified Ingredient","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Oculomucocutaneous Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"31 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":6072606,"Initial.FDA.Received.Date":"06/27/2006","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"27-JUN-2006","Suspect.Product.Names":"Lasix;Tylenol;Protonix;Neurontin;Ascriptin","Suspect.Product.Active.Ingredients":"Aspirin;Metoprolol;Gabapentin;Potassium Chloride;Pantoprazole Sodium;Furosemide;Acetaminophen;Amiodarone","Reason.for.Use":"-","Reactions":"Skin Hypoplasia;White Blood Cell Count Decreased;Systemic Candida;Stevens-Johnson Syndrome;Rash Erythematous;Dysphagia;Cholestasis;Oropharyngeal Pain;Haemoglobin Decreased;Graft Versus Host Disease;Biliary Tract Disorder;Diarrhoea;Sepsis;Hyperbilirubinaemia;Leukopenia;Platelet Count Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"82 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":6087029,"Initial.FDA.Received.Date":"07/10/2006","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"18-JUL-2006","Suspect.Product.Names":"Neurontin;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Gabapentin;Pantoprazole Sodium;Acetaminophen;Amiodarone Hydrochloride;Metoprolol Tartrate","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Candida Infection;Platelet Count Decreased;White Blood Cell Count Decreased;Systemic Candida;Rash Erythematous;Alpha Haemolytic Streptococcal Infection;Oropharyngeal Pain;Bone Marrow Failure;Sepsis;Oral Candidiasis;Hyperbilirubinaemia;Haemoglobin Decreased;Stevens-Johnson Syndrome;Graft Versus Host Disease;Cholestasis;Diarrhoea;Dysphagia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"82 YR","Sender":"Pfizer","Concomitant.Product.Names":"Potassium Chloride"}
{"Case.ID":6118458,"Initial.FDA.Received.Date":"08/30/2006","days.since.last.fda":51,"Event.Date":"","Latest.FDA.Received.Date":"30-AUG-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Isoniazid\\Rifampin","Reason.for.Use":"Pulmonary Tuberculosis","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"39 YR","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":6118457,"Initial.FDA.Received.Date":"08/30/2006","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"30-AUG-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Isoniazid\\Rifampin","Reason.for.Use":"Pulmonary Tuberculosis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"24 YR","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":6118456,"Initial.FDA.Received.Date":"08/30/2006","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"30-AUG-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Isoniazid\\Rifampin","Reason.for.Use":"Pulmonary Tuberculosis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"20 YR","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":6124936,"Initial.FDA.Received.Date":"08/31/2006","days.since.last.fda":1,"Event.Date":"09/19/2005","Latest.FDA.Received.Date":"31-AUG-2006","Suspect.Product.Names":"Bactrim Ds","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Cerebrovascular Accident;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"93 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6124105,"Initial.FDA.Received.Date":"09/01/2006","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"01-SEP-2006","Suspect.Product.Names":"Haldol;Seroquel;Prilosec;Avelox;Prozac;Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine;Fluoxetine Hydrochloride;Moxifloxacin Hydrochloride;Levodopa;Omeprazole Magnesium;Quetiapine Fumarate;Haloperidol","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6141332,"Initial.FDA.Received.Date":"09/20/2006","days.since.last.fda":19,"Event.Date":"09/02/2004","Latest.FDA.Received.Date":"20-SEP-2006","Suspect.Product.Names":"Belladonna Alkaloids W/ Phenobarbital","Suspect.Product.Active.Ingredients":"Atropine Sulfate\\Hyoscyamine Sulfate\\Phenobarbital\\Scopolamine Hydrobromide","Reason.for.Use":"-","Reactions":"Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Westward","Concomitant.Product.Names":"-"}
{"Case.ID":6149147,"Initial.FDA.Received.Date":"10/06/2006","days.since.last.fda":16,"Event.Date":"","Latest.FDA.Received.Date":"06-OCT-2006","Suspect.Product.Names":"Tarceva","Suspect.Product.Active.Ingredients":"Erlotinib Hydrochloride","Reason.for.Use":"Lung Cancer Metastatic","Reactions":"Stevens-Johnson Syndrome;Conjunctivitis;Mouth Haemorrhage;Dermatitis Acneiform","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Osi","Concomitant.Product.Names":"-"}
{"Case.ID":6169009,"Initial.FDA.Received.Date":"10/31/2006","days.since.last.fda":25,"Event.Date":"06/18/2005","Latest.FDA.Received.Date":"31-OCT-2006","Suspect.Product.Names":"Biaxin","Suspect.Product.Active.Ingredients":"Clarithromycin;Allopurinol","Reason.for.Use":"-","Reactions":"Skin Abrasion;Stevens-Johnson Syndrome;Dehydration;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6237685,"Initial.FDA.Received.Date":"11/13/2006","days.since.last.fda":13,"Event.Date":"10/01/2003","Latest.FDA.Received.Date":"13-NOV-2006","Suspect.Product.Names":"Levaquin;Zosyn","Suspect.Product.Active.Ingredients":"Piperacillin Sodium\\Tazobactam Sodium;Levofloxacin;Allopurinol;Cephalexin;Ciprofloxacin","Reason.for.Use":"Bacterial Infection;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Renal Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Johnson And Johnson","Concomitant.Product.Names":"Acetaminophen\\Pseudoephedrine Hydrochloride;Coumadin;Isosorbide;Carafate;Hydroxyzine;Claritin;Reglan;Ambien;Hydrocodone;Enalapril Maleate;Enalapril;Tylenol;Lasix;Zoloft;Atenolol;Aloe Vera Leaf;Protonix;Nexium;Digoxin"}
{"Case.ID":6169105,"Initial.FDA.Received.Date":"11/16/2006","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"16-NOV-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Valacyclovir Hydrochloride","Reason.for.Use":"Herpes Simplex","Reactions":"Nasal Mucosal Disorder;Mouth Ulceration;Conjunctival Hyperaemia;Pyrexia;Purpura;Rash Maculo-Papular;Respiratory Failure;Stevens-Johnson Syndrome;Lip Ulceration;Erythema Multiforme;Chills;Pain","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"55 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Acyclovir"}
{"Case.ID":6171172,"Initial.FDA.Received.Date":"11/21/2006","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"21-NOV-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Postoperative Care","Reactions":"Furuncle;Stevens-Johnson Syndrome;Blister;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":6174795,"Initial.FDA.Received.Date":"11/28/2006","days.since.last.fda":7,"Event.Date":"11/11/2006","Latest.FDA.Received.Date":"18-JAN-2007","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine;Tenofovir Disoproxil Fumarate;Emtricitabine","Reason.for.Use":"Hiv Infection","Reactions":"Blister;Cheilitis;Skin Reaction;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"50 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Ferrous Sulfate;Efavirenz"}
{"Case.ID":6198633,"Initial.FDA.Received.Date":"12/01/2006","days.since.last.fda":3,"Event.Date":"03/01/2005","Latest.FDA.Received.Date":"01-DEC-2006","Suspect.Product.Names":"Extended Phenytoin Sodium","Suspect.Product.Active.Ingredients":"Phenytoin Sodium;Cephalexin","Reason.for.Use":"Infection;Metastases To Central Nervous System;Seizure","Reactions":"Otorrhoea;Tinea Capitis;Oedema Peripheral;Skin Exfoliation;Stevens-Johnson Syndrome;Seizure;Swelling Face;Ear Infection;Confusional State;Pruritus","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Mylan","Concomitant.Product.Names":"Methylprednisolone;Ketoconazole;Hydromorphone Hydrochloride;Phenobarbital;Hydroxyzine;Dexamethasone Sodium Phosphate"}
{"Case.ID":6180836,"Initial.FDA.Received.Date":"12/07/2006","days.since.last.fda":6,"Event.Date":"09/19/2006","Latest.FDA.Received.Date":"07-DEC-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Furosemide;Allopurinol","Reason.for.Use":"Cardiac Failure;Gout","Reactions":"Renal Tubular Necrosis;Acute Kidney Injury;Stevens-Johnson Syndrome;Acute Respiratory Distress Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"81 YR","Sender":"Aventis","Concomitant.Product.Names":"Digoxin;Perindopril;Coumadin"}
{"Case.ID":6182016,"Initial.FDA.Received.Date":"12/08/2006","days.since.last.fda":1,"Event.Date":"11/13/2006","Latest.FDA.Received.Date":"20-AUG-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Tenofovir Disoproxil Fumarate;Emtricitabine;Nevirapine;Efavirenz","Reason.for.Use":"Hiv Infection;Pyrexia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"50 YR","Sender":"Gilead","Concomitant.Product.Names":"Ciprofloxacin;Ferrous Sulfate;Unspecified Ingredient"}
{"Case.ID":6202655,"Initial.FDA.Received.Date":"12/12/2006","days.since.last.fda":4,"Event.Date":"11/13/2006","Latest.FDA.Received.Date":"12-DEC-2006","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Efavirenz;Tenofovir;Nevirapine;Emtricitabine","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome;Palpitations;Psychotic Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"29 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6207343,"Initial.FDA.Received.Date":"01/03/2007","days.since.last.fda":22,"Event.Date":"","Latest.FDA.Received.Date":"03-JAN-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cefoperazone\\Sulbactam","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"Unspecified Ingredient;Cannabis Sativa Subsp. Indica Top"}
{"Case.ID":6218960,"Initial.FDA.Received.Date":"01/08/2007","days.since.last.fda":5,"Event.Date":"11/13/2006","Latest.FDA.Received.Date":"08-JAN-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Tenofovir;Efavirenz;Emtricitabine;Nevirapine","Reason.for.Use":"Hiv Infection","Reactions":"Psychotic Disorder;Palpitations;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"50 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6231860,"Initial.FDA.Received.Date":"01/25/2007","days.since.last.fda":17,"Event.Date":"12/25/2006","Latest.FDA.Received.Date":"25-JAN-2007","Suspect.Product.Names":"Lioresal","Suspect.Product.Active.Ingredients":"Baclofen","Reason.for.Use":"Muscle Spasticity","Reactions":"Sepsis;Stevens-Johnson Syndrome;Burns Second Degree;Drug Hypersensitivity","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"8 YR","Sender":"Medtronic","Concomitant.Product.Names":"-"}
{"Case.ID":6255823,"Initial.FDA.Received.Date":"02/23/2007","days.since.last.fda":29,"Event.Date":"02/12/2007","Latest.FDA.Received.Date":"23-FEB-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampicillin","Reason.for.Use":"Blood Culture Positive","Reactions":"Tachycardia;General Physical Health Deterioration;Hypotension;Myocarditis;Cardiac Failure;Tachypnoea;Pain;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"19 MTH","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6247556,"Initial.FDA.Received.Date":"02/28/2007","days.since.last.fda":5,"Event.Date":"10/24/2005","Latest.FDA.Received.Date":"28-FEB-2007","Suspect.Product.Names":"Leustatin","Suspect.Product.Active.Ingredients":"Cladribine","Reason.for.Use":"Constipation;Hypovitaminosis;Infection Prophylaxis;Lymphoplasmacytoid Lymphoma/Immunocytoma;Oedema Peripheral;Osteoporosis;Pyrexia","Reactions":"Platelet Count Decreased;Lymphoplasmacytoid Lymphoma/Immunocytoma;Neoplasm Malignant;White Blood Cell Count Decreased;Anaemia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Johnson And Johnson","Concomitant.Product.Names":"Cefozopran Hydrochloride;Gaster;Sulfamethoxazole\\Trimethoprim;Magnesium Oxide;Human Red Blood Cell;Meropenem;Isoniazid;Lenograstim;Decadron;Platelets;Alendronate Sodium;Lasix;Unspecified Ingredient;Ascorbic Acid"}
{"Case.ID":6265783,"Initial.FDA.Received.Date":"03/20/2007","days.since.last.fda":20,"Event.Date":"","Latest.FDA.Received.Date":"02-APR-2007","Suspect.Product.Names":"Lincocin","Suspect.Product.Active.Ingredients":"Lincomycin","Reason.for.Use":"Otitis Media Chronic","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"25 YR","Sender":"Pfizer","Concomitant.Product.Names":"Erythromycin;Clemastine Fumarate"}
{"Case.ID":6271753,"Initial.FDA.Received.Date":"03/27/2007","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"27-MAR-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin Hydrochloride","Reason.for.Use":"Product Used For Unknown Indication;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Bayer","Concomitant.Product.Names":"Piperacillin Sodium\\Tazobactam Sodium"}
{"Case.ID":6284410,"Initial.FDA.Received.Date":"04/10/2007","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"10-APR-2007","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Mental Disorder","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":6308973,"Initial.FDA.Received.Date":"05/03/2007","days.since.last.fda":23,"Event.Date":"09/05/2006","Latest.FDA.Received.Date":"03-MAY-2007","Suspect.Product.Names":"Keppra","Suspect.Product.Active.Ingredients":"Levetiracetam","Reason.for.Use":"Seizure","Reactions":"Respiratory Distress;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"31 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6337324,"Initial.FDA.Received.Date":"05/04/2007","days.since.last.fda":1,"Event.Date":"09/01/2004","Latest.FDA.Received.Date":"04-MAY-2007","Suspect.Product.Names":"Unasyn","Suspect.Product.Active.Ingredients":"Ampicillin Sodium\\Sulbactam Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":6336049,"Initial.FDA.Received.Date":"06/06/2007","days.since.last.fda":33,"Event.Date":"04/24/2007","Latest.FDA.Received.Date":"11-JUL-2007","Suspect.Product.Names":"Urso 250","Suspect.Product.Active.Ingredients":"Ursodiol;Levofloxacin;Sodium Bicarbonate\\Sodium Phosphate, Monobasic, Anhydrous;Acetaminophen","Reason.for.Use":"Constipation;Hepatic Function Abnormal;Infection;Pyrexia","Reactions":"Blood Pressure Decreased;Jaundice;Cardio-Respiratory Arrest;Stevens-Johnson Syndrome;Renal Failure;Fungal Infection;Hypoalbuminaemia;Hypovolaemia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Axcan","Concomitant.Product.Names":"Allopurinol;Lasix;Spironolactone;Isosorbide Dinitrate;Enalapril Maleate;Carvedilol"}
{"Case.ID":6335802,"Initial.FDA.Received.Date":"06/06/2007","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"06-JUN-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lansoprazole","Reason.for.Use":"-","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"66 YR","Sender":"Takeda","Concomitant.Product.Names":"-"}
{"Case.ID":6333946,"Initial.FDA.Received.Date":"06/08/2007","days.since.last.fda":2,"Event.Date":"","Latest.FDA.Received.Date":"08-JUN-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Renal Failure;Dialysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6359119,"Initial.FDA.Received.Date":"07/10/2007","days.since.last.fda":32,"Event.Date":"05/10/2007","Latest.FDA.Received.Date":"10-JUL-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Efavirenz;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Antifungal Prophylaxis;Hiv Infection","Reactions":"Stevens-Johnson Syndrome;Diarrhoea;Cardiac Arrest;Metabolic Disorder;Hepatic Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"50 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6362240,"Initial.FDA.Received.Date":"07/13/2007","days.since.last.fda":3,"Event.Date":"04/05/2007","Latest.FDA.Received.Date":"13-JUL-2007","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Urinary Tract Infection","Reactions":"Drug Hypersensitivity;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6362802,"Initial.FDA.Received.Date":"07/20/2007","days.since.last.fda":7,"Event.Date":"09/23/2006","Latest.FDA.Received.Date":"07-AUG-2007","Suspect.Product.Names":"Polaramine;Cercine;Humulin R;Tegretol;Voltaren;Multi Vitamin Infusion;Glycyrrhizin, Ammoniated;Solu-Medrol;Ropivacaine.;Mobic","Suspect.Product.Active.Ingredients":"Meloxicam;Ropivacaine Hydrochloride;Distigmine Bromide;Nicardipine;Cefotiam\\Mepivacaine;Methylprednisolone Sodium Succinate;Betamethasone Acetate\\Betamethasone Sodium Phosphate;Ammonium Glycyrrhizate;Lansoprazole;Flomoxef;Bromhexine;Omeprazole;Pazufloxacin;Flunitrazepam;Albumin Human;Sennosides;Ketoprofen;Doripenem Monohydrate;Magnesium Oxide;Aspirin;Edaravone;.Alpha.-Tocopherol\\.Alpha.-Tocopherol Acetate, Dl-\\Ascorbic Acid\\Biotin\\Cyanocobalamin\\Dexpanthenol\\Ergocalciferol\\Folic Acid\\Niacinamide\\Pyridoxine Hydrochloride\\Retinol\\Riboflavin 5'-Phosphate Sodium\\Thiamine;Phenobarbital;Loxoprofen Sodium;Sodium Picosulfate;Unspecified Ingredient;Amino Acids, Source Unspecified;Zolpidem Tartrate;Ozagrel;Zopiclone;Teprenone;Naproxen;Carbamazepine;Diclofenac Sodium;Insulin Human;Heparin Sodium;Diazepam;Dexchlorpheniramine Maleate","Reason.for.Use":"Cerebral Infarction;Constipation;Fluid Replacement;Gastric Ulcer;Gastritis;Hyperglycaemia;Hypertension;Infection;Infection Prophylaxis;Neurogenic Bladder;Nutritional Supplementation;Product Used For Unknown Indication;Prophylaxis;Pyrexia;Seizure Prophylaxis;Vitamin Supplementation","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":6362799,"Initial.FDA.Received.Date":"07/20/2007","days.since.last.fda":0,"Event.Date":"09/23/2006","Latest.FDA.Received.Date":"02-AUG-2007","Suspect.Product.Names":"Humulin R;Rinderon Vg;Cercine;Multi Vitamin Infusion;Voltaren;Tegretol;Albumin (Human);Polaramine;Solu-Medrol;Mobic","Suspect.Product.Active.Ingredients":"Distigmine Bromide;Meloxicam;Methylprednisolone Sodium Succinate;Ozagrel;Flunitrazepam;Zopiclone;Edaravone;Sodium Picosulfate;Zolpidem Tartrate;Magnesium Oxide;Ketoprofen;Ammonium Glycyrrhizate;Doripenem Monohydrate;Dexchlorpheniramine Maleate;Albumin Human;Unspecified Ingredient;Naproxen;Carbamazepine;Lansoprazole;Teprenone;Diclofenac Sodium;Pazufloxacin;Amino Acids, Source Unspecified;Heparin Sodium;.Alpha.-Tocopherol\\.Alpha.-Tocopherol Acetate, Dl-\\Ascorbic Acid\\Biotin\\Cyanocobalamin\\Dexpanthenol\\Ergocalciferol\\Folic Acid\\Niacinamide\\Pyridoxine Hydrochloride\\Retinol\\Riboflavin 5'-Phosphate Sodium\\Thiamine;Omeprazole;Bromhexine;Diazepam;Loxoprofen Sodium;Phenobarbital;Betamethasone Valerate\\Gentamicin Sulfate;Flomoxef;Sennosides;Insulin Human;Aspirin;Nicardipine","Reason.for.Use":"Asthma;Cerebral Infarction;Constipation;Fluid Replacement;Gastric Ulcer;Gastritis;Hepatic Function Abnormal;Hyperglycaemia;Hypertension;Infection;Infection Prophylaxis;Neurogenic Bladder;Nutritional Supplementation;Product Used For Unknown Indication;Pruritus;Pyrexia;Rash;Seizure Prophylaxis;Sputum Retention;Vitamin Supplementation;Wound Complication","Reactions":"Sepsis;Liver Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Roche","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":6371443,"Initial.FDA.Received.Date":"07/24/2007","days.since.last.fda":4,"Event.Date":"06/22/2007","Latest.FDA.Received.Date":"24-JUL-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Seizure","Reactions":"Encephalopathy;Stevens-Johnson Syndrome;Anaemia;Gastrointestinal Necrosis;Thrombocytopenia;Acute Respiratory Distress Syndrome;Toxic Epidermal Necrolysis;Septic Shock;Heart Rate Increased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"7 YR","Sender":"-","Concomitant.Product.Names":"Divalproex Sodium"}
{"Case.ID":6447819,"Initial.FDA.Received.Date":"10/16/2007","days.since.last.fda":84,"Event.Date":"10/04/2007","Latest.FDA.Received.Date":"23-APR-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Doxycycline;Erythromycin;Rimonabant","Reason.for.Use":"Lower Respiratory Tract Infection;Weight Decreased","Reactions":"Confusional State;Thrombocytopenia;Labile Blood Pressure;Acute Kidney Injury;Lower Respiratory Tract Infection;General Physical Health Deterioration;Hypotension;Proteus Infection;Stevens-Johnson Syndrome;Bronchopulmonary Aspergillosis;Drug Interaction;Corneal Abrasion;Mucosal Inflammation;Blood Potassium Increased;Enterobacter Infection;Toxic Shock Syndrome;Pneumonia Fungal;Eosinophilia;Dermatitis Exfoliative;Diarrhoea;Anaemia;Hypophagia;Depressed Level Of Consciousness","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"Sandoz","Concomitant.Product.Names":"Metformin Hydrochloride;Rosiglitazone;Furosemide;Glipizide;Lansoprazole;Prednisolone;Aspirin;Lisinopril;Ramipril;Hydrochlorothiazide;Miconazole;Amoxicillin;Cialis;Allopurinol;Chlorhexidine Gluconate;Atorvastatin;Budesonide"}
{"Case.ID":6464018,"Initial.FDA.Received.Date":"11/02/2007","days.since.last.fda":17,"Event.Date":"09/11/2006","Latest.FDA.Received.Date":"02-NOV-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Azithromycin Anhydrous","Reason.for.Use":"Upper Respiratory Tract Infection","Reactions":"Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"54 YR","Sender":"-","Concomitant.Product.Names":"Colace;Vitamins;Heparin;Sucralfate;Levaquin;Pantoprazole Sodium"}
{"Case.ID":6463445,"Initial.FDA.Received.Date":"11/02/2007","days.since.last.fda":0,"Event.Date":"09/11/2006","Latest.FDA.Received.Date":"02-NOV-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Azithromycin Anhydrous","Reason.for.Use":"Upper Respiratory Tract Infection","Reactions":"Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"54 YR","Sender":"-","Concomitant.Product.Names":"Heparin;Sucralfate;Levaquin;Vitamins;Pantoprazole Sodium;Colace"}
{"Case.ID":6465591,"Initial.FDA.Received.Date":"11/05/2007","days.since.last.fda":3,"Event.Date":"10/07/2007","Latest.FDA.Received.Date":"05-NOV-2007","Suspect.Product.Names":"Coreg","Suspect.Product.Active.Ingredients":"Carvedilol","Reason.for.Use":"Cardiac Disorder","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6501745,"Initial.FDA.Received.Date":"12/14/2007","days.since.last.fda":39,"Event.Date":"11/24/2007","Latest.FDA.Received.Date":"31-DEC-2007","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Oxaliplatin;Fluorouracil","Reason.for.Use":"Rectal Cancer","Reactions":"Diarrhoea;Acute Kidney Injury;Stevens-Johnson Syndrome;Leukopenia;Depressed Level Of Consciousness;Dehydration;Tachycardia;Blood Pressure Decreased;Multiple Organ Dysfunction Syndrome;Thrombocytopenia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"Sanofi","Concomitant.Product.Names":"Butylscopolamine Bromide;Verapamil Hydrochloride;Isovorin;Primperan;Deslanoside;Cefotiam Hydrochloride"}
{"Case.ID":6508246,"Initial.FDA.Received.Date":"12/18/2007","days.since.last.fda":4,"Event.Date":"09/28/2001","Latest.FDA.Received.Date":"18-DEC-2007","Suspect.Product.Names":"Rocephin","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium;Minocycline Hydrochloride;Levofloxacin","Reason.for.Use":"Gastric Ulcer;Hepatitis","Reactions":"Stevens-Johnson Syndrome;Pneumonia;Empyema","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"77 YR","Sender":"Roche","Concomitant.Product.Names":"Gaster;Ambroxol Hydrochloride;Carbocysteine;Unspecified Ingredient;Clenbuterol Hydrochloride;Theo-Dur"}
{"Case.ID":6517985,"Initial.FDA.Received.Date":"01/02/2008","days.since.last.fda":15,"Event.Date":"12/13/2007","Latest.FDA.Received.Date":"23-JAN-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Etodolac;Omeprazole","Reason.for.Use":"Gastrooesophageal Reflux Disease;Hyperlipidaemia;Hypertension;Pollakiuria;Postoperative Analgesia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"29227 DAY","Sender":"Astrazeneca","Concomitant.Product.Names":"Benidipine Hydrochloride;Simvastatin;Enalapril Maleate"}
{"Case.ID":6532095,"Initial.FDA.Received.Date":"01/22/2008","days.since.last.fda":20,"Event.Date":"04/19/2005","Latest.FDA.Received.Date":"22-JAN-2008","Suspect.Product.Names":"Norvasc","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Unspecified Ingredient;Losartan;Enoxaparin Sodium;Allopurinol;Nifedipine;Torsemide;Metoprolol Succinate;Prednisolone;Enalapril;Simvastatin;Metronidazole;Calcium Carbonate","Reason.for.Use":"Parenteral Nutrition;Product Used For Unknown Indication;Secondary Hypothyroidism;Sepsis;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"Roche","Concomitant.Product.Names":"Nebivolol;Rifampin;Vancomycin;Unspecified Ingredient;Moxonidine;Piperacillin.;Quinapril;Sulbactam"}
{"Case.ID":6534501,"Initial.FDA.Received.Date":"01/24/2008","days.since.last.fda":2,"Event.Date":"10/31/2003","Latest.FDA.Received.Date":"17-APR-2008","Suspect.Product.Names":"Simethicone (Dimethicone);Ciprofloxacin Extended-Release;Primaxin Im;Heparin;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Colchicine;Clarithromycin;Heparin Sodium;Vancomycin;Neomycin;Cilastatin Sodium\\Imipenem;Diclofenac;Ciprofloxacin\\Ciprofloxacin Hydrochloride;Dimethicone;Carvedilol","Reason.for.Use":"Cardiac Failure Congestive;Conjunctival Haemorrhage;Constipation;Diabetes Mellitus;Exophthalmos;Gastrointestinal Disorder;Infection;Pain;Parenteral Nutrition;Pericardial Effusion;Prophylaxis Against Gastrointestinal Ulcer;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"58 YR","Sender":"Merck","Concomitant.Product.Names":"Hetastarch In Sodium Chloride;Gentamicin Sulfate;Acetylcysteine;Prednisolone Sodium Succinate;Albumin (Human);Vioxx;Piritramide;Dexpanthenol;Dextrose;Ergocalciferol\\Phytonadione\\Vitamin A;Lactulose;Insulin Nos;Soybean Oil;Metronidazole;Dopamine Hydrochloride"}
{"Case.ID":7126250,"Initial.FDA.Received.Date":"01/25/2008","days.since.last.fda":1,"Event.Date":"04/19/2005","Latest.FDA.Received.Date":"25-JAN-2008","Suspect.Product.Names":"Tpn;Norvasc","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Enalapril;Enoxaparin Sodium;Prednisolone;Metronidazole;Simvastatin;Nifedipine;Allopurinol;Amino Acids\\Dextrose\\Electrolytes Nos\\Soybean Oil;Metoprolol Succinate;Torsemide;Losartan Potassium;Unspecified Ingredient;Calcium Carbonate","Reason.for.Use":"Diverticulitis;Hyperparathyroidism Secondary;Hypertension;Parenteral Nutrition;Renal Failure;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"Pfizer","Concomitant.Product.Names":"Moxonidine;Nebivolol Hydrochloride;Sulbactam;Piperacillin Sodium;Quinapril Hydrochloride"}
{"Case.ID":6550190,"Initial.FDA.Received.Date":"01/28/2008","days.since.last.fda":3,"Event.Date":"08/06/2004","Latest.FDA.Received.Date":"05-FEB-2008","Suspect.Product.Names":"Konakion;Nexium;Lasix;Pantozol;Fragmin;Placebo;Prograf;Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Metoclopramide;Lormetazepam;Tacrolimus;Sulbactam;Unspecified Ingredient;Piperacillin Sodium;Ciclopirox Olamine;Menaquinone 6;Acetaminophen;Ramipril;Tramadol Hydrochloride;Vancomycin;Sodium Chloride;Prednisolone;Acyclovir;Pramipexole Dihydrochloride;Meropenem;Midazolam Hydrochloride;Dalteparin Sodium;Pantoprazole Sodium;Prednisolone Sodium Succinate;Furosemide;Ciprofloxacin Hydrochloride;Esomeprazole Magnesium;Acetylcysteine;Phytonadione;Potassium Chloride;Glucose, Liquid;Pentazocine;Calcipotriene","Reason.for.Use":"Antiviral Prophylaxis;Endoscopic Retrograde Cholangiopancreatography;Extrapyramidal Disorder;Fluid Replacement;Fungal Infection;Hypertension;Hypokalaemia;Infection Prophylaxis;Nausea;Oedema;Pain;Prophylaxis;Prophylaxis Against Gastrointestinal Ulcer;Psoriasis;Respiratory Disorder;Restless Legs Syndrome;Sleep Disorder","Reactions":"Stevens-Johnson Syndrome;Oedema;Hypokalaemia;Toxic Epidermal Necrolysis;Nausea;Sleep Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"62 YR","Sender":"Pfizer","Concomitant.Product.Names":"Metoprolol Tartrate;Urso;Atropine Sulfate"}
{"Case.ID":6547644,"Initial.FDA.Received.Date":"02/07/2008","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"07-FEB-2008","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":6552042,"Initial.FDA.Received.Date":"02/13/2008","days.since.last.fda":6,"Event.Date":"12/15/2004","Latest.FDA.Received.Date":"13-FEB-2008","Suspect.Product.Names":"Imodium;Tavor (Lorazepam);Nexium;Albumin (Human);Ciprofloxacin Extended-Release;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Clemastine;Ciprofloxacin\\Ciprofloxacin Hydrochloride;Prednisone;Metoclopramide;Sodium Chloride;Prednisolone;Erythropoietin;Albumin Human;Esomeprazole Magnesium;Potassium Bicarbonate;Potassium Chloride;Sodium Bicarbonate;Torsemide;Calcium;Lorazepam;Metronidazole;Loperamide Hydrochloride;Acetaminophen;Calcium Chloride\\Potassium Chloride\\Sodium Chloride;Phytonadione;Enoxaparin Sodium;Metoprolol;Phenprocoumon","Reason.for.Use":"Blood Pressure Management;Cardiac Disorder;Cardiac Operation;Diarrhoea;Endocarditis;Gastric Disorder;Infection;Nephrotic Syndrome;Oedema;Prophylaxis;Pruritus;Restlessness;Secretion Discharge;Sleep Disorder Therapy;Therapeutic Skin Care Topical;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"Roche","Concomitant.Product.Names":"Pantozol;Novodigal (.Beta.-Acetyldigoxin);Fresubin;Clemastine;Meropenem;Fentanyl;Vancomycin;Furosemide;Nexium;Prednisone;Ambroxol Hydrochloride;Amiodarone;Rocephin;Midazolam Hydrochloride;Norepinephrine Bitartrate;Metoprolol;Benzalkonium Chloride\\Chlorhexidine Hydrochloride\\Dexpanthenol\\Domiphen Bromide;Paracodin [Dihydrocodeine Bitartrate];Aldactone"}
{"Case.ID":6553329,"Initial.FDA.Received.Date":"02/14/2008","days.since.last.fda":1,"Event.Date":"02/23/2005","Latest.FDA.Received.Date":"14-FEB-2008","Suspect.Product.Names":"Albumin (Human);Piperacillin.;Heparin;Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Norepinephrine Bitartrate;Heparin Sodium;Metoclopramide;Amino Acids\\Carbohydrates\\Minerals\\Soybean Oil\\Vitamins;Erythromycin;Pyridoxine Hydrochloride;Xylitol;Unspecified Ingredient;Dobutamine Hydrochloride;Glucose, Liquid;Piperacillin Sodium;Midazolam Hydrochloride;Albumin Human;Enoxaparin Sodium;Insulin Nos;Calcium;Dipyrone;Omeprazole;Furosemide;Caspofungin;Acetylcysteine;Spironolactone;Vancomycin;Piritramide;Aspirin;Sufentanil Citrate;Sulbactam","Reason.for.Use":"Fungal Infection;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"Pfizer","Concomitant.Product.Names":"Clinomel;Potassium Chloride;Unspecified Ingredient;Konakion;Levofloxacin;Ferrlecit;Cyanocobalamin;Hydrocortisone;Metoprolol Tartrate;Folic Acid;Clemastine;Fenoterol Hydrobromide\\Ipratropium Bromide;Metronidazole"}
{"Case.ID":6553942,"Initial.FDA.Received.Date":"02/15/2008","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"15-FEB-2008","Suspect.Product.Names":"Xeloda","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":6555434,"Initial.FDA.Received.Date":"02/18/2008","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"21-APR-2008","Suspect.Product.Names":"Arixtra","Suspect.Product.Active.Ingredients":"Fondaparinux Sodium","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Multiple Organ Dysfunction Syndrome;Rash;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":6555542,"Initial.FDA.Received.Date":"02/18/2008","days.since.last.fda":0,"Event.Date":"03/29/2005","Latest.FDA.Received.Date":"18-FEB-2008","Suspect.Product.Names":"Imodium;Multi-Vitamin;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Sodium Chloride;Enoxaparin Sodium;Metoclopramide;Dipyrone;Acetaminophen;Amitriptyline Hydrochloride;Nystatin;.Alpha.-Tocopherol Acetate, Dl-\\Ascorbic Acid\\Cyanocobalamin\\Fluoride Ion\\Folic Acid\\Niacin\\Pyridoxine\\Riboflavin\\Thiamine\\Vitamin A\\Vitamin D;Loperamide Hydrochloride;Menaquinone 6;Ceftriaxone;Bethanechol Chloride;Glyburide;Unspecified Ingredient;Sulfamethoxazole\\Trimethoprim;Magaldrate;Methylprednisolone","Reason.for.Use":"Collagen Disorder;Depression;Diabetes Mellitus;Diarrhoea;Dyspnoea;Infection;Nausea;Pain;Polyneuropathy;Prophylaxis;Pruritus;Skin Disorder;Thrombosis;Thrombosis Prophylaxis;Urinary Incontinence;Yersinia Infection","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Roche","Concomitant.Product.Names":"Prednisone;Voltaren;Avelox;Unspecified Ingredient;Marcumar;Xylitol;Isosorbide Mononitrate;Actrapid;Calcium Carbonate\\Calcium Glubionate\\Calcium Gluconate\\Calcium Lactobionate;Calcium Gluconate;Tpn;Hetastarch;Novalgin (Metamizole Sodium);Atorvastatin;.Alpha.-Lipoic Acid"}
{"Case.ID":6560846,"Initial.FDA.Received.Date":"02/25/2008","days.since.last.fda":7,"Event.Date":"03/17/2005","Latest.FDA.Received.Date":"25-FEB-2008","Suspect.Product.Names":"Imodium;Pantozol;Rocephin;Konakion","Suspect.Product.Active.Ingredients":"Phytonadione;Ceftriaxone Sodium;Enoxaparin Sodium;Magaldrate;Pantoprazole Sodium;Glyburide;Metoclopramide Hydrochloride;Acetaminophen;Loperamide Hydrochloride;Sulfamethoxazole\\Trimethoprim;Bethanechol Chloride;Dipyrone;Nystatin;Amitriptyline Hydrochloride","Reason.for.Use":"Abdominal Pain Upper;Antibiotic Prophylaxis;Bladder Disorder;Candida Infection;Collagen Disorder;Depression;Diabetes Mellitus;Diarrhoea;Dyspnoea;Gastrointestinal Disorder Therapy;Hypercholesterolaemia;Hypocalcaemia;Infection;Nausea;Pain;Polyneuropathy;Pruritus;Pyrexia;Skin Disorder;Thrombosis;Thrombosis Prophylaxis;Unevaluable Event;Vomiting;Yersinia Infection","Reactions":"Pain Of Skin;Pruritus;Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Mcneil","Concomitant.Product.Names":"Novalgin (Metamizole Sodium);Metoclopramide Hydrochloride;Marcumar;Avelox;.Alpha.-Lipoic Acid;Sodium Chloride;Atorvastatin;Methylprednisolone;Unspecified Ingredient;Prednisone;Calcium;Isosorbide Mononitrate;Multi-Vitamin;Xylitol;Actrapid;Tpn;Voltaren"}
{"Case.ID":6560546,"Initial.FDA.Received.Date":"02/25/2008","days.since.last.fda":0,"Event.Date":"07/22/2005","Latest.FDA.Received.Date":"25-FEB-2008","Suspect.Product.Names":"Trental;Heparin;Mcp;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Potassium Chloride\\Sodium Bicarbonate\\Sodium Chloride;Allopurinol;Metoclopramide Hydrochloride;Methimazole;Lactulose;Citalopram Hydrobromide;Heparin Sodium;Pentoxifylline;Aspirin;Dipyrone;Lisinopril","Reason.for.Use":"Atrial Fibrillation;Cardiac Failure;Constipation;Depression;Hypertension;Hyperthyroidism;Hyperuricaemia;Hyponatraemia;Nausea;Pain;Prophylaxis Against Gastrointestinal Ulcer;Pyrexia;Thrombosis Prophylaxis;Transient Ischaemic Attack","Reactions":"Lip Erosion;Oral Pain;Stevens-Johnson Syndrome;Rash Macular;Pyrexia;Pruritus;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"Aventis","Concomitant.Product.Names":"Acetaminophen;Trimipramine Maleate;Nitroglycerin;Aggrenox;Metoprolol Succinate;Calcium Chloride\\Magnesium Chloride\\Potassium Chloride\\Sodium Acetate\\Sodium Chloride;Sodium Chloride;Torsemide;Digitoxin"}
{"Case.ID":6560431,"Initial.FDA.Received.Date":"02/25/2008","days.since.last.fda":0,"Event.Date":"03/09/2005","Latest.FDA.Received.Date":"25-FEB-2008","Suspect.Product.Names":"Risperdal","Suspect.Product.Active.Ingredients":"Risperidone;Folic Acid;Citalopram Hydrobromide;Amoxicillin\\Clavulanate Potassium;Enoxaparin Sodium;Cyclophosphamide;Prednisolone;Mesna","Reason.for.Use":"Depression;Enteral Nutrition;Gastrointestinal Disorder Therapy;Medical Diet;Mineral Supplementation;Pain;Product Used For Unknown Indication;Prophylaxis;Pruritus;Restlessness;Systemic Lupus Erythematosus;Thrombosis Prophylaxis;Vitamin Supplementation","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"34 YR","Sender":"Johnson And Johnson","Concomitant.Product.Names":"Prednisone;Piritramide;Potassium Chloride;Cyanocobalamin;Pipamperone;Azathioprine;Pantozol;Calcium Carbonate;Gonadorelin"}
{"Case.ID":6563083,"Initial.FDA.Received.Date":"02/27/2008","days.since.last.fda":2,"Event.Date":"03/29/2005","Latest.FDA.Received.Date":"27-FEB-2008","Suspect.Product.Names":"Pantozol;Imodium","Suspect.Product.Active.Ingredients":"Loperamide Hydrochloride;Bethanechol Chloride;Sodium Chloride;Amitriptyline;Pantoprazole Sodium;Phytonadione;Magaldrate;Dipyrone;Acetaminophen;Glyburide;Ascorbic Acid\\Calcium Pantothenate\\Cyanocobalamin\\Pyridoxine Hydrochloride\\Riboflavin\\Thiamine Hydrochloride;Unspecified Ingredient;Nystatin;Methylprednisolone;Sulfamethoxazole\\Trimethoprim;Enoxaparin Sodium;Metoclopramide","Reason.for.Use":"Abdominal Pain Upper;Depression;Diabetes Mellitus;Diarrhoea;Genital Candidiasis;Infection;Nausea;Pain;Prophylaxis Against Gastrointestinal Ulcer;Pyrexia;Thrombosis Prophylaxis;Urinary Incontinence","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Aventis","Concomitant.Product.Names":"Calcium Gluconate;Glyburide;Actrapid;Tpn;Prednisone;Atorvastatin;Hetastarch;Voltaren;Novalgin (Metamizole Sodium);Calcium Glubionate;.Alpha.-Lipoic Acid;Avelox;Xylitol;Unspecified Ingredient;Dimethindene;Marcumar;Isosorbide Mononitrate"}
{"Case.ID":6565116,"Initial.FDA.Received.Date":"02/28/2008","days.since.last.fda":1,"Event.Date":"07/22/2005","Latest.FDA.Received.Date":"28-FEB-2008","Suspect.Product.Names":"Pantozol;Movicol;Aggrenox;Heparin;Trental","Suspect.Product.Active.Ingredients":"Pentoxifylline;Acetaminophen;Metoclopramide;Sodium Chloride;Heparin Sodium;Citalopram Hydrobromide;Trimipramine Maleate;Calcium Chloride\\Magnesium Chloride\\Potassium Chloride\\Sodium Acetate\\Sodium Chloride;Lactulose;Aspirin\\Dipyridamole;Lisinopril;Aspirin;Metoprolol Succinate;Polyethylene Glycol 3350\\Potassium Chloride\\Sodium Bicarbonate\\Sodium Chloride;Methimazole;Torsemide;Nitroglycerin;Pantoprazole Sodium;Allopurinol;Dipyrone;Digitoxin","Reason.for.Use":"Atrial Fibrillation;Atrial Flutter;Cardiac Failure;Cardiovascular Disorder;Constipation;Depression;Hypernatraemia;Hyperosmolar State;Hypertension;Hyperthyroidism;Hyperuricaemia;Hypovolaemia;Nausea;Pain;Pyrexia;Thrombosis Prophylaxis;Vomiting","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"Wyeth","Concomitant.Product.Names":"-"}
{"Case.ID":6565071,"Initial.FDA.Received.Date":"02/28/2008","days.since.last.fda":0,"Event.Date":"11/11/2004","Latest.FDA.Received.Date":"28-FEB-2008","Suspect.Product.Names":"Clopidogrel;Mcp;Pantozol;Tavor (Lorazepam)","Suspect.Product.Active.Ingredients":"Lorazepam;Pantoprazole Sodium;Metoprolol Succinate;Hydrochlorothiazide;Enoxaparin Sodium;Melperone Hydrochloride;Metoclopramide Hydrochloride;Ramipril;Loperamide Hydrochloride;Allopurinol;Clopidogrel Bisulfate;Digitoxin;Methimazole;Carbamazepine;Torsemide;Sodium Perchlorate Monohydrate","Reason.for.Use":"Acute Myocardial Infarction;Candida Infection;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Electrolyte Substitution Therapy;Fluid Replacement;Haemoglobin Decreased;Hypercholesterolaemia;Hypertension;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Nausea;Ocular Hyperaemia;Pain;Parotitis;Pneumonia;Polyuria;Prophylaxis Against Gastrointestinal Ulcer;Pruritus;Pyrexia;Renal Failure;Restlessness;Sedation;Skin Disorder;Sleep Disorder;Swollen Tongue;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"25960 DAY","Sender":"Astrazeneca","Concomitant.Product.Names":"Gramicidin\\Neomycin Sulfate\\Polymyxin B Sulfate;Amphotericin B;Metoprolol;Flunitrazepam;Levofloxacin;Brotizolam;Haloperidol;Potassium Carbonate\\Potassium Citrate;Novalgin (Metamizole Sodium);Diflucan;Hydrochlorothiazide\\Ramipril;Potassium Chloride;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate\\Sodium Acetate\\Sodium Chlori;Tazobactam;Furosemide;Lantus;Prednisolone Sodium Succinate;Clarithromycin;Ampicillin Sodium\\Sulbactam Sodium;Humalog;Perfalgan;Digitoxin;Aspirin;Ferrous Sulfate;Morphine;Atorvastatin;Human Red Blood Cell;Sodium Chloride;Promethazine Hydrochloride;Dermatop;Zyrtec;Mcp"}
{"Case.ID":6564798,"Initial.FDA.Received.Date":"02/28/2008","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"28-FEB-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Levofloxacin;Loxoprofen Sodium;Loperamide Hydrochloride","Reason.for.Use":"Abdominal Pain;Diarrhoea;Product Used For Unknown Indication;Pyrexia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"58 YR","Sender":"Mcneil","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":6568026,"Initial.FDA.Received.Date":"03/03/2008","days.since.last.fda":4,"Event.Date":"11/11/2004","Latest.FDA.Received.Date":"03-MAR-2008","Suspect.Product.Names":"Mcp;Tavor (Lorazepam);Clopidogrel;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Melperone Hydrochloride;Allopurinol;Sodium Perchlorate Monohydrate;Clopidogrel Bisulfate;Methimazole;Lorazepam;Digitoxin;Carbamazepine;Torsemide;Hydrochlorothiazide;Metoprolol Succinate;Loperamide Hydrochloride;Enoxaparin Sodium;Metoclopramide Hydrochloride;Ramipril","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Electrolyte Substitution Therapy;Gastric Disorder;Haemoglobin Decreased;Hypercholesterolaemia;Hypertension;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Nausea;Ocular Hyperaemia;Pain;Parotitis;Pneumonia;Polyuria;Prophylaxis;Pruritus;Pyrexia;Renal Failure;Skin Disorder;Sleep Disorder;Swollen Tongue;Thrombosis Prophylaxis","Reactions":"Mouth Ulceration;Nikolsky'S Sign;Stevens-Johnson Syndrome;Blister;Pneumonia;Lip Erosion;Skin Reaction;Ocular Hyperaemia;Pruritus;Conjunctivitis;Swollen Tongue","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Aventis","Concomitant.Product.Names":"Levofloxacin;Dermatop;Ampicillin Sodium\\Sulbactam Sodium;Atorvastatin;Human Red Blood Cell;Flunitrazepam;Novalgin (Metamizole Sodium);Piperacillin Sodium\\Tazobactam Sodium;Haloperidol;Potassium Chloride;Dextrose;Aspirin;Diflucan;Humalog;Sodium Chloride;Furosemide;Digitoxin;Dimethindene;Morphine;Brotizolam;Metoprolol;Clarithromycin;Hydrochlorothiazide\\Ramipril;Gramicidin\\Neomycin Sulfate\\Polymyxin B Sulfate;Pipamperone;Prednisolone Sodium Succinate;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate\\Sodium Acetate\\Sodium Chlori;Unspecified Ingredient;Ferro-Sanol Duodenal;Mcp;Zyrtec;Perfalgan;Lantus;Promethazine Hydrochloride"}
{"Case.ID":6583242,"Initial.FDA.Received.Date":"03/04/2008","days.since.last.fda":1,"Event.Date":"04/18/2003","Latest.FDA.Received.Date":"24-MAR-2008","Suspect.Product.Names":"Innohep;Mcp;Fexofenadine Hcl;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Carbamazepine;Fexofenadine Hydrochloride;Metoclopramide Hydrochloride;Clemastine;Benzthiazide\\Triamterene;Digoxin;Diazepam;Trimeprazine;Tinzaparin Sodium;Fenoterol\\Ipratropium;Theophylline Anhydrous;Digitoxin;Clonazepam;Prednisone","Reason.for.Use":"Asthma;Chronic Obstructive Pulmonary Disease;Generalised Tonic-Clonic Seizure;Hypertension;Nausea;Prophylaxis;Pruritus;Rash;Supraventricular Tachycardia;Thrombosis Prophylaxis","Reactions":"Nausea;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Pharmion","Concomitant.Product.Names":"Plavix;Depakene;Marcumar;Isoptin;Clobazam;Serevent Diskus"}
{"Case.ID":7399940,"Initial.FDA.Received.Date":"03/12/2008","days.since.last.fda":8,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"12-MAR-2008","Suspect.Product.Names":"Lantus;Pantozol;Tavor (Lorazepam);Lendorm;Humalog;Clopidogrel","Suspect.Product.Active.Ingredients":"Insulin Lispro;Clopidogrel Bisulfate;Sodium Perchlorate Monohydrate;Melperone Hydrochloride;Hydrochlorothiazide;Torsemide;Metoprolol Succinate;Citric Acid Monohydrate\\Potassium Bicarbonate\\Potassium Citrate;Metoprolol;Brotizolam;Carbamazepine;Potassium Chloride;Lorazepam;Digitoxin;Pantoprazole Sodium;Pipamperone;Insulin Glargine;Calcium Acetate\\Magnesium Acetate\\Potassium Chloride;Atorvastatin Calcium;Methimazole;Aminoxyacetic Acid\\Ferrous Sulfate;Glucose, Liquid;Aspirin;Sodium Chloride;Metoclopramide;Furosemide;Allopurinol;Ramipril;Enoxaparin Sodium;Clarithromycin;Loperamide","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Fluid Replacement;Hypercholesterolaemia;Hypertension;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Hypothyroidism;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Prophylaxis Against Gastrointestinal Ulcer;Renal Failure;Sleep Disorder;Thrombosis Prophylaxis","Reactions":"Pneumonia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Biovail","Concomitant.Product.Names":"Digitoxin;Novalgin (Metamizole Sodium);Haloperidol;Dermatop;Unspecified Ingredient;Diflucan;Levofloxacin;Zyrtec;Perfalgan;Morphine"}
{"Case.ID":6581426,"Initial.FDA.Received.Date":"03/14/2008","days.since.last.fda":2,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"18-APR-2008","Suspect.Product.Names":"Pantozol","Suspect.Product.Active.Ingredients":"Glucose, Liquid;Pantoprazole Sodium;Sodium Perchlorate Monohydrate;Pipamperone;Digitoxin;Furosemide;Melperone;Loperamide;Torsemide;Dimethindene Maleate;Clopidogrel Bisulfate;Ramipril;Metoprolol;Aspirin;Brotizolam;Allopurinol;Methimazole;Metoclopramide;Hydrochlorothiazide;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate;Clarithromycin;Insulin Glargine;Enoxaparin Sodium;Carbamazepine;Ferrous Sulfate;Potassium Chloride;Dipyrone;Metoprolol Succinate;Sodium Chloride;Lorazepam;Insulin Lispro;Atorvastatin Calcium","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Essential Hypertension;Fluid Replacement;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Ocular Hyperaemia;Pneumonia;Polyuria;Product Used For Unknown Indication;Prophylaxis Against Gastrointestinal Ulcer;Renal Failure;Skin Disorder;Sleep Disorder;Thrombosis Prophylaxis;Vomiting","Reactions":"Lip Erosion;Stevens-Johnson Syndrome;Swollen Tongue;Pruritus;Blister;Conjunctivitis;Purpura;Ocular Hyperaemia;Nikolsky'S Sign","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Abbott","Concomitant.Product.Names":"Amphotericin B;Morphine;Prednicarbate;Levofloxacin;Acetaminophen;Promethazine Hydrochloride;Piperacillin And Tazobactam;Digitoxin;Haloperidol;Prednisolone Sodium Succinate;Cetirizine Hydrochloride"}
{"Case.ID":6586008,"Initial.FDA.Received.Date":"03/17/2008","days.since.last.fda":3,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"13-APR-2008","Suspect.Product.Names":"Pantozol;Tavor (Lorazepam);Humalog;Lantus;Clopidogrel","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Potassium Chloride;Enoxaparin Sodium;Insulin Glargine;Methimazole;Insulin Lispro;Lorazepam;Loperamide;Pantoprazole Sodium;Furosemide;Sodium Perchlorate Monohydrate;Brotizolam;Atorvastatin;Ramipril;Allopurinol;Digitoxin;Ferrous Sulfate;Citric Acid Monohydrate\\Potassium Bicarbonate\\Potassium Citrate;Carbamazepine;Pipamperone;Melperone Hydrochloride;Glucose, Liquid;Metoprolol Succinate;Metoprolol;Aspirin;Sodium Chloride;Metoclopramide;Hydrochlorothiazide;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate\\Sodium Acetate\\Sodium Chlori;Torsemide;Clarithromycin","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Ocular Hyperaemia;Nikolsky'S Sign;Blister;Purpura;Pruritus;Oral Disorder;Swollen Tongue;Conjunctivitis;Stevens-Johnson Syndrome;Lip Erosion","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Novartis","Concomitant.Product.Names":"Diflucan;Perfalgan;Levofloxacin;Haloperidol;Prednisolone Sodium Succinate;Digitoxin;Promethazine Hydrochloride;Morphine;Novalgin (Metamizole Sodium);Unspecified Ingredient;Tazobactam;Flunitrazepam"}
{"Case.ID":6607528,"Initial.FDA.Received.Date":"03/21/2008","days.since.last.fda":4,"Event.Date":"04/02/2003","Latest.FDA.Received.Date":"21-MAR-2008","Suspect.Product.Names":"Aldactone;Nexium;Konakion","Suspect.Product.Active.Ingredients":"Sucralfate;Phytonadione;Metoclopramide;Diclofenac;Metamizole Sodium;Omeprazole;Esomeprazole Magnesium;Benfotiamine\\Pyridoxine;Calcium Carbonate\\Cholecalciferol;Spironolactone;Xipamide;Ibuprofen;Propranolol Hydrochloride;Ornithine Aspartate","Reason.for.Use":"Ascites;Gastric Ulcer;Gastritis Prophylaxis;Gastrooesophageal Reflux Disease;Helicobacter Infection;Hepatic Cirrhosis;Oedema;Osteoporosis;Pain;Portal Hypertension;Vitamin A;Vitamin K Deficiency","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Axcan","Concomitant.Product.Names":"-"}
{"Case.ID":6610269,"Initial.FDA.Received.Date":"03/28/2008","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"28-MAR-2008","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Urinary Tract Infection","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6618055,"Initial.FDA.Received.Date":"04/07/2008","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"09-JAN-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Schizophreniform Disorder","Reactions":"Respiratory Distress;Gastrointestinal Haemorrhage;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Acute Pulmonary Oedema;Renal Impairment;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"26 YR","Sender":"Apotex","Concomitant.Product.Names":"-"}
{"Case.ID":6623275,"Initial.FDA.Received.Date":"04/24/2008","days.since.last.fda":17,"Event.Date":"03/28/2008","Latest.FDA.Received.Date":"24-APR-2008","Suspect.Product.Names":"Depakene","Suspect.Product.Active.Ingredients":"Valproic Acid","Reason.for.Use":"Dyspnoea;Gastrointestinal Disorder;Herpes Zoster;Infection;Seizure Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Cardiac Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Abbott","Concomitant.Product.Names":"Piperacillin And Tazobactam;Albuterol;Acyclovir;Metoclopramide"}
{"Case.ID":6626678,"Initial.FDA.Received.Date":"04/28/2008","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"28-APR-2008","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"Pfizer","Concomitant.Product.Names":"Dexamethasone;Unspecified Ingredient"}
{"Case.ID":6638264,"Initial.FDA.Received.Date":"05/12/2008","days.since.last.fda":14,"Event.Date":"02/04/2008","Latest.FDA.Received.Date":"27-JUN-2008","Suspect.Product.Names":"Daraprim;Merrem Iv","Suspect.Product.Active.Ingredients":"Meropenem;Clindamycin Phosphate;Pyrimethamine","Reason.for.Use":"Brain Abscess;Cerebral Toxoplasmosis;Generalised Tonic-Clonic Seizure;Rash","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"13976 DAY","Sender":"Astrazeneca","Concomitant.Product.Names":"Oxatomide;Phenobarbital;Isoniazid;Mycobutin;Cyanocobalamin;Kaletra;Truvada;Keppra"}
{"Case.ID":6704217,"Initial.FDA.Received.Date":"07/10/2008","days.since.last.fda":59,"Event.Date":"06/27/2006","Latest.FDA.Received.Date":"10-JUL-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Drug Hypersensitivity;Eosinophilia;Erythema Multiforme;Fear;Injury;Anxiety;Stevens-Johnson Syndrome;Pain;Toxic Epidermal Necrolysis;Acute Generalised Exanthematous Pustulosis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Actavis Mid Atlantic","Concomitant.Product.Names":"-"}
{"Case.ID":6759876,"Initial.FDA.Received.Date":"07/11/2008","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"11-JUL-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Glyburide","Reason.for.Use":"Diabetes Mellitus","Reactions":"Giant Cell Arteritis;Jaundice Cholestatic;Hepatitis Cholestatic;Staphylococcal Infection;Stevens-Johnson Syndrome;Sudden Death;Toxic Skin Eruption;Haemophilus Infection;Pneumonia;Drug Hypersensitivity;Impaired Healing","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":6704549,"Initial.FDA.Received.Date":"07/21/2008","days.since.last.fda":10,"Event.Date":"06/27/2006","Latest.FDA.Received.Date":"21-JUL-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Drug Reaction With Eosinophilia And Systemic Symptoms;Skin Infection;Acute Generalised Exanthematous Pustulosis;Erythema Multiforme;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Drug Hypersensitivity;Dermatitis Bullous","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":6731594,"Initial.FDA.Received.Date":"08/07/2008","days.since.last.fda":17,"Event.Date":"03/13/2008","Latest.FDA.Received.Date":"07-AUG-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Zonisamide;Erlotinib","Reason.for.Use":"Lung Adenocarcinoma","Reactions":"Erythema Multiforme;Constipation;Neoplasm Malignant;Pain;Therapy Non-Responder;Stevens-Johnson Syndrome;Gastrointestinal Disorder;Viral Infection","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"75 YR","Sender":"Osi","Concomitant.Product.Names":"Gaster;Betamethasone;Dipyridamole"}
{"Case.ID":6735389,"Initial.FDA.Received.Date":"08/12/2008","days.since.last.fda":5,"Event.Date":"05/01/2008","Latest.FDA.Received.Date":"12-AUG-2008","Suspect.Product.Names":"Tarceva","Suspect.Product.Active.Ingredients":"Erlotinib Hydrochloride","Reason.for.Use":"Lung Adenocarcinoma","Reactions":"Stevens-Johnson Syndrome;Pneumonia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Osi","Concomitant.Product.Names":"Phenytoin;Diclofenac Sodium;Megestrol Acetate;Benzonatate"}
{"Case.ID":6725047,"Initial.FDA.Received.Date":"08/12/2008","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"12-AUG-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamivudine;Nelfinavir;Nevirapine","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome;Staphylococcal Infection;Septic Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":6733838,"Initial.FDA.Received.Date":"08/22/2008","days.since.last.fda":10,"Event.Date":"05/02/2008","Latest.FDA.Received.Date":"19-FEB-2009","Suspect.Product.Names":"Rocephin","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium;Allopurinol","Reason.for.Use":"Gout","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"81 YR","Sender":"Roche","Concomitant.Product.Names":"Eprex;Colchicine\\Opium;Omeprazole;Furosemide;Nicardipine Hydrochloride;Plavix;Rilmenidine"}
{"Case.ID":6785720,"Initial.FDA.Received.Date":"10/01/2008","days.since.last.fda":40,"Event.Date":"08/07/2006","Latest.FDA.Received.Date":"01-OCT-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cephalexin;Phenytoin Sodium","Reason.for.Use":"-","Reactions":"Emotional Distress;Erythema Multiforme;Drug Eruption;Multiple Organ Dysfunction Syndrome;Cardiac Arrest;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Acute Generalised Exanthematous Pustulosis;Anxiety;Drug Reaction With Eosinophilia And Systemic Symptoms;Fear","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":6782926,"Initial.FDA.Received.Date":"10/01/2008","days.since.last.fda":0,"Event.Date":"09/05/2008","Latest.FDA.Received.Date":"01-OCT-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Azithromycin Anhydrous;Penicillin V Potassium","Reason.for.Use":"Lymphadenopathy;Oropharyngeal Pain","Reactions":"Mucosal Haemorrhage;Systemic Inflammatory Response Syndrome;Stevens-Johnson Syndrome;Cardiac Arrest;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"62 YR","Sender":"-","Concomitant.Product.Names":"Allopurinol;Acular;Vicodin;Lisinopril And Hydrochlorothiazide;Moxifloxacin;Lidocaine;Clonidine;Skelaxin"}
{"Case.ID":6801045,"Initial.FDA.Received.Date":"10/15/2008","days.since.last.fda":14,"Event.Date":"03/14/2007","Latest.FDA.Received.Date":"29-APR-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lansoprazole","Reason.for.Use":"Gastric Ulcer;Gouty Arthritis;Ischaemic Stroke;Upper Gastrointestinal Haemorrhage","Reactions":"Hyperkalaemia;Respiratory Failure;Haemodialysis;Bacterial Infection;Urinary Tract Inflammation;Coagulopathy;Septic Shock;Gouty Arthritis;Gastric Ulcer;Stevens-Johnson Syndrome;Pneumonia;Electrolyte Imbalance;Ventricular Hypokinesia;Acute Myocardial Infarction;Renal Impairment","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"58 YR","Sender":"Takeda","Concomitant.Product.Names":"Indapamide;Clopidogrel;Celecoxib;Carbimazole;Fosinopril Sodium;Aspirin;Felodipine;Allopurinol"}
{"Case.ID":6797192,"Initial.FDA.Received.Date":"10/27/2008","days.since.last.fda":12,"Event.Date":"","Latest.FDA.Received.Date":"22-DEC-2008","Suspect.Product.Names":"Pred Forte;Relafen;Zymar;Acular","Suspect.Product.Active.Ingredients":"Ketorolac Tromethamine;Gatifloxacin;Nabumetone;Prednisolone Acetate","Reason.for.Use":"Postoperative Care;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Allergan","Concomitant.Product.Names":"Zantac;Norvasc"}
{"Case.ID":6817044,"Initial.FDA.Received.Date":"11/13/2008","days.since.last.fda":17,"Event.Date":"11/10/2008","Latest.FDA.Received.Date":"13-NOV-2008","Suspect.Product.Names":"Flagyl","Suspect.Product.Active.Ingredients":"Metronidazole\\Metronidazole Hydrochloride","Reason.for.Use":"Clostridial Infection","Reactions":"Drug Hypersensitivity;Sepsis;Wound;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6824379,"Initial.FDA.Received.Date":"11/26/2008","days.since.last.fda":13,"Event.Date":"10/01/2006","Latest.FDA.Received.Date":"04-AUG-2010","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Partial Seizures;Seizure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"52 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":6863572,"Initial.FDA.Received.Date":"12/11/2008","days.since.last.fda":15,"Event.Date":"07/05/2008","Latest.FDA.Received.Date":"11-DEC-2008","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Minocycline Hydrochloride","Reason.for.Use":"Acne","Reactions":"Drug Reaction With Eosinophilia And Systemic Symptoms;Lung Disorder;Myocarditis;Pericardial Haemorrhage;Diffuse Alveolar Damage;Cardiomyopathy;Rash;Sepsis;Brain Death;Stevens-Johnson Syndrome;Disseminated Intravascular Coagulation","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"17 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6851618,"Initial.FDA.Received.Date":"12/15/2008","days.since.last.fda":4,"Event.Date":"06/24/2007","Latest.FDA.Received.Date":"05-MAR-2009","Suspect.Product.Names":"Voltaren","Suspect.Product.Active.Ingredients":"Diclofenac Sodium;Allopurinol","Reason.for.Use":"Cardiac Failure;Constipation;Gastritis;Hypertension;Hyperuricaemia;Hypothermia;Pyrexia","Reactions":"Erythema;Condition Aggravated;Stevens-Johnson Syndrome;Rash;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Novartis","Concomitant.Product.Names":"Enalapril Maleate;Lasix;Teprenone;Micardis;Carvedilol;Norvasc;Aldactone;Sennosides A And B"}
{"Case.ID":6851620,"Initial.FDA.Received.Date":"12/15/2008","days.since.last.fda":0,"Event.Date":"06/02/2006","Latest.FDA.Received.Date":"15-DEC-2008","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Delirium Tremens;Diuretic Therapy;Haemolytic Anaemia;Hepatic Cirrhosis;Pneumonia","Reactions":"Rash Macular;Pruritus;Stevens-Johnson Syndrome;Pyrexia;Oral Mucosa Erosion;Pneumonia;Rash Pustular;Lip Erosion;Gastrointestinal Erosion","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"32 YR","Sender":"Novartis","Concomitant.Product.Names":"Avelox;Lasix;Clarithromycin;Prednisolone"}
{"Case.ID":6855510,"Initial.FDA.Received.Date":"12/17/2008","days.since.last.fda":2,"Event.Date":"05/08/2006","Latest.FDA.Received.Date":"17-DEC-2008","Suspect.Product.Names":"Sandostatin;Lasix;Perfalgan;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Minoxidil;Bisoprolol;Oxazepam;Amoxicillin\\Clavulanate Potassium;Acetaminophen;Lisinopril;Unspecified Ingredient;Acetylcysteine;Furosemide;Octreotide Acetate;Xipamide;Levothyroxine Sodium\\Potassium Iodide;Calcium Carbonate;Alfacalcidol;Clorazepate Dipotassium","Reason.for.Use":"Hyperparathyroidism Secondary;Hypertension;Pancreatitis;Prophylaxis;Pyrexia;Renal Failure;Respiratory Disorder;Sedation;Sepsis","Reactions":"Hepatic Failure;Ocular Hyperaemia;Blister;Mucosal Erosion;Sepsis;Pyrexia;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Erosive Oesophagitis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"64 YR","Sender":"Novartis","Concomitant.Product.Names":"Lisinopril;Petrolatum;Hydrocortisone;Vancomycin;Meropenem;Sodium Chloride;Bisoprolol Fumarate;Metronidazole"}
{"Case.ID":6893013,"Initial.FDA.Received.Date":"01/27/2009","days.since.last.fda":41,"Event.Date":"02/26/2008","Latest.FDA.Received.Date":"22-SEP-2009","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin;Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome;Cardiac Failure Congestive;Sepsis;Respiratory Failure;Pulmonary Oedema","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":6892812,"Initial.FDA.Received.Date":"01/27/2009","days.since.last.fda":0,"Event.Date":"03/01/2008","Latest.FDA.Received.Date":"25-MAR-2009","Suspect.Product.Names":"Dilantin-125","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Fall;Stevens-Johnson Syndrome;Cerebral Thrombosis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"80 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":6893014,"Initial.FDA.Received.Date":"01/27/2009","days.since.last.fda":0,"Event.Date":"09/01/2007","Latest.FDA.Received.Date":"27-JAN-2009","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Cardio-Respiratory Arrest;Obesity","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"57 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":6906293,"Initial.FDA.Received.Date":"02/10/2009","days.since.last.fda":14,"Event.Date":"05/14/2006","Latest.FDA.Received.Date":"10-FEB-2009","Suspect.Product.Names":"Lasix;Pantozol;Sandostatin;Augmentin","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium;Clorazepate Dipotassium;Sodium Chloride;Calcium Carbonate;Xipamide;Octreotide Acetate;Ascorbic Acid\\Calcium Pantothenate\\Folic Acid\\Pyridoxine Hydrochloride\\Riboflavin\\Thiamine Hydrochloride;Levothyroxine Sodium\\Potassium Iodide;Pantoprazole Sodium;Alfacalcidol;Acetylcysteine;Furosemide;Sodium Bicarbonate;Acetaminophen;Bisoprolol;Minoxidil;Lisinopril;Oxazepam","Reason.for.Use":"Blood Bicarbonate Decreased;Electrolyte Substitution Therapy;Fluid Replacement;Gastritis Prophylaxis;Hyperparathyroidism Secondary;Hypertension;Infection Prophylaxis;Iodine Deficiency;Pancreatitis;Pyrexia;Renal Failure;Secretion Discharge;Sedation;Sepsis;Vitamin B Complex Deficiency","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"Vancomycin"}
{"Case.ID":6915803,"Initial.FDA.Received.Date":"02/23/2009","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"23-FEB-2009","Suspect.Product.Names":"Dilantin-125","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":6965022,"Initial.FDA.Received.Date":"04/09/2009","days.since.last.fda":45,"Event.Date":"01/01/2009","Latest.FDA.Received.Date":"09-APR-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Seizure","Reactions":"Pneumonia;Mouth Ulceration;Oral Candidiasis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Valproate Sodium"}
{"Case.ID":6979333,"Initial.FDA.Received.Date":"04/10/2009","days.since.last.fda":1,"Event.Date":"01/19/2009","Latest.FDA.Received.Date":"18-JUN-2009","Suspect.Product.Names":"Celestamine;Herbal Nos;Predonine","Suspect.Product.Active.Ingredients":"Prednisolone;Mequitazine;Betamethasone;Herbals;Clarithromycin;Cefcapene;Unspecified Ingredient;Rebamipide;Betamethasone\\Dexchlorpheniramine Maleate;Irsogladine;Methylcobalamin;Acetaminophen;Olopatadine Hydrochloride;Cefditoren Pivoxil","Reason.for.Use":"Drug Eruption;Otitis Media Acute","Reactions":"Stevens-Johnson Syndrome;Endocarditis;Disseminated Intravascular Coagulation;Vena Cava Thrombosis;Sepsis;Splenic Infarction;Liver Disorder;Toxic Epidermal Necrolysis;Drug Ineffective;Transfusion-Related Acute Lung Injury;Cerebral Haemorrhage;Bacteraemia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"22 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6975317,"Initial.FDA.Received.Date":"04/15/2009","days.since.last.fda":5,"Event.Date":"04/10/2009","Latest.FDA.Received.Date":"15-APR-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Thiotepa;Etoposide;Carboplatin","Reason.for.Use":"-","Reactions":"Mucosal Inflammation;Pyrexia;Septic Shock;Toxic Epidermal Necrolysis;Multiple Organ Dysfunction Syndrome;Hepatic Failure;Cardiac Failure;Neutropenia;General Physical Health Deterioration;Stevens-Johnson Syndrome;Hypertension;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"4 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":6981486,"Initial.FDA.Received.Date":"04/22/2009","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"22-APR-2009","Suspect.Product.Names":"Cefepime;Vasotec","Suspect.Product.Active.Ingredients":"Enalapril Maleate;Minoxidil;Vancomycin Hydrochloride;Cefepime Hydrochloride;Allopurinol;Clopidogrel Bisulfate","Reason.for.Use":"Hypertension;Product Used For Unknown Indication","Reactions":"Toxic Epidermal Necrolysis;Urinary Tract Infection;General Physical Health Deterioration;Cardio-Respiratory Arrest;Angioedema;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Bta Pharm","Concomitant.Product.Names":"Acetaminophen\\Oxycodone Hydrochloride;Aspirin;Metoprolol;Acetaminophen;Pantoprazole Sodium;Nifedipine;Epoetin Alfa;Risperidone;Valsartan;Simvastatin;Furosemide;Nitroglycerin;Folic Acid;Clonidine"}
{"Case.ID":6988489,"Initial.FDA.Received.Date":"04/28/2009","days.since.last.fda":6,"Event.Date":"04/01/2008","Latest.FDA.Received.Date":"28-APR-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin Hydrochloride","Reason.for.Use":"Sepsis","Reactions":"Burns Third Degree;Dialysis;Renal Failure;Hepatic Failure;Acute Respiratory Distress Syndrome;Hallucination;Hypophagia;Bacterial Infection;Diabetes Mellitus;Fluid Intake Reduced;Stevens-Johnson Syndrome;Ocular Icterus","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"61 YR","Sender":"-","Concomitant.Product.Names":"Allopurinol"}
{"Case.ID":7012018,"Initial.FDA.Received.Date":"06/02/2009","days.since.last.fda":35,"Event.Date":"01/23/2009","Latest.FDA.Received.Date":"02-JUN-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amoxicillin;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Staphylococcal Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"30 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7008660,"Initial.FDA.Received.Date":"06/02/2009","days.since.last.fda":0,"Event.Date":"01/18/2009","Latest.FDA.Received.Date":"02-JUN-2009","Suspect.Product.Names":"Fulcaliq;Novolin R;Rocephin;Decadron;Meylon","Suspect.Product.Active.Ingredients":"Sodium Bicarbonate;Ammonium Glycyrrhizate;Lactobacillus Acidophilus;Meropenem;Ganciclovir Sodium;Dietary Supplement\\Probiotics;Menatetrenone;Dexamethasone;Albumin Human;Heparin Sodium;Lactase;Aspirin;Insulin Human;Ceftriaxone Sodium;Minerals;Nafamostat Mesylate;Amino Acids\\Carbohydrates\\Electrolytes Nos\\Vitamins;Famotidine;Soybean Oil;Amino Acids, Source Unspecified;Midazolam Hydrochloride;Teprenone;Mannitol","Reason.for.Use":"Arterial Catheterisation;Brain Oedema;Cytomegalovirus Infection;Liver Disorder;Malnutrition;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"4 MTH","Sender":"Roche","Concomitant.Product.Names":"Dietary Supplement\\Probiotics;Teprenone"}
{"Case.ID":7040960,"Initial.FDA.Received.Date":"06/19/2009","days.since.last.fda":17,"Event.Date":"","Latest.FDA.Received.Date":"19-JUN-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Anhedonia;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Fear;Pain;Emotional Distress;Drug Eruption;Drug Reaction With Eosinophilia And Systemic Symptoms;Erythema Multiforme;Anxiety;Acute Generalised Exanthematous Pustulosis;Injury","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Taro","Concomitant.Product.Names":"-"}
{"Case.ID":7029577,"Initial.FDA.Received.Date":"06/22/2009","days.since.last.fda":3,"Event.Date":"01/01/2009","Latest.FDA.Received.Date":"22-JUN-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Minoxidil","Reason.for.Use":"Antibiotic Therapy;Hypertension;Pain;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Watson","Concomitant.Product.Names":"Aspirin;Allopurinol;Clonidine;Folic Acid;Risperidone;Oxycodone And Acetaminophen;Paroxetine Hydrochloride;Cefepime;Epoetin Alfa;Valsartan;Fosinopril Sodium;Pantoprazole Sodium;Clopidogrel;Vancomycin;Simvastatin;Metoprolol;Furosemide;Nifedipine;Enalapril;Nitroglycerin;Doxercalciferol"}
{"Case.ID":7047125,"Initial.FDA.Received.Date":"06/29/2009","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"29-JUN-2009","Suspect.Product.Names":"Cefepime;Clopidogrel","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Fosinopril Sodium;Enalapril;Cefepime Hydrochloride;Vancomycin;Minoxidil;Allopurinol","Reason.for.Use":"Antibiotic Therapy;Hypertension;Product Used For Unknown Indication","Reactions":"Cerebrovascular Accident;Cardio-Respiratory Arrest;Toxic Epidermal Necrolysis;Platelet Count Decreased;Blood Pressure Increased;Urinary Tract Infection Staphylococcal;Haematocrit Decreased;Body Temperature Increased;Haemoglobin Decreased;Blood Creatinine Increased;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Par","Concomitant.Product.Names":"Clonidine;Simvastatin;Paroxetine Hydrochloride;Aspirin;Folic Acid;Nifedipine;Acetaminophen;Acetaminophen\\Oxycodone Hydrochloride;Epoetin Alfa;Risperidone;Nitroglycerin;Metoprolol"}
{"Case.ID":7069129,"Initial.FDA.Received.Date":"07/31/2009","days.since.last.fda":32,"Event.Date":"","Latest.FDA.Received.Date":"11-SEP-2009","Suspect.Product.Names":"Primaxin Im","Suspect.Product.Active.Ingredients":"Cilastatin Sodium\\Imipenem;Amphotericin B","Reason.for.Use":"Lymphoma","Reactions":"Respiratory Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"47 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":7636233,"Initial.FDA.Received.Date":"08/13/2009","days.since.last.fda":13,"Event.Date":"01/27/2009","Latest.FDA.Received.Date":"28-JUN-2011","Suspect.Product.Names":"Predonine;Celestamine","Suspect.Product.Active.Ingredients":"Betamethasone\\Dexchlorpheniramine Maleate;Betamethasone;Prednisolone;Cefcapene Pivoxil Hydrochloride;Cefditoren Pivoxil;Mequitazine;Irsogladine;Clarithromycin;Alpinia Katsumadai Fruit Extract;Rebamipide;Methylcobalamin;Unspecified Ingredient;Olopatadine Hydrochloride;Acetaminophen","Reason.for.Use":"Analgesic Therapy;Drug Eruption;Labyrinthitis;Otitis Media Acute;Prophylaxis Against Gastrointestinal Ulcer;Rhinitis Allergic","Reactions":"Toxic Epidermal Necrolysis;Disseminated Intravascular Coagulation;Endocarditis;Liver Disorder;Pelvic Venous Thrombosis;Splenic Infarction;Stevens-Johnson Syndrome;Continuous Haemodiafiltration;Bacteraemia;Mycoplasma Test Positive;Transfusion-Related Acute Lung Injury","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"22 YR","Sender":"Abbott","Concomitant.Product.Names":"Plasma, Fresh Frozen;Solu-Medrol"}
{"Case.ID":7107999,"Initial.FDA.Received.Date":"09/08/2009","days.since.last.fda":26,"Event.Date":"01/17/2007","Latest.FDA.Received.Date":"03-SEP-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamivudine\\Nevirapine\\Stavudine","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"1 YR","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":7136204,"Initial.FDA.Received.Date":"09/24/2009","days.since.last.fda":16,"Event.Date":"09/01/2009","Latest.FDA.Received.Date":"24-SEP-2009","Suspect.Product.Names":"Truvada","Suspect.Product.Active.Ingredients":"Emtricitabine\\Tenofovir Disoproxil Fumarate;Efavirenz","Reason.for.Use":"Hiv Infection","Reactions":"Oral Candidiasis;Abdominal Pain;Rash;Vomiting;Hepatomegaly;Dermatitis;Asthenia;Hypoglycaemia;Blood Pressure Diastolic Decreased;Coma Hepatic;Eating Disorder;Blood Albumin Decreased;Confusional State;Blood Creatine Increased;Stevens-Johnson Syndrome;Heart Rate Increased;Blood Bilirubin Increased;Stupor;Hepatitis;Hepatotoxicity;Blood Sodium Decreased;Jaundice;Hypoaesthesia;Hepatic Encephalopathy","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"29 YR","Sender":"-","Concomitant.Product.Names":"Rifampin;Ethambutol;Isoniazid;Pyrazinamide;Cotrimoxazole"}
{"Case.ID":7141208,"Initial.FDA.Received.Date":"09/28/2009","days.since.last.fda":4,"Event.Date":"06/17/2009","Latest.FDA.Received.Date":"28-SEP-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7167492,"Initial.FDA.Received.Date":"10/30/2009","days.since.last.fda":32,"Event.Date":"10/07/2009","Latest.FDA.Received.Date":"30-OCT-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Gout","Reactions":"Metabolic Acidosis;Pneumonia;Pyrexia;Acute Kidney Injury;Delirium;Tubulointerstitial Nephritis;Hypotension;Leukocytosis;Cardiac Arrest;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;International Normalised Ratio Increased;Multiple Organ Dysfunction Syndrome;Sepsis;Ventricular Fibrillation;Hallucination;Renal Tubular Necrosis;Henoch-Schonlein Purpura;Respiratory Failure;Coagulopathy;Nosocomial Infection;Disseminated Intravascular Coagulation;Haemolytic Uraemic Syndrome;Thrombocytopenic Purpura;Psychotic Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"-","Concomitant.Product.Names":"Coumadin;Azulfidine;Potassium;Lasix;Coreg;Synthroid;Aldactone;Cardura;Lipitor"}
{"Case.ID":7177092,"Initial.FDA.Received.Date":"11/13/2009","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"22-MAR-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Valproate Sodium;Lamotrigine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Drug Interaction;Incorrect Dose Administered","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Abbott","Concomitant.Product.Names":"-"}
{"Case.ID":7183964,"Initial.FDA.Received.Date":"11/18/2009","days.since.last.fda":5,"Event.Date":"10/27/2009","Latest.FDA.Received.Date":"18-NOV-2009","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Blood Uric Acid","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"94 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7186899,"Initial.FDA.Received.Date":"11/24/2009","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"24-NOV-2009","Suspect.Product.Names":"Dilantin-125","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":7193656,"Initial.FDA.Received.Date":"11/30/2009","days.since.last.fda":6,"Event.Date":"09/21/2009","Latest.FDA.Received.Date":"30-NOV-2009","Suspect.Product.Names":"Coartem","Suspect.Product.Active.Ingredients":"Artemether\\Lumefantrine;Acetaminophen;Amoxicillin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Skin Lesion","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"19 MTH","Sender":"Novartis","Concomitant.Product.Names":"Phenobarbital"}
{"Case.ID":7200498,"Initial.FDA.Received.Date":"12/04/2009","days.since.last.fda":4,"Event.Date":"01/01/2007","Latest.FDA.Received.Date":"04-DEC-2009","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Bipolar Disorder","Reactions":"Stevens-Johnson Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":7202432,"Initial.FDA.Received.Date":"12/07/2009","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"07-JUL-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amoxicillin","Reason.for.Use":"Upper Respiratory Tract Infection","Reactions":"Abdominal Distension;Stevens-Johnson Syndrome;Streptococcal Infection;Blister;Eye Pain;Genital Erosion;Lip Erosion;Diarrhoea;Hypothermia;Haematochezia;Toxic Epidermal Necrolysis;Gastritis Erosive;Erosive Oesophagitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":7221559,"Initial.FDA.Received.Date":"12/17/2009","days.since.last.fda":10,"Event.Date":"08/10/2009","Latest.FDA.Received.Date":"29-JAN-2010","Suspect.Product.Names":"Haldol","Suspect.Product.Active.Ingredients":"Haloperidol;Furosemide","Reason.for.Use":"Anxiety;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"87 YR","Sender":"Aventis","Concomitant.Product.Names":"Diltiazem Hydrochloride;Inipomp;Cartrol;Paroxetine Hydrochloride;Budesonide\\Formoterol;Potassium Chloride;Zopiclone"}
{"Case.ID":7232814,"Initial.FDA.Received.Date":"12/29/2009","days.since.last.fda":12,"Event.Date":"12/19/2009","Latest.FDA.Received.Date":"29-DEC-2009","Suspect.Product.Names":"Dianeal","Suspect.Product.Active.Ingredients":"Calcium Chloride\\Dextrose\\Magnesium Chloride\\Sodium Chloride\\Sodium Lactate;Unspecified Ingredient","Reason.for.Use":"Peritoneal Dialysis;Urinary Tract Infection","Reactions":"Urinary Tract Infection;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Baxter","Concomitant.Product.Names":"-"}
{"Case.ID":7261043,"Initial.FDA.Received.Date":"01/25/2010","days.since.last.fda":27,"Event.Date":"10/05/2009","Latest.FDA.Received.Date":"25-JAN-2010","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine;Carbamazepine","Reason.for.Use":"Seizure","Reactions":"Alopecia;Stevens-Johnson Syndrome;Organ Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"43 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7260972,"Initial.FDA.Received.Date":"01/29/2010","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"29-JAN-2010","Suspect.Product.Names":"Soriatane","Suspect.Product.Active.Ingredients":"Acitretin","Reason.for.Use":"Psoriasis","Reactions":"Death;Stevens-Johnson Syndrome;Cellulitis;Staphylococcal Infection","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":7275007,"Initial.FDA.Received.Date":"02/10/2010","days.since.last.fda":12,"Event.Date":"12/21/2009","Latest.FDA.Received.Date":"27-JUN-2011","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Cardiac Failure Chronic;Cerebral Infarction;Epilepsy","Reactions":"Oral Disorder;Multiple Organ Dysfunction Syndrome;Jaundice;Lung Disorder;Pyrexia;Oral Mucosal Erythema;Stevens-Johnson Syndrome;Drug Eruption;Hypophagia;Drug Reaction With Eosinophilia And Systemic Symptoms;Erythema;General Physical Health Deterioration","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Novartis","Concomitant.Product.Names":"Warfarin Sodium;Digoxin;Furosemide;Candesartan Cilexetil;Zantac;Lansoprazole;Adalat"}
{"Case.ID":7276373,"Initial.FDA.Received.Date":"02/11/2010","days.since.last.fda":1,"Event.Date":"01/14/2010","Latest.FDA.Received.Date":"09-MAR-2010","Suspect.Product.Names":"Xeloda","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Melaena;Haematemesis;Blister;Diarrhoea","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"77 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":7295326,"Initial.FDA.Received.Date":"02/19/2010","days.since.last.fda":8,"Event.Date":"01/31/2010","Latest.FDA.Received.Date":"19-FEB-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"31 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7309092,"Initial.FDA.Received.Date":"03/09/2010","days.since.last.fda":18,"Event.Date":"","Latest.FDA.Received.Date":"09-MAR-2010","Suspect.Product.Names":"Mitoxantrone","Suspect.Product.Active.Ingredients":"Mitoxantrone Hydrochloride;Rituximab;Fludarabine Phosphate;Dexamethasone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":7319714,"Initial.FDA.Received.Date":"03/15/2010","days.since.last.fda":6,"Event.Date":"03/01/2010","Latest.FDA.Received.Date":"15-MAR-2010","Suspect.Product.Names":"Arava","Suspect.Product.Active.Ingredients":"Leflunomide","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":7321696,"Initial.FDA.Received.Date":"03/16/2010","days.since.last.fda":1,"Event.Date":"03/04/2008","Latest.FDA.Received.Date":"24-JAN-2011","Suspect.Product.Names":"Fragmin;Zovirax;Nexium;Haldol;Tavor (Lorazepam);Insulin Human Nos;Ciloxan;Daraprim;Piperacillin And Tazobactam","Suspect.Product.Active.Ingredients":"Piperacillin Sodium\\Tazobactam Sodium;Levofloxacin;Acetaminophen;Pyrimethamine;Vancomycin;Ciprofloxacin Hydrochloride;Insulin Human;Esomeprazole Magnesium;Haloperidol;Lorazepam;Acyclovir;Aspirin;Ceftazidime;Dalteparin Sodium;Sulfadiazine;Clindamycin Hydrochloride","Reason.for.Use":"Ear Infection;Hallucination;Hyperglycaemia;Meningoencephalitis Herpetic;Pyrexia;Sepsis;Thrombosis Prophylaxis;Toxoplasmosis","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"42 YR","Sender":"Pfizer","Concomitant.Product.Names":"Nizoral;Leucovorin Calcium;Methylprednisolone Aceponate;Melperone Hydrochloride;Sorbitol;Vitamin B1;Sodium Chloride;Epirizole;Konakion;Thiamine Hydrochloride"}
{"Case.ID":7321695,"Initial.FDA.Received.Date":"03/16/2010","days.since.last.fda":0,"Event.Date":"02/04/2008","Latest.FDA.Received.Date":"16-MAR-2010","Suspect.Product.Names":"Insulin Human Nos;Ultiva;Lyrica;Nexium;Dulcolax (Bisacodyl)","Suspect.Product.Active.Ingredients":"Bisacodyl;Fluconazole;Heparin Sodium;Ciprofloxacin;Ketamine Hydrochloride;Levothyroxine Sodium;Esomeprazole Magnesium;Pregabalin;Metoprolol Succinate;Remifentanil Hydrochloride;Piperacillin Sodium\\Tazobactam Sodium;Propofol;Midazolam Hydrochloride;Metoprolol Tartrate;Insulin Human;Hydrocortisone;Furosemide","Reason.for.Use":"Arthritis;Constipation;Depression;Hyperglycaemia;Hypertension;Hypotension;Hypothyroidism;Pain;Polyuria;Prophylaxis Against Gastrointestinal Ulcer;Restlessness;Sepsis;Stupor;Thrombosis Prophylaxis","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"Wyeth","Concomitant.Product.Names":"Piritramide;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate\\Sodium Acetate\\Sodium Chlori;Fentanyl;Tpn Electrolytes;Sodium Chloride;Lorazepam;Potassium Chloride\\Sodium Chloride;Potassium Chloride;Calcium Chloride"}
{"Case.ID":7322960,"Initial.FDA.Received.Date":"03/17/2010","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"24-MAR-2010","Suspect.Product.Names":"Dianeal","Suspect.Product.Active.Ingredients":"Calcium Chloride\\Dextrose\\Magnesium Chloride\\Sodium Chloride\\Sodium Lactate","Reason.for.Use":"Peritoneal Dialysis","Reactions":"Infection;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"57 YR","Sender":"Baxter","Concomitant.Product.Names":"-"}
{"Case.ID":7349365,"Initial.FDA.Received.Date":"04/06/2010","days.since.last.fda":20,"Event.Date":"03/17/2010","Latest.FDA.Received.Date":"06-APR-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Pralatrexate","Reason.for.Use":"T-Cell Lymphoma Refractory","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"47 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7367080,"Initial.FDA.Received.Date":"04/15/2010","days.since.last.fda":9,"Event.Date":"02/18/2008","Latest.FDA.Received.Date":"15-APR-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin Sodium","Reason.for.Use":"-","Reactions":"Drug Eruption;Toxic Epidermal Necrolysis;Acute Generalised Exanthematous Pustulosis;Skin Reaction;Drug Reaction With Eosinophilia And Systemic Symptoms;Dermatitis Bullous;Sepsis;Erythema Multiforme;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Westward","Concomitant.Product.Names":"-"}
{"Case.ID":7371979,"Initial.FDA.Received.Date":"04/30/2010","days.since.last.fda":15,"Event.Date":"08/18/2008","Latest.FDA.Received.Date":"06-JUL-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ibuprofen;Moxonidine;Folic Acid;Ferrous Gluconate;Tolterodine Tartrate;Digoxin;Allopurinol;Povidone-Iodine;Aspirin;Dexamethasone Sodium Phosphate\\Neomycin Sulfate\\Polymyxin B Sulfate;Torsemide","Reason.for.Use":"Cardiac Failure;Conjunctivitis;Hypertension;Hyperuricaemia;Incontinence;Pain;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"87 YR","Sender":"Wyeth","Concomitant.Product.Names":"-"}
{"Case.ID":7415200,"Initial.FDA.Received.Date":"06/10/2010","days.since.last.fda":41,"Event.Date":"05/12/2001","Latest.FDA.Received.Date":"09-JUL-2010","Suspect.Product.Names":"Heparin","Suspect.Product.Active.Ingredients":"Heparin Sodium;Metoclopramide Hydrochloride;Etilefrine Hydrochloride;Pantoprazole Sodium;Loperamide;Pentazocine;Omeprazole;Mezlocillin Sodium;Prednisolone Sodium Succinate;Ciprofloxacin Hydrochloride;Dimenhydrinate;Penciclovir Sodium;Hymecromone;Metronidazole","Reason.for.Use":"Cholangitis;Cholelithiasis;Gastroenteritis;Hypotension;Pain;Peptic Ulcer;Product Used For Unknown Indication;Pruritus;Thrombosis Prophylaxis;Vomiting","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Circulatory Collapse","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"Mcneil","Concomitant.Product.Names":"-"}
{"Case.ID":7417034,"Initial.FDA.Received.Date":"06/11/2010","days.since.last.fda":1,"Event.Date":"04/15/2010","Latest.FDA.Received.Date":"11-JUN-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Meropenem","Reason.for.Use":"Osteomyelitis;Pain;Prophylaxis;Rash","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"48 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"Fexofenadine;Ezetimibe;Omeprazole;Acetaminophen;Spironolactone;Vancomycin;Amoxicillin\\Clavulanate Potassium;Irbesartan;Tiotropium Bromide;Symbicort;Enoxaparin Sodium;Tramadol;Gentamicin;Ciprofloxacin;Petrolatum;Pravastatin"}
{"Case.ID":7436369,"Initial.FDA.Received.Date":"06/25/2010","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"25-JUN-2010","Suspect.Product.Names":"Combivir","Suspect.Product.Active.Ingredients":"Lamivudine\\Zidovudine;Nevirapine","Reason.for.Use":"Human Immunodeficiency Virus Transmission;Prophylaxis","Reactions":"Hypersensitivity;Stevens-Johnson Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":7557060,"Initial.FDA.Received.Date":"07/16/2010","days.since.last.fda":21,"Event.Date":"","Latest.FDA.Received.Date":"16-JUL-2010","Suspect.Product.Names":"Celebrex","Suspect.Product.Active.Ingredients":"Celecoxib","Reason.for.Use":"-","Reactions":"Labelled Drug-Disease Interaction Medication Error;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":7532489,"Initial.FDA.Received.Date":"08/06/2010","days.since.last.fda":21,"Event.Date":"","Latest.FDA.Received.Date":"06-AUG-2010","Suspect.Product.Names":"Dilantin-125","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":7544611,"Initial.FDA.Received.Date":"08/17/2010","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"09-SEP-2010","Suspect.Product.Names":"Dianeal","Suspect.Product.Active.Ingredients":"Calcium Chloride\\Dextrose\\Magnesium Chloride\\Sodium Chloride\\Sodium Lactate","Reason.for.Use":"Peritoneal Dialysis","Reactions":"Hypertension;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"Baxter","Concomitant.Product.Names":"-"}
{"Case.ID":7605191,"Initial.FDA.Received.Date":"09/16/2010","days.since.last.fda":30,"Event.Date":"04/15/2010","Latest.FDA.Received.Date":"16-SEP-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Psoriasis","Reactions":"Metabolic Acidosis;Neutropenia;Sepsis;Acute Respiratory Distress Syndrome;Skin Reaction;Acute Kidney Injury;Ischaemic Hepatitis;Cardiac Arrest;Anaemia;Leukopenia;Dehydration;Thrombocytopenia;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"56 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7613800,"Initial.FDA.Received.Date":"09/24/2010","days.since.last.fda":8,"Event.Date":"10/02/2009","Latest.FDA.Received.Date":"24-SEP-2010","Suspect.Product.Names":"Cefepime","Suspect.Product.Active.Ingredients":"Cefepime Hydrochloride;Ciprofloxacin\\Ciprofloxacin Hydrochloride","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Rash;Blister;Cardiac Arrest;Stevens-Johnson Syndrome;Multiple Injuries","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"61 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7639710,"Initial.FDA.Received.Date":"10/26/2010","days.since.last.fda":32,"Event.Date":"","Latest.FDA.Received.Date":"26-OCT-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin;Aztreonam;Levofloxacin;Clindamycin","Reason.for.Use":"Cellulitis;Chronic Obstructive Pulmonary Disease","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"Ranbaxy","Concomitant.Product.Names":"-"}
{"Case.ID":7651885,"Initial.FDA.Received.Date":"11/01/2010","days.since.last.fda":6,"Event.Date":"01/01/2010","Latest.FDA.Received.Date":"10-NOV-2010","Suspect.Product.Names":"Lyrica;Revlimid","Suspect.Product.Active.Ingredients":"Lenalidomide;Pregabalin","Reason.for.Use":"Plasma Cell Myeloma","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":7665381,"Initial.FDA.Received.Date":"11/12/2010","days.since.last.fda":11,"Event.Date":"06/12/2008","Latest.FDA.Received.Date":"12-NOV-2010","Suspect.Product.Names":"Altace;Norvasc","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Hydrochlorothiazide;Ramipril;Bisoprolol Fumarate;Lansoprazole","Reason.for.Use":"-","Reactions":"Staphylococcal Sepsis;Erythema Multiforme;Skin Erosion;Pyrexia;Rash Macular;Blister;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"75 YR","Sender":"King","Concomitant.Product.Names":"-"}
{"Case.ID":7727149,"Initial.FDA.Received.Date":"11/24/2010","days.since.last.fda":12,"Event.Date":"10/07/2010","Latest.FDA.Received.Date":"24-NOV-2010","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Psoriasis","Reactions":"Rash;Stevens-Johnson Syndrome;Erythema Multiforme;Leukopenia;Thrombocytopenia;Hepatic Enzyme Increased;Anaemia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"89 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":7699597,"Initial.FDA.Received.Date":"12/08/2010","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"08-DEC-2010","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"-","Reactions":"Death;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":7754786,"Initial.FDA.Received.Date":"01/11/2011","days.since.last.fda":34,"Event.Date":"","Latest.FDA.Received.Date":"25-SEP-2017","Suspect.Product.Names":"Amoxicillin And Clavulanate Potassium","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"Pneumonia","Reactions":"Stevens-Johnson Syndrome;Tubulointerstitial Nephritis;Acute Hepatic Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"38 YR","Sender":"Ranbaxy","Concomitant.Product.Names":"-"}
{"Case.ID":7760284,"Initial.FDA.Received.Date":"01/13/2011","days.since.last.fda":2,"Event.Date":"08/18/2008","Latest.FDA.Received.Date":"21-JAN-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ferrous Gluconate;Ibuprofen;Folic Acid;Povidone-Iodine;Allopurinol;Torsemide;Moxonidine;Tolterodine Tartrate;Digoxin;Aspirin;Dexamethasone Sodium Phosphate\\Neomycin Sulfate\\Polymyxin B Sulfate","Reason.for.Use":"Cardiac Failure;Conjunctivitis;Hypertension;Hyperuricaemia;Incontinence;Pain;Thrombosis Prophylaxis","Reactions":"Fungal Infection;Multiple Organ Dysfunction Syndrome;Staphylococcal Infection;Stevens-Johnson Syndrome;Sepsis;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"87 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":7767892,"Initial.FDA.Received.Date":"01/20/2011","days.since.last.fda":7,"Event.Date":"02/04/2008","Latest.FDA.Received.Date":"20-JAN-2011","Suspect.Product.Names":"Dulcolax (Bisacodyl);Ultiva;Nexium;Insulin Human Nos;Piperacillin And Tazobactam;Lyrica","Suspect.Product.Active.Ingredients":"Pregabalin;Propofol;Furosemide;Levothyroxine Sodium;Ciprofloxacin;Hydrocortisone Sodium Succinate;Piperacillin Sodium\\Tazobactam Sodium;Insulin Human;Esomeprazole Magnesium;Ketamine;Metoprolol Tartrate;Midazolam Hydrochloride;Remifentanil Hydrochloride;Fluconazole;Metoprolol Succinate;Bisacodyl;Lorazepam;Heparin Sodium","Reason.for.Use":"Arthritis;Constipation;Hyperglycaemia;Hypertension;Hypothyroidism;Polyuria;Prophylaxis Against Gastrointestinal Ulcer;Restlessness;Stupor;Thrombosis Prophylaxis","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"59 YR","Sender":"Pfizer","Concomitant.Product.Names":"Calcium Chloride;Sodium Chloride;Potassium Chloride;Cafedrine Hydrochloride;Piritramide;Fentanyl"}
{"Case.ID":7771656,"Initial.FDA.Received.Date":"01/24/2011","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"31-JAN-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vincristine Sulfate;Etoposide;Rituximab;Thiotepa;Methotrexate;Cytarabine;Busulfan;Mycophenolate Mofetil;Procarbazine;Cyclophosphamide","Reason.for.Use":"Central Nervous System Lymphoma;Lupus Nephritis","Reactions":"Stevens-Johnson Syndrome;Central Nervous System Lymphoma;Bacterial Sepsis;Febrile Neutropenia;Bk Virus Infection;Posterior Reversible Encephalopathy Syndrome;Systemic Candida","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"20 YR","Sender":"Genentech","Concomitant.Product.Names":"-"}
{"Case.ID":7776800,"Initial.FDA.Received.Date":"01/27/2011","days.since.last.fda":3,"Event.Date":"05/15/2008","Latest.FDA.Received.Date":"27-JAN-2011","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin;Phenytoin Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":7776770,"Initial.FDA.Received.Date":"01/27/2011","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"27-JAN-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":7776757,"Initial.FDA.Received.Date":"01/27/2011","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"27-JAN-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":7810588,"Initial.FDA.Received.Date":"02/14/2011","days.since.last.fda":18,"Event.Date":"01/29/2011","Latest.FDA.Received.Date":"14-FEB-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital Sodium;Enoxaparin Sodium;Dexamethasone","Reason.for.Use":"Gastritis;Thrombosis Prophylaxis","Reactions":"Erythema Multiforme;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"63 YR","Sender":"Aventis","Concomitant.Product.Names":"Pantoprazole Sodium"}
{"Case.ID":7949501,"Initial.FDA.Received.Date":"04/28/2011","days.since.last.fda":73,"Event.Date":"","Latest.FDA.Received.Date":"20-MAY-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amoxicillin","Reason.for.Use":"Upper Respiratory Tract Infection","Reactions":"Gastritis Erosive;Toxic Epidermal Necrolysis;Large Intestinal Haemorrhage;Stevens-Johnson Syndrome;Streptococcus Test Positive;Diarrhoea;Hypothermia;Gastrointestinal Erosion;Erosive Oesophagitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Aurobindo","Concomitant.Product.Names":"-"}
{"Case.ID":7958441,"Initial.FDA.Received.Date":"05/05/2011","days.since.last.fda":7,"Event.Date":"03/31/2011","Latest.FDA.Received.Date":"18-NOV-2011","Suspect.Product.Names":"Emend","Suspect.Product.Active.Ingredients":"Aprepitant;Fluorouracil","Reason.for.Use":"Oesophageal Carcinoma;Prophylaxis","Reactions":"Oral Infection;Skin Infection;Agranulocytosis;Stevens-Johnson Syndrome;Stomatitis;International Normalised Ratio Abnormal;Dihydropyrimidine Dehydrogenase Deficiency;White Blood Cell Count Decreased;Disseminated Intravascular Coagulation;Platelet Count Decreased;Bone Marrow Failure;Activated Partial Thromboplastin Time Prolonged;International Normalised Ratio Decreased;Febrile Neutropenia;Hyperbilirubinaemia;Pneumonia;Acute Respiratory Distress Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"Merck","Concomitant.Product.Names":"Cisplatin;Humulin R;Haloperidol;Zofran;Adriacin"}
{"Case.ID":7931898,"Initial.FDA.Received.Date":"05/05/2011","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"05-MAY-2011","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":7953664,"Initial.FDA.Received.Date":"05/20/2011","days.since.last.fda":15,"Event.Date":"05/03/2011","Latest.FDA.Received.Date":"22-AUG-2011","Suspect.Product.Names":"Clopidogrel","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"87 YR","Sender":"Aventis","Concomitant.Product.Names":"Tamsulosin Hydrochloride;Enoxaparin Sodium;Ecotrin;Furosemide"}
{"Case.ID":8045319,"Initial.FDA.Received.Date":"07/20/2011","days.since.last.fda":61,"Event.Date":"","Latest.FDA.Received.Date":"20-JUL-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine;Topiramate","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":8065500,"Initial.FDA.Received.Date":"08/02/2011","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"08-AUG-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Omeprazole;Carbamazepine;Cilostazol","Reason.for.Use":"Restless Legs Syndrome;Tremor","Reactions":"Toxic Epidermal Necrolysis;Drug Interaction;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"Cetirizine Hydrochloride;Hydroxyzine Hydrochloride;Deflazacort;Sulpiride;Methylprednisolone"}
{"Case.ID":8088333,"Initial.FDA.Received.Date":"08/12/2011","days.since.last.fda":10,"Event.Date":"07/01/2011","Latest.FDA.Received.Date":"12-AUG-2011","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Treatment Failure;Death;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"11 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Depakene"}
{"Case.ID":8099482,"Initial.FDA.Received.Date":"08/22/2011","days.since.last.fda":10,"Event.Date":"03/27/2011","Latest.FDA.Received.Date":"12-SEP-2011","Suspect.Product.Names":"Clolar","Suspect.Product.Active.Ingredients":"Clofarabine;Cytarabine;Idarubicin Hydrochloride","Reason.for.Use":"Acute Myeloid Leukaemia;Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"58 YR","Sender":"Genzyme","Concomitant.Product.Names":"Valtrex;Amphotericin B"}
{"Case.ID":8117744,"Initial.FDA.Received.Date":"08/26/2011","days.since.last.fda":4,"Event.Date":"04/22/2011","Latest.FDA.Received.Date":"26-AUG-2011","Suspect.Product.Names":"Chantix","Suspect.Product.Active.Ingredients":"Varenicline Tartrate","Reason.for.Use":"Tobacco Abuse","Reactions":"Confusional State;Swelling Face;Oropharyngeal Pain;Rash;Stevens-Johnson Syndrome;Pyrexia;Lethargy;Cough;Dysphagia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"39 YR","Sender":"-","Concomitant.Product.Names":"Doxycycline;Lisinopril"}
{"Case.ID":8146361,"Initial.FDA.Received.Date":"08/29/2011","days.since.last.fda":3,"Event.Date":"02/17/2011","Latest.FDA.Received.Date":"21-SEP-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mirtazapine","Reason.for.Use":"Depression","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Schering Plough","Concomitant.Product.Names":"Mcp;Fentanyl"}
{"Case.ID":8111821,"Initial.FDA.Received.Date":"08/29/2011","days.since.last.fda":0,"Event.Date":"02/17/2011","Latest.FDA.Received.Date":"29-AUG-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mirtazapine","Reason.for.Use":"Decreased Appetite;Depression;Nausea;Tumour Pain","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Sandoz","Concomitant.Product.Names":"Mcp;Fentanyl;Metamizole Sodium"}
{"Case.ID":8118528,"Initial.FDA.Received.Date":"09/02/2011","days.since.last.fda":4,"Event.Date":"06/29/2011","Latest.FDA.Received.Date":"10-NOV-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Erythromycin;Clarithromycin","Reason.for.Use":"Lower Respiratory Tract Infection;Product Used For Unknown Indication","Reactions":"Rash Maculo-Papular;Stevens-Johnson Syndrome;Skin Exfoliation;Mouth Ulceration","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Watson","Concomitant.Product.Names":"Doxycycline;Citalopram;Perindopril;Omeprazole;Levothyroxine;Acetaminophen"}
{"Case.ID":8121432,"Initial.FDA.Received.Date":"09/06/2011","days.since.last.fda":4,"Event.Date":"08/13/2011","Latest.FDA.Received.Date":"11-OCT-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Meropenem","Reason.for.Use":"Sepsis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"77 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"Clindamycin"}
{"Case.ID":8147296,"Initial.FDA.Received.Date":"09/09/2011","days.since.last.fda":3,"Event.Date":"02/17/2011","Latest.FDA.Received.Date":"09-SEP-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mirtazapine","Reason.for.Use":"Depression","Reactions":"Stevens-Johnson Syndrome;Gamma-Glutamyltransferase Increased;Blood Creatinine Increased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Aurobindo","Concomitant.Product.Names":"Fentanyl Citrate;Fentanyl;Mcp"}
{"Case.ID":8160671,"Initial.FDA.Received.Date":"09/16/2011","days.since.last.fda":7,"Event.Date":"02/17/2011","Latest.FDA.Received.Date":"16-SEP-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mirtazapine","Reason.for.Use":"Depression","Reactions":"Blood Creatinine Increased;Stevens-Johnson Syndrome;Gamma-Glutamyltransferase Increased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Actavis Elizabeth","Concomitant.Product.Names":"-"}
{"Case.ID":8155396,"Initial.FDA.Received.Date":"09/26/2011","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"26-SEP-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Omeprazole;Cilostazol;Carbamazepine","Reason.for.Use":"Restless Legs Syndrome;Skin Lesion;Tremor","Reactions":"Septic Shock;Stevens-Johnson Syndrome;Drug Interaction;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Mylan","Concomitant.Product.Names":"Hydroxyzine;Sulpiride;Cetirizine Hydrochloride;Methylprednisolone;Deflazacort"}
{"Case.ID":8164137,"Initial.FDA.Received.Date":"09/30/2011","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"30-SEP-2011","Suspect.Product.Names":"Arimidex","Suspect.Product.Active.Ingredients":"Anastrozole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Astrazeneca","Concomitant.Product.Names":"-"}
{"Case.ID":8182211,"Initial.FDA.Received.Date":"10/04/2011","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"04-OCT-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Omeprazole;Cilostazol;Carbamazepine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Lymphopenia;Leukopenia;Enterobacter Test Positive;Staphylococcus Test Positive;Toxic Epidermal Necrolysis;Drug Interaction;Acinetobacter Test Positive;Cardio-Respiratory Arrest;Septic Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Dexcel","Concomitant.Product.Names":"Methylprednisolone;Cetirizine Hydrochloride;Hydroxyzine"}
{"Case.ID":8265150,"Initial.FDA.Received.Date":"11/28/2011","days.since.last.fda":55,"Event.Date":"","Latest.FDA.Received.Date":"28-NOV-2011","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Blood Disorder;Renal Failure;Bone Marrow Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"33 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":8266288,"Initial.FDA.Received.Date":"11/29/2011","days.since.last.fda":1,"Event.Date":"08/01/2007","Latest.FDA.Received.Date":"29-NOV-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Gout","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Vertex","Concomitant.Product.Names":"-"}
{"Case.ID":8284999,"Initial.FDA.Received.Date":"12/12/2011","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"12-DEC-2011","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Linezolid;Meropenem;Vancomycin","Reason.for.Use":"Pneumonia Bacterial;Sepsis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"18 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"Cyclophosphamide;Methylprednisolone"}
{"Case.ID":8284336,"Initial.FDA.Received.Date":"12/12/2011","days.since.last.fda":0,"Event.Date":"11/01/2011","Latest.FDA.Received.Date":"12-DEC-2011","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Epilepsy","Reactions":"Stevens-Johnson Syndrome;Drug Hypersensitivity;Sepsis;Multi-Organ Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"46 YR","Sender":"-","Concomitant.Product.Names":"Lamictal"}
{"Case.ID":8325154,"Initial.FDA.Received.Date":"01/06/2012","days.since.last.fda":25,"Event.Date":"","Latest.FDA.Received.Date":"06-JAN-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin Sodium;Fosphenytoin","Reason.for.Use":"Seizure","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Drug Reaction With Eosinophilia And Systemic Symptoms","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":8336047,"Initial.FDA.Received.Date":"01/13/2012","days.since.last.fda":7,"Event.Date":"02/17/2011","Latest.FDA.Received.Date":"13-JAN-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mirtazapine","Reason.for.Use":"Decreased Appetite;Depression;Nausea;Tumour Pain","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Teva","Concomitant.Product.Names":"Fentanyl;Mcp"}
{"Case.ID":8405448,"Initial.FDA.Received.Date":"02/02/2012","days.since.last.fda":20,"Event.Date":"","Latest.FDA.Received.Date":"02-FEB-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Omeprazole;Carbamazepine;Cilostazol","Reason.for.Use":"Resting Tremor;Restless Legs Syndrome","Reactions":"Nikolsky'S Sign;Stevens-Johnson Syndrome;Urticaria;Septic Shock;Cardio-Respiratory Arrest;Drug Interaction;Pruritus;Heart Rate Increased;Leukopenia;Acinetobacter Test Positive;Pyrexia;Toxic Epidermal Necrolysis;Staphylococcus Test Positive;Lymphopenia;Skin Exfoliation","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Actavis Totowa","Concomitant.Product.Names":"Hydroxyzine;Cetirizine;Methylphenidate"}
{"Case.ID":8429746,"Initial.FDA.Received.Date":"02/28/2012","days.since.last.fda":26,"Event.Date":"01/19/2011","Latest.FDA.Received.Date":"28-FEB-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"Pneumonia;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"44 YR","Sender":"Ranbaxy","Concomitant.Product.Names":"Vitamin B Complex;Nifedipine;Ferrous Fumarate;Metoprolol;Folic Acid;Calcium Carbonate;Furosemide"}
{"Case.ID":8456851,"Initial.FDA.Received.Date":"03/13/2012","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"13-MAR-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Trimethoprim","Reason.for.Use":"Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"89 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":8456694,"Initial.FDA.Received.Date":"03/13/2012","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"13-MAR-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"Urinary Tract Infection","Reactions":"Rash Erythematous;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"89 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":8463003,"Initial.FDA.Received.Date":"03/16/2012","days.since.last.fda":3,"Event.Date":"02/01/1999","Latest.FDA.Received.Date":"16-MAR-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sertraline Hydrochloride;Amitriptyline","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":8513385,"Initial.FDA.Received.Date":"04/03/2012","days.since.last.fda":18,"Event.Date":"03/04/2012","Latest.FDA.Received.Date":"16-MAY-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ibuprofen;Acetaminophen","Reason.for.Use":"Oropharyngeal Pain;Pain","Reactions":"Disease Complication;Neutrophil Count Decreased;White Blood Cell Count Decreased;Stevens-Johnson Syndrome;Platelet Count Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"17 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":8550747,"Initial.FDA.Received.Date":"04/30/2012","days.since.last.fda":27,"Event.Date":"","Latest.FDA.Received.Date":"30-APR-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital","Reason.for.Use":"Epilepsy","Reactions":"Pancytopenia;Confusional State;Urinary Tract Infection;Anxiety;Toxic Epidermal Necrolysis;Gastrointestinal Haemorrhage;Stevens-Johnson Syndrome;Device Related Infection","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"51 YR","Sender":"Actavis Elizabeth","Concomitant.Product.Names":"-"}
{"Case.ID":8560669,"Initial.FDA.Received.Date":"05/14/2012","days.since.last.fda":14,"Event.Date":"02/01/1999","Latest.FDA.Received.Date":"14-MAY-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sertraline Hydrochloride;Amitriptyline","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":8560646,"Initial.FDA.Received.Date":"05/14/2012","days.since.last.fda":0,"Event.Date":"07/01/2001","Latest.FDA.Received.Date":"14-MAY-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Valacyclovir Hydrochloride","Reason.for.Use":"Immunosuppressant Drug Therapy","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"52 YR","Sender":"Mylan","Concomitant.Product.Names":"Dexamethasone"}
{"Case.ID":8602357,"Initial.FDA.Received.Date":"05/24/2012","days.since.last.fda":10,"Event.Date":"03/01/2012","Latest.FDA.Received.Date":"24-MAY-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sertraline Hydrochloride;Amitriptyline Hydrochloride","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Endo","Concomitant.Product.Names":"-"}
{"Case.ID":8583774,"Initial.FDA.Received.Date":"05/29/2012","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"13-MAR-2013","Suspect.Product.Names":"Xeloda","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":8584186,"Initial.FDA.Received.Date":"05/29/2012","days.since.last.fda":0,"Event.Date":"07/01/2001","Latest.FDA.Received.Date":"29-MAY-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Valacyclovir Hydrochloride","Reason.for.Use":"Oral Herpes","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"52 YR","Sender":"Watson","Concomitant.Product.Names":"-"}
{"Case.ID":8583642,"Initial.FDA.Received.Date":"05/29/2012","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"29-MAY-2012","Suspect.Product.Names":"Xeloda","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":8639854,"Initial.FDA.Received.Date":"06/19/2012","days.since.last.fda":21,"Event.Date":"03/28/2012","Latest.FDA.Received.Date":"19-JUN-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin","Reason.for.Use":"Endocarditis Bacterial","Reactions":"Hypotension;Stevens-Johnson Syndrome;Pneumonia;Hypothermia;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"66 YR","Sender":"-","Concomitant.Product.Names":"Folic Acid;Darbepoetin Alfa;Metoprolol Tartrate;Enalapril;Aspirin;Ferrous Sulfate;Senna;Cinacalcet;Calcium Acetate;Rosuvastatin;Gabapentin"}
{"Case.ID":8658801,"Initial.FDA.Received.Date":"06/25/2012","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"25-JUN-2012","Suspect.Product.Names":"Onfi","Suspect.Product.Active.Ingredients":"Clobazam","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Lundbeck","Concomitant.Product.Names":"-"}
{"Case.ID":8695562,"Initial.FDA.Received.Date":"07/13/2012","days.since.last.fda":18,"Event.Date":"03/16/2011","Latest.FDA.Received.Date":"13-JUL-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Omeprazole","Reason.for.Use":"Gastric Haemorrhage","Reactions":"Aspartate Aminotransferase Increased;Pyrexia;Alanine Aminotransferase Increased;Hyperbilirubinaemia;Drug Reaction With Eosinophilia And Systemic Symptoms;Swelling Face;Renal Impairment;Erythema;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Hypogammaglobulinaemia;Pancreatic Enzymes Increased;Lymphadenopathy;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"54 YR","Sender":"Dexcel","Concomitant.Product.Names":"-"}
{"Case.ID":8673264,"Initial.FDA.Received.Date":"07/19/2012","days.since.last.fda":6,"Event.Date":"06/02/2012","Latest.FDA.Received.Date":"13-NOV-2012","Suspect.Product.Names":"Zocor","Suspect.Product.Active.Ingredients":"Simvastatin;Spironolactone;Clarithromycin;Bumetanide","Reason.for.Use":"Pneumonia;Pulmonary Embolism","Reactions":"Fluid Overload;Swelling;Scab;Toxic Epidermal Necrolysis;Acute Kidney Injury;Blood Creatinine Increased;Blister;Exfoliative Rash;Rash;Petechiae;Atrial Fibrillation;Rash Pruritic;Eczema;Rash Maculo-Papular;Dry Skin;Haemoglobin Decreased;Oedema Peripheral;Stevens-Johnson Syndrome;Hypersensitivity;Pruritus;Pain;Erythema","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Teva","Concomitant.Product.Names":"Bisoprolol;Cocodamol;Adenosine;Amoxicillin\\Clavulanate Potassium;Teicoplanin;Calcium Carbonate\\Cholecalciferol;Heparin;Dalteparin Sodium;Methotrexate;Amiodarone;Omeprazole;Gentamicin;Dioralyte;Furosemide;Diclofenac Diethylamine;Acetaminophen;Folic Acid;Candesartan;Clotrimazole;Warfarin;Tramadol;Metoclopramide"}
{"Case.ID":8714063,"Initial.FDA.Received.Date":"07/24/2012","days.since.last.fda":5,"Event.Date":"06/02/2012","Latest.FDA.Received.Date":"18-SEP-2012","Suspect.Product.Names":"Zocor","Suspect.Product.Active.Ingredients":"Simvastatin;Spironolactone;Bumetanide;Clarithromycin","Reason.for.Use":"Pneumonia","Reactions":"Atrial Fibrillation;Stevens-Johnson Syndrome;Fluid Overload;Hypersensitivity;Toxic Epidermal Necrolysis;Vasculitis;Haemodialysis;Haemoglobin Decreased;Acute Kidney Injury;Pulmonary Embolism","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Actavis Elizabeth","Concomitant.Product.Names":"Metoclopramide;Tramadol Hydrochloride;Adenosine;Clotrimazole;Omeprazole;Teicoplanin;Amoxicillin;Calcium Carbonate\\Cholecalciferol;Warfarin Sodium;Furosemide;Candesartan;Amoxicillin\\Clavulanate Potassium;Methotrexate;Heparin;Diclofenac;Bisoprolol;Folic Acid;Dioralyte;Gentamicin;Cocodamol;Amiodarone;Acetaminophen;Dalteparin;Clarithromycin"}
{"Case.ID":8681822,"Initial.FDA.Received.Date":"07/25/2012","days.since.last.fda":1,"Event.Date":"06/02/2012","Latest.FDA.Received.Date":"25-JUL-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate;Simvastatin;Bumetanide;Clarithromycin;Spironolactone","Reason.for.Use":"Pneumonia;Product Used For Unknown Indication;Pulmonary Embolism","Reactions":"Acute Kidney Injury;Stevens-Johnson Syndrome;Atrial Fibrillation;Fluid Overload;Haemoglobin Decreased;Pulmonary Fibrosis;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Mylan","Concomitant.Product.Names":"Diclofenac;Gentamicin;Metoclopramide;Warfarin Sodium;Potassium Chloride\\Sodium Bicarbonate\\Sodium Chloride;Amoxicillin\\Clavulanate Potassium;Furosemide;Clotrimazole;Dalteparin Sodium;Folic Acid;Omeprazole;Protein;Candesartan;Acetaminophen;Calcium Carbonate;Adenosine;Tramadol Hydrochloride;Heparin;Teicoplanin;Cocodamol;Amiodarone;Bisoprolol"}
{"Case.ID":8684345,"Initial.FDA.Received.Date":"07/26/2012","days.since.last.fda":1,"Event.Date":"06/02/2012","Latest.FDA.Received.Date":"24-OCT-2012","Suspect.Product.Names":"Zocor","Suspect.Product.Active.Ingredients":"Simvastatin;Bumetanide;Clarithromycin;Spironolactone","Reason.for.Use":"Pneumonia;Product Used For Unknown Indication;Pulmonary Embolism","Reactions":"Atrial Fibrillation;Oedema Peripheral;Fluid Overload;Rash Maculo-Papular;Toxic Epidermal Necrolysis;Swelling;Eczema;Rash;Hypersensitivity;Pruritus;Blood Creatinine Increased;Erythema;Dry Skin;Rash Pruritic;Pain;Haemoglobin Decreased;Scab;Stevens-Johnson Syndrome;Acute Kidney Injury;Exfoliative Rash;Blister;Petechiae","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Watson","Concomitant.Product.Names":"Amiodarone;Methotrexate;Diclofenac Diethylamine;Tramadol;Candesartan;Adenosine;Teicoplanin;Cocodamol;Calcium Carbonate\\Cholecalciferol;Warfarin;Bisoprolol;Omeprazole;Acetaminophen;Heparin;Dalteparin Sodium;Amoxicillin\\Clavulanic Acid;Gentamicin;Clotrimazole;Metoclopramide;Furosemide;Folic Acid"}
{"Case.ID":8686594,"Initial.FDA.Received.Date":"07/26/2012","days.since.last.fda":0,"Event.Date":"06/02/2012","Latest.FDA.Received.Date":"02-OCT-2012","Suspect.Product.Names":"Zocor","Suspect.Product.Active.Ingredients":"Simvastatin;Unspecified Ingredient;Clarithromycin","Reason.for.Use":"Pneumonia;Pulmonary Embolism","Reactions":"Swelling;Pruritus;Exfoliative Rash;Blood Creatinine Increased;Fluid Overload;Toxic Epidermal Necrolysis;Rash Maculo-Papular;Oedema Peripheral;Atrial Fibrillation;Stevens-Johnson Syndrome;Scab;Rash Pruritic;Blister;Haemoglobin Decreased;Rash;Petechiae;Eczema;Hypersensitivity;Dry Skin;Pain;Erythema;Acute Kidney Injury","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"79 YR","Sender":"Merck","Concomitant.Product.Names":"Metoclopramide;Diclofenac Diethylamine;Methotrexate;Adenosine;Acetaminophen And Codeine;Dalteparin Sodium;Amoxicillin\\Clavulanate Potassium;Folic Acid;Teicoplanin;Gentamicin;Warfarin;Dioralyte;Bisoprolol;Furosemide;Tramadol Hydrochloride;Calcium Carbonate\\Cholecalciferol;Candesartan;Heparin;Omeprazole;Amiodarone;Acetaminophen;Clotrimazole"}
{"Case.ID":8702109,"Initial.FDA.Received.Date":"08/03/2012","days.since.last.fda":8,"Event.Date":"01/01/2012","Latest.FDA.Received.Date":"03-AUG-2012","Suspect.Product.Names":"Aricept","Suspect.Product.Active.Ingredients":"Donepezil Hydrochloride;Azithromycin Anhydrous","Reason.for.Use":"-","Reactions":"Rash;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Eisai","Concomitant.Product.Names":"-"}
{"Case.ID":8710705,"Initial.FDA.Received.Date":"08/07/2012","days.since.last.fda":4,"Event.Date":"01/01/2012","Latest.FDA.Received.Date":"07-AUG-2012","Suspect.Product.Names":"Aricept","Suspect.Product.Active.Ingredients":"Donepezil Hydrochloride;Azithromycin Anhydrous","Reason.for.Use":"Dementia Alzheimer'S Type","Reactions":"Rash;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"85 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":8718885,"Initial.FDA.Received.Date":"08/10/2012","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"10-AUG-2012","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Renal Failure;Stevens-Johnson Syndrome;Bone Marrow Failure;Blood Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"33 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":8750661,"Initial.FDA.Received.Date":"08/22/2012","days.since.last.fda":12,"Event.Date":"04/28/1947","Latest.FDA.Received.Date":"22-AUG-2012","Suspect.Product.Names":"Enbrel","Suspect.Product.Active.Ingredients":"Etanercept","Reason.for.Use":"Psoriasis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"0 YR","Sender":"-","Concomitant.Product.Names":"Prednisolone"}
{"Case.ID":8763831,"Initial.FDA.Received.Date":"08/31/2012","days.since.last.fda":9,"Event.Date":"08/22/2012","Latest.FDA.Received.Date":"31-AUG-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vemurafenib","Reason.for.Use":"Malignant Melanoma","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":8780107,"Initial.FDA.Received.Date":"09/04/2012","days.since.last.fda":4,"Event.Date":"08/22/2012","Latest.FDA.Received.Date":"04-SEP-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vemurafenib","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":8800346,"Initial.FDA.Received.Date":"09/21/2012","days.since.last.fda":17,"Event.Date":"","Latest.FDA.Received.Date":"21-SEP-2012","Suspect.Product.Names":"Enbrel","Suspect.Product.Active.Ingredients":"Etanercept","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Toxicity To Various Agents;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Amgen","Concomitant.Product.Names":"-"}
{"Case.ID":8837373,"Initial.FDA.Received.Date":"10/12/2012","days.since.last.fda":21,"Event.Date":"12/28/1998","Latest.FDA.Received.Date":"12-OCT-2012","Suspect.Product.Names":"Rocephin;Konakion;Dusodril","Suspect.Product.Active.Ingredients":"Nafronyl Oxalate;Erythromycin;Phytonadione;Ceftriaxone Sodium;Furosemide;Heparin Sodium;Piperacillin Sodium\\Tazobactam Sodium;Citric Acid Monohydrate\\Potassium Bicarbonate\\Potassium Citrate;Diltiazem Hydrochloride;Valerian;Sodium Polystyrene Sulfonate;Fluconazole;Digitoxin;Benazepril Hydrochloride;Vancomycin;Albumin Human;Omeprazole;Nitrazepam;Cilastatin Sodium\\Imipenem;Trimipramine Maleate","Reason.for.Use":"Aortic Valve Incompetence;Cardiac Failure;Hyperkalaemia;Hypertension;Hypokalaemia;Ill-Defined Disorder;Restlessness;Sepsis;Stoma Care;Thrombosis Prophylaxis","Reactions":"Sepsis;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Pfizer","Concomitant.Product.Names":"Phytonadione;Roxithromycin;Pantoprazole Sodium;Acetaminophen;Heparin;Spironolactone;Human Red Blood Cell;Piretanide;Lactulose;Lansoprazole"}
{"Case.ID":8840259,"Initial.FDA.Received.Date":"10/15/2012","days.since.last.fda":3,"Event.Date":"01/01/2010","Latest.FDA.Received.Date":"13-NOV-2012","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Bipolar Disorder;Bipolar I Disorder;Hyperlipidaemia;Insomnia","Reactions":"Aspartate Aminotransferase Increased;Thrombin-Antithrombin Iii Complex Increased;Platelet Count Decreased;Prothrombin Time Prolonged;Rash Papular;Disseminated Intravascular Coagulation;Blood Urea Increased;Erythema;C-Reactive Protein Increased;Prothrombin Level Decreased;Fibrin D Dimer Increased;Antithrombin Iii Decreased;Alanine Aminotransferase Increased;Face Oedema;Stevens-Johnson Syndrome;Monocyte Percentage Decreased;Malaise;Toxic Epidermal Necrolysis;Blood Creatinine Increased;Gamma-Glutamyltransferase Increased;Neutrophil Percentage Increased;General Physical Health Deterioration;Pyrexia;Blood Alkaline Phosphatase Increased;Feeling Abnormal;Drug Reaction With Eosinophilia And Systemic Symptoms;Renal Impairment;Blood Lactate Dehydrogenase Increased;Multiple Organ Dysfunction Syndrome;Lymphocyte Percentage Decreased;Hepatic Function Abnormal","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"51 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Brotizolam;Valproate Sodium;Livalo;Lithium Carbonate;Zopiclone"}
{"Case.ID":8880099,"Initial.FDA.Received.Date":"11/01/2012","days.since.last.fda":17,"Event.Date":"","Latest.FDA.Received.Date":"01-NOV-2012","Suspect.Product.Names":"Phenytoin Sodium Extended","Suspect.Product.Active.Ingredients":"Phenytoin Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Taro","Concomitant.Product.Names":"-"}
{"Case.ID":8887233,"Initial.FDA.Received.Date":"11/05/2012","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"05-NOV-2012","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Anticoagulant Therapy;Antifungal Prophylaxis;Antiviral Prophylaxis;Immunosuppressant Drug Therapy","Reactions":"Multiple Organ Dysfunction Syndrome;Acute Respiratory Distress Syndrome;Renal Failure;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"66 YR","Sender":"Teva","Concomitant.Product.Names":"Prograf;Cellcept;Pantozol;Heparin;Lamivudine"}
{"Case.ID":8909861,"Initial.FDA.Received.Date":"11/15/2012","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"29-NOV-2012","Suspect.Product.Names":"Allegra","Suspect.Product.Active.Ingredients":"Fexofenadine Hydrochloride;Unspecified Ingredient","Reason.for.Use":"Adult T-Cell Lymphoma/Leukaemia;Pruritus;Rash;Skin Disorder","Reactions":"Skin Disorder;Skin Exfoliation;Ocular Hyperaemia;Stevens-Johnson Syndrome;Blister;Rash;Erythema;Skin Lesion;Oropharyngeal Pain;Lip Erosion;Toxic Epidermal Necrolysis;Eye Pruritus;Pruritus","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"60 YR","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":8929271,"Initial.FDA.Received.Date":"11/26/2012","days.since.last.fda":11,"Event.Date":"07/25/2012","Latest.FDA.Received.Date":"26-NOV-2012","Suspect.Product.Names":"Treanda","Suspect.Product.Active.Ingredients":"Bendamustine Hydrochloride","Reason.for.Use":"Chronic Lymphocytic Leukaemia","Reactions":"Rash;Staphylococcal Infection;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"66 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":8971490,"Initial.FDA.Received.Date":"12/18/2012","days.since.last.fda":22,"Event.Date":"07/17/2011","Latest.FDA.Received.Date":"18-DEC-2012","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Nerve Compression","Reactions":"Rash Erythematous;Rash Vesicular;Skin Exfoliation;Sepsis;Stevens-Johnson Syndrome;Rash Pustular;Coma;Acute Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"68 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":9063658,"Initial.FDA.Received.Date":"02/13/2013","days.since.last.fda":57,"Event.Date":"02/03/2013","Latest.FDA.Received.Date":"01-MAR-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Clofarabine","Reason.for.Use":"Acute Myeloid Leukaemia;Hyperpyrexia;Mouth Ulceration;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Shock;Renal Failure;Acute Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"40 YR","Sender":"Genzyme","Concomitant.Product.Names":"Furosemide;Cubicin;Itraconazole;Clindamycin;Tazobactam;Piperacillin Sodium\\Tazobactam Sodium;Cytarabine;Vancomycin;Ampicillin;Meropenem;Omeprazole;Allopurinol;Tropisetron"}
{"Case.ID":9124380,"Initial.FDA.Received.Date":"02/27/2013","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"27-FEB-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampicillin","Reason.for.Use":"-","Reactions":"Visual Impairment;Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"40 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":9165342,"Initial.FDA.Received.Date":"03/15/2013","days.since.last.fda":16,"Event.Date":"","Latest.FDA.Received.Date":"15-MAR-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ampicillin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"40 YR","Sender":"Bristol Myers Squibb","Concomitant.Product.Names":"-"}
{"Case.ID":9261995,"Initial.FDA.Received.Date":"04/29/2013","days.since.last.fda":45,"Event.Date":"","Latest.FDA.Received.Date":"29-APR-2013","Suspect.Product.Names":"Gatifloxacin Sesquihydrate","Suspect.Product.Active.Ingredients":"Gatifloxacin;Moxifloxacin","Reason.for.Use":"Product Used For Unknown Indication;Stevens-Johnson Syndrome","Reactions":"Death;Influenza Like Illness;Stevens-Johnson Syndrome;Asthenia;Pyrexia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"67 YR","Sender":"Allergan","Concomitant.Product.Names":"Corticosteroid Nos;Immune Globulin Nos"}
{"Case.ID":9270442,"Initial.FDA.Received.Date":"05/03/2013","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"03-MAY-2013","Suspect.Product.Names":"Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Death;Hypersensitivity;Unevaluable Event;Weight Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Mutual","Concomitant.Product.Names":"-"}
{"Case.ID":9284471,"Initial.FDA.Received.Date":"05/10/2013","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"10-MAY-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ramipril;Lansoprazole","Reason.for.Use":"-","Reactions":"Sepsis;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"Amlodipine;Hydrochlorothiazide"}
{"Case.ID":9304899,"Initial.FDA.Received.Date":"05/21/2013","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"21-MAY-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lansoprazole","Reason.for.Use":"-","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Takeda","Concomitant.Product.Names":"Amlodipine;Hydrochlorothiazide"}
{"Case.ID":9322784,"Initial.FDA.Received.Date":"06/01/2013","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"01-JUN-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ceftriaxone","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Skin Infection;Shock;Stevens-Johnson Syndrome;Pneumonia;Multiple Organ Dysfunction Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":9335388,"Initial.FDA.Received.Date":"06/05/2013","days.since.last.fda":4,"Event.Date":"05/03/2013","Latest.FDA.Received.Date":"05-JUN-2013","Suspect.Product.Names":"Epilim","Suspect.Product.Active.Ingredients":"Valproate Sodium;Nevirapine","Reason.for.Use":"Mania;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"28 YR","Sender":"Abbott","Concomitant.Product.Names":"Zidovudine;Risperidone;Lamivudine;Valproate Sodium"}
{"Case.ID":9339544,"Initial.FDA.Received.Date":"06/10/2013","days.since.last.fda":5,"Event.Date":"10/18/2009","Latest.FDA.Received.Date":"10-JUN-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methylprednisolone","Reason.for.Use":"-","Reactions":"Infection;Stevens-Johnson Syndrome;Overdose;Dialysis;Victim Of Crime;Victim Of Abuse","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"74 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":9412867,"Initial.FDA.Received.Date":"07/22/2013","days.since.last.fda":42,"Event.Date":"","Latest.FDA.Received.Date":"25-SEP-2014","Suspect.Product.Names":"Piperacillin.","Suspect.Product.Active.Ingredients":"Piperacillin Sodium;Hydrocortisone;Ceftriaxone;Meropenem;Dexamethasone;Prednisolone;Corticosteroid Nos;Glycyrrhizin","Reason.for.Use":"Rash;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Reactions":"Stevens-Johnson Syndrome;Skin Exfoliation;Rash;Toxic Epidermal Necrolysis;Escherichia Test Positive;Staphylococcus Test Positive;Drug Ineffective;Generalised Oedema","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Sandoz","Concomitant.Product.Names":"Cefozopran;Fosfomycin"}
{"Case.ID":9442512,"Initial.FDA.Received.Date":"08/06/2013","days.since.last.fda":15,"Event.Date":"","Latest.FDA.Received.Date":"06-AUG-2013","Suspect.Product.Names":"Mabthera","Suspect.Product.Active.Ingredients":"Rituximab","Reason.for.Use":"Immune Thrombocytopenia","Reactions":"Pyrexia;Disturbance In Attention;Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Roche","Concomitant.Product.Names":"Levodopa"}
{"Case.ID":9450021,"Initial.FDA.Received.Date":"08/09/2013","days.since.last.fda":3,"Event.Date":"07/16/2013","Latest.FDA.Received.Date":"09-AUG-2013","Suspect.Product.Names":"Unasyn","Suspect.Product.Active.Ingredients":"Ampicillin Sodium\\Sulbactam Sodium;Allopurinol","Reason.for.Use":"Hyperuricaemia;Pyrexia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Pfizer","Concomitant.Product.Names":"Benserazide Hydrochloride\\Levodopa;Aspirin;Zolpidem Tartrate;Levemir;Bisoprolol Fumarate;Furosemide;Apidra;Lansoprazole"}
{"Case.ID":9460249,"Initial.FDA.Received.Date":"08/15/2013","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"15-AUG-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Calcium Metabolism Disorder;Diabetes Mellitus;Product Used For Unknown Indication;Prophylaxis;Vasculitis","Reactions":"Stevens-Johnson Syndrome;Cardiac Arrest","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Watson","Concomitant.Product.Names":"Digoxin;Prednisolone;Bisoprolol;Calcium Carbonate;Atorvastatin;Bumetanide;Omeprazole;Acetaminophen;Cyclophosphamide;Alfacalcidol;Hydralazine;Isosorbide"}
{"Case.ID":9553791,"Initial.FDA.Received.Date":"09/12/2013","days.since.last.fda":28,"Event.Date":"","Latest.FDA.Received.Date":"12-SEP-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Apotex","Concomitant.Product.Names":"-"}
{"Case.ID":9527795,"Initial.FDA.Received.Date":"09/13/2013","days.since.last.fda":1,"Event.Date":"07/23/2013","Latest.FDA.Received.Date":"13-SEP-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Terbinafine","Reason.for.Use":"-","Reactions":"Myocardial Infarction;Pneumonia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"Ariad","Concomitant.Product.Names":"-"}
{"Case.ID":9557470,"Initial.FDA.Received.Date":"09/24/2013","days.since.last.fda":11,"Event.Date":"08/16/2013","Latest.FDA.Received.Date":"06-JAN-2014","Suspect.Product.Names":"Sertraline","Suspect.Product.Active.Ingredients":"Sertraline Hydrochloride","Reason.for.Use":"Depression","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"69 YR","Sender":"Aurobindo","Concomitant.Product.Names":"Prednisolone;Methotrexate"}
{"Case.ID":9610856,"Initial.FDA.Received.Date":"10/09/2013","days.since.last.fda":15,"Event.Date":"08/25/2013","Latest.FDA.Received.Date":"23-OCT-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Hyperuricaemia","Reactions":"Anuria;Skin Exfoliation;Acute Kidney Injury;Urticaria;Hypotension;Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Sandoz","Concomitant.Product.Names":"Trazodone;Torsemide;Pantoprazole;Furosemide;Unspecified Ingredient"}
{"Case.ID":9648861,"Initial.FDA.Received.Date":"10/28/2013","days.since.last.fda":19,"Event.Date":"09/21/2013","Latest.FDA.Received.Date":"28-OCT-2013","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Meropenem;Vancomycin","Reason.for.Use":"Cellulitis","Reactions":"Stevens-Johnson Syndrome;Skin Reaction","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Sandoz","Concomitant.Product.Names":"Clindamycin;Imipenem;Piperacillin Sodium\\Tazobactam Sodium;Dextrose;Amikacin;Haldol;Calcium Chloride\\Potassium Chloride\\Sodium Chloride\\Sodium Lactate"}
{"Case.ID":9661056,"Initial.FDA.Received.Date":"10/31/2013","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"31-OCT-2013","Suspect.Product.Names":"Lamictal","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Epilepsy","Reactions":"Ulcer;Skin Ulcer;Rash;Stevens-Johnson Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Glaxosmithkline","Concomitant.Product.Names":"Unspecified Ingredient"}
{"Case.ID":9670483,"Initial.FDA.Received.Date":"11/06/2013","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"06-NOV-2013","Suspect.Product.Names":"Xeloda","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"Osteosarcoma","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"58 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":9744449,"Initial.FDA.Received.Date":"12/10/2013","days.since.last.fda":34,"Event.Date":"","Latest.FDA.Received.Date":"12-DEC-2013","Suspect.Product.Names":"Epilim","Suspect.Product.Active.Ingredients":"Valproate Sodium","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"24 YR","Sender":"Abbvie","Concomitant.Product.Names":"-"}
{"Case.ID":9798474,"Initial.FDA.Received.Date":"01/06/2014","days.since.last.fda":27,"Event.Date":"11/25/2013","Latest.FDA.Received.Date":"06-JAN-2014","Suspect.Product.Names":"Busulfex","Suspect.Product.Active.Ingredients":"Busulfan;Cyclophosphamide","Reason.for.Use":"Product Used For Unknown Indication;Transplant","Reactions":"Stevens-Johnson Syndrome;Colitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"65 YR","Sender":"Otsuka","Concomitant.Product.Names":"Digoxin;Mesna;Propranolol Hydrochloride;Levofloxacin;Ceftazidime;Calcium Phosphate, Dibasic, Anhydrous\\Magnesium Glycerophosphate\\Phosphoric Acid\\Sodium Phosphate, Dibasic;Zovirax;Tramadol Hydrochloride"}
{"Case.ID":9828685,"Initial.FDA.Received.Date":"01/17/2014","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"17-JAN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Rituximab;Bendamustine","Reason.for.Use":"Chronic Lymphocytic Leukaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":9882563,"Initial.FDA.Received.Date":"02/07/2014","days.since.last.fda":21,"Event.Date":"","Latest.FDA.Received.Date":"07-FEB-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Zonisamide","Reason.for.Use":"Seizure Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Eisai","Concomitant.Product.Names":"-"}
{"Case.ID":9890463,"Initial.FDA.Received.Date":"02/11/2014","days.since.last.fda":4,"Event.Date":"01/13/2014","Latest.FDA.Received.Date":"11-FEB-2014","Suspect.Product.Names":"Aldara","Suspect.Product.Active.Ingredients":"Imiquimod","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"72 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":9995962,"Initial.FDA.Received.Date":"03/11/2014","days.since.last.fda":28,"Event.Date":"01/15/2013","Latest.FDA.Received.Date":"11-MAR-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cloxacillin Sodium;Ceftazidime Sodium;Omeprazole","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"10 YR","Sender":"Ucb","Concomitant.Product.Names":"-"}
{"Case.ID":10044260,"Initial.FDA.Received.Date":"03/28/2014","days.since.last.fda":17,"Event.Date":"","Latest.FDA.Received.Date":"28-MAR-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cyclophosphamide;Rituximab;Fludarabine Phosphate","Reason.for.Use":"Allogenic Stem Cell Transplantation","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Aventis","Concomitant.Product.Names":"Radiation Therapy"}
{"Case.ID":10235879,"Initial.FDA.Received.Date":"06/12/2014","days.since.last.fda":76,"Event.Date":"05/05/2014","Latest.FDA.Received.Date":"12-JUN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"Cellulitis;Oropharyngeal Candidiasis","Reactions":"Stevens-Johnson Syndrome;Cellulitis;Toxic Epidermal Necrolysis;Rash Papular;Macule","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"-","Concomitant.Product.Names":"Vitamins;Flonase;Artificial Tears;Norco"}
{"Case.ID":10248678,"Initial.FDA.Received.Date":"06/18/2014","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"18-JUN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin","Reason.for.Use":"Pneumonia","Reactions":"Gastrointestinal Haemorrhage;Sepsis;Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"Fresenius Medical Care","Concomitant.Product.Names":"-"}
{"Case.ID":10243678,"Initial.FDA.Received.Date":"06/18/2014","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"18-JUN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Off Label Use;Pneumonia","Reactions":"Toxic Epidermal Necrolysis;Respiratory Failure;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"91 YR","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":10243492,"Initial.FDA.Received.Date":"06/18/2014","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"18-JUN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Urinary Tract Infection","Reactions":"Sepsis;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":10262284,"Initial.FDA.Received.Date":"06/26/2014","days.since.last.fda":8,"Event.Date":"","Latest.FDA.Received.Date":"26-JUN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Pneumonia","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"91 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":10262092,"Initial.FDA.Received.Date":"06/26/2014","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"26-JUN-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":10285909,"Initial.FDA.Received.Date":"07/09/2014","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"09-JUL-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Pneumonia","Reactions":"Stevens-Johnson Syndrome;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"91 YR","Sender":"Ranbaxy","Concomitant.Product.Names":"-"}
{"Case.ID":10285906,"Initial.FDA.Received.Date":"07/09/2014","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"09-JUL-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Urinary Tract Infection","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"68 YR","Sender":"Ranbaxy","Concomitant.Product.Names":"-"}
{"Case.ID":10299938,"Initial.FDA.Received.Date":"07/11/2014","days.since.last.fda":2,"Event.Date":"","Latest.FDA.Received.Date":"11-JUL-2014","Suspect.Product.Names":"Ertapenem.","Suspect.Product.Active.Ingredients":"Ertapenem Sodium;Vancomycin","Reason.for.Use":"Febrile Neutropenia;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"75 YR","Sender":"Baxter","Concomitant.Product.Names":"-"}
{"Case.ID":10348397,"Initial.FDA.Received.Date":"07/29/2014","days.since.last.fda":18,"Event.Date":"","Latest.FDA.Received.Date":"29-JUL-2014","Suspect.Product.Names":"Nuvigil","Suspect.Product.Active.Ingredients":"Armodafinil","Reason.for.Use":"Circadian Rhythm Sleep Disorder","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":10364929,"Initial.FDA.Received.Date":"08/06/2014","days.since.last.fda":8,"Event.Date":"06/26/2014","Latest.FDA.Received.Date":"27-OCT-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Gout;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"71 YR","Sender":"Sandoz","Concomitant.Product.Names":"Novalgin (Metamizole Sodium);Nitroglycerin;Xyzal;Prednisolone;Fluconazole;Nebivolol;Polyethylene Glycol 3350\\Potassium Chloride\\Sodium Bicarbonate\\Sodium Chloride"}
{"Case.ID":10419276,"Initial.FDA.Received.Date":"08/29/2014","days.since.last.fda":23,"Event.Date":"","Latest.FDA.Received.Date":"29-AUG-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Nevirapine;Lamivudine;Zidovudine","Reason.for.Use":"Hiv Infection","Reactions":"Death;Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"28 YR","Sender":"Glaxosmithkline","Concomitant.Product.Names":"-"}
{"Case.ID":10519749,"Initial.FDA.Received.Date":"10/15/2014","days.since.last.fda":47,"Event.Date":"","Latest.FDA.Received.Date":"15-OCT-2014","Suspect.Product.Names":"Abilify","Suspect.Product.Active.Ingredients":"Aripiprazole","Reason.for.Use":"Depression","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"5 DEC","Sender":"Bristol Myers Squibb","Concomitant.Product.Names":"-"}
{"Case.ID":10559451,"Initial.FDA.Received.Date":"10/30/2014","days.since.last.fda":15,"Event.Date":"","Latest.FDA.Received.Date":"30-OCT-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Epilepsy","Reactions":"Tachycardia;Myocardial Necrosis;Cardiac Failure;Hypersensitivity;Tachyarrhythmia;Stevens-Johnson Syndrome;Lower Respiratory Tract Infection;Cardiac Arrest;Cardiogenic Shock","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"41 YR","Sender":"Validus","Concomitant.Product.Names":"-"}
{"Case.ID":10586089,"Initial.FDA.Received.Date":"11/15/2014","days.since.last.fda":16,"Event.Date":"","Latest.FDA.Received.Date":"21-NOV-2014","Suspect.Product.Names":"Childrens Motrin","Suspect.Product.Active.Ingredients":"Ibuprofen","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Death","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"5 YR","Sender":"Mcneil","Concomitant.Product.Names":"-"}
{"Case.ID":10586276,"Initial.FDA.Received.Date":"11/17/2014","days.since.last.fda":2,"Event.Date":"01/12/2014","Latest.FDA.Received.Date":"17-NOV-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate;Mercaptopurine","Reason.for.Use":"Chemotherapy","Reactions":"Mucosal Inflammation;Product Prescribing Error;Blister;Stevens-Johnson Syndrome;Respiratory Tract Haemorrhage;Cardiac Arrest;Rash;Pancytopenia;Toxicity To Various Agents","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"16 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":10614848,"Initial.FDA.Received.Date":"12/01/2014","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"28-OCT-2015","Suspect.Product.Names":"Mircera","Suspect.Product.Active.Ingredients":"Methoxy Polyethylene Glycol-Epoetin Beta","Reason.for.Use":"Chronic Kidney Disease","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"39 YR","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":10618245,"Initial.FDA.Received.Date":"12/02/2014","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"02-DEC-2014","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Aspirin;Ranitidine;Ciprofloxacin","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"Lupin","Concomitant.Product.Names":"-"}
{"Case.ID":10666781,"Initial.FDA.Received.Date":"12/19/2014","days.since.last.fda":17,"Event.Date":"10/13/2014","Latest.FDA.Received.Date":"19-DEC-2014","Suspect.Product.Names":"Revlimid","Suspect.Product.Active.Ingredients":"Lenalidomide","Reason.for.Use":"Myelodysplastic Syndrome","Reactions":"Culture Urine Positive;Staphylococcus Test Positive;Stevens-Johnson Syndrome;Clostridium Test Positive;Hypotension;Klebsiella Test Positive;Respiratory Distress;Blood Culture Positive;Tachycardia;Therapy Non-Responder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":10678113,"Initial.FDA.Received.Date":"12/29/2014","days.since.last.fda":10,"Event.Date":"12/10/2014","Latest.FDA.Received.Date":"21-JAN-2015","Suspect.Product.Names":"Stivarga","Suspect.Product.Active.Ingredients":"Regorafenib","Reason.for.Use":"Colorectal Cancer;Constipation;Drug Toxicity Prophylaxis;Hypertension","Reactions":"Disseminated Intravascular Coagulation;Cardiac Failure;Stevens-Johnson Syndrome;Renal Failure;Hepatic Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"66 YR","Sender":"Bayer","Concomitant.Product.Names":"Magnesium Oxide;Diovan"}
{"Case.ID":10763210,"Initial.FDA.Received.Date":"01/28/2015","days.since.last.fda":30,"Event.Date":"","Latest.FDA.Received.Date":"28-JAN-2015","Suspect.Product.Names":"Rituxan","Suspect.Product.Active.Ingredients":"Rituximab;Bendamustine","Reason.for.Use":"Chronic Lymphocytic Leukaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Genentech","Concomitant.Product.Names":"-"}
{"Case.ID":10796061,"Initial.FDA.Received.Date":"02/16/2015","days.since.last.fda":19,"Event.Date":"12/14/2014","Latest.FDA.Received.Date":"15-APR-2015","Suspect.Product.Names":"Abilify;Nu-Lotan;Depakene","Suspect.Product.Active.Ingredients":"Valproic Acid;Losartan Potassium;Mitiglinide;Famotidine;Voglibose;Pravastatin Sodium;Aripiprazole;Allopurinol;Trazodone Hydrochloride;Nicardipine Hydrochloride","Reason.for.Use":"Agitation;Delirium;Diabetes Mellitus;Dyslipidaemia;Hypertension;Hyperuricaemia;Insomnia;Irritability","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"77 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":10903693,"Initial.FDA.Received.Date":"03/04/2015","days.since.last.fda":16,"Event.Date":"09/03/2014","Latest.FDA.Received.Date":"04-MAR-2015","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Bumetanide","Reason.for.Use":"Oedema","Reactions":"Purulence;Pyrexia;Acidosis;Eye Irritation;Eye Discharge;Ocular Hyperaemia;Laboratory Test Interference;Documented Hypersensitivity To Administered Product;Cardiac Arrest;Stevens-Johnson Syndrome;Eye Pain;Stress;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"86 YR","Sender":"-","Concomitant.Product.Names":"Aspirin;Lyrica;Allopurinol;Amlodipine;Carvedilol;Zocor;Accupril;Viagra;Omeprazole"}
{"Case.ID":10926637,"Initial.FDA.Received.Date":"03/16/2015","days.since.last.fda":12,"Event.Date":"","Latest.FDA.Received.Date":"16-MAR-2015","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium;Methylprednisolone;Prednisone;Ivermectin;Doxycycline","Reason.for.Use":"Product Used For Unknown Indication;Pyrexia;Strongyloidiasis","Reactions":"Drug Reaction With Eosinophilia And Systemic Symptoms;Stevens-Johnson Syndrome;Pseudomonal Sepsis;Strongyloidiasis;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"29 YR","Sender":"Hospira","Concomitant.Product.Names":"-"}
{"Case.ID":10956040,"Initial.FDA.Received.Date":"03/26/2015","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"26-MAY-2015","Suspect.Product.Names":"Intelence","Suspect.Product.Active.Ingredients":"Etravirine","Reason.for.Use":"Hiv Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Janssen","Concomitant.Product.Names":"-"}
{"Case.ID":10977521,"Initial.FDA.Received.Date":"03/30/2015","days.since.last.fda":4,"Event.Date":"01/12/2014","Latest.FDA.Received.Date":"30-MAR-2015","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mercaptopurine;Methotrexate","Reason.for.Use":"Chemotherapy","Reactions":"Product Prescribing Error;Respiratory Tract Haemorrhage;Mucosal Inflammation;Stevens-Johnson Syndrome;Cardiac Arrest;Pancytopenia;Toxicity To Various Agents;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"16 YR","Sender":"Nova Laboratories","Concomitant.Product.Names":"-"}
{"Case.ID":10990331,"Initial.FDA.Received.Date":"04/06/2015","days.since.last.fda":7,"Event.Date":"","Latest.FDA.Received.Date":"28-MAY-2015","Suspect.Product.Names":"Lasix","Suspect.Product.Active.Ingredients":"Furosemide","Reason.for.Use":"-","Reactions":"Acute Respiratory Distress Syndrome;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":11058007,"Initial.FDA.Received.Date":"04/22/2015","days.since.last.fda":16,"Event.Date":"09/08/2014","Latest.FDA.Received.Date":"22-APR-2015","Suspect.Product.Names":"Bumex","Suspect.Product.Active.Ingredients":"Bumetanide","Reason.for.Use":"Oedema Peripheral","Reactions":"Cardiac Arrest;Stevens-Johnson Syndrome;Ventricular Fibrillation;Hypersensitivity;Acidosis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"86 YR","Sender":"-","Concomitant.Product.Names":"Zocor;Carvedilol;Amlodipine;Allopurinol;Viagra;Accupril;Aspirin;Omeprazole;Lyrica"}
{"Case.ID":11069039,"Initial.FDA.Received.Date":"04/27/2015","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"14-JAN-2016","Suspect.Product.Names":"Cefotaxime;Avelox","Suspect.Product.Active.Ingredients":"Moxifloxacin Hydrochloride;Cefotaxime Sodium;Losartan;Cortisone Acetate","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":11128064,"Initial.FDA.Received.Date":"05/21/2015","days.since.last.fda":24,"Event.Date":"","Latest.FDA.Received.Date":"20-MAY-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol;Bendamustine;Rituximab","Reason.for.Use":"Follicular Lymphoma;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"Dr Reddys","Concomitant.Product.Names":"Dexamethasone;Lorazepam;Prochlorperazine;Levothyroxine;Palonosetron.;Aspirin;Vitamin D Nos"}
{"Case.ID":11340098,"Initial.FDA.Received.Date":"08/05/2015","days.since.last.fda":76,"Event.Date":"","Latest.FDA.Received.Date":"05-AUG-2015","Suspect.Product.Names":"Treanda","Suspect.Product.Active.Ingredients":"Bendamustine Hydrochloride;Allopurinol;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"B-Cell Lymphoma;Pneumocystis Jirovecii Pneumonia;Tumour Lysis Syndrome","Reactions":"Febrile Neutropenia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"76 YR","Sender":"Teva","Concomitant.Product.Names":"Dexamethasone;Vitamin D Nos;Metoclopramide;Lorazepam;Ondansetron;Rabeprazole;Zopiclone"}
{"Case.ID":11522392,"Initial.FDA.Received.Date":"09/18/2015","days.since.last.fda":44,"Event.Date":"","Latest.FDA.Received.Date":"18-SEP-2015","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol;Rituximab;Bendamustine","Reason.for.Use":"B-Cell Lymphoma;Product Used For Unknown Indication;Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"78 YR","Sender":"Apotex","Concomitant.Product.Names":"Prochlorperazine;Levothyroxine Sodium;Aspirin;Dexamethasone;Lorazepam;Palonosetron.;Ergocalciferol"}
{"Case.ID":11682025,"Initial.FDA.Received.Date":"10/29/2015","days.since.last.fda":41,"Event.Date":"","Latest.FDA.Received.Date":"29-OCT-2015","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Azithromycin Anhydrous","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Bronchiolitis;Drug-Induced Liver Injury;Bronchiectasis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":11829845,"Initial.FDA.Received.Date":"12/12/2015","days.since.last.fda":44,"Event.Date":"","Latest.FDA.Received.Date":"22-DEC-2015","Suspect.Product.Names":"Perjeta","Suspect.Product.Active.Ingredients":"Pertuzumab;Thrombomodulin Alfa;Trastuzumab;Meropenem;Docetaxel","Reason.for.Use":"Breast Cancer;Febrile Neutropenia","Reactions":"Skin Erosion;Cytomegalovirus Enterocolitis;Respiratory Failure;Erythema;Stevens-Johnson Syndrome;Immune Reconstitution Inflammatory Syndrome;Cytomegalovirus Infection Reactivation;Roseolovirus Test Positive","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"Astrazeneca","Concomitant.Product.Names":"-"}
{"Case.ID":11847712,"Initial.FDA.Received.Date":"12/17/2015","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"17-DEC-2015","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Diclofenac","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Skin Erosion;Depressed Level Of Consciousness;Rash;Oliguria;Nasopharyngitis;Oedema;Vomiting;Erythema;Pyrexia;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"76 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":11856124,"Initial.FDA.Received.Date":"12/21/2015","days.since.last.fda":4,"Event.Date":"12/04/2015","Latest.FDA.Received.Date":"30-MAR-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Docetaxel;Pertuzumab;Trastuzumab","Reason.for.Use":"Premedication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"49 YR","Sender":"Roche","Concomitant.Product.Names":"Acetaminophen;Ranitidine;Dexamethasone;Ondansetron"}
{"Case.ID":11940174,"Initial.FDA.Received.Date":"01/22/2016","days.since.last.fda":32,"Event.Date":"","Latest.FDA.Received.Date":"22-JAN-2016","Suspect.Product.Names":"Plavix","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Metoprolol","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"87 YR","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":11944935,"Initial.FDA.Received.Date":"01/25/2016","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"25-JAN-2016","Suspect.Product.Names":"Plavix","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Metoprolol","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"87 YR","Sender":"Aurobindo","Concomitant.Product.Names":"-"}
{"Case.ID":11979651,"Initial.FDA.Received.Date":"01/29/2016","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"29-JAN-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Urinary Tract Infection;Wound Infection","Reactions":"Toxic Epidermal Necrolysis;Septic Shock;Stevens-Johnson Syndrome;Hypotension;Multiple Organ Dysfunction Syndrome;Respiratory Failure","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"Westward","Concomitant.Product.Names":"Vancomycin;Doxycycline;Piperacillin Sodium\\Tazobactam Sodium"}
{"Case.ID":11994849,"Initial.FDA.Received.Date":"02/03/2016","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"03-FEB-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"Product Used For Unknown Indication;Urinary Tract Infection","Reactions":"Septic Shock;Multiple Organ Dysfunction Syndrome;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"Hospira","Concomitant.Product.Names":"Fluoxetine;Vancomycin;Pregabalin;Methadone;Trazodone;Bisacodyl;Amitriptyline;Hydrocortisone;Ranitidine;Loratadine;Polyethylene Glycols;Docusate Sodium\\Senna Leaf;Piperacillin And Tazobactam;Camphor (Synthetic)\\Menthol"}
{"Case.ID":12099298,"Initial.FDA.Received.Date":"02/19/2016","days.since.last.fda":16,"Event.Date":"11/15/2015","Latest.FDA.Received.Date":"19-FEB-2016","Suspect.Product.Names":"Tarceva","Suspect.Product.Active.Ingredients":"Erlotinib Hydrochloride","Reason.for.Use":"Terminal State","Reactions":"Palpitations;Oral Pain;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"-","Concomitant.Product.Names":"-"}
{"Case.ID":12093049,"Initial.FDA.Received.Date":"02/19/2016","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"19-FEB-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Cardiac Failure;Diabetes Mellitus;Hypertension;Psoriasis","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"54 YR","Sender":"Fresenius Kabi","Concomitant.Product.Names":"Lisinopril;Aspirin;Insulin Nos;Metoprolol;Prednisone"}
{"Case.ID":12113814,"Initial.FDA.Received.Date":"02/25/2016","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"25-FEB-2016","Suspect.Product.Names":"Ketorolac","Suspect.Product.Active.Ingredients":"Ketorolac Tromethamine;Acetaminophen;Sulfamethoxazole\\Trimethoprim;Pantoprazole Sodium;Clarithromycin;Ciprofloxacin;Phenytoin;Ceftriaxone;Lamotrigine;Phenobarbital;Carbamazepine;Acetaminophen\\Codeine Phosphate;Allopurinol;Levofloxacin;Amoxicillin;Naproxen","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":12120362,"Initial.FDA.Received.Date":"02/26/2016","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"26-FEB-2016","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine;Zidovudine;Lamivudine","Reason.for.Use":"Prophylaxis Against Hiv Infection","Reactions":"Stevens-Johnson Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"-"}
{"Case.ID":12183161,"Initial.FDA.Received.Date":"03/16/2016","days.since.last.fda":19,"Event.Date":"02/22/2016","Latest.FDA.Received.Date":"16-MAR-2016","Suspect.Product.Names":"Revlimid","Suspect.Product.Active.Ingredients":"Lenalidomide;Dexamethasone;Bortezomib","Reason.for.Use":"Plasma Cell Myeloma;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"56 YR","Sender":"Celgene","Concomitant.Product.Names":"Allopurinol"}
{"Case.ID":12350960,"Initial.FDA.Received.Date":"05/10/2016","days.since.last.fda":55,"Event.Date":"","Latest.FDA.Received.Date":"10-MAY-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Diclofenac","Reason.for.Use":"Arthritis;Product Used For Unknown Indication","Reactions":"Multiple Organ Dysfunction Syndrome;Sepsis;Hepatic Failure;Stevens-Johnson Syndrome;Off Label Use;Hepatitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"Iroko Pharm","Concomitant.Product.Names":"Fluoxetine;Levothyroxine"}
{"Case.ID":12537647,"Initial.FDA.Received.Date":"07/07/2016","days.since.last.fda":58,"Event.Date":"12/13/2014","Latest.FDA.Received.Date":"07-JUL-2016","Suspect.Product.Names":"Dilantin","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"52 YR","Sender":"Pfizer","Concomitant.Product.Names":"Metoprolol;Aspirin;Insulin Nos;Perindopril;Simvastatin;Amlodipine"}
{"Case.ID":12576342,"Initial.FDA.Received.Date":"07/20/2016","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"20-JUL-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Drug-Induced Liver Injury;Stevens-Johnson Syndrome;Cholestatic Liver Injury","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Unichem","Concomitant.Product.Names":"-"}
{"Case.ID":12637022,"Initial.FDA.Received.Date":"08/09/2016","days.since.last.fda":20,"Event.Date":"","Latest.FDA.Received.Date":"09-AUG-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Doxycycline;Piperacillin Sodium\\Tazobactam Sodium;Ceftaroline;Vancomycin;Linezolid;Ciprofloxacin","Reason.for.Use":"Antibiotic Therapy;Meningitis;Sepsis;Staphylococcal Infection","Reactions":"Septic Shock;Drug Reaction With Eosinophilia And Systemic Symptoms;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis;Staphylococcal Bacteraemia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"Fresenius Kabi","Concomitant.Product.Names":"-"}
{"Case.ID":12647511,"Initial.FDA.Received.Date":"08/12/2016","days.since.last.fda":3,"Event.Date":"01/05/2015","Latest.FDA.Received.Date":"12-AUG-2016","Suspect.Product.Names":"Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Product Used For Unknown Indication;Seizure","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"66 YR","Sender":"Novartis","Concomitant.Product.Names":"Ranitidine;Alfuzosin;Dutasteride;Simvastatin"}
{"Case.ID":12657480,"Initial.FDA.Received.Date":"08/16/2016","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"16-AUG-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin Hydrochloride;Doxycycline","Reason.for.Use":"-","Reactions":"Cardiac Failure;Acute Kidney Injury;Tubulointerstitial Nephritis;Hepatitis;Thyroiditis;Drug Reaction With Eosinophilia And Systemic Symptoms;Stevens-Johnson Syndrome;Septic Shock;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"69 YR","Sender":"Ani","Concomitant.Product.Names":"-"}
{"Case.ID":12667874,"Initial.FDA.Received.Date":"08/19/2016","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"19-AUG-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Mebendazole","Reason.for.Use":"Helminthic Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"4 YR","Sender":"Janssen","Concomitant.Product.Names":"-"}
{"Case.ID":12679312,"Initial.FDA.Received.Date":"08/24/2016","days.since.last.fda":5,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"14-MAY-2018","Suspect.Product.Names":"Humalog;Lantus;Pantozol;Clopidogrel","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Atorvastatin;Pantoprazole Sodium;Methimazole;Allopurinol;Melperone Hydrochloride;Potassium Citrate;Torsemide;Clarithromycin;Sodium Perchlorate;Dextrose;Ferrous Sulfate;Metoprolol;Insulin Glargine;Brotizolam;Insulin Lispro;Metoclopramide;Potassium Chloride;Ramipril;Loperamide;Pipamperone;Carbamazepine;Hydrochlorothiazide;Enoxaparin Sodium;Aspirin;Sodium Chloride;Lorazepam;Digitoxin;Metoprolol Succinate;Furosemide;Electrolytes Nos","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Nikolsky'S Sign;Oral Disorder;Purpura;Ocular Hyperaemia;Lip Erosion;Swollen Tongue;Stevens-Johnson Syndrome;Pruritus;Blister;Conjunctivitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Bayer","Concomitant.Product.Names":"Levofloxacin;Haloperidol;Digitoxin;Tazobactam;Morphine;Perfalgan;Novalgin (Metamizole Sodium);Dermatop;Zyrtec;Dimethindene;Gramicidin\\Neomycin Sulfate\\Polymyxin B Sulfate;Promethazine Hydrochloride;Ampicillin Sodium\\Sulbactam Sodium;Prednisolone Sodium Succinate;Diflucan;Flunitrazepam"}
{"Case.ID":12716981,"Initial.FDA.Received.Date":"09/06/2016","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"06-SEP-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Drug Reaction With Eosinophilia And Systemic Symptoms;Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Sebela","Concomitant.Product.Names":"-"}
{"Case.ID":12928586,"Initial.FDA.Received.Date":"11/10/2016","days.since.last.fda":65,"Event.Date":"10/10/2016","Latest.FDA.Received.Date":"19-NOV-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Constipation Prophylaxis;Diuretic Therapy;Gastrointestinal Disorder;Hypertension;Hyperuricaemia;Postoperative Analgesia","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"Lupin","Concomitant.Product.Names":"Furosemide;Amlodipine;Calonal;Aldactone;Famotidine;Herbals;Febuxostat;Carvedilol"}
{"Case.ID":12986515,"Initial.FDA.Received.Date":"11/29/2016","days.since.last.fda":19,"Event.Date":"04/03/2016","Latest.FDA.Received.Date":"29-NOV-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Itraconazole;Fluconazole","Reason.for.Use":"Oesophageal Candidiasis","Reactions":"Blister;Stevens-Johnson Syndrome;Urticaria;Rash;Acute Kidney Injury;Atrial Fibrillation;Hypotension","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"73 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"Irinotecan"}
{"Case.ID":12998321,"Initial.FDA.Received.Date":"12/03/2016","days.since.last.fda":4,"Event.Date":"09/18/2016","Latest.FDA.Received.Date":"03-DEC-2016","Suspect.Product.Names":"Arcoxia;Tegretol","Suspect.Product.Active.Ingredients":"Carbamazepine;Etoricoxib","Reason.for.Use":"Arthritis;Neuralgia","Reactions":"Oral Pain;Rash;Fungal Infection;Malaise;Vulvovaginal Pain;Septic Shock;Cellulitis;Vulvovaginal Pruritus;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"81 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"Insulin Nos;Panadol"}
{"Case.ID":13011869,"Initial.FDA.Received.Date":"12/09/2016","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"28-DEC-2016","Suspect.Product.Names":"Gazyva;Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Chlorambucil;Obinutuzumab;Allopurinol","Reason.for.Use":"Chronic Lymphocytic Leukaemia;Product Used For Unknown Indication","Reactions":"Pyrexia;Stevens-Johnson Syndrome;Hyperaemia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":13024197,"Initial.FDA.Received.Date":"12/13/2016","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"13-DEC-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Dapsone","Reason.for.Use":"-","Reactions":"Drug-Induced Liver Injury;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"North Creek Pharmaceuticals","Concomitant.Product.Names":"-"}
{"Case.ID":13056490,"Initial.FDA.Received.Date":"12/22/2016","days.since.last.fda":9,"Event.Date":"","Latest.FDA.Received.Date":"22-DEC-2016","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Warfarin;Sulfamethoxazole\\Trimethoprim","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;International Normalised Ratio Increased;Glomerulonephritis Rapidly Progressive","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"60 YR","Sender":"Ani","Concomitant.Product.Names":"-"}
{"Case.ID":13094853,"Initial.FDA.Received.Date":"01/06/2017","days.since.last.fda":15,"Event.Date":"","Latest.FDA.Received.Date":"06-JAN-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Docetaxel;Cyclophosphamide","Reason.for.Use":"Breast Cancer;Chemotherapy","Reactions":"Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome;Pneumonia;Disseminated Intravascular Coagulation","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"60 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":13096082,"Initial.FDA.Received.Date":"01/09/2017","days.since.last.fda":3,"Event.Date":"12/04/2016","Latest.FDA.Received.Date":"25-MAY-2017","Suspect.Product.Names":"Cancidas;Kardegic;Bactrim;Amlodipine","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Sulfamethoxazole\\Trimethoprim;Valganciclovir;Pantoprazole;Aspirin Dl-Lysine;Caspofungin Acetate;Tramadol Hydrochloride;Colistin Sulfate;Ciprofloxacin;Methylprednisolone;Gentamicin;Imipenem;Vancomycin","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Pancytopenia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Roche","Concomitant.Product.Names":"Tacrolimus;Prednisone;Amikacin;Urapidil;Fosfomycin;Mycophenolic Acid;Calciparine"}
{"Case.ID":13103975,"Initial.FDA.Received.Date":"01/11/2017","days.since.last.fda":2,"Event.Date":"","Latest.FDA.Received.Date":"11-JAN-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cefadroxil","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"86 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":13108022,"Initial.FDA.Received.Date":"01/12/2017","days.since.last.fda":1,"Event.Date":"12/06/2016","Latest.FDA.Received.Date":"12-JAN-2017","Suspect.Product.Names":"Bactrim;Kardegic;Amlodipine;Cancidas","Suspect.Product.Active.Ingredients":"Caspofungin Acetate;Methylprednisolone Sodium Succinate;Valganciclovir;Colistimethate Sodium;Amlodipine Besylate;Aspirin Dl-Lysine;Gentamicin;Ciprofloxacin;Pantoprazole;Vancomycin;Sulfamethoxazole\\Trimethoprim;Imipenem;Tramadol","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Pancytopenia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Aurobindo","Concomitant.Product.Names":"-"}
{"Case.ID":13112063,"Initial.FDA.Received.Date":"01/13/2017","days.since.last.fda":1,"Event.Date":"12/06/2016","Latest.FDA.Received.Date":"13-JAN-2017","Suspect.Product.Names":"Amlodipine;Cancidas;Kardegic;Bactrim","Suspect.Product.Active.Ingredients":"Sulfamethoxazole\\Trimethoprim;Aspirin Dl-Lysine;Caspofungin Acetate;Amlodipine Besylate;Ciprofloxacin;Valganciclovir Hydrochloride;Colistimethate Sodium;Pantoprazole;Tramadol Hydrochloride;Gentamicin;Imipenem;Methylprednisolone;Vancomycin","Reason.for.Use":"-","Reactions":"Pancytopenia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":13122784,"Initial.FDA.Received.Date":"01/17/2017","days.since.last.fda":4,"Event.Date":"12/06/2016","Latest.FDA.Received.Date":"17-JAN-2017","Suspect.Product.Names":"Bactrim;Cancidas;Amlodipine;Kardegic","Suspect.Product.Active.Ingredients":"Aspirin Dl-Lysine;Imipenem;Amlodipine Besylate;Vancomycin;Colistin Sulfate;Gentamicin;Tramadol;Valganciclovir;Caspofungin Acetate;Methylprednisolone;Sulfamethoxazole\\Trimethoprim;Ciprofloxacin;Pantoprazole","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Pancytopenia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":13136503,"Initial.FDA.Received.Date":"01/22/2017","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"22-JAN-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Valganciclovir;Pantoprazole;Vancomycin;Tramadol;Cilastatin Sodium\\Imipenem;Ciprofloxacin;Methylprednisolone","Reason.for.Use":"Enterobacter Infection;Infection;Product Used For Unknown Indication","Reactions":"Pancytopenia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"Amikacin;Nicardipine;Cancidas;Urapidil;Bactrim;Fosfomycin;Kardegic;Calciparine;Gentamicin;Colistimethate Sodium;Meropenem;Amlodipine"}
{"Case.ID":13360397,"Initial.FDA.Received.Date":"03/22/2017","days.since.last.fda":59,"Event.Date":"02/22/2017","Latest.FDA.Received.Date":"20-JUN-2017","Suspect.Product.Names":"Omnipaque","Suspect.Product.Active.Ingredients":"Iohexol","Reason.for.Use":"Atrial Fibrillation;Blood Cholesterol Increased;Cough;Dyspnoea;Hypertension;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Ge Healthcare","Concomitant.Product.Names":"Bisoprolol;Simvastatin;Warfarin;Fusidic Acid;Allopurinol;Valsartan;Doxycycline"}
{"Case.ID":13415451,"Initial.FDA.Received.Date":"04/06/2017","days.since.last.fda":15,"Event.Date":"","Latest.FDA.Received.Date":"06-APR-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Acetaminophen","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Fresenius Kabi","Concomitant.Product.Names":"-"}
{"Case.ID":13668127,"Initial.FDA.Received.Date":"06/19/2017","days.since.last.fda":74,"Event.Date":"06/05/2017","Latest.FDA.Received.Date":"19-JUN-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Gout","Reactions":"Metabolic Disorder;Stevens-Johnson Syndrome;Lactic Acidosis;Dialysis;Toxic Epidermal Necrolysis;Headache","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"78 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"-"}
{"Case.ID":13697303,"Initial.FDA.Received.Date":"06/28/2017","days.since.last.fda":9,"Event.Date":"05/23/2016","Latest.FDA.Received.Date":"28-JUN-2017","Suspect.Product.Names":"Factive","Suspect.Product.Active.Ingredients":"Gemifloxacin Mesylate","Reason.for.Use":"Chronic Obstructive Pulmonary Disease;Dementia;Gastric Ulcer;Respiratory Failure;Sinusitis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"Lg Life Sciences","Concomitant.Product.Names":"Memantine Hydrochloride;Prednisolone;Lansoprazole"}
{"Case.ID":13741961,"Initial.FDA.Received.Date":"07/11/2017","days.since.last.fda":13,"Event.Date":"","Latest.FDA.Received.Date":"11-JUL-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Sebela","Concomitant.Product.Names":"-"}
{"Case.ID":13744353,"Initial.FDA.Received.Date":"07/12/2017","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"22-DEC-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Acute Kidney Injury","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"83 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":13754000,"Initial.FDA.Received.Date":"07/14/2017","days.since.last.fda":2,"Event.Date":"06/02/2016","Latest.FDA.Received.Date":"14-JUL-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Gemifloxacin;Lansoprazole;Memantine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Arteriosclerosis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"80 YR","Sender":"Allergan","Concomitant.Product.Names":"-"}
{"Case.ID":13784338,"Initial.FDA.Received.Date":"07/24/2017","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"24-JUL-2017","Suspect.Product.Names":"Rimstar","Suspect.Product.Active.Ingredients":"Ethambutol\\Isoniazid\\Pyrazinamide\\Rifamycin","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Hepatic Failure","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":13859907,"Initial.FDA.Received.Date":"08/11/2017","days.since.last.fda":18,"Event.Date":"","Latest.FDA.Received.Date":"08-AUG-2018","Suspect.Product.Names":"Entresto","Suspect.Product.Active.Ingredients":"Sacubitril\\Valsartan","Reason.for.Use":"Left Ventricular Failure","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":13869215,"Initial.FDA.Received.Date":"08/15/2017","days.since.last.fda":4,"Event.Date":"08/25/2013","Latest.FDA.Received.Date":"15-AUG-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Hyperuricaemia","Reactions":"Acute Kidney Injury;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"83 YR","Sender":"Teva","Concomitant.Product.Names":"Furosemide;Pantoprazole Sodium;Trazodone;Torsemide"}
{"Case.ID":13944413,"Initial.FDA.Received.Date":"09/07/2017","days.since.last.fda":23,"Event.Date":"","Latest.FDA.Received.Date":"07-SEP-2017","Suspect.Product.Names":"Rituxan","Suspect.Product.Active.Ingredients":"Rituximab;Bendamustine","Reason.for.Use":"Chronic Lymphocytic Leukaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":13961561,"Initial.FDA.Received.Date":"09/12/2017","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"12-SEP-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Epilepsy","Reactions":"Cardiac Arrest;Respiratory Distress;Loss Of Consciousness;Stevens-Johnson Syndrome;Myocarditis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"43 YR","Sender":"Epic Pharm","Concomitant.Product.Names":"-"}
{"Case.ID":13968414,"Initial.FDA.Received.Date":"09/14/2017","days.since.last.fda":2,"Event.Date":"","Latest.FDA.Received.Date":"05-OCT-2017","Suspect.Product.Names":"Sporanox","Suspect.Product.Active.Ingredients":"Itraconazole","Reason.for.Use":"Hypertension;Hyperuricaemia;Onychomycosis","Reactions":"Death;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Janssen","Concomitant.Product.Names":"Allopurinol;Candesartan"}
{"Case.ID":14124742,"Initial.FDA.Received.Date":"10/25/2017","days.since.last.fda":41,"Event.Date":"","Latest.FDA.Received.Date":"25-OCT-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Cipla","Concomitant.Product.Names":"-"}
{"Case.ID":14190573,"Initial.FDA.Received.Date":"11/14/2017","days.since.last.fda":20,"Event.Date":"","Latest.FDA.Received.Date":"14-NOV-2017","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Bendamustine","Reason.for.Use":"Splenic Marginal Zone Lymphoma","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"Allopurinol;Rituximab"}
{"Case.ID":14243626,"Initial.FDA.Received.Date":"12/01/2017","days.since.last.fda":17,"Event.Date":"","Latest.FDA.Received.Date":"01-DEC-2017","Suspect.Product.Names":"Stivarga","Suspect.Product.Active.Ingredients":"Regorafenib","Reason.for.Use":"Colorectal Cancer Metastatic","Reactions":"Stevens-Johnson Syndrome;Rash;Palmar-Plantar Erythrodysaesthesia Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"22 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":14362454,"Initial.FDA.Received.Date":"01/08/2018","days.since.last.fda":38,"Event.Date":"12/20/2017","Latest.FDA.Received.Date":"15-FEB-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenobarbital;Lamotrigine;Valproic Acid","Reason.for.Use":"Post Stroke Epilepsy;Product Used For Unknown Indication","Reactions":"Hyperpyrexia;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Cipla","Concomitant.Product.Names":"Carvedilol;Aspirin Dl-Lysine"}
{"Case.ID":14407689,"Initial.FDA.Received.Date":"01/17/2018","days.since.last.fda":9,"Event.Date":"12/04/2017","Latest.FDA.Received.Date":"17-JAN-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Doxycycline","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Rash","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"64 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"-"}
{"Case.ID":14400952,"Initial.FDA.Received.Date":"01/17/2018","days.since.last.fda":0,"Event.Date":"06/18/2017","Latest.FDA.Received.Date":"17-JAN-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Naproxen Sodium","Reason.for.Use":"Analgesic Therapy","Reactions":"Stevens-Johnson Syndrome;Blister;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"49 YR","Sender":"Bayer","Concomitant.Product.Names":"Mirtazapine;Omeprazole;Cocodamol;Morphine Sulfate;Dexamethasone"}
{"Case.ID":14612809,"Initial.FDA.Received.Date":"03/08/2018","days.since.last.fda":50,"Event.Date":"","Latest.FDA.Received.Date":"08-MAR-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"-","Reactions":"Death;Stevens-Johnson Syndrome;Acute Respiratory Distress Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"74 YR","Sender":"Bayer","Concomitant.Product.Names":"Digoxin;Ambroxol Hydrochloride;Nicorandil;Isosorbide Dinitrate;Warfarin;Spironolactone;Tripelennamine;Adalat Cc"}
{"Case.ID":14656107,"Initial.FDA.Received.Date":"03/19/2018","days.since.last.fda":11,"Event.Date":"","Latest.FDA.Received.Date":"02-APR-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Carbamazepine","Reason.for.Use":"Epilepsy","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Vomiting","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"14 YR","Sender":"Novartis","Concomitant.Product.Names":"Epival"}
{"Case.ID":14695602,"Initial.FDA.Received.Date":"03/29/2018","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"29-MAR-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Pantoprazole","Reason.for.Use":"Gastrointestinal Haemorrhage","Reactions":"Sepsis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"74 YR","Sender":"Teva","Concomitant.Product.Names":"Lisinopril;Vitamin D3;Aspirin;Donepezil;Hydrochlorothiazide;Sucralfate"}
{"Case.ID":14716918,"Initial.FDA.Received.Date":"04/04/2018","days.since.last.fda":6,"Event.Date":"02/24/2018","Latest.FDA.Received.Date":"05-JUL-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Rifampin;Gentamicin;Vancomycin","Reason.for.Use":"Diabetes Mellitus;Pneumonitis;Product Used For Unknown Indication","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"76 YR","Sender":"Bausch And Lomb","Concomitant.Product.Names":"Aspirin\\Clopidogrel;Esomeprazole Sodium;Amlodipine;Humalog;Bisoprolol Fumarate;Lasix;Mycostatin;Potassium Chloride;Beclomethasone Dipropionate;Atorvastatin;Nitroglycerin;Plavix;Lantus;Aspirin"}
{"Case.ID":14778760,"Initial.FDA.Received.Date":"04/19/2018","days.since.last.fda":15,"Event.Date":"","Latest.FDA.Received.Date":"19-APR-2018","Suspect.Product.Names":"Remicade","Suspect.Product.Active.Ingredients":"Infliximab","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Janssen","Concomitant.Product.Names":"-"}
{"Case.ID":14801209,"Initial.FDA.Received.Date":"04/24/2018","days.since.last.fda":5,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"24-APR-2018","Suspect.Product.Names":"Lantus;Humalog;Pantozol;Clopidogrel","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Dextrose;Hydrochlorothiazide;Metoprolol Succinate;Allopurinol;Pantoprazole Sodium;Sodium Chloride;Aspirin;Melperone Hydrochloride;Ferrous Sulfate;Insulin Lispro;Insulin Glargine;Ramipril;Furosemide;Loperamide;Metoclopramide;Potassium Citrate;Digitoxin;Electrolytes Nos;Clarithromycin;Enoxaparin Sodium;Methimazole;Brotizolam;Torsemide;Potassium Chloride;Pipamperone;Lorazepam;Sodium Perchlorate Monohydrate;Atorvastatin;Carbamazepine;Metoprolol","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Product Used For Unknown Indication;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Conjunctivitis;Blister;Purpura;Lip Erosion;Nikolsky'S Sign;Ocular Hyperaemia;Swollen Tongue;Oral Disorder;Stevens-Johnson Syndrome;Pruritus","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Eli Lilly And Co","Concomitant.Product.Names":"Tazobactam;Sultamicillin Tosylate;Digitoxin;Diflucan;Flunitrazepam;Dermatop;Haloperidol;Acetaminophen\\Caffeine\\Propyphenazone;Promethazine Hydrochloride;Levofloxacin;Morphine;Zyrtec;Prednisolone Sodium Succinate;Perfalgan;Dimethindene"}
{"Case.ID":14841455,"Initial.FDA.Received.Date":"05/03/2018","days.since.last.fda":9,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"29-MAY-2018","Suspect.Product.Names":"Lantus;Humalog;Clopidogrel;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Clarithromycin;Atorvastatin;Brotizolam;Potassium Chloride;Sodium Chloride;Aspirin;Loperamide;Metoprolol Succinate;Clopidogrel Bisulfate;Carbamazepine;Electrolytes Nos;Hydrochlorothiazide;Potassium Citrate;Melperone Hydrochloride;Insulin Lispro;Digitoxin;Ramipril;Insulin Glargine;Methimazole;Torsemide;Ferrous Sulfate;Dextrose;Pipamperone;Metoprolol;Lorazepam;Furosemide;Allopurinol;Sodium Perchlorate;Enoxaparin Sodium;Metoclopramide","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Product Used For Unknown Indication;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome;Conjunctivitis;Blister;Purpura;Lip Erosion;Oral Disorder;Nikolsky'S Sign;Pruritus;Ocular Hyperaemia;Swollen Tongue","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Aurobindo","Concomitant.Product.Names":"Haloperidol;Zyrtec;Novalgin (Metamizole Sodium);Morphine;Dermatop;Diflucan;Ampicillin Sodium\\Sulbactam Sodium;Perfalgan;Dimethindene;Tazobactam;Promethazine Hydrochloride;Prednisolone Sodium Succinate;Levofloxacin;Flunitrazepam;Digitoxin"}
{"Case.ID":14846967,"Initial.FDA.Received.Date":"05/04/2018","days.since.last.fda":1,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"29-MAY-2018","Suspect.Product.Names":"Clopidogrel;Lantus;Humalog;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Ferrous Sulfate;Sodium Perchlorate;Insulin Lispro;Atorvastatin;Hydrochlorothiazide;Furosemide;Torsemide;Clarithromycin;Allopurinol;Ramipril;Metoclopramide;Carbamazepine;Aspirin;Metoprolol;Sodium Chloride;Metoprolol Succinate;Insulin Glargine;Potassium Chloride;Brotizolam;Dextrose;Pipamperone;Clopidogrel Bisulfate;Lorazepam;Electrolytes Nos;Potassium Citrate;Melperone Hydrochloride;Digitoxin;Loperamide;Enoxaparin Sodium;Methimazole","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Product Used For Unknown Indication;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Oral Disorder;Nikolsky'S Sign;Swollen Tongue;Pruritus;Stevens-Johnson Syndrome;Blister;Lip Erosion;Ocular Hyperaemia;Purpura;Conjunctivitis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Baxter","Concomitant.Product.Names":"Levofloxacin;Flunitrazepam;Haloperidol;Dermatop;Dimethindene;Morphine;Digitoxin;Diflucan;Tazobactam;Promethazine Hydrochloride;Perfalgan;Novalgin (Metamizole Sodium);Zyrtec;Prednisolone Sodium Succinate;Ampicillin Sodium\\Sulbactam Sodium"}
{"Case.ID":14852768,"Initial.FDA.Received.Date":"05/07/2018","days.since.last.fda":3,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"07-MAY-2018","Suspect.Product.Names":"Humalog;Pantozol;Lantus;Clopidogrel","Suspect.Product.Active.Ingredients":"Clopidogrel Bisulfate;Sodium Perchlorate;Hydrochlorothiazide;Metoprolol;Dextrose;Potassium Chloride;Sodium Chloride;Insulin Glargine;Enoxaparin Sodium;Carbamazepine;Aspirin;Pantoprazole Sodium;Clarithromycin;Atorvastatin;Methimazole;Electrolytes Nos;Pipamperone;Insulin Lispro;Allopurinol;Loperamide;Torsemide;Ferrous Sulfate;Metoprolol Succinate;Ramipril;Brotizolam;Metoclopramide;Digitoxin;Lorazepam;Melperone Hydrochloride;Furosemide;Potassium Citrate","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Product Used For Unknown Indication;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Lip Erosion;Conjunctivitis;Ocular Hyperaemia;Oral Disorder;Swollen Tongue;Stevens-Johnson Syndrome;Blister;Nikolsky'S Sign;Pruritus;Purpura","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Fresenius Kabi","Concomitant.Product.Names":"Perfalgan;Digitoxin;Levofloxacin;Haloperidol;Novalgin (Metamizole Sodium);Ampicillin Sodium\\Sulbactam Sodium;Flunitrazepam;Tazobactam;Gramicidin\\Neomycin Sulfate\\Polymyxin B Sulfate;Promethazine Hydrochloride;Diflucan;Morphine;Zyrtec;Dermatop;Prednisolone Sodium Succinate;Dimethindene"}
{"Case.ID":14861530,"Initial.FDA.Received.Date":"05/08/2018","days.since.last.fda":1,"Event.Date":"11/11/2004","Latest.FDA.Received.Date":"08-MAY-2018","Suspect.Product.Names":"Clopidogrel;Humalog;Ferro-Sanol Duodenal;Lantus;Tavor (Lorazepam);Pantozol","Suspect.Product.Active.Ingredients":"Clarithromycin;Pantoprazole Sodium;Ramipril;Brotizolam;Metoclopramide;Lorazepam;Metoclopramide Hydrochloride;Torsemide;Methimazole;Insulin Glargine;Metoprolol;Hydrochlorothiazide;Pipamperone;Sodium Perchlorate;Metoprolol Succinate;Atorvastatin;Ferrous Glycine Sulfate;Loperamide;Potassium Citrate;Insulin Lispro;Electrolytes Nos;Enoxaparin Sodium;Clopidogrel Bisulfate;Carbamazepine;Potassium Chloride;Digitoxin;Melperone Hydrochloride;Furosemide;Allopurinol;Aspirin;Sodium Chloride","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Candida Infection;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Electrolyte Substitution Therapy;Fluid Replacement;Haemoglobin Decreased;Hypercholesterolaemia;Hypertension;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Nausea;Ocular Hyperaemia;Pain;Parotitis;Pneumonia;Polyuria;Product Used For Unknown Indication;Prophylaxis Against Gastrointestinal Ulcer;Pruritus;Pyrexia;Renal Failure;Restlessness;Sedation;Skin Disorder;Sleep Disorder;Swollen Tongue;Thrombosis Prophylaxis","Reactions":"Purpura;Lip Erosion;Ocular Hyperaemia;Pruritus;Oral Disorder;Conjunctivitis;Nikolsky'S Sign;Blister;Stevens-Johnson Syndrome;Swollen Tongue","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Aralez Pharmaceuticals","Concomitant.Product.Names":"Pipamperone;Levofloxacin;Perfalgan;Haloperidol;Tazobactam;Sultamicillin Tosylate;Sodium Chloride;Furosemide;Ampho-Moronal;Metoprolol;Hydrochlorothiazide\\Ramipril;Aspirin;Flunitrazepam;Human Red Blood Cell;Piperacillin Sodium\\Tazobactam Sodium;Potassium Chloride;Dimethindene;Acetaminophen\\Caffeine\\Propyphenazone;Morphine;Zyrtec;Prednicarbate;Potassium Carbonate\\Potassium Citrate;Kcl;Diflucan;Dextrose"}
{"Case.ID":14907803,"Initial.FDA.Received.Date":"05/17/2018","days.since.last.fda":9,"Event.Date":"","Latest.FDA.Received.Date":"17-MAY-2018","Suspect.Product.Names":"Clopidogrel;Humalog;Lantus;Pantozol","Suspect.Product.Active.Ingredients":"Brotizolam;Pantoprazole Sodium;Insulin Glargine;Insulin Lispro;Potassium Chloride;Dextrose;Clarithromycin;Metoprolol;Ramipril;Atorvastatin;Loperamide;Sodium Chloride;Allopurinol;Metoclopramide;Furosemide;Enoxaparin Sodium;Aspirin;Melperone Hydrochloride;Digitoxin;Haloperidol;Clopidogrel Bisulfate;Methimazole;Hydrochlorothiazide;Pipamperone;Metoprolol Succinate;Ferrous Sulfate;Carbamazepine;Lorazepam;Potassium Citrate;Torsemide;Sodium Perchlorate","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Product Used For Unknown Indication;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Johnson And Johnson","Concomitant.Product.Names":"Ampicillin Sodium\\Sulbactam Sodium;Promethazine Hydrochloride;Zyrtec;Morphine;Dimethindene;Dermatop;Diflucan;Prednisolone Sodium Succinate;Levofloxacin;Flunitrazepam;Perfalgan;Novalgin (Metamizole Sodium);Tazobactam"}
{"Case.ID":14920809,"Initial.FDA.Received.Date":"05/21/2018","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"21-MAY-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Toxic Epidermal Necrolysis;Haemorrhage;Skin Infection;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"39 YR","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":14992793,"Initial.FDA.Received.Date":"06/09/2018","days.since.last.fda":19,"Event.Date":"06/18/2017","Latest.FDA.Received.Date":"09-JUN-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Naproxen","Reason.for.Use":"Analgesic Therapy","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome;Blister","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"49 YR","Sender":"Teva","Concomitant.Product.Names":"Mirtazapine;Morphine Sulfate;Dexamethasone;Omeprazole;Cocodamol"}
{"Case.ID":15011011,"Initial.FDA.Received.Date":"06/14/2018","days.since.last.fda":5,"Event.Date":"02/02/2018","Latest.FDA.Received.Date":"05-OCT-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Hyperuricaemia;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Sandoz","Concomitant.Product.Names":"Nebivolol;Levothyroxine Sodium;Lasix;Coumadin;Telmisartan"}
{"Case.ID":15098596,"Initial.FDA.Received.Date":"07/02/2018","days.since.last.fda":18,"Event.Date":"11/22/2017","Latest.FDA.Received.Date":"02-JUL-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amikacin","Reason.for.Use":"Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"92 YR","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":15140328,"Initial.FDA.Received.Date":"07/13/2018","days.since.last.fda":11,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"24-JUL-2018","Suspect.Product.Names":"Clopidogrel;Humalog;Lantus;Pantozol","Suspect.Product.Active.Ingredients":"Pantoprazole Sodium;Furosemide;Metoprolol Tartrate;Lorazepam;Allopurinol;Electrolytes Nos;Pipamperone;Dextrose;Clarithromycin;Ferrous Sulfate;Aspirin;Torsemide;Enoxaparin Sodium;Ramipril;Insulin Glargine;Methimazole;Atorvastatin;Insulin Lispro;Hydrochlorothiazide;Metoclopramide;Metoprolol;Clopidogrel Bisulfate;Brotizolam;Melperone Hydrochloride;Loperamide;Potassium Chloride;Sodium Chloride;Sodium Perchlorate;Carbamazepine;Potassium Citrate;Digitoxin","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Pneumonia;Polyuria;Product Used For Unknown Indication;Renal Failure;Sleep Disorder;Thrombosis;Thrombosis Prophylaxis","Reactions":"Blister;Nikolsky'S Sign;Pruritus;Stevens-Johnson Syndrome;Purpura;Ocular Hyperaemia;Conjunctivitis;Lip Erosion;Swollen Tongue;Oral Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Sandoz","Concomitant.Product.Names":"Dermatop;Prednisolone Sodium Succinate;Levofloxacin;Novalgin (Metamizole Sodium);Dimethindene;Haloperidol;Zyrtec;Promethazine Hydrochloride;Tazobactam;Morphine;Perfalgan;Ampicillin Sodium\\Sulbactam Sodium;Diflucan;Flunitrazepam"}
{"Case.ID":15206266,"Initial.FDA.Received.Date":"07/27/2018","days.since.last.fda":14,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"06-OCT-2018","Suspect.Product.Names":"Clopidogrel;Ferro-Sanol Duodenal;Pantozol;Humalog;Lantus","Suspect.Product.Active.Ingredients":"Insulin Glargine;Pipamperone Hydrochloride;Melperone Hydrochloride;Insulin Lispro;Atorvastatin;Aspirin;Pantoprazole Sodium;Enoxaparin Sodium;Sodium Perchlorate;Metamizole Sodium;Brotizolam;Furosemide;Digitoxin;Ferrous Glycine Sulfate;Ramipril;Clopidogrel Bisulfate;Carbamazepine;Dextrose;Hydrochlorothiazide;Clarithromycin;Metoprolol;Loperamide;Sodium Chloride;Lorazepam;Allopurinol;Metoclopramide;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate\\Sodium Acetate\\Sodium Chlori;Electrolytes Nos;Torsemide;Potassium Citrate;Methimazole;Hydrochlorothiazide\\Metoprolol Succinate;Potassium Chloride;Ferrous Sulfate","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Ocular Hyperaemia;Pneumonia;Polyuria;Product Used For Unknown Indication;Prophylaxis Against Gastrointestinal Ulcer;Renal Failure;Skin Disorder;Sleep Disorder;Thrombosis Prophylaxis;Vomiting","Reactions":"Purpura;Pruritus;Swollen Tongue;Nikolsky'S Sign;Stevens-Johnson Syndrome;Conjunctivitis;Blister;Lip Erosion;Ocular Hyperaemia;Oral Disorder","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Abbvie","Concomitant.Product.Names":"Tazobactam;Prednisolone Sodium Succinate;Flunitrazepam;Levofloxacin;Promethazine Hydrochloride;Novalgin (Metamizole Sodium);Piperacillin And Tazobactam;Amphotericin B;Diflucan;Cetirizine Hydrochloride;Zyrtec;Morphine;Dermatop;Dimethindene;Haloperidol;Perfalgan;Ampicillin Sodium\\Sulbactam Sodium"}
{"Case.ID":15232035,"Initial.FDA.Received.Date":"08/02/2018","days.since.last.fda":6,"Event.Date":"11/04/2004","Latest.FDA.Received.Date":"04-OCT-2018","Suspect.Product.Names":"Clopidogrel;Lantus;Pantozol;Humalog;Ferro-Sanol Duodenal","Suspect.Product.Active.Ingredients":"Ferrous Glycine Sulfate;Methimazole;Lorazepam;Metoprolol;Furosemide;Clarithromycin;Brotizolam;Melperone Hydrochloride;Torsemide;Insulin Lispro;Pantoprazole Sodium;Ferrous Sulfate;Metamizole Sodium;Metoclopramide;Loperamide;Insulin Glargine;Hydrochlorothiazide\\Metoprolol Succinate;Aspirin;Ramipril;Potassium Citrate;Pipamperone Hydrochloride;Potassium Chloride;Hydrochlorothiazide;Clopidogrel Bisulfate;Sodium Chloride;Calcium Acetate\\Magnesium Acetate\\Potassium Acetate\\Sodium Acetate\\Sodium Chlori;Allopurinol;Electrolytes Nos;Digitoxin;Dextrose;Enoxaparin Sodium;Atorvastatin;Sodium Perchlorate;Carbamazepine","Reason.for.Use":"Acute Myocardial Infarction;Agitation;Cardiac Failure;Confusional State;Diabetes Mellitus;Diarrhoea;Disorientation;Essential Hypertension;Fluid Replacement;Gastrointestinal Ulcer;Hypercholesterolaemia;Hyperthyroidism;Hyperuricaemia;Hypoglycaemia;Hypokalaemia;Mineral Supplementation;Nausea;Ocular Hyperaemia;Pneumonia;Polyuria;Product Used For Unknown Indication;Prophylaxis Against Gastrointestinal Ulcer;Renal Failure;Skin Disorder;Sleep Disorder;Thrombosis Prophylaxis;Vomiting","Reactions":"Conjunctivitis;Stevens-Johnson Syndrome;Swollen Tongue;Lip Erosion;Pruritus;Oral Disorder;Purpura;Nikolsky'S Sign;Blister;Ocular Hyperaemia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Mylan","Concomitant.Product.Names":"Amphotericin B;Flunitrazepam;Dimethindene;Promethazine Hydrochloride;Cetirizine Hydrochloride;Perfalgan;Piperacillin And Tazobactam;Prednisolone Sodium Succinate;Levofloxacin;Digitoxin;Dermatop;Morphine;Tazobactam;Ampicillin Sodium\\Sulbactam Sodium;Novalgin (Metamizole Sodium);Diflucan;Zyrtec;Haloperidol"}
{"Case.ID":15319204,"Initial.FDA.Received.Date":"08/26/2018","days.since.last.fda":24,"Event.Date":"07/04/2017","Latest.FDA.Received.Date":"26-AUG-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol;Colchicine","Reason.for.Use":"Gout","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":15342343,"Initial.FDA.Received.Date":"09/02/2018","days.since.last.fda":7,"Event.Date":"07/04/2017","Latest.FDA.Received.Date":"02-SEP-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Colchicine;Allopurinol","Reason.for.Use":"Gout","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":15351063,"Initial.FDA.Received.Date":"09/05/2018","days.since.last.fda":3,"Event.Date":"07/04/2017","Latest.FDA.Received.Date":"19-OCT-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Colchicine;Allopurinol","Reason.for.Use":"Gout","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"Ranbaxy","Concomitant.Product.Names":"-"}
{"Case.ID":15518172,"Initial.FDA.Received.Date":"10/17/2018","days.since.last.fda":42,"Event.Date":"","Latest.FDA.Received.Date":"12-FEB-2019","Suspect.Product.Names":"Lyrica","Suspect.Product.Active.Ingredients":"Pregabalin;Vancomycin Hydrochloride;Rivaroxaban;Ceftriaxone","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":15516812,"Initial.FDA.Received.Date":"10/17/2018","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"17-OCT-2018","Suspect.Product.Names":"Amaryl","Suspect.Product.Active.Ingredients":"Glimepiride;Rivaroxaban;Pregabalin;Ceftriaxone;Vancomycin","Reason.for.Use":"Diabetes Mellitus","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"Sanofi Aventis","Concomitant.Product.Names":"-"}
{"Case.ID":15536959,"Initial.FDA.Received.Date":"10/22/2018","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"22-OCT-2018","Suspect.Product.Names":"Xarelto","Suspect.Product.Active.Ingredients":"Rivaroxaban","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"73 YR","Sender":"Janssen","Concomitant.Product.Names":"Ceftriaxone;Vancomycin Hydrochloride;Glimepiride;Pregabalin"}
{"Case.ID":15627507,"Initial.FDA.Received.Date":"11/16/2018","days.since.last.fda":25,"Event.Date":"05/15/2018","Latest.FDA.Received.Date":"16-NOV-2018","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Levofloxacin","Reason.for.Use":"Impaired Healing","Reactions":"Malaise;Stevens-Johnson Syndrome;Decreased Appetite","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"-"}
{"Case.ID":15682669,"Initial.FDA.Received.Date":"12/03/2018","days.since.last.fda":17,"Event.Date":"10/06/2017","Latest.FDA.Received.Date":"03-DEC-2018","Suspect.Product.Names":"Folotyn","Suspect.Product.Active.Ingredients":"Pralatrexate","Reason.for.Use":"Peripheral T-Cell Lymphoma Unspecified","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"Not Specified","Sender":"Spectrum","Concomitant.Product.Names":"-"}
{"Case.ID":15815211,"Initial.FDA.Received.Date":"01/12/2019","days.since.last.fda":40,"Event.Date":"02/02/2018","Latest.FDA.Received.Date":"10-MAR-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Hyperuricaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"77 YR","Sender":"Accord","Concomitant.Product.Names":"Levothyroxine Sodium;Lasix;Nebivolol;Coumadin"}
{"Case.ID":15869014,"Initial.FDA.Received.Date":"01/25/2019","days.since.last.fda":13,"Event.Date":"07/24/2018","Latest.FDA.Received.Date":"25-JAN-2019","Suspect.Product.Names":"Calonal","Suspect.Product.Active.Ingredients":"Acetaminophen;Clarithromycin;Dextromethorphan Hydrobromide;Ramatroban;Domperidone","Reason.for.Use":"Antipyresis;Antitussive Therapy;Infection;Product Used For Unknown Indication;Vomiting","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"12 YR","Sender":"Abbvie","Concomitant.Product.Names":"-"}
{"Case.ID":15879665,"Initial.FDA.Received.Date":"01/28/2019","days.since.last.fda":3,"Event.Date":"12/18/2018","Latest.FDA.Received.Date":"25-APR-2019","Suspect.Product.Names":"Nexavar","Suspect.Product.Active.Ingredients":"Sorafenib","Reason.for.Use":"Hepatocellular Carcinoma","Reactions":"Staphylococcal Sepsis;Toxic Skin Eruption;Stevens-Johnson Syndrome;Staphylococcal Bacteraemia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Bayer","Concomitant.Product.Names":"Glucophage;Caffeine;Doliprane;Rilmenidine Phosphate;Hydrochlorothiazide;Ketoprofen;Rilmenidine;Hydrochlorothiazide\\Irbesartan;Irbesartan;Acetaminophen;Lamaline (Acetaminophen\\Caffeine\\Opium)"}
{"Case.ID":16047339,"Initial.FDA.Received.Date":"02/08/2019","days.since.last.fda":11,"Event.Date":"01/14/2019","Latest.FDA.Received.Date":"08-FEB-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Pembrolizumab","Reason.for.Use":"Transitional Cell Carcinoma","Reactions":"Stevens-Johnson Syndrome;Aspiration;Packed Red Blood Cell Transfusion;Blood Ph Decreased","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"76 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"Escitalopram;Sodium Chloride;Dronabinol;Dexamethasone;Folic Acid;Estradiol;Furosemide;Ondansetron;Rosuvastatin;Allopurinol;Pantoprazole"}
{"Case.ID":15990213,"Initial.FDA.Received.Date":"02/21/2019","days.since.last.fda":13,"Event.Date":"07/24/2018","Latest.FDA.Received.Date":"21-FEB-2019","Suspect.Product.Names":"Calonal","Suspect.Product.Active.Ingredients":"Acetaminophen;Clarithromycin;Dextromethorphan Hydrobromide;Domperidone;Ramatroban","Reason.for.Use":"Antipyresis;Antitussive Therapy;Infection;Product Used For Unknown Indication;Vomiting","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"12 YR","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":16003800,"Initial.FDA.Received.Date":"02/26/2019","days.since.last.fda":5,"Event.Date":"07/04/2017","Latest.FDA.Received.Date":"26-FEB-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol;Colchicine","Reason.for.Use":"Gout","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"84 YR","Sender":"Accord","Concomitant.Product.Names":"-"}
{"Case.ID":16114470,"Initial.FDA.Received.Date":"03/25/2019","days.since.last.fda":27,"Event.Date":"08/02/1996","Latest.FDA.Received.Date":"25-MAR-2019","Suspect.Product.Names":"Cytotec","Suspect.Product.Active.Ingredients":"Misoprostol;Cilastatin Sodium\\Imipenem;Tobramycin Sulfate;Ganciclovir Sodium;Furosemide;Midazolam Hydrochloride;Human Cytomegalovirus Immune Globulin","Reason.for.Use":"Abdominal Discomfort;Antiviral Prophylaxis;Biliary Colic;Fluid Replacement;Gastrointestinal Disorder;Haemorrhage;Hypoglycaemia;Hypokalaemia;Hypolipidaemia;Hypophosphataemia;Hypovitaminosis;Immunosuppression;Malnutrition;Mineral Deficiency;Oedema;Pain;Parenteral Nutrition;Prophylaxis;Respiratory Disorder;Sedation;Thrombosis Prophylaxis","Reactions":"Circulatory Collapse;Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"54 YR","Sender":"Merck","Concomitant.Product.Names":"Magnesium Aspartate\\Potassium Aspartate;Amphotericin B;Albumin Human;Piritramide;Cyclosporine;Gentamicin;Potassium Chloride;Thymocyte Immune Globulin Nos;Methylprednisolone;Nadroparin Calcium;Egg Phospholipids\\Glycerin\\Soybean Oil;Azathioprine;Ursodiol;Fentanyl;Dextrose;Ranitidine;Dopamine;Polymyxin;Potassium Phosphate, Dibasic;Cernevit;Acetylcysteine;Trasylol;Human Plasma"}
{"Case.ID":16119712,"Initial.FDA.Received.Date":"03/26/2019","days.since.last.fda":1,"Event.Date":"03/11/1994","Latest.FDA.Received.Date":"26-MAR-2019","Suspect.Product.Names":"Heparin;Lasix","Suspect.Product.Active.Ingredients":"Furosemide;Piritramide;Potassium Bicarbonate\\Potassium Citrate;Dimethicone;Heparin Sodium;Midazolam Hydrochloride;Acetaminophen;Sodium Bicarbonate\\Sodium Phosphate, Monobasic, Anhydrous;Acetylcysteine;Beclomethasone Dipropionate;Ketamine Hydrochloride;Cilastatin Sodium\\Imipenem;Promethazine Hydrochloride;Prednisolone Sodium Succinate;Piretanide;Reproterol Hydrochloride;Sucralfate;Droperidol;Ciprofloxacin Hydrochloride;Lactulose;Ambroxol Hydrochloride;Theophylline Anhydrous;Cisapride;Nitrendipine;Bambuterol Hydrochloride","Reason.for.Use":"Abdominal Distension;Asthma;Constipation;Essential Hypertension;Gastrointestinal Disorder;General Symptom;Mental Disorder;Oedema;Pyrexia;Respiratory Disorder;Thrombosis","Reactions":"Respiratory Failure;Respiratory Disorder;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"63 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":16126300,"Initial.FDA.Received.Date":"03/28/2019","days.since.last.fda":2,"Event.Date":"03/01/2019","Latest.FDA.Received.Date":"28-MAR-2019","Suspect.Product.Names":"Keppra","Suspect.Product.Active.Ingredients":"Levetiracetam;Methylprednisolone;Acyclovir;Amoxicillin;Ceftriaxone Sodium","Reason.for.Use":"Epilepsy;Listeriosis;Meningoencephalitis Herpetic;Pneumonia;Vasculitis","Reactions":"Stevens-Johnson Syndrome;Multiple Organ Dysfunction Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"Ucb","Concomitant.Product.Names":"-"}
{"Case.ID":16163125,"Initial.FDA.Received.Date":"04/05/2019","days.since.last.fda":8,"Event.Date":"","Latest.FDA.Received.Date":"05-APR-2019","Suspect.Product.Names":"Diflucan","Suspect.Product.Active.Ingredients":"Fluconazole;Ciprofloxacin Hydrochloride;Teicoplanin","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"82 YR","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":16184344,"Initial.FDA.Received.Date":"04/10/2019","days.since.last.fda":5,"Event.Date":"12/31/2018","Latest.FDA.Received.Date":"10-APR-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Gabapentin","Reason.for.Use":"Occipital Neuralgia","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"70 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"-"}
{"Case.ID":16177882,"Initial.FDA.Received.Date":"04/10/2019","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"10-APR-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Prednisolone Sodium Phosphate","Reason.for.Use":"Vasculitis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Edenbridge Pharmaceuticals","Concomitant.Product.Names":"-"}
{"Case.ID":16186544,"Initial.FDA.Received.Date":"04/11/2019","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"11-APR-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Cyclophosphamide;Rituximab;Vincristine;Doxorubicin;Prednisolone","Reason.for.Use":"Leukaemia","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":16367873,"Initial.FDA.Received.Date":"04/22/2019","days.since.last.fda":11,"Event.Date":"03/22/2019","Latest.FDA.Received.Date":"22-APR-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"Colon Cancer Metastatic","Reactions":"Stevens-Johnson Syndrome;Pyrexia;Sepsis;Thrombocytopenia;Rash;Leukopenia","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"68 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"-"}
{"Case.ID":16408711,"Initial.FDA.Received.Date":"05/02/2019","days.since.last.fda":10,"Event.Date":"04/13/2019","Latest.FDA.Received.Date":"02-MAY-2019","Suspect.Product.Names":"Abraxane","Suspect.Product.Active.Ingredients":"Paclitaxel;Olanzapine;Vancomycin","Reason.for.Use":"Breast Cancer Metastatic;Febrile Neutropenia","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"34 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"-"}
{"Case.ID":16268539,"Initial.FDA.Received.Date":"05/03/2019","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"03-MAY-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Divalproex Sodium","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Unichem","Concomitant.Product.Names":"-"}
{"Case.ID":16344932,"Initial.FDA.Received.Date":"05/22/2019","days.since.last.fda":19,"Event.Date":"05/01/2014","Latest.FDA.Received.Date":"22-MAY-2019","Suspect.Product.Names":"Childrens Tylenol;Childrens Motrin","Suspect.Product.Active.Ingredients":"Ibuprofen;Acetaminophen","Reason.for.Use":"Decreased Appetite;Pyrexia;Vomiting","Reactions":"Stevens-Johnson Syndrome;Product Use In Unapproved Indication;Death","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"3 YR","Sender":"Johnson And Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":16410132,"Initial.FDA.Received.Date":"06/10/2019","days.since.last.fda":19,"Event.Date":"01/06/2012","Latest.FDA.Received.Date":"10-JUN-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Temozolomide","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"37 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":16679470,"Initial.FDA.Received.Date":"08/07/2019","days.since.last.fda":58,"Event.Date":"07/17/2019","Latest.FDA.Received.Date":"07-AUG-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ceftriaxone","Reason.for.Use":"Pneumonitis","Reactions":"Dyspnoea;Stevens-Johnson Syndrome;Dermatitis Exfoliative Generalised","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"95 YR","Sender":"Sandoz","Concomitant.Product.Names":"-"}
{"Case.ID":16720822,"Initial.FDA.Received.Date":"08/20/2019","days.since.last.fda":13,"Event.Date":"03/09/2019","Latest.FDA.Received.Date":"20-AUG-2019","Suspect.Product.Names":"Keppra","Suspect.Product.Active.Ingredients":"Levetiracetam;Methylprednisolone;Ceftriaxone Sodium;Acyclovir;Amoxicillin","Reason.for.Use":"Epilepsy;Listeriosis;Meningoencephalitis Herpetic;Pneumonia;Vasculitis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"Mylan","Concomitant.Product.Names":"-"}
{"Case.ID":16765914,"Initial.FDA.Received.Date":"09/03/2019","days.since.last.fda":14,"Event.Date":"","Latest.FDA.Received.Date":"12-SEP-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":16807512,"Initial.FDA.Received.Date":"09/13/2019","days.since.last.fda":10,"Event.Date":"","Latest.FDA.Received.Date":"13-SEP-2019","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"Hiv Infection;Product Used For Unknown Indication","Reactions":"Conjunctivitis;Stevens-Johnson Syndrome;Erythema Multiforme;Oral Mucosal Blistering","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Zidovudine;Lamivudine;Cotrimoxazole"}
{"Case.ID":16807986,"Initial.FDA.Received.Date":"09/16/2019","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"16-SEP-2019","Suspect.Product.Names":"Viramune","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"Hiv Infection;Product Used For Unknown Indication","Reactions":"Rash;Pruritus;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Boehringer Ingelheim","Concomitant.Product.Names":"Lamivudine;Sulfamethoxazole\\Trimethoprim;Zidovudine"}
{"Case.ID":16941495,"Initial.FDA.Received.Date":"10/21/2019","days.since.last.fda":35,"Event.Date":"","Latest.FDA.Received.Date":"21-OCT-2019","Suspect.Product.Names":"Amlodipine","Suspect.Product.Active.Ingredients":"Amlodipine Besylate;Rabeprazole;Pyrazinamide;Investigational Product;Tetanus Antitoxin;Tropicamide;Acetaminophen;Phenobarbital;Fentanyl;Dabigatran","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Johnson And Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":16947164,"Initial.FDA.Received.Date":"10/22/2019","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"22-OCT-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Nevirapine","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Erythema Multiforme;Conjunctivitis;Stevens-Johnson Syndrome;Oral Mucosal Blistering","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Mylan","Concomitant.Product.Names":"Zidovudine;Lamivudine;Cotrimoxazole"}
{"Case.ID":16944988,"Initial.FDA.Received.Date":"10/22/2019","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"22-OCT-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Phenytoin","Reason.for.Use":"Seizure","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"68 YR","Sender":"Pfizer","Concomitant.Product.Names":"Hydromorphone;Ranitidine;Dexamethasone"}
{"Case.ID":16949505,"Initial.FDA.Received.Date":"10/23/2019","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"24-OCT-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Acetaminophen","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Hepatic Failure;Death;Stevens-Johnson Syndrome;Anaphylactic Reaction;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Johnson And Johnson","Concomitant.Product.Names":"-"}
{"Case.ID":17134917,"Initial.FDA.Received.Date":"12/10/2019","days.since.last.fda":48,"Event.Date":"","Latest.FDA.Received.Date":"10-DEC-2019","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ciprofloxacin","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Hypoalbuminaemia;Sepsis;Stevens-Johnson Syndrome;Dysphagia","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"67 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":17158155,"Initial.FDA.Received.Date":"12/16/2019","days.since.last.fda":6,"Event.Date":"","Latest.FDA.Received.Date":"18-MAR-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Fludarabine Phosphate","Reason.for.Use":"Chemotherapy","Reactions":"Mucosal Inflammation;Skin Exfoliation;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Pfizer","Concomitant.Product.Names":"-"}
{"Case.ID":17334684,"Initial.FDA.Received.Date":"01/28/2020","days.since.last.fda":43,"Event.Date":"","Latest.FDA.Received.Date":"28-JAN-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Vancomycin","Reason.for.Use":"Product Used For Unknown Indication;Urinary Tract Infection Staphylococcal","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"83 YR","Sender":"Baxter","Concomitant.Product.Names":"Warfarin;Famotidine;Gentamicin;Furosemide;Humulin Nos;Promethazine;Isosorbide Mononitrate;Droperidol"}
{"Case.ID":17713321,"Initial.FDA.Received.Date":"04/27/2020","days.since.last.fda":90,"Event.Date":"","Latest.FDA.Received.Date":"27-APR-2020","Suspect.Product.Names":"Adempas","Suspect.Product.Active.Ingredients":"Riociguat","Reason.for.Use":"Pulmonary Arterial Hypertension","Reactions":"Toxic Epidermal Necrolysis;Intensive Care;Stevens-Johnson Syndrome;Haemorrhage Intracranial","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"86 YR","Sender":"Bayer","Concomitant.Product.Names":"-"}
{"Case.ID":17710829,"Initial.FDA.Received.Date":"04/27/2020","days.since.last.fda":0,"Event.Date":"","Latest.FDA.Received.Date":"27-APR-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate Sodium","Reason.for.Use":"Acute Lymphocytic Leukaemia","Reactions":"Mucosal Inflammation;Pancytopenia;Stevens-Johnson Syndrome;Septic Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"193 MTH","Sender":"Pfizer","Concomitant.Product.Names":"Cytarabine"}
{"Case.ID":17803085,"Initial.FDA.Received.Date":"05/19/2020","days.since.last.fda":22,"Event.Date":"","Latest.FDA.Received.Date":"19-MAY-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Acute Lymphocytic Leukaemia;Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome;Pancytopenia;Mucosal Inflammation;Septic Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"16 YR","Sender":"Novartis","Concomitant.Product.Names":"Cytarabine"}
{"Case.ID":17817754,"Initial.FDA.Received.Date":"05/22/2020","days.since.last.fda":3,"Event.Date":"","Latest.FDA.Received.Date":"22-MAY-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Fludarabine Phosphate","Reason.for.Use":"Chemotherapy","Reactions":"Stevens-Johnson Syndrome;Skin Exfoliation;Neoplasm Progression;Mucosal Inflammation","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":17825769,"Initial.FDA.Received.Date":"05/26/2020","days.since.last.fda":4,"Event.Date":"","Latest.FDA.Received.Date":"08-JUL-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate","Reason.for.Use":"Acute Lymphocytic Leukaemia","Reactions":"Mucosal Inflammation;Pancytopenia;Stevens-Johnson Syndrome;Septic Shock","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"16 YR","Sender":"Teva","Concomitant.Product.Names":"Cytarabine"}
{"Case.ID":17916202,"Initial.FDA.Received.Date":"06/19/2020","days.since.last.fda":24,"Event.Date":"","Latest.FDA.Received.Date":"19-JUN-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Bevacizumab;Capecitabine","Reason.for.Use":"Colorectal Cancer Metastatic","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":17940663,"Initial.FDA.Received.Date":"06/24/2020","days.since.last.fda":5,"Event.Date":"","Latest.FDA.Received.Date":"24-JUN-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ceftriaxone Sodium","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"71 YR","Sender":"Novartis","Concomitant.Product.Names":"-"}
{"Case.ID":18012549,"Initial.FDA.Received.Date":"07/13/2020","days.since.last.fda":19,"Event.Date":"","Latest.FDA.Received.Date":"13-JUL-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Isoniazid","Reason.for.Use":"Pulmonary Tuberculosis","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"68 YR","Sender":"Novartis","Concomitant.Product.Names":"Pyrazinamide;Rifampin;Ethambutol"}
{"Case.ID":18137332,"Initial.FDA.Received.Date":"08/12/2020","days.since.last.fda":30,"Event.Date":"","Latest.FDA.Received.Date":"12-AUG-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Epilepsy","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"33 YR","Sender":"Alkem","Concomitant.Product.Names":"-"}
{"Case.ID":18267709,"Initial.FDA.Received.Date":"09/15/2020","days.since.last.fda":34,"Event.Date":"","Latest.FDA.Received.Date":"15-SEP-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Acyclovir","Reason.for.Use":"Oral Herpes","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"26 YR","Sender":"Amneal","Concomitant.Product.Names":"-"}
{"Case.ID":18354915,"Initial.FDA.Received.Date":"10/07/2020","days.since.last.fda":22,"Event.Date":"","Latest.FDA.Received.Date":"07-OCT-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Capecitabine;Bevacizumab","Reason.for.Use":"Colorectal Cancer Metastatic","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Roche","Concomitant.Product.Names":"-"}
{"Case.ID":18500230,"Initial.FDA.Received.Date":"11/12/2020","days.since.last.fda":36,"Event.Date":"","Latest.FDA.Received.Date":"12-NOV-2020","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Enfortumab Vedotin","Reason.for.Use":"-","Reactions":"Toxic Epidermal Necrolysis;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Fda-Ctu","Concomitant.Product.Names":"Aspirin;Cetirizine;Magnesium Oxide;Losartan;Compazine"}
{"Case.ID":18722206,"Initial.FDA.Received.Date":"01/11/2021","days.since.last.fda":60,"Event.Date":"","Latest.FDA.Received.Date":"11-JAN-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Lamotrigine","Reason.for.Use":"Bipolar Disorder","Reactions":"Multiple Organ Dysfunction Syndrome;Thrombosis;Stevens-Johnson Syndrome;Coagulopathy","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"Not Specified","Sender":"Unichem","Concomitant.Product.Names":"-"}
{"Case.ID":18758552,"Initial.FDA.Received.Date":"01/19/2021","days.since.last.fda":8,"Event.Date":"01/01/2020","Latest.FDA.Received.Date":"19-JAN-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Piperacillin Sodium\\Tazobactam Sodium;Amoxicillin\\Clavulanic Acid","Reason.for.Use":"-","Reactions":"C-Reactive Protein Increased;Liver Function Test Increased;Urticaria;Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"65 YR","Sender":"Teva","Concomitant.Product.Names":"-"}
{"Case.ID":18895104,"Initial.FDA.Received.Date":"02/15/2021","days.since.last.fda":27,"Event.Date":"01/02/2021","Latest.FDA.Received.Date":"15-FEB-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Amoxicillin","Reason.for.Use":"Product Used For Unknown Indication","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"92 YR","Sender":"Teva","Concomitant.Product.Names":"Nicardipine Hydrochloride;Kardegic;Ramipril;Esomeprazole.;Urapidil;Sotalol;Potassium Chloride"}
{"Case.ID":19072625,"Initial.FDA.Received.Date":"03/30/2021","days.since.last.fda":43,"Event.Date":"","Latest.FDA.Received.Date":"30-MAR-2021","Suspect.Product.Names":"Invanz","Suspect.Product.Active.Ingredients":"Ertapenem Sodium","Reason.for.Use":"-","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"55 YR","Sender":"Merck","Concomitant.Product.Names":"-"}
{"Case.ID":19078251,"Initial.FDA.Received.Date":"03/31/2021","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"31-MAR-2021","Suspect.Product.Names":"Keytruda","Suspect.Product.Active.Ingredients":"Pembrolizumab","Reason.for.Use":"Lung Neoplasm Malignant","Reactions":"Stevens-Johnson Syndrome;Toxic Epidermal Necrolysis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"60 YR","Sender":"Merck","Concomitant.Product.Names":"Trazodone Hydrochloride;Ranitidine;Hydromorphone;Fragmin;Hydroxyzine;Citalopram;Oxazepam;Verapamil Hydrochloride;Ciclesonide;Celebrex;Tylenol;Perindopril;Alvesco;Metoclopramide;Prednisone;Pantoprazole Sodium;Lansoprazole;Dexamethasone"}
{"Case.ID":19084922,"Initial.FDA.Received.Date":"04/01/2021","days.since.last.fda":1,"Event.Date":"","Latest.FDA.Received.Date":"01-APR-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Methotrexate Sodium;Ciprofloxacin","Reason.for.Use":"Incision Site Cellulitis;Pemphigoid","Reactions":"Blister;White Blood Cell Count Decreased;Pruritus;Drug Interaction;Neutropenia;Stevens-Johnson Syndrome;Off Label Use;Blood Creatinine Increased;Skin Exfoliation","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"84 YR","Sender":"Pfizer","Concomitant.Product.Names":"Hydrocortisone;Metronidazole;Midazolam;Furosemide;Leucovorin;Vancomycin;Meropenem;Granulocyte Colony-Stimulating Factor Nos;Sodium Chloride;Pantoprazole;Sodium Bicarbonate;Septra;Clobetasol;Ceftriaxone"}
{"Case.ID":19150124,"Initial.FDA.Received.Date":"04/17/2021","days.since.last.fda":16,"Event.Date":"01/15/2020","Latest.FDA.Received.Date":"17-APR-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Atrial Fibrillation;Gout;Myocardial Ischaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"79 YR","Sender":"Novartis","Concomitant.Product.Names":"Warfarin Sodium;Bisoprolol;Febuxostat"}
{"Case.ID":19172337,"Initial.FDA.Received.Date":"04/23/2021","days.since.last.fda":6,"Event.Date":"01/15/2020","Latest.FDA.Received.Date":"23-APR-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Atrial Fibrillation;Gout;Myocardial Ischaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"79 YR","Sender":"Teva","Concomitant.Product.Names":"Bisoprolol;Warfarin Sodium"}
{"Case.ID":19381327,"Initial.FDA.Received.Date":"06/07/2021","days.since.last.fda":45,"Event.Date":"01/15/2020","Latest.FDA.Received.Date":"07-JUN-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Allopurinol","Reason.for.Use":"Atrial Fibrillation;Gout;Myocardial Ischaemia","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"79 YR","Sender":"Accord","Concomitant.Product.Names":"Warfarin Sodium;Febuxostat;Allopurinol;Bisoprolol"}
{"Case.ID":19488381,"Initial.FDA.Received.Date":"07/02/2021","days.since.last.fda":25,"Event.Date":"","Latest.FDA.Received.Date":"12-AUG-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Capecitabine","Reason.for.Use":"Pancreatic Carcinoma Metastatic","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Male","Patient.Age":"70 YR","Sender":"Roche","Concomitant.Product.Names":"Amlodipine;Glimepiride"}
{"Case.ID":19497463,"Initial.FDA.Received.Date":"07/06/2021","days.since.last.fda":4,"Event.Date":"06/23/2021","Latest.FDA.Received.Date":"06-JUL-2021","Suspect.Product.Names":"Cotellic;Zelboraf","Suspect.Product.Active.Ingredients":"Vemurafenib;Cobimetinib","Reason.for.Use":"Malignant Melanoma","Reactions":"Stevens-Johnson Syndrome","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"54 YR","Sender":"Fda-Ctu","Concomitant.Product.Names":"Prednisone;Norco;Vitamins;Triamcinolone;Saccharomyces Cerevisiae;Escitalopram;Morphine;Dexamethasone;Famotidine;Dicyclomine;Oxycontin;Ondansetron;Levothyroxine;Loperamide;Metoclopramide;Vitamin C;Prochlorperazine;Magnesium"}
{"Case.ID":19773764,"Initial.FDA.Received.Date":"09/01/2021","days.since.last.fda":57,"Event.Date":"","Latest.FDA.Received.Date":"01-SEP-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Ondansetron;Amoxicillin\\Clavulanate Potassium","Reason.for.Use":"Abdominal Pain;Pharyngitis","Reactions":"Hepatic Failure;Stevens-Johnson Syndrome;Sepsis","Serious":"Serious","Outcomes":"Died","Sex":"Female","Patient.Age":"46 YR","Sender":"Fresenius Kabi","Concomitant.Product.Names":"Morphine;Lidocaine;Esketamine;Dexamethasone"}
{"Case.ID":19808479,"Initial.FDA.Received.Date":"09/09/2021","days.since.last.fda":8,"Event.Date":"05/20/2021","Latest.FDA.Received.Date":"09-SEP-2021","Suspect.Product.Names":"-","Suspect.Product.Active.Ingredients":"Rituximab;Vancomycin","Reason.for.Use":"Hypothyroidism;Non-Hodgkin'S Lymphoma;Urinary Tract Infection","Reactions":"Stevens-Johnson Syndrome;Cardiac Arrest;Mucosal Inflammation;Drug Eruption;Skin Exfoliation;Rash Erythematous","Serious":"Serious","Outcomes":"Died","Sex":"Not Specified","Patient.Age":"Not Specified","Sender":"Celltrion","Concomitant.Product.Names":"Levothyroxine Sodium"}