Please choose an event type to view the corresponding MedsFacts report:

RESPIRATORY FAILURE ( 9 FDA reports)
AGGRESSION ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
RESTLESSNESS ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
BILIARY TRACT OPERATION ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
DEATH ( 3 FDA reports)
CATARACT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
CHOLANGITIS SUPPURATIVE ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
STRESS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INTUBATION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)

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