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DRUG TOXICITY ( 39 FDA reports)
COMPLETED SUICIDE ( 16 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
VOMITING ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
ANTICHOLINERGIC SYNDROME ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POISONING ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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