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COMPLETED SUICIDE ( 161 FDA reports)
DRUG TOXICITY ( 86 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 44 FDA reports)
CARDIAC ARREST ( 27 FDA reports)
INTENTIONAL DRUG MISUSE ( 25 FDA reports)
INTENTIONAL MISUSE ( 21 FDA reports)
RESPIRATORY ARREST ( 20 FDA reports)
HEPATIC FAILURE ( 19 FDA reports)
HYPOTENSION ( 16 FDA reports)
DEATH ( 15 FDA reports)
OVERDOSE ( 14 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
DRUG ABUSE ( 10 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
CONVULSION ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
DRUG SCREEN POSITIVE ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
COMA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
VOMITING ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
TACHYPNOEA ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
POISONING ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APNOEA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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