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COMPLETED SUICIDE ( 93 FDA reports)
CARDIO-RESPIRATORY ARREST ( 49 FDA reports)
CARDIAC ARREST ( 46 FDA reports)
RESPIRATORY ARREST ( 45 FDA reports)
MULTIPLE DRUG OVERDOSE ( 22 FDA reports)
INTENTIONAL DRUG MISUSE ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
INTENTIONAL MISUSE ( 10 FDA reports)
DRUG SCREEN POSITIVE ( 9 FDA reports)
CONVULSION ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
COMA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
ALCOHOL USE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
ABSCESS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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