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

OVERDOSE ( 17 FDA reports)
LIVER INJURY ( 8 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 6 FDA reports)
HEPATIC NECROSIS ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
COMA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
BLISTER ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
LACTATE PYRUVATE RATIO INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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