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

PYREXIA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ANURIA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
CRYSTALLURIA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
VOMITING ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
COMA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)

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