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

CYTOLYTIC HEPATITIS ( 13 FDA reports)
NEUTROPENIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
CHOLESTASIS ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
RASH ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
MICROLITHIASIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
ANURIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
GRANULOCYTES MATURATION ARREST ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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