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HEPATIC STEATOSIS ( 11 FDA reports)
CHOLESTASIS ( 10 FDA reports)
ADENOVIRAL HEPATITIS ( 8 FDA reports)
CYTOLYTIC HEPATITIS ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
PANCREATITIS ACUTE ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
HERPES SIMPLEX ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
SYSTEMIC CANDIDA ( 6 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PRIMARY HYPOGONADISM ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MEDIASTINUM NEOPLASM ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
MASS ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PUNCTURE SITE INFECTION ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICELLA ( 1 FDA reports)

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