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

STOMATITIS ( 17 FDA reports)
PYREXIA ( 16 FDA reports)
VOMITING ( 16 FDA reports)
HYPERPYREXIA ( 15 FDA reports)
STOMATITIS NECROTISING ( 13 FDA reports)
DIARRHOEA ( 12 FDA reports)
OEDEMA ( 12 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
ANURIA ( 7 FDA reports)
BACTERAEMIA ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
BACTERIAL SEPSIS ( 6 FDA reports)
BURKITT'S LYMPHOMA ( 6 FDA reports)
ENTEROCOCCAL SEPSIS ( 6 FDA reports)
MUCOSAL INFLAMMATION ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 5 FDA reports)
APHONIA ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HYDRONEPHROSIS ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
OROPHARYNGITIS FUNGAL ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INFUSION SITE HAEMORRHAGE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MYELITIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
EPIDIDYMITIS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RASH ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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