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

PYREXIA ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ECTHYMA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
PERIORBITAL OEDEMA ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
B-LYMPHOCYTE ABNORMALITIES ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MYELOBLAST COUNT INCREASED ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLASMINOGEN DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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