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

DYSPNOEA ( 7 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
VOMITING ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
GLIOSIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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