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ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
DEATH ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
FALL ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 5 FDA reports)
ANGIOPLASTY ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
INFECTION ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RED BLOOD CELL ABNORMALITY ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NEOPLASM OF THYMUS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBELLAR HYPOPLASIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHLAMYDIA IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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