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

MYALGIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
FALL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARAESTHESIA MUCOSAL ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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