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

FEBRILE NEUTROPENIA ( 11 FDA reports)
NEUTROPENIA ( 10 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
HYPERPYREXIA ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
EROSIVE BALANITIS ( 3 FDA reports)
EXTRAVASATION ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MASTECTOMY ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)

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