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

DIPLOPIA ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
MALIGNANT PITUITARY TUMOUR ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
PITUITARY TUMOUR RECURRENT ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CEREBRAL FUNGAL INFECTION ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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