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

ANAEMIA ( 5 FDA reports)
ASTHENIA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
TRANSURETHRAL BLADDER RESECTION ( 2 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER MASS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
MALAISE ( 2 FDA reports)
HYPOTENSION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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