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MULTIPLE INJURIES ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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