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MYOCARDIAL INFARCTION ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FALL ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)

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