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

OEDEMA PERIPHERAL ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)

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