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

MYOCARDIAL INFARCTION ( 7 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
INFECTION ( 3 FDA reports)
RENAL FAILURE ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)

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