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

HEPATIC FAILURE ( 18 FDA reports)
HYPOTENSION ( 18 FDA reports)
ILEUS ( 18 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 18 FDA reports)
NEUROLOGICAL SYMPTOM ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
RENAL FAILURE ( 18 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 18 FDA reports)
SEPTIC SHOCK ( 18 FDA reports)
FUNGAL SEPSIS ( 16 FDA reports)
URETEROSTOMY SITE DISCOMFORT ( 16 FDA reports)
MYOCARDIAL INFARCTION ( 12 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
CEREBRAL HAEMORRHAGE ( 10 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
CARDIAC DISORDER ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
TUMOUR HAEMORRHAGE ( 6 FDA reports)
PNEUMONIA ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
CARDIAC ENZYMES INCREASED ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
NECROSIS ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PITYRIASIS ( 3 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SEROMA ( 3 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)

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