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

VOMITING ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
RECTAL CANCER ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FUNGAL PERITONITIS ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 3 FDA reports)
SCAR ( 3 FDA reports)
ANGIOPATHY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MULTIPLE EPIPHYSEAL DYSPLASIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SKIN STRIAE ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use