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

THROMBOCYTOPENIA ( 5 FDA reports)
SHUNT OCCLUSION ( 5 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
POST PROCEDURAL URINE LEAK ( 4 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
VITAMIN B12 ABNORMAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
SHOCK ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)

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