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

PNEUMONIA ( 8 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
BRONCHOPLEURAL FISTULA ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
VITAMIN K DEFICIENCY ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HETEROPHORIA ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
FALL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)

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