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

SEPSIS ( 14 FDA reports)
HEPATIC FAILURE ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
LIVER DISORDER ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
RENAL FAILURE ( 11 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
BONE MARROW FAILURE ( 8 FDA reports)
ENTEROCOCCAL INFECTION ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
REPERFUSION INJURY ( 8 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
ABDOMINAL INFECTION ( 6 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SURGICAL PROCEDURE REPEATED ( 4 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
HAEMATOMA INFECTION ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
INJURY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SCAR ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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