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

CARDIAC ARREST ( 10 FDA reports)
PYREXIA ( 9 FDA reports)
WOUND INFECTION ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
JOINT DISLOCATION ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 4 FDA reports)
CHILLS ( 4 FDA reports)
RENAL FAILURE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
ASCITES ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
RASH ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)

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