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CATHETER RELATED COMPLICATION ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)

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