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ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)

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