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

WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
URINARY RETENTION ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYST ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
PAIN ( 2 FDA reports)
VOMITING ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
FALL ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DEATH ( 1 FDA reports)
INFECTION ( 1 FDA reports)

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