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

DRUG INTERACTION ( 7 FDA reports)
AGRANULOCYTOSIS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
RENAL DISORDER ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHEST PAIN ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
FALL ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)

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