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

ATRIAL FIBRILLATION ( 9 FDA reports)
SUDDEN DEATH ( 7 FDA reports)
PNEUMONIA ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
PAIN ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
DEATH ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
ANGER ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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