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

PYREXIA ( 5 FDA reports)
SPLENECTOMY ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
TETANY ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)

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