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

VISUAL IMPAIRMENT ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
FOREIGN BODY IN EYE ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)

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