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

ABASIA ( 8 FDA reports)
SALIVARY HYPERSECRETION ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
NEPHROLITHIASIS ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
OFF LABEL USE ( 5 FDA reports)
HYPOTENSION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
FALL ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)

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