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

RENAL FAILURE ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
APHASIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)

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