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IN-STENT ARTERIAL RESTENOSIS ( 8 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
FATIGUE ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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