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HEPATITIS C ( 3 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
CERULOPLASMIN INCREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)

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