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DRUG INTERACTION ( 4 FDA reports)
PORTAL HYPERTENSION ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
VOMITING ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
GLIAL SCAR ( 1 FDA reports)

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