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ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
COMA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
CAROTID ANEURYSM RUPTURE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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