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| (koe-less-TIE-ruh-meen) |
| LoCHOLEST, LoCHOLEST Light, Prevalite, Questran, Questran Light |
| Class: Antihyperlipidemic/Bile acid sequestrant |
Action Increases removal of bile acids from body by forming insoluble complexes in intestine, which are then excreted in feces. As body loses bile acids, it converts cholesterol from blood to bile acid, thus lowering serum cholesterol.
Indications Reduction of serum cholesterol in patients with primary hypercholesterolemia; relief of pruritus associated with partial biliary obstruction. Unlabeled use(s): Treatment of antibiotic-induced pseudomembranous colitis, bile salt-mediated diarrhea and digitalis toxicity.
Contraindications Hypersensitivity to bile acid sequestering resins; complete biliary obstruction.
ADULTS: PO 4 g 1 to 6 times/day; generally given 3 to 4 times/day.
Acetaminophen, amiodarone, corticosteroids, digitalis glycosides, HMG-CoA reductase inhibitors (eg, fluvastatin), methotrexate, some NSAIDs (eg, piroxicam), propranolol, thiazide diuretics, ursodiol, warfarin, and other drugs: Cholestyramine may interfere with the absorption of many drugs, especially those listed. Fats and fat-soluble vitamins A, D, E, and K: Cholestyramine may interfere with normal fat absorption and digestion; consider supplementation with these vitamins and with folic acid. Iopanoic acid: Coadministration may result in abnormal cholecystography.
Lab Test Interferences Increased serum phosphorus and chloride; decreased serum sodium and potassium.
DERM: Rash; irritation of skin, tongue, and perianal area. GI: Constipation (can be severe and at times accompanied by fecal impaction); aggravation of hemorrhoids; abdominal pain and distention; bleeding; belching; flatulence; nausea; vomiting; diarrhea; heartburn; anorexia; steatorrhea. HEMA: Bleeding tendencies related to vitamin K deficiency; folic acid deficiency. META: Fat-soluble vitamin deficiencies; hyperchloremic acidosis and increased urinary calcium excretion; osteoporosis.
Pregnancy: Safety not established. Lactation: Undetermined. Children: Safety and efficacy not established. Carcinogenesis: Incidence of intestinal tumors in studies was greater in cholestyramine-treated rats than in controls; relevance to clinical practice is not known.
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