Maa: Yhdysvallat
Kieli: englanti
Lähde: NLM (National Library of Medicine)
NADOLOL (UNII: FEN504330V) (NADOLOL - UNII:FEN504330V), BENDROFLUMETHIAZIDE (UNII: 5Q52X6ICJI) (BENDROFLUMETHIAZIDE - UNII:5Q52X6ICJI)
Pfizer Laboratories Div Pfizer Inc
NADOLOL
NADOLOL 40 mg
ORAL
PRESCRIPTION DRUG
CORZIDE (Nadolol and Bendroflumethiazide Tablets) is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including the classes to which this drug principally belongs. There are no controlled trials demonstrating risk reduction with CORZIDE. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program's Joint National Committee on Prevention, Detection, Ev
CORZIDE (Nadolol and Bendroflumethiazide Tablets) Round, biconvex tablets are white to bluish white with dark blue specks. Each tablet has a full bisect bar. Tablet identification numbers: 40 mg/5 mg combination embossed with KPI/283 on the scored side and Corzide 40/5 on the other; 80 mg/5 mg combination embossed with KPI/284 on the scored side and Corzide 80/5 on the other. Keep bottle tightly closed. Store at room temperature; avoid excessive heat. Rx Only
New Drug Application
CORZIDE- NADOLOL AND BENDROFLUMETHIAZIDE TABLET PFIZER LABORATORIES DIV PFIZER INC ---------- CORZIDE® (NADOLOL AND BENDROFLUMETHIAZIDE TABLETS) DESCRIPTION CORZIDE (Nadolol and Bendroflumethiazide Tablets) for oral administration combines two antihypertensive agents: CORGARD (nadolol), a nonselective beta-adrenergic blocking agent, and NATURETIN (bendroflumethiazide), a thiazide diuretic-antihypertensive. Formulations: 40 mg and 80 mg nadolol per tablet combined with 5 mg bendroflumethiazide. Inactive ingredients: cellulose, colorant (FD&C Blue No. 2), lactose, magnesium stearate, povidone, sodium starch glycolate, and starch. NADOLOL Nadolol is a white crystalline powder. It is freely soluble in ethanol, soluble in hydrochloric acid, slightly soluble in water and in chloroform, and very slightly soluble in sodium hydroxide. Nadolol is designated chemically as 1-(_tert_-butylamino)-3-{(5,6,7,8-tetrahydro-_cis_-6,7-dihydroxy-1-naphthyl)oxy}- 2-propanol. Structural formula: C H NO MW 309.4 0 CAS-4 2200-33-9 BENDROFLUMETHIAZIDE Bendroflumethiazide is a white crystalline powder. It is soluble in alcohol and in sodium hydroxide, and insoluble in hydrochloric acid, water, and chloroform. Bendroflumethiazide is designated chemically as 3-benzyl-3,4-dihydro-6-(trifluoromethyl)-2_H_-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide. Structural formula: ® ® 17 27 4 C H F N O S MW 4 21.4 1 CAS-73-4 8-3 CLINICAL PHARMACOLOGY NADOLOL Nadolol is a nonselective beta-adrenergic receptor blocking agent. Clinical pharmacology studies have demonstrated beta-blocking activity by showing (1) reduction in heart rate and cardiac output at rest and on exercise, (2) reduction of systolic and diastolic blood pressure at rest and on exercise, (3) inhibition of isoproterenol-induced tachycardia, and (4) reduction of reflex orthostatic tachycardia. Nadolol specifically competes with beta-adrenergic receptor agonists for available beta receptor sites; it inhibits both the beta receptors located chiefly in cardiac muscle and the beta recept Lue koko asiakirja