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Hydrodiuril (Hydrochlorothiazide) - Description and Clinical Pharmacology

 
 



DESCRIPTION

HydroDIURIL * (Hydrochlorothiazide) is a diuretic and antihypertensive. It is the 3,4-dihydro derivative of chlorothiazide. Its chemical name is 6-chloro-3,4-dihydro-2 H -1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide. Its empirical formula is C7H8ClN3O4S2 and its structural formula is:

It is a white, or practically white, crystalline powder with a molecular weight of 297.74, which is slightly soluble in water, but freely soluble in sodium hydroxide solution.

HydroDIURIL is supplied as 25 mg and 50 mg tablets for oral use. Each tablet contains the following inactive ingredients: calcium phosphate, FD&C Yellow 6, gelatin, lactose, magnesium stearate, starch and talc.


*Registered trademark of MERCK & CO., INC.

CLINICAL PHARMACOLOGY

The mechanism of the antihypertensive effect of thiazides is unknown. HydroDIURIL does not usually affect normal blood pressure.

HydroDIURIL affects the distal renal tubular mechanism of electrolyte reabsorption. At maximal therapeutic dosage all thiazides are approximately equal in their diuretic efficacy.

HydroDIURIL increases excretion of sodium and chloride in approximately equivalent amounts. Natriuresis may be accompanied by some loss of potassium and bicarbonate.

After oral use diuresis begins within 2 hours, peaks in about 4 hours and lasts about 6 to 12 hours.

Pharmacokinetics and Metabolism

HydroDIURIL is not metabolized but is eliminated rapidly by the kidney. When plasma levels have been followed for at least 24 hours, the plasma half-life has been observed to vary between 5.6 and 14.8 hours. At least 61 percent of the oral dose is eliminated unchanged within 24 hours. Hydrochlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.

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