1962
DOI: 10.1136/bmj.2.5307.756
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Triamterene, a New Diuretic Drug--I

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1963
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Cited by 48 publications
(8 citation statements)
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“…Similar results were obtained with triamterene. 3 The third comparison, in a normal human subject, again revealed a qualitative similarity between the two compounds. Amiloride (40 mg.) proved more potent than 200 mg. of triamterene in promoting sodium loss and water diuresis but produced closely similar effects on urinary potassium and bicarbonate excretion and on urinary pH.…”
Section: Discussionmentioning
confidence: 83%
“…Similar results were obtained with triamterene. 3 The third comparison, in a normal human subject, again revealed a qualitative similarity between the two compounds. Amiloride (40 mg.) proved more potent than 200 mg. of triamterene in promoting sodium loss and water diuresis but produced closely similar effects on urinary potassium and bicarbonate excretion and on urinary pH.…”
Section: Discussionmentioning
confidence: 83%
“…Triamterene differs from the thiazide diuretics in that it does not produce a significant potassium diuresis and, in fact, may suppress the excretion of potassium (Crosley et al 1962; Baba et al 1962 a ). It is therefore unlikely to produce hypokalaemia with its associated portal systemic encephalopathy.…”
Section: Discussionmentioning
confidence: 99%
“…A new diuretic agent, triamterene (SKF 8542, ‘Dytac‘, 2, 4, 7‐triamino‐6‐phenylpteridine) has recently been described in the treatment of fluid retention due to various causes (Donnelly et al 1962; Crosley et al 1962; Baba et al 1962; Shaldon and Ryder 1962). We report its use in six patients with ascites due to cirrhosis of the liver.…”
Section: Introductionmentioning
confidence: 99%
“…On this account it was originally regarded as an aldosterone antagonist, but further investigations showed that it exerted this effect after adrenalectomy when no mineralocorticoid was given and also in men taking an excess of sodium chloride to depress the adrenal secretion of aldosterone (Liddle, 1961 ;Baba et al, 1962a;Cattell and Havard, 1962). The effect is presumably directly on the nephron, and one site of action must lie in the distal tubule where the drug depresses the absorption of sodium and the exchange of potassium for sodium.…”
Section: Metabolic Disturbancesmentioning
confidence: 99%