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  2. Spironolactone - Wikipedia

    en.wikipedia.org/wiki/Spironolactone

    1.7 Polyuria: 2: 0.6: 8: 1.2 Fatigue/lethargy: 1: 0.3: ≥12 a: ≥1.8 Footnotes: a = Precise values unavailable due to inadequate reporting. b = Not monitored in most studies. Description: Side effects of spironolactone (25–400 mg/day) with ≥1% incidence in a 2017 hybrid systematic review of clinical studies of spironolactone for acne ...

  3. Talk:Spironolactone - Wikipedia

    en.wikipedia.org/wiki/Talk:Spironolactone

    June 2, 2007. 2(2) 189-199. Rathnayake D, Sinclair R. “Innovative use of spironolactone as an antiandrogen in the treatment of female pattern hair loss.” Dermatol Clin.

  4. Pharmacodynamics of spironolactone - Wikipedia

    en.wikipedia.org/wiki/Pharmacodynamics_of...

    7α-Thiomethylspironolactone, the major active form of spironolactone. It accounts for about 80% of the potassium-sparing effect of spironolactone. [1] [2] [3] Canrenone, the second major active form of spironolactone. It accounts for around 10 to 25% of the potassium-sparing effect of spironolactone. [4

  5. 7α-Thiospironolactone - Wikipedia

    en.wikipedia.org/wiki/7α-thiospironolactone

    Spironolactone is a prodrug with a short terminal half-life of 1.4 hours. [ 5 ] [ 6 ] [ 7 ] The active metabolites of spironolactone have extended terminal half-lives of 13.8 hours for 7α-TMS, 15.0 hours for 6β-OH-7α-TMS, and 16.5 hours for canrenone, and accordingly, these metabolites are responsible for the therapeutic effects of the drug.

  6. Mineralocorticoid receptor antagonist - Wikipedia

    en.wikipedia.org/wiki/Mineralocorticoid_receptor...

    Spironolactone has shorter half-life (t1/2 = 1.3-1.4 hours) than eplerenone (t1/2 = 4–6 hours). Eplerenone goes through rapid metabolism by the liver to inactive metabolites (t1/2 = 4–6 hours). However, spironolactone is metabolized to three active metabolites, which give it prolonged activity (13.8 – 16. 5 hours).

  7. Spirolactone - Wikipedia

    en.wikipedia.org/wiki/Spirolactone

    SC-5233 (6,7-dihydrocanrenone), the C17α propanoic acid lactone of testosterone (androst-4-en-17β-ol-3-one), is the unsubstituted parent or prototype compound of the spirolactones, and is one of a few of the simplest members of the series along with SC-8109 (the 19-demethyl analogue of SC-5233) and canrenone (the 1,2-didehydro analogue of SC ...

  8. Category:Spironolactone - Wikipedia

    en.wikipedia.org/wiki/Category:Spironolactone

    Pages in category "Spironolactone" The following 10 pages are in this category, out of 10 total. ... This page was last edited on 25 October 2020, at 01:19 (UTC).

  9. Potassium-sparing diuretic - Wikipedia

    en.wikipedia.org/wiki/Potassium-sparing_diuretic

    Potassium-sparing diuretics or antikaliuretics [1] refer to drugs that cause diuresis without causing potassium loss in the urine. [2] They are typically used as an adjunct in management of hypertension, cirrhosis, and congestive heart failure. [3] The steroidal aldosterone antagonists can also be used for treatment of primary hyperaldosteronism.