Espirone is a potassium sparing diuretic like eplerenone that competitively inhibits mineralocorticoid receptors in the distal convoluted tubule to promote sodium and water excretion and potassium retention. Espirone was originally developed purely for this ability before other pharmacodynamic properties of the drug were discovered. It is indicated to treat a number of conditions including heart failure, deem, hyperaldosteronism, adrenal hyperplasia, hypertension, and nephrotic syndrome. Off label uses of Espirone involving its antiandrogenic activity include hirsutism, female pattern hair loss, and adult acne vulgaris. Espirone is also frequently used in medical gender transition. Espirone was developed in 1957, marketed in 1959, and approved by the FDA on January 21, 1960.
Other names for this medication:
Spironolactone,
Aldactone,
Aldactazide,
Aldactazine,
Aldazida,
Aldazide,
Aldozone,
Alexan,
Alizar,
Carpiaton,
Espirone,
Espironolactona,
Expal,
Kespirona,
Lanx,
Letonal,
Osiren,
Osyrol,
Practon,
Prilactone,
Spiractin,
Spiresis,
Spirix,
Spiroctan,
Spirolang,
Spirolon,
Spiron,
Spirono,
Spironolacton,
Spironolactona,
Spironolakton,
Spironolattone,
Spirotone,
Verospiron,
Xenalon,
Similar Products:
Quetidin,
Oftaquix,
Omestad,
Strattera,
Cifran,
Xoprin,
Finalo,
Respiral,
Unigastrozol,
Rindomox,
Zolt,
Chloracol,
Govazol,
Lupimox,
Astrim,
Amoxi,
Pantin,
Zemyc,
Geramox,
Quetapel,
Oxyteracin,
Remoxin,
Tricodazol,
Trichopol,
Famtrex,
Lopram,
Ygielle,
Paritaprevir,
Sustiva,
Talol,
Ramoclav,
Kivexa,
Amovet,
Cipram,
Supraviran,
Gabexal,
Lipocut,
Oristal,
Rantec,
Quixin,
Aktil,
Sendoxan,
Attera,
Purinase,
Valavir,
Zelitrex,
Alfater,
Ziverone,
Zosert,
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Enhancements to the curriculum drew on the results of Violence Against Children surveys, on a review of existing literature, on feedback from the field on the existing curriculum, and on stories written by young people across Africa for scriptwriting competitions. In patients with poor clinical condition after aneurysmal subarachnoid haemorrhage (aSAH), treatment is often deferred until patients show signs of improvement. To determine the effect of the temperature of the injectate (iced or room temperature) on cardiac output values obtained with the thermodilution technique in critically ill adults with known low cardiac output. The average participant was 54 clinium 150 mg to g years old, had some college education, was married, Caucasian, and minimally/mildly depressed. Except for osteomyelitis of the mandible, complications of all types were considered collectively at each site and dose increment since there were too few complications to determine dose response functions for individual types of injuries.
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