Danazol in hemophilia

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A two-week trial of high-dose danazol combined with aminocaproic acid in 20 adults with hemophilia showed increased factor levels in only two patients, failing to demonstrate broad therapeutic efficacy.

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Abstract

To the Editor.— In a recent article Garewal et al1demonstrated that danazol, an attenuated androgen, given at a dose of 600 mg daily for eight to 14 weeks, is not useful in the treatment of factor VIII—deficient and factor IX—deficient hemophilic patients. Some hemophilic patients experienced abnormal bleeding with danazol—a problem attributed to increased fibrinolysis.1,2 Subjects and Methods.— In 1984, we undertook a two-week trial of danazol in 800-mg/day oral doses, in addition to aminocaproic acid in 10-g/day oral doses as an inhibitor of fibrinolysis. The subjects were 20 adults with hemophilia and no factor VIII inhibitor, nor evidence of active bleeding. Eighteen cases had moderate to mild hemophilia A (3.2% to 10% of factor VIII), and two cases had moderate hemophilia B (3% and 4.2% of factor IX). Two of the 20 patients showed an increase in deficient factor levels: one with an initial factor VIII

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MeSH descriptors

Danazol Hemophilia A Hemophilia B Pregnadienes Adult Aminocaproic Acid Aminocaproic Acid Danazol Danazol Fibrinolysis Fibrinolysis Hemophilia A Hemophilia B Humans Male Pregnadienes

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last seen: 2026-08-26T06:23:00.087416+00:00
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