The use of danazol as a treatment of endometriosis

In: Modern Approaches to Endometriosis · 1991 · pp. 239–255 · doi:10.1007/978-94-011-3864-2_13 · W2281391140
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This chapter reviews the clinical pharmacology of danazol, its mode of action, and its therapeutic applications for treating endometriosis.

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Abstract

During the past 50 years, the medical management of endometriosis has evolved from a primitive clinical art utilizing agents with poor specificity, to a scientific endeavour utilizing pharmacological compounds that are highly specific in their molecular actions and extensively studied in randomized clinical trials. The first medical regimens developed to treat endometriosis utilized high-dose testosterone propionate1 or high-dose diethylstilboesterol2. These regimens were moderately effective in the treatment of endometriosis, but they were associated with major unwanted side-effects, such as virilization in the case of testosterone proprionate therapy1. In the late 1950s Kistner introduced progestin-only3 and pseudopregnancy4 regimens for the treatment of endometriosis. These regimens remained the standard medical therapy until danazol (Figure 13.1) was approved for use in 1976. This chapter will review the clinical pharmacology of danazol, including its mode of action and its therapeutic applications. Preview Unable to display preview. Download preview PDF. Similar content being viewed by others

References

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The use of danazol as a treatment of endometriosis. In: Thomas, E.J., Rock, J.A. (eds) Modern Approaches to Endometriosis. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3864-2_13 Download citation DOI: https://doi.org/10.1007/978-94-011-3864-2_13 Publisher Name: Springer, Dordrecht Print ISBN: 978-94-010-5719-6 Online ISBN: 978-94-011-3864-2 eBook Packages: Springer Book Archive

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