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National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Health Sciences Policy; Committee on the Clinical Utility of Treating Patients with Compounded Bioidentical Hormone Replacement Therapy; Jackson LM, Parker RM, Mattison DR, editors. The Clinical Utility of Compounded Bioidentical Hormone Therapy: A Review of Safety, Effectiveness, and Use. Washington (DC): National Academies Press (US); 2020 Jul 1.

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The Clinical Utility of Compounded Bioidentical Hormone Therapy: A Review of Safety, Effectiveness, and Use.

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Appendix HBoxed Warnings on U.S. Food and Drug Administration–Approved Estrogen and Testosterone Products

All U.S. Food and Drug Administration (FDA)-approved estrogen-containing products (Stefanick, 2005) and topical testosterone products (FDA, 2015) must contain a boxed warning that provides the prescriber and patient with safety warnings for the most serious adverse events associated with the use of these products. See Figures H-1 and H-2 for the boxed warning for FDA-approved estrogen-containing and topical testosterone products, respectively.

FIGURE H-1. Boxed warning included with FDA-approved estrogen-containing products.

FIGURE H-1

Boxed warning included with FDA-approved estrogen-containing products. SOURCE: NLM, 2020a.

FIGURE H-2. Boxed warning included with FDA-approved topical testosterone products.

FIGURE H-2

Boxed warning included with FDA-approved topical testosterone products. SOURCE: NLM, 2020b.

REFERENCES

Copyright 2020 by the National Academy of Sciences. All rights reserved.
Bookshelf ID: NBK562883

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