Medspas Begin Offering Addyi for Low Libido as FDA Weighs Post-Menopausal Approval

Three mature women with white flowers, celebrating body positivity and aging gracefully
Addyi, originally approved for premenopausal women, is now under FDA Priority Review for potential use in postmenopausal women experiencing low sexual desire.
Courtesy of oneinchpunch at Adobe Stock

Sprout Pharmaceuticals, the manufacturers behind Addyi, a FDA-approved pill for pre-menopausal women experiencing low sexual desire, has gained priority review by the FDA for the pill’s implication on post-menopause. Given the aesthetic industry’s portfolio of treatments, designated to address vaginal health and hormonal shifts, this medication is already seeing itself in practices, as medspas increasingly become a one-stop for medications, like GLP-1, that address biological concerns connected to outward comfort and appearance. 

Menopause affects women’s sexual health vastly, as lower estrogen levels can lead to vaginal dryness and discomfort, and the mood changes associated sometimes affect women's libido. Despite this fact, in the United States, the National Institutes of Health (NIH) allocates 11% of its budget to women’s health research [1], and women’s sexual health is widely understudied compared to men. 

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