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Itisha Arya

Addyi: FDA Approves Libido-Boosting Drug For Postmenopausal Women – What Does It Mean for Women’s Sexual Health?

libido boosting drug menopause

U.S. health authorities have widened the approval of a closely debated medication designed to increase female libido, allowing the once-daily pill to be used by women over the age of 65. The decision, announced on Monday by the <span>Food and Drug Administration</span>, extends the drug’s use to older women who have already gone through menopause. The pill, <span>Addyi</span>, was originally cleared a decade ago for premenopausal women experiencing emotional distress linked to a low sex drive. Anisha Mathur, Founding Partner at Shepherd Law Associates, explained the development and what it means.

Addyi, also known by its generic name flibanserin, is an FDA-approved prescription drug used to treat <span>hypoactive sexual desire disorder</span>, or HSDD, in women. HSDD refers to a long-term or recurring lack of sexual desire that leads to emotional distress or strain in relationships and cannot be explained by another medical condition, relationship difficulties, or medication side effects, according to the Cleveland Clinic.

Marketed by Sprout Pharmaceuticals, Addyi was once expected to become a major breakthrough in women’s health. However, the drug faced setbacks due to side effects such as dizziness and nausea. It also carries a strong safety warning about alcohol use. The <span>FDA</span>’s boxed warning, its strictest caution, notes that consuming alcohol while taking Addyi can lead to dangerously low blood pressure and fainting.

<h2>What Is Hypoactive Sexual Desire Disorder?</h2>

Hypoactive Sexual Desire Disorder, or HSDD, involves an ongoing reduction or absence of sexual thoughts, fantasies, and interest in sexual activity that causes significant personal distress or relationship tension. It is a common form of sexual dysfunction seen in both women and men. People with HSDD may experience low libido, little response to sexual stimulation, or a tendency to avoid sex altogether. Possible contributing factors include stress, relationship challenges, mental health conditions, certain medications, hormonal shifts, or past trauma.

The condition, which describes a distressing lack of sexual desire, has been recognised since the 1990s and is believed to affect a large number of women in the United States, based on survey data. After the commercial success of Viagra for men in the 1990s, pharmaceutical companies invested heavily in finding treatments for female sexual dysfunction. Diagnosis, however, remains complex because libido is influenced by many factors. After menopause, declining hormone levels bring biological changes and medical symptoms that further complicate assessment.

<h2>Addyi: FDA Approves Libido-Boosting Drug For Postmenopausal Women</h2>

U.S. health regulators have now expanded the approval of the controversial libido drug, allowing women over 65 to take the once-daily pill. The FDA’s announcement broadens its use to include older postmenopausal women.

According to CNN, diagnosing HSDD is challenging because sexual desire is affected by multiple physical, emotional, and psychological factors, particularly after menopause. Physicians are expected to rule out issues such as relationship stress, underlying medical conditions, depression, and other mental health disorders before prescribing the medication. The diagnosis itself remains debated, with some psychologists arguing that low sexual desire should not automatically be treated as a medical condition.

Before its approval in 2015, the FDA rejected Addyi twice, citing limited effectiveness and concerns over side effects. Its eventual approval followed a strong lobbying effort by the manufacturer and advocacy groups like Even the Score, which positioned the lack of treatment options for female libido as an issue of gender equality in healthcare.

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U.S. health authorities have widened the approval of a closely debated medication designed to increase female libido, allowing the once-daily pill to be used by women over the age of 65. The decision, announced on Monday by the Food and Drug Administration, extends the drug’s use to older women who have already gone through menopause. The pill, Addyi, was originally cleared a decade ago for premenopausal women experiencing emotional distress linked to a low sex drive. Anisha Mathur, Founding Partner at Shepherd Law Associates, explained the development and what it means.What Is Addyi?Addyi, also known by its generic name flibanserin, is an FDA-approved prescription drug used to treat hypoactive sexual desire disorder, or HSDD, in women. HSDD refers to a long-term or recurring lack of sexual desire that leads to emotional distress or strain in relationships and cannot be explained by another medical condition, relationship difficulties, or medication side effects, according to the Cleveland Clinic.Marketed by Sprout Pharmaceuticals, Addyi was once expected to become a major breakthrough in women’s health. However, the drug faced setbacks due to side effects such as dizziness and nausea. It also carries a strong safety warning about alcohol use. The FDA’s boxed warning, its strictest caution, notes that consuming alcohol while taking Addyi can lead to dangerously low blood pressure and fainting.What Is Hypoactive Sexual Desire Disorder?Hypoactive Sexual Desire Disorder, or HSDD, involves an ongoing reduction or absence of sexual thoughts, fantasies, and interest in sexual activity that causes significant personal distress or relationship tension. It is a common form of sexual dysfunction seen in both women and men. People with HSDD may experience low libido, little response to sexual stimulation, or a tendency to avoid sex altogether. Possible contributing factors include stress, relationship challenges, mental health conditions, certain medications, hormonal shifts, or past trauma.The condition, which describes a distressing lack of sexual desire, has been recognised since the 1990s and is believed to affect a large number of women in the United States, based on survey data. After the commercial success of Viagra for men in the 1990s, pharmaceutical companies invested heavily in finding treatments for female sexual dysfunction. Diagnosis, however, remains complex because libido is influenced by many factors. After menopause, declining hormone levels bring biological changes and medical symptoms that further complicate assessment.Addyi: FDA Approves Libido-Boosting Drug For Postmenopausal WomenU.S. health regulators have now expanded the approval of the controversial libido drug, allowing women over 65 to take the once-daily pill. The FDA’s announcement broadens its use to include older postmenopausal women.According to CNN, diagnosing HSDD is challenging because sexual desire is affected by multiple physical, emotional, and psychological factors, particularly after menopause. Physicians are expected to rule out issues such as relationship stress, underlying medical conditions, depression, and other mental health disorders before prescribing the medication. The diagnosis itself remains debated, with some psychologists arguing that low sexual desire should not automatically be treated as a medical condition.Before its approval in 2015, the FDA rejected Addyi twice, citing limited effectiveness and concerns over side effects. Its eventual approval followed a strong lobbying effort by the manufacturer and advocacy groups like Even the Score, which positioned the lack of treatment options for female libido as an issue of gender equality in healthcare.

fda approves libido-boosting drug for postmenopausal women – what does it mean for women’s sexual health?

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Addyi: FDA Approves Libido-Boosting Drug For Postmenopausal Women – What Does It Mean for Women’s Sexual Health?

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Addyi: FDA Approves Libido-Boosting Drug For Postmenopausal Women – What Does It Mean for Women’s Sexual Health?