Is PT-141 or Addyi Better for Low Libido in Women?
Is PT-141 or Addyi better for low libido in women?
Reviewed by Taylor Anderson, RN
Aesthetic Registered Nurse
Taylor Anderson is an aesthetic registered nurse and a reviewer for Hot or Nothing.
Updated September 6, 2026
Quick answer
Neither option produced a large average increase in desire; trials showed only small average gains in satisfying experiences and distress about low desire. These results were in premenopausal women with acquired, generalized HSDD that causes distress, not in low desire due to another medical condition, relationship issues, or a drug effect.
In this guide
Key takeaways
- Addyi is a once-daily bedtime pill, while Vyleesi is an as-needed injection used only around sex.
- Addyi requires avoiding alcohol until the day after each dose and carries a boxed warning for low blood pressure and fainting, while Vyleesi briefly affects blood pressure and heart rate and has no alcohol interaction.
- Nausea after Vyleesi often starts soon after the shot and lasts a few hours, with flushing and headache also common, so day-to-day feel differs from a daily pill.
Neither PT-141 nor Addyi gives most women a large lift in desire. Both showed only small average gains in trials of low sexual desire that causes distress, which clinicians call hypoactive sexual desire disorder or HSDD. Addyi is a nightly pill with risks of low blood pressure and fainting plus an alcohol rule, while PT-141 sold as Vyleesi is a shot you use only around sex with mainly nausea and flushing and no alcohol interaction.
How much did libido actually improve?
An analysis of the approval trial data found Addyi added about one extra satisfying sexual experience every two months compared with placebo, while bremelanotide added none on that count approval-data analysis.
In two 24-week trials that together included 1,267 women with a mean age of 39, bremelanotide 1.75 mg lowered distress about low desire by 0.33 points more than placebo, a small change with an effect size of 0.27 2020 RECONNECT review. In plain terms, women felt a little less bothered on average, not strongly desirous again.
Those averages come from studies in premenopausal women whose low desire was acquired and generalized. It developed after a period of usual desire and it occurred in most situations. Averages hide wide variation, and the studies did not identify who would respond more.
How do you take them and what feels different?
You take Addyi once daily at bedtime. It carries a boxed warning for low blood pressure and fainting, and the label directs you to avoid alcohol until the next day FDA Addyi label.
You inject Vyleesi under the skin as needed before sex, not daily. Each dose briefly raises blood pressure and lowers heart rate. Readings usually return to usual within 12 hours, so the label directs prescribers to consider heart risk before starting it and during use FDA Vyleesi label.
Day to day effects differ. In trials with 627 women on Vyleesi and 620 on placebo, nausea occurred in 40% compared with 1.3%, flushing in 20.3%, headache in 11.3% and vomiting in 4.8% FDA Vyleesi label. Nausea began a median 30 minutes after the shot and lasted a median 2.4 hours, and the review noted bremelanotide has few to no drug interactions and no adverse interaction with alcohol, unlike flibanserin 2020 RECONNECT review.
Which trade-off might suit you better?
A nightly pill may fit you if you prefer no shots and you can avoid alcohol until the day after each bedtime dose. Addyi labeling now covers women under 65 with acquired generalized HSDD that causes distress and is not due to another condition, relationship strain or a drug effect FDA Addyi label.
An as-needed shot may fit you if you want treatment only around sex and you want no alcohol restriction. Vyleesi labeling covers premenopausal women with the same distressing pattern of acquired generalized HSDD FDA Vyleesi label. The cost of that flexibility is a high chance of short-lived nausea or flushing after each use.
The HOD quiz asks about menopause stage, alcohol use, blood pressure history and dosing preference and sends your answers for clinician review to check fit.
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How much improvement did trials show?
On average, improvement was small. Addyi added about one extra satisfying sexual experience every two months compared with placebo, while bremelanotide added none on that measure, and distress about low desire eased only slightly on average.
How do dosing and timing differ?
Addyi is taken once daily at bedtime. Vyleesi is injected under the skin as needed before sex, not every day.
How do alcohol rules and heart-related risks differ?
Addyi has a boxed warning for low blood pressure and fainting and directs avoiding alcohol until the next day. Each Vyleesi dose briefly raises blood pressure and lowers heart rate, usually returning to usual within 12 hours, with no alcohol interaction, but prescribers consider heart risk before and during use.
Who are Addyi and Vyleesi labeled for?
Both are for acquired, generalized low desire that causes distress and is not due to another condition, relationship strain, or a drug effect. Addyi labeling covers women under 65, while Vyleesi labeling covers premenopausal women.
Keep reading
Sources (10)
- VYLEESI (bremelanotide injection) - accessdata.fda.gov U.S. Food and Drug Administration (.gov) https://www.accessdata.fda.gov › label · accessdata.fda.gov · captured September 6, 2026
- Bremelanotide and flibanserin for low sexual desire in women: the fallacy of regulatory precedent. · pubmed.ncbi.nlm.nih.gov · captured September 6, 2026
- ADDYI (flibanserin) - accessdata.fda.gov · accessdata.fda.gov · captured September 6, 2026
- ADDYI (flibanserin) tablets LABEL - accessdata.fda.gov · accessdata.fda.gov · captured September 6, 2026
- Bremelanotide and flibanserin for low sexual desire in women: the fallacy of regulatory precedent | Request PDF · researchgate.net · captured September 6, 2026
- (060) Comparison of Prescribing and Google Trends Between Bremelanotide (Vyleesi®) and Flibanserin (Addyi®) for Female Hypoactive Sexual Desire Disorder · researchgate.net · captured September 6, 2026
- PT-141 (Bremelanotide) Clinical Trials: FDA Approval, Phase 3 Data & HSDD Evidence | CompoundReview · compoundreview.com · captured September 6, 2026
- Bremelanotide and flibanserin for low sexual desire in women · ovid.com · captured September 6, 2026
- PT-141 for Women: How Bremelanotide Works for Female Libido · formblends.com · captured September 6, 2026
- Bremelanotide for Hypoactive Sexual Desire Disorder - T. S. Sathyanarayana Rao, Chittaranjan Andrade, 2020 · journals.sagepub.com · captured September 6, 2026
