


PT-141 10mg
🔬 What Is PT-141?
PT-141 (generic name bremelanotide) is a synthetic peptide derived from Melanotan II.
Unlike Viagra or Cialis (which work on blood flow), PT-141 acts in the brain by stimulating melanocortin receptors (MC3R & MC4R) that regulate sexual arousal.
It does not require sexual stimulation to be effective.
📌 FDA Status
Approved in the U.S. as Vyleesi (2019).
Indication: Premenopausal women with hypoactive sexual desire disorder (HSDD).
Also used off-label for men with erectile dysfunction (ED), especially when PDE-5 inhibitors (Viagra, Cialis) don’t work.
⚙️ Mechanism of Action
Activates melanocortin receptors in the hypothalamus, enhancing sexual desire and arousal pathways.
In men, this translates into improved erectile function, and in women, enhanced libido and satisfaction.
Effects begin in 30–60 minutes and can last 6–12 hours, sometimes longer.
⚠️ Side Effects
Most common:
Nausea (up to 40%)
Flushing
Headache
Injection site reactions
Other considerations:
Can cause a temporary increase in blood pressure and reduction in heart rate. Not recommended for those with uncontrolled hypertension or cardiovascular disease.
Some users experience darkening of moles or skin with repeated use (due to melanocortin receptor activity).
✅ Key Takeaways
PT-141 = Bremelanotide, a melanocortin receptor agonist.
Main effect: Increases sexual desire/arousal (women) and erectile function (men, off-label).
Dose: Typically 1.75 mg SC (FDA) or 0.5–2 mg SC (clinic use).
Side effects: Nausea, flushing, temporary BP changes.
Unique: Works centrally in the brain—not via blood vessels like Viagra.
🔬 What Is PT-141?
PT-141 (generic name bremelanotide) is a synthetic peptide derived from Melanotan II.
Unlike Viagra or Cialis (which work on blood flow), PT-141 acts in the brain by stimulating melanocortin receptors (MC3R & MC4R) that regulate sexual arousal.
It does not require sexual stimulation to be effective.
📌 FDA Status
Approved in the U.S. as Vyleesi (2019).
Indication: Premenopausal women with hypoactive sexual desire disorder (HSDD).
Also used off-label for men with erectile dysfunction (ED), especially when PDE-5 inhibitors (Viagra, Cialis) don’t work.
⚙️ Mechanism of Action
Activates melanocortin receptors in the hypothalamus, enhancing sexual desire and arousal pathways.
In men, this translates into improved erectile function, and in women, enhanced libido and satisfaction.
Effects begin in 30–60 minutes and can last 6–12 hours, sometimes longer.
⚠️ Side Effects
Most common:
Nausea (up to 40%)
Flushing
Headache
Injection site reactions
Other considerations:
Can cause a temporary increase in blood pressure and reduction in heart rate. Not recommended for those with uncontrolled hypertension or cardiovascular disease.
Some users experience darkening of moles or skin with repeated use (due to melanocortin receptor activity).
✅ Key Takeaways
PT-141 = Bremelanotide, a melanocortin receptor agonist.
Main effect: Increases sexual desire/arousal (women) and erectile function (men, off-label).
Dose: Typically 1.75 mg SC (FDA) or 0.5–2 mg SC (clinic use).
Side effects: Nausea, flushing, temporary BP changes.
Unique: Works centrally in the brain—not via blood vessels like Viagra.