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doi: 10.3390/ijms22137138 114 SaeedNHamzahIHAl-GharrawiSAR
This finding ultimately led to the development of bremelanotide (Vyleesi), approved by the FDA in 2019 for hypoactive sexual desire disorder (HSDD) in premenopausal women
The most frequently reported adverse effects are gastrointestinal in nature and typically occur during the dose-escalation phase
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