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Melanotan 2 has no marketing authorization from the FDA, the EMA, or any comparable regulator, and (as noted above) the FDA approval of the Melanotan-2-derived molecule bremelanotide/Vyleesi does not launder Melanotan 2 into an approved product

doi:10.1080/14656566.2024.2436595 Mikdachi H, Dunsmoor-Su R

In the UK, a patient must also be reapproved for GLP-1 usage after every two years of prescription

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Notably, GLP-1RAs slow the transit time of the gastrointestinal (GI) tract and suppress appetite, which could displace nutrient intake and result in mineral and vitamin deficiencies

published in Womens Health evaluated bremelanotide across three doses (0.75 mg, 1.25 mg, 1.75 mg) in premenopausal women with HSDD