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The questions that remain unanswered include the actual prevalence of sexual side effects (we do not know if it affects 5 percent or 30 percent of women), whether certain doses are more likely to cause sexual dysfunction than others, whether compounded semaglutide formulations produce different sexual side effect profiles than brand-name versions, whether specific pharmacy sources or compounding pharmacies produce formulations with different tolerability profiles, and whether pre-treatment screening can identify women at higher risk for sexual dysfunction on GLP-1 agonists

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Structurebased sitespecific pegylation of fibroblast growth factor 2 facilitates rational selection of conjugate sites

Conversely, among GLP-1RA non-users with HbA1c 7.5% (957 of 3747

Before matching, patients in the trial eligible and expanded populations initiating semaglutide or tirzepatide were younger, more likely to be white and were more frequently prescribed sulfonylureas compared to sitagliptin or dulaglutide users