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While semaglutide demonstrated a favorable safety and tolerability profile and was associated with modest changes in AD-related biomarkers, including plasma high-sensitivity C-reactive protein and AD-relevant cerebrospinal fluid biomarkers, it did not demonstrate superiority over placebo on the primary clinical endpoint, change in the clinical dementia ratingsum of boxes (CDR-SB) score at week 104 68

In summary: most people tolerate sermorelin well

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Uncertain side effects and safety profile

2024 FAERS Study The FDAs Adverse Event Reporting System, or FAERS, is an open-access database that gathers voluntary reports about possible drug side effects from both healthcare professionals and the public