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Neither peptide is approved by the FDA or comparable regulators as a hair-loss treatment, and neither has completed a human efficacy trial for that purpose

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What the Study Could Not Capture The researchers note several important limitations

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[12] Post-marketing surveillance data from the FDA Adverse Event Reporting System (FAERS) indicate that serious hepatic adverse events with semaglutide are rare, though such spontaneous reporting systems have inherent limitations and cannot establish true incidence or definitive causality