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They did so by evaluating reports of hair loss in the FDA Adverse Event Reporting System, known as FAERS, specifically focusing on data from 2022 to 2023 The authors performed a technique known as a disproportionality analysis of alopecia reports related to semaglutide, tirzepatide, and other GLP-1/gastric inhibitory polypeptide (GIP) receptor agonists within the FDA Adverse Event Reporting System, known as FAERS
2020;01(Sup4):S1722
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