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The CV outcome trials (CVOT) (Figure 1) of all the GLP-1 RAs (liraglutide, semaglutide, dulaglutide, albiglutide, extended-release exenatide, and lixisenatide) (Table 1)
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Once weekly dulaglutide had the greatest number of total adverse events, but the lowest percentage of cutaneous adverse events at 3.75%, which researchers noted could reflect higher prescription rates rather than increased dermatologic risk
10.1002/(SICI)1098-2744(199911)26:3 3.0.CO;2-K Mol
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