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The FDA has issued guidance documents, warning letters, and taken enforcement actions against companies making inappropriate drug claims or selling adulterated products

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Fifth, other studies have reported high one-year discontinuation rates (64.8% in non-T2DM and 46.5% in T2DM cohorts) and low 1-year re-initiation rates of GLP-1RA (36.3% in non-T2DM and 47.3% in T2DM cohorts), largely contributed by moderate or severe incident gastrointestinal adverse events and lower income status [107,108,109,110,111]

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