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[2] [7] These findings led regulatory authorities, including the Medicines and Healthcare products Regulatory Agency (MHRA) and the European Medicines Agency (EMA), to include specific warnings and precautions in the prescribing information for all GLP-1 medications

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What stood out was the nontrivial percentage of users who reported symptoms that may not be fully reflected in current drug labeling or routine adverse-event reporting

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A minor delay in gastric emptying in the early postprandial phase is also involved in the mechanism of blood glucose-lowering effect of GLP-1 RAs [8]