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Taste alterations, including bad taste in the mouth, are not listed among the common adverse reactions (occurring in 5% of patients) in the FDA-approved prescribing information for semaglutide products
In the CY 2022 PFS final rule (86 FR 65542 through 65544), we finalized a new requirement at 414.1400(b)(1)(ii) to state that, beginning with the CY 2023 performance period/2025 MIPS payment year, qualified clinical data registries (QCDRs) and qualified registries (as these terms are defined at 414.1305) must support MVPs that are applicable to the MVP participants on whose behalf they submit MIPS data
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