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Nonetheless, these symptoms led to discontinuation of treatment in 4-8% of patients enrolled in completed obesity trials for semaglutide (Novo Nordisk), and the dual GLP-1/GIP receptor agonist tirzepatide (Eli Lilly)
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Relevant sources include: Alba M, Fintini D, Sagazio A, et al
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Biosimilar interchangeability the designation required for automatic pharmacy substitution is the most commercially important regulatory designation in the BPCIA framework and remains structurally difficult to obtain
Effective November 1, 2023 select peptides will not be availablemake your voice heard to change this FDA mandate that impacts patient care
