Deadlines to halt production of compounded tirzepatide have since taken effect, but orders to stop compounded semaglutide production remain held up in court
(This is associative evidence and may reflect confounding by indication, surveillance patterns, and glycaemic differences.) For post-marketing pharmacovigilance, FAERS-based analyses of semaglutide identify multiple safety signals (e.g., gastrointestinal obstruction-related terms, dehydration/volume depletion in some GLP-1RA analyses), but vulvovaginal dryness/infection/discharge/pain are not prominent as labelled risks in the major semaglutide FAERS disproportionality paper retrieved here
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4A), and the results revealed an upregulation of IRE1 (an ER stress marker), indicating ER stress activation, reduced p62 levels, and increased LC3BII levels within 012 h of PFOS treatment
