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Stephanie Lambson, quoted by ACMT, noted that compounded vial-based products introduce particular risk because they lack the auto-calibrated pen mechanism of the branded products: "It's up to the patients to draw out the correct amount of medication to administer to themselves, and this is where we've seen a lot of the errors." What the Evidence Shows and What It Does Not MedicalDaily Evidence Check Study type: Retrospective analysis of national poison center database records (20122023) Participants: All reported GLP-1 receptor agonist exposures in national poison center data Published in: Journal of Medical Toxicology (2026), Volume 22, pages 275285 (DOI: 10.1007/s13181-026-01121-z) What it found: Poison control calls involving semaglutide surged more than five-fold after FDA weight-loss approval

Hydrops fetalis associated with erythrocyte G-6-PD deficiency and maternal ingestion of fava beans and ascorbic acid

doi: 10.1074/jbc.M109.015487

Yuan et al., 2008