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Real-world data from the FDA Adverse Event Reporting System shows that 77.44% of gastrointestinal side effects occur within the first 30 days, with a median onset time of just 1 day

Cumulative 36-month NAION incidence hit 8.9% in the diabetic semaglutide cohort versus 1.8% in comparators

Most of these studies were conducted exclusively in male rodents

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Results from Eli Lilly's Phase III study for the GLP-1 are being presented at the ADA's 85th Scientific Sessions in June and additionally published in a journal

In summary, its specifically recommended to avoid breastfeeding when taking oral semaglutide