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Diabetes 61 , 364371, doi:10.2337/db11-1019 (2012)

Gastrointestinal adverse events (most commonly nausea, vomiting, diarrhea, constipation, and dyspepsia) were mild to moderate, transient, and dose dependent, occurring in 7480% of participants with oral semaglutide 2550 mg, with higher frequency and discontinuation rates seen at the 50 mg dose during dose escalation [30, 31]

Meyer et al., 2007

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Clinical research settings: Some practitioners offer BPC-157 in research or clinical investigation settings where regulatory requirements differ

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