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The percentages of participants who experienced AE leading to treatment discontinuation as well as of those who experienced gastrointestinal AE with oral semaglutide 50 mg (Tables 2 and 3) were similar to those observed with subcutaneous semaglutide 2.4 mg (in STEP-1 and STEP-2 trials 67% discontinued treatment due to AE, 3444% experienced nausea, 2132% diarrhoea and 2225% vomiting) [11, 29]

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The inclusion of benzyl alcohol allows multiple withdrawals from the same vial, reducing waste and making it more practical for ongoing peptide use or research applications

Better memory was also demonstrated by GIP-transgenic mice, which is most likely connected to increased neurogenesis [23]