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Clin Cancer Res 11S:205, 2005

Always follow the dosing and safety instructions carefully when administering peptide therapy to ensure optimal results and minimize the risk of complications

Dihexa is not approved by the FDA or EMA

It could be speculated that this increased discontinuation rate vs all comparators, including GLP-1 RAs, may be possibly attributed to the severity of gastrointestinal adverse events experienced with tirzepatide 15 mg, considering that the incidence of gastrointestinal adverse events was similar between tirzepatide and GLP-1 RAs

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