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For retatrutide specifically, as it remains an investigational medicine, any adverse events experienced within a clinical trial setting should be reported directly to the trial sponsor and principal investigator in accordance with the trial protocol

10.1155%2F2021%2F5160728 Xiu-Juan Y, Qing-Qing L, Hong-Yi Q, Chen-Feng J, Sheng-Liang C (2020) The impact of stigma on medication adherence in patients with functional dyspepsia

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Esbensen AJ, Schworer EK, Hartley SL