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Survodutide (BI 456906) is an investigational compound currently in Phase 3 clinical trials and has not been approved by the MHRA, FDA, or any regulatory authority for human use

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The most common adverse events occurring in 5% of participants were nausea, diarrhea, constipation, injection-site reaction, dosing error, vomiting, and dizziness in the ixekizumab and tirzepatide concomitant treatment arm, and injection-site reaction, dosing error, and nasopharyngitis in the ixekizumab monotherapy arm.

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Kapseln Ergnzung zur Nahrung 69,49 (2.573,70 / kg, inkl

Common drawbacks include nausea, digestive symptoms, fatigue during dose increases, and cost