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The sites confirmed as appropriate for GLP-1 class drugs (abdomen, thigh, upper arm) apply to retatrutide's subcutaneous route regardless of whether delivery is via pen or syringe
Singh AK, Chattopadhyay R, Chakravarty B, Chaudhury K
The published TRIUMPH-1 and TRIUMPH-4 data suggest discontinuation rates due to adverse events climb with dose, and that the 12 mg arm of retatrutide has shown the highest discontinuation figures of the three compounds at their respective top doses in published Phase 3 trials [2][10]
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