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Event Phase 2 Rate (12 mg group) Phase 2 Rate (Placebo) Nausea 45.8% 11.6% Diarrhea 33.3% 9.3% Vomiting 22.2% 2.3% Constipation 16.7% 7.0% Decreased appetite 22.2% 2.3% The nausea incidence at the highest dose a nausea percentage of roughly 46% makes it the single most reported adverse event in retatrutide clinical trials 2026 data

For longer storage, prepare single-use aliquots at -20C

In contrast, in the Si-DSS group, the weight increased on the 1st day after DSS administration and then decreased after the 3rd day

These questions, discussed with your healthcare team, help determine if GLP-1 optimization makes sense or if you should proceed directly to fertility treatment

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