RETA (retatrutide) talk is everywhere right now. I’ve been hearing the buzz that it could be up for FDA approval in early 2026. While the exact timing isn’t confirmed, retatrutide is still in Phase 3, with many projections pointing toward a filing around –early 2026. Either way, this drug is a big deal in the GLP-1 world. RETA is a triple agonist (GLP-1 + GIP + glucagon), which is part of why there’s so much excitement around its metabolic potential. My personal experience: I tried to switch from tirzepatide to RETA a few months ago. I started conservatively at 0.5 mg once weekly, but within about two days of the first dose I had a noticeably raised heart rate. Because I already deal with anxiety, that combo wasn’t a good mix for me. I took a break and tried again — same result. So for now, RETA just doesn’t seem to match my biology. Why this might happen: Because RETA activates the glucagon receptor, it may increase energy expenditure, and clinical data have shown dose-related increases in heart rate that researchers are still working to fully understand. Also may be longer to see full appetite suppression because of the metabolic activation. I’m sharing this to normalize something important: Even the most exciting next-gen meds aren’t one-size-fits-all. See the full chart below for some clinical data I combined :) I’d love to hear your experiences — especially if you tried it and: - loved it - couldn’t tolerate it - noticed heart rate changes or little appetite? - found a better fit staying with tirzepatide or semaglutide. (Educational discussion only — not medical advice.)