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Although most patients experience grade 1-2 pneumonitis, it can rapidly escalate to a grade 3-4 irAE with a high mortality rate (50%-60%)

What are the key differences between CagriSema and Retatrutide

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Retatrutide is still completing its phase 3 trial program, with FDA approval estimated for 2027 or 2028

Reactions that warrant attention include persistent swelling or redness lasting more than 24 hours, significant pain beyond the initial injection moment, the development of hard nodules that do not resolve within a day or two, fever or systemic symptoms following injection, or any sign of infection at the injection site including warmth, pus, or spreading redness

Many clients begin gradually before adjusting usage to suit their needs