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As of early 2025, the FDA had received more than 455 adverse event reports involving compounded semaglutide and more than 320 involving compounded tirzepatide figures that the agency now cites as active justification for enforcement
This is particularly concerning given the lack of ingredient transparency
I would hope they would do the right thing but based on all the social media comments expressing the same exact treatment to multiple others Im not sure they are listening and if they arethey just really dont care about anything but making a profit for a service they fail to deliver.
Injecting immediately after reconstitution risks administering cold solution, which causes sharp burning pain and vasoconstriction at the injection site
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