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Friday: The FDA Drops the Hammer On February 6th, one day after the HIMS launch, FDA Commissioner Martin Makary issued a statement that may be the most consequential regulatory action in the compounded GLP-1 saga to date

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Immediately discontinue use and contact your physician if any adverse reactions occur

In addition, in a new set of experiments, we used an alternative protocol: we first gave cilostamide, then added 100 nM nifedipine, and then added retatrutide

At this concentration, a 500 mcg dose equals 0.2 mL (20 units on an insulin syringe)