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The Bottom Line The appeal of needle-free GLP-1 options is understandable, but the current evidence does not support sublingual semaglutide drops or weight loss patches as effective alternatives to proven treatments
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The FDA said Friday that it will start taking action against compounders for violations in the next 60 to 90 days, depending on the type of facility, in order to "avoid unnecessary disruption to patient treatment." "Now that the FDA has determined the drug shortage for semaglutide has been resolved, we will continue to offer access to personalized treatments as allowed by law to meet patient needs," Hims & Hers CEO Andrew Dudum posted Friday on X
I would like to see rigorous clinical trials before approval
Clinical Evidence: What the Research Actually Shows Human clinical trials on NAD supplementation remain limited