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Nothing has been filed with the FDA, the FDA has not accepted anything, there is no PDUFA date, and there is no approval
Serious Health Complications Linked to Zepbound Some Zepbound patients in West Virginia have reported having serious side effects and health complications
One analysis of these same trials reported the overall average weight loss on Contrave to be a little over 4%
The "minimal initial benefit" group (approximately 5-10% of users) reported limited improvements during treatment making discontinuation effects irrelevant, typically explained by inadequate product quality with degraded or low-concentration GHK-Cu, inappropriate application technique reducing absorption, unrealistic expectations exceeding what any topical can achieve, severe underlying pathology requiring medical intervention beyond cosmetic peptides, or individual non-responsiveness to copper peptide treatment for genetic or physiological reasons
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