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Assessing the association between GLP-1 receptor agonist use and diabetic retinopathy through the FDA adverse event reporting system

As regulators, providers, and patients navigate these developments, Empower continues to be a leading voice helping shape the conversation around peptide therapy, quality standards, and regulatory policy

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Kothare PA, Soon DKW, Linnebjerg H, Park S, Chan C, Yeo A, et al

Potential concerns include: Counterfeit products Improper storage conditions Unknown ingredients Lack of medical supervision Incorrect dosage administration Increased risk of complications Patients should avoid self-administering injectable treatments and seek care from qualified medical professionals