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FDA Drug Recalls and Warnings: Illegal GLP-1 Sales and Misleading Marketing by Novo Nordisk and Eli Lilly
21.27
The FDA has sent 30 warning letters to telehealth companies for falsely marketing compounded GLP-1s, which are not FDA-approved and can pose risks to patients. FULL STORY:🔗https://tinyurl.com/3ztf9uj2
28.32
FDA Escalates Enforcement Against Compounded GLP-1 Marketing
21.31
FDA warns against compounded GLP-1 medications
28.09
The FDA has issued warning letters to multiple companies marketing compounded Retatrutide, an investigational drug from Eli Lilly still in Phase II trials. While early studies have shown promising weight-loss results, Retatrutide
23.67
FDA Sends 30 Warning Letters To Continue Clampdown on Compounded GLP-1s
25.13
Congress Introduces SAFE Drugs Act of 2025, Expanding FDA Oversight of Compounded GLP-1 Drugs and Telehealth Providers
23.32
02105-1/asset/8468e457-0c7f-4e4c-9b6d-2202dbefa9cb/main.assets/gr1_lrg.jpg "GLP-1 receptor agonists and next-generation incretin-based medications: metabolic, cardiovascular, and renal benefits")
