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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
26.99
Lilly, Novo, Hims Get FDA Warnings About Misleading Drug Communications
22.22
Why the FDA Issued 30 Warning Letters to Telehealth Sites Marketing Compounded GLP-1s
28.10
The FDA has removed semaglutide injection products (GLP-1) from the shortage list, ending the temporary rule that allowed pharmacies to compound these medications, often used for weight loss. Compounded drugs are custom-made
20.96
Report: FDA must enforce rules on compounded GLP-1s
27.91
FDA alerts health care providers, compounders and patients of dosing errors associated with compounded injectable semaglutide products
28.14
September 15, 2025: Telehealth company must stop implying its compounded GLP-1 is FDA-approved, warns FDA – Partnership for Safe Medicines
27.95
