Serious adverse events related to supplements should be reported to the FDA through the MedWatch program, and manufacturers are legally required to report serious adverse events to the FDA
Starting January 1, 2026 , several major insurance providers, including Blue Cross Blue Shield (BCBS), Cigna, Harvard Pilgrim, and UnitedHealthcare, will implement changes to their coverage of GLP-1 medications
Responding to an ET query, a Novo spokesperson said: "We strive to introduce the latest innovations here as early as possible
Nearly 7% of the overweight or obese patients taking semaglutide had NAION, compared to only 0.8% of patients who were not taking semaglutide
Increased sensitivity to sweet, sour and salty taste in some participants was reported after RYGB as well as vertical sleeve gastrectomy, although these appear to be more common in RYGB [8283]