The FDA regulatory gap Under the Dietary Supplement Health and Education Act (DSHEA), supplements operate in a fundamentally different regulatory environment than pharmaceuticals
Off-Label Marketing Risk Manufacturers of GLP-1 medications may face regulatory scrutiny and legal risks if they promote their products for off-label use or disseminate inaccurate and misleading information
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Some participants discontinued treatment due to adverse effects, and approximately 1218% of trial participants dropped out, often due to side effects
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There is an increased risk of gall bladder disease with semaglutide and tirzepatide, and rapid weight loss is a contributor to that complication [18, 19]