It is not intended for human consumption, diagnostic, or therapeutic use
As we age, collagen levels naturally decline, leading to sagging and fine lines
It's crucial for individuals to discuss their medical history and any existing conditions with their healthcare provider before undergoing IV therapy to ensure safety and minimize risks
These cutting-edge therapies deliver powerful vitamins, minerals, and oxygen directly into your bloodstream, bypassing the digestive system for maximum absorption and immediate results
L., Carter, R
Sermorelin's FDA Journey: Approved, Discontinued, and Compounded Sermorelin acetate (Geref) was FDA-approved in 1997 for pediatric GHD 1 and in 1990 for diagnostic use.26 The manufacturer discontinued Geref in 2008 due to "manufacturing difficulties," not safety or efficacy concerns.12 In 2013, the FDA confirmed it wasn't withdrawn for safety/effectiveness, allowing for potential generic approvals.12 Currently, Sermorelin is primarily available as a compounded medication 3, which is permitted but not individually FDA-approved like mass-produced drugs.22 5.2
