What to Know About GLP-1 Medications and Weight Management Programs
Learn how Eden connects patients to licensed providers to explore GLP-1 medications as part of medical weight management programs.
Learn how semaglutide salt differs from FDA-approved GLP-1 meds. Understand the safety, risks, and why consulting a licensed provider matters.
Eden is a digital platform that connects individuals with licensed healthcare providers. Eden does not manufacture or dispense medications.
As interest in GLP-1 medications continues to grow, licensed healthcare providers and patients may encounter lesser-known versions of semaglutide, such as semaglutide sodium or semaglutide acetate—commonly referred to as semaglutide salt forms. These versions are not used in any FDA-approved semaglutide medication and have drawn attention from regulators due to questions around quality, safety, and oversight.
This guide explains how semaglutide salt differs from the FDA-approved base form and why it’s important to speak with a licensed healthcare provider before starting any GLP-1 therapy.
Semaglutide is a prescription medication in the GLP-1 receptor agonist class. It mimics a naturally occurring hormone that may help:
These effects, when delivered through FDA-approved formulations, have been clinically studied to support metabolic health in individuals with certain conditions.
FDA-approved semaglutide medications include:
For a peer-reviewed summary of semaglutide’s therapeutic uses, see: Semaglutide in type 2 diabetes care (PubMed).
These medications are only available by prescription and should be used under the supervision of a licensed healthcare provider.
Semaglutide salt refers to chemically modified forms of semaglutide combined with other compounds such as sodium or acetate. These salt versions:
⚠️ FDA Safety Note: In 2023, the FDA publicly warned that semaglutide sodium and semaglutide acetate have been listed by the FDA as not eligible for compounding exemptions under Section 503A of the FDCA. The agency emphasized that unapproved forms may pose risks due to uncertain quality, identity, and potency.
When prescribed by a licensed provider in its FDA-approved form, semaglutide may cause:
Each FDA-approved formulation also includes specific formulation technologies (e.g., SNAC in Rybelsus®), which may enhance bioavailability and maintain therapeutic effects.
When prescribed by a licensed provider in its FDA-approved form, semaglutide may cause:
Less common but serious side effects may include:
These effects have been observed in FDA-reviewed clinical trials of the semaglutide base form, such as those submitted for Ozempic®, Wegovy®, and Rybelsus®.
There are no published clinical trials evaluating the safety profile of semaglutide salt forms in humans.
Ongoing GLP-1 research explores:
To date, there are no published human clinical trials validating the safety or effectiveness of semaglutide salt forms (such as sodium or acetate).
Before starting GLP-1 therapy, consider asking:
Ozempic®, Wegovy®, and Rybelsus® are registered trademarks of Novo Nordisk A/S. This content is for educational purposes only and is not affiliated with or endorsed by Novo Nordisk.
Disclaimer: The FDA does not approve compounded medications for safety, quality, or manufacturing. Prescriptions and a medical evaluation are required for certain products. The information provided on this blog is for general informational purposes only. It is not intended as a substitute for professional advice from a qualified healthcare professional and should not be relied upon as personal health advice. The information contained in this blog is not meant to diagnose, treat, cure, or prevent any disease. Readers are advised to consult with a qualified healthcare professional for any medical concerns, including side effects. Use of this blog's information is at your own risk. The blog owner is not responsible for any adverse effects or consequences resulting from the use of any suggestions or information provided in this blog.