Founding Partner
The World Health Organization (WHO) has issued a formal safety alert confirming that semaglutide medications, including Ozempic®, Wegovy®, and Rybelsus® are associated with a very rare but serious risk of permanent vision loss caused by non-arteritic anterior ischemic optic neuropathy (NAION). This announcement follows a detailed review by the European Medicines Agency (EMA) and WHO’s own Advisory Committee on Safety of Medicinal Products (ACSoMP).
NAION is a serious and irreversible eye condition that can result in sudden blindness. According to WHO, the risk is now supported by data from clinical trials, real-world case reports, post-marketing surveillance, and medical literature. Patients using semaglutide are now officially advised to discontinue treatment if NAION is diagnosed, and to immediately consult a doctor if any changes in vision occur during use.
This alert represents a pivotal moment in semaglutide safety oversight and opens the door for thousands of injured patients to pursue legal accountability for their vision loss.
Non-arteritic anterior ischemic optic neuropathy (NAION) is a form of optic nerve damage that occurs when blood flow to the optic nerve is interrupted. Unlike other types of vision loss, NAION typically develops suddenly and without pain, often noticed upon waking. It most commonly affects just one eye and causes a partial or complete loss of vision that is usually permanent.
Key facts about NAION:
Semaglutide is a GLP-1 receptor agonist, originally developed for treating type 2 diabetes and later expanded to manage obesity. It works by slowing gastric emptying and regulating insulin and appetite, but its full systemic effects are still under investigation. The vision loss warning is the latest—and one of the most serious—emerging safety signals.
In May 2025, the EMA’s Pharmacovigilance Risk Assessment Committee (PRAC) completed a comprehensive evaluation of the NAION risk and semaglutide. Their review included:
Based on this evidence, the EMA determined that NAION occurs at a frequency of up to 1 in 10,000 patients, classifying it as a “very rare” but serious side effect. As a result, the EMA ordered mandatory labeling updates for all semaglutide products, including new language in the Summary of Product Characteristics (SmPC) and patient Package Leaflet.
According to the EMA:
“Data from epidemiological studies indicate an increased risk for non-arteritic anterior ischaemic optic neuropathy (NAION) during treatment with semaglutide. There is no identified time interval for when NAION may develop following the start of treatment. A sudden loss of vision should lead to ophthalmological examination, and treatment with semaglutide should be discontinued if NAION is confirmed.”
WHO’s ACSoMP echoed these conclusions and recommended that the Risk Management Plan for semaglutide be formally updated to include NAION. This includes enhanced pharmacovigilance activities and safety warnings to inform healthcare providers and patients of this irreversible threat.
According to the WHO, the VigiBase global database has received reports of patients in multiple countries developing NAION after taking Ozempic, Wegovy, or Rybelsus. These case safety reports reflect real-world harm and highlight the global scale of the risk.
While the frequency is considered “very rare,” the sheer volume of semaglutide users worldwide—estimated in the tens of millions—means that thousands of individuals may face this vision risk. The WHO warning is designed to raise awareness among healthcare providers, pharmacists, and regulators worldwide.
If you are currently taking Ozempic, Wegovy, or Rybelsus, or recently stopped using one of these medications, it is critical to be aware of the following:
Parker Waichman LLP represents patients across the United States who have developed NAION, permanent vision loss, or blindness after using semaglutide drugs. The firm is actively filing lawsuits and investigating claims that manufacturers failed to adequately warn consumers about these risks.
“People trusted that these medications were safe for use,” said Jason Goldstein, Senior Litigation Counsel at Parker Waichman LLP. “This new EMA and WHO confirmation underscores what we have been seeing through our clients’ experiences—sudden, devastating loss of vision that changes lives forever.”
Lawsuits may seek compensation for:
If you or a loved one suffered sudden vision loss, NAION, or blindness after taking Ozempic, Wegovy, or Rybelsus, you may be eligible for financial compensation. The national legal team at Parker Waichman LLP is investigating these claims and fighting to hold drug manufacturers accountable for failing to warn patients about the irreversible risks associated with their products.
Call 1-800-YOUR-LAWYER (1-800-968-7529) now for a free consultation. You don’t have to go through this alone. Let our experienced attorneys help you understand your rights and take legal action to protect your future. Regardless of your location or where your injury occurred, our nationwide Ozempic NAION Vision Loss Law Firm is ready to assist you.
Parker Waichman LLP
Our law firm is ready to represent you in your injury case. We’ve helped many New York residents as well as those needing help nationwide. Contact our team for a free case consultation today.
We have the experience and the skilled litigators to win your case. Contact us and speak with a real attorney who can help you.
Parker Waichman LLP
6 Harbor Park Drive
Port Washington, NY 11050
Parker Waichman LLP
201 Old Country Road – Suite 145
Melville, NY 11747
Parker Waichman LLP
300 Cadman Plaza West
One Pierrepont Plaza, 12th Floor
Brooklyn, NY 11201
Parker Waichman LLP
27299 Riverview Center Boulevard, Suite 108
Bonita Springs, FL 34134
We handle mass torts cases nationwide. Please contact our office to learn more.