Injury guide

NAION

Updated Oct 6, 202617 sources

NAION is damage to the eye’s main nerve from poor blood flow. It usually causes sudden loss of sight in one eye.

What the public record says

These are cited sources. Their inclusion does not imply that they endorse People’s Justice or reviewed this page.

U.S. Food and Drug Administration · U.S. Department of Health and Human Services · Publisher of the quarterly list of potential signals of serious risks from its adverse event system (FAERS, now AEMS); page last updated March 31, 2025

“Non-arteritic anterior ischemic optic neuropathy (NAION) FDA is evaluating the need for regulatory action.”

FDA: Potential signals of serious risks, October to December 2024 (opens in a new tab) · Mar 31, 2025 · Checked Oct 5, 2026

U.S. District Court for the Eastern District of Pennsylvania · Federal trial court (Case Management Order No. 12) · Court handling MDL No. 3163; summary of the claims, not a ruling

“suffer from non-arteritic anterior ischemic optic neuropathy (NAION), a condition that results in sudden, permanent vision loss.”

E.D. Pa.: Case Management Order No. 12, MDL No. 3163 (July 2, 2026) (opens in a new tab) · Jul 2, 2026 · Checked Oct 5, 2026

The evidence and its limits

U.S. Food and Drug Administration · 2025

FDA quarterly list of potential signals of serious risks, October to December 2024 (entry: GLP-1 receptor agonists and NAION)

Design:
Agency review
Participants:
Reports to FDA’s adverse event system (FAERS, now called AEMS) for the GLP-1 receptor agonist drug class.
Finding:
FDA identified NAION as a potential signal of a serious risk and is evaluating the need for regulatory action (status as of March 6, 2025).
Main limitation
FDA says these signals are based wholly or in part on reports in its adverse event system, and FDA is still evaluating them. FDA says a listing does not mean it has concluded that the drug has the risk.

Read the source: FDA quarterly list of potential signals of serious risks, October to December 2024 (entry: GLP-1 receptor agonists and NAION) (opens in a new tab) · Checked Oct 5, 2026

The short answer

What is NAION?
NAION is damage to the optic nerve from poor blood flow. The optic nerve carries what the eye sees to the brain. NAION usually causes a sudden, painless loss of sight in one eye. [1]
What are the signs of NAION, and when should I see a doctor?
The main sign is a sudden loss of sight in one eye, often with no pain. Get emergency eye care for any sudden loss of sight, even if it comes back. Talk to your doctor before you stop or change any medicine. [2]
How do doctors diagnose NAION?
An eye doctor does a full eye exam. It checks how sharp your sight is, your side vision, your color vision and how your pupils react to light. The doctor also looks at the back of the eye. [3]
Which records show a NAION diagnosis?
Records from your eye doctor show the diagnosis. Exam notes list your sight scores, side vision test and pupil checks. Notes or pictures from the dilated exam can show a swollen optic nerve. [3]

What rules a case out

Not covered by this case

  • This page is not medical advice. Talk to your doctor before you stop or change any medicine.
  • It does not cover the stomach and bowel claims about GLP-1 drugs, which are a separate group of cases.

NAION is damage to the eye’s main nerve from poor blood flow. It usually causes sudden loss of sight in one eye. Here is how it is found and what the GLP-1 drug lawsuits claim.

What is NAION?

NAION is damage to the optic nerve from poor blood flow. The optic nerve carries what the eye sees to the brain. NAION usually causes a sudden, painless loss of sight in one eye.

NAION is short for non-arteritic anterior ischemic optic neuropathy. Ischemic means poor blood flow. Anterior means the damage is at the front of the nerve, at the spot doctors call the optic disc. Non-arteritic means it is not caused by arteritis, such as giant cell arteritis (also called temporal arteritis).

It mostly affects people in their 50s or older. The National Library of Medicine lists causes of this kind of nerve damage that include hardened arteries and diabetes.

MedlinePlus says poor blood flow is the most common cause of optic nerve atrophy, and that damage from optic nerve atrophy cannot be reversed.

What are the signs of NAION, and when should I see a doctor?

The main sign is a sudden loss of sight in one eye, often with no pain. Get emergency eye care for any sudden loss of sight, even if it comes back. Talk to your doctor before you stop or change any medicine.

MedlinePlus says to tell your eye doctor right away about any change in vision. The Ozempic label also tells patients to contact their doctor if their vision changes during treatment.

FDA has said that when a drug shows up on its list of possible risks under review, it is not telling patients to stop the drug.

How do doctors diagnose NAION?

An eye doctor does a full eye exam. It checks how sharp your sight is, your side vision, your color vision and how your pupils react to light. The doctor also looks at the back of the eye.

Drops widen the pupils so the doctor can see inside the eye. This is called a dilated eye exam. The doctor may also check the pressure in the eye.

In NAION, the front of the optic nerve is often swollen, with tiny spots of bleeding. Imaging tests may also be used.

Which records show a NAION diagnosis?

Records from your eye doctor show the diagnosis. Exam notes list your sight scores, side vision test and pupil checks. Notes or pictures from the dilated exam can show a swollen optic nerve.

Pharmacy and prescription records show which drug you took and when. The court in the NAION cases has asked for records that confirm proof of use and proof of diagnosis.

HHS says patients may get copies of their records, such as test results and images. A provider normally has up to 30 days to respond, and cannot refuse because you have not paid a bill.

What does research say about GLP-1 drugs and NAION?

FDA listed a “potential signal of a serious risk” of NAION for GLP-1 drugs like Ozempic. FDA says it “is evaluating the need for regulatory action” on it. A listing does not mean FDA found that the drugs cause NAION.

The listing was in FDA’s report for late 2024 and covered the whole group of GLP-1 drugs, such as Ozempic and Wegovy. FDA gave that status as of March 6, 2025. FDA says these signals are based wholly or in part on reports in its adverse event system. We did not find a later FDA update on it.

The Ozempic label revised in May 2026 does not warn about NAION, and FDA’s label database found no Ozempic label that mentions optic neuropathy. Its eye warning is about problems from diabetic eye disease.

We found no court ruling that GLP-1 drugs cause NAION. The court has set early steps on that question. Requests to keep out expert opinions, and requests to decide the cases without a trial, are due by July 2, 2027.

Who brings NAION claims in the GLP-1 drug cases?

People who took GLP-1 drugs and later lost sight from NAION bring these claims. They say drugs such as Ozempic, Wegovy, Saxenda and Trulicity caused it. Whether a person has a claim depends on their own records and facts.

In December 2025, the federal NAION cases were grouped before Judge Karen S. Marston in Pennsylvania. A panel of federal judges kept them as their own group, apart from the GLP-1 stomach and bowel cases, to make them easier to track. The same judge handles both groups.

In July 2026, the court ordered early work on two shared questions: whether the drugs can cause NAION, and whether federal drug-label rules block the claims about warnings.

Can a family member get records for someone with NAION?

Often, yes. A health care power of attorney lets someone make health care choices for an adult. That person can then get the records that go with that role. A court can also name a guardian.

If the person has died, the executor or administrator of the estate may get the records needed to handle it. A provider may also share some facts with a relative who was involved in the person’s care or in paying for it. State law decides who can act.

If a person with NAION has died of any cause, the wrongful death case page explains in general how those claims work.

Sources

  1. NLM MeSH: Optic neuropathy, ischemic
  2. MedlinePlus: Vision problems
  3. MedlinePlus: Optic nerve atrophy
  4. FDA: Potential signals of serious risks, October to December 2024
  5. JPML transfer order, GLP-1 RA NAION MDL No. 3163 (Dec. 15, 2025)
  6. E.D. Pa.: GLP-1 RA MDL No. 3163 court pageE.D. Pa.: GLP-1 RA MDL No. 3163 court page · court
  7. MedlinePlus: Optic nerve disordersMedlinePlus: Optic nerve disorders · regulator
  8. FDA: About potential signals of serious risksFDA: About potential signals of serious risks · regulator
  9. FDA: Ozempic prescribing information (revised May 2026)FDA: Ozempic prescribing information (revised May 2026) · regulator
  10. NEI: Get a dilated eye examNEI: Get a dilated eye exam · regulator
  11. E.D. Pa.: Case Management Order No. 12, MDL No. 3163 (July 2, 2026)E.D. Pa.: Case Management Order No. 12, MDL No. 3163 (July 2, 2026) · court
  12. HHS: Your right to access your health informationHHS: Your right to access your health information · regulator
  13. openFDA: Semaglutide label searchopenFDA: Semaglutide label search · regulator
  14. E.D. Pa.: Case Management Order No. 14, MDL No. 3163 (Aug. 27, 2026), copy on CourtListenerE.D. Pa.: Case Management Order No. 14, MDL No. 3163 (Aug. 27, 2026), copy on CourtListener · court
  15. HHS: Personal representatives under HIPAAHHS: Personal representatives under HIPAA · regulator
  16. HHS: Health information of deceased individualsHHS: Health information of deceased individuals · regulator
  17. eCFR: 45 CFR 164.502(g), personal representativeseCFR: 45 CFR 164.502(g), personal representatives · regulator

Checked against 17 primary sources by People's Justice editors · Updated

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