Injury guide

UPDATED FEB 2026

Ozempic Vision Loss (NAION)

Part of the Ozempic / GLP-1 investigation

The short answer

Studies show semaglutide users face 4-8x higher risk of NAION — sudden, painless, permanent vision loss. The EMA required European warnings in 2024, but U.S. labels still do not include a NAION warning.

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What Is NAION?

Non-arteritic anterior ischemic optic neuropathy (NAION) is caused by sudden loss of blood flow to the optic nerve, resulting in painless, often irreversible vision loss. It typically affects one eye at a time and can range from mild visual field loss to near-total blindness. NAION is the most common cause of sudden optic nerve-related vision loss in adults over 50.

The Semaglutide-NAION Connection

A July 2024 JAMA Ophthalmology study found semaglutide users had dramatically elevated NAION risk: 8.9% among diabetic patients (vs 1.8% non-semaglutide) and 6.7% among weight-loss patients (vs 0.8%). A Danish/Norwegian cohort study of 424,000+ patients confirmed that semaglutide more than doubled NAION risk compared to SGLT2 inhibitors.

The Failure-to-Warn Gap

The European Medicines Agency (EMA) required NAION warnings on European semaglutide labels in August 2024. Novo Nordisk has not added equivalent warnings to U.S. labels — creating a clear failure-to-warn argument. A separate NAION MDL (3163) was established in December 2025.

Legal Claims for NAION

NAION claims are among the highest-value claims in the GLP-1 litigation because vision loss is permanent and profoundly life-altering. Key evidence: ophthalmology records documenting NAION diagnosis, timeline showing diagnosis occurred during semaglutide use, and absence of other NAION risk factors.

Research & evidence

Scientific Evidence

cohort

Risk of Non-Arteritic Anterior Ischemic Optic Neuropathy in Patients Prescribed Semaglutide

Hathaway JT, Shah MP, Hathaway DB, et al. (2024). JAMA Ophthalmology

Key findings

  • Type 2 diabetes patients: 8.9% NAION risk on semaglutide vs 1.8% on non-semaglutide medications
  • Weight-loss patients: 6.7% NAION risk vs 0.8% on alternatives
  • Risk was highest in first year of use
  • Findings confirmed by Danish/Norwegian cohort study of 424,000+ patients
  • EMA required European label update; Novo Nordisk has not updated U.S. labels
cohort

Risk of Gastrointestinal Adverse Events Associated With GLP-1 Receptor Agonists for Weight Loss

Sodhi M, Rezaeianzadeh R, Kezouh A, Bhatt M (2023). JAMA

Key findings

  • Gastroparesis hazard ratio: 3.67 (95% CI 1.15-11.90)
  • Bowel obstruction hazard ratio: 4.22 (95% CI 1.02-17.40)
  • Pancreatitis hazard ratio: 9.09 (95% CI 1.25-66.00)
  • Study population was non-diabetic weight-loss patients — directly relevant to majority of MDL plaintiffs
  • Findings were robust across sensitivity analyses
meta-analysis

GLP-1 Receptor Agonists and Gallbladder Disease: A Systematic Review of Randomized Controlled Trials

Multiple authors (systematic review) (2024). Clinical Gastroenterology and Hepatology

Key findings

  • 37% increased relative risk of gallbladder disease across 76 RCTs
  • Risk was more pronounced with higher doses and greater weight loss
  • Rapid weight loss mechanism contributes to gallstone formation
  • Risk increased with duration of GLP-1 agonist use
  • Findings support inclusion of gallbladder disease in GLP-1 litigation claims

FAQ

Frequently Asked Questions

36 QUESTIONS

Over 3,100 lawsuits allege that Novo Nordisk (maker of Ozempic, Wegovy, Rybelsus) and Eli Lilly (maker of Mounjaro, Zepbound) failed to adequately warn patients and doctors about severe side effects including gastroparesis (stomach paralysis), bowel obstruction, pancreatitis, and vision loss (NAION). The cases are consolidated in MDL 3094 in the Eastern District of Pennsylvania.

Dive deeper

Related Guides

7 GUIDES

The full investigation

Part of the Ozempic / GLP-1 Investigation