In-depth guide

UPDATED FEB 2026

Ozempic, Wegovy & Mounjaro Lawsuits

Part of the Ozempic / GLP-1 investigation

The short answer

The GLP-1 MDL consolidates claims against both Novo Nordisk (Ozempic, Wegovy) and Eli Lilly (Mounjaro, Zepbound). All semaglutide and tirzepatide products are at issue.

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Which Drugs Are Included?

The MDL covers all GLP-1 receptor agonist drugs including: Ozempic (semaglutide injection for diabetes), Wegovy (semaglutide 2.4mg for weight loss), Rybelsus (oral semaglutide), Mounjaro (tirzepatide for diabetes), Zepbound (tirzepatide for weight loss), Trulicity (dulaglutide), and other GLP-1 agonists. The legal theories are the same regardless of which specific drug you used.

Novo Nordisk vs Eli Lilly

Novo Nordisk manufactures semaglutide products (Ozempic, Wegovy, Rybelsus). Eli Lilly manufactures tirzepatide products (Mounjaro, Zepbound). Both are defendants in MDL 3094. Combined 2024 GLP-1 revenue exceeded $40 billion. Both face identical failure-to-warn allegations.

Off-Label vs Approved Use

Many patients used Ozempic off-label for weight loss before Wegovy was approved. Off-label use does not bar legal claims — the failure-to-warn theory applies regardless of whether the drug was prescribed on-label (diabetes, approved weight loss) or off-label (weight loss using diabetes formulation). The key question is whether the manufacturer adequately warned about the risks.

The Two MDLs

GI injury claims (gastroparesis, bowel obstruction, pancreatitis) are in MDL 3094 (E.D. Pennsylvania). NAION vision-loss claims are in MDL 3163 (consolidated December 2025). If you have both GI and vision injuries, your attorney can file in both proceedings.

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