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Zepbound® Lawsuit

Zepbound® users have experienced severe side effects and drug injuries. If you took the medication and suffered harm, you may be eligible for a Zepbound lawsuit.

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Case Overview

Zepbound® (tirzepatide) users have experienced severe gastrointestinal injuries and vision loss after using the GLP-1 medication. Those harmed are filing Zepbound lawsuits against the drug’s maker, Eli Lilly, for personal injuries and product liability. These cases have been divided into two separate federal multidistrict litigations (MDLs).

Important Zepbound lawsuit updates

  • August 2026: Zepbound MDL numbers rose. The gastrointestinal injury MDL added 80 cases since July, bringing the number of pending actions to 3,928. The vision loss MDL added 54 cases, bringing the number of pending actions to 200.
  • June 2026: Presiding Judge Karen Marston held a Science Day for the vision loss MDL. Both sides presented scientific evidence about GLP-1s and eye conditions. This will affect how evidence is presented once the trial begins. 
  • December 2025: The court separated gastrointestinal injury claims and vision loss claims to create two GLP-1 MDLs: MDL No. 3094 (gastrointestinal injuries) and MDL No. 3163 (vision loss). 

Key takeaways about Zepbound lawsuits

  • Zepbound is an FDA-approved injectable prescription medication used to treat overweight or obese adults.
  • Zepbound users have reported serious gastrointestinal health issues, including gastroparesis and gastroenteritis. Users also report severe eye conditions and vision loss. Despite disclosing some side effects, the drug’s manufacturer downplayed the severity of these risks.
  • Zepbound lawsuits are proceeding in two MDL dockets in federal courts. The MDLs include claims against Zepbound and its sister drugs, Mounjaro® and Trulicity®. Motley Rice attorneys are reviewing new claims.

What is Zepbound?

Zepbound is an injectable prescription medication made by the pharmaceutical company Eli Lilly. Its active ingredient is tirzepatide. The U.S. Food and Drug Administration (FDA) approved Zepbound in 2023 to treat obesity in adults. Patients must also have at least one weight-related condition, which can include high blood pressure, type 2 diabetes or high cholesterol.

Zepbound is a dual receptor agonist drug. It mimics the body’s glucose-dependent insulinotropic polypeptide (GIP) receptor and glucagon-like peptide-1 receptor agonists (GLP-1 RAs). It works by controlling insulin and blood sugar and slowing stomach emptying.

Why are people filing lawsuits against Zepbound?

People filing Zepbound lawsuits claim that tirzepatide side effects caused them severe injuries. The lawsuits address Eli Lilly’s product liability, claiming that the company knew or should have known about medication dangers but failed to warn healthcare providers and consumers.

In addition to Zepbound, GLP-1 litigation includes Eli Lilly’s Mounjaro® (also made with tirzepatide) and Trulicity® (dulaglutide). Lawsuits also name Ozempic®, Wegovy®, and Rybelsus®, all made by Novo Nordisk with the active ingredient semaglutide. They also name Novo Nordisk’s Saxenda® and Victoza® (liraglutide).

The allegations in these lawsuits include the following:

  • Breach of express and implied warranties claims: The drugs failed to perform safely as promised in product labeling and promotions.
  • Failure to warn claims: If doctors had been given adequate warnings, they would not have prescribed the drugs or would have monitored patients differently.
  • Negligent misrepresentation and fraud claims: Manufacturers intentionally downplayed severe drug side effects, claiming nausea and other symptoms as “minor” or “temporary” in marketing campaigns to drive profits.

What injuries are alleged in Zepbound lawsuits?

Several severe Zepbound side effects and drug injuries have been tied to using the medication, calling Zepbound’s safety into question. Many of these side effects were not listed or were not adequately listed on GLP-1 drug warning labels. 
 

Lawsuits allege that Zepbound and similar medications have caused plaintiffs to experience several side effects.

Vision injuries

  • Non-arteritic anterior ischemic optic neuropathy (NAION)
  • Optic nerve damage
  • Sudden or permanent vision loss

Read more: GLP-1 vision loss injuries and lawsuits ->

Gastrointestinal injuries

Other serious injuries and complications

  • Acute kidney injury and kidney failure
  • Biliary complications (problems or blockages in the liver, gallbladder and bile ducts)
  • Blood clots, deep vein thrombosis (DVT) and pulmonary embolism (PE)
  • Cholecystitis (swelling and irritation of the gallbladder)
  • Gallstones and increased gallbladder disease risk
  • Pancreatitis and pancreatic cancer
  • Severe dehydration and malnutrition
  • Thyroid C-cell tumors 

Contact a GLP-1 RA attorney

If you or a loved one has suffered from a serious side effect that wasn’t on the label of a GLP-1 RA drug, you may be eligible to file a lawsuit.

For more information, contact our team by filling out our online form or call 1.800.768.4026.

What is the status of Zepbound lawsuits in 2026?

One of the most significant Zepbound lawsuit updates for 2026 is the division of claims into two MDLs. The first, formed in 2024, consolidates claims over gastrointestinal injuries. This MDL, In re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAs) Products Liability Litigation, MDL No. 3094, had 3,928 pending actions as of August 2026.

The second, In re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAs) Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) Products Liability Litigation, MDL 3163, consolidates claims over NAION and vision loss. It was formed in December 2025 after the court divided these cases from the gastrointestinal injury and gastroparesis litigation. As of August 2026, it had 200 pending actions.

U.S. District Judge Karen S. Marston is presiding over both MDLs in the U.S. District Court for the Eastern District of Pennsylvania. The litigations are still in the discovery, motion and trial-planning phases. Motley Rice GLP-1 attorneys have lead roles in both MDLs.

Is there a Zepbound class action lawsuit?

There’s no Zepbound class action lawsuit. Instead, several claims regarding the GLP-1 drug have been consolidated into MDLs. 

Class actions and MDLs are both types of mass-tort lawsuits. MDLs temporarily consolidate cases to determine pre-trial matters, but each case in the MDL remains separate and receives its own ruling. With a class action, cases are consolidated into a class, represented by one or more plaintiffs. The case ruling applies to all members of the class.

Have there been Zepbound lawsuit settlements?

There are currently no Zepbound lawsuit settlements. Any potential Zepbound lawsuit settlement amounts will depend on the specifics of each individual case. In general, compensation may include pain and suffering, medical expenses and lost wages. 

Who may qualify to file a Zepbound lawsuit?

Whether or not you qualify for a Zepbound lawsuit will depend on your use of the drug, type of injury and medical history. To determine your eligibility, a Motley Rice Zepbound lawyer may consider the following evidence for a GLP-1 lawsuit:

  • Proof of Zepbound use: You’ll need evidence that your doctor prescribed Zepbound or another GLP-1 to you for an FDA-approved purpose. Typically, you’ll need to have taken the medication as directed for at least 30 days. 
  • Proof of injury: You’ll need medical records and objective diagnostic testing (such as blood tests, MRIs or CT scans) showing you have a GLP-1-related condition, such as gastroparesis or NAION. You’ll also need medical records documenting your side effects and symptoms. They’ll need to show that your health problem began while taking or shortly after stopping Zepbound. 
  • Proof of damages: You’ll need evidence that your drug injury resulted in surgery, hospitalization or other significant treatment, leading to pain and suffering, medical damages and lost wages from missed work. 

Having the above does not guarantee that you have a viable Zepbound claim. Lawsuit eligibility is determined on a case-by-case basis.

Zepbound lawsuit news and recent updates

08.03.26

GLP-1 MDLs continue to add new cases

MDL No. 3094 rose to 3,928 pending actions.

MDL No. 3163 rose to 200 pending actions.

06.02.26

Court holds Science Day in GLP-1 vision loss litigation

Judge Karen Marston held a Science Day in the vision loss MDL No. 3163. Lawyers and experts from both sides of the case were given the chance to educate the court about NAION, the available epidemiological studies, possible biological mechanisms and the regulatory history of GLP-1 drugs.

02.23.26

Judge names lead lawyers

Judge Marston officially appointed the leadership structure for the vision loss MDL No. 3163. She named Motley Rice’s Jonathan Orent as Co-Lead Counsel.Attorney Grace Chandler was also appointed to the Plaintiffs’ Executive Committee. 

12.04.25

The JPML creates vision loss MDL

The U.S. Judicial Panel on Multidistrict Litigation issued a transfer order separating GLP-1 vision loss claims from gastrointestinal injury claims. The order created MDL No. 3163. Judge Karen Marston will preside over both MDLs.

08.15.25

Judge orders gastric emptying studies

Judge Karen Marston ordered that any plaintiff filing a GLP-1 gastroparesis claim must prove their diagnosis with a properly performed gastric emptying study.

07.01.25

July report showed increase in MDL cases

The GLP-1 RA MDL now has 1,997 pending actions.

06.02.25

June MDL numbers grew

There are now 1,882 pending actions in the GLP-1 MDL.

05.30.25

FDA warned users of unapproved GLP-1 drugs

The FDA published a notice stating their concerns over unapproved GLP-1 medications used for weight loss. They advised patients to obtain a prescription from their doctor and fill that prescription at a state-licensed pharmacy. They also recommended patients visit the FDA BeSafeRx webpage for additional resources to safely buy prescription medications online.

05.01.25

MDL numbers increased leading into May

As of May 2, the GLP-1 MDL rose to 1,809 pending actions.

04.01.25

April report showed MDL case growth

The GLP-1 MDL now has 1,685 pending actions.

03.31.25

Zepbound adverse events reported

The FDA Adverse Event Reporting System (FAERS) reported 15,344 Zepbound adverse events since 2023. This included 730 serious cases and 16 deaths.

03.05.25

Judge halted production of compounded Zepbound

A federal judge issued a decision ruling that compounding pharmacies could no longer make and sell their own versions of Eli Lilly’s drugs Zepbound and Mounjaro.

03.03.25

MDL numbers grew leading into March

There are now 1,521 pending actions in the GLP-1 RA MDL.

02.03.25

February report showed increased MDL numbers

The GLP-1 MDL increased to 1,443 pending actions.

01.30.25

Tirzepatide linked to vision issues and eye conditions

A study published in JAMA Ophthalmology analyzed nine participants taking either semaglutide or tirzepatide drugs. The results of this small study showed that seven patients developed nonarteritic anterior ischemic optic neuropathy (NAION), one developed a stroke in the retina and one patient experienced swelling in both optic nerves.

01.24.25

Novo Nordisk and Eli Lilly tried to dismiss claims

Drug manufacturers Novo Nordisk and Eli Lilly filed a motion to dismiss almost all of the non-gastrointestinal claims in the GLP-1 MDL. This filing didn’t apply to any claims related to the manufacturers not properly warning patients of gastrointestinal issues. Novo Nordisk and Eli Lilly stated that “Plaintiffs fail to translate these broad allegations into viable causes of action for fraud or breach of warranty.”

01.02.25

January MDL numbers grew

As of January 2, there were 1,331 pending actions in the GLP-1 MDL.

12.20.24

Warning label updated to include new risk

The FDA has updated the Zepbound warning label to include information on the increased risk of developing pancreatitis for individuals who are taking Zepbound.

12.02.24

2024 GLP-1 RA MDL numbers

GLP-1 RA MDL pending actions increased dramatically throughout 2024 and are expected to grow into 2025.
December 2024: 1,300 pending actions
November 2024: 1,221 pending actions
October 2024: 1,090 pending actions
September 2024: 869 pending actions
August 2024: 346 pending actions
July 2024: 105 pending actions
June 2024: 101 pending actions
May 2024: 87 pending actions
April 2024: 74 pending actions
March 2024: 58 pending actions

12.01.24

DVT and blood clots not included as injuries in MDL

Deep vein thrombosis (DVT) and blood clot cases will not be included as injuries in In re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAS) Products Liability Litigation MDL No. 3094. Individuals may still pursue these cases in other venues if they’ve experienced these injuries. Contact GLP-1 RA Motley Rice attorneys Sara Couch or Jonathan Orent.

11.13.24

Plaintiffs filed master complaint in Pennsylvania

Plaintiffs filed a master complaint in the sprawling multidistrict litigation centralized in the Eastern District of Pennsylvania accusing manufacturers Novo Nordisk and Eli Lilly of failing to warn them about the various health risks associated with their medications, including Zepbound.

10.18.24

Zepbound warning label updated with new risk

The warning label on Zepbound and other medications like Ozempic, Wegovy, Rybelsus, Saxenda, Victoza and Mounjaro was updated to include a new warning regarding pulmonary aspiration during general anesthesia or deep sedation.

10.02.24

FDA removed Tirzepatide from drug shortages list

The FDA removed Tirzepatide from the drug shortages list, which may impact availability for patients who were receiving the drug through compounding pharmacies. Drugs made by compounding pharmacies aren’t included in the federal MDL.

05.01.24

Motley Rice attorneys appointed to MDL

Motley Rice attorney Jonathan Orent was named MDL No. 3094 Co-Lead Counsel, and Motley Rice attorney Sara Couch was named Chair of Marketing Discovery, Plaintiffs Executive Committee.

02.15.24

GLP-1 RA MDL is established

Zepbound lawsuits were consolidated with cases against similar drugs in MDL No. 3094, called In re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAS) Products Liability Litigation.

11.08.23

FDA approved Zepbound for weight management

The FDA approved Zepbound medication for chronic weight management in obese or overweight adults. The Zepbound injection should be used alongside a reduced calorie diet and increased amounts of physical exercise.

View Full Timeline

Frequently asked questions about Zepbound lawsuits

Can I file a lawsuit if I took Zepbound?

You may be eligible to file a Zepbound lawsuit if you have proof that you took the medication as prescribed and developed a related medical condition. You’ll need evidence, including diagnostic testing, medical records and proof of damages.

How long does a Zepbound lawsuit take?

There is no set timeline for how long a Zepbound lawsuit might take. The stages of an MDL include the discovery phase, pre-trial motions and negotiations. All of these can take time. The court’s schedule will also be a factor. However, you must file your claim before the statute of limitations in your state expires. These laws limit the time you have to take legal action.

Do I need a lawyer to file a Zepbound lawsuit?

You can legally file a Zepbound lawsuit on your own (pro se). But multidistrict litigation is complex, and working with a lawyer can benefit you in many ways. A Motley Rice Zepbound attorney could review your potential claim, help you gather evidence to support your case and litigate on your behalf.

Our GLP-1 and medical drug litigation experience

Motley Rice prescription drug and device attorneys have represented thousands of patients harmed by dangerous prescription and over-the-counter drugs. If you believe a diabetes or weight loss medication like Zepbound injured you or someone you love, our lawyers may be able to help.

Read more on our medical drug litigation experience

Do not stop taking a prescribed medication without first consulting with your doctor. Discontinuing a prescribed medication without your doctor’s advice can result in injury or death. Zepbound, Mounjaro, Trulicity, Ozempic, Rybelsus, Wegovy, Victoza and Saxenda remain approved by the U.S. Food and Drug Administration.

What is Zepbound?

Why are people filing lawsuits against Zepbound?

What injuries are alleged in Zepbound lawsuits?

What is the status of Zepbound lawsuits in 2026?

Who may qualify to file a Zepbound lawsuit?

Zepbound lawsuit news and recent updates

Frequently asked questions about Zepbound lawsuits

Our GLP-1 and medical drug litigation experience

About the Authors

Sources
  1. Australian Government, Department of Health and Aged Care. Inactive ingredients, the unsung players in medicine.
  2. Cleveland Clinic. GLP-1 Agonists. 
  3. Eli Lilly. What is Zepbound® (tirzepatide) injection?
  4. Eli Lilly. Zepbound Medication Guide.
  5. Fanshier A, Crews B, Garrett M, Johnson J. Tirzepatide: A Novel Glucose-Dependent Insulinotropic Polypeptide/Glucagon-Like Peptide 1 Receptor Agonist for the Treatment of Type 2 Diabetes: The First Twincretin. Clinical Diabetes. 2023 March: 41(3): 367-377.
  6. Harvard Health Publishing. GLP-1 diabetes and weight-loss drug side effects: “Ozempic face” and more.
  7. The Hill. Federal judge stops compounded copies of Eli Lilly weight loss, diabetes drugs.
  8. Judicial Panel on Multidistrict Litigation. Pending MDLs.
  9. Katz BJ, Lee MS, Lincoff NS. Ophthalmic complications associated with the antidiabetic drugs semaglutide and tirzepatide. JAMA Ophthalmol [Internet]. 2025 Jan 30.
  10. Law.com. Ozempic Defendants Seek to Shave 'Tacked On' Claims From MDL Complaint.
  11. Law.com. Ozempic MDL Plaintiffs Say Eli Lilly, Novo Nordisk Hid Risks.
  12. Mayo Clinic. Tirzepatide (Subcutaneous Route).
  13. Novo Nordisk. Ozempic.
  14. Ramírez-Mejía MM, Ponciano-Rodriguez G, Eslam M, Méndez-Sánchez N. GLP-1 receptor agonists and gallbladder disease risk: insights into molecular mechanisms and clinical implications. Ther Adv Endocrinol Metab. 2025 Dec 23;16
  15. Rodriguez P, Cartwright B, Gratzl S. Semaglutide vs Tirzepatide for Weight Loss in Adults with Overweight or Obesity. JAMA Internal Medicine. 2024 July: 2024.2525.
  16. Saxenda. Saxenda.
  17. ScienceDirect. Pulmonary Aspiration.
  18. Sodhi M, Rezaeianzadeh R, Kezouh A. Risk of Gastrointestinal Adverse Events Associated With Glucagon-Like Peptide-1 Receptor Agonists for Weight Loss. JAMA. 2023 Oct. 330(18):1795-1797.
  19. UC Health. FDA officials warn of fake weight loss drugs and ban compounded versions of popular medications.
  20. UC Health. What is Zepbound? Does this new weight loss drug work better than Wegovy and Ozempic? Will it cut costs?
  21. U.S. District Court Eastern District of Pennsylvania. IN RE: GLUCAGON-LIKE PEPTIDE-1 RECEPTOR AGONISTS (GLP-1 RAS) PRODUCTS LIABILITY LITIGATION.
  22. U.S. District Court for the Eastern District of Pennsylvania. MDL 3163 In Re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAs) Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) Products Liability Litigation.
  23. U.S. District Court for the Eastern District of Pennsylvania. MDL 3094 In Re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAS) Products Liability Litigation (GI Injuries).
  24. United States District Court, Eastern District of Pennsylvania. MDL 3094 In Re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAS) Products Liability Litigation.
  25. U.S. Food and Drug Administration. Drug Safety-related Labeling Changes (SrLC).
  26. U.S. Food and Drug Administration. FDA Adverse Events Reporting System (FAERS) Public Dashboard.
  27. U.S. Food and Drug Administration. FDA Approves New Medication for Chronic Weight Management.
  28. U.S. Food and Drug Administration. FDA clarifies policies for compounders as national GLP-1 supply begins to stabilize.
  29. U.S. Food and Drug Administration. FDA’s Concerns with Unapproved GLP-1 Drugs Used for Weight Loss.
  30. U.S. Judicial Panel on Multidistrict Litigation. MDL Statistics Report - Distribution of Pending MDL Dockets by Actions Pending. (07/01/2026).
  31. U.S. Judicial Panel on Multidistrict Litigation. MDL Statistics Report - Distribution of Pending MDL Dockets by Actions Pending. (08/03/2026). 
  32. U.S. Judicial Panel on Multidistrict Litigation. Pending MDLs.
  33. Wegovy. Wegovy Dosing Schedule.
  34. Zepbound. What is Zepbound.
  35. Zepbound. Your Weekly Zepbound Routine.
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