
The GLP-1 MDL had 1,685 pending actions.
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People are filing Mounjaro lawsuits after experiencing severe, unlisted gastrointestinal problems like gastroparesis, gastroenteritis and intestinal obstructions.
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Mounjaro™ is a type 2 diabetes drug created by Eli Lilly, which is also often used as a weight-loss aid. Mounjaro lawsuits have been filed across the country by people who allege serious health issues like gastroparesis (stomach paralysis). People harmed by Mounjaro may be eligible to file a lawsuit.
Mounjaro is a type 2 diabetes drug developed by Eli Lilly. The drug is taken once weekly through an injection. Patients start with a low dosage of 2.5 mg and increase at regular intervals under the supervision of their doctor. Mounjaro was approved by the U.S. Food and Drug Administration (FDA) in 2022.
The active ingredient in Mounjaro is tirzepatide. It simulates two separate types of hormones. This makes the drug both:
These two hormones help regulate blood sugar levels. They help the brain understand when to increase or decrease insulin production.
Mounjaro can make people feel full and decrease appetite, which sometimes results in weight loss. In this way, Mounjaro’s active ingredient, tirzepatide, is similar to semaglutide, the active ingredient in Ozempic®, Rybelsus® and Wegovy®.
Doctors and researchers are still unsure why semaglutide and tirzepatide are effective weight loss drugs, so research is ongoing.
Mounjaro, like Ozempic, isn’t approved by the FDA for weight loss. Using Mounjaro for weight loss is an off-label use and may come with safety risks.
Doctors sometimes prescribe medicine for a non-FDA approved purpose. This is called “off-label” use because it’s not specified on the insert inside the drug’s package. Off-label use might present additional risks not listed on the drug’s label.
In November 2023, the FDA approved Zepbound, another tirzepatide drug manufactured and sold by Eli Lilly. Eli Lilly created Zepbound to handle the growing off-label weight-loss use of Mounjaro.
Zepbound is nearly identical to Mounjaro, but with a different prescribed dosage of tirzepatide. However, it is specifically approved for weight loss, not diabetes management.
While all medicines come with warnings about potential side effects, many people are concerned about health issues that aren’t on Mounjaro’s warning label.
Many of these side effects are gastrointestinal problems:
Gastroparesis: This condition is sometimes referred to as “paralyzed stomach,” “stomach paralysis,” or “delayed gastric emptying.” It may cause a person’s stomach to slow or stop moving food through the digestive system. The delayed gastric emptying keeps food in the stomach, leading to potential complications. These complications include abdominal pain, acid reflux, nausea, vomiting and more. It may result in weight loss, malnutrition and severe dehydration.
Mounjaro’s label does warn users that it can cause severe gastrointestinal issues and isn’t recommended for people who have preexisting gastroparesis. But gastroparesis is not listed as a side effect on the warning label. These gastrointestinal conditions, which can severely impact a person’s life, are the basis of some personal injury lawsuits.
Other gastrointestinal issues have also been linked to GLP-1 drugs like Mounjaro. Chronic cyclical vomiting and intestinal obstructions are other serious Mounjaro side effects.
People are filing Mounjaro lawsuits against Eli Lilly. These lawsuits allege serious harm from using the type 2 diabetes drug. The plaintiffs say that they’ve suffered conditions such as gastroparesis and that Eli Lilly failed to warn users about these serious risks.
Mounjaro lawsuits include claims of:
Plaintiffs in a Mounjaro lawsuit may seek damages for:
The specific actions and damages of any Mounjaro lawsuit will depend on the facts of the case. Speaking with a Mounjaro lawyer can help you understand if you’re eligible to file a lawsuit against Eli Lilly.
Lawsuits against Eli Lilly for Mounjaro are currently being litigated in the U.S. District Court for the Eastern District of Pennsylvania as part of a larger multidistrict litigation (MDL). This MDL is known as In re: Glucagon-Like Peptide-1 Receptor Agonists (GLP-1 RAs) Products Liability Litigation, MDL No. 3094.
Plaintiffs who allege harm from taking GLP-1 RA drugs such as Ozempic, Rybelsus, Wegovy, Mounjaro and Trulicity have filed lawsuits as part of the MDL.
The purpose of an MDL is to help federal courts efficiently handle claims against similar defendants. Grouping clients together makes MDLs similar to class action lawsuits despite important differences:
If you or a loved one experienced an adverse side effect after taking Mounjaro, you may be eligible to sue Eli Lilly, the manufacturer of Mounjaro.
Call 1.800.768.4026 to contact attorneys Sara Couch and Jonathan Orent for more information or to discuss a potential Mounjaro claim.
If you’ve taken Mounjaro as directed by a doctor and experienced one or more digestive side effects, you may be eligible to file a Mounjaro lawsuit. Individuals who developed gastroparesis while using Mounjaro should consider speaking with an attorney to explore possible legal action against Eli Lilly.
People who may be eligible for a case include those who:
Determining eligibility for a Mounjaro lawsuit may be complicated. Speaking with an attorney who has experience handling medical drug claims can help you understand if you have a valid claim. An attorney can tell you what steps you need to take to file a Mounjaro suit.
If you’re eligible, a Mounjaro lawyer at Motley Rice can help you by:
The medical drug lawyers at Motley Rice have experience helping people navigate lawsuits for diabetes medications. Consider reaching out for a free consultation today.
04.02.25
The GLP-1 MDL had 1,685 pending actions.
02.03.25
By February 3, 2025, there were 1,443 pending actions in the MDL against GLP-1 drug manufacturers.
01.24.25
Drug manufacturers Novo Nordisk and Eli Lilly asked to dismiss almost all the non-gastrointestinal claims in the GLP-1 lawsuit. However, this doesn’t apply to any claims related to them not properly warning users of gastrointestinal issues. Their argument states that “Plaintiffs fail to translate these broad allegations into viable causes of action for fraud or breach of warranty.”
12.18.24
The FDA published a notice stating their concerns over people taking unapproved GLP-1 drugs. They noted that compounded drugs are not FDA-approved and explained their recommendations for using these types of drugs.
12.01.24
Deep vein thrombosis and blood clot cases will not be included as injuries in the GLP-1 RA MDL. People may still pursue these cases in other venues if they’ve experienced these injuries. Contact GLP-1 RA attorney Sara Couch or Jonathan Orent.
12.01.24
December 2024: 1,300 pending actions were in the MDL.
November 2024: Pending actions in the MDL grew to 1,221.
October 2024: The MDL had just under 1,100 pending cases.
August 2024: More than 346 cases were pending in the MDL.
April 2024: The number of pending actions in MDL 3094 grew to 74.
11.13.24
Patients accused Novo Nordisk and Eli Lilly of failing to warn them about the risks associated with Ozempic and other such medications. They filed a massive master complaint in the sprawling multidistrict litigation centralized in the Eastern District of Pennsylvania.
11.01.24
The warning labels on Ozempic, Wegovy, Rybelsus, Saxenda, Victoza, Mounjaro and Zepbound were updated to include pulmonary aspiration during general anesthesia or deep sedation.
10.02.24
On October 2, 2024, tirzepatide was removed from the FDA Drug Shortages List. Tirzepatide drugs, including Mounjaro, were on the list from December 2022 to October 2024. When a drug is on the shortages list, compounders may be able to make their own version of that drug, if they meet certain federal requirements. Removing tirzepatide from the list may impact availability for people who received the drug through compounding pharmacies. Note that drugs made by compounding pharmacies are not included in the federal MDL.
10.01.24
The FDA Adverse Events Reporting System (FAERS) showed 35,220 adverse events blamed on Mounjaro since 2022. That included 3,271 serious cases and, among those cases, 133 deaths.
05.01.24
Motley Rice attorneys Jonathan Orent and Sara Couch were appointed to key positions on the Plaintiffs’ Executive Committee in MDL 3094. They serve as co-lead counsel and chair of Marketing Discovery, respectively.
02.01.24
Multiple U.S. district courts consolidated similar lawsuits related to glucagon-like peptide-1 receptor agonists (GLP-1 RAs), like Mounjaro, into MDL 3094.
No, a Mounjaro class action lawsuit has not been filed as of February 2025, but a Mounjaro GLP-1 MDL has been created.
MDLs are similar to class action lawsuits in that multiple plaintiffs’ claims against specific defendants are consolidated before one court. However, unlike class actions, each plaintiff’s case in an MDL remains individually active. MDL cases can go to trial and any verdicts or settlements can be specific to the harm that each plaintiff has suffered. Class action awards are split between all plaintiffs.
The difference between Ozempic and Mounjaro is their active ingredient. Ozempic is a formulation of semaglutide, a GLP-1 receptor agonist, and is FDA-approved to reduce cardiovascular risks. Mounjaro is a formulation of tirzepatide, a GIP receptor and GLP-1 receptor agonist. They are both approved to help people with type 2 diabetes.
Ozempic and Mounjaro are both the subjects of ongoing litigation for injuries.
Read more about the risks of Ozempic.
The difference between Wegovy and Mounjaro is in their active ingredients. Wegovy, like Ozempic, uses the GLP-1 receptor agonist semaglutide. Mounjaro uses tirzepatide, which is both a GLP-1 receptor agonist and GIP receptor. Wegovy, unlike Mounjaro and Ozempic, has been approved for weight loss by the FDA.
Novo Nordisk, manufacturer of Wegovy and Ozempic, and Eli Lilly, manufacturer of Mounjaro, are defendants in personal injury lawsuits.
Our medical attorneys have represented thousands of patients seriously hurt by dangerous prescription and over-the-counter drugs. We understand that as a patient or family member, what you know about your or a loved one’s medications may be limited.
If you believe a medicine made you sick or hurt you, our attorneys have the resources needed to thoroughly investigate and:
Learn more about our law firm’s medical drug lawsuit experience here.
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. Ozempic, Wegovy, Mounjaro and Rybelsus remain approved by the U.S. Food and Drug Administration.
Read more important Mounjaro lawsuit updates
What is Mounjaro?
Health concerns over Mounjaro
Why are people filing lawsuits against Mounjaro?
Who can file a Mounjaro lawsuit?
How do I join a Mounjaro lawsuit?
Mounjaro lawsuits timeline
Frequently asked questions about Mounjaro lawsuits
Our medical drug litigation experience