Our firm is about people. That is our motto and that will always be our reality.
We do our best to get to know our clients, understand their situations, and get them the compensation they deserve.
At TorHoerman Law, we believe that if we continue to focus on the people that we represent, and continue to be true to the people that we are – justice will always be served.
Without our team, we would’nt be able to provide our clients with anything close to the level of service they receive when they work with us.
The TorHoerman Law Team commits to the sincere belief that those injured by the misconduct of others, especially large corporate profit mongers, deserve justice for their injuries.
Our team is what has made TorHoerman Law a very special place since 2009.
Wegovy lawsuits are being filed against Novo Nordisk on behalf of individuals who developed serious gastrointestinal issues and/or vision damage.
Two federal multidistrict litigations have been established for injury claims involving GLP-1 drugs, one for gastrointestinal problems and one for vision loss (NAION).
Our lawyers are actively accepting new clients for the Wegovy injury lawsuits.
Wegovy lawsuit claims center on allegations that Novo Nordisk failed to adequately warn patients and prescribing physicians about serious risks linked to semaglutide.
Lawsuits filed in federal court allege injuries including gastroparesis, persistent vomiting, intestinal obstruction, ileus, other gastrointestinal complications, and NAION-related vision loss.
TorHoerman Law is reviewing claims from individuals who have been harmed by GLP-1 medications, including Wegovy.
Wegovy and other GLP-1 weight loss medications have become widely used, but federal lawsuits now allege that some patients were not adequately warned about serious gastrointestinal and vision-related injuries.
Plaintiffs claim that drug makers failed to provide sufficient warnings about gastrointestinal adverse events such as gastroparesis, ileus, intestinal obstruction, persistent vomiting, dehydration, and related complications.
Some claims and safety reviews also involve NAION, a rare optic nerve condition associated with sudden vision loss.
The potential risks at issue are especially serious because delayed gastric emptying can persist beyond ordinary nausea or short-term digestive discomfort.
People pursuing Wegovy claims may have required emergency care, hospitalization, diagnostic testing, specialist treatment, long-term dietary changes, or time away from work.
Federal GLP-1 injury lawsuits are being coordinated in multidistrict litigation, while individual claims remain tied to each person’s medication history, diagnosis, treatment, and damages.
Financial compensation may be available when the evidence supports a product liability claim.
Our legal team can review prescription records, medical history, diagnosis, and injury timeline to determine whether a Wegovy or GLP-1 claim may qualify.
If you or a loved one developed gastroparesis, intestinal blockage, persistent vomiting, severe gastrointestinal complications, or sudden vision loss after using Wegovy or another GLP-1 medication, you may be eligible to file a Wegovy lawsuit.
Contact TorHoerman Law today for a free consultation.
Use the chat feature on this page to find out if you qualify for the Wegovy lawsuit.
Wegovy is part of a drug class known as glucagon like peptide 1 receptor agonists, which affect appetite, insulin signaling, and stomach emptying.
The same delayed gastric emptying that helps some patients eat less is central to current lawsuits alleging severe gastrointestinal problems involving the digestive tract.
Wegovy prescribing information states that the drug delays gastric emptying, has been associated with gastrointestinal adverse events that are sometimes severe, and is not recommended for patients with severe gastroparesis.
Researchers found that GLP-1 agonists used for weight loss were associated with increased risks of pancreatitis, gastroparesis, and bowel obstruction compared with bupropion-naltrexone, although that study should be understood as observational rather than definitive proof of causation.
Clinical trials and prescribing information also identify common gastrointestinal reactions such as nausea, vomiting, diarrhea, constipation, abdominal pain, bloating, and related symptoms.
Federal lawsuits allege that drug makers failed to adequately warn patients and physicians about the severity and persistence of these risks.

Serious injuries and symptoms discussed in Wegovy and GLP-1 litigation may include:
These allegations do not mean every patient who used Wegovy has a claim.
A potential lawsuit usually depends on prescription history, dose timing, symptom onset, diagnosis, medical testing, hospitalization, prior gastrointestinal history, and damages.
People with severe or persistent symptoms should seek medical care rather than stopping or changing medication without professional guidance.
TorHoerman Law can review whether the medical records and treatment timeline support a Wegovy or GLP-1 injury claim.
Wegovy lawsuits allege that semaglutide and other GLP 1 receptor agonists can cause or contribute to severe gastrointestinal injuries in some users, including gastroparesis, ileus, intestinal obstruction, persistent vomiting, dehydration, and malnutrition.
Gastroparesis occurs when the stomach muscles do not move food normally through the digestive tract, which can cause nausea, vomiting, bloating, abdominal pain, early fullness, and difficulty keeping food down.
Wegovy prescribing information states that the drug delays gastric emptying, has been associated with gastrointestinal adverse reactions that are sometimes severe, and is not recommended in patients with severe gastroparesis.
Researchers have reported an association between GLP-1 drugs used for weight loss and increased risk of gastroparesis, bowel obstruction, and pancreatitis, although the study was observational and does not by itself prove causation.

Plaintiffs allege that many patients were not adequately warned that delayed gastric emptying could become severe, prolonged, or medically disruptive.
Some recent safety reviews have also examined whether Wegovy linked risks may include NAION, a rare optic nerve condition that can cause sudden vision loss; in 2025, the European Medicines Agency concluded that NAION is a very rare side effect of semaglutide medicines.
The main federal Wegovy litigation remains focused on gastrointestinal injuries, while NAION-related allegations should be evaluated separately based on medical records, diagnosis, timing, and prescribing history.
Patients with persistent vomiting, severe abdominal pain, dehydration, inability to tolerate food, bowel-obstruction symptoms, or sudden vision changes should seek medical care promptly.
Recent safety reviews have examined whether semaglutide medicines, including Wegovy, may be associated with non-arteritic anterior ischemic optic neuropathy, or NAION.
NAION involves reduced blood flow to the optic nerve and can cause sudden, painless vision loss in one eye.
In 2025, the European Medicines Agency recommended updating semaglutide product information to include NAION as a very rare side effect.

This issue should be evaluated separately from the gastrointestinal injury claims centralized in MDL No. 3094 because the medical evidence, injury pattern, and claim criteria may differ.
Wegovy users who experienced sudden vision changes or lost vision should seek medical care promptly and preserve prescription records, ophthalmology records, diagnostic testing, and treatment history.
Wegovy lawsuits involve allegations that Novo Nordisk failed to adequately warn about serious gastrointestinal disorders linked to semaglutide use. Federal GLP-1 injury cases are centralized in MDL No. 3094 in the Eastern District of Pennsylvania and include claims involving Wegovy, Ozempic, Rybelsus, Trulicity, and Mounjaro.
Wegovy prescribing information states that the drug delays gastric emptying and has been associated with gastrointestinal adverse reactions that are sometimes severe.
Wegovy gastroparesis claims focus on whether delayed gastric emptying progressed into severe or persistent injury, including stomach paralysis, chronic vomiting, ileus, or bowel obstruction.
Scientific studies have reported associations between GLP-1 drugs used for weight loss and increased rates of gastroparesis, bowel obstruction, and pancreatitis, though each claim still depends on individual medical proof.
There is not a Wegovy class action lawsuit: each person’s claim remains tied to their prescription history, diagnosis, treatment course, and damages.
Vision-loss claims involving NAION are also being reviewed, but those injuries should be evaluated separately from the gastrointestinal claims in the federal MDL.

Current Wegovy lawsuit allegations may involve:
No Wegovy settlement has been reached, and there is no confirmed average settlement amount for Wegovy claims at this stage.
Lawyers involved in these cases estimate that GLP-1 lawsuit settlement amounts may range from $50,000 to over $700,000, depending on injury severity, medical evidence, and the impact on the person’s life.
These figures are projections, not guaranteed outcomes, and are based on how similar dangerous drug lawsuits have been valued in prior mass tort litigation.
Wegovy claims involving hospitalization, long-term gastroparesis, intestinal obstruction, persistent vomiting, malnutrition, future medical care, or permanent impairment may be valued differently than claims involving shorter-term symptoms.
Settlement value may also depend on prescription history, diagnosis, treatment records, causation evidence, lost income, and available damages.
Any future Wegovy settlement would be evaluated based on the specific facts of each claim, not a fixed payout schedule.
No, there is not a class action lawsuit for injuries and health problems associated with the use of Ozempic and Wegovy or other weight loss drugs.
Lawsuits for both Ozempic and Wegovy, as well as other semaglutide drugs, are being consolidated into a single federal court under a process known as multidistrict litigation (MDL).
The Judicial Panel on Multidistrict Litigation (JPML) certified the establishment of the Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAS) Products Liability Litigation (MDL 3094) in the US District Court for the Eastern District of Pennsylvania.
The MDL involves personal injury actions stemming from GLP-1 RAs, including Novo Nordisk drugs Ozempic, Wegovy, and Rybelsus, and Eli Lilly drugs Trulicity and Mounjaro.
MDL and class action are separate and distinct legal processes.
The litigation provides an avenue for those with Wegovy and Ozempic Lawsuits to seek compensation in an organized and unified manner.
Within an MDL, your case remains individual and in the event of a settlement, a successful claim would be compensated according to the unique facts and circumstances of the case.
This is different from class action lawsuits, where claims are combined together into one legal action and the relief is generally determined on a classwide basis, subject to the structure of the class action.
The GLP-1 gastrointestinal injury MDL includes claims involving Novo Nordisk and Eli Lilly products.
Novo Nordisk manufactures Ozempic, Wegovy, and Rybelsus.
Eli Lilly manufactures Trulicity and Mounjaro.
Plaintiffs allege that these manufacturers failed to adequately warn about severe gastrointestinal risks, including gastroparesis, ileus, intestinal obstruction, pseudo-obstruction, and related injuries.
People who used Wegovy, or similar GLP-1 medications and later developed serious gastrointestinal injuries may have a potential claim, depending on diagnosis, timing, medical history, warning information, and other facts.
Lawsuits are now being filed on behalf of those who have developed severe gastroparesis and other serious injuries from taking Ozempic, Wegovy, and other GLP 1 RA medications.

If you were prescribed Wegovy or other semaglutide drugs and developed stomach paralysis, intestinal blockage, or other conditions affecting gastric emptying, you may be eligible to file a Wegovy Lawsuit.
Contact our lawyers today for a free consultation.
You can also use the chatbot on this page for a free case evaluation.
Lawyers will help their clients throughout the legal process, assisting them with gathering and retaining crucial evidence and assessing their damages.
Evidence is important because a Wegovy claim must connect medication use, timing, diagnosis, injury severity, and damages.
It is essential that patients who have used these drugs retain any related medical documentation and further evidence to support their claims.
This is a part of the legal process you can begin on your own, but an experienced lawyer will help you gather and retain evidence.

Possible evidence in a Wegovy Lawsuit may include:
This evidence can help build a strong case by demonstrating the direct connection between Wegovy use and the adverse health outcomes experienced by the patient
Damages are the losses allegedly caused by the injury. In Wegovy claims, damages depend on diagnosis, treatment, symptom duration, hospitalization, work impact, and long-term medical needs.
Your lawyer will help you to assess and calculate damages.

Possible damages in a Wegovy Lawsuit may include:
TorHoerman Law is reviewing claims involving Wegovy and other GLP-1 medications where users developed gastroparesis, intestinal obstruction, persistent vomiting, severe gastrointestinal complications, or NAION-related vision loss.
Our national law firm can evaluate prescription history, diagnosis, treatment records, hospitalization history, and the timeline between medication use and injury.

A Wegovy lawyer from TorHoerman Law can explain whether the facts may support a product liability claim and what evidence may be needed.
Contact TorHoerman Law today for a free case review.
Use the chat feature on this page to find out if you qualify for the Wegovy lawsuit.
Wegovy was developed specifically for non-diabetic patients who were seeking a long term weight management solution.
Wegovy regulates appetite by mimicking the GLP-1 hormone, which increases insulin secretion, slows gastric emptying, and reduces appetite, helping individuals to feel fuller longer and eat less.
This mechanism helps regulate blood sugar levels and reduce body weight effectively.
According to health insurance claim records, Wegovy and other similar drugs are some of the most highly prescribed drugs in the country as of late.
Wegovy has been associated with serious gastrointestinal complications, including stomach paralysis and intestinal obstruction, leading to numerous reports of these issues to the FDA.
A study published in the Journal of the American Medical Association found that users of semaglutide, the active ingredient in Wegovy, face a threefold increased risk of stomach paralysis compared to those using oral weight loss drugs.
The FDA updated warning labels for these drugs due to the fact that a statistically significant number of patients developed severe gastroparesis and intestinal blockage (ileus).
Potential health problems linked to these two drugs, as well as other GLP 1 drugs, include:
Individuals who have used Wegovy and subsequently developed severe gastrointestinal issues, such as gastroparesis or intestinal blockages, may be eligible to file a lawsuit.
These lawsuits allege that the manufacturers, Novo Nordisk and Eli Lilly, failed to adequately warn users about the severe risks associated with their medications.
If you or a loved one have suffered from these side effects, consulting with a lawyer can help determine your eligibility to file a claim.
Wegovy prescribing information warns about several serious risks and adverse reactions associated with semaglutide use.
The label includes a boxed warning regarding thyroid C-cell tumors based on rodent studies and states that Wegovy should not be used in patients with a personal or family history of medullary thyroid carcinoma or MEN 2.
Other warnings involve severe gastrointestinal adverse reactions, delayed gastric emptying, pancreatitis, gallbladder problems, acute kidney injury related to dehydration, increased heart rate, hypoglycemia when used with certain diabetes medications, and suicidal behavior or thinking.
The label also states that Wegovy is not recommended in patients already diagnosed with severe gastroparesis.
Commonly reported side effects in clinical trials included nausea, vomiting, diarrhea, constipation, abdominal pain, headache, fatigue, dizziness, bloating, belching, hair loss, and dry mouth.
Wegovy is administered at a higher dose of semaglutide compared to Ozempic, with the maximum dose of Wegovy being 2.4 mg per week, while Ozempic’s maximum dose is 1.0 mg per week.
Wegovy and Ozempic both contain the active ingredient semaglutide, but Wegovy is specifically approved for chronic weight management, while Ozempic is approved for the treatment of type 2 diabetes.
Both Wegovy and Ozempic are glucagon-like peptide-1 (GLP-1) receptor agonists, but the key differences lie in their approved uses, dosing regimens, and concentrations of semaglutide.
Clinical trials have shown that approximately 44% of Wegovy users reported nausea, compared to 20% of Ozempic users, indicating a higher incidence of gastrointestinal side effects with Wegovy.
Wegovy has been linked to an increased risk of vision problems, specifically non-arteritic anterior ischemic optic neuropathy (NAION), which can lead to sudden vision loss due to reduced blood flow to the optic nerve.
Recent studies suggest that Wegovy users are 4 to 7 times more likely to develop NAION compared to non-users.
Owner & Attorney - TorHoerman Law
Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
Since 2009, we have successfully collected over $4 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?
At TorHoerman Law, we believe that if we continue to focus on the people that we represent, and continue to be true to the people that we are – justice will always be served.
Do you believe you’re entitled to compensation?
Use our Instant Case Evaluator to find out in as little as 60 seconds!
In this case, we obtained a verdict of $495 Million for our client’s child who was diagnosed with Necrotizing Enterocolitis after consuming baby formula manufactured by Abbott Laboratories.
In this case, we were able to successfully recover $20 Million for our client after they suffered a Toxic Tort Injury due to chemical exposure.
In this case, we were able to successfully recover $103.8 Million for our client after they suffered a COX-2 Inhibitors Injury.
In this case, we were able to successfully recover $4 Million for our client after they suffered a Traumatic Brain Injury while at daycare.
In this case, we were able to successfully recover $2.8 Million for our client after they suffered an injury due to a Defective Heart Device.
Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
Since 2009, we have successfully collected over $4 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?