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.
Victoza lawsuit claims center on allegations that the diabetes medication liraglutide, part of the GLP-1 receptor agonist class, is associated with serious and potentially life-altering complications.
Current litigation involving GLP-1 medications focuses primarily on severe gastrointestinal injuries, including gastroparesis, ileus, and intestinal obstruction, as well as emerging reports of possible vision loss in certain patients.
TorHoerman Law is reviewing claims involving Victoza and other GLP-1 drugs for individuals who experienced significant medical complications after use.
Victoza is a prescription diabetes drug manufactured by Novo Nordisk that belongs to a class of medications known as GLP-1 receptor agonists.
It works by helping regulate blood sugar levels through increased insulin release and slowed gastric emptying, and it is administered as a once-daily injectable medication.
Many patients taking Victoza report gastrointestinal side effects, and some claims allege that serious complications may develop after prolonged use.
Reported injuries linked to Victoza’s health risks include severe abdominal pain, gastroparesis, intestinal obstruction, and other conditions involving impaired digestive function.
Emerging investigations involving GLP-1 drugs also include allegations of vision loss in certain patients, including serious optic nerve injuries.
In earlier years, legal investigations involving Victoza primarily centered on acute pancreatitis and allegations of pancreatic and thyroid cancer.
Some lawsuits have alleged Novo Nordisk failed to warn patients and doctors about the full scope of Victoza’s health risks and potential risks associated with the drug’s mechanism of action.
Today, lawyers are investigating Victoza alongside Ozempic, Wegovy, Saxenda, Trulicity, and other GLP-1 medications based on the broader pattern of gastrointestinal injury claims now driving GLP-1 litigation.
If you or a loved one experienced severe gastrointestinal complications, persistent abdominal pain, vision changes, acute pancreatitis, or other serious medical problems after taking Victoza, you may be entitled to pursue compensation.
Contact TorHoerman Law for a free consultation to understand your legal options.
You can also use the chat feature on this page to find out if you qualify for the Victoza lawsuit.
TorHoerman Law is no longer accepting clients for this litigation.
Victoza is a GLP-1 receptor agonist prescribed to help manage type 2 diabetes by stimulating insulin production and reducing glucagon levels after meals.
It is administered by injection and is designed to support blood sugar control, but the drug’s effects on gastric emptying and digestive function have become central to modern safety concerns.
Many Victoza users report nausea, vomiting, constipation, and other gastrointestinal issues, but lawsuits focus on allegations that some patients developed far more severe complications than routine digestive discomfort.
Current claims allege that the side effects of Victoza may include serious gastrointestinal motility disorders that can lead to emergency hospitalization, surgical intervention, or long-term impairment.
In many cases, plaintiffs claim they suffered injuries after prolonged use, and that these outcomes were not properly disclosed through adequate warnings.
While Victoza was historically associated with concerns involving acute pancreatitis and pancreatic cancer risks, litigation now increasingly treats it as part of the broader GLP-1 drug category facing scrutiny across multiple products.
Plaintiffs allege that manufacturers understood the drug’s potential side effects but failed to provide clear and direct warning language about the severity of certain complications.
These lawsuits have expanded into state and federal courts as more patients report similar patterns of injury and medical diagnosis after use.

Current allegations in the GLP-1 litigation commonly involve claims that:
These allegations are not limited to Victoza, but Victoza has become part of this broader litigation because its mechanism of action overlaps with other GLP-1 medications now facing coordinated claims.
Plaintiffs argue that the same physiological effect that improves blood sugar control, delayed digestion, may also contribute to severe medical events in vulnerable patients.
Some lawsuits also claim that doctors and patients would have made different prescribing decisions if stronger warnings had been provided earlier.
As more medical records are reviewed, attorneys continue investigating whether there is a consistent pattern linking Victoza to serious gastrointestinal injury outcomes.
TorHoerman Law is reviewing claims involving Victoza users who suffered injuries after using the drug and is evaluating whether the manufacturer provided adequate warnings regarding these risks.
There are still legal claims and some lawsuits related to Victoza and pancreatic cancer or pancreatitis, but the landscape has changed over time and is not dominated by a single active “pancreatic cancer lawsuit” MDL as it once was.
Earlier litigation involving Victoza and other incretin mimetics included claims that the drug was linked to pancreatic cancer, pancreatitis, and other serious conditions, and some of these claims were consolidated in federal court, though many were dismissed or resolved years ago.
Regulatory and scientific evidence has not established a definitive causal link between Victoza and pancreatic cancer in humans, and newer clinical analyses generally do not confirm a strong association, though some plaintiffs’ attorneys continue to pursue individual claims.
Victoza’s prescribing information does include warnings about pancreatitis, and regulatory updates have focused on monitoring and communication rather than definitive cancer causation findings.

Victoza also carries a black box warning for the risk of thyroid C-cell tumors based on animal studies, and while the development of medullary thyroid carcinoma in humans remains uncertain, this risk factor continues to be part of safety discussions.
Other serious adverse effects such as gallbladder disease are recognized in clinical trials but are not typically central to cancer litigation.
Some plaintiffs’ firms still review and file individual cases in state and federal courts for patients who developed pancreatic cancer, acute pancreatitis, or other serious health issues following Victoza use, but these are generally pursued outside of a large centralized pancreatic cancer MDL at this time.
While no settlements specific to Victoza injury claims have been finalized, projected compensation figures can be informed by settlement estimates in litigation involving other diabetes medications in the GLP-1 class.
Projected settlement amounts range from approximately $50,000 for less severe injuries to over $700,000 for more serious and long-term medical complications, depending on documented harm and evidence of impact on quality of life.
These projected figures reflect how large-scale pharmaceutical injury claims have been valued in multidistrict litigation contexts, and they provide a framework for understanding what Victoza claimants might pursue.
The ultimate value of any individual settlement will depend on factors such as the extent of injuries, medical costs, lost income, and the strength of evidence linking the injury to medication use.

Projected settlement range examples from comparable GLP-1 litigation:
These projections are estimates, not guarantees, and actual outcomes for Victoza injury claims will vary based on individual case details.
An experienced attorney can evaluate your specific circumstances to estimate a potential settlement range tailored to your injuries and evidence.
GLP-1 weight loss and diabetes drugs have become the subject of growing legal scrutiny as researchers and regulators continue evaluating whether these medications may carry an increased risk of serious adverse health outcomes in certain patients.
Victoza, a GLP-1 receptor agonist manufactured by Novo Nordisk, has remained part of this discussion due to its long history of safety monitoring and reported complications.
Ongoing litigation has led to more explicit warnings regarding pancreatitis, thyroid C-cell tumors, and gallbladder disease on Victoza’s label.
The FDA required a black box warning on the drug’s label due to the risk of thyroid tumors in animal studies, and this warning continues to shape how the drug is prescribed and monitored.
Patients taking Victoza have reported a higher incidence of pancreatitis compared to those using other diabetes medications, raising concerns about whether some patients face heightened pancreatic injury risks.

As litigation has expanded to include a broader range of GLP-1 products, plaintiffs and medical experts have increasingly focused on gastrointestinal motility disorders and other complications that may involve long-term impairment.
Patients are advised to discuss severe abdominal pain, persistent vomiting, or rapid changes in vision with their healthcare provider immediately, as these symptoms may signal potentially serious medical conditions.
While research continues and causation remains disputed in court, these reported injuries have become central to why GLP-1 drugs are now being investigated in coordinated litigation nationwide.
Gastroparesis, sometimes described as stomach paralysis, is one of the most serious gastrointestinal injuries alleged in GLP-1 drug litigation.
This condition occurs when the stomach’s normal muscle contractions slow or stop, preventing food from moving through the digestive tract properly.
Plaintiffs in GLP-1 lawsuits claim that delayed gastric emptying, a known pharmacological effect of these medications, may contribute to severe digestive dysfunction in certain patients.
In some cases, individuals report persistent nausea, vomiting, malnutrition, and dehydration that require hospitalization or surgical intervention.
These complications often become life-altering when symptoms do not resolve after the medication is discontinued.

Common gastrointestinal injuries alleged in GLP-1 litigation include:
Vision loss has emerged as a separate and serious area of concern in GLP-1 drug litigation, distinct from claims involving gastrointestinal injuries.
Certain observational studies and post-market safety reviews have examined a potential association between GLP-1 medications and non-arteritic anterior ischemic optic neuropathy, commonly referred to as NAION.
NAION is a condition involving reduced blood flow to the optic nerve and can result in sudden, permanent vision loss in one or both eyes.
While causation has not been definitively established, researchers have noted patterns that warrant further investigation, particularly in patients with underlying risk factors.

As a result, lawsuits alleging vision loss linked to GLP-1 drugs have begun to proceed on a separate legal track from the gastrointestinal litigation.
These claims are being coordinated through consolidated proceedings focused specifically on ophthalmic injuries and optic nerve damage.
Plaintiffs allege that manufacturers failed to adequately warn patients and providers about the potential risk of serious vision-related side effects associated with these medications.
Qualifying for a Victoza lawsuit generally depends on whether a patient suffered serious health problems after using the medication and whether medical records support a plausible link to Victoza use.
Many personal injury claims involve severe gastrointestinal complications, including gastroparesis, intestinal obstruction, ileus, or persistent vomiting that required emergency treatment or hospitalization.
Other claims may involve pancreatitis, gallbladder disease, or other medically documented complications identified in safety warnings associated with Victoza.
Some individuals are also pursuing claims involving vision loss, including optic nerve injuries such as NAION, though these cases are still developing and remain the subject of ongoing litigation.

To qualify, patients typically need proof of prescription use, a clear diagnosis, and treatment records showing the extent of the injury and resulting medical intervention.
Timing often matters, including when symptoms began, whether they worsened over time, and whether they persisted after discontinuing the drug.
Claims may be stronger when the injury resulted in long-term impairment, surgical procedures, significant financial losses, or permanent health limitations.
TorHoerman Law is reviewing Victoza cases to determine whether the facts support a product liability claim based on the injuries reported and the warnings provided at the time of use.
Strong evidence is often the deciding factor in whether a Victoza lawsuit can move forward and whether a claim can be valued accurately.
These cases typically require clear medical documentation showing when a patient started Victoza, when symptoms began, and how the condition progressed.
Victoza attorneys also look for proof that the injury required significant medical treatment, hospitalization, or long-term follow-up care.
Without complete records, it becomes harder to demonstrate causation, damages, and the full impact of the injury.

Common evidence used in Victoza lawsuits includes:
Damages are the measurable harms a patient suffers as a result of a serious injury, including both financial losses and the physical impact of the condition.
In a Victoza lawsuit, lawyers evaluate damages by reviewing medical records, treatment costs, wage loss documentation, and evidence showing how the injury affected a person’s daily life.
Compensation is typically based on the severity of the injury, the length of recovery, and whether the patient faces permanent limitations or ongoing medical needs.
Attorneys also consider whether the injury required hospitalization, surgery, long-term medication, or specialist care, since these factors often increase case value.
The goal is to calculate a compensation demand that reflects both the direct economic losses and the lasting personal consequences of the injury.

Potential compensation in a Victoza lawsuit may include:
Victoza lawsuits involve serious allegations of gastrointestinal injury, pancreatitis, and other medical complications that may leave patients facing long-term health consequences and substantial financial losses.
These cases require careful review of medical records, prescription history, and the full timeline of symptoms and treatment.
TorHoerman Law is investigating claims involving Victoza and other GLP-1 medications to determine whether patients may have grounds to pursue compensation.

If you or a loved one suffered a severe medical complication after using Victoza, legal action may be available depending on the facts of your case.
Contact TorHoerman Law today to discuss your potential claim in a free and confidential consultation.
You can also use the chat feature on this page to find out if you qualify for the Victoza lawsuit.
There is not currently a traditional Victoza class action lawsuit for personal injury claims involving health complications like pancreatitis or gastroparesis; instead, individual Victoza lawsuits alleging injury have been centralized into multidistrict litigation (MDL) so that similar cases can proceed together while each plaintiff retains an individual claim.
In product liability matters involving Victoza’s safety, the MDL process accommodates hundreds of separate lawsuits without collapsing them into a single class action with uniform outcomes.
Lawsuits alleging vision loss, such as NAION, are also being organized in consolidated proceedings but remain individual claims rather than a class action.
Separately, there is a proposed class action lawsuit filed by a drug wholesaler alleging anticompetitive conduct by Novo Nordisk to delay generic Victoza entry into the market, seeking damages on behalf of purchasers rather than patients injured by the drug.
That proposed class action focuses on market and pricing issues, not personal injury from use of the medication.
As with all litigation, the presence of an MDL or a pending class claim can evolve over time, and anyone considering a claim should consult experienced counsel to understand available legal avenues.
No, there is no current, active FDA recall of Victoza that would remove the drug entirely from the U.S. market.
Victoza remains available by prescription for patients with type 2 diabetes and continues to be regulated by the US Food and Drug Administration (FDA) as a legally marketed medication.
There was a prior recall of certain Victoza lots in 2021 due to temperature control issues during distribution, but that recall was terminated in 2022 after the affected products were removed or corrected.
Aside from that isolated distribution recall, the FDA has not issued a recall Victoza for safety reasons such as an undisclosed defect or imminent risk to patients.
Reports discussing safety risks like pancreatitis, gallbladder disease, or thyroid C-cell tumors have led to label changes and black box warnings, not to a formal recall of all Victoza products.
Patient and provider guidance continues to emphasize monitoring for serious symptoms rather than avoiding the drug outright.
Should any recall be announced in the future, it would be published on the FDA’s official recall databases and communicated through healthcare channels.
Victoza lawsuits are being filed because patients allege that the drug manufacturer failed to provide adequate warnings about serious health risks associated with the medication.
Victoza is manufactured by Novo Nordisk and was first approved for the market in 2010, and it has since been widely prescribed for type 2 diabetes management.
The original MDL for Victoza began in 2013, but most federal claims linking Victoza to pancreatic and thyroid cancer were dismissed in 2021, and the MDL was formally dismissed in 2022 due to insufficient evidence from the plaintiffs’ sole expert witness.
Despite those dismissals, litigation regarding Victoza remains active, particularly concerning gastroparesis, kidney failure, vision loss, and other gastrointestinal injuries now being investigated in broader GLP-1 proceedings.
Common reasons Victoza lawsuits are being filed today include:
Individuals may qualify to file a Victoza lawsuit if they were prescribed and used the medication and later developed a serious medical condition that may be linked to its known or alleged risks.
Most current claims involve severe gastrointestinal injuries such as gastroparesis, ileus, intestinal obstruction, or persistent vomiting requiring hospitalization or surgical intervention.
Some individuals are also pursuing claims involving kidney failure related to dehydration, or vision loss such as non-arteritic anterior ischemic optic neuropathy.
To qualify, a person typically must have medical records confirming both Victoza use and a documented diagnosis of the injury.
The strength of a claim often depends on the timing of symptoms, the severity of the condition, and whether the injury resulted in long-term impairment or substantial financial loss.
An experienced attorney can review prescription history, medical documentation, and the overall circumstances to determine whether a viable product liability claim may exist.
Yes, Victoza has been the subject of cancer-related lawsuits and regulatory scrutiny, particularly involving allegations of pancreatic cancer and thyroid cancer risk.
The FDA initiated an investigation into Victoza’s potential link to pancreatic cancer in 2013 after safety concerns emerged, and Victoza has been associated with an increased risk of pancreatic cancer in some studies and adverse event reporting, prompting continued evaluation.
The FDA also required a black box warning on Victoza’s label due to concerns about thyroid tumors in animal studies, which has remained a central issue in safety discussions.
However, most federal claims linking Victoza to pancreatic and thyroid cancer were dismissed in 2021 due to insufficient scientific evidence to support causation in court.
Despite ongoing safety concerns and investigations, Victoza remains available on the market and continues to be prescribed for type 2 diabetes.
Separately, Victoza may cause gallbladder disease, including gallbladder stones and cholecystitis, which can require surgery, and these complications may also be relevant in certain injury claims.
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?