Attorney Jessica Paluch-Hoerman, founder of TruLaw, has over 28 years of experience as a personal injury and mass tort attorney, and previously worked as an international tax attorney at Deloitte. Jessie collaborates with attorneys nationwide — enabling her to share reliable, up-to-date legal information with our readers.
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A Belviq Lawsuit may apply to you or your loved one if the diet drug Belviq or Belviq XR was taken prior to a cancer diagnosis.
An experienced Belviq lawyer will be able to assist in protecting your legal rights.
The Food and Drug Administration announced that the popular weight-loss drug Belviq (lorcaserin) would be pulled from the United States market as of February 2020.
Researchers found increased reported cancer rates in people who took Belviq. FDA officials recommend that Belviq users immediately stop taking the medication.
Belviq is a popular prescription weight-loss drug sold and produced by Eisai Inc. Belviq works by altering the brain chemical signals responsible for appetite.
The drug is prescribed in combination with exercise and a healthy diet to help adults who are overweight or obese.
The medication does not treat underlying health conditions.
Belviq is a 10 mg prescription tablet that patients take two times a day.
Belviq XR is the extended-release form taken once daily.
The FDA requested Belviq be pulled from the U.S. market because of the drug’s ties to increased cancer rates.
FDA researchers conducted a study on the drug and found that approximately 7.7 percent of patients that took Belviq were diagnosed with cancer compared to 7.1 percent of placebo recipients.
The FDA also found that the longer a patient was on Belviq, the greater his or her risk was of developing cancer.
TruLaw recommends finding out if you qualify for a Belviq Lawsuit instantly using the Bevliq Case Qualification tool.
A Belviq Lawyer may be able to assist with compensation for injuries and medical bills while protecting your legal rights.
The FDA reported increased rates of pancreatic, lung, and colorectal cancers in Belviq and Belviq XR users.
In January, the FDA announced that Belviq and Belviq XR cancer risks were strong enough to call for the drugs’ removal from the U.S. market.
The agency said it still cannot definitively conclude that Belviq and Belviq cause cancer.
However, officials said the medications’ risks outweigh the benefits and that people taking Belviq should stop immediately.
Belviq and Belviq XR have been tied to numerous other side effects.
These include headaches, fatigue, dizziness, nausea, dry mouth, and constipation.
Patients with diabetes who take Belviq / Belviq XR might also experience coughing, back pain, and hypoglycemia.
The drug can also cause slowed heartbeat and heart valve issues.
The medications were rejected by the European Medicines Agency in 2012 due to safety concerns.
Belviq is classified as a Schedule IV controlled substance by the Drug Enforcement Agency.
This means the drug carries risks of dependence.
People who take higher doses than prescribed can experience hallucinations, euphoria, and slowed thinking.
The medication can also adversely interact with other prescriptions.
Note that Belviq / Belviq XR were only approved for people who are overweight (a body-mass index between 27 and 30) or obese (a body-mass index over 30) and have high cholesterol, high blood pressure, or diabetes.
To find out if a Belviq Lawsuit is right for you visit our Bevlviq Instant Case Report Tool or contact TruLaw at (888) 477-3804 to speak with a Belviq Lawyer.
The U.S. Food and Drug Administration requested that Belviq, the popular weight-loss medication, be voluntarily pulled from U.S. markets after clinical safety trials tied the drug to increased cancer rates.
Eisai Inc., the medication’s manufacturer, submitted to requests and pulled the drug from the market.
FDA officials said cancer risks tied to Belviq are significant enough to call for the medication’s removal from markets.
Since the drug’s approval, researchers have been conducting a five-year study analyzing its safety profile.
The researchers discovered approximately 7.7 percent of Belviq users had a cancer diagnosis versus the 7.1 percent who took a placebo.
FDA officials said people taking Belviq should stop immediately.
Patients should speak with a health professional to find different weight-loss drugs and weight-management programs.
Patients should dispose of Belviq at a drug take-back site or in their household waste using the following techniques:
The FDA is not requiring special cancer screenings for people who took Belviq.
Patients should still undergo regular recommended cancer screenings.
Patients should contact their healthcare provider with any questions.
The FDA said healthcare providers should immediately stop dispensing and prescribing Belviq and Belviq XR to patients.
Providers should contact any patients currently taking the medication to inform them of the clinical trial results and ask them to stop taking the drug.
Providers should help patients find alternative medications and weight-loss strategies.
To help the FDA track Belviq safety issues, the agency encourages patients and health professionals to report adverse reactions and side effects to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program.
Information can be submitted through:
If you took Belviq or Belviq XR and developed cancer or other adverse side effects, you could be eligible for a Belviq / Belviq XR lawsuit.
If you took Belviq or Belviq XR and were diagnosed with colorectal, pancreatic, or lung cancer, we will work to seek the following damages for you:
Hiring an experienced Belviq lawyer is critical for earning full compensation for the suffering endured by you or your loved one.
TruLaw will work with you to successfully pursue your bad drug lawsuit.
We offer free, zero-obligation case consultations for all potential Belviq lawsuit clients.
Find out if you qualify instantly or Contact TruLaw today to learn about your potential case and legal options.
Managing Attorney & Owner
With over 25 years of legal experience, Jessica Paluch-Hoerman is an Illinois lawyer, a CPA, and a mother of three. She spent the first decade of her career working as an international tax attorney at Deloitte.
In 2009, Jessie co-founded her own law firm with her husband – which has scaled to over 30 employees since its conception.
In 2016, Jessie founded TruLaw, which allows her to collaborate with attorneys and legal experts across the United States on a daily basis. This hypervaluable network of experts is what enables her to share the most reliable, accurate, and up-to-date legal information with our readers!
Here, at TruLaw, we’re committed to helping victims get the justice they deserve.
Alongside our partner law firms, we have successfully collected over $3 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?
At TruLaw, we fiercely combat corporations that endanger individuals’ well-being. If you’ve suffered injuries and believe these well-funded entities should be held accountable, we’re here for you.
With TruLaw, you gain access to successful and seasoned lawyers who maximize your chances of success. Our lawyers invest in you—they do not receive a dime until your lawsuit reaches a successful resolution!
AFFF Lawsuit claims are being filed against manufacturers of aqueous film-forming foam (AFFF), commonly used in firefighting.
Claims allege that companies such as 3M, DuPont, and Tyco Fire Products failed to adequately warn users about the potential dangers of AFFF exposure — including increased risks of various cancers and diseases.
Depo Provera Lawsuit claims are being filed by individuals who allege they developed meningioma (a type of brain tumor) after receiving Depo-Provera birth control injections.
A 2024 study found that women using Depo-Provera for at least 1 year are five times more likely to develop meningioma brain tumors compared to those not using the drug.
Suboxone Tooth Decay Lawsuit claims are being filed against Indivior, the manufacturer of Suboxone, a medication used to treat opioid addiction.
Claims allege that Indivior failed to adequately warn users about the potential dangers of severe tooth decay and dental injuries associated with Suboxone’s sublingual film version.
Social Media Harm Lawsuits are being filed against social media companies for allegedly causing mental health issues in children and teens.
Claims allege that companies like Meta, Google, ByteDance, and Snap designed addictive platforms that led to anxiety, depression, and other mental health issues without adequately warning users or parents.
Transvaginal Mesh Lawsuits are being filed against manufacturers of transvaginal mesh products used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI).
Claims allege that companies like Ethicon, C.R. Bard, and Boston Scientific failed to adequately warn about potential dangers — including erosion, pain, and infection.
Bair Hugger Warming Blanket Lawsuits involve claims against 3M — alleging their surgical warming blankets caused severe infections and complications (particularly in hip and knee replacement surgeries).
Plaintiffs claim 3M failed to warn about potential risks — despite knowing about increased risk of deep joint infections since 2011.
Baby Formula NEC Lawsuit claims are being filed against manufacturers of cow’s milk-based baby formula products.
Claims allege that companies like Abbott Laboratories (Similac) and Mead Johnson & Company (Enfamil) failed to warn about the increased risk of necrotizing enterocolitis (NEC) in premature infants.
Here, at TruLaw, we’re committed to helping victims get the justice they deserve.
Alongside our partner law firms, we have successfully collected over $3 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?