Personal Injury Attorney
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Defective Drug and Medical Devices

Belviq and Belviq XR (lorcaserin)

Photograph: two feet on a white bathroom scale.

The U.S. Food and Drug Administration (“FDA”) has just requested that Eisai, Inc. (a Japanese drug company with U.S. headquarters in New Jersey), withdraw its weight-loss drug Belviq and Belviq XR from the U.S. market because of an increased occurrence of cancers observed among users.  The FDA Notice is available by link here:

https://www.fda.gov/drugs/fda-drug-safety-podcasts/fda-requests-withdrawal-weight-loss-drug-belviq-belviq-xr-lorcaserin-market

A copy of the notice of withdrawal by Eisai, Inc., manufacturer of Belviq and Belviq XR, is available here:

https://us.eisai.com/

The FDA has issued this safety communication regarding Belviq and Belviq XR (lorcaserin), which are indicated for chronic weight management in adults with BMI 30 or BMI 27 with at least one weight-related comorbidity, when combined with diet and exercise.  Belviq was approved in 2012 and Belviq XR was approved in 2016.

FDA stated in issuing the market withdrawal of this drug: “When FDA approved lorcaserin [Belviq] in 2012, we required the drug manufacturer [Eisai] to conduct a clinical trial to evaluate the risk of cardiovascular problems.  A range of cancer types was reported, with several different types of cancers occurring more frequently in the lorcaserin group, including pancreatic, colorectal, and lung.”

As a result of this increased cancer risk, the FDA recommends that patients should stop taking Belviq and Belviq XR (lorcaserin) and talk to their health professionals about alternative weight-loss medicines and weight management programs.  In a related move, the FDA is directing that healthcare professionals stop prescribing and dispensing Belviq and Belviq XR (lorcaserin) to patients.

If you or someone you know in New York State is or was:

(i) An adult; and

(ii) Experienced primary pancreatic cancer; (ii) primary colorectal cancer; and/or (iii) primary lung cancer, and

(iii) Had at least six (6) months of collective (not necessarily continuous) exposure to Belviq or Belviq XR, and

(iv) Ingested Belviq or Belviq XR within seven (7) years of their cancer diagnosis,

You or the person you know may have a claim for monetary damages in compensation for the cancers caused by exposure to these weight-loss medications.

WHAT TO DO NEXT AND WHY CHOOSE JAMES T. SNYDER LAW?

If you or someone you know in New York State has been injured by or died from pancreatic, colorectal, or lung cancer while or after taking Belviq or Belviq XR weight-loss medication, you, the person you know and/or the deceased’s estate may be entitled to compensation.  But if you’ve seen ads on TV or are searching the internet for an attorney to help -- you may be completely bewildered or confused by all the Google search results, 800 numbers, faceless law firms, etc. 

If so, you’ve come to the right place. 

We can help you personally.  We’ve helped so many people who have been injured through the negligence of others, including those injured in mass tort claims.  People want someone to talk to for free, to answer their questions and sort through their options, without a fee or obligation -- it’s a comfort and a relief.  Don’t be intimidated or afraid to ask.  We’ll help.        

So for a free, no-obligation personal and confidential consultation about your legal rights or those of another or a deceased in New York regarding a primary cancer diagnosis linked to taking Belviq or Belviq XR, call us at 315-884-8888 or fill out and send in the easy-to-complete form below. 

Learn more.  Learn your rights.  Fill out and submit this simple form today -- we promise to respond immediately and in full confidentiality.