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Drug Eluting Stents

Were you looking for FDA Issues Warning for Transvascular Autonomic Modulation (TVAM) lawsuits?


Lawyers are currently investigating the numbers of stent-related cardiac events linked to drug eluting stents. Drug eluting stents are also known as medicated or drug-coated stents. Medicated stents are, unlike bare metal stents, coated in drugs intended to inhibit cell growth to prevent restenosis (re-blocking of the artery).


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Drug Eluting Stents' Side Effects

drug eluting stentsManufacturers of these stents include Boston Scientific (Taxus stent) and Cordis, a subsidiary of Johnson & Johnson (Cypher stent). Medicated stents are increasingly common, projected to represent 88% of all stents sold in the US in 2005.

Drug Eluting Stents have been linked to side effects such as thrombosis and severe allergic reactions.

Stents were originally developed to open arteries clogged with plaque. A treatment called angioplasty was developed whereby doctors expanded clogged arteries with tiny balloons, but about half the time the arteries re-closed.

In an attempt to solve the problem, doctors used the balloon to expand a tiny wire mesh sleeve, called a stent, inside the artery to keep it open. This helped a bit, but in 20-30% of cases, cells grew over the wire and the arteries re-closed.

The next solution was to coat the stents with a drug that prevented cell growth. These drug eluting stents (DES) cut the restenosis rate to about 5%. However, a new problem developed - by stopping cell growth, pieces of the stent could stick out of the artery and create a perfect place for a blood clot to form and cause a fatal heart attack.

The drug-coated stents have also been linked to a higher death rate due to cardiac events such as heart attack when compared to metal stents without a drug coating. The associated blood clots may occur up to thirty days after the heart stent was implanted. It is estimated that 2,000 Americans die each year due to drug eluting stents.

While allergic reactions may also occur, including pain, hives, and fever, along with difficult breathing and blood pressure issues, the law firm is interested in investigating only those cases that relate to post-stent implantation cardiac events. The strongest cases involve death with autopsy showing a blood clot inside the stent.

Drug Eluting Stent Lawyers

If you or a loved one has suffered a heart attack or stroke after having a drug eluting stent implanted, please click the link below to send your Drug Eluting Stents claim to a lawyer for a free evaluation.
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Angioplasty TVAM, Doctors and the FDA
Angioplasty TVAM, Doctors and the FDA
May 19, 2017
Washington, DC: Angioplasty was designed as a safe alternative to open heart surgery, but a procedure using balloon angioplasty devices called transvascular autonomic modulation (TVAM) is not safe, which the FDA has warned of repeatedly. Some doctors, however, believe its benefits outweigh the risks involved.

FDA Warns Against Off Label Angioplasty Treatment Known as TVAM
FDA Warns Against Off Label Angioplasty Treatment Known as TVAM
April 17, 2017
Dallas, TX The FDA is taking the unusual step of calling out a specific doctor and warning people to steer clear of the use of TVAM angioplasty as a treatment for serious illnesses such as Parkinson’s disease, Multiple Sclerosis and other autonomic disorders.

Jury Still Out on Safety of Drug Eluting Stents
Jury Still Out on Safety of Drug Eluting Stents
October 20, 2008
Washington, DC When the US Food and Drug Administration (FDA) approved 'Endeavor,' the drug-coated Medtronic stent earlier this year, it did so amidst a storm of controversy as to whether or not the stents promote potentially dire blood clots in heart attack patients. Drug eluting stents are still under FDA scrutiny, but as 2008 dawned there was little conclusive evidence to prove the suspicion as fact.


Posted by

i had 2 stents put in may of 2005 i’m pretty sure i have 2 stents that are recalled i had 2 more put in 2008 so i have 4 stents and would like to know if i’m eligible for a settlement

Posted by

I suffered a heart attack on August 4 and was administered clot busting medication to keep me alive at Kenora Hospital in Kenora Ontario. On August 7 I was then transferred to St. Boniface Hospital in Winnipeg Manitoba where an angiogram and ultrasound was performed.
The heart attack had damaged my heart and was attributed to a blood clot that formed in my Taxus stent. I am now on Warfarin to ensure no clots form in my heart chamber and then am looking at a lifetime of Plavix and aspirin. I have also lost my drivers license for the next 30 days. I also face a future of uncertainty regarding the Taxus stent and possible side effects and risks.


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