Because Expericence Matters

Heart Stents

In the United States, coronary artery diseases are the leading cause of death among men and women. The American Heart Association reports that about every 29 seconds, someone in the U.S. suffers from a coronary artery disease-related event, and about every minute someone dies from such an event. One way to fix clogged arteries-- that can cause chest pains, sudden heart attacks and strokes-- is the use of heart stents. Every year, when hundreds of thousands of people need procedures to open up their arteries, this procedure is usually performed with heart stents.

Once a heart stent has been implanted into the heart arteries, it becomes part of the artery itself and remains there permanently. In November 2004, a Duke University Medical Center study-- presented at the American Heart Association’s scientific sessions-- showed heart stents do not improve the long-term survival rates of heart patients, even when drug-coated heart stents are used.

The findings were especially alarming considering the existing controversy surrounding the safety of heart stents. In April 2003, the subsidiary of Johnson & Johnson, Cordis Corporation, received FDA approval to market there Cypher drug-coated heart stents. In less than six months following FDA approval, at least 290 people had suffered life-threatening injury and 60 people had died due to heart stent side effects. The FDA issued two major warnings about this product in 2003, yet the heart stents remained on the market.

These serious injuries and deaths suffered by patients with Cypher heart stents were largely caused by blood clots. These Cordis-Johnson and Johnson heart stents pose a high risk of causing blood clots around the stent. Stent thrombosis has a high risk of causing a heart attack. In addition to these serious risks, Cyper heart stents have also been linked to severe allergic reactions, of which the FDA received at least 50 adverse drug reaction reports in 2003 alone.

In March 2004, competitor Boston Scientific received FDA approval to market Taxus drug-coated heart stents. Less than six months later, the company announced a partial recall of the Taxus heart stents due to safety concerns. As worries mounted, the Taxus heart stent recall grew to over 100,000 recalled heart stents. At least three people have died, and dozens more injured, because of serious Taxus heart stent side effects.

Despite the serious dangers associated with both brands of drug-coated heart stents, these dangerous pharmaceutical products remain on the market. While these stents provide a great benefit to those who suffer coronary artery disease, they can also cause serious and life-threatening side effects.

If you or a loved one has been injured after receiving a heart stent, please contact us to learn more about your legal rights and options. You may be eligible to seek compensation for your losses and suffering.

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