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Vioxx & Heart Disease

 

The Risks Of Vioxx

Almost every prescription drug on the market has some significant side effects, with some more severe than others. Usually, the doctors will weigh the risks of possible side effects to the benefits of the treatment when deciding a patient’s need for the drug. However, when the high incident risk between Vioxx and heart disease was discovered, the drug was pulled from the market.

There are some non-steroidal anti-inflammatory drugs, used for pain, have been available over the counter for may years, and sold under a variety of names such as ibuprofen and naproxen. All of them are labeled with a warning that they might cause stomach ulcers and other problems. This is because of the cyclooxygenase (COX) inhibitors, which are part of the products, inhibit what is referred to COX-1, which can produce an enzyme which is responsible for the protection of the stomach lining.

Researchers have discovered a way to block COX-2 production and not COX-1, which showed promise of a pain reliever that did not have the same side effects that cause stomach problems. The COX-2 enzyme, on the other hand, also blocks the production of prostaglandin, and anti-clotting agent. When the effects of Vioxx and heart disease began to appear, there were additional warnings added to the drug’s label.

The manufacturer informed the approving agency, the FDA, this tie-in of Vioxx, and heart disease was only common in patients with a high risk of coronary events, and under a physician’s guidance was safe for use by those without a severe risk, reducing the threat linked to Vioxx and heart disease.

Drug Recalled From Market

When further studies showed an increase of heart attacks in patients who take Vioxx and heart disease histories increased four times. An editorial in the New England Journal of Medicine claimed the makers of Vioxx were aware of increased threat of those taking Vioxx and heart disease. Those claims were the major cause of the additional warnings placed on labels.

Due to the increased incidents of those taking Vioxx and heart disease events such as heart attack and stroke, Vioxx was pulled from the market in 2005, after six years of existence on the market.

The increased scrutiny tying Vioxx and heart disease is the leading factor in drawing the manufacturer into numerous lawsuits around the country. The families of people with histories of major coronary events, who were taking Vioxx and died, have taken legal action claiming the tie-in of Vioxx and heart disease is responsible for their loved-ones deaths.

 

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