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1stlawyerinfo.com primary objective is to provide you with the support and vioxx lawyer resources, vioxx attorney information necessary to handle your legal issues. One of the biggest ways we achieve this goal is by helping you contact a qualified legal professional free vioxx lawyers information, vioxx attorneys solutions and counselor near you, who can inform you of your legal rights and options.
A Vioxx attorney offers clients expertise in the side effects of this common arthritis pain medication. Vioxx attorneys are familiar with the very specific regulations that govern medical products liability; a Vioxx attorney can usually provide more accurate information than a regular attorney.

The advantage to retaining a Vioxx attorney is that the victim will be represented by an attorney who understands their problems. Experienced Vioxx attorneys understand the long-term implications of the side-effects for plaintiffs and their families, which means Vioxx attorneys are prepared to fight to ensure that their clients receive full and proper compensation. Many Vioxx attorneys are able to obtain large settlements from defendant corporations without having to go to trial. Vioxx attorneys can also help victims and their families form reasonable expectations and make sound decisions.

A Vioxx attorney has experience representing victims of Vioxx side effects, such as cardiac arrest. An experienced Vioxx attorney fully understands the implications of this serious problem, and the liability of manufacturers. Consulting a Vioxx attorney early on can help victims receive appropriate medical treatment and legal representation. An experienced Vioxx attorney is likely available in your area, and can discuss the merits of your case at no charge.

Vioxx Attorney and Class Action Lawsuit Information on Heart Attack Drug Vioxx.
Merck said that data from the trial showed the increased risk of heart attack and other cardiovascular complications began 18 months after patients started taking Vioxx. The data comes from a three-year study aimed at showing that Vioxx at a 25 milligram dose prevents recurrence of polyps in the colon and rectum. The trial was stopped after Merck discovered the higher heart risk compared to patients taking dummy pills.

FDA VIOXX STUDY
The FDA was informed by Merck & Co., Inc. on September 27, 2004, that the Data Safety Monitoring Board for an ongoing long-term study of Vioxx (APPROVe) had recommended that the study be stopped early for safety reasons. The study was being conducted in patients at risk for developing recurrent colon polyps. The study showed an increased risk of cardiovascular events (including heart attack and stroke) in patients on Vioxx compared to placebo, particularly those who had been taking the drug for longer than 18 months. Based on this new safety information, Merck and FDA officials met the next day, September 28, 2004, and during that meeting FDA was informed that Merck was voluntarily withdrawing Vioxx from the market place.

The risk that an individual patient taking Vioxx will suffer a heart attack or stroke related to the drug is very small. Patients who are currently taking Vioxx should contact their physician for guidance regarding discontinuation and alternative therapies.

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