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Vioxx
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Vioxx® is a non-steroidal anti-inflammatory drug prescribed for arthritis and menstrual cramps. It is made by the pharmaceutical giant Merck & Co., the second-largest drug manufacturer/distributor in the United States. Vioxx® was approved by the Food and Drug Administration (FDA) in 1999, and was withdrawn from the market in September 2004 after it was linked to increases in the occurrence of heart attack and stroke among its users. More than 10,000 lawsuits have been initiated against Merck regarding these very serious Vioxx® side effects. Several of the earlier lawsuits have resulted in verdicts against Merck. At Phillips and Associates, Vioxx® specialist lawyers can tell you about these cases in greater detail.
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Vioxx was a medication sold for the treatment of acute pain and relief of osteoarthritis and other conditions. It was manufactured and sold by Merck and Company. Merck is a world wide pharmaceutical company with its headquarters in New Jersey. All cases involving claims concerning Vioxx have been assigned by the New Jersey Supreme Court to the Honorable Carol E. Higbee for coordinated management in Atlantic County, New Jersey. On September 30, 2004, Merck & Co., Inc. voluntarily recalled Vioxx from the market.
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Do not take Vioxx if you have had severe allergic reaction to aspirin or any medicine containing aspirin or to a nonsteroidal anti-inflammatory drug (such as Feldene, Motrin, Naprosyn, Clinoril). A severe reaction includes a severe rash, hives, breathing difficulties, or dizziness. If you have a question about whether you are allergic to Vioxx or if a certain medicine is a nonsteroidal anti-inflammatory drug, contact your doctor or pharmacist. If you experience difficulty breathing; tightness of chest; swelling of eyelids, face, or lips; or if you develop a rash or hives, tell your doctor immediately. Do not take any more doses of Vioxx unless your doctor tells you to do so. DO NOT exceed the recommended dose or take Vioxx for longer than prescribed without checking with your doctor. Keep ALL doctor and laboratory appointments while you are using Vioxx.
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Some people who have experienced damaging side effects of taking the drug Vioxx have filed individual lawsuits, while others are going to be part of a proposed class action lawsuit. On August 19, 2005, a Texas jury held drug giant Merck & Co. liable in the heart-related death of 59-year-old Wal-Mart produce manager Robert Ernst, a marathon runner who took its prescription painkiller Vioxx, slapping the company with a $253.4 million judgment.
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Reporting your Vioxx injury can help others avoid health problems.The FDA has already taken steps to force Vioxx manufacturers Merck & Co. to disclose the risks associated with this drug. Changes in medication labels have been made, along with orders to cease misleading advertising practices. Doctors are ... beginning to speak out and to inform their patients about the actual benefits, cost, and problems of Vioxx and Celebrex. Hiring a Vioxx attorney may be a valuable step in the right direction. Each case brought against Merck can help secure tighter drug regulation, fewer acts of drug fraud, and more comprehensive drug research laws.
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The FDA has released a memo indicating that Vioxx® might have contributed to 27,785 heart attacks and deaths from 1999 through 2003. The memo was authored by Dr. David Graham, an associate director of the FDA's office of drug safety. It was based on a sample of patient records from a study conducted with Kaiser Permanente. The memo concludes that people taking Vioxx® were more likely to have heart attacks or die from sudden cardiac arrest than people taking Celebrex®. Dr. Graham's e-mail and meeting notes suggests that his efforts to publish his views were delayed by top officials at the FDA. Several recent articles have ... suggested that Merck and the FDA should have withdrawn Vioxx® from the market as early as 2000.
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