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Vioxx News Article
December 8, 2005
Associated Press, "New England Journal: Merck Concealed Data"
          Vioxx maker Merck & Co. concealed heart attacks suffered by three patients during a clinical study of the now-withdrawn painkiller in a report on the study published in the New England Journal of Medicine in 2000, the journal wrote in an editorial released Thursday.
          The editorial, written by the journal's editor in chief, Dr. Jeffrey M. Drazen, executive editor Dr. Gregory D. Curfman and a third doctor, also alleges the study's authors deleted other relevant data before submitting their article for publication.
          "Taken together, these inaccuracies and deletions call into question the integrity of the data on adverse cardiovascular events in this article," the doctors wrote.
          Adverse cardiovascular events include heart attacks, strokes and deaths. Findings of the study in question have been a key part of testimony in the three product liability trials to date over the withdrawn drug, including one being deliberated Thursday by a federal jury in Texas.
          Merck spokesman Chris Loder said the Whitehouse Station, N.J.-based company would issue a statement in response to the editorial Thursday.
          Excluding the three heart attacks "made certain calculations and conclusions in the article incorrect," the doctors wrote, adding that they have asked the report's authors to submit a correction to the journal.
          Merck withdrew Vioxx, once one of its top-selling drugs, from the market on Sept. 30, 2004 after other research showed the popular arthritis drug doubled risks of heart attacks and stroke with long-term use. The company now faces at least 7,000 lawsuits over Vioxx and legal liability some analysts have estimated at up to $50 billion. Those problems were part of the reason Merck last week announced plans to cut 7,000 jobs and close eight manufacturing and research facilities around the world as the first step in a sweeping reorganization.

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For our personal injury Vioxx cases, we bring a team of experienced lawyers. In addition, we have on staff multiple nurses, legal assistants, scientific analysts and case clerks to assist our Vioxx attorneys. Learn more about advantages we offer patients with Vioxx problems and injuries.
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We have a nationwide team of experienced injury Vioxx lawyers assigned to Vioxx trials.
We provide individual attentive service. Learn more about our firm.
We have retained the leading national medical experts on Vioxx and have a staff of nurses to assist the prosecution of the claims of our clients.
We have been contacted by thousands of Vioxx drug patients nationwide as part of the Vioxx litigation. We have represented patients who ingested prescription drugs with dangerous, undisclosed side effects in personal injury lawsuits across America, including residents of Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming.
Persons living outside the United States who have been injured by an American product manufactured may also in certain cases file Vioxx lawsuits for compensation for heart attacks and strokes in United States courts.

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Vioxx Recall: The international prescription drug company Merck announced in September 2004 the worldwide withdrawal of the arthritis medication Rofecoxib, sold in most countries under the brand name Vioxx, because a study showed an increased risk of heart attack and stroke.

Vioxx Trial: Patients who have suffered injuries due to Vioxx have filed litigation against Merck for selling Vioxx even though Merck allegedly was aware of Vioxx's dangerous side effects.