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Vioxx News Article
August 2, 2005
Los Angeles Times, "Pathologist Deals Blow to Merck in Vioxx Lawsuit"

          Jurors in the Vioxx trial heard testimony Monday from a pathologist who said the death of a man taking the drug was more than likely caused by a heart attack - damaging Merck & Co.'s defense in the first Vioxx liability case to reach trial.
          
The videotaped testimony from Dr. Maria Araneta, a former assistant coroner for the Johnson County medical examiner's office near Fort Worth, was shown to the jury almost immediately after the Texas Supreme Court denied Merck's attempt to stop jurors from hearing it.
          
Merck, the drug's New Jersey-based maker, was relying heavily on Araneta's autopsy report, which said that Robert Ernst, 59, died as a result of an arrhythmia, or irregular heartbeat, secondary to clogged arteries. Merck says no studies show a link between taking Vioxx and a higher risk of arrhythmia.
         
In the deposition, Araneta said she thought Ernst's 2001 death from arrhythmia was more than likely caused by a heart attack.
         
Neither her report nor Ernst's death certificate identify a heart attack as the cause of his death.
         
Merck attorney Joseph Piorkowski asked Araneta whether she was changing her conclusion in the autopsy report.
         
"I'm not changing my opinion, I'm just explaining it further," she said. "That's the autopsy report, but it's not the end of the story."


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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.