Vioxx Settlement |
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Jury Finds Merck Responsible in Vioxx Lawsuit Involving Long-Term User |
November 9, 2007—Merck announced that is has offered $4.85 billion to settle 27,000 lawsuits filed by people claiming injuries after taking Vioxx.
Vioxx was removed from the market in September 2004 after several studies revealed that the drug was associated with a substantially greater risk of heart attacks and strokes. |
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April 5, 2006—A New Jersey jury found that Vioxx caused the heart attack
suffered by a long-term user of the drug. This was the first case to reach trial involving
a plaintiff who had used Vioxx for a lengthy period. The jury awarded the man $4.5 million
in damages.
The same jury rejected the claims of another man who argued his heart attack
also was caused by Vioxx. That person was awarded just $45, reimbursement for his prescription
costs.
In February 2006, a federal jury in New Orleans decided
Merck was not responsible for the death of a man who used Vioxx for less than one month before
dying of a heart attack.
The New Jersey verdict illustrates the problems Merck will face in cases involving
plaintiffs who used the drug for longer periods of time. Merck already has acknowledged that
the risk of cardiovascular problems increases the longer a person is on the drug.
Merck's legal strategy underscores the need for those harmed by Vioxx to select
aggressive trial lawyers to protect their legal rights. We encourage you to learn more about
our Vioxx lawyers and how our firm can help you if you or a loved one suffered a heart attack
or stroke while using Vioxx. |
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Merck Issues Vioxx Recall
After Clinical Study Shows Increase in Heart Attacks, Strokes
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Vioxx Lawyers |
Merck & Co. conducted
a clinical study involving 2,600 patients to determine whether
Vioxx was effective in preventing colon cancer. Merck halted
the study before its conclusion after it became clear that
Vioxx increased the risk of heart attacks and other serious
cardiovascular problems.
On August 26, 2004, just one month prior to
the withdrawal, Merck released a press releasing contending
that the drug was safe. The company said it stood behind the
"overall safety and cardiovascular safety" of Vioxx.
Merck attacked studies from other research groups that found
a link between Vioxx and heart attacks, strokes,
blood clots, and other serious side
effects.
More than 84 million have taken the drug worldwide
and it is believed more than 2 million were taking the arthritis
drug at the time of the recall. The widespread use was the
result of an aggressive marketing campaign by Vioxx. Merck
spent approximately $100 million per year promoting the dangerous
drug. Most of this money was spent after researchers already
had reported a link between Vioxx and heart problems.
The FDA has estimated that Vioxx may be responsible
for as many as 27,000 heart attacks and cardiac deaths between
1999 and 2003. The FDA reached this number by analyzing a
database of 1.4 million patients in the Kaiser Permanente
health care system. That analysis also led to the finding
that Vioxx users were more likely to suffer a heart attack
or sudden cardiac death than those who took a competing drug.
The problems with Vioxx began before the drug
was approved for sale in the United States. Pre-approval trials
to determine the safety of the drug lasted less than 12 months,
in spite of the fact that many people taking Vioxx for arthritis
would use the drug for a much longer period of time. |
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Martin
& Jones has represented hundreds of victims in legal claims
against manufacturers of dangerous pharmaceuticals.
We encourage you to learn more about
our Vioxx lawyers. |
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Vioxx News |
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Congress Launches
Hearing Over Vioxx Withdrawal |
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Visit the Vioxx News page for the latest
developments on Vioxx lawsuits.
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On November
18, 2004, Congress began hearings intended to assess the FDA's
decision not to recall Vioxx years before the drug finally
was pulled from the market. Dr. Graham, the Associate Director
for Science in the FDA's Office of Drug Safety testified that
the agency is "incapable of protecting America against
another Vioxx."
In alarming testimony, Dr. Graham estimated
that Vioxx had caused between 88,000 and 139,000 cases of
heart attack and stroke. These numbers are significantly greater
than the 27,000 estimate announced by the FDA in October 2004.
During the hearing, one senator expressed concern
that the FDA was "too cozy" with drug companies.
Many policymakers believe an independent drug safety office
should be created to review the safety of medications following
FDA approval.
The fallout has extended beyond Merck and Vioxx.
Our law firm is representing people harmed by Bextra,
a prescription arthritis drug belonging to the same family
of pharmaceuticals as Vioxx. The FDA forced a Bextra
recall less than a year following the announcement of
the Vioxx withdrawal.
We encourage you to learn how weakened
FDA regulations harmed Vioxx patients. |
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The New York Times 
Merck Agrees to Pay $4.85 Billion in Vioxx Claims
November 9, 2007
Reuters 
Jury Awards $4.5 Million in Vioxx Verdict Against Merck
April 5, 2006
MarketWatch 
After Vioxx Victory, Merck Faces Bigger Legal Test
February 21, 2006
MSNBC 
Merck Wins Retrial of Federal Vioxx Lawsuit
February 18, 2006
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Vioxx Lawyers |
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Current Lawsuits |
Martin
& Jones has been successfully representing injured
men, women and children since 1982. We are proud to represent
people from all walks of life, and the law firm has the experience
and resources to aggressively do so, regardless of the size
and resources of the offending company. We have a reputation
for taking on tough, serious cases and have successfully represented
individuals in claims against 30 of the 100 largest corporations
in America.
With a wealth of experience acquired over the
past two decades, Martin & Jones is committed to providing
the highest standard of representation possible for our clients
throughout the country. This commitment is reflected by the
diverse and extensive experience of our lawyers and by the
diligence of our law firm's staff of experienced paralegals,
adjusters, legal assistants and other support personnel.
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Asbestos
Cerebral Palsy
Guidant Heart Devices
Ketek
Kugel Mesh Patch
Nickel and Chromium Exposure
Panacryl
Permax
Renu
Vioxx
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©
2007 by Martin & Jones
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