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Possible Class Action Lawsuit against Vioxx
Aug-19-05 - Recently a jury awarded
$253.4 million in damages to a man who died of arrhythmia or irregular
heartbeat, after approximately eight months of Vioxx use.
This, despite the fact that the manufacturer claims it studied whether
Vioxx caused arrhythmias in nine clinical trials before the drug went
on the market, and determined that there was “no clinically meaningful
differences" in patients who took the pain killer versus a placebo
or other NSAID medication.
Nevertheless, counsel for the deceased victim’s wife and plaintiff,
stated that her husband died too quickly for his heart to show damage.
He also pointed to Merck’s own highly recognized medical reference,
The Merck Manual, which itself states that arrhythmias play a role
in more than ninety percent of all heart attacks.
If you consulted a lawyer who declined your case due to lack of
myocardial infarction, or you completed a form on this site that indicated
a rhythm disorder and you did not receive a response from an attorney,
please submit your complaint to us and clearly note your arrythmia
issue.
Jul-02-03 - Vioxx (Rofecoxib) is a Cox-2 inhibitor that was
approved by the US Food and Drug Administration in 1999 for the treatment
of arthritis, osteoarthritis, menstrual pain and for the management
of acute pain in adults. Serious concerns have been raised in recent
months regarding the use of Vioxx, Vioxx side effects
on kidney and cardiovascular health, and the increased risk of heart
attack and stroke.
Vioxx is an anti-inflammatory drug, which means it reduces
internal inflammation. Vioxx, along with Aspirin, is part
of the class of drugs known as nonsteroidal anti-inflammatory drugs
(NSAID) - i.e. it is not a steroid. Vioxx is analgesic, (it eliminates
pain) and it is antipyretic (it reduces fevers). Its active ingredient
is rofecoxib.
Vioxx withdrawn from the market
Vioxx was pulled off the shelves worldwide in September 2004
after a clinical study confirmed concerns that it raises the risk
of heart attack and stroke, which can lead to serious and permanent
injuries and death. More than 2 million people worldwide are using
Vioxx.
Complications begin approximately 18 months after patients start taking
Vioxx. Previous clinical trials had linked Vioxx to an increase
in blood clots and other cardiovascular problems, including heart
attack, chest pain related to heart disease, stroke and sudden death.
Vioxx users were more than twice as likely to experience heart problems
than patients using the control drug.
The results of clinical studies with one drug in a given class do
not necessarily apply to other drugs in the same class. All NSAIDs
have some risks, such as gastrointestinal (stomach) bleeding, and
liver and kidney toxicity, when taken chronically.
Vioxx advisory from FDA
Doctors are being told to take patients off Vioxx. Please talk to
your Doctor as soon as possible about switching to another drug. The
FDA has issued a public health advisory, and plans to work closely
with Merck to coordinate the withdrawal of Vioxx from the
US market.
FDA Public Health Advisory
The FDA public health advisory on Vioxx safety. [US
FDA]
Vioxx In the News
Judge denies mistrial request by Merck lawyers in second Vioxx lawsuit
claiming that Vioxx caused a New Jersey man's heart attack in 2001.
(Oct-03-05) [CNN]
Due to hurricane Katrina federal Vioxx cases are being moved from
New Orleans to Houston. (Sep-06-05) [TALLAHASSEE
DEMOCRAT]
New Jersey Vioxx trial is set. (Aug-30-05) [REUTERS]
Jury Awards Widow $253.4 million in Vioxx Trial (Aug-19-05) [BUSINESS
WEEK]
Merck Vioxx Suit Certified as Class Action by New Jersey Judge [BLOOMBERG]
Internal documents show that Merck considered reformulating Vioxx
in 2000 to reduce cardiovascular side effects after a study found
patients were five times more likely to have heart attacks than those
on the generic naproxen. (June-23-05) [SAN
FRANCISCO CHRONICLE]
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