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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. |
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| Below are summaries of press articles on the Vioxx trials and Vioxx class action. For a concise review of the Vioxx recall and how patients with Vioxx side effects may file a Vioxx lawsuit and obtain compensation, please visit our main page. |
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| August
24, 2002 |
The
Orange County Register (Santa Ana, California),
"Some worry 'better' painkillers may have negative
side effects"
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Seven years ago, Ruth Carvajal gave up her thriving
housecleaning business to battle miserable pain
from rheumatoid arthritis. The arthritis had more
or less crippled her hands, distorted her posture,
especially along her hips, tortured her every
step and robbed her of peaceful sleep.
Carvajal, 61, of Santa Ana, Calif., tried many medications
but eventually found relief only in Celebrex. The prescription
drug, along with Vioxx and newcomer Bextra, is among
a class of pain medications called cox-2 inhibitors.
Hailed as better painkillers when they debuted in 1998,
cox-2 inhibitors are now being scrutinized to determine
whether they increase risk of heart attacks and whether
they pose a lower risk of adverse effects than conventional
prescription pain medications.
The FDA underscored the question of risks in April when
it established labeling changes for Vioxx, after a large-scale
study on the drug. That study found that Vioxx carried
a lower risk of gastrointestinal adverse effects compared
with naproxen but also unexpectedly found that those
who took Vioxx had a higher risk of a heart attack.
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| May
27, 2002 |
The
Associated Press, "New studies add to
debate over arthritis drugs and suspected risk of heart
attacks"
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Three new studies are adding to a raging debate over
whether the popular arthritis pain reliever Vioxx increases
the risk of heart attack.
The editor of the Archives of Internal Medicine, which
published the studies in its May 27 edition, says the
results offer reassuring evidence that drugs like Vioxx
and Celebrex are not bad for the heart.
But cardiologist Dr. Eric Topol of the Cleveland Clinic
said the Food and Drug Administration's order last month
for new precautions on Vioxx's label is still warranted.
Topol took part in an analysis last year of data that
showed Vioxx users faced double the risk of serious
cardiovascular problems, including stroke and heart
attack. He said the newest research leaves the question
"far from settled."
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| April
15, 2002 |
USA
Today, "Drug dilemma confronts arthritis
sufferers"
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Arthritis
patients looking for pain relief may start feeling as
if they have to choose between two evils: a bleeding
ulcer from some drugs, maybe a higher risk of heart
attack from another.
The
Food and Drug Administration announced last week that
Vioxx -- Merck's blockbuster painkiller, with $ 1.9
billion in sales last year -- would include new information
on its label. The FDA said Merck can claim that Vioxx
has fewer gastrointestinal (GI) complications than one
older non-steroidal anti-inflammatory drug, naproxen.
But the FDA also decided that the Vioxx label must mention
that it might be linked to an increased risk of heart
attack or high blood pressure.
More
than a year ago, an FDA advisory committee recommended
adding the heart disease information to Vioxx's label
after hearing presentations by agency scientists.
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| April
12, 2002 |
The
New York Times, "Merck to Revise Label
Information for Vioxx"
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Merck
& Company said yesterday that it would revise
prescribing information for its Vioxx painkiller to
show both cardiovascular risks and a benefit in reducing
side effects like ulcers in arthritis patients.
Merck
will include information on higher risks of heart
attacks for Vioxx patients, compared with the risk
in patients taking an older painkiller, naproxen.
The Food and Drug Administration will also allow changes
in the drug's label to reflect results from a study
showing that Vioxx patients had fewer gastrointestinal
side effects than patients on naproxen. Vioxx had
sales of $2.6 billion last year.
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| Lieff Cabraser: Experienced Product Liability Lawyers |
| Founded in 1972, Lieff Cabraser Heimann & Bernstein,
LLP is an over fifty attorney law firm with offices in San Francisco, New
York and Nashville. For the last five years, the National Law Journal has
recognized Lieff Cabraser as one of the top plaintiffs law firms
in America. |
| For our personal injury cases, we bring a team of experienced lawyers. Each client is assigned a partner and an associate. In addition, we have on staff multiple nurses, legal assistants, scientific analysts and case clerks to assist the attorneys. |
| We have represented thousands of patients who ingested prescription drugs with dangerous undisclosed side effects, and patients who received defective medical devices 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. |
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Lieff
Cabraser Heimann & Bernstein, LLP
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| Trademark Notice |
| "Vioxx" is
a registered trademark of Merck. Lieff Cabraser Heimann & Bernstein,
LLP is in no way affiliated with Merck, and the Vioxx
trademark is used solely for informational purposes. |
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Copyright © 2007 Lieff Cabraser Heimann & Bernstein, LLP |
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Merck
Agrees to Resolve U.S. VIOXX® Product
Liability Lawsuits
November 9, 2007
Merck & Co., Inc.
announced that
it has entered into
an agreement to resolve
state and federal myocardial
infarction (MI) and
ischemic stroke claims
already filed against
the Company in the
United States. More... |
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