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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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| December
31, 2003 |
Biotech
Week, "Merck, a textbook case of pharmaceutical
industry woes"
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The
problems besetting pharmaceutical giant Merck &
Co. also plague most of its competitors: falling profits,
patent expirations, generic competition, the lack
of new blockbuster drugs and pressures to make medicines
more affordable. But
the contrast to the heady days and double-digit profit
growth of the 1990s is particularly striking at Merck,
which has fallen in just a few years from the world's
biggest drug maker to No. 3 as competitors merged
and leapfrogged ahead.
"The
key to success in this industry is novel medicines and
medicines that are priced competitively," said
Merck's chairman.
But
this fall Merck canceled testing of the fourth drug
in mid- or late-stage development since February, one
of which was expected to be its first entrant in the
lucrative antidepressant market. Merck also announced
an unprecedented layoff of 4400 workers - 7% of its
global work force - as part of a drive to make the company
more efficient.
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| December
31, 2003 |
CBS
Market Watch, "Merck seeks OK for
new arthritis medication"
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Merck
& Co. shares rose Wednesday after the company resubmitted
a U.S. marketing application for Arcoxia, a highly anticipated
arthritis medication.
For
the year, Merck shares are down 18 percent because of
concerns that the drugmaker doesn't have enough new
promising medications in development.
Re-filing
of the application, announced late Tuesday, had been
expected. Merck CEO Raymond Gilmartin affirmed in early
December that the No. 3 pharmaceutical company was on
track to resubmit Arcoxia to the Food and Drug Administration
before the end of the month.
Merck
had withdrawn the initial application for Arcoxia in
March 2002 to gather more information about its potential
to treat an inflammatory condition of the spine.
Arcoxia,
which is already available in 38 countries, is seen
as the next-generation version of Vioxx, Merck's blockbuster
arthritis medication.
Merck
has forecast that combined 2004 sales of Vioxx and Arcoxia
will be between $2.6 billion and $2.8 billion.
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| December
30, 2003 |
AFX
News Limited, "Merck seeks OK for new arthritis
medication"
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Merck
& Co. said late Tuesday it had resubmitted to the
FDA a marketing application for Arcoxia, an arthritis
medication. Merck had withdrawn the initial application
for Arcoxia in March 2002 to gather more information
about its potential to treat an inflammatory condition
of the spine. The No. 3 drugmaker is positioning Arcoxia
as the next-generation version of its arthritis blockbuster
Vioxx.
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| December
21, 2003 |
Heart
Disease Weekly, "Inflammation: Vioxx
shows no effect on markers of cardiovascular disease"
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In
the largest randomized controlled trial yet of the effect
of a COX-2 inhibitor on the function of blood vessels
and markers of inflammation, including C-reactive protein,
rofecoxib (brand name Vioxx) did not appear to have
any favorable or adverse effects in patients with coronary
artery disease who were receiving low-dose aspirin,
according to a new study.
"I
was surprised that rofecoxib had no effect, as I had
originally hypothesized that it would both improve endothelial
dysfunction and reduce signs of inflammation,"
said Lawrence M. Title, MD at the Queen Elizabeth II
Health Sciences Center in Halifax, Nova Scotia, Canada.
"I was more surprised that we saw no effect on
the markers of inflammation, including high-sensitivity
C-reactive protein (CRP), given that rofecoxib is an
anti-inflammatory drug," he added.
The
study appeared in the Journal of the American College
of Cardiology.
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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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