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Jurors award $47.5 million in Vioxx decision
March 13, 2007 (Associated Press) – “Merck & Co.’s painkiller Vioxx contributed
to an Idaho postal worker’s heart attack, a jury in Atlantic City ruled Monday,
reversing the verdict in the man’s first trial and hitting Merck with a total of
$47.5 million in damages."
Forbes: June 29, 2006 - Key Vioxx 18-month Usage Claim Withdrawn by Journal,
Dealing Significant Potential Blow To Merck
Merck Found Liable For Man's Death In Vioxx Trial
August 19 2005 - Bloomberg - Merck & Co. must pay more than $253 million to
the family of a Texas man who died after taking the company's Vioxx painkiller.
Merck Pharmaceuticals Withdraws Popular Arthritis
Drug Vioxx from Market
See
Our Vioxx Alert Video
To view the current status of the litigation, see our articles, First
Vioxx Trial Verdict and Cases Challenge
18-Month Damage Claim and Analysts
Predict Merck’s Vioxx Liabilities Could Hit $50 Billion.
Merck withdrew Vioxx, its arthritis treatment, after a study
showed it increased the risk of heart attack and stroke.
In addition to heart attacks and strokes, Vioxx
has also been associated with several other life-threatening side effects,
including blood clots, angina and nonbacterial meningitis, severe intestinal
damage, ulcerations and bleeding, and kidney damage.
Merck & Co. announced the
immediate, voluntary worldwide withdrawal after a three-year colon cancer
clinical trial revealed that 18 months after patients started taking Vioxx, test
results showed an increased risk of heart attacks and other cardiovascular
complications.
Many recent Vioxx lawsuits bring to light questions as to when Merck was first
made aware that fatal side effects were associated with Vioxx, and whether the
company failed to inform public health authorities of these side effects, in a
timely manner.
In addition to heart attacks, strokes, and cardiac damage,
patients taking Vioxx have experienced the following Vioxx side effects:
-
Serious Kidney Problems: Serious
kidney problems may lead to acute kidney failure
-
Serious Liver Problems: Symptoms
of liver problems include nausea, tiredness, itching, tenderness in the
upper right abdomen and flu-like symptoms.
-
Allergic reactions: Symptoms
include swelling of face, lips, tongue, and throat which can cause
difficulty breathing or swallowing.
-
The FDA reports that Vioxx has
also been linked to at least five cases of a non-bacterial type of
meningitis, a rare but serious side effect.
These conditions may come about
suddenly with few or no symptoms. If left untreated, hospitalization or even
death can occur.
Merck extensively marketed Vioxx as highly safe and effective, while
minimizing its risks compared to other drugs on the market.
If you or a
loved one have taken Vioxx and have suffered any side effects, you may have a
legal right to compensation.
In a study of more than 8,000
patients that compared the COX-2 inhibitor rofecoxib (Vioxx) with the
traditional NSAID naproxen, the risk of cardiovascular problems, including heart
attack, chest pain related to heart disease, stroke, sudden death and blood
clots, was more than two times higher in the rofecoxib group than in the
naproxen group.
Vioxx and Celebrex are classified as
and known as COX-2 inhibitors, or coxibs. COX-2 inhibitors, like older drugs
such as ibuprofen and naproxen, are nonsteroidal anti-inflammatory drugs, or
NSAIDs. Older NSAIDs reduce inflammation by blocking an enzyme called COX-2, but
they also block another enzyme called COX-1. This enzyme helps protect the
lining of the stomach, so blocking COX-2 can cause stomach irritation. COX-2
inhibitors only block COX-2, leaving the stomach-protecting COX-1 alone.
The annual rates of heart attack in
both the Celebrex (celecoxib) and Vioxx (rofecoxib) studies were increased
compared to a review of studies containing a total of more than 48,000 patients.
In those studies, 0.52% of patients taking an inactive placebo pill had a heart
attack each year. The annual rate of heart attack was 0.74% for patients taking
rofecoxib and 0.80% for those taking celecoxib.
The researches believe that until
more research is done, doctors should use caution in prescribing Vioxx and
Celebrex to patients with heart disease.
FDA Drug
Safety Report
More
Informative Links.
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