Avandia
Avandia is one of the most popular treatments of Type 2,
or adult-onset diabetes – the most common form of the
disease. It has been on the market since 1999, and is used
by millions of people worldwide each year. It is available
by prescription only, under the brand names of Avandia, or
in combination with other drugs as Avandamet and Avandryl.
Avandia (rosiglitazone) works by lowering blood sugar
levels, which can cause complications such as kidney and eye
damage by increasing the body's sensitivity to insulin.
However, recent studies have linked its use to congestive
heart failure, hepatitis and liver failure.
A May 2007 study published in the New England Journal of
Medicine concluded that the drug raises the risk of heart
attack by 43 percent. Based on those results, the U.S. Food
and Drug Administration (FDA) issued a safety alert on the
drug. The FDA subsequently asked for a black-box warning
about congestive heart failure be added to the labels of
Avandia and a related drug, Actos.
In its May safety alert, the U.S. Food and Drug
Administration said patients taking Avandia, especially
those with heart disease or at high risk of heart attack,
should talk to their doctor about the risks. Lawsuits
concerning Avandia have resulted because of the serious side
affects associated with its use.
Avandia, manufactured by GlaxoSmithKline Plc, was approved
by the FDA in 1999, generates billions of dollars in sales.
The New England Journal of Medicine study detailed a recent
analysis of clinical trials that suggested that the drug
significantly increases the risk of heart attacks and
cardiovascular death. The study was conducted by doctors at
the renowned Cleveland Clinic. The trials compared patients
taking Avandia with those not using the drug. The results
indicate that Avandia users had an increase of
cardiac-related deaths by 64 percent and 43 percent increase
in heart attacks.
The consumer group Public Citizen has said that it had
repeatedly warned the Glaxo and the FDA about the dangers of
Avandia, stating that the drug should only be a
“last-choice” option for the treatment of type 2 diabetes
because studies have shown it to cause serious cardiac
problems.
Type 2 diabetes affects more than 20 million Americans, and
is a leading cause of coronary heart disease, blindness,
kidney failure and limb amputation. According to the
American Diabetes Association, in type 2 diabetes, either
the body does not produce enough insulin or the cells ignore
the insulin. Insulin is necessary for the body to be able to
use sugar. Sugar is the basic fuel for the cells in the
body, and insulin takes the sugar from the blood into the
cells. When glucose builds up in the blood instead of going
into cells, it can cause two problems:
- Right away, your cells may be starved for energy.
- Over time, high blood glucose levels may hurt your
eyes, kidneys, nerves or heart.
People who have taken Avandia may not know if they have been
harmed. If you or a loved one has taken Avandia and no side
effects were noticed, it is still possible the drug will
have an adverse effect. The defect of the drug is latent and
can manifest itself at any time. If you are currently taking
Avandia, of have taken any form of it in the past, we urge
you speak with a medical professional immediately. Then,
contact the Virginia law firm of Epperly & Follis, P.C. Our
firm handles product liability cases, which includes
pharmaceutical drugs like Avandia, as well as medical
devices.
Contact Epperly & Follis today for a free consultation at
1-888-703-0109 or (804) 648-6480, or contact us via our
online Contact Form.