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[T1414]Types Of Bone Fracture
by Peter Kent, Pet
The study, which was conducted by researchers at the University of East Anglia in Norwich, evaluated the risks of bone density degradation among women who consumed the diabetic therapy treatment. The CMAJ article reported that of the 13,715 individuals involved in the 10 randomized clinical trials, a large number had "a significantly increased risk of fractures".

Women who consumed the drugs were found to have an increased loss of bone mineral density among their lumbar spine, located just above the tailbone.

The study found no risk of bone density loss among men, but women who were already at risk for developing bone fractures were said to be affected with one out of every 21 women developing the condition, while those women not at a predisposed bone fracture risk were said to be affected with one out of every 55 women developing bone density loss.

How Thiazolidinediones Work

Approximately 4 million Americans currently consumed a type of thiazolidineodiones. Of the thiazolidinediones or glitazones class are Actos and Competact (piglitazone) and Avandia and Advandamet (rosiglitazones). According to the Medicines and Healthcare Products Regulatory (MHRA) organization the therapies, "work by reducing insulin resistance and helping the body use the insulin it produces; the MHRA is a regulatory body in the United Kingdom that is of similar nature to the U.S. Food and Drug Administration (FDA).

The following are additional safety concerns and side effects associated with the consumption of these medications, according to the MHRA:

* hypersensitivity

* cardiac failure

* hepatic impairment

* macular oedema

* bone fracture

Avandia Side Effects

Of the thiazolidinediones, is the commonly prescribed Avandia therapy from GlaxoSmithKline, which was released in May 1999. Besides bone fractures as a risk stemming from Avandia consumption, there are several additional side effects including:

* weight gain

* cold

* cough

* headache

* inflammation of sinuses

* back pain

* swelling, fluid retention

* cardiac arrest

Although Avandia has repeated made numerous headlines for the controversy surrounding its use, it remains on the market. Researchers who conducted the study explained that "these drugs need stronger warnings about potential side effects," according to a Washington Post article on the study.

Those who have become victims of the thiazolidinediones drug class may find it necessary to develop an Avandia class action lawsuit in which a return of money may be awarded to a victim for the damaged endured. Many pharmaceutical attorneys will offer free legal consultations as to the development of such litigation.

To determine the details of a potential Avandia lawsuit, victims can obtain information from an experienced pharmaceutical attorney.

Swiss researchers recently concluded that Avandia, a type 2 diabetes drug, nearly doubles the chances of osteoporosis and bone fracture among patients who take the drug and is increased for patients taking the drug for more than a year. The results of the study come on heels of controversy surrounding the drug's link to increased heart disease and various studies warning of potential risks related to bone degradation.

The type 2 diabetes drug was introduced to the market in 1999 from GlaxoSmithKline, and has been reportedly prescribed to nearly 3.5 million Americans suffering from the disease. Avandia was once considered one of the most popular treatments until results of several clinical trials reported in the news in 2007 determined a strong connection of the drug to cardiomyopathy and cardiovascular disease. One study, published by the Cleveland Clinic, found a 43 percent increase for patients developing these various heart diseases. Dr. John Buse, an expert on diabetes, has openly stated that Avandia may have been responsible for approximately 83,000 preventable myocardial infarctions over the last few years.

Additional studies then began to surface linking the drug to an increased risk of osteoporosis, although many of the studies did not have definitive proof of the connection until the recent Swiss study was published. The Swiss study determined patients on Avandia and Actos, which is also part of the Avandia class of drugs known as thiazolidinediones, doubled and, in some cases, tripled the ?odds of non-spine fractures? among patients, according to news reports. For patients who took the drug for 12 to 18 months, this risk increased, and for those on the drug longer than two years were found to be at the highest risk of bone fracture and osteoporosis.

Osteoporosis is a disease characterized by loss of bone density and leads to abnormally porous bones, thus increasing the fragility of bones and an increase of fractures and breaks. A bone diseased with osteoporosis will have a density similar to that of a sponge, whereas healthy bones have a brick-consistent density level. Bones are made up of collagen, calcium and protein to ensure strength. Avandia was found to inhibit the development of osteoclasts and osteoblasts, which are cells that induce the redevelopment of healthy bone over time. Nearly 18 million U.S. citizens are at risk for osteoporosis. While taking Avandia, that risk has been suggested to only increase.

The Swiss researchers used medical records of over 1,000 diabetic patients who were diagnosed with bone fractures between the years of 1994 and 2005. The medical records included diagnosis of fractures for these patients from British physicians, and the research was compared to a control group of diabetics that did were not diagnosed with bone fractures during that time. Avandia, once an extremely popular form of type 2 diabetes treatment, now is rapidly declining in popularity and in sales because of surfacing side effects. Most recently, the U.S. Food and Drug Administration (FDA) conducted a routine inspection that brought about information of results being withheld on the drug, thus the FDA issued manufacturers GlaxoSmithKline a warning letter.

However, the risk of osteoporosis and Avandia consumption has not be recognized by the FDA. In fact, the FDA has only responded to the controversial heart disease link by placing a black box warning on Avandia prescriptions, which some health experts consider to be a mild slap on the wrist considering the severe safety issues associated with the drug and many of these individuals are advocating removal of the drug from the market. The black box warning is the strongest label given by the FDA and warns of significant risk and the potential for life-threatening risks associated with taking a drug.

Individuals who have taken Avandia and who were adversely affected by the side effects of osteoporosis and bone fracture should speak with a pharmaceutical attorney about developing Avandia litigation to potentially receive monetary compensation for the medical bills incurred at the cost of the Avandia side effects.
Article Source : Pg. 29

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Both Peter Kent & Alan Haburchak are contributors for EditorialToday. The above articles have been edited for relevancy and timeliness. All write-ups, reviews, tips and guides published by EditorialToday.com and its partners or affiliates are for informational purposes only. They should not be used for any legal or any other type of advice. We do not endorse any author, contributor, writer or article posted by our team.

Peter Kent has sinced written about articles on various topics from Exhaust, Fitness and Health. For more information on Avandia visit or
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