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Avandia, an oral medication used to treat type-2 diabetes, has been found to increase the chances that individuals taking this drug will develop severe, potentially life-threatening side effects. To date, the Food and Drug Administration (FDA) has not issued a formal recall on Avandia.
However, in August 2008, a medical journal entitled Heart published a study that:
In response to this research, the FDA mandated that GlaxoSmithKline (the maker of Avandia) include “black box” warnings on all Avandia packaging. Black box warnings are the most serious warnings issued by the FDA, as they indicate that a drug has the potential to cause severe injury, permanent disability and/or death.
Following this mandate, the FDA voted 8 to 7 against issuing an Avandia recall.
Some of the serious injuries associated with Avandia use (and used as a basis of urging an Avandia drug recall) include:
Without treatment, some of these side effects – particularly heart attack, CHF and severe allergic reaction – can be fatal.
Avandia patients with the highest risk of sustaining these side effects include those with a history of:
Additionally, diabetic patients who do NOT eat healthfully and do NOT exercise regularly will also have a greater risk of developing severe Avandia side effects.
Patients who sustain serious side effects after taking Avandia should:
To encourage injured Avandia patients to learn more about their legal rights and entitlements, Avandia lawyers:
For more information about Avandia recall and other defective drugs, please contact an Avandia lawyer today.
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