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Drugs & Medical Devices Avandia Legal Options News & Warnings

JAMA Report, 12.7.07

in this section: 6.6.07 Study | FDA Warning, 5.22.07 | Black Box Warning | JAMA Report, 12.7.07


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Breaking News: Report in the Journal of American Medical Association Finds Older Patients using Avandia at Risk of Serious Heart Problems, Death

BREAKING NEWS: A study in the December 12, 2007 issue of the Journal of the American Medical Association (JAMA) has found that older patients treated with diabetes medications known as thiazolidinediones (which include rosiglitazone, brand name Avandia) had a significantly increased risk of heart attack, congestive heart failure and death, compared with the use of other drugs.

The study's authors conclude that the results present further evidence that drugs such as Avandia may cause more harm than good.

The study included 159,026 individuals with diabetes. Users of medicines with rosiglitazone had a 60 percent increased risk of heart failure; a 40 percent increased risk of heart attack; and a 29 percent increased risk of death.

If you or a loved one has suffered cardiac complications after ingesting Avandia, you deserve the guidance of a knowledgeable drug attorney. Get a free case review by filling out the form below.

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Did you experience cardiovascular problems after taking Avandia?
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Did you suffer a bone fracture after taking either Avandia or Actos?
Please provide detail about your bone fracture injury, including the date of the injury, how the fracture occured and what bone(s) were affected.
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see also:

6.6.07 Study Study Designed to Debunk Risks Raises Questions About Avandia Medicine
Avandia Medicine Still Has Serious Heart Risks, Doctors Warn

Black Box Warning FDA: Manufacturer of Avandia Strengthens Warning on Heart Failure Risk
FDA Says GlaxoSmithKline Will Include Boxed Warning on Avandia Label

FDA Warning, 6.6.07 FDA Issues Strictest Warning on Prescription Diabetes Drug Avandia
FDA Calls for Toughest Warning to be Placed on Avandia Prescription

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