Avandia® Warning

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Made and distributed by GlaxoSmithKline, Avandia® is an oral diabetes medication that helps those with type-2 diabetes better control their blood glucose levels. However, since its release in 1999, Avandia® has been found increase patients' risk of:

  • stroke
  • bone fractures (particularly in the hands and/or feet)
  • congestive heart failure
  • heart attack

Although the Food and Drug Administration (FDA) has yet to officially recall Avandia®, it has issued two national Avandia® warnings (on March 21, 2007 and May 23, 2007) to alert the public about the dangerous side effects associated with this medication (In 2008, Avandia® warnings weren't issued).

In the latest warning, the FDA required that the Avandia® drug warning label be upgraded to a "black box warning," the most serious type of warning label indicating the drug can cause life threatening side effects.

Information on the Avandia® Warning Label

To ensure that patients are aware of the risks associated with taking the Avandia® drug, warning labels include the following information:

  • Avoid drinking alcohol when taking Avandia®, as alcohol consumption can increase patients' risk of developing severe cases of hypoglycemia (dangerously low blood sugar).
  • Before taking Avandia®, tell your doctor if you have a history of stroke, heart problems and/or liver disease, as these conditions may affect your dosage (or prevent you from being able to safely take Avandia®).
  • Do NOT take Avandia® if you are pregnant, breastfeeding or thinking of becoming pregnant, as the effects of this medication on unborn babies is currently unknown.
  • Do NOT take Avandia® if you have type-1 diabetes, as this medication is only for the treatment of type-2 diabetes.
  • Do NOT take Avandia® if you are in a state of diabetic ketoacidosis (a potentially fatal condition in which a severe lack of insulin results in dangerously high blood sugar levels).

Other Avandia® Warnings

In addition to the above precautions, the 2007 Avandia® warnings also alert patients to seek immediate medical attention should they start to develop any combination of the following symptoms:

  • blurry vision
  • chest pain
  • dark urine and/or clay-colored feces
  • frequent urination
  • general information
  • increased appetite
  • nausea
  • paralysis on one side of the body
  • rapid weight gain
  • sweating
  • weakness
  • breathing difficulties (particularly shortness of breath)

These symptoms can indicate that patients are developing serious Avandia® side effects. Emergency medical care will be necessary to prevent further, possibly life threatening complications.

Avandia® Lawsuits

Despite FDA Avandia® drug alerts and warnings, some patients will still be injured after using Avandia®. These individuals will likely have a legal claim against GlaxoSmithKline and may be entitled to compensation for their:

  • past and future medical bills
  • ongoing treatments and medications
  • emotional pain and suffering
  • living expenses, lost wages

To encourage affected individuals to evaluate and pursue their cases, experienced Avandia® attorneys offer free consultations and work on contingency, meaning there is no fees unless a settlement is awarded.

If You Have Been Injured by Avandia®

Have you or a loved one been injured after taking Avandia®? If so, contact us to speak with an experienced Avandia® attorney who specializes in drug recall litigation & lawsuits. Let us help you win the compensation you need and deserve.

Free Consultation Use this form to request a free consultation with a qualified attorney near you.
Have you or a loved one experienced one of the following?
Heart Attack
Stroke
Congestive Heart Failure
Macular Edema
Other Ailments
If the person taking Avandia died, please list the cause of death as stated on the death certificate and state whether there was an autopsy.

Was there a hospitalization for any reason while taking Avandia?

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