The Story Of Our Firm | En Español
 Home    Lawyers   Litigation   Why Choose Us?   Results   Search

Drugs Avandia Research Center

FDA Safety Information

in this section: Firm's Press Release, 10.1.07 | Another FDA Warning? 10.24.07 | avandia drug warning | Study Reveals Risks, 6.6.07 | FDA Warning, 5.22.07 | Secret Avandia Vote | Veterans Affairs: Avandia | FDA Approval of Avandia | NEJM Study | Warning Letter, 2001 | Sales Plunge | NEJM Update, 6.5.07 | FDA Safety Information | FDA Warning, 6.6.07 | Scientists Silenced | Dallas Lawsuit | Patients Switch Meds | Avandia Prescriptions Fall | Updated Study, 7.12.07 | Avandia Panel, 7.25.07 | Second Black Box? | Senators Testify | Experts Cite Risks | Black Box Warning | 9.12.07 Study Analysis | Actos Study | Arkansas Lawsuit | Weakens Bones | JAMA Report, 12.7.07 | Avandia Diabetes Pills | Avandia Warning


Bookmark This Page Print This Page Email This Page

FDA Releases New Safety Info on Diabetes Drug Avandia and Side Effects

The following is updated safety information from the Food and Drug Administration's website. Concerns have been voiced side effects, about a possible increased chance of heart attack and heart-related deaths in patients taking Avandia--generic name rosiglitazone--an ingredient in three drugs used to treat type 2 diabetes: Avandia, Avandaryl, and Avandamet.

What Patients Should Do
If you are a patient taking rosiglitazone:
Do not stop taking Avandia, Avandaryl or Avandamet without first talking to your doctor about this new information. Discuss the best individualized treatment plan for your diabetes and other medical conditions. Remember that the best treatment plan is a team approach between you and your doctor. There is agreement by several organizations that the overall level of risk appears to be small, but that the risk deserves serious attention and follow-up. They are:

American Association of Clinical Endocrinologists
American College of Cardiology
American Diabetes Association
American Heart Association
Endocrine Society
FDA agrees with these organizations and is conducting a thorough investigation.

What We Know

  • FDA and GlaxoSmithKline (GSK), the maker of rosiglitazone, have long recognized that use of drugs containing this ingredient may be associated with certain heart problems. This information has been included in the prescribing information for all rosiglitazone-containing products since 2001.
  • New information regarding fluid-related heart problems has been updated since 2001 and included in the prescribing information for all three drugs--most recently in 2006.
  • GSK combined the data from 42 clinical studies to look at the chance of other heart problems with rosiglitazone, analyzed the data, and submitted the results of this analysis to FDA, which is conducting its own analysis of these data.
  • These combined data raise the possibility of a new risk from rosiglitazone, related to the heart. This possible risk, while important, appears to be small.
  • There are over 14,000 people in these studies, and about 2/3 of them were treated with rosiglitazone. Rosiglitazone is in a class of drugs called thiazolidinediones (TZDs). The other approved drug in this group is pioglitazone (Actos). These are two different drugs, and FDA is evaluating whether they have the same or different heart-related risks.
  • Swelling and fluid retention may occur with both drugs, so neither should be used in patients with troublesome heart failure.

    What FDA is Doing
  • Conducting its own analysis of GSK's combined data, including a detailed review of the patient information from the 42 studies.
  • Considering the results of these data along with all other published and unpublished studies regarding rosiglitazone use and other diabetes drugs to determine the chance of heart problems. Continuing to update the public as the agency receives new information, completes its analyses, and reaches conclusions based on those analyses.

    Type 2 Diabetes:
  • Is a serious and life-threatening disease
  • Affects about 18 to 20 million Americans
  • Is a leading cause of coronary heart disease, blindness, kidney failure and limb amputation
  • Is usually treated first with diet and exercise, and if they are not enough, FDA-approved medications, including metformin, sulfonylureas, thiazolidinediones, insulin, and several newer drugs, to lower blood glucose levels Differs among each person, so treatment must be individualized.

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

    Click To Talk To Us Online

    Please complete the following questionnaire:

    When did you start taking Avandia?
    What cardiovascular problems did you experience with the drug?
    What was the date you experienced cardiac complications?
    Did you have any cardiovascular disease before taking Avandia?
    Do you smoke?
    How did you learn of Weitz & Luxenberg?
    Contact Name
    Email Address
    Phone Number (optional)


  • see also:

    Patients Switch Meds Physicians Take Patients off Avandia Medicine, Citing its Heart Risks
    Fearing the Cardiovascular Risks, Doctors Take Patients off Avandia

    Weakens Bones Diabetes Drug Avandia Could Weaken Bones--Get a Free Legal Review
    Study: Type 2 Diabetes Med Avandia May Contribute to Fracture of Bones

    News & Warnings Avandia Breaking News: Glaxo Warned in 2001 about Misleading Marketing
    Bloomberg News: FDA Warned Glaxo about Avandia Marketing in 2001


    Name Phone Email
    Do you have a legal question? Ask us!   strictly confidential
    Your Question

    Click here
    for a free case review



    $53 million verdict — brake mechanic suffering from mesothelioma

    $13.5 million verdict — one of the very first Vioxx trial cases

    $15 million settlement — man wound up a paraplegic due to negligent hospital care

    $37 million verdict — 2 asbestos lung cancer plaintiffs

    $47 million verdict — boilermaker who died from mesothelioma

    $75 million verdict — historic consolidated trial involving men who had worked at the Brooklyn Navy Yard in the 1940s and 1950s

    $12.7 million verdict — iron worker who was injured due to unsafe working conditions

    $64.65 million award — 4 asbestos plaintiffs

    $17.5 million — consolidated trial of 5 mesothelioma victims

    $25 million jury verdict — brake reliner

    $5.8 million settlement — failure to perform timely C-Section

    $30 million verdict — 7 former power-plant workers suffering from asbestos-related illnesses

    $6 million settlement — pediatric malpractice case

    $14 million consolidated verdict — 5 asbestos-related cancer suits: shipyards/powerhouses/construction

    $8 million settlement — obstetrical malpractice resulted in neurological deficits

    $3.5 million — 2 asbestos exposure cases

    $600,000 settlement — motor vehicle negligence resulting in serious injury

    $44 million verdict — 5 asbestos cases, including $11.6 million awarded to widow of sheet metal worker who died of mesothelioma

    $1.6 million settlement — suicide after premature hospital discharge

    $2.6 million settlement — ill-fitting prosthesis caused decubitus ulcers

    $1.5 million settlement — construction worker fell off elevated train tracks

    $750,000 settlement — defective construction equipment resulted in serious injury to worker



    Ask a Free Question:
    Were you injured?

    check for your response [login]
    For legal help anywhere in the U.S.
    A nationally-recognized personal injury law firm, Weitz & Luxenberg is committed to helping clients win cases, get the compensation to which they’re entitled and continue with their lives. In just over 20 years, we’ve collected more than $1.3 billion for plaintiffs.