Onglyza Lawsuit

Manufactured by AstraZeneca, Onglyza is a medication used to treat type 2 diabetes. The primary purpose of this medication is to regulate insulin levels after a patient eats. This may be used in conjunction with other medications or used alone. But it is intended only for treating type 2 diabetes and not for treating patients who are suffering from diabetic ketoacidosis. Onglyza was approved by the FDA in 2009.

While it was considered safe at that time by many patients and doctors, there is increasing academic evidence that the drug increases a user’s risks for cardiovascular problems, some of which can be fatal. This is why more patients are speaking with an Onglyza lawyer about their potential for filing a lawsuit. The Food and Drug Administration has been a critical component of raising the alarm about the potential harm associated with Onglyza.

Patients who have been injured by this medication allege that:

  • The company did not safely market this medication
  • The company knew about the dangers of this drug but failed to warn the public and marketed it anyways
  • The company manufactured a dangerous drug to begin with

Patients and family members who have suffered injuries as a result of taking Onglyza may be entitled to compensation in the form of wrongful death expenses, punitive damages, medical costs, pain and suffering and lost wages. Every potential case of medical injury associated with a dangerous or defective drug needs to be evaluated separately. This is why it is essential to set up a consultation with an Onglyza lawyer sooner rather than later.

FDA Warns Patients About Potential Onglyza Risks

In 2015, an FDA panel required that AstraZeneca place an additional warning about Onglyza on the label that would warn patients about a potential risk of heart failure.

This is a result of the SAVOR study involving nearly 16,500 patients. In this study, 1,220 of these patients were associated with a major cardiovascular event. In this study the manufacturer was responsible for indicating that Onglyza could not increase heart failure or other cardiovascular risk by more than 30%. This study indicates that patients taking Onglyza were found to have a 27% higher risk of hospitalization for heart failure when compared with those patients in the controlled group.

Although the manufacturer met this required threshold, the FDA panelists shared that more details were necessary in order to determine the actual risk of death. If you or someone you know has recently suffered heart failure or another major cardiovascular event after taking Onglyza or a similar medication, you may have grounds to file a lawsuit for compensation.

Some of the symptoms of heart failure include:

  • Fatigue
  • Persistent wheezing or cough
  • Irregular heart rate
  • Swelling of feet, hands or ankles
  • Difficulty breathing

This most recent study is not the first time that Onglyza has been called into question. In 2013 a separate study indicated that use of Onglyza was linked with a higher risk of pancreatic cancer. Pancreatic cancer was identified in individuals who took Onglyza, especially males over the age of 60 who took the drug for between 1 and 6 months and also took the drug Simvastatin. More than 2,600 individuals participated in this study and 19 of them had pancreatic cancer.

More on Onglyza Lawsuits

Many Onglyza users and their family members have decided to take legal action by filing claims as a result of the medications linked to unanticipated health issues. Users of Onglyza allege that they have suffered serious medical conditions as a result of their use of the drugs and that the manufacturer was aware of these risks but chose not to share it with the public. Some users have already filed lawsuits against AstraZeneca after experiencing health problems associated with their Onglyza use.

Many have been successful in recovering damages for lost wages, pain and suffering and medical costs. If you have recently lost a loved one as a result of his or her use of Onglyza or suspected use of Onglyza, family members may be eligible to recover expenses associated with wrongful death. Contact an experienced attorney today.

Notwithstanding claims relating to this product, the drug/medical device remains approved by the U.S. FDA.


Since its establishment in 1999, Seeger Weiss has led some of the most complex and high-profile litigations in the U.S.