Oxbryta Lawsuits

If you or a loved one took Oxbryta for 30 days or more between 2018 and the present, and developed vaso-occlusive crisis (sickle cell crisis), stroke, organ failure, heart attack or death, contact Ankin Law right away. We are currently investigating cases to determine whether injured patients have viable Oxbryta lawsuits. Free consultations are available to help you get started.

Call us at (312) 600-0000 to discuss your case and explore your legal options.

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Why Are People Filing Oxbryta Lawsuits?

Oxbryta lawsuits stem from allegations that the manufacturers Global Blood Therapeutics and Pfizer failed to adequately warn patients and healthcare providers about the risks associated with the medication. Even though Pfizer is voluntarily recalling Oxbryta, key legal claims include:

Inadequate Warnings and Labeling

Many lawsuits allege that Global Blood Therapeutics and Pfizer did not provide sufficient warnings about the risks and severe side effects of Oxbryta. Patients argue that had they been fully informed, they might have chosen alternative treatments.

Negligence in Testing and Approval

Plaintiffs claim that the manufacturer rushed the approval process for Oxbryta, prioritizing market availability over patient safety. Insufficient clinical trials and limited long-term safety data are common points of contention.

Failure to Monitor Post-Market Safety

Ongoing monitoring of a drug’s safety is critical after FDA approval. Lawsuits allege that Global Blood Therapeutics and Pfizer failed to adequately monitor and address adverse events reported by patients and healthcare providers.

Despite Pfizer’s voluntary withdrawal of Oxbryta, people who suffered severe health complications after taking the medication can still file lawsuits to recover compensation. A recall does not eliminate liability for harm caused by the drug. If you suffered injuries from Oxbryta, you may have legal options to seek compensation for medical expenses, pain, and other damages. 

Do the Risks Outweigh the Benefits?

Oxbryta (voxelotor) is an oral medication that was approved by the U.S. Food and Drug Administration (FDA) in 2019 to treat sickle cell disease in patients aged 12 and older. Sickle cell disease is a genetic blood disorder that affects the shape and function of red blood cells. It can lead to severe pain, organ damage, and other life-threatening complications. Oxbryta was developed to improve the quality of life for patients by addressing the root cause of the disease. Manufactured by Global Blood Therapeutics, and later bought out by Pfizer, Oxbryta works by increasing hemoglobin levels and reducing the destruction of red blood cells.

However, emerging reports, clinical studies, and postmarketing data suggest that the medication may cause adverse effects that outweigh its intended benefits. 

After numerous instances of Oxbryta patients developing vaso-occlusive crisis, organ damage, and other complications, Pfizer voluntarily recalled Oxbryta from the market in September 2024.

Reported Side Effects and Risks Associated With Oxbryta

While Oxbryta has been praised for its innovative approach to treating sickle cell disease, some patients have reported side effects, including:

  • Headaches
  • Diarrhea
  • Fatigue
  • Nausea

These symptoms, while uncomfortable, are generally manageable. However, some individuals have experienced serious, and even life-threatening complications while using the medication, including:

Legal Rights for Victims of Oxbryta (Voxelotor)

If you used voxelotor and experienced severe complications, you may be eligible to file an Oxbryta lawsuit against Global Blood Therapeutics, Pfizer, or both. Taking legal action can help you recover compensation for losses and hold the companies accountable.

Types of Compensation Available

Medical Expenses:

You may be entitled to compensation for hospital stays, treatments, and ongoing care related to Oxbryta complications.

Lost Wages:

If you missed from work due to health issues caused by the medication, you may be reimbursed for the income you lost.

Pain and Suffering:

Compensation may also be available for physical and emotional distress caused by the medication.

Wrongful Death:

If your loved one passed away due to complications caused by Oxbryta, you may pursue claims for loss of companionship and financial support.

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    Steps to Take If You’ve Been Affected by Oxbryta

    If you believe you’ve suffered harm due to Oxbryta, it’s important to take action promptly to protect your health and your legal rights.

    1. Seek Medical Attention: Document your symptoms, seek medical advice from your healthcare provider, and receive the recommended treatment for any health complications.
    2. Preserve Evidence: Keep records of your Oxbryta prescriptions, medical visits, and any communication with healthcare providers.

    Contact Ankin Law: Call us at (312) 600-0000 to schedule a free consultation. We’ll evaluate your case and provide guidance on the next steps.

    Frequently Asked Questions About Oxbryta Lawsuits

    1

    Who Can File an Oxbryta Lawsuit?

    Anyone who has suffered serious side effects or complications after taking Oxbryta for over 30 days between 2018 and the present may be eligible to file a lawsuit. Family members of deceased victims may also have grounds for legal action.

    2

    How Long Do I Have to File a Claim?

    The statute of limitations for filing a product liability claim in Illinois is typically two years from the date of injury, or the date the person knew about the injury. Exceptions exist, however, and your deadline may be shorter or longer. Contact Ankin Law to ensure your claim is filed on time.

    3

    What Evidence Is Needed for a Lawsuit?

    Key evidence includes medical records, proof of Oxbryta prescriptions, and documentation of adverse effects. Our attorneys will help gather and organize the necessary information to build a strong case.

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    Very pleased with all the help that Scott Goldstein has afforded me. During the process of my case, Scott continued to go the extra mile repeatedly. I feel that Scott is an excellent lawyer. When Scott is unavailable, his assistant is always there to answer any questions I had. I highly recommend Scott Goldstein and Ankin Law Firm.

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    If you or a loved one took Oxbryta for at least 30 days, and you were diagnosed with vaso-occlusive crisis (sickle cell crisis), stroke, organ failure, or heart attack, or your loved one died, don’t wait to seek legal assistance. Call us today at (312) 600-0000 for a free consultation. Let us help you hold negligent manufacturers accountable.