In September 2024, pharmaceutical manufacturer Pfizer issued a global recall of Oxbryta, a medication that provided critical treatment to patients with sickle cell disease. Millions of people around the world struggle with this condition, and Oxbryta has served as a ground-breaking treatment by helping hemoglobin retain oxygen more effectively, which reduces the sickling process that causes red blood cells to become crescent-shaped and cluster together. However, research showed that the medication’s risks significantly outweighed these benefits. Oxbryta injury lawsuits have been filed, reflecting the harm caused to countless patients who used the medication in the past.
Oxbryta May Lead to Vaso-Occlusive Events
Vaso-occlusive crises (VOCs) are some of the most severe complications of sickle cell disease. These events occur when misshapen red blood cells cluster together and block blood vessels, preventing oxygen from reaching vital tissues and organs. VOCs can strike without warning, causing excruciating pain, organ damage, and in severe cases, death.
Recent clinical data revealed an alarming increase in these life-threatening events among Oxbryta users—proving that the medication may cause the very complications that it was designed to prevent. Oxbryta demonstrated such a dangerous safety profile of potential side effects that Pfizer had no choice but to recall the drug from the market.
What to Do If You Were Taking Oxbryta
If you are currently taking Oxbryta, speak to your doctor immediately to learn how you can safely stop using the medication and transition to an alternative treatment. Abruptly stopping the medication without medical supervision could trigger severe complications, so make sure to seek advice first.
Your doctor will evaluate your medical history and risk factors to determine the most appropriate treatment. During your transition, maintain detailed records of all symptoms, side effects, medical visits, and treatments related to your Oxbryta use. Document any VOCs, hospitalizations, or other adverse events that you experienced while taking the medication, including the dates, duration, and severity of symptoms.
Legal Options for Patients Harmed by Oxbryta
Drug manufacturers are required to disclose all potential risks associated with a medication, and when they fail to do so, they can be held legally liable. Former Oxbryta patients have now begun to file lawsuits against Pfizer for the harm that they suffered due to these dangerous side effects. If you have experienced serious complications—or lost a loved one due to Oxbryta use—you may be entitled to financial compensation.
A dangerous drug lawsuit allows you to hold the manufacturer accountable for the damages that you endured due to the undisclosed side effects. Your settlement may cover:
- Medical expenses
- Lost wages and benefits
- Disability accommodations
- Pain and suffering
- Loss of quality of life
- Funeral and burial expenses
Pursuing an Oxbryta lawsuit can provide financial support while holding pharmaceutical companies accountable for putting profits over patient safety. If you are unsure whether you qualify, an attorney can evaluate the strength of your case and assess your legal options.
Take Action with Shapiro Legal Group, PLLC
Victims of Oxbryta-related complications deserve justice, and an attorney can relentlessly pursue the accountability and compensation that they need to move forward. Shapiro Legal Group, PLLC is currently representing former patients nationwide in their lawsuits against Pfizer.
If you have been affected by this medication, trust our Oxbryta lawsuit attorneys to guide you through the process. Contact us at (800) 220-0984 for a confidential consultation to discuss your potential Oxbryta claim and learn how we can help secure the settlement you deserve.