If you or a loved one has suffered health issues after taking the medication Oxbryta, our dedicated personal injury lawyers are here to help. Oxbryta, a drug prescribed to treat sickle cell disease, was developed to improve the lives of those struggling with this chronic illness. However, recent reports have raised serious safety concerns, leading to a manufacturer recall that has left patients and families worried about potential health risks. If this has impacted you or a loved one, you may need the assistance of an Oxbryta recall lawyer.
FDA Oxbryta Recall Notice
“Pfizer Inc., the manufacturer of Oxbryta, announced it is voluntarily withdrawing the medication from the market, ceasing distribution, and discontinuing all active clinical trials and expanded access programs for Oxbryta because recent data indicate the benefit of Oxbryta does not outweigh the risks for the sickle cell patient population,” an FDA notice for the Oxbryta recall revealed on September 26, 2024.
“In postmarketing clinical trials of Oxbryta, Pfizer reported a higher rate of vaso-occlusive crisis (severe pain caused by sickled red blood cells blocking blood flow and oxygen delivery to tissues) in patients with sickle cell disease receiving Oxbryta compared to placebo,” the notice continued.
Ultimately, there were also more deaths in the Oxbryta treatment group when compared to the placebo group in these studies. “Pfizer also observed a higher rate of vaso-occlusive crisis in patients with sickle cell disease receiving Oxbryta in two real-world registry studies,” the notice said. “Based on the totality of clinical data, Pfizer has determined the benefit of Oxbryta does not outweigh the risk.”
What Is a Vaso-Occlusive Crisis?
“A vaso-occlusive crisis, or VOC, occurs when sickled red blood cells block blood flow to the point that tissues become deprived of oxygen,” Sickle Cell Disease News reported.
“This in turn sets in motion an inflammatory response as the body tries to rectify the problem. The result is substantial pain, which can affect any part of the body, but most commonly occurs in the back, chest, or extremities.”
There were higher rates of vaso-occlusive crisis reported by Pfizer in patients who took Oxbryta compared to those taking a placebo. Sadly, some patients who trusted this medication reported adverse effects that impacted their quality of life and caused severe complications.
“VOC is the most common cause of hospitalization related to SCD,” according to Sickle Cell Disease News. “In addition to causing acute pain, these crises can set the stage for further health complications, such as arthritis, kidney failure, and strokes.”
What Should Patients Taking Oxbryta Do?
“Health care professionals should stop prescribing Oxbryta,” the FDA recall notice advised. “Patients and caregivers should contact their health care professional about stopping Oxbryta and starting another treatment option.”
Fortunately, the agency noted, “There are other FDA-approved medications for the treatment of sickle cell disease, which health care professionals may prescribe as an alternative treatment to Oxbryta.”
If you have been affected by the Oxbryta recall, you may be entitled to compensation for medical bills, lost wages, pain and suffering, and other damages resulting from the harm caused by this drug. It is recommended that you contact an Oxbryta attorney to learn more about your legal options.
Oxbryta Cases – Eligible Injuries
Phillips Law Group is currently investigating potential Oxbryta claims. If you or a loved one has been diagnosed with a variant of sickle cell disease, were prescribed Oxbryta, and took it at least once daily, you may have an eligible claim.
If you have medical documentation that shows increased vaso-occlusive crises, a diagnosis of acute chest syndrome that is new or has recently worsened, or documentation showing hepatic failure, blood clots, arthritis or bone necrosis, kidney failure, priapism, stroke, vision loss, pulmonary hypertension, splenic sequestration, sleep disordered breathing like sleep apnea, leg ulcers, and severe infections such as pneumonia, or your loved one died after consistent use of Oxbryta, you may be qualified to take legal action.
Please contact our firm without delay to determine your options.
How Phillips Law Group Can Help with an Oxbryta Recall Case
At Phillips Law Group, we have years of experience in seeking justice for individuals harmed by dangerous or defective pharmaceutical products. Our experienced legal team will work to investigate your case, gather evidence, and hold the manufacturers accountable. We understand how devastating it is to face health complications after trusting a prescription drug, and we’re committed to providing compassionate, effective legal support for you every step of the way.
If you believe that Oxbryta has negatively impacted your health, don’t face the fight alone. Our personal injury lawyers have the resources and experience necessary to pursue justice and compensation on your behalf. We have been a trusted voice in the Arizona community for years, have a proven record of success, and our team wants to help.
Contact us today for a free, no-obligation consultation with an Oxbryta recall lawyer. We’re here to answer your questions, explain your rights, and take the first steps toward holding the responsible parties accountable for their actions. Call 602-222-2222 to learn more now.
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