Oxbryta Lawsuit Litigation Updates

December 3, 2024

• Oxbryta Withdrawal Underscores Long-Standing Concerns: Pfizer's recent decision to withdraw Oxbryta from global markets highlights long-held concerns about the drug's safety and effectiveness. Regulatory agencies and health authorities, including the UK's National Institute for Health and Care Excellence (NICE), had previously expressed reservations about Oxbryta's cost-effectiveness and clinical benefits. This withdrawal could strengthen the position of those pursuing lawsuits related to Oxbryta's side effects.

November 19, 2024

• European Regulators Recommend Halting Oxbryta Sales: The European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use has recommended suspending the marketing authorization for Oxbryta, a sickle cell disease drug. This decision raises further concerns about the drug's safety profile and could influence regulatory actions in other countries.

November 9, 2024

• New Oxbryta Lawsuit Alleges Increased Health Risks: A new lawsuit filed in California claims that the sickle cell disease drug Oxbryta caused severe health complications, including an increase in vaso-occlusive crises and a stroke. The plaintiff alleges that the manufacturers, Global Blood Therapeutics and Pfizer, failed to adequately warn about these risks despite knowledge of potential adverse effects. The lawsuit seeks damages for various claims, including strict liability, negligence, and breach of warranty.

Oxbryta Linked to Serious Health Risks: File a Lawsuit Today

Oxbryta, a medication for sickle cell disease, has recently been linked to a higher risk of vaso-occlusive crises (VOCs) and other serious health issues. This has led to many patients who took Oxbryta seeking information and legal help.

But you don't have to face this alone. You have rights. At Injury Claims, we connect you with experienced attorneys who will help you understand your legal options and pursue the compensation you deserve if you've been harmed by Oxbryta.

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Oxbryta Recall Information

On September 26, 2024, the U.S. Food and Drug Administration (FDA) announced that Pfizer, the manufacturer of Oxbryta, had issued a voluntary recall of the medication.

This recall was initiated due to recent studies that showed an increased risk of VOCs and death in patients taking Oxbryta compared to those taking a placebo.  

Oxbryta Use and Increased Health Risks

Studies have shown a possible connection between Oxbryta use and an increased risk of VOCs, a painful and dangerous complication of sickle cell disease. VOCs happen when sickled red blood cells block blood flow, causing severe pain and potentially damaging organs.

The possible link between Oxbryta and these complications raises questions about whether patients were adequately informed of the medication's risks.

What Is a Vaso-Occlusive Crisis (VOC)?

A VOC, also known as a pain crisis, is a common and serious complication of sickle cell disease. It occurs when sickled red blood cells obstruct blood flow to tissues and organs.

Symptoms of a VOC can include:

• Severe pain, often in the bones, chest, and abdomen;
• Swelling in the hands and feet;
• Fever;
• Fatigue; and
• Shortness of breath.

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Symptoms To Watch Out For

If you've been taking Oxbryta, it's important to be aware of the potential symptoms of VOCs and other complications. Seek immediate medical attention if you experience:

• Sudden onset of severe pain,
• Swelling in the hands or feet,
• Fever,
• Difficulty breathing,
• Chest pain, and
• Changes in vision.

Oxbryta Lawsuits

Patients who experienced VOCs, other health problems, or the death of a loved one after taking Oxbryta are taking legal action against the drug's manufacturer.

They claim the manufacturer failed to properly warn about the potential risks. These lawsuits seek to hold the manufacturer responsible and secure compensation for medical costs, lost income, and pain and suffering.

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