Oxbryta (voxelotor) is a prescription medication developed by Global Blood Therapeutics (GBT) and approved by the FDA in 2019 to treat sickle cell disease (SCD). While it helps reduce sickling of red blood cells, serious liver damage and other side effects have been reported.
Key Facts About Oxbryta:
Multiple studies and FDA reports suggest Oxbryta may cause severe liver injury, including:
Key Evidence:
The FDA has issued multiple warnings about Oxbryta’s risks:
Side Effect | Frequency |
Liver damage | 5-10% of patients |
Headaches | 20-30% |
Nausea & vomiting | 15-25% |
Fatigue | 10-20% |
FDA Actions:
Patients are filing lawsuits alleging:
Potential Settlement Estimates:
Case Type | Expected Compensation |
Liver injury (mild) | $100,000 – $500,000 |
Liver failure (severe) | $1M – $5M+ |
Wrongful death | $2M – $10M+ |
Note: No global settlement yet, but cases are being filed.
You may qualify if:
✔ Took Oxbryta for at least 3 months
✔ Diagnosed with liver damage, hepatitis, or liver failure
✔ Experienced hospitalization or ongoing treatment
Even if you still take Oxbryta, you may have a claim.
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Yes, typically 1-3 years from diagnosis (varies by state).
Yes, if you have liver damage.
You may file a wrongful death lawsuit.
If you or a loved one suffered liver damage from Oxbryta, contact CollectiveClaim today for a free consultation.
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