If you or a loved one used the drug Zinbryta to treat MS and developed a worsening, inflammatory brain disorder, such as encephalitis, meningoencephalitis or death resulting from these injuries, you may qualify for compensation from the manufacturer of the drug.
Zinbryta was pulled from the market after it was linked to 12 reports of patients who suffered “serious brain disorders,” including 3 patients in the United States who developed encephalitis. Other patients suffered life-threatening brain inflammation, meningoencephalitis, or death.
The FDA cited “concern about the drug’s evolving benefit/risk profile” while announcing Zinbryta’s withdrawal in the U.S. and around the world.
Zinbryta (daclizumab) is a multiple sclerosis injection drug that was introduced in 2016, for the treatment of adult patients with relapsing forms of multiple sclerosis.
Zinbryta (daclizumab) is made and marketed by Biogen and AbbVie. Zinbryta first received FDA approval pursuant to Biologic License Application (BLA: 761029) in May of 2016. Zinbryta is a humanized monoclonal antibody that is self-administered as an injection for the treatment of Multiple Sclerosis.
In March of 2018 Biogen published a letter directed towards physicians and surgeons giving notice that Zinbryta would be withdrawn from the market and would no longer be available as of April 30, 2018.
The European Medicines Agency akso announced a recall of the drug after recording 12 reports of severe inflammatory brain disorders that developed after Zinbryta use, including at least three fatal cases.
Symptoms of brain inflammation can include:
Did you or a loved one suffer an inflammatory brain disorder, such as Encephalitis, Meningoencephalitis, Sudden Brain Inflammation or Wrongful Death after using the recalled drug Zinbryta to treat MS?
Find out if you may qualify for compensation.
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