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Injection Treatment When the Body Makes Too Many Eosinophils

Fasenra (benralizumab) for hypereosinophilic syndrome

Health Canada/FDA Approved · United States, Canada, European Union · September 3, 2026

Condition: Hypereosinophilic Syndrome

Who this is for

Health Canada and the FDA have labelled Fasenra for hypereosinophilic syndrome. Japan and Switzerland have too. The UK SmPC already carries the wording. The European Union (EU) approved it on 3 July 2026. Toronto has an open paediatric trial. Authorized is not funded.

Next clinical step

Health Canada and the US Food and Drug Administration (FDA) have approved this medicine. In Canada and the United States, ask your doctor or a specialist whether it suits you. They can write a prescription. Insurance or public drug plan coverage is not guaranteed. In the European Union, authorisation is not confirmed; see Possible routes below if any are listed.

Ways to access this treatment

General resources for further research

AI-produced discussion aid; not prescribing instructions. Approval does not establish coverage. Full article: https://medcelerator.com/articles/fasenra-benralizumab-hypereosinophilic-syndrome