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Anakinra authorized to treat severe coronavirus disease 2019; Sepsis breakthrough or time to reflect?
INTRODUCTION: The European Medicines Agency (EMA) and the United States Food and Drug Administration (FDA) announced conditions for using recombinant human interleukin-1 receptor antagonist (rhIL-1ra) to treat hospitalized patients with Coronavirus disease 2019 (COVID-19) and risk for progression. T...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620707/ https://www.ncbi.nlm.nih.gov/pubmed/37928695 http://dx.doi.org/10.3389/fmicb.2023.1250483 |