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首页> 外文期刊>Health affairs >Biosimilar Filgrastim Uptake And Costs Among Commercially Insured, Medicare Advantage
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Biosimilar Filgrastim Uptake And Costs Among Commercially Insured, Medicare Advantage

机译:商业保险人对生物仿制药非格司亭的吸收和成本,Medicare Advantage

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摘要

In 2015 the Food and Drug Administration approved filgrastim-sndz (Zarxio), the first US biosimilar. Following rapid uptake, by March 2018 filgrastim-sndz accounted for 47 percent of filgrastim administrations among commercially insured and 42 percent among Medicare Advantage beneficiaries. The initial cost difference between the originator and biosimilar was 31 percent in the former population but negligible in the latter.
机译:2015年,美国食品药品监督管理局(FDA)批准了非格司亭-SNDZ(Zarxio),这是美国首个生物类似药。随着快速采用,到2018年3月,非格司亭-sndz占商业保险人非格司亭给药的47%,在Medicare Advantage受益人中占42%。在前者中,原研药和生物仿制药之间的初始成本差异为31%,但在后者中可以忽略不计。

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  • 来源
    《Health affairs》 |2019年第11期|1887-1892|共6页
  • 作者单位

    Univ Minnesota, Carlson Sch Management, Finance Dept, Minneapolis, MN 55455 USA;

    Univ Minnesota, Sch Publ Hlth, Div Hlth Policy & Management, Minneapolis, MN 55455 USA;

    Mayo Clin, Div Hematol, Med, Rochester, MN USAUniv Minnesota, Coll Pharm, Pharmaceut Care & Hlth Syst, Minneapolis, MN 55455 USAUniv Minnesota, Div Hematol Oncol & Transplantat, Med Sch, Minneapolis, MN USAMayo Clin, Dept Hlth Care Policy & Res, Rochester, MN USA;

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  • 原文格式 PDF
  • 正文语种 英语
  • 中图分类 预防医学、卫生学;
  • 关键词

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