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Mythologising

机译:神话化

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摘要

In the world of pharmaceutical companies and drug regulatory agencies, people often talk about "a drug's life cycle".They refer to its "international birth date" and the "family" it belongs to, they attribute "paternity" to a particular inventor (although the drug is sometimes an "orphan",..), and they follow its "development" intently.They are proud when "it has demonstrated its efficacy. They are thrilled when "it obtains" marketing authorisation (MA), as if this were a qualification bestowed by a sympathetic or unsupportive panel of examiners. As time goes by, the drug may be suspected of being "responsible" tor a particular adverse effect, so studies are requested, again and again, to make sure that an innocent drug is not wrongfully blamed. And finally they mourn its "death". The poor drug, once so "promising", becomes another victim of a heartless, merciless pharmacovigilance system...
机译:在制药公司和药品监管机构的世界中,人们经常谈论“药物的生命周期”。他们指的是“国际出生日期”和其所属的“家庭”,他们将“父子关系”归因于特定的发明家(尽管该药有时是“孤儿药”,但他们会专心地遵循其“发展”。当“已证明其功效”时,他们会感到自豪。当“获得”市场许可(MA)时,他们会为之兴奋。随着时间的流逝,这种药物可能被怀疑对某种特定的不良反应是“负责任的”,因此,要求进行一次又一次的研究,以确保这种药物是无害的。药物没有被错误地责备,最后他们哀悼了它的“死亡”,这种可怜的药物曾经如此“有前途”,却成为无情,无情的药物警戒系统的另一个受害者。

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  • 来源
    《Prescrire international》 |2014年第149期|共1页
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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
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