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为什么药物安全性不应次于疗效。

Why drug safety should not take a back seat to efficacy.

出版信息

PLoS Med. 2011 Sep;8(9):e1001097. doi: 10.1371/journal.pmed.1001097. Epub 2011 Sep 27.

DOI:10.1371/journal.pmed.1001097
PMID:21984875
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3181229/
Abstract

The editors argue that methodological challenges in monitoring the safety of prescription medications should not mean that drug safety be considered less important than efficacy.

摘要

编辑们认为,监测处方药物安全性的方法学挑战不应意味着药物安全性不如疗效重要。

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本文引用的文献

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PLoS Med. 2011 Sep;8(9):e1001098. doi: 10.1371/journal.pmed.1001098. Epub 2011 Sep 27.
2
Meta-analyses of adverse effects data derived from randomised controlled trials as compared to observational studies: methodological overview.随机对照试验与观察性研究中不良反应数据的荟萃分析:方法学概述。
PLoS Med. 2011 May;8(5):e1001026. doi: 10.1371/journal.pmed.1001026. Epub 2011 May 3.
3
Postmarketing studies of drug safety.药物安全性的上市后研究。
BMJ. 2011 Feb 8;342:d342. doi: 10.1136/bmj.d342.
4
Drug-review deadlines and safety problems.药物审查期限与安全问题。
N Engl J Med. 2008 Mar 27;358(13):1354-61. doi: 10.1056/NEJMsa0706341.
5
Clinical trial registration--looking back and moving ahead.临床试验注册——回顾与展望
N Engl J Med. 2007 Jun 28;356(26):2734-6. doi: 10.1056/NEJMe078110. Epub 2007 Jun 4.
6
Potential for conflict of interest in the evaluation of suspected adverse drug reactions: a counterpoint.评估疑似药物不良反应时利益冲突的可能性:一种反对观点
JAMA. 2004 Dec 1;292(21):2643-6. doi: 10.1001/jama.292.21.2643. Epub 2004 Nov 22.
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Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients.药物不良反应作为入院原因:对18820例患者的前瞻性分析。
BMJ. 2004 Jul 3;329(7456):15-9. doi: 10.1136/bmj.329.7456.15.