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1
Postmarketing surveillance of adverse drug reactions in general practice. II: Prescription-event monitoring at the University of Southampton.全科医疗中药物不良反应的上市后监测。II:南安普顿大学的处方事件监测。
Br Med J (Clin Res Ed). 1981 Apr 11;282(6271):1216-7. doi: 10.1136/bmj.282.6271.1216.
2
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Terminology in prescription-event monitoring.处方事件监测中的术语。
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Safety of zafirlukast: results of a postmarketing surveillance study on 7976 patients in England.扎鲁司特的安全性:一项针对英格兰7976名患者的上市后监测研究结果
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引用本文的文献

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2
Intensive Monitoring Studies for Assessing Medicines: A Systematic Review.用于评估药物的强化监测研究:一项系统评价
Front Med (Lausanne). 2019 Jul 19;6:147. doi: 10.3389/fmed.2019.00147. eCollection 2019.
3
The hope, hype and reality of Big Data for pharmacovigilance.大数据用于药物警戒的希望、炒作与现实。
Ther Adv Drug Saf. 2018 Jan;9(1):5-11. doi: 10.1177/2042098617736422. Epub 2017 Oct 31.
4
A survey of adverse drug reactions in family practice.家庭医疗中的药物不良反应调查。
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Clarification of terminology in drug safety.药物安全性术语的阐释
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Linking pharmacovigilance with pharmacogenetics.将药物警戒与药物遗传学联系起来。
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7
Comparison of losartan with ACE inhibitors and dihydropyridine calcium channel antagonists: a pilot study of prescription-event monitoring in Japan.氯沙坦与血管紧张素转换酶抑制剂及二氢吡啶类钙通道拮抗剂的比较:日本处方事件监测的一项初步研究。
Drug Saf. 2002;25(11):811-21. doi: 10.2165/00002018-200225110-00005.
8
Postmarketing studies: the work of the Drug Safety Research Unit.上市后研究:药物安全研究单位的工作
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Pharmacoeconomic consequences of measurement and modification of hospital drug use.医院用药计量与调整的药物经济学后果
Pharmacoeconomics. 1992 Jul;2(1):15-33. doi: 10.2165/00019053-199202010-00004.
10
The way towards adverse event monitoring in clinical trials.临床试验中不良事件监测的方法。
Drug Saf. 1993 Mar;8(3):251-62. doi: 10.2165/00002018-199308030-00006.

全科医疗中药物不良反应的上市后监测。II:南安普顿大学的处方事件监测。

Postmarketing surveillance of adverse drug reactions in general practice. II: Prescription-event monitoring at the University of Southampton.

作者信息

Inman W H

出版信息

Br Med J (Clin Res Ed). 1981 Apr 11;282(6271):1216-7. doi: 10.1136/bmj.282.6271.1216.

DOI:10.1136/bmj.282.6271.1216
PMID:6788140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1505289/
Abstract

An independent, non-regulatory drug surveillance research unit has been established at the University of Southampton. Its first task will be to set up a prescription-event monitoring scheme in general practice to enable the pattern of adverse events, as distinct from suspected adverse reactions associated with new drugs to be compared with that of older medicines. Prescriptions for selected drugs will identify patients and a simple questionnaire, designed to be completed in under five minutes, will be used to obtain the required information. Medical opinions about causation need not be given, and the scheme will not interfere with normal prescribing practice.

摘要

南安普敦大学设立了一个独立的、非监管性的药物监测研究单位。其首要任务将是在全科医疗中建立一个处方事件监测计划,以便将新药相关不良事件的模式(有别于疑似不良反应)与老药的模式进行比较。选定药物的处方将识别患者,一份设计为在五分钟内完成的简单问卷将用于获取所需信息。无需给出关于因果关系的医学意见,该计划也不会干扰正常的处方行为。