• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

制定药品不良反应报告术语的使用要求。

Establishing requirements for the use of terms for reporting adverse drug reactions.

作者信息

Venulet J

机构信息

Council for International Organizations of Medical Sciences, Geneva, Switzerland.

出版信息

Int J Clin Pharmacol Res. 1992;12(2):61-4.

PMID:1428299
Abstract

The establishment of a project for the standardization of international reporting of adverse drug reactions (ADR), sponsored by the Council for International Organizations of Medical Sciences is described. The need to establish requirements for properly diagnosing a given suspected ADR and to describe it with the correct terms is demonstrated. However in view of the difficulties involved, it is suggested that the present deliberate approach needs to be reconsidered.

摘要

本文描述了由国际医学科学组织理事会发起的一个关于药品不良反应(ADR)国际报告标准化项目的设立情况。文中表明了确立正确诊断特定疑似药品不良反应并使用正确术语进行描述的要求的必要性。然而,鉴于其中涉及的困难,建议重新考虑当前这种审慎的方法。

相似文献

1
Establishing requirements for the use of terms for reporting adverse drug reactions.制定药品不良反应报告术语的使用要求。
Int J Clin Pharmacol Res. 1992;12(2):61-4.
2
Establishing requirements for the use of terms for reporting adverse drug reactions (ADR). Consultant, Council for International Organizations of Medical Sciences (CIOMS), World Health Organization.制定药品不良反应(ADR)报告术语的使用要求。医学科学国际组织理事会(CIOMS)顾问,世界卫生组织。
Mater Med Pol. 1993 Jan-Mar;25(1):45-6.
3
Points of view on adverse drug reactions terminology.关于药品不良反应术语的观点。
Therapie. 1998 Mar-Apr;53(2):145-9.
4
[International reporting of adverse drug reactions. Final report of CIOMS ADR Working Group].
Therapie. 1991 May-Jun;46(3):173-8.
5
International reporting on adverse drug reactions: the CIOMS project. CIOMS ADR Working Group.国际药品不良反应报告:CIOMS项目。CIOMS药品不良反应工作组
Int J Clin Pharmacol Ther Toxicol. 1990 Apr;28(4):133-8.
6
[Adverse drug reactions definitions and terminology].[药品不良反应的定义和术语]
Harefuah. 2001 Dec;140(12):1181-6, 1228.
7
Mapping of the WHO-ART terminology on Snomed CT to improve grouping of related adverse drug reactions.将世界卫生组织药物不良反应术语集(WHO-ART)映射到医学系统命名法临床术语(Snomed CT)以改进相关药品不良反应的分组
Stud Health Technol Inform. 2006;124:833-8.
8
Building an ontology of adverse drug reactions for automated signal generation in pharmacovigilance.构建用于药物警戒中自动信号生成的药物不良反应本体。
Comput Biol Med. 2006 Jul-Aug;36(7-8):748-67. doi: 10.1016/j.compbiomed.2005.04.009. Epub 2005 Sep 26.
9
Definitions and basic requirements for the use of terms for reporting adverse drug reactions (X): gastrointestinal system disorders.
Pharmacoepidemiol Drug Saf. 1998 Jul;7(4):281-7. doi: 10.1002/(SICI)1099-1557(199807/08)7:4<281::AID-PDS325>3.0.CO;2-W.
10
Basic requirements for the use of terms for reporting adverse drug reactions (VIII): renal and urinary system disorders.药品不良反应报告术语使用的基本要求(八):肾脏和泌尿系统疾病
Pharmacoepidemiol Drug Saf. 1997 May;6(3):203-11. doi: 10.1002/(SICI)1099-1557(199705)6:3<203::AID-PDS265>3.0.CO;2-I.