• 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

药物不良反应:第一部分。

Adverse drug reactions: Part I.

作者信息

Wooten James M

机构信息

Department of Medicine, University of Missouri-Kansas City, Kansas City, MO, USA.

出版信息

South Med J. 2010 Oct;103(10):1025-8; quiz 1029. doi: 10.1097/SMJ.0b013e3181f0c866.

DOI:10.1097/SMJ.0b013e3181f0c866
PMID:20818299
Abstract

Pharmacovigilance is the process of identifying, monitoring, and effectively reducing adverse drug reactions. Adverse drug reactions (ADRs) are an important consideration when assessing a patient's health. The proliferation of new pharmaceuticals means that the incidence of ADRs is increasing. The goal for all health care providers must be to minimize the risk of ADRs as much as possible. Steps to achieve this include understanding the pharmacology for all drugs prescribed and proactively assessing and monitoring those patients at greatest risk for developing an ADR. Groups at greatest risk for developing ADRs include the elderly, children, and pregnant patients, as well as others. Pharmacovigilance must effectively be practiced by all health providers in order to avoid ADRs.

摘要

药物警戒是识别、监测并有效减少药物不良反应的过程。在评估患者健康状况时,药物不良反应是一个重要的考量因素。新药物的不断涌现意味着药物不良反应的发生率正在上升。所有医疗保健提供者的目标必须是尽可能降低药物不良反应的风险。实现这一目标的步骤包括了解所有处方药的药理学知识,并主动评估和监测那些发生药物不良反应风险最高的患者。发生药物不良反应风险最高的群体包括老年人、儿童、孕妇以及其他人群。所有医疗保健提供者都必须切实有效地开展药物警戒工作,以避免药物不良反应的发生。

相似文献

1
Adverse drug reactions: Part I.药物不良反应:第一部分。
South Med J. 2010 Oct;103(10):1025-8; quiz 1029. doi: 10.1097/SMJ.0b013e3181f0c866.
2
Adverse drug reactions: part II.
South Med J. 2010 Nov;103(11):1138-45; quiz 1146-7. doi: 10.1097/SMJ.0b013e3181f5ecb5.
3
Safety of fibrinogen concentrate: analysis of more than 27 years of pharmacovigilance data.纤维蛋白原浓缩物的安全性:超过 27 年药物警戒数据的分析。
Thromb Haemost. 2015 Apr;113(4):759-71. doi: 10.1160/TH14-06-0514. Epub 2014 Dec 11.
4
Adverse drug reactions to self-medication: a study in a pharmacovigilance database.自我药疗的药物不良反应:一项基于药物警戒数据库的研究
Fundam Clin Pharmacol. 2015 Oct;29(5):517-20. doi: 10.1111/fcp.12140. Epub 2015 Aug 24.
5
[Analysis of adverse reactions and pharmacovigilance research to parenterally administered shuxuening].注射用舒血宁不良反应分析及药物警戒研究
Zhongguo Zhong Yao Za Zhi. 2013 Sep;38(18):3013-8.
6
Safety and outcomes of test doses for the evaluation of adverse drug reactions: a 5-year retrospective review.药物不良反应评估中测试剂量的安全性和结果:一项 5 年回顾性研究。
J Allergy Clin Immunol Pract. 2014 Nov-Dec;2(6):768-74. doi: 10.1016/j.jaip.2014.08.001. Epub 2014 Sep 10.
7
Adverse drug reactions - allergy? side-effect? intolerance?药物不良反应——过敏?副作用?不耐受?
Aust Fam Physician. 2013 Jan-Feb;42(1-2):12-6.
8
[Pharmacovigilance of parenterally administered salvianolate based on analysis of spontaneous reporting system data].基于自发报告系统数据分析的注射用丹参酚酸的药物警戒
Zhongguo Zhong Yao Za Zhi. 2013 Sep;38(18):3003-7.
9
[Significance of age, sex, kidney function, atopy and number of prescriptions for the occurrence of adverse drug reactions, studied by multivariate statistical methods. Results from the Comprehensive Hospital Drug Monitoring Berne (CHDMB)].
Schweiz Med Wochenschr. 1984 Dec 8;114(49):1854-7.
10
[Adverse drug reactions and prescription errors: morbi-mortality].药物不良反应与处方错误:疾病死亡率
Medicina (B Aires). 2013;73(2):111-8.

引用本文的文献

1
A qualitative exploration of pharmacovigilance policy implementation in Jordan, Oman, and Kuwait using Matland's ambiguity-conflict model.采用 Matland 的歧义-冲突模型对约旦、阿曼和科威特的药物警戒政策实施进行定性探索。
Global Health. 2021 Aug 30;17(1):97. doi: 10.1186/s12992-021-00751-y.
2
DNA damage by Withanone as a potential cause of liver toxicity observed for herbal products of (Ashwagandha).作为(印度人参)草药产品所观察到的肝脏毒性的潜在原因,睡茄内酯对DNA的损伤。
Curr Res Toxicol. 2021 Feb 16;2:72-81. doi: 10.1016/j.crtox.2021.02.002. eCollection 2021.
3
Impact of protocol change on individual factors related to course of adverse reactions to chemotherapy for breast cancer.
方案变更对乳腺癌化疗不良反应发生发展相关个体因素的影响。
Support Care Cancer. 2020 Jan;28(1):395-403. doi: 10.1007/s00520-019-04841-x. Epub 2019 May 6.
4
Reduction in exacerbation of COPD in patients of advanced age using the Japanese Kampo medicine Dai-kenchu-to: a retrospective cohort study.使用日本汉方药物大建中汤减少老年慢性阻塞性肺疾病患者的病情加重:一项回顾性队列研究
Int J Chron Obstruct Pulmon Dis. 2018 Dec 27;14:129-139. doi: 10.2147/COPD.S181916. eCollection 2019.
5
Consumer Narratives in ADR Reporting: An Important Aspect of Public Health? Experiences from Reports to a Swedish Consumer Organization.药品不良反应报告中的消费者叙述:公共卫生的一个重要方面?来自向瑞典一个消费者组织报告的经验
Front Public Health. 2015 Sep 1;3:211. doi: 10.3389/fpubh.2015.00211. eCollection 2015.
6
Renal xenobiotic transporter expression is altered in multiple experimental models of nonalcoholic steatohepatitis.在非酒精性脂肪性肝炎的多个实验模型中,肾脏外源性物质转运体的表达发生了改变。
Drug Metab Dispos. 2015 Feb;43(2):266-72. doi: 10.1124/dmd.114.060574. Epub 2014 Dec 8.
7
Drug disposition alterations in liver disease: extrahepatic effects in cholestasis and nonalcoholic steatohepatitis.肝病中的药物处置改变:胆汁淤积和非酒精性脂肪性肝炎的肝外效应。
Expert Opin Drug Metab Toxicol. 2014 Sep;10(9):1209-19. doi: 10.1517/17425255.2014.936378. Epub 2014 Jul 3.
8
Modeling human nonalcoholic steatohepatitis-associated changes in drug transporter expression using experimental rodent models.利用实验性啮齿动物模型模拟人类非酒精性脂肪性肝炎相关的药物转运体表达变化。
Drug Metab Dispos. 2014 Apr;42(4):586-95. doi: 10.1124/dmd.113.055996. Epub 2014 Jan 2.
9
Variations in ATP-binding cassette transporter regulation during the progression of human nonalcoholic fatty liver disease.人非酒精性脂肪性肝病进展过程中三磷酸腺苷结合盒转运体调控的变化。
Drug Metab Dispos. 2011 Dec;39(12):2395-402. doi: 10.1124/dmd.111.041012. Epub 2011 Aug 30.