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Response to "Evaluating Adverse Events in Databases".

作者信息

Calapai Fabrizio, Mannucci Carmen, Cardia Luigi, Currò Mariaconcetta, Calapai Gioacchino, Esposito Emanuela, Ammendolia Ilaria

机构信息

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.

出版信息

Pharmacol Res Perspect. 2023 Oct;11(5):e01127. doi: 10.1002/prp2.1127.

DOI:10.1002/prp2.1127
PMID:37589310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10433452/
Abstract
摘要

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Drug Saf. 2023 Jul;46(7):625-636. doi: 10.1007/s40264-023-01302-7. Epub 2023 Jun 6.
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Evolution of adverse drug reactions reporting systems: paper based to software based.药物不良反应报告系统的演变:从纸质到软件。
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Chances and Challenges of Registry-Based Pharmacovigilance in Multiple Sclerosis: Lessons Learnt from the Implementation of the Multicenter REGIMS Registry.基于登记的药物警戒在多发性硬化症中的机遇与挑战:从多中心 REGIMS 登记研究实施中吸取的经验教训。
Drug Saf. 2021 Jan;44(1):7-15. doi: 10.1007/s40264-020-01007-1. Epub 2020 Oct 23.
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Some concerns about adverse event reporting in randomized clinical trials.关于随机临床试验中不良事件报告的一些担忧。
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