A realworld pharmacovigilance study of trazodone based on the FDA adverse event reporting system

A realworld pharmacovigilance study of trazodone based on the FDA adverse event reporting system

Abstract To explore and analyze the potential adverse event (AE) signals of trazodone, with reference to the safe clinical use of drugs. Based on the FDA Adverse Event Reporting System (FAERS), the AE data of trazodone were extracted from the first quarter of 2004 to the second quarter of 2024, and...

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Bibliographic Details
Main Authors:	Yong Yu, Xin Sun, Liqun Hao, Xiaoyan Zhang, Yankui Guo
Format:	Article
Language:	English
Published:	Nature Portfolio 2025-02-01
Series:	Scientific Reports
Subjects:	Trazodone FDA adverse event reporting system Adverse drug reaction Data mining
Online Access:	https://doi.org/10.1038/s41598-025-89632-7
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