Drug-induced sinusoidal obstruction syndrome: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System (FEARS)

Drug-induced sinusoidal obstruction syndrome: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System (FEARS)

Abstract Background Hepatic Sinusoidal Obstruction Syndrome (SOS) represents a rare but serious adverse drug reaction. This study aimed to identify the medications most frequently associated with SOS risk through the analysis of the United States Food and Drug Administration (FDA) Adverse Event Repo...

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Bibliographic Details
Main Authors: Cuicui Sun, Xiaoyan Yang, Lili Wang, Linlin Tang, Jinhua Chen
Format: Article
Language:English
Published: BMC 2025-07-01
Series:BMC Pharmacology and Toxicology
Subjects:
LiverTox®
Pharmacovigilance
Proportional reporting ratio (PRR)
Reported odds ratio (ROR)
Sinusoidal Obstruction Syndrome (SOS)
United States Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database
Online Access:https://doi.org/10.1186/s40360-025-00965-5
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https://doi.org/10.1186/s40360-025-00965-5

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