A Disproportionality Analysis of Adverse Events Caused by Pexidartinib from the FDA Adverse Event Reporting System
August 2025
in “
Scientific Reports
”
Studysummary This study analyzed pexidartinib-associated adverse events from FDA data and reported common events such as hepatic issues and systemic reactions. It highlighted sex-specific susceptibilities and reinforced the need for risk mitigation and long-term monitoring in tenosynovial giant cell tumor management.
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