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Drug safety assessments advocate intervention strategies, including dose control, to mitigate toxicity ( The FDA Adverse Event Reporting System (FAERS) serves as a national post-marketing surveillance tool and one of the worlds largest pharmacovigilance databases, designed to systematically capture spontaneous safety reports for therapeutic agents ( 2 Patients and methods 2.1 Data sources and procedures Available data related to pexidartinib were extracted and analyzed from the FAERS database ( There was no need for specific ethical approval and informed consent, as no direct human intervention or human sample collection was required

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