2023
DOI: 10.3389/fphar.2023.1194545
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Safety analysis of pemigatinib leveraging the US Food and Drug administration adverse event reporting system

Abstract: Background: Cholangiocarcinoma (CCA) is a highly lethal and aggressive epithelial tumor of the hepatobiliary system. A poor prognosis, propensity for relapse, low chance of cure and survival are some of its hallmarks. Pemigatinib, the first targeted treatment for CCA in the United States, has been demonstrated to have a significant response rate and encouraging survival data in early-phase trials. The adverse events (AEs) of pemigatinib must also be determined.Objective: To understand more deeply the safety of… Show more

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Cited by 10 publications
(4 citation statements)
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“…This study has some limitations that should be considered. First, although ROR and PRR have high stability and specificity, BCPNN has higher sensitivity, stability, and specificity than ROR and PRR ( Zhang et al, 2023 ). To make our results more robust, we used four algorithms to filter the AEs associated with the use of epirubicin: PRR, ROR, BCPNN, and EBGM.…”
Section: Discussionmentioning
confidence: 99%
“…This study has some limitations that should be considered. First, although ROR and PRR have high stability and specificity, BCPNN has higher sensitivity, stability, and specificity than ROR and PRR ( Zhang et al, 2023 ). To make our results more robust, we used four algorithms to filter the AEs associated with the use of epirubicin: PRR, ROR, BCPNN, and EBGM.…”
Section: Discussionmentioning
confidence: 99%
“…In the FAERS database, reported drugs are categorized into four types: Primary Suspect Drug (PS), Secondary Suspect Drug (SS), Concomitant Drug (C), and Interacting (I). To enhance the accuracy of the analysis and mitigate the effects of concomitant drug use, the AE role code was retained only when the PS drug was identi ed as "famciclovir" 13 . Throughout this research, we discovered 432 cases of AE reports with famciclovir classi ed as the PS drug.…”
Section: Methodsmentioning
confidence: 99%
“…The drugs reported in FAERS were categorized into four modalities: PS (primary suspect), SS (second suspect), C (concomitant), and I (interacting). To enhance the precision of the analyses and eliminate the influence of concurrent medications, the AEs role code was preserved exclusively for instances where the PS drug was identified as 'mepolizumab' (Zhang et al, 2023). The highest level of terminology used for coding all AEs in the report is the System Organ Class (SOC) based on the Medical Dictionary for Regulatory Activities (MedDRA,version 26.0).…”
Section: Methodsmentioning
confidence: 99%