<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li D</submitter><funding>the Education Reform Project of Chongqing Municipal Education Commission</funding><funding>the Research Incubation Project of the Third Affiliated Hospital of Chongqing Medical University</funding><pagination>20420986241274909</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11380128</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The use of antineoplastic agents is one of the important triggers of tumor lysis syndrome (TLS), but there is still a lack of comprehensive understanding of antineoplastic agents that may trigger TLS and the TLS risk differences between different antineoplastic agents.&lt;h4>Objectives&lt;/h4>This study aims to investigate the TLS risk of different antineoplastic agents and provide reference information for clinical practice.&lt;h4>Design&lt;/h4>Real-world adverse events data in the FDA Adverse Event Reporting System (FAERS) database were used as the basis for the disproportionality analysis.&lt;h4>Methods&lt;/h4>We reviewed the TLS reports in the FAERS database from 2004 to 2022 to summarize an antineoplastic agent list that was reported to trigger TLS, based on which we conducted dispro</pubmed_abstract><journal>Therapeutic advances in drug safety</journal><pubmed_title>Assessing the risk of tumor lysis syndrome associated with the use of antineoplastic agents: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database.</pubmed_title><pmcid>PMC11380128</pmcid><funding_grant_id>234035</funding_grant_id><funding_grant_id>KY22038</funding_grant_id><pubmed_authors>Du Q</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Du D</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Qin C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Assessing the risk of tumor lysis syndrome associated with the use of antineoplastic agents: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database.</name><description>&lt;h4>Background&lt;/h4>The use of antineoplastic agents is one of the important triggers of tumor lysis syndrome (TLS), but there is still a lack of comprehensive understanding of antineoplastic agents that may trigger TLS and the TLS risk differences between different antineoplastic agents.&lt;h4>Objectives&lt;/h4>This study aims to investigate the TLS risk of different antineoplastic agents and provide reference information for clinical practice.&lt;h4>Design&lt;/h4>Real-world adverse events data in the FDA Adverse Event Reporting System (FAERS) database were used as the basis for the disproportionality analysis.&lt;h4>Methods&lt;/h4>We reviewed the TLS reports in the FAERS database from 2004 to 2022 to summarize an antineoplastic agent list that was reported to trigger TLS, based on which we conducted dispro</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-05-29T11:55:04.57Z</modification><creation>2025-04-05T13:57:12.596Z</creation></dates><accession>S-EPMC11380128</accession><cross_references><pubmed>39247253</pubmed><doi>10.1177/20420986241274909</doi></cross_references></HashMap>