DC FieldValueLanguage
dc.contributor.authorSchreier, Tobias-
dc.contributor.authorTropmann-Frick, Marina-
dc.contributor.authorBöhm, Ruwen-
dc.date.accessioned2026-10-16T10:22:07Z-
dc.date.available2026-10-16T10:22:07Z-
dc.date.issued2024-
dc.identifier.issn1610-1995en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12738/20251-
dc.description.abstractTraditionally, disproportionality analysis (DPA) methods are employed for signal detection in pharmacovigilance, but these methods utilize only a limited portion of the data available from spontaneous event reports (SERs). This research aims to enhance signal detection by applying machine learning (ML) methods that can leverage additional data. We create a dataset by integrating SER data from the FDA Adverse Event Reporting System (FAERS) with biological and chemical data from DrugBank, and information on known adverse drug reactions (ADRs) from Side Effect Resource (SIDER). The known ADRs from SIDER are used to label the dataset for ML training. Using the AutoML library TPOT, ML models are trained on this dataset. Our findings indicate that ML models, even when trained with the same features as DPA methods, achieve higher recall and precision. Moreover, incorporating additional features related to drugs and events significantly boosts the performance of ML models. Analysis using the explainable AI (XAI) technique SHAP reveals that the drug name, event name, and fifth-level ATC code are the most influential features for model predictions. These ML models offer a promising alternative or supplement to conventional DPA methods for signal detection in pharmacovigilance.en
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofDatenbank-Spektrumen_US
dc.subjectMachine Learningen_US
dc.subjectSignal Detectionen_US
dc.subjectAdverse Drug Reactionen_US
dc.subjectDisproportionality Analysisen_US
dc.subjectPharmacovigilanceen_US
dc.subject.ddc004: Informatiken_US
dc.titleIntegration of FAERS, DrugBank and SIDER data for machine learning-based detection of adverse drug reactionsen
dc.typeArticleen_US
dc.description.versionPeerRevieweden_US
tuhh.container.endpage242en_US
tuhh.container.issue3en_US
tuhh.container.startpage233en_US
tuhh.container.volume24en_US
tuhh.note.internharvest 2026-09-23; persons: 0000-0003-1623-5309,0009-0003-7345-7394; openalex: W4403245102; orcid: 0009-0003-7345-7394/177810790-
tuhh.oai.showtrueen_US
tuhh.publication.instituteDepartment Informatiken_US
tuhh.publication.instituteForschungs- und Transferzentrum Smart Systemsen_US
tuhh.publication.instituteFakultät Technik und Informatiken_US
tuhh.publisher.doi10.1007/s13222-024-00486-1-
tuhh.type.opus(wissenschaftlicher) Artikel-
dc.rights.cchttps://creativecommons.org/licenses/by/4.0/en_US
dc.type.casraiJournal Article-
dc.type.diniarticle-
dc.type.driverarticle-
dc.type.statusinfo:eu-repo/semantics/publishedVersionen_US
dcterms.DCMITypeText-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.creatorGNDSchreier, Tobias-
item.creatorGNDTropmann-Frick, Marina-
item.creatorGNDBöhm, Ruwen-
item.openairetypeArticle-
item.creatorOrcidSchreier, Tobias-
item.creatorOrcidTropmann-Frick, Marina-
item.creatorOrcidBöhm, Ruwen-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
crisitem.author.deptDepartment Informatik (ehemalig, aufgelöst 10.2025)-
crisitem.author.deptDepartment Informatik (ehemalig, aufgelöst 10.2025)-
crisitem.author.orcid0000-0003-1623-5309-
crisitem.author.parentorgFakultät Technik und Informatik (ehemalig, aufgelöst 10.2025)-
crisitem.author.parentorgFakultät Technik und Informatik (ehemalig, aufgelöst 10.2025)-
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