Evidence map›Paper›PMID 40908272›Full record

ArticlePharmacoepidemiology and drug safety2025

Aioli: Standardising Drugs in the FDA Adverse Event Reporting System (FAERS) to RxNorm and Anatomical Therapeutic Chemical (ATC) Codes.

Rowan E Parry, Victor Pera, Katia M C Verhamme, Marcel de Wilde, Erik M van Mulligen, Jan A Kors

Abstract read
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Article in Pharmacoepidemiology and drug safety, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rowan E ParryDepartment of Medical Informatics, Erasmus University Medical Center, Rotterdam, the Netherlands.
Victor PeraDepartment of Medical Informatics, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-0786-4712
Katia M C VerhammeDepartment of Medical Informatics, Erasmus University Medical Center, Rotterdam, the Netherlands.
Marcel de WildeDepartment of Medical Informatics, Erasmus University Medical Center, Rotterdam, the Netherlands.
Erik M van MulligenDepartment of Medical Informatics, Erasmus University Medical Center, Rotterdam, the Netherlands.
Jan A KorsDepartment of Medical Informatics, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-4929-026X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe Food and Drug Administration Adverse Event Reporting System (FAERS) is an important source of information on suspected adverse drug reactions, but does not standardise drugs. The Adverse Event Open Learning Through Universal Standardization (AEOLUS) System Provides Standardisation of drugs in FAERS to RxNorm, but its coverage leaves room for improvement and mapping accuracy has not been established. Furthermore, drugs are not mapped to the Anatomical Therapeutic Chemical (ATC) Classification System, which is frequently used in pharmacovigilance studies. Here we develop and evaluate the Aioli system, an extension of AEOLUS, to increase the mapping of drugs in FAERS to RxNorm, and to provide mappings to the ATC coding system.

methodsSeveral changes and extensions were made to the AEOLUS mapping process to increase the number of drugs standardized to RxNorm. Information in FAERS fields about ingredient, route, dose amount, dose form, and dose unit was used to map to the most appropriate ATC code. Mapping accuracy was assessed on an evaluation set of 122 FAERS records.

resultsAioli mapped 94.1% of drug names in FAERS to RxNorm, compared to 90.4% by AEOLUS. In addition, Aioli mapped 80.4% of drug names to ATC codes. Evaluation showed high accuracies, with 92.2% correct mappings to RxNorm and 94.0% to ATC.

conclusionsWe have developed and evaluated the Aioli system that maps drugs in the FAERS database to RxNorm and ATC codes. With increased coverage of drugs and the mapping to ATC, Aioli further improves the usability of FAERS data in pharmacovigilance studies.

Indexed as

Adverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse ReactionsHumansPharmacovigilanceUnited StatesUnited States Food and Drug AdministrationATC classificationdrug standardisationFAERSRxNorm

Identifiers

PMID40908272
PMCPMC12411121

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.