Can FHIR support standardization in post-market safety surveillance?

Research output: Chapter in Book/Report/Conference proceedingChapter


The Fast Healthcare Interoperability Resources (FHIR) contain multiple data-exchange standards that aim at optimizing healthcare information exchange. One of them, the FHIR AdverseEvent, may support post-market safety surveillance. We examined its readiness using the Food and Drug Administration's (FDA) Adverse Event Reporting System (FAERS). Our methodology focused on mapping the public FAERS data fields to the FHIR AdverseEvent Resource elements and developing a software tool to automate this process. We mapped directly nine and indirectly two of the twenty-six FAERS elements, while six elements were assigned default values. This exploration further revealed opportunities for adding extra elements to the FHIR standard, based on critical FAERS pieces of information reviewed at the FDA. The existing version of the FHIR AdverseEvent Resource may standardize some of the FAERS information but has to be modified and extended to maximize its value in post-market safety surveillance.

Original languageEnglish (US)
Title of host publicationPublic Health and Informatics
Subtitle of host publicationProceedings of MIE 2021
PublisherIOS Press
Number of pages5
ISBN (Electronic)9781643681856
ISBN (Print)9781643681849
StatePublished - Jul 1 2021


  • Adverse Drug Event
  • FHIR
  • Post-market Safety Surveillance

ASJC Scopus subject areas

  • General Medicine


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