FHIR Adverse Event Resource
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Project Number Project Number 1240
FHIR Resource Proposal AdverseEvent_FHIR_Resource_Proposal
Project Name FHIR Adverse Event Resource
Project Sponsor(s) RCRIM Work Group and Patient Care WG
Contents
Description
Project Scope Statement - Project 1240
Objectives / Deliverables
To enhance patient safety, it is noted that many countries have strong needs to exchange product safety information between varieties of stakeholders in the healthcare domain. Currently many regulatory agencies collect safety reports of adverse drug reactions, adverse events, infections, contamination and other incidents from consumers, pharmaceutical companies and healthcare professionals.
The AdverseEvent resource will address the exchange of the following types of information:
1) Individual Case Safety Report (ICSR): Framework for data exchange and information sharing by providing a common messaging format for transmission of Individual Case Safety Reports (ICSR) for adverse drug reactions (ADR), adverse events (AE), product problems and consumer complaints that may occur upon the administration or use of one or more products or substances. The reports can relate to a specific subject or may be used to relay an issue or finding related to a specific substance, product or device.
2) (Not in current standard) – Individual Occurrence Report (IOR): The identification and characterization of exceptional events related to patient care, patient safety, protocol implementation, and service delivery. Examples might be falling out of bed, slipping on a wet floor, inappropriate use of restraints.
Meeting Details
Next scheduled meeting: Friday, October 21, 2016 at 10 AM TO 11 AM Eastern
Web Meeting at http://www.webex.com
Meeting number: 196 412 889
Direct WebEx Meeting Link:
HL7 Teleconference Line:
Phone Number: +1 770-657-9270
Participant Passcode: 7485962
Meeting Agendas / Minutes / Presentations / Publications
Links are to PDF files. Download, or open in a new Tab or Window.
- TO COME Call 9 > FHIR AdverseEvent Resource Conf Call on 2016-09-02: Agenda and Minutes
Call 8 > FHIR AdverseEvent Resource Conf Call on 2016-08-12: Agenda and Minutes
Call 6 > FHIR AdverseEvent Resource Conf Call on 2016-06-24: Agenda and Minutes
Call 5 > FHIR AdverseEvent Resource Conf Call on 2016-06-17: Agenda and Minutes
Call 4 > FHIR AdverseEvent Resource Conf Call on 2016-06-10: Agenda and Minutes
Call 3 > FHIR AdverseEvent Resource Conf Call on 2016-06-03: Agenda and Minutes
Call 2 > FHIR AdverseEvent Resource Conf Call on 2016-05-27: Agenda and Minutes
Call 1 > FHIR AdverseEvent Resource Conf Call on 2016-05-20: Agenda and Minutes
PRESENTATIONS
Call 6 > Presentation, FDA Adverse Event Reporting, Dr. Mitra Rocca, 2016-06-24
PUBLICATIONS
Publication by Stella Stergiopoulos et al. from Tufts, "A Survey of Adverse Event Reporting Practices Among US Healthcare Professionals" http://link.springer.com/article/10.1007/s40264-016-0455-4
Project Requirements
FHIR AdverseEvent Resource Data Elements Draft as of 2016-10-14
Project References
FHIR Event Resource Pattern
Guidance on standard syntax issued by the FHIR team for any Resource that details event information.
FHIR_Event_Resource_Pattern.pdf, July 5, 2016
Based on TANSI/HL7 V3 ICSRP1, R2-2012
HL7 Version 3 Standard: Pharmacovigilance - Individual Case Safety Report
ICSR Part 1: The Framework for Adverse Event Reporting, R2
http://www.hl7.org/implement/standards/product_brief.cfm?product_id=266
ICSR Part 2: Human Pharmaceutical Reporting Requirements for ICSR, R2
http://www.hl7.org/implement/standards/product_brief.cfm?product_id=267 (medicinals only)
AHRQ Patient Safety Common Format Guidelines
https://www.psoppc.org/psoppc_web/publicpages/supportingDocsV1.2
FHIR W5 Guidelines:
http://hl7-fhir.github.io/w5.html
