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 adverse event 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 ICSRs 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
Fridays 10 AM to 11 AM Eastern
Conference Call Information: Phone Number: +1 770-657-9270 Participant Passcode: 7485962
Web Meeting Info (does not include audio connection)
www.webex.com - meeting number 622 569 796 password - Meeting
Direct Meeting Link: Link
Next scheduled meeting: Friday, May 27, 2016 at 10 AM EDT
Meeting Agendas/Minutes
FHIR AE Resource Agenda and Minutes 2016 5 20
Project Requirements
FHIR AE Spreadsheet as of 2-16 5 20
Project References
Based on TANSI/HL7 V3 ICSRP1, R2-2012 HL7 Version 3 Standard: Pharmacovigilance - Individual Case Safety Report, Part 1: The Framework for Adverse Event Reporting, R2 (revise and partition ANSI/HL7 V3 RRCS, R1-2005)1/31/2012
ICSR Part 1 is http://www.hl7.org/implement/standards/product_brief.cfm?product_id=266 ICSR Part 2 is http://www.hl7.org/implement/standards/product_brief.cfm?product_id=267. (medicinals only)
