Evidence Based Medicine on FHIR Implementation Guide, published by HL7 International / Clinical Decision Support. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ballot3 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/ebm/ and changes regularly. See the Directory of published versions
| Official URL: https://fevir.net/resources/EvidenceVariable/367898 | Version: 1.0.0-ballot3 | ||||
| Standards status: Informative | Computable Name: Rate_of_Adverse_Events_of_Special_Interest_NCT03640312 | ||||
| Other Identifiers: FEvIR Object Identifier: FEvIR Object Identifier#367898, FEvIR Linking Identifier: NCT03640312-otherOutcome-2, OID:2.16.840.1.113883.4.642.40.44.24.181 | |||||
Copyright/Legal: Copyright the Authors else Computable Publishing LLC. Noncommercial use permitted with CC BY-NC-SA 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/). Commercial use permitted as agreed in Terms of Use (https://fevir.net/termsofuse). |
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Rate of pre-specified adverse events that are known side effects of active ingredients at the participant level.
version: 31; Last updated: 2026-09-08 12:21:25+0000
Profile: VariableDefinition
ArtifactPublicationStatus: Active
url: EvidenceVariable Rate of Adverse Events of Special Interest (NCT03640312)
identifier: FEvIR Object Identifier/367898, FEvIR Linking Identifier/NCT03640312-otherOutcome-2, Uniform Resource Identifier (URI)/urn:oid:2.16.840.1.113883.4.642.40.44.24.181
version: 1.0.0-ballot3
name: Rate_of_Adverse_Events_of_Special_Interest_NCT03640312
title: Rate of Adverse Events of Special Interest (NCT03640312)
citeAs:
Rate of Adverse Events of Special Interest (NCT03640312) [Database Entry: FHIR EvidenceVariable Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 367898. Revised 2026-09-08. Available at: https://fevir.net/resources/EvidenceVariable/367898. Computable resource at: https://fevir.net/resources/EvidenceVariable/367898#json.
status: Active
date: 2026-11-05 14:34:28+0000
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
publisher: HL7 International / Clinical Decision Support
contact: HL7 International / Clinical Decision Support: http://www.hl7.org/Special/committees/dss
description:
Rate of pre-specified adverse events that are known side effects of active ingredients at the participant level.
copyright:
Copyright the Authors else Computable Publishing LLC. Noncommercial use permitted with CC BY-NC-SA 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/). Commercial use permitted as agreed in Terms of Use (https://fevir.net/termsofuse).
| Concept |
| Rate of Adverse Events of Special Interest Rate of pre-specified adverse events that are known side effects of active ingredients at the participant level. |
handling: Evidence variable handling not specified
| Text |
| 12 weeks |