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
| Computable Name: | ||||
version: 30; Last updated: 2026-09-02 17:12:13+0000
Profile: VariableDefinition
ArtifactPublicationStatus: Active
url: https://fevir.net/resources/EvidenceVariable/367897
identifier: FEvIR Object Identifier/367897, FEvIR Linking Identifier/NCT03640312-otherOutcome-1
name: Percentage_of_Participants_With_Potentially_Related_Adverse_Events_NCT03640312
title: Percentage of Participants With Potentially Related Adverse Events (NCT03640312)
citeAs:
Percentage of Participants With Potentially Related Adverse Events (NCT03640312) [Database Entry: FHIR EvidenceVariable Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 367897. Revised 2026-09-02. Available at: https://fevir.net/resources/EvidenceVariable/367897. Computable resource at: https://fevir.net/resources/EvidenceVariable/367897#json.
status: Active
author: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter:
publisher: Computable Publishing LLC
contact: support@computablepublishing.com
description:
Percentage of participants with occurrence of any potentially related adverse event (pre-specified as in study procedures). Defined as: At least possibly related to study drug.
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 |
| Percentage of Participants With Potentially Related Adverse Events Percentage of participants with occurrence of any potentially related adverse event (pre-specified as in study procedures). Defined as: At least possibly related to study drug. |
handling: Evidence variable handling not specified
| Text |
| 12 weeks |