Reference record for OID 2.16.840.1.113883.11.21026

Parent
2.16.840.1.113883.11 (valueSets)
Node code
21026
Node names
  • AdverseEventCRSerCrit
  • adverse-event-clinical-research-seriousness-criteria
Numeric OID
2.16.840.1.113883.11.21026
URN notation
urn:oid:2.16.840.1.113883.11.21026
ASN.1 notation

{2 16 840 1 113883 11 21026}

  • {joint-iso-itu-t(2) country(16) us(840) organization(1) hl7(113883) valueSets(11) adverse-event-clinical-research-seriousness-criteria(21026)}
  • {joint-iso-itu-t(2) country(16) us-joint(840) organization(1) hl7(113883) valueSets(11) adverse-event-clinical-research-seriousness-criteria(21026)}
  • {joint-iso-ccitt(2) country(16) us(840) organization(1) hl7(113883) valueSets(11) adverse-event-clinical-research-seriousness-criteria(21026)}
  • {joint-iso-ccitt(2) country(16) us-joint(840) organization(1) hl7(113883) valueSets(11) adverse-event-clinical-research-seriousness-criteria(21026)}
OID-IRI notation
  • /2/16/840/1/113883/11/21026
  • /Country/840/1/113883/11/21026
  • /Joint-ISO-ITU-T/16/840/1/113883/11/21026
Named path variants
  • /joint-iso-itu-t/country/us/organization/hl7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-itu-t/country/us/organization/hl7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-itu-t/country/us/organization/HL7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-itu-t/country/us/organization/HL7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-itu-t/country/us-joint/organization/hl7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-itu-t/country/us-joint/organization/hl7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-itu-t/country/us-joint/organization/HL7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-itu-t/country/us-joint/organization/HL7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-ccitt/country/us/organization/hl7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-ccitt/country/us/organization/hl7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-ccitt/country/us/organization/HL7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-ccitt/country/us/organization/HL7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-ccitt/country/us-joint/organization/hl7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-ccitt/country/us-joint/organization/hl7/valueSets/adverse-event-clinical-research-seriousness-criteria
  • /joint-iso-ccitt/country/us-joint/organization/HL7/valueSets/AdverseEventCRSerCrit
  • /joint-iso-ccitt/country/us-joint/organization/HL7/valueSets/adverse-event-clinical-research-seriousness-criteria

Descriptions

AdverseEventCRSerCrit, adverse-event-clinical-research-seriousness-criteria — HL7 Terminology

Action criteria usually associated with serious events that pose a threat to a patient's life or functioning. Adverse Events criteria to expand on the seriousness of the adverse event. Typically used in reporting for Clinical Research, post-market surveillance (e.g. Form FDA 3500A MedWatch). The adverse event seriousness criteria value set is based on the ICH E2D Post-Approval Safety Data Management: Definitions and Standards for Expedited Reporting guidance (https://database.ich.org/sites/default/files/E2D_Guideline.pdf). For information on ICH see https://admin.ich.org/sites/default/files/inline-files/OID_Information_Paper_1.pdf from the INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE (ICH) document ICH E2B(R3), the Electronic Transmission of Individual Case Safety Reports (ICSRs) Implementation Guide Data Elements and Message Specification, and ICH M8, the Electronic Common Technical Document

Source records

AdverseEventCRSerCrit, adverse-event-clinical-research-seriousness-criteria

Status in source: active.

Names: AdverseEventCRSerCrit, adverse-event-clinical-research-seriousness-criteria

Technical details
{
  "url": "http://terminology.hl7.org/ValueSet/adverse-event-clinical-research-seriousness-criteria",
  "date": "2023-07-28T19:27:19+00:00",
  "title": "Adverse Event Clinical Research Seriousness Criteria",
  "status": "active",
  "contact": [
    {
      "telecom": [
        {
          "value": "http://hl7.org",
          "system": "url"
        },
        {
          "value": "hq@HL7.org",
          "system": "email"
        }
      ]
    }
  ],
  "version": "1.0.0",
  "copyright": "This material derives from the HL7 Terminology THO. THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license.html",
  "publisher": "Health Level Seven International",
  "experimental": false,
  "resource_type": "ValueSet",
  "oid_identifier": {
    "value": "urn:oid:2.16.840.1.113883.11.21026",
    "system": "urn:ietf:rfc:3986"
  }
}

First Registration Authority (inferred from ancestor 2.16.840.1.113883)

W. Ted Klein

Current Registration Authority (inferred from ancestor 2.16.840.1)

Karen Hughes

Siblings (1453)

OIDNameDirect childrenDescendantsDescription
2.16.840.1.113883.11.19617 actRelationshipObjective, ActRelationshipObjective00
2.16.840.1.113883.11.19618 packagedDrugProductEntity, PackagedDrugProductEntity00
2.16.840.1.113883.11.19619 authorizationIssueManagementCode, AuthorizationIssueManagementCode00
2.16.840.1.113883.11.19620 actAdministrativeAuthorizationDetectedIssueCode, ActAdministrativeAuthorizationDetectedIssueCode00
2.16.840.1.113883.11.19621 actAdministrativeRuleDetectedIssueCode, ActAdministrativeRuleDetectedIssueCode00
2.16.840.1.113883.11.19622 individualCaseSafetyReportType, IndividualCaseSafetyReportType00
2.16.840.1.113883.11.19623 deviceGenericType, DeviceGenericType00
2.16.840.1.113883.11.19624 individualCaseSafetyReportSenderType, IndividualCaseSafetyReportSenderType00
2.16.840.1.113883.11.19625 individualCaseSafetyReportValueDomains, IndividualCaseSafetyReportValueDomains00
2.16.840.1.113883.11.19626 caseSeriousnessCriteria, CaseSeriousnessCriteria00
2.16.840.1.113883.11.19627 subjectReaction, SubjectReaction00
2.16.840.1.113883.11.19628 productCharacterization, ProductCharacterization00
2.16.840.1.113883.11.19629 pertinentReactionRelatedness, PertinentReactionRelatedness00
2.16.840.1.113883.11.19630 subjectReactionOutcome, SubjectReactionOutcome00
2.16.840.1.113883.11.19631 subjectReactionEmphasis, SubjectReactionEmphasis00
2.16.840.1.113883.11.19632 deviceManufacturerEvaluationResult, DeviceManufacturerEvaluationResult00
2.16.840.1.113883.11.19633 deviceManufacturerEvaluationInterpretation, DeviceManufacturerEvaluationInterpretation00
2.16.840.1.113883.11.19634 deviceManufacturerEvaluationMethod, DeviceManufacturerEvaluationMethod00
2.16.840.1.113883.11.19635 reactionActionTaken, ReactionActionTaken00
2.16.840.1.113883.11.19636 reasonForNotEvaluatingDevice, ReasonForNotEvaluatingDevice00
2.16.840.1.113883.11.19637 deviceOperatorType, DeviceOperatorType00
2.16.840.1.113883.11.19638 acknowledgementDetailCode, AcknowledgementDetailCode00
2.16.840.1.113883.11.19639 acknowledgementDetailSyntaxErrorCode, AcknowledgementDetailSyntaxErrorCode00
2.16.840.1.113883.11.19640 acknowledgementDetailNotSupportedCode, AcknowledgementDetailNotSupportedCode00
2.16.840.1.113883.11.19641 workPlaceAddressUse, WorkPlaceAddressUse00
2.16.840.1.113883.11.19642 actDisciplinaryActionCode, ActDisciplinaryActionCode00
2.16.840.1.113883.11.19643 relatedLinkType, RelatedLinkType00
2.16.840.1.113883.11.19644 x-ClinicalStatementObservationMood00 x_ClinicalStatementObservationMood
2.16.840.1.113883.11.19645 x-ClinicalStatementSubstanceMood00 x_ClinicalStatementSubstanceMood
2.16.840.1.113883.11.19646 x-ClinicalStatementSupplyMood00 x_ClinicalStatementSupplyMood
2.16.840.1.113883.11.19647 x-ClinicalStatementProcedureMood00 x_ClinicalStatementProcedureMood
2.16.840.1.113883.11.19648 x-ClinicalStatementEncounterMood00 x_ClinicalStatementEncounterMood
2.16.840.1.113883.11.19649 x-ClinicalStatementActMood00 x_ClinicalStatementActMood
2.16.840.1.113883.11.19650 responseMode, ResponseMode00
2.16.840.1.113883.11.19652 resourceGroupEntityType, ResourceGroupEntityType00
2.16.840.1.113883.11.19656 x-LabProcessCodes00 x_LabProcessCodes
2.16.840.1.113883.11.19657 x-LabProcessClassCodes00 x_LabProcessClassCodes
2.16.840.1.113883.11.19658 actObservationVerificationCode, ActObservationVerificationCode00
2.16.840.1.113883.11.19659 actInfoPersistCode, ActInfoPersistCode00
2.16.840.1.113883.11.19660 actSpecimenLabelCode, ActSpecimenLabelCode00
2.16.840.1.113883.11.19661 actSpecimenManifestCode, ActSpecimenManifestCode00
2.16.840.1.113883.11.19662 actSpecimenAccessionCode, ActSpecimenAccessionCode00
2.16.840.1.113883.11.19663 actSpecimenTransportCode, ActSpecimenTransportCode00
2.16.840.1.113883.11.19664 actClassStorage, ActClassStorage00
2.16.840.1.113883.11.19665 actClassProcedure, ActClassProcedure00
2.16.840.1.113883.11.19666 actClassSpecimenCollection, ActClassSpecimenCollection00
2.16.840.1.113883.11.19667 x-AdministeredSubstance00 x_AdministeredSubstance
2.16.840.1.113883.11.19668 x-Medicine00 x_Medicine
2.16.840.1.113883.11.19669 actInjuryCode, ActInjuryCode00
2.16.840.1.113883.11.19670 x-DeterminerInstanceKind00 x_DeterminerInstanceKind