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
2.16.840.1.113883.11.19395 x-RoleClassPayeePolicyRelationship00 x_RoleClassPayeePolicyRelationship
2.16.840.1.113883.11.19397 actInvoiceElementCode, ActInvoiceElementCode00
2.16.840.1.113883.11.19398 actInvoiceGroupCode, ActInvoiceGroupCode00
2.16.840.1.113883.11.19399 actInvoiceRootGroupCode, ActInvoiceRootGroupCode00
2.16.840.1.113883.11.19400 actInvoiceInterGroupCode, ActInvoiceInterGroupCode00
2.16.840.1.113883.11.19401 actInvoiceDetailCode, ActInvoiceDetailCode00
2.16.840.1.113883.11.19402 actInvoiceDetailDrugProductCode, ActInvoiceDetailDrugProductCode00
2.16.840.1.113883.11.19404 actInvoiceDetailClinicalProductCode, ActInvoiceDetailClinicalProductCode00
2.16.840.1.113883.11.19405 actInvoiceDetailClinicalServiceCode, ActInvoiceDetailClinicalServiceCode00
2.16.840.1.113883.11.19406 actInvoiceDetailPreferredAccommodationCode, ActInvoiceDetailPreferredAccommodationCode00
2.16.840.1.113883.11.19407 actInvoiceDetailGenericCode, ActInvoiceDetailGenericCode00
2.16.840.1.113883.11.19408 actInvoiceDetailGenericProviderCode, ActInvoiceDetailGenericProviderCode00
2.16.840.1.113883.11.19409 actInvoiceDetailTaxCode, ActInvoiceDetailTaxCode00
2.16.840.1.113883.11.19410 actInvoiceDetailGenericModifierCode, ActInvoiceDetailGenericModifierCode00
2.16.840.1.113883.11.19411 actInvoiceDetailGenericAdjudicatorCode, ActInvoiceDetailGenericAdjudicatorCode00
2.16.840.1.113883.11.19412 actInvoiceAdjudicationPaymentCode, ActInvoiceAdjudicationPaymentCode00
2.16.840.1.113883.11.19413 actInvoiceAdjudicationPaymentSummaryCode, ActInvoiceAdjudicationPaymentSummaryCode00
2.16.840.1.113883.11.19414 actInvoiceAdjudicationPaymentGroupCode, ActInvoiceAdjudicationPaymentGroupCode00
2.16.840.1.113883.11.19415 x-ActInvoiceDetailPharmacyCode00 x_ActInvoiceDetailPharmacyCode
2.16.840.1.113883.11.19416 x-ActInvoiceDetailPreferredAccommodationCode00 x_ActInvoiceDetailPreferredAccommodationCode
2.16.840.1.113883.11.19417 researchSubjectRoleBasis, ResearchSubjectRoleBasis00
2.16.840.1.113883.11.19427 hL7TriggerEventCode, HL7TriggerEventCode00
2.16.840.1.113883.11.19428 actFinancialDetectedIssueCode, ActFinancialDetectedIssueCode00
2.16.840.1.113883.11.19429 actAdministrativeDetectedIssueCode, ActAdministrativeDetectedIssueCode00
2.16.840.1.113883.11.19430 actFinancialDetectedIssueManagementCode, ActFinancialDetectedIssueManagementCode00
2.16.840.1.113883.11.19431 actAdministrativeDetectedIssueManagementCode, ActAdministrativeDetectedIssueManagementCode00
2.16.840.1.113883.11.19432 canadianActInvoiceDetailClinicalProductCode, CanadianActInvoiceDetailClinicalProductCode00
2.16.840.1.113883.11.19433 canadianActProcedureCode, CanadianActProcedureCode00
2.16.840.1.113883.11.19434 canadianActInvoiceDetailClinicalServiceCode, CanadianActInvoiceDetailClinicalServiceCode00
2.16.840.1.113883.11.19435 canadianProductEntityType, CanadianProductEntityType00
2.16.840.1.113883.11.19436 canadianDiagnosisCode, CanadianDiagnosisCode00
2.16.840.1.113883.11.19437 canadianWorkInjuryOrDiseaseCode, CanadianWorkInjuryOrDiseaseCode00
2.16.840.1.113883.11.19438 injuryActSite, InjuryActSite00
2.16.840.1.113883.11.19439 canadianActInjurySite, CanadianActInjurySite00
2.16.840.1.113883.11.19440 actBillableTreatmentPlanCode, ActBillableTreatmentPlanCode00
2.16.840.1.113883.11.19441 actClassExtract, ActClassExtract00
2.16.840.1.113883.11.19442 actClassComposition, ActClassComposition00
2.16.840.1.113883.11.19443 actClassOrganizer, ActClassOrganizer00
2.16.840.1.113883.11.19444 actClassEntry, ActClassEntry00
2.16.840.1.113883.11.19445 actClassContainer, ActClassContainer00
2.16.840.1.113883.11.19446 x-ActRelationshipEntry00 x_ActRelationshipEntry
2.16.840.1.113883.11.19447 x-ActRelationshipEntryRelationship00 x_ActRelationshipEntryRelationship
2.16.840.1.113883.11.19449 hL7ITSVersionCode, HL7ITSVersionCode00
2.16.840.1.113883.11.19450 dedicatedServiceDeliveryLocationRoleType, DedicatedServiceDeliveryLocationRoleType00
2.16.840.1.113883.11.19451 incidentalServiceDeliveryLocationRoleType, IncidentalServiceDeliveryLocationRoleType00
2.16.840.1.113883.11.19452 dedicatedNonClinicalLocationRoleType, DedicatedNonClinicalLocationRoleType00
2.16.840.1.113883.11.19453 uSEncounterDischargeDisposition, USEncounterDischargeDisposition00
2.16.840.1.113883.11.19454 uSEncounterReferralSource, USEncounterReferralSource00
2.16.840.1.113883.11.19455 state, State00
2.16.840.1.113883.11.19456 x-ActEncounterReason00 x_ActEncounterReason