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
2.16.840.1.113883.11.19721 observationIssueTriggerCodedObservationType, ObservationIssueTriggerCodedObservationType00
2.16.840.1.113883.11.19722 observationIssueTriggerMeasuredObservationType, ObservationIssueTriggerMeasuredObservationType00
2.16.840.1.113883.11.19723 patientCharacteristicObservationType, PatientCharacteristicObservationType00
2.16.840.1.113883.11.19724 issueTriggerObservationValue, IssueTriggerObservationValue00
2.16.840.1.113883.11.19725 actNoImmunizationReason, ActNoImmunizationReason00
2.16.840.1.113883.11.19726 actSupplyFulfillmentRefusalReason, ActSupplyFulfillmentRefusalReason00
2.16.840.1.113883.11.19727 substanceAdminSubstitutionNotAllowedReason, SubstanceAdminSubstitutionNotAllowedReason00
2.16.840.1.113883.11.19728 medicationGeneralizationRoleType, MedicationGeneralizationRoleType00
2.16.840.1.113883.11.19729 activeIngredientDrugEntityType, ActiveIngredientDrugEntityType00
2.16.840.1.113883.11.19730 vaccineEntityType, VaccineEntityType00
2.16.840.1.113883.11.19731 actMedicationDocumentCode, ActMedicationDocumentCode00
2.16.840.1.113883.11.19732 humanSubstanceAdministrationSite, HumanSubstanceAdministrationSite00
2.16.840.1.113883.11.19733 actPrivilegeCategorization, ActPrivilegeCategorization00
2.16.840.1.113883.11.19734 observationIndicationType, ObservationIndicationType00
2.16.840.1.113883.11.19735 indicationValue, IndicationValue00
2.16.840.1.113883.11.19736 symptomValue, SymptomValue00
2.16.840.1.113883.11.19737 otherIndicationValue, OtherIndicationValue00
2.16.840.1.113883.11.19738 actTransportationModeCode, ActTransportationModeCode00
2.16.840.1.113883.11.19739 actPatientTransportationModeCode, ActPatientTransportationModeCode00
2.16.840.1.113883.11.19740 ambulance, Ambulance00
2.16.840.1.113883.11.19741 coverageEligibilityReason, CoverageEligibilityReason00 Reason or rationale for why a person is eligibile for benefits under an insurance policy or program
2.16.840.1.113883.11.19742 x-VeryBasicConfidentialityKind00 x_VeryBasicConfidentialityKind
2.16.840.1.113883.11.19743 x-PhysicalVerbalParticipationMode00 x_PhysicalVerbalParticipationMode
2.16.840.1.113883.11.19744 x-SubstitutionConditionNoneOrUnconditional00 x_SubstitutionConditionNoneOrUnconditional
2.16.840.1.113883.11.19745 x-PhoneOrEmailURLScheme00 x_PhoneOrEmailURLScheme
2.16.840.1.113883.11.19746 x-PhoneURLScheme00 x_PhoneURLScheme
2.16.840.1.113883.11.19747 referralReasonCode, ReferralReasonCode00
2.16.840.1.113883.11.19748 nonPerformanceReasonCode, NonPerformanceReasonCode00
2.16.840.1.113883.11.19749 x-MedicationOrImmunization00 x_MedicationOrImmunization
2.16.840.1.113883.11.19750 queryParameterValue, QueryParameterValue00
2.16.840.1.113883.11.19751 immunizationForecastDate00 ImmunizationForecastDate
2.16.840.1.113883.11.19752 HL7FormatCodes, v3-HL7FormatCodes, hl7formatcodesvs00
2.16.840.1.113883.11.19753 uscore-cc00
2.16.840.1.113883.11.19754 genderIdentity00
2.16.840.1.113883.11.19755 personalPronouns00
2.16.840.1.113883.11.19756 icaoSex00
2.16.840.1.113883.11.19757 rsgField00
2.16.840.1.113883.11.21013 DrugEntity, v3-DrugEntity00
2.16.840.1.113883.11.21014 ManufacturerModelNameExample, v3-ManufacturerModelNameExample00
2.16.840.1.113883.11.21015 SoftwareNameExample, v3-SoftwareNameExample00
2.16.840.1.113883.11.21025 AdverseEventClinicalResearchOutcomes, adverse-event-clinical-research-outcomes00
2.16.840.1.113883.11.21027 AdverseEventClinicalResearchGrades, adverse-event-clinical-research-grades00
2.16.840.1.113883.11.21028 AdverseEventClinicalResearchCausalityRelatedness, adverse-event-clinical-research-causality-relatedness00
2.16.840.1.113883.11.21029 JurisdictionValueSet, jurisdiction00
2.16.840.1.113883.11.21034 ProcedureTypeCodes, procedure-type00
2.16.840.1.113883.11.21035 DiagnosisTypeCodes, diagnosistype00
2.16.840.1.113883.11.21037 MedicalManagementType, medical-management-type00
2.16.840.1.113883.11.21038 ImmunizationFunction, immunization-function00
2.16.840.1.113883.11.21041 ClaimAdjudicationBasisCategories, claim-adjudication-basis-categories00
2.16.840.1.113883.11.21042 USClaimInformationCategoryCodes, us-claim-information-category00