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Packagehl7.fhir.uv.xver-r4.r4b
Resource TypeCodeSystem
IdCodeSystem-v2-0252.json
FHIR VersionR4B

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Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: CodeSystem v2-0252

This code system http://terminology.hl7.org/CodeSystem/v2-0252 defines the following codes:

CodeDisplayNederlands (Dutch, nl)
AW Abatement of event after product withdrawnVermindering gebeurtenis na terugtrekken product
BE Event recurred after product reintroducedGebeurtenis trad opnieuw op na herintroductie product
DR Dose response observedDosis reactie geobserveerd
EX Alternative explanations for the event availableAlternatieve verklaringen voor gebeurtenis beschikbaar
IN Event occurred after product introducedGebeurtenis trad op na introductie product
LI Literature reports association of product with eventLiteratuur vermeldt koppeling van product met gebeurtenis
OE Occurrence of event was confirmed by objective evidenceOptreden van gebeurtenis is bevestigd door objectief bewijs
OT OtherAnders
PL Effect observed when patient receives placeboEffect geobserveerd wanneer patiënt placebo krijgt
SE Similar events in past for this patientVergelijkbare gebeurtenissen in verleden voor deze patiënt
TC Toxic levels of product documented in blood or body fluidsToxische niveaus van product gedocumenteerd in bloed of lichaamssappen

Source1

{
  "resourceType": "CodeSystem",
  "id": "v2-0252",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
      "valueCode": "external"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm",
      "valueInteger": 0
    },
    {
      "extension": [
        {
          "url": "packageId",
          "valueId": "hl7.fhir.uv.xver-r4.r4b"
        },
        {
          "url": "version",
          "valueString": "0.0.1-snapshot-2"
        }
      ],
      "url": "http://hl7.org/fhir/StructureDefinition/package-source"
    },
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode": "fhir"
    }
  ],
  "url": "http://terminology.hl7.org/CodeSystem/v2-0252",
  "version": "2.9",
  "name": "v2.0252",
  "title": "v2 Causality Observations",
  "status": "active",
  "experimental": false,
  "date": "2025-09-13T16:11:23-04:00",
  "publisher": "FHIR Infrastructure",
  "contact": [
    {
      "name": "FHIR Infrastructure",
      "telecom": [
        {
          "system": "url",
          "value": "http://www.hl7.org/Special/committees/fiwg"
        }
      ]
    }
  ],
  "description": "FHIR Value set/code system definition for HL7 v2 table 0252 ( Causality Observations)",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code": "001",
          "display": "World"
        }
      ]
    }
  ],
  "content": "complete",
  "concept": [
    {
      "code": "AW",
      "display": "Abatement of event after product withdrawn",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Vermindering gebeurtenis na terugtrekken product"
        }
      ]
    },
    {
      "code": "BE",
      "display": "Event recurred after product reintroduced",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Gebeurtenis trad opnieuw op na herintroductie product"
        }
      ]
    },
    {
      "code": "DR",
      "display": "Dose response observed",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Dosis reactie geobserveerd"
        }
      ]
    },
    {
      "code": "EX",
      "display": "Alternative explanations for the event available",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Alternatieve verklaringen voor gebeurtenis beschikbaar"
        }
      ]
    },
    {
      "code": "IN",
      "display": "Event occurred after product introduced",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Gebeurtenis trad op na introductie product"
        }
      ]
    },
    {
      "code": "LI",
      "display": "Literature reports association of product with event",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Literatuur vermeldt koppeling van product met gebeurtenis"
        }
      ]
    },
    {
      "code": "OE",
      "display": "Occurrence of event was confirmed by objective evidence",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Optreden van gebeurtenis is bevestigd door objectief bewijs"
        }
      ]
    },
    {
      "code": "OT",
      "display": "Other",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Anders"
        }
      ]
    },
    {
      "code": "PL",
      "display": "Effect observed when patient receives placebo",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Effect geobserveerd wanneer patiënt placebo krijgt"
        }
      ]
    },
    {
      "code": "SE",
      "display": "Similar events in past for this patient",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Vergelijkbare gebeurtenissen in verleden voor deze patiënt"
        }
      ]
    },
    {
      "code": "TC",
      "display": "Toxic levels of product documented in blood or body fluids",
      "designation": [
        {
          "language": "nl",
          "use": {
            "system": "http://terminology.hl7.org/CodeSystem/designation-usage",
            "code": "display"
          },
          "value": "Toxische niveaus van product gedocumenteerd in bloed of lichaamssappen"
        }
      ]
    }
  ]
}