Adverse Event Clinical Research R4 Backport
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This page is part of the Adverse Event Clinical Research R4 Backport (v1.0.0-ballot: STU 1 Ballot 1) based on FHIR R4. . For a full list of available versions, see the Directory of published versions

: AdverseEvent Severity or Grade Value Set - JSON Representation

Page standards status: Informative

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{
  "resourceType" : "ValueSet",
  "id" : "adverse-event-severity-or-grade-vs",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This value set contains 8 concepts</p><table class=\"codes\"><tr><td><b>Level</b></td><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>System</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a name=\"null-null\"> </a>1</td><td style=\"white-space:nowrap\">\u00a0\u00a0<i title=\"This code is not selectable ('Abstract')\"/></td><td/><td>Severity codes</td><td/></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-1\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-1\">1</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Mild</td><td><div><p>An experience that is usually transient, and requires no special treatment or intervention. The event does not generally interfere with usual daily activities. Includes transient laboratory test alterations.</p>\n</div></td></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-2\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-2\">2</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Moderate</td><td><div><p>An experience that is alleviated with simple therapeutic treatments. The event impacts usual daily activities. Includes laboratory test alterations indicating injury, but without long-term risk.</p>\n</div></td></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-3\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-3\">3</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Severe</td><td><div><p>An adverse event experience that requires intensive therapeutic intervention and interrupts usual daily activities.</p>\n</div></td></tr><tr><td><a name=\"null-null\"> </a>1</td><td style=\"white-space:nowrap\">\u00a0\u00a0<i title=\"This code is not selectable ('Abstract')\"/></td><td/><td>Grade codes</td><td/></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-1\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-1\">1</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Mild</td><td><div><p>An experience that is usually transient, and requires no special treatment or intervention. The event does not generally interfere with usual daily activities. Includes transient laboratory test alterations.</p>\n</div></td></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-2\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-2\">2</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Moderate</td><td><div><p>An experience that is alleviated with simple therapeutic treatments. The event impacts usual daily activities. Includes laboratory test alterations indicating injury, but without long-term risk.</p>\n</div></td></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-3\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-3\">3</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Severe</td><td><div><p>An adverse event experience that requires intensive therapeutic intervention and interrupts usual daily activities.</p>\n</div></td></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-4\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-4\">4</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Life Threatening or Disabling</td><td><div><p>Any adverse event that places the patient, in the view of the initial reporter, at immediate risk of death from the adverse event as it occurred, i.e., it does not include an adverse experience that, had it occurred in a more severe form, might have caused death.</p>\n</div></td></tr><tr><td><a name=\"http---hl7.org-fhir-uv-ae-research-backport-ig-CodeSystem-adverse-event-severity-or-grade-cs-5\"> </a>2</td><td style=\"white-space:nowrap\">\u00a0\u00a0\u00a0\u00a0<a href=\"CodeSystem-adverse-event-severity-or-grade-cs.html#adverse-event-severity-or-grade-cs-5\">5</a></td><td>http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs</td><td>Death Related to Adverse Event</td><td><div><p>The termination of life associated with an adverse event.</p>\n</div></td></tr></table></div>"
  },
  "extension" : [
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status",
      "valueCode" : "informative",
      "_valueCode" : {
        "extension" : [
          {
            "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-conformance-derivedFrom",
            "valueCanonical" : "http://hl7.org/fhir/uv/ae-research-backport-ig/ImplementationGuide/hl7.fhir.uv.ae-research-backport-ig"
          }
        ]
      }
    }
  ],
  "url" : "http://hl7.org/fhir/uv/ae-research-backport-ig/ValueSet/adverse-event-severity-or-grade-vs",
  "version" : "1.0.0-ballot",
  "name" : "AdverseEventSeverityOrGrade",
  "title" : "AdverseEvent Severity or Grade Value Set",
  "status" : "draft",
  "experimental" : true,
  "date" : "2023-07-28T19:53:38+00:00",
  "publisher" : "HL7 International - Biomedical Research and Regulation, Vulcan AdverseEvent groups",
  "contact" : [
    {
      "name" : "Biomedical Research and Regulation WG",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://hl7.org/Special/committees/rcrim"
        }
      ]
    }
  ],
  "description" : "This value set includes codes that indicate severity of the adverse event or grade.",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code" : "001"
        }
      ]
    }
  ],
  "compose" : {
    "include" : [
      {
        "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
        "filter" : [
          {
            "property" : "parent",
            "op" : "in",
            "value" : "severity, grade"
          }
        ]
      }
    ]
  },
  "expansion" : {
    "timestamp" : "2022-05-22T13:56:07Z",
    "total" : 8,
    "offset" : 0,
    "parameter" : [
      {
        "name" : "version",
        "valueString" : "1.00"
      }
    ],
    "contains" : [
      {
        "abstract" : true,
        "display" : "Severity codes",
        "contains" : [
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "1",
            "display" : "Mild"
          },
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "2",
            "display" : "Moderate"
          },
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "3",
            "display" : "Severe"
          }
        ]
      },
      {
        "abstract" : true,
        "display" : "Grade codes",
        "contains" : [
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "1",
            "display" : "Mild"
          },
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "2",
            "display" : "Moderate"
          },
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "3",
            "display" : "Severe"
          },
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "4",
            "display" : "Life Threatening or Disabling"
          },
          {
            "system" : "http://hl7.org/fhir/uv/ae-research-backport-ig/CodeSystem/adverse-event-severity-or-grade-cs",
            "code" : "5",
            "display" : "Death Related to Adverse Event"
          }
        ]
      }
    ]
  }
}