{
  "resourceType": "CodeSystem",
  "id": "administration-subpotent-reason",
  "meta": {
    "lastUpdated": "2023-03-26T15:21:02.749+11:00",
    "profile": [
      "http://hl7.org/fhir/StructureDefinition/shareablecodesystem"
    ]
  },
  "text": {
    "status": "generated",
    "div": "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This code system <code>http://hl7.org/fhir/CodeSystem/administration-subpotent-reason</code> defines the following codes:</p><table class=\"codes\"><tr><td><b>Lvl</b></td><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td>1</td><td style=\"white-space:nowrap\">partialdose<a name=\"administration-subpotent-reason-partialdose\"> </a></td><td>Partial Dose</td><td>The full amount of the dose was not administered to the patient.</td></tr><tr><td>2</td><td style=\"white-space:nowrap\">  vomited<a name=\"administration-subpotent-reason-vomited\"> </a></td><td>Vomited</td><td>The patient vomited part of the dose.</td></tr><tr><td>1</td><td style=\"white-space:nowrap\">coldchainbreak<a name=\"administration-subpotent-reason-coldchainbreak\"> </a></td><td>Cold Chain Break</td><td>The medication experienced a cold chain break.</td></tr><tr><td>1</td><td style=\"white-space:nowrap\">recall<a name=\"administration-subpotent-reason-recall\"> </a></td><td>Manufacturer Recall</td><td>The medication was recalled by the manufacturer.</td></tr><tr><td>1</td><td style=\"white-space:nowrap\">adversestorage<a name=\"administration-subpotent-reason-adversestorage\"> </a></td><td>Adverse Storage</td><td>The medication experienced adverse storage conditions.</td></tr><tr><td>1</td><td style=\"white-space:nowrap\">expired<a name=\"administration-subpotent-reason-expired\"> </a></td><td>Expired Product</td><td>The medication was expired at the time of administration.</td></tr></table></div>"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode": "phx"
    }
  ],
  "url": "http://hl7.org/fhir/CodeSystem/administration-subpotent-reason",
  "identifier": [
    {
      "system": "urn:ietf:rfc:3986",
      "value": "urn:oid:2.16.840.1.113883.4.642.4.2001"
    }
  ],
  "version": "5.0.0",
  "name": "AdministrationSubPotentReason",
  "title": "Administration SubPotent Reason",
  "status": "active",
  "experimental": false,
  "publisher": "HL7 International",
  "description": "This value set is provided as an example. The value set to instantiate this attribute should be drawn from a robust terminology code system that consists of or contains concepts to support the medication administration process.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code": "001",
          "display": "World"
        }
      ]
    }
  ],
  "caseSensitive": true,
  "hierarchyMeaning": "is-a",
  "content": "complete",
  "concept": [
    {
      "code": "partialdose",
      "display": "Partial Dose",
      "definition": "The full amount of the dose was not administered to the patient.",
      "concept": [
        {
          "code": "vomited",
          "display": "Vomited",
          "definition": "The patient vomited part of the dose."
        }
      ]
    },
    {
      "code": "coldchainbreak",
      "display": "Cold Chain Break",
      "definition": "The medication experienced a cold chain break."
    },
    {
      "code": "recall",
      "display": "Manufacturer Recall",
      "definition": "The medication was recalled by the manufacturer."
    },
    {
      "code": "adversestorage",
      "display": "Adverse Storage",
      "definition": "The medication experienced adverse storage conditions."
    },
    {
      "code": "expired",
      "display": "Expired Product",
      "definition": "The medication was expired at the time of administration."
    }
  ]
}