UFIS-SWE-IG
0.1.0 - ci-build

UFIS-SWE-IG, published by UNICOM. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/joofio/ufis-swe-ig/ and changes regularly. See the Directory of published versions

: Stesolid-10mg-Solution-SE-IS-RA - JSON Representation

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{
  "resourceType" : "RegulatedAuthorization",
  "id" : "Stesolid-10mg-Solution-SE-IS-RA",
  "meta" : {
    "profile" : [
      🔗 "http://unicom-project.eu/fhir/StructureDefinition/PPLRegulatedAuthorization"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: RegulatedAuthorization Stesolid-10mg-Solution-SE-IS-RA</b></p><a name=\"Stesolid-10mg-Solution-SE-IS-RA\"> </a><a name=\"hcStesolid-10mg-Solution-SE-IS-RA\"> </a><a name=\"hcStesolid-10mg-Solution-SE-IS-RA-en-US\"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/fhir/marketingAuthorizationNumber</code>/9292</p><p><b>subject</b>: <a href=\"MedicinalProductDefinition-Stesolid-10mg-Solution-SE-IS-MPD.html\">MedicinalProductDefinition: identifier = http://ema.europa.eu/fhir/mpId#SE-100000064-00009292,http://ema.europa.eu/fhir/eurdId#1029; domain = Human use; status = Current; combinedPharmaceuticalDoseForm = Rectal solution; indication = Stesolid rektallösning är speciellt användbart vid manifesta kramper, som feberkramper, tetanus och  eklampsi, vid status epilepticus samt för premedicinering och sedering. Stesolid rektallösning är  indicerat också i andra akuta situationer då snabb, ångestdämpande eller sederande effekt önskas.; legalStatusOfSupply = Medicinal product subject to special medical prescription; classification = N05BA01</a></p><p><b>type</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/220000000060 220000000061}\">Marketing Authorisation</span></p><p><b>region</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000000002 100000000535}\">Kingdom of Sweden</span></p><p><b>status</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000072049 100000072099}\">Valid</span></p><p><b>statusDate</b>: 1977-11-18</p><p><b>holder</b>: <a href=\"Organization-LOC-100001873.html\">Organization Actavis Group PTC ehf.</a></p><h3>Cases</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Type</b></td><td><b>Date[x]</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{https://ema.europa.eu/fhir/authorisationDateType dateOfFirstAuthorisation}\">First Authorisation</span></td><td>1977-11-18</td></tr></table></div>"
  },
  "identifier" : [
    {
      "system" : "http://ema.europa.eu/fhir/marketingAuthorizationNumber",
      "value" : "9292"
    }
  ],
  "subject" : [
    {
      🔗 "reference" : "MedicinalProductDefinition/Stesolid-10mg-Solution-SE-IS-MPD"
    }
  ],
  "type" : {
    "coding" : [
      {
        "system" : "https://spor.ema.europa.eu/v1/lists/220000000060",
        "code" : "220000000061",
        "display" : "Marketing Authorisation"
      }
    ]
  },
  "region" : [
    {
      "coding" : [
        {
          "system" : "https://spor.ema.europa.eu/v1/lists/100000000002",
          "code" : "100000000535",
          "display" : "Kingdom of Sweden"
        }
      ]
    }
  ],
  "status" : {
    "coding" : [
      {
        "system" : "https://spor.ema.europa.eu/v1/lists/100000072049",
        "code" : "100000072099",
        "display" : "Valid"
      }
    ]
  },
  "statusDate" : "1977-11-18",
  "holder" : {
    🔗 "reference" : "Organization/LOC-100001873"
  },
  "case" : {
    "type" : {
      "coding" : [
        {
          "system" : "https://ema.europa.eu/fhir/authorisationDateType",
          "code" : "dateOfFirstAuthorisation",
          "display" : "First Authorisation"
        }
      ]
    },
    "dateDateTime" : "1977-11-18"
  }
}