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

: Sandimmun50mgmlkoncentrat-SE-PLC-MPD - XML Representation

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<MedicinalProductDefinition xmlns="http://hl7.org/fhir">
  <id value="Sandimmun50mgmlkoncentrat-SE-PLC-MPD"/>
  <meta>
    <profile
             value="http://unicom-project.eu/fhir/StructureDefinition/PPLMedicinalProductDefinition"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: MedicinalProductDefinition Sandimmun50mgmlkoncentrat-SE-PLC-MPD</b></p><a name="Sandimmun50mgmlkoncentrat-SE-PLC-MPD"> </a><a name="hcSandimmun50mgmlkoncentrat-SE-PLC-MPD"> </a><a name="hcSandimmun50mgmlkoncentrat-SE-PLC-MPD-en-US"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/fhir/mpId</code>/SE-100003469-00010263, <code>http://ema.europa.eu/fhir/eurdId</code>/745</p><p><b>domain</b>: <span title="Codes:{https://spor.ema.europa.eu/v1/lists/100000000004 100000000012}">Human use</span></p><p><b>status</b>: <span title="Codes:{https://spor.ema.europa.eu/v1/lists/200000005003 200000005004}">Current</span></p><p><b>combinedPharmaceuticalDoseForm</b>: <span title="Codes:{https://spor.ema.europa.eu/v1/lists/200000000004~200000000006~200000000007~200000000008 100000073871}">Concentrate for solution for infusion</span></p><p><b>indication</b>: </p><div><p>Transplantationsindikationer  Organtransplantation  För prevention av transplantatavstötning efter organtransplantation.   Behandling av cellmedierad transplantatavstötning hos patienter som tidigare fått annan immunsuppressiv behandling.   Benmärgstransplantation  För prevention av transplantatavstötning efter allogen benmärgs- och stamcellstransplantation.   Profylax eller behandling av graft-versus-host disease (GVHD).</p>
</div><p><b>legalStatusOfSupply</b>: <span title="Codes:{https://spor.ema.europa.eu/v1/lists/100000072051 100000072084}">Medicinal product subject to medical prescription</span></p><p><b>classification</b>: <span title="Codes:{https://spor.ema.europa.eu/v1/lists/100000093533 100000096879}">ciclosporin</span></p><blockquote><p><b>name</b></p><p><b>productName</b>: Sandimmun 50 mg/ml koncentrat till infusionsvätska, lösning</p><blockquote><p><b>part</b></p><p><b>part</b>: Sandimmun</p><p><b>type</b>: <span title="Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000002}">Invented name part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: 50 mg/ml</p><p><b>type</b>: <span title="Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000004}">Strength part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: koncentrat till infusionsvätska, lösning</p><p><b>type</b>: <span title="Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000005}">Pharmaceutical dose form part</span></p></blockquote><h3>Usages</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Country</b></td><td><b>Language</b></td></tr><tr><td style="display: none">*</td><td><span title="Codes:{https://spor.ema.europa.eu/v1/lists/100000000002 100000000535}">Kingdom of Sweden</span></td><td><span title="Codes:{urn:ietf:bcp:47 sv}">Swedish</span></td></tr></table></blockquote></div>
  </text>
  <identifier>
    <system value="http://ema.europa.eu/fhir/mpId"/>
    <value value="SE-100003469-00010263"/>
  </identifier>
  <identifier>
    <system value="http://ema.europa.eu/fhir/eurdId"/>
    <value value="745"/>
  </identifier>
  <domain>
    <coding>
      <system value="https://spor.ema.europa.eu/v1/lists/100000000004"/>
      <code value="100000000012"/>
      <display value="Human use"/>
    </coding>
  </domain>
  <status>
    <coding>
      <system value="https://spor.ema.europa.eu/v1/lists/200000005003"/>
      <code value="200000005004"/>
      <display value="Current"/>
    </coding>
  </status>
  <combinedPharmaceuticalDoseForm>
    <coding>
      <system
              value="https://spor.ema.europa.eu/v1/lists/200000000004~200000000006~200000000007~200000000008"/>
      <code value="100000073871"/>
      <display value="Concentrate for solution for infusion"/>
    </coding>
  </combinedPharmaceuticalDoseForm>
  <indication
              value="Transplantationsindikationer  Organtransplantation  För prevention av transplantatavstötning efter organtransplantation.   Behandling av cellmedierad transplantatavstötning hos patienter som tidigare fått annan immunsuppressiv behandling.   Benmärgstransplantation  För prevention av transplantatavstötning efter allogen benmärgs- och stamcellstransplantation.   Profylax eller behandling av graft-versus-host disease (GVHD)."/>
  <legalStatusOfSupply>
    <coding>
      <system value="https://spor.ema.europa.eu/v1/lists/100000072051"/>
      <code value="100000072084"/>
      <display value="Medicinal product subject to medical prescription"/>
    </coding>
  </legalStatusOfSupply>
  <classification>
    <coding>
      <system value="https://spor.ema.europa.eu/v1/lists/100000093533"/>
      <code value="100000096879"/>
      <display value="ciclosporin"/>
    </coding>
  </classification>
  <name>
    <productName
                 value="Sandimmun 50 mg/ml koncentrat till infusionsvätska, lösning"/>
    <part>
      <part value="Sandimmun"/>
      <type>
        <coding>
          <system value="http://spor.ema.europa.eu/v1/lists/220000000000"/>
          <code value="220000000002"/>
          <display value="Invented name part"/>
        </coding>
      </type>
    </part>
    <part>
      <part value="50 mg/ml"/>
      <type>
        <coding>
          <system value="http://spor.ema.europa.eu/v1/lists/220000000000"/>
          <code value="220000000004"/>
          <display value="Strength part"/>
        </coding>
      </type>
    </part>
    <part>
      <part value="koncentrat till infusionsvätska, lösning"/>
      <type>
        <coding>
          <system value="http://spor.ema.europa.eu/v1/lists/220000000000"/>
          <code value="220000000005"/>
          <display value="Pharmaceutical dose form part"/>
        </coding>
      </type>
    </part>
    <usage>
      <country>
        <coding>
          <system value="https://spor.ema.europa.eu/v1/lists/100000000002"/>
          <code value="100000000535"/>
          <display value="Kingdom of Sweden"/>
        </coding>
      </country>
      <language>
        <coding>
          <system value="urn:ietf:bcp:47"/>
          <code value="sv"/>
          <display value="Swedish"/>
        </coding>
      </language>
    </usage>
  </name>
</MedicinalProductDefinition>