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

: HydrokortisonOrifarm20mgTablett-SE-PLC-MPD - XML Representation

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<MedicinalProductDefinition xmlns="http://hl7.org/fhir">
  <id value="HydrokortisonOrifarm20mgTablett-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 HydrokortisonOrifarm20mgTablett-SE-PLC-MPD</b></p><a name="HydrokortisonOrifarm20mgTablett-SE-PLC-MPD"> </a><a name="hcHydrokortisonOrifarm20mgTablett-SE-PLC-MPD"> </a><a name="hcHydrokortisonOrifarm20mgTablett-SE-PLC-MPD-en-US"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/fhir/mpId</code>/SE-100002342-00054330, <code>http://ema.europa.eu/fhir/eurdId</code>/10855</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 100000073664}">Tablet</span></p><p><b>indication</b>: </p><div><p>Substitutionsbehandling vid kongenital binjurebarkshyperplasi hos barn.  Behandling av binjurebarkinsufficiens hos barn och ungdomar under 18 år.  Akut behandling av svår astma, överkänslighetsreaktioner mot läkemedel, serumsjuka, angioneurotiskt ödem och anafylaxi hos vuxna och barn.  Hydrokortison Orifarm är avsett för vuxna och barn i åldern 1 månad till 18 år där tablettberedning bedöms lämplig.</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 100000096043}">hydrocortisone</span></p><blockquote><p><b>name</b></p><p><b>productName</b>: Hydrokortison Orifarm 20 mg Tablett</p><blockquote><p><b>part</b></p><p><b>part</b>: Hydrokortison Orifarm</p><p><b>type</b>: <span title="Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000003}">Scientific name part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: 20 mg</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>: tablett</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-100002342-00054330"/>
  </identifier>
  <identifier>
    <system value="http://ema.europa.eu/fhir/eurdId"/>
    <value value="10855"/>
  </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="100000073664"/>
      <display value="Tablet"/>
    </coding>
  </combinedPharmaceuticalDoseForm>
  <indication
              value="Substitutionsbehandling vid kongenital binjurebarkshyperplasi hos barn.  Behandling av binjurebarkinsufficiens hos barn och ungdomar under 18 år.  Akut behandling av svår astma, överkänslighetsreaktioner mot läkemedel, serumsjuka, angioneurotiskt ödem och anafylaxi hos vuxna och barn.  Hydrokortison Orifarm är avsett för vuxna och barn i åldern 1 månad till 18 år där tablettberedning bedöms lämplig."/>
  <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="100000096043"/>
      <display value="hydrocortisone"/>
    </coding>
  </classification>
  <name>
    <productName value="Hydrokortison Orifarm 20 mg Tablett"/>
    <part>
      <part value="Hydrokortison Orifarm"/>
      <type>
        <coding>
          <system value="http://spor.ema.europa.eu/v1/lists/220000000000"/>
          <code value="220000000003"/>
          <display value="Scientific name part"/>
        </coding>
      </type>
    </part>
    <part>
      <part value="20 mg"/>
      <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="tablett"/>
      <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>