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

: TramadolRetardActavis100mgdepot-SE-PLC-ING04 - XML Representation

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<Ingredient xmlns="http://hl7.org/fhir">
  <id value="TramadolRetardActavis100mgdepot-SE-PLC-ING04"/>
  <meta>
    <profile
             value="http://unicom-project.eu/fhir/StructureDefinition/PPLIngredient"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: Ingredient TramadolRetardActavis100mgdepot-SE-PLC-ING04</b></p><a name="TramadolRetardActavis100mgdepot-SE-PLC-ING04"> </a><a name="hcTramadolRetardActavis100mgdepot-SE-PLC-ING04"> </a><a name="hcTramadolRetardActavis100mgdepot-SE-PLC-ING04-en-US"> </a><p><b>status</b>: Active</p><p><b>for</b>: </p><ul><li><a href="MedicinalProductDefinition-TramadolRetardActavis100mgdepot-SE-PLC-MPD.html">MedicinalProductDefinition: identifier = http://ema.europa.eu/fhir/mpId#SE-100000064-00024560,http://ema.europa.eu/fhir/eurdId#3002; domain = Human use; status = Current; combinedPharmaceuticalDoseForm = Prolonged-release tablet; indication = Behandling av måttlig till svår smärta.; legalStatusOfSupply = Medicinal product subject to medical prescription; classification = tramadol</a></li><li><a href="ManufacturedItemDefinition-TramadolRetardActavis100mgdepot-SE-PLC-MID.html">ManufacturedItemDefinition: status = active; manufacturedDoseForm = Prolonged-release tablet; unitOfPresentation = Tablet</a></li><li><a href="AdministrableProductDefinition-TramadolRetardActavis100mgdepot-SE-PLC-APD.html">AdministrableProductDefinition: status = active; administrableDoseForm = Prolonged-release tablet</a></li></ul><p><b>role</b>: <span title="Codes:{https://spor.ema.europa.eu/v1/lists/100000072050 100000072082}">Excipient</span></p><blockquote><p><b>substance</b></p><h3>Codes</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Concept</b></td></tr><tr><td style="display: none">*</td><td><span title="Codes:{https://spor.azure-api.net/sms/api/v2/SubstanceDefinition 100000092242}">Silica, colloidal anhydrous</span></td></tr></table></blockquote></div>
  </text>
  <status value="active"/>
  <for>🔗 
    <reference
               value="MedicinalProductDefinition/TramadolRetardActavis100mgdepot-SE-PLC-MPD"/>
  </for>
  <for>🔗 
    <reference
               value="ManufacturedItemDefinition/TramadolRetardActavis100mgdepot-SE-PLC-MID"/>
  </for>
  <for>🔗 
    <reference
               value="AdministrableProductDefinition/TramadolRetardActavis100mgdepot-SE-PLC-APD"/>
  </for>
  <role>
    <coding>
      <system value="https://spor.ema.europa.eu/v1/lists/100000072050"/>
      <code value="100000072082"/>
      <display value="Excipient"/>
    </coding>
  </role>
  <substance>
    <code>
      <concept>
        <coding>
          <system
                  value="https://spor.azure-api.net/sms/api/v2/SubstanceDefinition"/>
          <code value="100000092242"/>
          <display value="Silica, colloidal anhydrous"/>
        </coding>
      </concept>
    </code>
  </substance>
</Ingredient>