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

: CefuroximMIP-750mg-Powder-SE-IS-APD - JSON Representation

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{
  "resourceType" : "AdministrableProductDefinition",
  "id" : "CefuroximMIP-750mg-Powder-SE-IS-APD",
  "meta" : {
    "profile" : [
      🔗 "http://unicom-project.eu/fhir/StructureDefinition/PPLAdministrableProductDefinition"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: AdministrableProductDefinition CefuroximMIP-750mg-Powder-SE-IS-APD</b></p><a name=\"CefuroximMIP-750mg-Powder-SE-IS-APD\"> </a><a name=\"hcCefuroximMIP-750mg-Powder-SE-IS-APD\"> </a><a name=\"hcCefuroximMIP-750mg-Powder-SE-IS-APD-en-US\"> </a><p><b>status</b>: Active</p><p><b>formOf</b>: <a href=\"MedicinalProductDefinition-CefuroximMIP-750mg-Powder-SE-IS-MPD.html\">MedicinalProductDefinition: identifier = http://ema.europa.eu/fhir/mpId#SE-100003467-00046356,http://ema.europa.eu/fhir/eurdId#615; domain = Human use; status = Current; combinedPharmaceuticalDoseForm = Powder for solution for injection; indication = Cefuroxim MIP är avsett för behandling av nedanstående infektioner hos vuxna och barn,  även nyfödda (från födelsen).  • Samhällsförvärvad pneumoni.  • Akut exacerbation av kronisk bronkit.  • Komplicerade urinvägsinfektioner, även pyelonefrit.  • Mjukdelsinfektioner: cellulit, erysipelas och sårinfektioner.  • Intraabdominella infektioner.  • Profylax mot infektion inför gastrointestinal (även esofageal), ortopedisk, kardiovaskulär  och gynekologisk operation (även kejsarsnitt).  Vid behandling och förebyggande av infektioner då det är mycket troligt att anaeroba  organismer påträffas ska cefuroxim administreras tillsammans med ett lämpligt antianaerobt  antibiotikum.  Hänsyn ska tas till officiella riktlinjer om lämplig användning av antibakteriella medel.; legalStatusOfSupply = Medicinal product subject to medical prescription; classification = J01DC02</a></p><p><b>administrableDoseForm</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/200000000004 100000073863}\">Solution for injection</span></p><p><b>producedFrom</b>: <a href=\"ManufacturedItemDefinition-CefuroximMIP-750mg-Powder-SE-IS-MID.html\">ManufacturedItemDefinition: status = active; manufacturedDoseForm = Powder for solution for injection; unitOfPresentation = Vial</a></p><h3>RouteOfAdministrations</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Code</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000073345 100000073600}, {https://spor.ema.europa.eu/v1/lists/100000073345 100000073611}\">Intramuscular use</span></td></tr></table></div>"
  },
  "status" : "active",
  "formOf" : [
    {
      🔗 "reference" : "MedicinalProductDefinition/CefuroximMIP-750mg-Powder-SE-IS-MPD"
    }
  ],
  "administrableDoseForm" : {
    "coding" : [
      {
        "system" : "https://spor.ema.europa.eu/v1/lists/200000000004",
        "code" : "100000073863",
        "display" : "Solution for injection"
      }
    ]
  },
  "producedFrom" : [
    {
      🔗 "reference" : "ManufacturedItemDefinition/CefuroximMIP-750mg-Powder-SE-IS-MID"
    }
  ],
  "routeOfAdministration" : [
    {
      "code" : {
        "coding" : [
          {
            "system" : "https://spor.ema.europa.eu/v1/lists/100000073345",
            "code" : "100000073600",
            "display" : "Intramuscular use"
          },
          {
            "system" : "https://spor.ema.europa.eu/v1/lists/100000073345",
            "code" : "100000073611",
            "display" : "Intravenous use"
          }
        ]
      }
    }
  ]
}