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
{
"resourceType" : "AdministrableProductDefinition",
"id" : "Fragmin-5000IE-Solution-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 Fragmin-5000IE-Solution-SE-IS-APD</b></p><a name=\"Fragmin-5000IE-Solution-SE-IS-APD\"> </a><a name=\"hcFragmin-5000IE-Solution-SE-IS-APD\"> </a><a name=\"hcFragmin-5000IE-Solution-SE-IS-APD-en-US\"> </a><p><b>status</b>: Active</p><p><b>formOf</b>: <a href=\"MedicinalProductDefinition-Fragmin-5000IE-Solution-SE-IS-MPD.html\">MedicinalProductDefinition: identifier = http://ema.europa.eu/fhir/mpId#SE-100001390-00010756,http://ema.europa.eu/fhir/eurdId#922; domain = Human use; status = Current; combinedPharmaceuticalDoseForm = Solution for injection in pre-filled syringe; indication = Behandling av akut djup ventrombos och lungemboli när trombolytisk behandling eller kirurgi inte är aktuell. Trombosprofylax-antikoagulation vid extrakorporeal cirkulation under hemodialys och hemofiltration. Trombosprofylax vid kirurgi. Profylax till patienter med kraftigt ökad risk för venös tromboembolism och som är tillfälligt immobiliserade pga akut sjukdomstillstånd som t ex hjärtinsufficiens, andningsinsufficiens, allvarlig infektion. Instabil kranskärlssjukdom (instabil angina och icke Q-vågsinfarkt). Cancerpatienter: Behandling och sekundärprevention av djup ventrombos och lungemboli.; legalStatusOfSupply = Medicinal product subject to medical prescription; classification = B01AB04</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-Fragmin-5000IE-Solution-SE-IS-MID.html\">ManufacturedItemDefinition: status = active; manufacturedDoseForm = Solution for injection; unitOfPresentation = Syringe</a></p><blockquote><p><b>routeOfAdministration</b></p><p><b>code</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000073345 100000073611}\">Intravenous use</span></p></blockquote><blockquote><p><b>routeOfAdministration</b></p><p><b>code</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000073345 100000073633}\">Subcutaneous use</span></p></blockquote><blockquote><p><b>routeOfAdministration</b></p><p><b>code</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000073345 100000075556}\">Extracorporeal use</span></p></blockquote></div>"
},
"status" : "active",
"formOf" : [
{
🔗 "reference" : "MedicinalProductDefinition/Fragmin-5000IE-Solution-SE-IS-MPD"
}
],
"administrableDoseForm" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/200000000004",
"code" : "100000073863",
"display" : "Solution for injection"
}
]
},
"producedFrom" : [
{
🔗 "reference" : "ManufacturedItemDefinition/Fragmin-5000IE-Solution-SE-IS-MID"
}
],
"routeOfAdministration" : [
{
"code" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000073345",
"code" : "100000073611",
"display" : "Intravenous use"
}
]
}
},
{
"code" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000073345",
"code" : "100000073633",
"display" : "Subcutaneous use"
}
]
}
},
{
"code" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000073345",
"code" : "100000075556",
"display" : "Extracorporeal use"
}
]
}
}
]
}