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" : "Ingredient",
"id" : "TramadolRetardActavis100mgdepot-SE-PLC-ING04",
"meta" : {
"profile" : [
🔗 "http://unicom-project.eu/fhir/StructureDefinition/PPLIngredient"
]
},
"text" : {
"status" : "generated",
"div" : "<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>"
},
"status" : "active",
"for" : [
{
🔗 "reference" : "MedicinalProductDefinition/TramadolRetardActavis100mgdepot-SE-PLC-MPD"
},
{
🔗 "reference" : "ManufacturedItemDefinition/TramadolRetardActavis100mgdepot-SE-PLC-MID"
},
{
🔗 "reference" : "AdministrableProductDefinition/TramadolRetardActavis100mgdepot-SE-PLC-APD"
}
],
"role" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000072050",
"code" : "100000072082",
"display" : "Excipient"
}
]
},
"substance" : {
"code" : {
"concept" : {
"coding" : [
{
"system" : "https://spor.azure-api.net/sms/api/v2/SubstanceDefinition",
"code" : "100000092242",
"display" : "Silica, colloidal anhydrous"
}
]
}
}
}
}