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: Cefuroxime-MIP-1500mg-EE-MPD - JSON Representation
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{
"resourceType" : "MedicinalProductDefinition",
"id" : "Cefuroxime-MIP-1500mg-EE-MPD",
"meta" : {
"profile" : [
"http://unicom-project.eu/fhir/StructureDefinition/PPLMedicinalProductDefinition"
]
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative: MedicinalProductDefinition</b><a name=\"Cefuroxime-MIP-1500mg-EE-MPD\"> </a></p><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Resource MedicinalProductDefinition "Cefuroxime-MIP-1500mg-EE-MPD" </p><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-PPLMedicinalProductDefinition.html\">PPL Medicinal Product profile</a></p></div><p><b>identifier</b>: id: EE-100009199-27834, id: EE0000002</p><p><b>domain</b>: Human use <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-domain-ema-cs.html\">Domain EMA</a>#100000000012)</span></p><p><b>status</b>: Current <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-recordStatus-ema-cs.html\">Record Status EMA SPOR</a>#200000005004)</span></p><p><b>combinedPharmaceuticalDoseForm</b>: Powder for solution for injection/infusion <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-pharmaceutical-dose-form-ema-cs.html\">Pharmaceutical Dose Form EMA</a>#100000116186)</span></p><p><b>legalStatusOfSupply</b>: Medicinal Product subject to medical prescription <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-legal-status-for-the-supply-ema-cs.html\">Legal Status for the Supply EMA</a>#100000072084)</span></p><p><b>classification</b>: Cefuroxime <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-ATC-Human-EMA.html\">ATC Human EMA</a>#100000096183)</span>, cefuroxime <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"http://terminology.hl7.org/5.0.0/CodeSystem-v3-WC.html\">WHO ATC</a>#J01DC02)</span></p><blockquote><p><b>name</b></p><p><b>productName</b>: Cefuroxime MIP 1500 mg, süste-/infusioonilahuse pulber</p><blockquote><p><b>namePart</b></p><p><b>part</b>: Cefuroxime MIP</p><p><b>type</b>: Invented name part <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (220000000000#220000000002)</span></p></blockquote><blockquote><p><b>namePart</b></p><p><b>part</b>: 1500 MG</p><p><b>type</b>: Strength part <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (220000000000#220000000004)</span></p></blockquote><h3>CountryLanguages</h3><table class=\"grid\"><tr><td>-</td><td><b>Country</b></td><td><b>Language</b></td></tr><tr><td>*</td><td>Republic of Estonia <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-country-ema-cs.html\">Country EMA</a>#100000000388)</span></td><td>Estonian <span style=\"background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki\"> (<a href=\"CodeSystem-language-ema-cs.html\">Language EMA</a>#100000072172)</span></td></tr></table></blockquote></div>"
},
"identifier" : [
{
"system" : "http://ema.europa.eu/fhir/mpId",
"value" : "EE-100009199-27834"
},
{
"system" : "http://ema.europa.eu/fhir/pmsId",
"value" : "EE0000002"
}
],
"domain" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000000004",
"code" : "100000000012",
"display" : "Human use"
}
]
},
"status" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/200000005003",
"code" : "200000005004",
"display" : "Current"
}
]
},
"combinedPharmaceuticalDoseForm" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/200000000004",
"code" : "100000116186",
"display" : "Powder for solution for injection/infusion"
}
]
},
"legalStatusOfSupply" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000072051",
"code" : "100000072084",
"display" : "Medicinal Product subject to medical prescription"
}
]
},
"classification" : [
{
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000093533",
"code" : "100000096183",
"display" : "Cefuroxime"
}
]
},
{
"coding" : [
{
"system" : "http://www.whocc.no/atc",
"code" : "J01DC02",
"display" : "cefuroxime"
}
]
}
],
"name" : [
{
"productName" : "Cefuroxime MIP 1500 mg, süste-/infusioonilahuse pulber",
"namePart" : [
{
"part" : "Cefuroxime MIP",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/220000000000",
"code" : "220000000002",
"display" : "Invented name part"
}
]
}
},
{
"part" : "1500 MG",
"type" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/220000000000",
"code" : "220000000004",
"display" : "Strength part"
}
]
}
}
],
"countryLanguage" : [
{
"country" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000000002",
"code" : "100000000388",
"display" : "Republic of Estonia"
}
]
},
"language" : {
"coding" : [
{
"system" : "https://spor.ema.europa.eu/v1/lists/100000072057",
"code" : "100000072172",
"display" : "Estonian"
}
]
}
}
]
}
]
}
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