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

: Zeldox20mgmlpulvervatskainjek-SE-PLC-MPD - JSON Representation

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{
  "resourceType" : "MedicinalProductDefinition",
  "id" : "Zeldox20mgmlpulvervatskainjek-SE-PLC-MPD",
  "meta" : {
    "profile" : [
      🔗 "http://unicom-project.eu/fhir/StructureDefinition/PPLMedicinalProductDefinition"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: MedicinalProductDefinition Zeldox20mgmlpulvervatskainjek-SE-PLC-MPD</b></p><a name=\"Zeldox20mgmlpulvervatskainjek-SE-PLC-MPD\"> </a><a name=\"hcZeldox20mgmlpulvervatskainjek-SE-PLC-MPD\"> </a><a name=\"hcZeldox20mgmlpulvervatskainjek-SE-PLC-MPD-en-US\"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/fhir/mpId</code>/SE-100023206-00015002, <code>http://ema.europa.eu/fhir/eurdId</code>/3146</p><p><b>domain</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000000004 100000000012}\">Human use</span></p><p><b>status</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/200000005003 200000005004}\">Current</span></p><p><b>combinedPharmaceuticalDoseForm</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/200000000004~200000000006~200000000007~200000000008 100000073868}\">Powder and solvent for solution for injection</span></p><p><b>indication</b>: </p><div><p>Ziprasidon injektionsvätska, lösning är indicerat för snabb kontroll av agiterade patienter med schizofreni, när peroral terapi inte är lämpligt, under maximalt tre på varandra följande dagar.   Behandling med ziprasidon injektionsvätska, lösning bör upphöra och peroralt ziprasidon initieras så snart det är kliniskt lämpligt.</p>\n</div><p><b>legalStatusOfSupply</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000072051 100000072084}\">Medicinal product subject to medical prescription</span></p><p><b>classification</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000093533 100000097488}\">ziprasidone</span></p><blockquote><p><b>name</b></p><p><b>productName</b>: Zeldox 20 mg/ml pulver och vätska till injektionsvätska, lösning</p><blockquote><p><b>part</b></p><p><b>part</b>: Zeldox</p><p><b>type</b>: <span title=\"Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000002}\">Invented name part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: 20 mg/ml</p><p><b>type</b>: <span title=\"Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000004}\">Strength part</span></p></blockquote><blockquote><p><b>part</b></p><p><b>part</b>: pulver och vätska till injektionsvätska, lösning</p><p><b>type</b>: <span title=\"Codes:{http://spor.ema.europa.eu/v1/lists/220000000000 220000000005}\">Pharmaceutical dose form part</span></p></blockquote><h3>Usages</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Country</b></td><td><b>Language</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000000002 100000000535}\">Kingdom of Sweden</span></td><td><span title=\"Codes:{urn:ietf:bcp:47 sv}\">Swedish</span></td></tr></table></blockquote></div>"
  },
  "identifier" : [
    {
      "system" : "http://ema.europa.eu/fhir/mpId",
      "value" : "SE-100023206-00015002"
    },
    {
      "system" : "http://ema.europa.eu/fhir/eurdId",
      "value" : "3146"
    }
  ],
  "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/200000000004~200000000006~200000000007~200000000008",
        "code" : "100000073868",
        "display" : "Powder and solvent for solution for injection"
      }
    ]
  },
  "indication" : "Ziprasidon injektionsvätska, lösning är indicerat för snabb kontroll av agiterade patienter med schizofreni, när peroral terapi inte är lämpligt, under maximalt tre på varandra följande dagar.   Behandling med ziprasidon injektionsvätska, lösning bör upphöra och peroralt ziprasidon initieras så snart det är kliniskt lämpligt.",
  "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" : "100000097488",
          "display" : "ziprasidone"
        }
      ]
    }
  ],
  "name" : [
    {
      "productName" : "Zeldox 20 mg/ml pulver och vätska till injektionsvätska, lösning",
      "part" : [
        {
          "part" : "Zeldox",
          "type" : {
            "coding" : [
              {
                "system" : "http://spor.ema.europa.eu/v1/lists/220000000000",
                "code" : "220000000002",
                "display" : "Invented name part"
              }
            ]
          }
        },
        {
          "part" : "20 mg/ml",
          "type" : {
            "coding" : [
              {
                "system" : "http://spor.ema.europa.eu/v1/lists/220000000000",
                "code" : "220000000004",
                "display" : "Strength part"
              }
            ]
          }
        },
        {
          "part" : "pulver och vätska till injektionsvätska, lösning",
          "type" : {
            "coding" : [
              {
                "system" : "http://spor.ema.europa.eu/v1/lists/220000000000",
                "code" : "220000000005",
                "display" : "Pharmaceutical dose form part"
              }
            ]
          }
        }
      ],
      "usage" : [
        {
          "country" : {
            "coding" : [
              {
                "system" : "https://spor.ema.europa.eu/v1/lists/100000000002",
                "code" : "100000000535",
                "display" : "Kingdom of Sweden"
              }
            ]
          },
          "language" : {
            "coding" : [
              {
                "system" : "urn:ietf:bcp:47",
                "code" : "sv",
                "display" : "Swedish"
              }
            ]
          }
        }
      ]
    }
  ]
}