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

: Altermol-500mg30mg-Tablet-SE-IS-MPD - JSON Representation

Raw json | Download


{
  "resourceType" : "MedicinalProductDefinition",
  "id" : "Altermol-500mg30mg-Tablet-SE-IS-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 Altermol-500mg30mg-Tablet-SE-IS-MPD</b></p><a name=\"Altermol-500mg30mg-Tablet-SE-IS-MPD\"> </a><a name=\"hcAltermol-500mg30mg-Tablet-SE-IS-MPD\"> </a><a name=\"hcAltermol-500mg30mg-Tablet-SE-IS-MPD-en-US\"> </a><p><b>identifier</b>: <code>http://ema.europa.eu/fhir/mpId</code>/SE-100001659-00050802, <code>http://ema.europa.eu/fhir/eurdId</code>/851</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 100000073664}\">Tablet</span></p><p><b>indication</b>: </p><div><p>Opiodkänslig smärta när enbart perifert verkande analgetika inte är tillräcklig. Kodein är indicerat för vuxna, ungdomar och barn äldre än 12 år för behandling av akut måttlig smärta, som  inte anses kunna lindras av andra analgetika såsom paracetamol eller ibuprofen (enbart).</p>\n</div><p><b>legalStatusOfSupply</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000072051 100000072085}\">Medicinal product subject to special medical prescription</span></p><p><b>classification</b>: <span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/100000116677 100000093533}\">N02AJ06</span></p><blockquote><p><b>name</b></p><p><b>productName</b>: Altermol 500 mg/30 mg Tablett</p><blockquote><p><b>part</b></p><p><b>part</b>: Altermol</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>: 500 mg/30 mg</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>: Tablett</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><h3>Characteristics</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Type</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:{https://spor.ema.europa.eu/v1/lists/200000003186 200000003187}\">combined therapeutic medicine / device</span></td></tr></table></div>"
  },
  "identifier" : [
    {
      "system" : "http://ema.europa.eu/fhir/mpId",
      "value" : "SE-100001659-00050802"
    },
    {
      "system" : "http://ema.europa.eu/fhir/eurdId",
      "value" : "851"
    }
  ],
  "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" : "100000073664",
        "display" : "Tablet"
      }
    ]
  },
  "indication" : "Opiodkänslig smärta när enbart perifert verkande analgetika inte är tillräcklig. Kodein är indicerat för vuxna, ungdomar och barn äldre än 12 år för behandling av akut måttlig smärta, som  inte anses kunna lindras av andra analgetika såsom paracetamol eller ibuprofen (enbart).",
  "legalStatusOfSupply" : {
    "coding" : [
      {
        "system" : "https://spor.ema.europa.eu/v1/lists/100000072051",
        "code" : "100000072085",
        "display" : "Medicinal product subject to special medical prescription"
      }
    ]
  },
  "classification" : [
    {
      "coding" : [
        {
          "system" : "https://spor.ema.europa.eu/v1/lists/100000116677",
          "code" : "100000093533",
          "display" : "N02AJ06"
        }
      ]
    }
  ],
  "name" : [
    {
      "productName" : "Altermol 500 mg/30 mg Tablett",
      "part" : [
        {
          "part" : "Altermol",
          "type" : {
            "coding" : [
              {
                "system" : "http://spor.ema.europa.eu/v1/lists/220000000000",
                "code" : "220000000002",
                "display" : "Invented name part"
              }
            ]
          }
        },
        {
          "part" : "500 mg/30 mg",
          "type" : {
            "coding" : [
              {
                "system" : "http://spor.ema.europa.eu/v1/lists/220000000000",
                "code" : "220000000004",
                "display" : "Strength part"
              }
            ]
          }
        },
        {
          "part" : "Tablett",
          "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"
              }
            ]
          }
        }
      ]
    }
  ],
  "characteristic" : [
    {
      "type" : {
        "coding" : [
          {
            "system" : "https://spor.ema.europa.eu/v1/lists/200000003186",
            "code" : "200000003187",
            "display" : "combined therapeutic medicine / device"
          }
        ]
      }
    }
  ]
}