This page is part of the FHIR Specification (v4.0.1: R4 - Mixed Normative and STU) in it's permanent home (it will always be available at this URL). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Not linked to any defined compartments |
Raw XML (canonical form + also see XML Format Specification)
Example of medicinalproduct (id = "example")
<?xml version="1.0" encoding="UTF-8"?> <MedicinalProduct xmlns="http://hl7.org/fhir"> <id value="example"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"><p> <b> Generated Narrative with Details</b> </p> <p> <b> id</b> : example</p> <p> <b> identifier</b> : {mpid}</p> <p> <b> productClassification</b> : WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02 <span> (Details : {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem code 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02' = 'WHOAnatomicalTherapeuticCh emicalATCClassificationSystem|B01AF02)</span> </p> <p> <b> attachedDocument</b> : <a> DocumentReference/example</a> </p> <p> <b> masterFile</b> : <a> DocumentReference/example</a> </p> <blockquote> <p> <b> name</b> </p> <p> <b> productName</b> : Equilidem 2.5 mg film-coated tablets</p> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : Equilidem</p> <p> <b> type</b> : INV (Details: [not stated] code INV = 'INV', stated as 'null')</p> </blockquote> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : 2.5 mg</p> <p> <b> type</b> : STR (Details: [not stated] code STR = 'STR', stated as 'null')</p> </blockquote> <blockquote> <p> <b> namePart</b> </p> <p> <b> part</b> : film-coated tablets</p> <p> <b> type</b> : FRM (Details: [not stated] code FRM = 'FRM', stated as 'null')</p> </blockquote> <h3> CountryLanguages</h3> <table> <tr> <td> -</td> <td> <b> Country</b> </td> <td> <b> Jurisdiction</b> </td> <td> <b> Language</b> </td> </tr> <tr> <td> *</td> <td> EU <span> (Details : {http://ema.europa.eu/example/countryCode code 'EU' = 'EU)</span> </td> <td> EU <span> (Details : {http://ema.europa.eu/example/jurisdictionCode code 'EU' = 'EU)</span> </td> <td> EN <span> (Details : {http://ema.europa.eu/example/languageCode code 'EN' = 'EN)</span> </td> </tr> </table> </blockquote> <h3> ManufacturingBusinessOperations</h3> <table> <tr> <td> -</td> <td> <b> OperationType</b> </td> <td> <b> AuthorisationReferenceNumber</b> </td> <td> <b> EffectiveDate</b> </td> <td> <b> Manufacturer</b> </td> <td> <b> Regulator</b> </td> </tr> <tr> <td> *</td> <td> Batchrelease <span> (Details : {http://ema.europa.eu/example/manufacturingOperationType code 'Batchrelease' = 'Batchrelease)</span> </td> <td> 1324TZ</td> <td> 15/03/2013</td> <td> <a> Organization/example</a> </td> <td> <a> Organization/example</a> </td> </tr> </table> </div> </text> <identifier> <system value="http://ema.europa.eu/example/MPID"/> <value value="{mpid}"/> </identifier> <productClassification> <coding> <system value="http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem"/> <code value="WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02"/> </coding> </productClassification> <attachedDocument> <reference value="DocumentReference/example"/> </attachedDocument> <masterFile> <reference value="DocumentReference/example"/> </masterFile> <name> <productName value="Equilidem 2.5 mg film-coated tablets"/> <namePart> <part value="Equilidem"/> <type> <code value="INV"/> </type> </namePart> <namePart> <part value="2.5 mg"/> <type> <code value="STR"/> </type> </namePart> <namePart> <part value="film-coated tablets"/> <type> <code value="FRM"/> </type> </namePart> <countryLanguage> <country> <coding> <system value="http://ema.europa.eu/example/countryCode"/> <code value="EU"/> </coding> </country> <jurisdiction> <coding> <system value="http://ema.europa.eu/example/jurisdictionCode"/> <code value="EU"/> </coding> </jurisdiction> <language> <coding> <system value="http://ema.europa.eu/example/languageCode"/> <code value="EN"/> </coding> </language> </countryLanguage> </name> <manufacturingBusinessOperation> <operationType> <coding> <system value="http://ema.europa.eu/example/manufacturingOperationType"/> <code value="Batchrelease"/> </coding> </operationType> <authorisationReferenceNumber> <system value="http://ema.europa.eu/example/manufacturingAuthorisationReferenceNumber"/> <value value="1324TZ"/> </authorisationReferenceNumber> <effectiveDate value="2013-03-15"/> <manufacturer> <reference value="Organization/example"/> </manufacturer> <regulator> <reference value="Organization/example"/> </regulator> </manufacturingBusinessOperation> </MedicinalProduct>
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.