This page is part of the FHIR Specification (v4.1.0: Release 4B Ballot #1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B
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)
Basic details of a product, only using MedicinalProductDefinition and no other resources (id = "equilidem-basics")
<?xml version="1.0" encoding="UTF-8"?> <MedicinalProductDefinition xmlns="http://hl7.org/fhir"> <id value="equilidem-basics"/> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <p> <b> Generated Narrative </b> </p> <p> <b> Id </b> : equilidem-basics </p> <p> <b> Identifier </b> : Equilidem25 </p> <p> <b> Combined Pharmaceutical Dose Form </b> : <span title="Codes: {http://example.org.uk/fhir/dosefom tablet}"> tablet </span> </p> <p> <b> Indication </b> : Prevention of venous thromboembolic events (VTE) in adult patients who have undergone elective hip or knee replacement surgery. Prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (NVAF), with one or more risk factors, such as prior stroke or transient ischaemic attack (TIA); age ≥ 75 years; hypertension; diabetes mellitus; symptomatic heart failure (NYHA Class >= II). Treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE), and prevention of recurrent DVT and PE in adults. </p> <p> <b> Legal Status Of Supply </b> : <span title="Codes: {http://example.org.uk/fhir/legalstatusofsupply POM}"> Prescription only medicine </span> </p> <p> <b> Classification </b> : <span title="Codes: {http://www.whocc.no/atc/example B01A}"> ATC: B01A </span> </p> <p> <b> Ingredient </b> : </p> <ul> <li> <span> Equilidonium Phosphate </span> </li> <li> <span> Calcium Carbonate </span> </li> </ul> <h3> Names </h3> <table class="grid"> <tr> <td> - </td> <td> <b> Product Name </b> </td> </tr> <tr> <td> * </td> <td> Equilidem 2.5 mg film-coated tablets </td> </tr> </table> <h3> Cross References </h3> <table class="grid"> <tr> <td> - </td> <td> <b> Product </b> </td> </tr> <tr> <td> * </td> <td> Link to generic equivalent </td> </tr> </table> <h3> Manufacturing/Business Operations </h3> <table class="grid"> <tr> <td> - </td> <td> <b> Manufacturer </b> </td> </tr> <tr> <td> * </td> <td> <span> EquiliDrugCo Inc. </span> </td> </tr> </table> </div> </text> <identifier> <system value="http://example.org.uk/fhir/product"/> <value value="Equilidem25"/> </identifier> <combinedPharmaceuticalDoseForm> <coding> <system value="http://example.org.uk/fhir/dosefom"/> <code value="tablet"/> </coding> </combinedPharmaceuticalDoseForm> <indication value="Prevention of venous thromboembolic events (VTE) in adult patients who have undergone elective hip or knee replacement surgery. Prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (NVAF), with one or more risk factors, such as prior stroke or transient ischaemic attack (TIA); age ≥ 75 years; hypertension; diabetes mellitus; symptomatic heart failure (NYHA Class >= II). Treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE), and prevention of recurrent DVT and PE in adults."/> <legalStatusOfSupply> <coding> <system value="http://example.org.uk/fhir/legalstatusofsupply"/> <code value="POM"/> <display value="Prescription only medicine"/> </coding> </legalStatusOfSupply> <classification> <coding> <system value="http://www.whocc.no/atc/example"/> <code value="B01A"/> </coding> </classification> <ingredient> <reference> <display value="Equilidonium Phosphate"/> </reference> </ingredient> <ingredient> <reference> <display value="Calcium Carbonate"/> </reference> </ingredient> <name> <productName value="Equilidem 2.5 mg film-coated tablets"/> </name> <crossReference> <product> <reference> <reference value="MedicinalProductDefinition/genericEquilidonium"/> </reference> </product> </crossReference> <operation> <organization> <display value="EquiliDrugCo Inc."/> <!-- licence holder would use RegulatedAuthorization --> </organization> </operation> </MedicinalProductDefinition>
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.