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Vocabulary Work Group | Maturity Level: N/A | Standards Status: Informative |
Raw XML (canonical form + also see XML Format Specification)
Identifies what sort of change is permitted or has occurred between the therapy that was ordered and the therapy that was/will be provided.
<?xml version="1.0" encoding="UTF-8"?> <CodeSystem xmlns="http://hl7.org/fhir"> <id value="v3-substanceAdminSubstitution"/> <meta> <lastUpdated value="2018-08-12T00:00:00.000+10:00"/> </meta> <text> <status value="generated"/> <div xmlns="http://www.w3.org/1999/xhtml"> <p> Release Date: 2018-08-12</p> <table class="grid"> <tr> <td> <b> Level</b> </td> <td> <b> Code</b> </td> <td> <b> Display</b> </td> <td> <b> Definition</b> </td> </tr> <tr> <td> 1</td> <td> <span style="color: grey"> <i> (_ActSubstanceAdminSubstitutionCode)</i> </span> <b> <i> Abstract</i> </b> </td> <td> <a name="v3-substanceAdminSubstitution-_ActSubstanceAdminSubstitutionCode">Â </a> </td> <td> Description: Substitution occurred or is permitted with another product that may potentially have different ingredients, but having the same biological and therapeutic effects. <br/> </td> </tr> <tr> <td> 2</td> <td> Â Â E <a name="v3-substanceAdminSubstitution-E"> </a> </td> <td> equivalent</td> <td> Description: Substitution occurred or is permitted with another bioequivalent and therapeutically equivalent product. <br/> </td> </tr> <tr> <td> 3</td> <td> Â Â Â Â EC <a name="v3-substanceAdminSubstitution-EC"> </a> </td> <td> equivalent composition</td> <td> Description: <br/> Substitution occurred or is permitted with another product that is a: <br/> pharmaceutical alternative containing the same active ingredient but is formulated with different salt, ester pharmaceutical equivalent that has the same active ingredient, strength, dosage form and route of administration Examples: <br/> Pharmaceutical alternative: Erythromycin Ethylsuccinate for Erythromycin Stearate Pharmaceutical equivalent: Lisonpril for Zestril </td> </tr> <tr> <td> 4</td> <td> Â Â Â Â Â Â BC <a name="v3-substanceAdminSubstitution-BC"> </a> </td> <td> brand composition</td> <td> Description: <br/> Substitution occurred or is permitted between equivalent Brands but not Generics <br/> Examples: <br/> Zestril for Prinivil Coumadin for Jantoven </td> </tr> <tr> <td> 4</td> <td> Â Â Â Â Â Â G <a name="v3-substanceAdminSubstitution-G"> </a> </td> <td> generic composition</td> <td> Description: Substitution occurred or is permitted between equivalent Generics but not Brands <br/> Examples: <br/> Lisnopril (Lupin Corp) for Lisnopril (Wockhardt Corp) </td> </tr> <tr> <td> 3</td> <td> Â Â Â Â TE <a name="v3-substanceAdminSubstitution-TE"> </a> </td> <td> therapeutic alternative</td> <td> Description: Substitution occurred or is permitted with another product having the same therapeutic objective and safety profile. <br/> Examples: <br/> ranitidine for Tagamet </td> </tr> <tr> <td> 4</td> <td> Â Â Â Â Â Â TB <a name="v3-substanceAdminSubstitution-TB"> </a> </td> <td> therapeutic brand</td> <td> Description: Substitution occurred or is permitted between therapeutically equivalent Brands but not Generics <br/> > Examples: <br/> Zantac for Tagamet </td> </tr> <tr> <td> 4</td> <td> Â Â Â Â Â Â TG <a name="v3-substanceAdminSubstitution-TG"> </a> </td> <td> therapeutic generic</td> <td> Description: Substitution occurred or is permitted between therapeutically equivalent Generics but not Brands <br/> > Examples: <br/> Ranitidine for cimetidine </td> </tr> <tr> <td> 2</td> <td> Â Â F <a name="v3-substanceAdminSubstitution-F"> </a> </td> <td> formulary</td> <td> Description: This substitution was performed or is permitted based on formulary guidelines. <br/> </td> </tr> <tr> <td> 2</td> <td> Â Â N <a name="v3-substanceAdminSubstitution-N"> </a> </td> <td> none</td> <td> No substitution occurred or is permitted. <br/> </td> </tr> </table> </div> </text> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status"> <valueCode value="external"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm"> <valueInteger value="0"/> </extension> <url value="http://terminology.hl7.org/CodeSystem/v3-substanceAdminSubstitution"/> <identifier> <system value="urn:ietf:rfc:3986"/> <value value="urn:oid:2.16.840.1.113883.5.1070"/> </identifier> <version value="2018-08-12"/> <name value="v3.substanceAdminSubstitution"/> <title value="v3 Code System substanceAdminSubstitution"/> <status value="active"/> <experimental value="false"/> <date value="2018-08-12T00:00:00+10:00"/> <publisher value="HL7, Inc"/> <contact> <telecom> <system value="url"/> <value value="http://hl7.org"/> </telecom> </contact> <description value=" Identifies what sort of change is permitted or has occurred between the therapy that was ordered and the therapy that was/will be provided."/> <caseSensitive value="true"/> <valueSet value="http://terminology.hl7.org/ValueSet/v3-substanceAdminSubstitution"/> <hierarchyMeaning value="is-a"/> <content value="complete"/> <property> <code value="notSelectable"/> <uri value="http://hl7.org/fhir/concept-properties#notSelectable"/> <description value="Indicates that the code is abstract - only intended to be used as a selector for other concepts"/> <type value="boolean"/> </property> <concept> <code value="_ActSubstanceAdminSubstitutionCode"/> <display value="ActSubstanceAdminSubstitutionCode"/> <definition value="Description: Substitution occurred or is permitted with another product that may potentially have different ingredients, but having the same biological and therapeutic effects."/> <property> <code value="notSelectable"/> <valueBoolean value="true"/> </property> <concept> <code value="E"/> <display value="equivalent"/> <definition value="Description: Substitution occurred or is permitted with another bioequivalent and therapeutically equivalent product."/> <concept> <code value="EC"/> <display value="equivalent composition"/> <definition value="Description: Substitution occurred or is permitted with another product that is a: pharmaceutical alternative containing the same active ingredient but is formulated with different salt, ester pharmaceutical equivalent that has the same active ingredient, strength, dosage form and route of administration Examples: Pharmaceutical alternative: Erythromycin Ethylsuccinate for Erythromycin Stearate Pharmaceutical equivalent: Lisonpril for Zestril"/> <concept> <code value="BC"/> <display value="brand composition"/> <definition value="Description: Substitution occurred or is permitted between equivalent Brands but not Generics Examples: Zestril for Prinivil Coumadin for Jantoven"/> </concept> <concept> <code value="G"/> <display value="generic composition"/> <definition value="Description: Substitution occurred or is permitted between equivalent Generics but not Brands Examples: Lisnopril (Lupin Corp) for Lisnopril (Wockhardt Corp)"/> </concept> </concept> <concept> <code value="TE"/> <display value="therapeutic alternative"/> <definition value="Description: Substitution occurred or is permitted with another product having the same therapeutic objective and safety profile. Examples: ranitidine for Tagamet"/> <concept> <code value="TB"/> <display value="therapeutic brand"/> <definition value="Description: Substitution occurred or is permitted between therapeutically equivalent Brands but not Generics > Examples: Zantac for Tagamet"/> </concept> <concept> <code value="TG"/> <display value="therapeutic generic"/> <definition value="Description: Substitution occurred or is permitted between therapeutically equivalent Generics but not Brands > Examples: Ranitidine for cimetidine"/> </concept> </concept> </concept> <concept> <code value="F"/> <display value="formulary"/> <definition value="Description: This substitution was performed or is permitted based on formulary guidelines."/> </concept> <concept> <code value="N"/> <display value="none"/> <definition value="No substitution occurred or is permitted."/> </concept> </concept> </CodeSystem>
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.