Generated Narrative: StructureDefinition MedicinalProductModel Name Flags Card. Type Description & Constraints MedicinalProductModel 0..* Base Medicinal product (model) Instances of this logical model can be the target of a Reference #xD; identifyingCode[x] 0..* Identifier or product code for the product, independently of the level of product. If several identifiers are specified, they shall not have conflicting meanings or very different granularities. #xD; identifyingCodeCodeableConcept CodeableConcept #xD; identifyingCodeIdentifier Identifier #xD; classification 0..* CodeableConcept Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) #xD; productName 0..1 string Name of the product (full name, invented name, other). When the product has different names, the appropriate one for the context should be used. Translations of names can be provided. #xD; marketingAuthorisationHolder 0..1 Base Marketing authorisation holder of manufacturer of the medicinal product. Relevant for identifying the exact product. #xD; organizationName 0..1 string Name of the organisation holding the authorisation for marketing/mahufacturing #xD; organizationIdentifier 0..* Identifier Identifier of the organisation and/or its physical location #xD; doseForm 0..1 CodeableConcept Dose form(s) on a product level. Dose form for a single package item is defined below. #xD; packSize 0..* Quantity Overall amount of product in one package (100ml; 20 tablets; 1 creme & 6 pessaries) #xD; item 0..* Base A medication item. For combination packs, this can be manufactured items with each item having its own dose form and ingredients+strengths defined #xD; doseForm 0..1 CodeableConcept Dose form #xD; ingredient 1..* Base Ingredients #xD; role[x] 0..1 Role (active ingredient, excipient). Typically excipients are not needed, so by default active ingredients are expected. #xD; roleBoolean boolean #xD; roleCodeableConcept CodeableConcept #xD; substance 1..1 CodeableConcept Substance #xD; strengthInfo 0..1 Base Concentration or presentation strength #xD; strength 1..1 Ratio Concentration or presentation strength of the precise active ingredient #xD; basisOfStrengthSubstance 0..1 CodeableConcept Substance that the strength refers to, if different from the main substance #xD; unitOfPresentation 0..1 CodeableConcept Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package. #xD; containedQuantity 0..1 Ratio Manufactured item quantity for liquids (3ml/vial) #xD; amount 0..1 Quantity Number of such manufactured items in this product (5 vials) #xD; device 0..* Base Administration device included in the product #xD; deviceQuantity 1..1 Quantity Number of such devices #xD; device[x] 1..1 Device coded #xD; deviceCodeableConcept CodeableConcept #xD; deviceReference Reference(Device) #xD; characteristic 0..* Base Other features of the product #xD; type 1..1 CodeableConcept A code expressing the type of characteristic #xD; value[x] 0..1 Description of the characteristic #xD; valueBoolean boolean #xD; valueCodeableConcept CodeableConcept #xD; valueString string #xD; valueQuantity Quantity #xD; valueDateTime dateTime #xD; = 0)">valueUnsignedInt unsignedInt #xD; valueDecimal decimal #xD; valueRatio Ratio #xD; batch 0..1 Base Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request. #xD; lotNumber 0..1 string Batch identifier of the medicinal product #xD; expirationDate 0..1 dateTime Batch expiration date of the medicinal product. #xD; serialNumber 0..1 string Serial Number of the medicinal product. #xD; Documentation for this format
Integrating the Healthcare Enterprise (IHE)
Logical model for prescribed/dispensed medication. The model is shared by statements, requests, dispensations, and treatment lines. Each of those may have different restrictions in FHIR profile.
IHE http://www.ihe.net/Governance/#Intellectual_Property
Identifier or product code for the product, independently of the level of product. If several identifiers are specified, they shall not have conflicting meanings or very different granularities.
Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.)
Name of the product (full name, invented name, other). When the product has different names, the appropriate one for the context should be used. Translations of names can be provided.
Marketing authorisation holder of manufacturer of the medicinal product. Relevant for identifying the exact product.
Name of the organisation holding the authorisation for marketing/mahufacturing
Identifier of the organisation and/or its physical location
Dose form(s) on a product level. Dose form for a single package item is defined below.
Overall amount of product in one package (100ml; 20 tablets; 1 creme & 6 pessaries)
A medication item. For combination packs, this can be manufactured items with each item having its own dose form and ingredients+strengths defined
Role (active ingredient, excipient). Typically excipients are not needed, so by default active ingredients are expected.
Concentration or presentation strength of the precise active ingredient
Substance that the strength refers to, if different from the main substance
Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package.
Manufactured item quantity for liquids (3ml/vial)
Number of such manufactured items in this product (5 vials)
Administration device included in the product
A code expressing the type of characteristic
Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
Batch identifier of the medicinal product
Batch expiration date of the medicinal product.