Name Flags Card. Type Description & Constraints PrescribedProductModel1 0..* Base DRAFT: Flattened Medicinal Product on ePrescription. Focused on an authorised product. This logical model cannot be the target of a reference identifier 0..* Class Identifier(s) for the product type 1..1 CD Type of identifier, e.g. PCID, PhPID, MPID, VMP, VMPP, BE-VMPG... identifier 1..1 II Identifier marketingAuthorisationHolder 0..1 ST MAH name - do we need more? classification 0..* Class Classification atc 1..1 CD ATC code otherClassification 1..1 CD Any other classification fullName 0..* ST Name of the product doseForm 0..1 CD Dose form (authorised/combined dose form for full product) packSize 0..* PQ Overall amount (100ml; 20 tablets; 1 tube & 6 pessaries) manufacturedItem 1..* Class Actual product description. Repeated for products that contain multiple different items itemQuantity 1..1 PQ Quantity of such items in the package containedQuantity 0..1 PQ Amount of product per unit of presentation when applicable (3ml vial) unitOfPresentation 0..* CD Unit of presentation for the manufactured item doseForm 1..1 CD Manufactured dose form ingredient 0..* Class Active/relevant(?) ingredients role 1..1 CD ingredient role substance 1..1 CD Substance strengthInfo 1..* Class Concentration or presentation strength strength 1..* RTO Concentration or presentation strength of the precise active ingredient referenceStrength 0..* Class Reference strength; according to the substance+strength type above referenceSubstance 1..1 CD Substance for reference strength strength 1..1 RTO Reference strength device 0..* Class Administrative device included in the product device 1..1 CD Separate device included in the package, not the container of the product itemQuantity 1..1 PQ Number of such devices Documentation for this format
DRAFT: Flattened Medicinal Product on ePrescription. Focused on an authorised product.
Integrating the Healthcare Enterprise (IHE)
DRAFT. eP/eD/PS medicinal product as a implementation-agnostic logical model
IHE http://www.ihe.net/Governance/#Intellectual_Property
All FHIR elements must have a @value or children
hasValue() or (children().count() > id.count())
Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.
Extensions are always sliced by (at least) url
Additional content defined by implementations
May be used to represent additional information that is not part of the basic definition of the element. To make the use of extensions safe and managable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.
There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.
Must have either extensions or value[x], not both
Extensions that cannot be ignored even if unrecognized
May be used to represent additional information that is not part of the basic definition of the element and that modifies the understanding of the element in which it is contained and/or the understanding of the containing element's descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and managable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions. Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).
Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the [definition of modifier extensions](http://hl7.org/fhir/R5/extensibility.html#modifierExtension).
Modifier extensions are expected to modify the meaning or interpretation of the element that contains them
Type of identifier, e.g. PCID, PhPID, MPID, VMP, VMPP, BE-VMPG...
Dose form (authorised/combined dose form for full product)
Overall amount (100ml; 20 tablets; 1 tube & 6 pessaries)
Actual product description. Repeated for products that contain multiple different items
Amount of product per unit of presentation when applicable (3ml vial)
Unit of presentation for the manufactured item
Concentration or presentation strength of the precise active ingredient
Reference strength; according to the substance+strength type above
Administrative device included in the product
Separate device included in the package, not the container of the product