Generated Narrative: StructureDefinition MyHealthEuMedicationEpd Name Flags Card. Type Description & Constraints MyHealthEuMedicationEpd 0..* MyHealthEuMedication Prescribed Medication model Elements defined in Ancestors:<a href="http://www.xt-ehr.eu/fhir/models/0.3.0/StructureDefinition-EHDSMedication.html" title="An identifier (e.g. from EMA SPOR PMS or national registry) or a code (e.g. from SNOMED CT or national code system) for the product (virtual product, branded product, or package). If several identifiers are specified, they shall not have conflicting meanings or very different granularities. An identifier might not exist e.g. for substance-based prescriptions.">identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch, identifyingCode[x], classification, productName, description, batch #xD; marketingAuthorisationHolder O 0..1 Base Marketing authorisation holder of the medicinal product. Relevant for identifying the exact product. If the product does not have a marketing authorisation, the manufacturer information may be used. Obligations Actor MAY:able-to-populate MyHealth@EU Handler #xD; item #xD; doseForm O 0..1 CodeableConcept Administrable or manufactured item dose form, depending on the type of medication definition. This should not include combined dose forms. Obligations Actor Source MAY:able-to-populate & SHALL:handle MyHealth@EU HandlerMyHealth@EU Handler from Medication model #xD; ingredient O 1..* Base Ingredients Obligations Actor Source SHOULD:handle & SHALL:handle MyHealth@EU HandlerMyHealth@EU Handler from Medication model #xD; isActive O 0..1 boolean Marks whether the ingredient is considered an active ingredient. Excipients are typically not needed, and by default only active ingredients are expected. Obligations Actor SHALL:handle MyHealth@EU Handler #xD; substance O 1..1 CodeableConcept Substance Obligations Actor SHALL:handle MyHealth@EU Handler #xD; strengthInfo #xD; strength O 1..1 Ratio Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHOULD:handle MyHealth@EU Handler #xD; containedQuantity O 0..1 Ratio Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor Source MAY:able-to-populate & SHOULD:handle MyHealth@EU HandlerMyHealth@EU Handler from Medication model #xD; amount O 0..1 Quantity Number of such items in this product (5 vials). The combined amount of all items will be considered to be the total package size. Obligations Actor Source MAY:able-to-populate & SHOULD:handle MyHealth@EU HandlerMyHealth@EU Handler from Medication model #xD; packageType O 0..1 CodeableConcept Type of package of the medication item Obligations Actor Source MAY:able-to-populate & SHOULD:handle MyHealth@EU HandlerMyHealth@EU Handler from Medication model #xD; Documentation for this format
MyHealth@EU refined model for prescribed medication information
Copyright European Union, represented by the European Commission - DG SANTE. Licenced under CC-BY-4.0.
An identifier (e.g. from EMA SPOR PMS or national registry) or a code (e.g. from SNOMED CT or national code system) for the product (virtual product, branded product, or package). If several identifiers are specified, they shall not have conflicting meanings or very different granularities. An identifier might not exist e.g. for substance-based prescriptions.
Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.)
Current trade name (authorised name) of the product. When medication is specified by a CodeableConcept, the name may be omitted when available as the display name of the concept.
Marketing authorisation holder of the medicinal product. Relevant for identifying the exact product. If the product does not have a marketing authorisation, the manufacturer information may be used.
Name of the organisation holding the authorisation for marketing/manufacturing
Identifier of the organisation and/or its physical location
Dose form at the package level (e.g. authorised dose form), corresponding to IDMP Combined Pharmaceutical Dose Form (this includes terms from EDQM Combination Pack or Combined Dose Form lists). Dose form for a single package item is defined in item.doseForm.
Textual description of the product, e.g. including package description.
UCUM for units of measure. EDQM Standard Terms for units of presentation.
A medication item. For combination packs, this can be multiple manufactured items with each item having its own dose form and ingredients+strengths defined
Administrable or manufactured item dose form, depending on the type of medication definition. This should not include combined dose forms.
Marks whether the ingredient is considered an active ingredient. Excipients are typically not needed, and by default only active ingredients are expected.
Strength of the product - amount of substance per unit
Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet'
Substance that the strength refers to, especially when different from .item.strength.substance
Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package.
Manufactured item quantity per one item (3 ml / 1 vial)
Number of such items in this product (5 vials). The combined amount of all items will be considered to be the total package size.
Administration device included in the product. Devices that are not inside the medication package are excluded.
Additional features of the product (e.g. reimbursable, sugar-free, easy-open cap, score-lined). It is expected that implementers will define a valueset supporting their use cases.
A code expressing the type of characteristic.
Description of the characteristic value.
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.