MyHealth@Eu Electronic Prescription and Dispense - Local Development build (v0.1.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

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Logical Model: Medication model

MyHealthEu refined base model for medication information

Usages:

• Use this Logical Model: Medication dispense model

You can also check for usages in the FHIR IG Statistics

Formal Views of Profile Content

Description of Profiles, Differentials, Snapshots and how the different presentations work.

• Key Elements Table
• Differential Table
• Snapshot Table
• Statistics/References
• All

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHealthEuMedication		0..*	EHDSMedication	Medication model Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch
identifyingCode[x]	O	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. Obligations Actor MAY:able-to-populate EHDSI Handler
identifyingCodeCodeableConcept			CodeableConcept
identifyingCodeIdentifier			Identifier
classification	O	0..*	CodeableConcept	Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) Binding Description: (preferred): WHO ATC Obligations Actor MAY:able-to-populate EHDSI Handler
productName	O	0..1	string	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. Obligations Actor MAY:able-to-populate EHDSI Handler
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 EHDSI Handler
organisationName		0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm		0..1	CodeableConcept	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. Binding Description: (preferred): EDQM Standard Terms
description		0..1	string	Textual description of the product, e.g. including package description. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation.
item		0..*	Base	A medication item. For combination packs, this can be multiple manufactured items with each item having its own dose form and ingredients+strengths defined
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. Binding Description: (preferred): EDQM Standard Terms Obligations Actor SHALL:handle EHDSI Handler
ingredient	O	1..*	Base	Ingredients Obligations Actor SHALL:handle EHDSI Handler
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 EHDSI Handler
substance		1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS
strengthInfo		0..1	Base	Strength of the product - amount of substance per unit
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 EHDSI Handler
basisOfStrengthSubstance		0..1	CodeableConcept	Substance that the strength refers to, especially when different from .item.strength.substance Binding Description: (preferred): EMA SPOR SMS
unitOfPresentation		0..1	CodeableConcept	Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package. Binding Description: (preferred): EDQM Standard Terms
containedQuantity	O	0..1	Ratio	Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor SHOULD:handle EHDSI Handler
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. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation. Obligations Actor SHOULD:handle EHDSI Handler
packageType	O	0..1	CodeableConcept	Type of package of the medication item Binding Description: (preferred): EDQM Standard Terms for packaging. Obligations Actor SHOULD:handle EHDSI Handler
device		0..*	Base	Administration device included in the product. Devices that are not inside the medication package are excluded.
deviceQuantity		1..1	Quantity	Number of such devices
device[x]		1..1		Device coded
deviceCodeableConcept			CodeableConcept
deviceEHDSDevice			EHDSDevice
characteristic		0..*	Base	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.
type		1..1	CodeableConcept	A code expressing the type of characteristic.
value[x]		0..1		Description of the characteristic value.
valueBoolean			boolean
valueCodeableConcept			CodeableConcept
valueString			string
valueQuantity			Quantity
valueDateTime			dateTime
valueInteger			integer
valueDecimal			decimal
valueRatio			Ratio
batch		0..1	Base	Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
lotNumber		0..1	string	Batch identifier of the medicinal product.
expirationDate		0..1	dateTime	Batch expiration date of the medicinal product.
Documentation for this format

Terminology Bindings

Path	Status	Usage	ValueSet	Version	Source
MyHealthEuMedication.​classification	Base	preferred		Not State	Unknown
MyHealthEuMedication.​doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​description	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.substance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.strengthInfo.​basisOfStrengthSubstance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.unitOfPresentation	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.amount	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.packageType	Base	preferred		Not State	Unknown

This structure is derived from EHDSMedication

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHealthEuMedication		0..*	EHDSMedication	Medication model Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch
identifyingCode[x]	O	0..*	CodeableConcept, Identifier	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. Obligations Actor MAY:able-to-populate EHDSI Handler
classification	O	0..*	CodeableConcept	Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) Obligations Actor MAY:able-to-populate EHDSI Handler
productName	O	0..1	string	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. Obligations Actor MAY:able-to-populate EHDSI Handler
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 EHDSI Handler
item
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 SHALL:handle EHDSI Handler
ingredient	O	1..*	Base	Ingredients Obligations Actor SHALL:handle EHDSI Handler
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 EHDSI Handler
strengthInfo
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 EHDSI Handler
containedQuantity	O	0..1	Ratio	Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor SHOULD:handle EHDSI Handler
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 SHOULD:handle EHDSI Handler
packageType	O	0..1	CodeableConcept	Type of package of the medication item Obligations Actor SHOULD:handle EHDSI Handler
Documentation for this format

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHealthEuMedication		0..*	EHDSMedication	Medication model Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch
identifyingCode[x]	O	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. Obligations Actor MAY:able-to-populate EHDSI Handler
identifyingCodeCodeableConcept			CodeableConcept
identifyingCodeIdentifier			Identifier
classification	O	0..*	CodeableConcept	Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) Binding Description: (preferred): WHO ATC Obligations Actor MAY:able-to-populate EHDSI Handler
productName	O	0..1	string	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. Obligations Actor MAY:able-to-populate EHDSI Handler
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 EHDSI Handler
organisationName		0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm		0..1	CodeableConcept	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. Binding Description: (preferred): EDQM Standard Terms
description		0..1	string	Textual description of the product, e.g. including package description. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation.
item		0..*	Base	A medication item. For combination packs, this can be multiple manufactured items with each item having its own dose form and ingredients+strengths defined
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. Binding Description: (preferred): EDQM Standard Terms Obligations Actor SHALL:handle EHDSI Handler
ingredient	O	1..*	Base	Ingredients Obligations Actor SHALL:handle EHDSI Handler
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 EHDSI Handler
substance		1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS
strengthInfo		0..1	Base	Strength of the product - amount of substance per unit
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 EHDSI Handler
basisOfStrengthSubstance		0..1	CodeableConcept	Substance that the strength refers to, especially when different from .item.strength.substance Binding Description: (preferred): EMA SPOR SMS
unitOfPresentation		0..1	CodeableConcept	Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package. Binding Description: (preferred): EDQM Standard Terms
containedQuantity	O	0..1	Ratio	Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor SHOULD:handle EHDSI Handler
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. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation. Obligations Actor SHOULD:handle EHDSI Handler
packageType	O	0..1	CodeableConcept	Type of package of the medication item Binding Description: (preferred): EDQM Standard Terms for packaging. Obligations Actor SHOULD:handle EHDSI Handler
device		0..*	Base	Administration device included in the product. Devices that are not inside the medication package are excluded.
deviceQuantity		1..1	Quantity	Number of such devices
device[x]		1..1		Device coded
deviceCodeableConcept			CodeableConcept
deviceEHDSDevice			EHDSDevice
characteristic		0..*	Base	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.
type		1..1	CodeableConcept	A code expressing the type of characteristic.
value[x]		0..1		Description of the characteristic value.
valueBoolean			boolean
valueCodeableConcept			CodeableConcept
valueString			string
valueQuantity			Quantity
valueDateTime			dateTime
valueInteger			integer
valueDecimal			decimal
valueRatio			Ratio
batch		0..1	Base	Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
lotNumber		0..1	string	Batch identifier of the medicinal product.
expirationDate		0..1	dateTime	Batch expiration date of the medicinal product.
Documentation for this format

Terminology Bindings

Path	Status	Usage	ValueSet	Version	Source
MyHealthEuMedication.​classification	Base	preferred		Not State	Unknown
MyHealthEuMedication.​doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​description	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.substance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.strengthInfo.​basisOfStrengthSubstance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.unitOfPresentation	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.amount	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.packageType	Base	preferred		Not State	Unknown

This structure is derived from EHDSMedication

Summary

Key Elements View

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHealthEuMedication		0..*	EHDSMedication	Medication model Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch
identifyingCode[x]	O	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. Obligations Actor MAY:able-to-populate EHDSI Handler
identifyingCodeCodeableConcept			CodeableConcept
identifyingCodeIdentifier			Identifier
classification	O	0..*	CodeableConcept	Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) Binding Description: (preferred): WHO ATC Obligations Actor MAY:able-to-populate EHDSI Handler
productName	O	0..1	string	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. Obligations Actor MAY:able-to-populate EHDSI Handler
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 EHDSI Handler
organisationName		0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm		0..1	CodeableConcept	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. Binding Description: (preferred): EDQM Standard Terms
description		0..1	string	Textual description of the product, e.g. including package description. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation.
item		0..*	Base	A medication item. For combination packs, this can be multiple manufactured items with each item having its own dose form and ingredients+strengths defined
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. Binding Description: (preferred): EDQM Standard Terms Obligations Actor SHALL:handle EHDSI Handler
ingredient	O	1..*	Base	Ingredients Obligations Actor SHALL:handle EHDSI Handler
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 EHDSI Handler
substance		1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS
strengthInfo		0..1	Base	Strength of the product - amount of substance per unit
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 EHDSI Handler
basisOfStrengthSubstance		0..1	CodeableConcept	Substance that the strength refers to, especially when different from .item.strength.substance Binding Description: (preferred): EMA SPOR SMS
unitOfPresentation		0..1	CodeableConcept	Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package. Binding Description: (preferred): EDQM Standard Terms
containedQuantity	O	0..1	Ratio	Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor SHOULD:handle EHDSI Handler
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. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation. Obligations Actor SHOULD:handle EHDSI Handler
packageType	O	0..1	CodeableConcept	Type of package of the medication item Binding Description: (preferred): EDQM Standard Terms for packaging. Obligations Actor SHOULD:handle EHDSI Handler
device		0..*	Base	Administration device included in the product. Devices that are not inside the medication package are excluded.
deviceQuantity		1..1	Quantity	Number of such devices
device[x]		1..1		Device coded
deviceCodeableConcept			CodeableConcept
deviceEHDSDevice			EHDSDevice
characteristic		0..*	Base	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.
type		1..1	CodeableConcept	A code expressing the type of characteristic.
value[x]		0..1		Description of the characteristic value.
valueBoolean			boolean
valueCodeableConcept			CodeableConcept
valueString			string
valueQuantity			Quantity
valueDateTime			dateTime
valueInteger			integer
valueDecimal			decimal
valueRatio			Ratio
batch		0..1	Base	Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
lotNumber		0..1	string	Batch identifier of the medicinal product.
expirationDate		0..1	dateTime	Batch expiration date of the medicinal product.
Documentation for this format

Terminology Bindings

Path	Status	Usage	ValueSet	Version	Source
MyHealthEuMedication.​classification	Base	preferred		Not State	Unknown
MyHealthEuMedication.​doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​description	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.substance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.strengthInfo.​basisOfStrengthSubstance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.unitOfPresentation	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.amount	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.packageType	Base	preferred		Not State	Unknown

Differential View

This structure is derived from EHDSMedication

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHealthEuMedication		0..*	EHDSMedication	Medication model Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch
identifyingCode[x]	O	0..*	CodeableConcept, Identifier	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. Obligations Actor MAY:able-to-populate EHDSI Handler
classification	O	0..*	CodeableConcept	Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) Obligations Actor MAY:able-to-populate EHDSI Handler
productName	O	0..1	string	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. Obligations Actor MAY:able-to-populate EHDSI Handler
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 EHDSI Handler
item
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 SHALL:handle EHDSI Handler
ingredient	O	1..*	Base	Ingredients Obligations Actor SHALL:handle EHDSI Handler
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 EHDSI Handler
strengthInfo
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 EHDSI Handler
containedQuantity	O	0..1	Ratio	Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor SHOULD:handle EHDSI Handler
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 SHOULD:handle EHDSI Handler
packageType	O	0..1	CodeableConcept	Type of package of the medication item Obligations Actor SHOULD:handle EHDSI Handler
Documentation for this format

Snapshot View

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHealthEuMedication		0..*	EHDSMedication	Medication model Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch
identifyingCode[x]	O	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. Obligations Actor MAY:able-to-populate EHDSI Handler
identifyingCodeCodeableConcept			CodeableConcept
identifyingCodeIdentifier			Identifier
classification	O	0..*	CodeableConcept	Classification (e.g. ATC; narcotic/psychotropic; orphan drug; etc.) Binding Description: (preferred): WHO ATC Obligations Actor MAY:able-to-populate EHDSI Handler
productName	O	0..1	string	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. Obligations Actor MAY:able-to-populate EHDSI Handler
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 EHDSI Handler
organisationName		0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm		0..1	CodeableConcept	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. Binding Description: (preferred): EDQM Standard Terms
description		0..1	string	Textual description of the product, e.g. including package description. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation.
item		0..*	Base	A medication item. For combination packs, this can be multiple manufactured items with each item having its own dose form and ingredients+strengths defined
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. Binding Description: (preferred): EDQM Standard Terms Obligations Actor SHALL:handle EHDSI Handler
ingredient	O	1..*	Base	Ingredients Obligations Actor SHALL:handle EHDSI Handler
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 EHDSI Handler
substance		1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS
strengthInfo		0..1	Base	Strength of the product - amount of substance per unit
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 EHDSI Handler
basisOfStrengthSubstance		0..1	CodeableConcept	Substance that the strength refers to, especially when different from .item.strength.substance Binding Description: (preferred): EMA SPOR SMS
unitOfPresentation		0..1	CodeableConcept	Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package. Binding Description: (preferred): EDQM Standard Terms
containedQuantity	O	0..1	Ratio	Manufactured item quantity per one item (3 ml / 1 vial) Obligations Actor SHOULD:handle EHDSI Handler
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. Binding Description: (preferred): UCUM for units of measure. EDQM Standard Terms for units of presentation. Obligations Actor SHOULD:handle EHDSI Handler
packageType	O	0..1	CodeableConcept	Type of package of the medication item Binding Description: (preferred): EDQM Standard Terms for packaging. Obligations Actor SHOULD:handle EHDSI Handler
device		0..*	Base	Administration device included in the product. Devices that are not inside the medication package are excluded.
deviceQuantity		1..1	Quantity	Number of such devices
device[x]		1..1		Device coded
deviceCodeableConcept			CodeableConcept
deviceEHDSDevice			EHDSDevice
characteristic		0..*	Base	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.
type		1..1	CodeableConcept	A code expressing the type of characteristic.
value[x]		0..1		Description of the characteristic value.
valueBoolean			boolean
valueCodeableConcept			CodeableConcept
valueString			string
valueQuantity			Quantity
valueDateTime			dateTime
valueInteger			integer
valueDecimal			decimal
valueRatio			Ratio
batch		0..1	Base	Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
lotNumber		0..1	string	Batch identifier of the medicinal product.
expirationDate		0..1	dateTime	Batch expiration date of the medicinal product.
Documentation for this format

Terminology Bindings

Path	Status	Usage	ValueSet	Version	Source
MyHealthEuMedication.​classification	Base	preferred		Not State	Unknown
MyHealthEuMedication.​doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​description	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.doseForm	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.substance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.ingredient.strengthInfo.​basisOfStrengthSubstance	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.unitOfPresentation	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.amount	Base	preferred		Not State	Unknown
MyHealthEuMedication.​item.packageType	Base	preferred		Not State	Unknown

This structure is derived from EHDSMedication

Summary

Other representations of profile: CSV, Excel