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: test LM without items

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. Model is suitable for generic/virtual medications as well as branded/real products.

Usages:

• This Logical Model is not used by any profiles in this Implementation Guide

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
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Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHmedicationNoItems		0..*	EHDSMedication	Medication: test LM without items Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch Instances of this logical model can be the target of a Reference
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	O	0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing Obligations Actor MAY:able-to-populate EHDSI Handler
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm	O	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 Obligations Actor SHALL:handle EHDSI Handler
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	O	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 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	O	1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS Obligations Actor SHALL:handle EHDSI Handler
strengthInfo	O	0..1	Base	Strength of the product - amount of substance per unit Obligations Actor SHALL:handle EHDSI Handler
strength	O	1..1	Ratio	Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHALL: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. 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
Documentation for this format

Terminology Bindings

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

This structure is derived from EHDSMedication

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHmedicationNoItems		0..*	EHDSMedication	Medication: test LM without items Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch Instances of this logical model can be the target of a Reference
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
organisationName	O	0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing Obligations Actor MAY:able-to-populate EHDSI Handler
doseForm	O	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. Obligations Actor SHALL:handle EHDSI Handler
item	O	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 Obligations Actor SHALL:handle EHDSI Handler
doseForm		0..0		Administrable or manufactured item dose form, depending on the type of medication definition. This should not include combined dose forms.
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	O	1..1	CodeableConcept	Substance Obligations Actor SHALL:handle EHDSI Handler
strengthInfo	O	0..1	Base	Strength of the product - amount of substance per unit Obligations Actor SHALL:handle EHDSI Handler
strength	O	1..1	Ratio	Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHALL:handle EHDSI Handler
basisOfStrengthSubstance		0..0		Substance that the strength refers to, especially when different from .item.strength.substance
unitOfPresentation		0..0		Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package.
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
device		0..0		Administration device included in the product. Devices that are not inside the medication package are excluded.
characteristic		0..0		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.
batch		0..0		Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
Documentation for this format

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHmedicationNoItems		0..*	EHDSMedication	Medication: test LM without items Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch Instances of this logical model can be the target of a Reference
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	O	0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing Obligations Actor MAY:able-to-populate EHDSI Handler
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm	O	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 Obligations Actor SHALL:handle EHDSI Handler
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	O	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 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	O	1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS Obligations Actor SHALL:handle EHDSI Handler
strengthInfo	O	0..1	Base	Strength of the product - amount of substance per unit Obligations Actor SHALL:handle EHDSI Handler
strength	O	1..1	Ratio	Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHALL: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. 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
Documentation for this format

Terminology Bindings

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

This structure is derived from EHDSMedication

Summary

Prohibited: 6 elements

Key Elements View

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHmedicationNoItems		0..*	EHDSMedication	Medication: test LM without items Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch Instances of this logical model can be the target of a Reference
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	O	0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing Obligations Actor MAY:able-to-populate EHDSI Handler
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm	O	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 Obligations Actor SHALL:handle EHDSI Handler
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	O	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 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	O	1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS Obligations Actor SHALL:handle EHDSI Handler
strengthInfo	O	0..1	Base	Strength of the product - amount of substance per unit Obligations Actor SHALL:handle EHDSI Handler
strength	O	1..1	Ratio	Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHALL: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. 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
Documentation for this format

Terminology Bindings

Path	Status	Usage	ValueSet	Version	Source
MyHmedicationNoItems.​classification	Base	preferred		Not State	Unknown
MyHmedicationNoItems.​doseForm	Base	preferred		Not State	Unknown
MyHmedicationNoItems.​description	Base	preferred		Not State	Unknown
MyHmedicationNoItems.​item.ingredient.substance	Base	preferred		Not State	Unknown
MyHmedicationNoItems.​item.amount	Base	preferred		Not State	Unknown
MyHmedicationNoItems.​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
MyHmedicationNoItems		0..*	EHDSMedication	Medication: test LM without items Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch Instances of this logical model can be the target of a Reference
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
organisationName	O	0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing Obligations Actor MAY:able-to-populate EHDSI Handler
doseForm	O	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. Obligations Actor SHALL:handle EHDSI Handler
item	O	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 Obligations Actor SHALL:handle EHDSI Handler
doseForm		0..0		Administrable or manufactured item dose form, depending on the type of medication definition. This should not include combined dose forms.
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	O	1..1	CodeableConcept	Substance Obligations Actor SHALL:handle EHDSI Handler
strengthInfo	O	0..1	Base	Strength of the product - amount of substance per unit Obligations Actor SHALL:handle EHDSI Handler
strength	O	1..1	Ratio	Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHALL:handle EHDSI Handler
basisOfStrengthSubstance		0..0		Substance that the strength refers to, especially when different from .item.strength.substance
unitOfPresentation		0..0		Unit of presentation for the manufactured item (tablet, vial, tube). Typically, the smallest countable object in the package.
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
device		0..0		Administration device included in the product. Devices that are not inside the medication package are excluded.
characteristic		0..0		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.
batch		0..0		Batch information of a medicinal product. Typically recorded during dispense or administration, rarely known or relevant for a prescription/request.
Documentation for this format

Snapshot View

Name	Flags	Card.	Type	Description & Constraints    Filter: Bindings Constraints Obligations
MyHmedicationNoItems		0..*	EHDSMedication	Medication: test LM without items Elements defined in Ancestors:identifyingCode[x], classification, productName, marketingAuthorisationHolder, doseForm, description, item, device, characteristic, batch Instances of this logical model can be the target of a Reference
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	O	0..1	string	Name of the organisation holding the authorisation for marketing/manufacturing Obligations Actor MAY:able-to-populate EHDSI Handler
organisationIdentifier		0..*	Identifier	Identifier of the organisation and/or its physical location
doseForm	O	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 Obligations Actor SHALL:handle EHDSI Handler
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	O	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 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	O	1..1	CodeableConcept	Substance Binding Description: (preferred): EMA SPOR SMS Obligations Actor SHALL:handle EHDSI Handler
strengthInfo	O	0..1	Base	Strength of the product - amount of substance per unit Obligations Actor SHALL:handle EHDSI Handler
strength	O	1..1	Ratio	Concentration or presentation strength, e.g '100 mg/1 ml' or '500 mg per 1 tablet' Obligations Actor SHALL: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. 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
Documentation for this format

Terminology Bindings

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

This structure is derived from EHDSMedication

Summary

Prohibited: 6 elements

Other representations of profile: CSV, Excel