This page is part of the FHIR Specification (v4.6.0: R5 Draft Ballot - see ballot notes). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B

15.5 Resource AdministrableProductDefinition - Content

Biomedical Research and Regulation

Work Group

Maturity Level: 1

Trial Use

Security Category: Anonymous

Compartments: Not linked to any defined compartments

A medicinal product in the final form which is suitable for administering to a patient (after any mixing of multiple components, dissolution etc. has been performed).

15.5.1 Scope and Usage

For an overview of this resource and others in the Medication Definition domain, also see the module page

A medicinal product may consist of several items, which need to be combined or processed before administration to the patient. This resource covers the ready-for-use administrable product - the components of which are ManufacturedItemDefinition resources. Note that often the administrable product is the same as the manufactured item.

This resource represents the final form of the product; hence it details properties such as the route, that only apply to the final product. It is a definitional resource, representing the properties of a product, but not the actual instance given to someone. When necessary to record that, a Medication resource is used.

15.5.2 References

This resource is referenced by MedicinalProductDefinition and PlanDefinition.

This resource does not implement any patterns.

Structure

Name	Flags	Card.	Type	Description & Constraints
AdministrableProductDefinition	TU		DomainResource	A medicinal product in the final form which is suitable for administering to a patient (after any mixing of multiple components, dissolution etc. has been performed) Elements defined in Ancestors: id, meta, implicitRules, language, text, contained, extension, modifierExtension
identifier	Σ	0..*	Identifier	An identifier for the administrable product
subject	Σ	0..*	Reference(MedicinalProductDefinition)	The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product
administrableDoseForm	Σ	0..1	CodeableConcept	The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing
unitOfPresentation	Σ	0..1	CodeableConcept	The units of presentation for the administrable product, for example 'tablet'
producedFrom	Σ	0..*	Reference(ManufacturedItemDefinition)	The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients
ingredient	Σ	0..*	Reference(Ingredient)	The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)
device	Σ	0..*	Reference(DeviceDefinition)	A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged
property	Σ	0..*	BackboneElement	Characteristics e.g. a products onset of action
type	Σ	1..1	CodeableConcept	A code expressing the type of characteristic
value[x]	Σ	0..1		A value for the characteristic
valueCodeableConcept			CodeableConcept
valueQuantity			Quantity
valueDate			date
valueBoolean			boolean
valueAttachment			Attachment
status	Σ	0..1	CodeableConcept	The status of characteristic e.g. assigned or pending
routeOfAdministration	Σ	1..*	BackboneElement	The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route
code	Σ	1..1	CodeableConcept	Coded expression for the route
firstDose	Σ	0..1	Quantity	The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement
maxSingleDose	Σ	0..1	Quantity	The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement
maxDosePerDay	Σ	0..1	Quantity	The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered
maxDosePerTreatmentPeriod	Σ	0..1	Ratio	The maximum dose per treatment period that can be administered
maxTreatmentPeriod	Σ	0..1	Duration	The maximum treatment period during which an Investigational Medicinal Product can be administered
targetSpecies	Σ	0..*	BackboneElement	A species for which this route applies
code	Σ	1..1	CodeableConcept	Coded expression for the species
withdrawalPeriod	Σ	0..*	BackboneElement	A species specific time during which consumption of animal product is not appropriate
tissue	Σ	1..1	CodeableConcept	Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk
value	Σ	1..1	Quantity	A value for the time
supportingInformation	Σ	0..1	string	Extra information about the withdrawal period
Documentation for this format

UML Diagram (Legend)

XML Template

<AdministrableProductDefinition xmlns="http://hl7.org/fhir"> 
 <!-- from Resource: id, meta, implicitRules, and language -->
 <!-- from DomainResource: text, contained, extension, and modifierExtension -->
 <identifier><!-- 0..* Identifier An identifier for the administrable product --></identifier>
 <subject><!-- 0..* Reference(MedicinalProductDefinition) The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product --></subject>
 <administrableDoseForm><!-- 0..1 CodeableConcept The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing --></administrableDoseForm>
 <unitOfPresentation><!-- 0..1 CodeableConcept The units of presentation for the administrable product, for example 'tablet' --></unitOfPresentation>
 <producedFrom><!-- 0..* Reference(ManufacturedItemDefinition) The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients --></producedFrom>
 <ingredient><!-- 0..* Reference(Ingredient) The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s) --></ingredient>
 <device><!-- 0..* Reference(DeviceDefinition) A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged --></device>
 <property>  <!-- 0..* Characteristics e.g. a products onset of action -->
  <type><!-- 1..1 CodeableConcept A code expressing the type of characteristic --></type>
  <value[x]><!-- 0..1 CodeableConcept|Quantity|date|boolean|Attachment A value for the characteristic --></value[x]>
  <status><!-- 0..1 CodeableConcept The status of characteristic e.g. assigned or pending --></status>
 </property>
 <routeOfAdministration>  <!-- 1..* The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route -->
  <code><!-- 1..1 CodeableConcept Coded expression for the route --></code>
  <firstDose><!-- 0..1 Quantity The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement --></firstDose>
  <maxSingleDose><!-- 0..1 Quantity The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement --></maxSingleDose>
  <maxDosePerDay><!-- 0..1 Quantity The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered --></maxDosePerDay>
  <maxDosePerTreatmentPeriod><!-- 0..1 Ratio The maximum dose per treatment period that can be administered --></maxDosePerTreatmentPeriod>
  <maxTreatmentPeriod><!-- 0..1 Duration The maximum treatment period during which an Investigational Medicinal Product can be administered --></maxTreatmentPeriod>
  <targetSpecies>  <!-- 0..* A species for which this route applies -->
   <code><!-- 1..1 CodeableConcept Coded expression for the species --></code>
   <withdrawalPeriod>  <!-- 0..* A species specific time during which consumption of animal product is not appropriate -->
    <tissue><!-- 1..1 CodeableConcept Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk --></tissue>
    <value><!-- 1..1 Quantity A value for the time --></value>
    <supportingInformation value="[string]"/><!-- 0..1 Extra information about the withdrawal period -->
   </withdrawalPeriod>
  </targetSpecies>
 </routeOfAdministration>
</AdministrableProductDefinition>

JSON Template

{
  "resourceType" : "AdministrableProductDefinition",
  // from Resource: id, meta, implicitRules, and language
  // from DomainResource: text, contained, extension, and modifierExtension
  "identifier" : [{ Identifier }], // An identifier for the administrable product
  "subject" : [{ Reference(MedicinalProductDefinition) }], // The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product
  "administrableDoseForm" : { CodeableConcept }, // The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing
  "unitOfPresentation" : { CodeableConcept }, // The units of presentation for the administrable product, for example 'tablet'
  "producedFrom" : [{ Reference(ManufacturedItemDefinition) }], // The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients
  "ingredient" : [{ Reference(Ingredient) }], // The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)
  "device" : [{ Reference(DeviceDefinition) }], // A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged
  "property" : [{ // Characteristics e.g. a products onset of action
    "type" : { CodeableConcept }, // R!  A code expressing the type of characteristic
    // value[x]: A value for the characteristic. One of these 5:
    "valueCodeableConcept" : { CodeableConcept },
    "valueQuantity" : { Quantity },
    "valueDate" : "<date>",
    "valueBoolean" : <boolean>,
    "valueAttachment" : { Attachment },
    "status" : { CodeableConcept } // The status of characteristic e.g. assigned or pending
  }],
  "routeOfAdministration" : [{ // R!  The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route
    "code" : { CodeableConcept }, // R!  Coded expression for the route
    "firstDose" : { Quantity }, // The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement
    "maxSingleDose" : { Quantity }, // The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement
    "maxDosePerDay" : { Quantity }, // The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered
    "maxDosePerTreatmentPeriod" : { Ratio }, // The maximum dose per treatment period that can be administered
    "maxTreatmentPeriod" : { Duration }, // The maximum treatment period during which an Investigational Medicinal Product can be administered
    "targetSpecies" : [{ // A species for which this route applies
      "code" : { CodeableConcept }, // R!  Coded expression for the species
      "withdrawalPeriod" : [{ // A species specific time during which consumption of animal product is not appropriate
        "tissue" : { CodeableConcept }, // R!  Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk
        "value" : { Quantity }, // R!  A value for the time
        "supportingInformation" : "<string>" // Extra information about the withdrawal period
      }]
    }]
  }]
}

Turtle Template

@prefix fhir: <http://hl7.org/fhir/> .


[ a fhir:AdministrableProductDefinition;
  fhir:nodeRole fhir:treeRoot; # if this is the parser root

  # from Resource: .id, .meta, .implicitRules, and .language
  # from DomainResource: .text, .contained, .extension, and .modifierExtension
  fhir:AdministrableProductDefinition.identifier [ Identifier ], ... ; # 0..* An identifier for the administrable product
  fhir:AdministrableProductDefinition.subject [ Reference(MedicinalProductDefinition) ], ... ; # 0..* The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product
  fhir:AdministrableProductDefinition.administrableDoseForm [ CodeableConcept ]; # 0..1 The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing
  fhir:AdministrableProductDefinition.unitOfPresentation [ CodeableConcept ]; # 0..1 The units of presentation for the administrable product, for example 'tablet'
  fhir:AdministrableProductDefinition.producedFrom [ Reference(ManufacturedItemDefinition) ], ... ; # 0..* The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients
  fhir:AdministrableProductDefinition.ingredient [ Reference(Ingredient) ], ... ; # 0..* The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)
  fhir:AdministrableProductDefinition.device [ Reference(DeviceDefinition) ], ... ; # 0..* A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged
  fhir:AdministrableProductDefinition.property [ # 0..* Characteristics e.g. a products onset of action
    fhir:AdministrableProductDefinition.property.type [ CodeableConcept ]; # 1..1 A code expressing the type of characteristic
    # AdministrableProductDefinition.property.value[x] : 0..1 A value for the characteristic. One of these 5
      fhir:AdministrableProductDefinition.property.valueCodeableConcept [ CodeableConcept ]
      fhir:AdministrableProductDefinition.property.valueQuantity [ Quantity ]
      fhir:AdministrableProductDefinition.property.valueDate [ date ]
      fhir:AdministrableProductDefinition.property.valueBoolean [ boolean ]
      fhir:AdministrableProductDefinition.property.valueAttachment [ Attachment ]
    fhir:AdministrableProductDefinition.property.status [ CodeableConcept ]; # 0..1 The status of characteristic e.g. assigned or pending
  ], ...;
  fhir:AdministrableProductDefinition.routeOfAdministration [ # 1..* The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route
    fhir:AdministrableProductDefinition.routeOfAdministration.code [ CodeableConcept ]; # 1..1 Coded expression for the route
    fhir:AdministrableProductDefinition.routeOfAdministration.firstDose [ Quantity ]; # 0..1 The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement
    fhir:AdministrableProductDefinition.routeOfAdministration.maxSingleDose [ Quantity ]; # 0..1 The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement
    fhir:AdministrableProductDefinition.routeOfAdministration.maxDosePerDay [ Quantity ]; # 0..1 The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered
    fhir:AdministrableProductDefinition.routeOfAdministration.maxDosePerTreatmentPeriod [ Ratio ]; # 0..1 The maximum dose per treatment period that can be administered
    fhir:AdministrableProductDefinition.routeOfAdministration.maxTreatmentPeriod [ Duration ]; # 0..1 The maximum treatment period during which an Investigational Medicinal Product can be administered
    fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies [ # 0..* A species for which this route applies
      fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.code [ CodeableConcept ]; # 1..1 Coded expression for the species
      fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod [ # 0..* A species specific time during which consumption of animal product is not appropriate
        fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod.tissue [ CodeableConcept ]; # 1..1 Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk
        fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod.value [ Quantity ]; # 1..1 A value for the time
        fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod.supportingInformation [ string ]; # 0..1 Extra information about the withdrawal period
      ], ...;
    ], ...;
  ], ...;
]

Changes since R3

This resource did not exist in Release 2

This analysis is available as XML or JSON.

Structure

Name	Flags	Card.	Type	Description & Constraints
AdministrableProductDefinition	TU		DomainResource	A medicinal product in the final form which is suitable for administering to a patient (after any mixing of multiple components, dissolution etc. has been performed) Elements defined in Ancestors: id, meta, implicitRules, language, text, contained, extension, modifierExtension
identifier	Σ	0..*	Identifier	An identifier for the administrable product
subject	Σ	0..*	Reference(MedicinalProductDefinition)	The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product
administrableDoseForm	Σ	0..1	CodeableConcept	The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing
unitOfPresentation	Σ	0..1	CodeableConcept	The units of presentation for the administrable product, for example 'tablet'
producedFrom	Σ	0..*	Reference(ManufacturedItemDefinition)	The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients
ingredient	Σ	0..*	Reference(Ingredient)	The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)
device	Σ	0..*	Reference(DeviceDefinition)	A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged
property	Σ	0..*	BackboneElement	Characteristics e.g. a products onset of action
type	Σ	1..1	CodeableConcept	A code expressing the type of characteristic
value[x]	Σ	0..1		A value for the characteristic
valueCodeableConcept			CodeableConcept
valueQuantity			Quantity
valueDate			date
valueBoolean			boolean
valueAttachment			Attachment
status	Σ	0..1	CodeableConcept	The status of characteristic e.g. assigned or pending
routeOfAdministration	Σ	1..*	BackboneElement	The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route
code	Σ	1..1	CodeableConcept	Coded expression for the route
firstDose	Σ	0..1	Quantity	The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement
maxSingleDose	Σ	0..1	Quantity	The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement
maxDosePerDay	Σ	0..1	Quantity	The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered
maxDosePerTreatmentPeriod	Σ	0..1	Ratio	The maximum dose per treatment period that can be administered
maxTreatmentPeriod	Σ	0..1	Duration	The maximum treatment period during which an Investigational Medicinal Product can be administered
targetSpecies	Σ	0..*	BackboneElement	A species for which this route applies
code	Σ	1..1	CodeableConcept	Coded expression for the species
withdrawalPeriod	Σ	0..*	BackboneElement	A species specific time during which consumption of animal product is not appropriate
tissue	Σ	1..1	CodeableConcept	Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk
value	Σ	1..1	Quantity	A value for the time
supportingInformation	Σ	0..1	string	Extra information about the withdrawal period
Documentation for this format

UML Diagram (Legend)

XML Template

<AdministrableProductDefinition xmlns="http://hl7.org/fhir"> 
 <!-- from Resource: id, meta, implicitRules, and language -->
 <!-- from DomainResource: text, contained, extension, and modifierExtension -->
 <identifier><!-- 0..* Identifier An identifier for the administrable product --></identifier>
 <subject><!-- 0..* Reference(MedicinalProductDefinition) The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product --></subject>
 <administrableDoseForm><!-- 0..1 CodeableConcept The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing --></administrableDoseForm>
 <unitOfPresentation><!-- 0..1 CodeableConcept The units of presentation for the administrable product, for example 'tablet' --></unitOfPresentation>
 <producedFrom><!-- 0..* Reference(ManufacturedItemDefinition) The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients --></producedFrom>
 <ingredient><!-- 0..* Reference(Ingredient) The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s) --></ingredient>
 <device><!-- 0..* Reference(DeviceDefinition) A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged --></device>
 <property>  <!-- 0..* Characteristics e.g. a products onset of action -->
  <type><!-- 1..1 CodeableConcept A code expressing the type of characteristic --></type>
  <value[x]><!-- 0..1 CodeableConcept|Quantity|date|boolean|Attachment A value for the characteristic --></value[x]>
  <status><!-- 0..1 CodeableConcept The status of characteristic e.g. assigned or pending --></status>
 </property>
 <routeOfAdministration>  <!-- 1..* The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route -->
  <code><!-- 1..1 CodeableConcept Coded expression for the route --></code>
  <firstDose><!-- 0..1 Quantity The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement --></firstDose>
  <maxSingleDose><!-- 0..1 Quantity The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement --></maxSingleDose>
  <maxDosePerDay><!-- 0..1 Quantity The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered --></maxDosePerDay>
  <maxDosePerTreatmentPeriod><!-- 0..1 Ratio The maximum dose per treatment period that can be administered --></maxDosePerTreatmentPeriod>
  <maxTreatmentPeriod><!-- 0..1 Duration The maximum treatment period during which an Investigational Medicinal Product can be administered --></maxTreatmentPeriod>
  <targetSpecies>  <!-- 0..* A species for which this route applies -->
   <code><!-- 1..1 CodeableConcept Coded expression for the species --></code>
   <withdrawalPeriod>  <!-- 0..* A species specific time during which consumption of animal product is not appropriate -->
    <tissue><!-- 1..1 CodeableConcept Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk --></tissue>
    <value><!-- 1..1 Quantity A value for the time --></value>
    <supportingInformation value="[string]"/><!-- 0..1 Extra information about the withdrawal period -->
   </withdrawalPeriod>
  </targetSpecies>
 </routeOfAdministration>
</AdministrableProductDefinition>

JSON Template

{
  "resourceType" : "AdministrableProductDefinition",
  // from Resource: id, meta, implicitRules, and language
  // from DomainResource: text, contained, extension, and modifierExtension
  "identifier" : [{ Identifier }], // An identifier for the administrable product
  "subject" : [{ Reference(MedicinalProductDefinition) }], // The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product
  "administrableDoseForm" : { CodeableConcept }, // The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing
  "unitOfPresentation" : { CodeableConcept }, // The units of presentation for the administrable product, for example 'tablet'
  "producedFrom" : [{ Reference(ManufacturedItemDefinition) }], // The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients
  "ingredient" : [{ Reference(Ingredient) }], // The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)
  "device" : [{ Reference(DeviceDefinition) }], // A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged
  "property" : [{ // Characteristics e.g. a products onset of action
    "type" : { CodeableConcept }, // R!  A code expressing the type of characteristic
    // value[x]: A value for the characteristic. One of these 5:
    "valueCodeableConcept" : { CodeableConcept },
    "valueQuantity" : { Quantity },
    "valueDate" : "<date>",
    "valueBoolean" : <boolean>,
    "valueAttachment" : { Attachment },
    "status" : { CodeableConcept } // The status of characteristic e.g. assigned or pending
  }],
  "routeOfAdministration" : [{ // R!  The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route
    "code" : { CodeableConcept }, // R!  Coded expression for the route
    "firstDose" : { Quantity }, // The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement
    "maxSingleDose" : { Quantity }, // The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement
    "maxDosePerDay" : { Quantity }, // The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered
    "maxDosePerTreatmentPeriod" : { Ratio }, // The maximum dose per treatment period that can be administered
    "maxTreatmentPeriod" : { Duration }, // The maximum treatment period during which an Investigational Medicinal Product can be administered
    "targetSpecies" : [{ // A species for which this route applies
      "code" : { CodeableConcept }, // R!  Coded expression for the species
      "withdrawalPeriod" : [{ // A species specific time during which consumption of animal product is not appropriate
        "tissue" : { CodeableConcept }, // R!  Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk
        "value" : { Quantity }, // R!  A value for the time
        "supportingInformation" : "<string>" // Extra information about the withdrawal period
      }]
    }]
  }]
}

Turtle Template

@prefix fhir: <http://hl7.org/fhir/> .


[ a fhir:AdministrableProductDefinition;
  fhir:nodeRole fhir:treeRoot; # if this is the parser root

  # from Resource: .id, .meta, .implicitRules, and .language
  # from DomainResource: .text, .contained, .extension, and .modifierExtension
  fhir:AdministrableProductDefinition.identifier [ Identifier ], ... ; # 0..* An identifier for the administrable product
  fhir:AdministrableProductDefinition.subject [ Reference(MedicinalProductDefinition) ], ... ; # 0..* The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product
  fhir:AdministrableProductDefinition.administrableDoseForm [ CodeableConcept ]; # 0..1 The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing
  fhir:AdministrableProductDefinition.unitOfPresentation [ CodeableConcept ]; # 0..1 The units of presentation for the administrable product, for example 'tablet'
  fhir:AdministrableProductDefinition.producedFrom [ Reference(ManufacturedItemDefinition) ], ... ; # 0..* The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients
  fhir:AdministrableProductDefinition.ingredient [ Reference(Ingredient) ], ... ; # 0..* The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)
  fhir:AdministrableProductDefinition.device [ Reference(DeviceDefinition) ], ... ; # 0..* A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged
  fhir:AdministrableProductDefinition.property [ # 0..* Characteristics e.g. a products onset of action
    fhir:AdministrableProductDefinition.property.type [ CodeableConcept ]; # 1..1 A code expressing the type of characteristic
    # AdministrableProductDefinition.property.value[x] : 0..1 A value for the characteristic. One of these 5
      fhir:AdministrableProductDefinition.property.valueCodeableConcept [ CodeableConcept ]
      fhir:AdministrableProductDefinition.property.valueQuantity [ Quantity ]
      fhir:AdministrableProductDefinition.property.valueDate [ date ]
      fhir:AdministrableProductDefinition.property.valueBoolean [ boolean ]
      fhir:AdministrableProductDefinition.property.valueAttachment [ Attachment ]
    fhir:AdministrableProductDefinition.property.status [ CodeableConcept ]; # 0..1 The status of characteristic e.g. assigned or pending
  ], ...;
  fhir:AdministrableProductDefinition.routeOfAdministration [ # 1..* The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route
    fhir:AdministrableProductDefinition.routeOfAdministration.code [ CodeableConcept ]; # 1..1 Coded expression for the route
    fhir:AdministrableProductDefinition.routeOfAdministration.firstDose [ Quantity ]; # 0..1 The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement
    fhir:AdministrableProductDefinition.routeOfAdministration.maxSingleDose [ Quantity ]; # 0..1 The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement
    fhir:AdministrableProductDefinition.routeOfAdministration.maxDosePerDay [ Quantity ]; # 0..1 The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered
    fhir:AdministrableProductDefinition.routeOfAdministration.maxDosePerTreatmentPeriod [ Ratio ]; # 0..1 The maximum dose per treatment period that can be administered
    fhir:AdministrableProductDefinition.routeOfAdministration.maxTreatmentPeriod [ Duration ]; # 0..1 The maximum treatment period during which an Investigational Medicinal Product can be administered
    fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies [ # 0..* A species for which this route applies
      fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.code [ CodeableConcept ]; # 1..1 Coded expression for the species
      fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod [ # 0..* A species specific time during which consumption of animal product is not appropriate
        fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod.tissue [ CodeableConcept ]; # 1..1 Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk
        fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod.value [ Quantity ]; # 1..1 A value for the time
        fhir:AdministrableProductDefinition.routeOfAdministration.targetSpecies.withdrawalPeriod.supportingInformation [ string ]; # 0..1 Extra information about the withdrawal period
      ], ...;
    ], ...;
  ], ...;
]

Changes since Release 3

This resource did not exist in Release 2

This analysis is available as XML or JSON.

See the Profiles & Extensions and the alternate definitions: Master Definition XML + JSON, XML Schema/Schematron + JSON Schema, ShEx (for Turtle) + see the extensions, the spreadsheet version & the dependency analysis a

15.5.4 Search Parameters

Search parameters for this resource. The common parameters also apply. See Searching for more information about searching in REST, messaging, and services.

Name	Type	Description	Expression	In Common
device	reference	A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged	AdministrableProductDefinition.device (DeviceDefinition)
dose-form	token	The administrable dose form, i.e. the dose form of the final product after necessary reconstitution or processing	AdministrableProductDefinition.administrableDoseForm
identifier	token	An identifier for the administrable product	AdministrableProductDefinition.identifier
ingredient	reference	The ingredients of this administrable medicinal product. Sometimes it may be appropriate to specify these via the associated manufactured item(s)	AdministrableProductDefinition.ingredient (Ingredient)
manufactured-item	reference	The manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solution item). Note that these are not raw ingredients	AdministrableProductDefinition.producedFrom (ManufacturedItemDefinition)
route	token	Coded expression for the route	AdministrableProductDefinition.routeOfAdministration.code
subject	reference	The medicinal product that this is an administrable form of. This is not a reference to the item(s) that make up this administrable form - it is the whole product	AdministrableProductDefinition.subject (MedicinalProductDefinition)
target-species	token	Coded expression for the species	AdministrableProductDefinition.routeOfAdministration.targetSpecies.code