This page is part of the FHIR Specification (v4.5.0: R5 Preview #3). 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

11.15 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 pharmaceutical product described in terms of its composition and dose form.

11.15.1 Scope and Usage

Qualitative and quantitative composition of a Medicinal Product in the dose form approved for administration in line with the regulated product information

Note that in many instances, the pharmaceutical product is equal to the manufactured item. However, there are instances where the manufactured item must undergo a transformation before being administered to the patient (as the pharmaceutical product) and the two are not equal.

11.15.2 References

This resource is referenced by MedicinalProductDefinition.

This resource does not implement any patterns.

Structure

Name	Flags	Card.	Type	Description & Constraints
AdministrableProductDefinition	Σ TU		DomainResource	A pharmaceutical product described in terms of its composition and dose form Elements defined in Ancestors: id, meta, implicitRules, language, text, contained, extension, modifierExtension
identifier	Σ	0..*	Identifier	An identifier for the pharmaceutical medicinal product
subject	Σ	0..*	Reference(MedicinalProductDefinition)	The product that this is a pharmaceutical product of
administrableDoseForm	Σ	0..1	CodeableConcept	The administrable dose form, after necessary reconstitution
unitOfPresentation	Σ	0..1	CodeableConcept	Todo
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 pharmaceutical product
device	Σ	0..*	Reference(DeviceDefinition)	Accompanying device
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 pharmaceutical product is taken into or makes contact with the body
code	Σ	1..1	CodeableConcept	Coded expression for the route
firstDose	Σ	0..1	Quantity	The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement
maxSingleDose	Σ	0..1	Quantity	The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation
maxDosePerTreatmentPeriod	Σ	0..1	Ratio	The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation
maxTreatmentPeriod	Σ	0..1	Duration	The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation
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 pharmaceutical medicinal product --></identifier>
 <subject><!-- 0..* Reference(MedicinalProductDefinition) The product that this is a pharmaceutical product of --></subject>
 <administrableDoseForm><!-- 0..1 CodeableConcept The administrable dose form, after necessary reconstitution --></administrableDoseForm>
 <unitOfPresentation><!-- 0..1 CodeableConcept Todo --></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 pharmaceutical product --></ingredient>
 <device><!-- 0..* Reference(DeviceDefinition) Accompanying device --></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 pharmaceutical product is taken into or makes contact with the body -->
  <code><!-- 1..1 CodeableConcept Coded expression for the route --></code>
  <firstDose><!-- 0..1 Quantity The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement --></firstDose>
  <maxSingleDose><!-- 0..1 Quantity The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation --></maxDosePerDay>
  <maxDosePerTreatmentPeriod><!-- 0..1 Ratio The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation --></maxDosePerTreatmentPeriod>
  <maxTreatmentPeriod><!-- 0..1 Duration The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation --></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 pharmaceutical medicinal product
  "subject" : [{ Reference(MedicinalProductDefinition) }], // The product that this is a pharmaceutical product of
  "administrableDoseForm" : { CodeableConcept }, // The administrable dose form, after necessary reconstitution
  "unitOfPresentation" : { CodeableConcept }, // Todo
  "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 pharmaceutical product
  "device" : [{ Reference(DeviceDefinition) }], // Accompanying device
  "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 pharmaceutical product is taken into or makes contact with the body
    "code" : { CodeableConcept }, // R!  Coded expression for the route
    "firstDose" : { Quantity }, // The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement
    "maxSingleDose" : { Quantity }, // The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation
    "maxDosePerTreatmentPeriod" : { Ratio }, // The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation
    "maxTreatmentPeriod" : { Duration }, // The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation
    "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 pharmaceutical medicinal product
  fhir:AdministrableProductDefinition.subject [ Reference(MedicinalProductDefinition) ], ... ; # 0..* The product that this is a pharmaceutical product of
  fhir:AdministrableProductDefinition.administrableDoseForm [ CodeableConcept ]; # 0..1 The administrable dose form, after necessary reconstitution
  fhir:AdministrableProductDefinition.unitOfPresentation [ CodeableConcept ]; # 0..1 Todo
  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 pharmaceutical product
  fhir:AdministrableProductDefinition.device [ Reference(DeviceDefinition) ], ... ; # 0..* Accompanying device
  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 pharmaceutical product is taken into or makes contact with the body
    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 in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement
    fhir:AdministrableProductDefinition.routeOfAdministration.maxSingleDose [ Quantity ]; # 0..1 The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation
    fhir:AdministrableProductDefinition.routeOfAdministration.maxDosePerTreatmentPeriod [ Ratio ]; # 0..1 The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation
    fhir:AdministrableProductDefinition.routeOfAdministration.maxTreatmentPeriod [ Duration ]; # 0..1 The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation
    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	Σ TU		DomainResource	A pharmaceutical product described in terms of its composition and dose form Elements defined in Ancestors: id, meta, implicitRules, language, text, contained, extension, modifierExtension
identifier	Σ	0..*	Identifier	An identifier for the pharmaceutical medicinal product
subject	Σ	0..*	Reference(MedicinalProductDefinition)	The product that this is a pharmaceutical product of
administrableDoseForm	Σ	0..1	CodeableConcept	The administrable dose form, after necessary reconstitution
unitOfPresentation	Σ	0..1	CodeableConcept	Todo
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 pharmaceutical product
device	Σ	0..*	Reference(DeviceDefinition)	Accompanying device
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 pharmaceutical product is taken into or makes contact with the body
code	Σ	1..1	CodeableConcept	Coded expression for the route
firstDose	Σ	0..1	Quantity	The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement
maxSingleDose	Σ	0..1	Quantity	The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation
maxDosePerTreatmentPeriod	Σ	0..1	Ratio	The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation
maxTreatmentPeriod	Σ	0..1	Duration	The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation
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 pharmaceutical medicinal product --></identifier>
 <subject><!-- 0..* Reference(MedicinalProductDefinition) The product that this is a pharmaceutical product of --></subject>
 <administrableDoseForm><!-- 0..1 CodeableConcept The administrable dose form, after necessary reconstitution --></administrableDoseForm>
 <unitOfPresentation><!-- 0..1 CodeableConcept Todo --></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 pharmaceutical product --></ingredient>
 <device><!-- 0..* Reference(DeviceDefinition) Accompanying device --></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 pharmaceutical product is taken into or makes contact with the body -->
  <code><!-- 1..1 CodeableConcept Coded expression for the route --></code>
  <firstDose><!-- 0..1 Quantity The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement --></firstDose>
  <maxSingleDose><!-- 0..1 Quantity The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation --></maxDosePerDay>
  <maxDosePerTreatmentPeriod><!-- 0..1 Ratio The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation --></maxDosePerTreatmentPeriod>
  <maxTreatmentPeriod><!-- 0..1 Duration The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation --></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 pharmaceutical medicinal product
  "subject" : [{ Reference(MedicinalProductDefinition) }], // The product that this is a pharmaceutical product of
  "administrableDoseForm" : { CodeableConcept }, // The administrable dose form, after necessary reconstitution
  "unitOfPresentation" : { CodeableConcept }, // Todo
  "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 pharmaceutical product
  "device" : [{ Reference(DeviceDefinition) }], // Accompanying device
  "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 pharmaceutical product is taken into or makes contact with the body
    "code" : { CodeableConcept }, // R!  Coded expression for the route
    "firstDose" : { Quantity }, // The first dose (dose quantity) administered in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement
    "maxSingleDose" : { Quantity }, // The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation
    "maxDosePerTreatmentPeriod" : { Ratio }, // The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation
    "maxTreatmentPeriod" : { Duration }, // The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation
    "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 pharmaceutical medicinal product
  fhir:AdministrableProductDefinition.subject [ Reference(MedicinalProductDefinition) ], ... ; # 0..* The product that this is a pharmaceutical product of
  fhir:AdministrableProductDefinition.administrableDoseForm [ CodeableConcept ]; # 0..1 The administrable dose form, after necessary reconstitution
  fhir:AdministrableProductDefinition.unitOfPresentation [ CodeableConcept ]; # 0..1 Todo
  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 pharmaceutical product
  fhir:AdministrableProductDefinition.device [ Reference(DeviceDefinition) ], ... ; # 0..* Accompanying device
  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 pharmaceutical product is taken into or makes contact with the body
    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 in humans can be specified, for a product under investigation, using a numerical value and its unit of measurement
    fhir:AdministrableProductDefinition.routeOfAdministration.maxSingleDose [ Quantity ]; # 0..1 The maximum single dose that can be administered as per the protocol of a clinical trial 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 as per the protocol referenced in the clinical trial authorisation
    fhir:AdministrableProductDefinition.routeOfAdministration.maxDosePerTreatmentPeriod [ Ratio ]; # 0..1 The maximum dose per treatment period that can be administered as per the protocol referenced in the clinical trial authorisation
    fhir:AdministrableProductDefinition.routeOfAdministration.maxTreatmentPeriod [ Duration ]; # 0..1 The maximum treatment period during which an Investigational Medicinal Product can be administered as per the protocol referenced in the clinical trial authorisation
    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

11.15.4 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	Accompanying device	AdministrableProductDefinition.device (DeviceDefinition)
dose-form	token	The administrable dose form, after necessary reconstitution	AdministrableProductDefinition.administrableDoseForm
identifier	token	An identifier for the pharmaceutical medicinal product	AdministrableProductDefinition.identifier
ingredient	reference	The ingredients of this administrable pharmaceutical product	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 product that this is a pharmaceutical product of	AdministrableProductDefinition.subject (MedicinalProductDefinition)
target-species	token	Coded expression for the species	AdministrableProductDefinition.routeOfAdministration.targetSpecies.code