MedicinalProductDefinition

Trial Use 3 Specialized — Medication Definition

Detailed definition of a medicinal product, typically for uses other than direct patient care (e.g. regulatory use, drug catalogs, to support prescribing, adverse events management etc.).

Endpoints

devhttps://api.sandbox.ovok.com/fhir/R5/MedicinalProductDefinition

Interaction	Method	Path
Read	GET	/fhir/R5/MedicinalProductDefinition/[id]
Vread	GET	/fhir/R5/MedicinalProductDefinition/[id]/_history/[vid]
Update	PUT	/fhir/R5/MedicinalProductDefinition/[id]
Patch	PATCH	/fhir/R5/MedicinalProductDefinition/[id]
Delete	DELETE	/fhir/R5/MedicinalProductDefinition/[id]
Create	POST	/fhir/R5/MedicinalProductDefinition
Search	GET	/fhir/R5/MedicinalProductDefinition?...
History	GET	/fhir/R5/MedicinalProductDefinition/[id]/_history
Type-history	GET	/fhir/R5/MedicinalProductDefinition/_history

Top-level elements

Element	Type(s)	Cardinality	Description
identifier	Identifier	0..*	Business identifier for this product. Could be an MPID
type	CodeableConcept	0..1	Regulatory type, e.g. Investigational or Authorized
domain	CodeableConcept	0..1	If this medicine applies to human or veterinary uses
version	string	0..1	A business identifier relating to a specific version of the product
status	CodeableConcept	0..1	The status within the lifecycle of this product record modifier
statusDate	dateTime	0..1	The date at which the given status became applicable
description	markdown	0..1	General description of this product
combinedPharmaceuticalDoseForm	CodeableConcept	0..1	The dose form for a single part product, or combined form of a multiple part product
route	CodeableConcept	0..*	The path by which the product is taken into or makes contact with the body
indication	markdown	0..1	Description of indication(s) for this product, used when structured indications are not required
legalStatusOfSupply	CodeableConcept	0..1	The legal status of supply of the medicinal product as classified by the regulator
additionalMonitoringIndicator	CodeableConcept	0..1	Whether the Medicinal Product is subject to additional monitoring for regulatory reasons
specialMeasures	CodeableConcept	0..*	Whether the Medicinal Product is subject to special measures for regulatory reasons
pediatricUseIndicator	CodeableConcept	0..1	If authorised for use in children
classification	CodeableConcept	0..*	Allows the product to be classified by various systems
marketingStatus	MarketingStatus	0..*	Marketing status of the medicinal product, in contrast to marketing authorization
packagedMedicinalProduct	CodeableConcept	0..*	Package type for the product
comprisedOf	Reference	0..*	Types of medicinal manufactured items and/or devices that this product consists of, such as tablets, capsule, or syringes
ingredient	CodeableConcept	0..*	The ingredients of this medicinal product - when not detailed in other resources
impurity	CodeableReference	0..*	Any component of the drug product which is not the chemical entity defined as the drug substance, or an excipient in the drug product
attachedDocument	Reference	0..*	Additional documentation about the medicinal product
masterFile	Reference	0..*	A master file for the medicinal product (e.g. Pharmacovigilance System Master File)
contact	BackboneElement	0..*	A product specific contact, person (in a role), or an organization
clinicalTrial	Reference	0..*	Clinical trials or studies that this product is involved in
code	Coding	0..*	A code that this product is known by, within some formal terminology
name	BackboneElement	1..*	The product's name, including full name and possibly coded parts
crossReference	BackboneElement	0..*	Reference to another product, e.g. for linking authorised to investigational product
operation	BackboneElement	0..*	A manufacturing or administrative process for the medicinal product
characteristic	BackboneElement	0..*	Key product features such as "sugar free", "modified release"

Resource-specific search parameters

Parameter	Type	Description
characteristic	token	Allows the key product features to be recorded, such as "sugar free", "modified release", "parallel import"
characteristic-type	token	A category for the characteristic
contact	reference	A product specific contact, person (in a role), or an organization
domain	token	If this medicine applies to human or veterinary uses
identifier	token	Business identifier for this product. Could be an MPID
ingredient	token	An ingredient of this product
master-file	reference	A master file for to the medicinal product (e.g. Pharmacovigilance System Master File)
name	string	The full product name
name-language	token	Language code for this name
product-classification	token	Allows the product to be classified by various systems
status	token	The status within the lifecycle of this product record. A high-level status, this is not intended to duplicate details carried elsewhere such as legal status, or authorization status
type	token	Regulatory type, e.g. Investigational or Authorized

Reference

• Official FHIR R5 spec: MedicinalProductDefinition
• Maturity: Trial Use 3 (FMM 3).