@medplum/fhirtypes
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Medplum FHIR Type Definitions
97 lines (86 loc) • 3.71 kB
TypeScript
/*
* This is a generated file
* Do not edit manually.
*/
import { CodeableConcept } from './CodeableConcept';
import { Extension } from './Extension';
import { Period } from './Period';
/**
* The marketing status describes the date when a medicinal product is
* actually put on the market or the date as of which it is no longer
* available.
*/
export interface MarketingStatus {
/**
* Unique id for the element within a resource (for internal references).
* This may be any string value that does not contain spaces.
*/
id?: string;
/**
* May be used to represent additional information that is not part of
* the basic definition of the element. To make the use of extensions
* safe and manageable, there is a strict set of governance applied to
* the definition and use of extensions. Though any implementer can
* define an extension, there is a set of requirements that SHALL be met
* as part of the definition of the extension.
*/
extension?: Extension[];
/**
* May be used to represent additional information that is not part of
* the basic definition of the element and that modifies the
* understanding of the element in which it is contained and/or the
* understanding of the containing element's descendants. Usually
* modifier elements provide negation or qualification. To make the use
* of extensions safe and manageable, there is a strict set of governance
* applied to the definition and use of extensions. Though any
* implementer can define an extension, there is a set of requirements
* that SHALL be met as part of the definition of the extension.
* Applications processing a resource are required to check for modifier
* extensions.
*
* Modifier extensions SHALL NOT change the meaning of any elements on
* Resource or DomainResource (including cannot change the meaning of
* modifierExtension itself).
*/
modifierExtension?: Extension[];
/**
* The country in which the marketing authorisation has been granted
* shall be specified It should be specified using the ISO 3166 ‑ 1
* alpha-2 code elements.
*/
country: CodeableConcept;
/**
* Where a Medicines Regulatory Agency has granted a marketing
* authorisation for which specific provisions within a jurisdiction
* apply, the jurisdiction can be specified using an appropriate
* controlled terminology The controlled term and the controlled term
* identifier shall be specified.
*/
jurisdiction?: CodeableConcept;
/**
* This attribute provides information on the status of the marketing of
* the medicinal product See ISO/TS 20443 for more information and
* examples.
*/
status: CodeableConcept;
/**
* The date when the Medicinal Product is placed on the market by the
* Marketing Authorisation Holder (or where applicable, the
* manufacturer/distributor) in a country and/or jurisdiction shall be
* provided A complete date consisting of day, month and year shall be
* specified using the ISO 8601 date format NOTE “Placed on the market”
* refers to the release of the Medicinal Product into the distribution
* chain.
*/
dateRange: Period;
/**
* The date when the Medicinal Product is placed on the market by the
* Marketing Authorisation Holder (or where applicable, the
* manufacturer/distributor) in a country and/or jurisdiction shall be
* provided A complete date consisting of day, month and year shall be
* specified using the ISO 8601 date format NOTE “Placed on the market”
* refers to the release of the Medicinal Product into the distribution
* chain.
*/
restoreDate?: string;
}