Generated Narrative: StructureDefinition MyHealthEuVaccination Name Flags Card. Type Description & Constraints MyHealthEuVaccination 0..* MyHealthEuImmunisation MyHealth@EU Vaccination - Logical Model Elements defined in Ancestors:header, diseaseOrAgentTargeted, vaccine, administeredProduct, administrationTime, administeringCentre, administrator, note, diseaseOrAgentTargeted, vaccine, administeredProduct, administrationTime, administeringCentre, administrator, note #xD; diseaseOrAgentTargeted O 0..* CodeableConcept Disease or agent that the vaccination provides protection against (e.g. 76902006 Tetanus). Obligations Actor Source MAY:able-to-populate & SHOULD:handle MyHealth@EU HandlerMyHealth@EU Handler from Immunisation model #xD; doseNumber 0..1 CodeableConcept Dose number #xD; vaccinationCountry 1..1 CodeableConcept Country where the vaccination was administered #xD; nextVaccinationDate 0..1 date Expected date for the next vaccination #xD; adverseEvent 0..1 Base Section: Adverse event (extended) #xD; presenceOfAdverseEvent 0..1 boolean Presence of adverse event #xD; reportedAdverseEvent 0..1 string Reported adverse event #xD; adverseEventCode 0..1 CodeableConcept Adverse event code #xD; observations 0..1 string Observations #xD; Documentation for this format
Logical model representing the EU Vaccination as defined by the MyHealth@EU specification.
Copyright European Union, represented by the European Commission - DG SANTE. Licenced under CC-BY-4.0.
Business identifier for the object, unique within its system. Supporting disambiguation between different contexts (systems/countries).
The author of the immunisation statement.
Date and optionally time of authoring/issuing
Status of the immunisation event (completed, not-done).
Source of information (e.g. patient, patient's proxy). Used in case the patient has authored the information or the author has submitted patient-stated information.
Language in which the resource is written. Language is expressed by the IETF language tag.
Disease or agent that the vaccination provides protection against (e.g. 76902006 Tetanus).
Type of immunisation, e.g. J07AM01 Tetanus toxoid; or 871803007 Hepatitis A and Hepatitis B virus antigens only vaccine product.
Administered medicinal product (e.g. TETAVAX suspension for injection), including batch/lot details when necessary.
The date and optionally the exact time when the vaccination was administered.
Administering centre or a health authority responsible for the vaccination event
Health professional responsible for administering the immunisation product.
Any additional free-text information about the immunisation
Any additional free-text information about the immunisation. It can be used for next vaccination date and dose number, among other details.
Country where the vaccination was administered
Information about adverse events following vaccination
Description of the adverse events associated to the vaccination act, completed with Adverse event code.
The adverse events associated to the vaccination act, completed with Adverse event code.
Standardized code corresponding to the medical problem of the adverse event.
Presence of other annotations or observation that are relevant to the vaccination event.