BeModelVaccinationReduced

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

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.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

The patient that has received the vaccination.

The professional that administered the medication. Use code "unknown" if not known.

The details of the product that was administered

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

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.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

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).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

The code of the product that was administered. This can be just text (not desired), or a code (e.g. 1696392 = Neisvac C Dos 0,5ml).

The description of the product that was administered.

The lot number

The business identifier(s) for the vaccination entry - This is an optional attribute, used for example to track an entry throughout its lifecycle, or across vaults.

The date and/or time when the vaccine administration has been administered or presumed to be administered

The date and time when the administration of the vaccine was recorded - typically used when the vaccine event is recorded a posteriori.

The number or quantity of product(s) that was administered - e.g. 1/2 dose, etc.

The target disease for this vaccination.

Any noted side effect from this vaccination.

Is the vaccination due to pre or post exposition prophylaxis?

BeModelVaccinationReduced

The patient that has received the vaccination.

The professional that administered the medication. Use code "unknown" if not known.

The details of the product that was administered

The code of the product that was administered. This can be just text (not desired), or a code (e.g. 1696392 = Neisvac C Dos 0,5ml).

The description of the product that was administered.

The lot number

The business identifier(s) for the vaccination entry - This is an optional attribute, used for example to track an entry throughout its lifecycle, or across vaults.

The date and/or time when the vaccine administration has been administered or presumed to be administered

The date and time when the administration of the vaccine was recorded - typically used when the vaccine event is recorded a posteriori.

The number or quantity of product(s) that was administered - e.g. 1/2 dose, etc.

The target disease for this vaccination.

Any noted side effect from this vaccination.

Is the vaccination due to pre or post exposition prophylaxis?

BeModelVaccinationReduced

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

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.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

The patient that has received the vaccination.

The professional that administered the medication. Use code "unknown" if not known.

The details of the product that was administered

Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces.

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.

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

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).

There can be no stigma associated with the use of extensions by any application, project, or standard - regardless of the institution or jurisdiction that uses or defines the extensions. The use of extensions is what allows the FHIR specification to retain a core level of simplicity for everyone.

Modifier extensions allow for extensions that cannot be safely ignored to be clearly distinguished from the vast majority of extensions which can be safely ignored. This promotes interoperability by eliminating the need for implementers to prohibit the presence of extensions. For further information, see the definition of modifier extensions.

The code of the product that was administered. This can be just text (not desired), or a code (e.g. 1696392 = Neisvac C Dos 0,5ml).

The description of the product that was administered.

The lot number

The business identifier(s) for the vaccination entry - This is an optional attribute, used for example to track an entry throughout its lifecycle, or across vaults.

The date and/or time when the vaccine administration has been administered or presumed to be administered

The date and time when the administration of the vaccine was recorded - typically used when the vaccine event is recorded a posteriori.

The number or quantity of product(s) that was administered - e.g. 1/2 dose, etc.

The target disease for this vaccination.

Any noted side effect from this vaccination.

Is the vaccination due to pre or post exposition prophylaxis?