Release 4

This page is part of the FHIR Specification (v4.0.1: R4 - Mixed Normative and STU) in it's permanent home (it will always be available at this URL). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

Biomedical Research and Regulation Work GroupMaturity Level: 0 Trial UseSecurity Category: Anonymous Compartments: Not linked to any defined compartments

Detailed Descriptions for the elements in the MedicinalProductUndesirableEffect resource.

MedicinalProductUndesirableEffect
Element IdMedicinalProductUndesirableEffect
Definition

Describe the undesirable effects of the medicinal product.

Cardinality0..*
TypeDomainResource
Summarytrue
MedicinalProductUndesirableEffect.subject
Element IdMedicinalProductUndesirableEffect.subject
Definition

The medication for which this is an indication.

Cardinality0..*
TypeReference(MedicinalProduct | Medication)
Summarytrue
MedicinalProductUndesirableEffect.symptomConditionEffect
Element IdMedicinalProductUndesirableEffect.symptomConditionEffect
Definition

The symptom, condition or undesirable effect.

Cardinality0..1
TypeCodeableConcept
Summarytrue
MedicinalProductUndesirableEffect.classification
Element IdMedicinalProductUndesirableEffect.classification
Definition

Classification of the effect.

Cardinality0..1
TypeCodeableConcept
Summarytrue
MedicinalProductUndesirableEffect.frequencyOfOccurrence
Element IdMedicinalProductUndesirableEffect.frequencyOfOccurrence
Definition

The frequency of occurrence of the effect.

Cardinality0..1
TypeCodeableConcept
Summarytrue
MedicinalProductUndesirableEffect.population
Element IdMedicinalProductUndesirableEffect.population
Definition

The population group to which this applies.

Cardinality0..*
TypePopulation
Summarytrue