ID

40058

Beschrijving

The form corresponds to an incomplete version of FHIR Resource AdverseEvent, v4.0.1. It contains all data elements that query a medical issue. The file was created for analysis purposes. https://www.hl7.org/fhir/resourcelist.html 02.01.2020

Link

https://www.hl7.org/fhir/resourcelist.html

Trefwoorden

Versies (1)
  1. 10-03-20 10-03-20 -
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HL7 FHIR

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10 maart 2020

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Licentie

Creative Commons BY-NC 4.0
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FHIR v4.0.1

Engels

Resource Adverse Event (0)

1 Formulieren  
AdverseEvent
Beschrijving

AdverseEvent

Alias
UMLS CUI-1
C0877248
Whether the event actually happened, or just had the potential to.
Beschrijving

Note that this is independent of whether anyone was affected or harmed or how severely.

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0237400
UMLS CUI [1,3]
C1709305
UMLS CUI [2,1]
C0877248
UMLS CUI [2,2]
C3245505
UMLS CUI [2,3]
C1709305
The overall type of event, intended for search and filtering purposes.
Beschrijving

AdverseEvent.category

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0332307
This element defines the specific type of event that occurred or that was prevented from occurring.
Beschrijving

AdverseEvent.event

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C1521902
UMLS CUI [1,4]
C1709305
UMLS CUI [2,1]
C0877248
UMLS CUI [2,2]
C0332307
UMLS CUI [2,3]
C1521902
UMLS CUI [2,4]
C1292733
This subject or group impacted by the event.
Beschrijving

AdverseEvent.subject

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0681850
UMLS CUI [2,1]
C0877248
UMLS CUI [2,2]
C1705429
The date (and perhaps time) when the adverse event occurred.
Beschrijving

AdverseEvent.date

Datatype

datetime

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0011008
Estimated or actual date the AdverseEvent began, in the opinion of the reporter.
Beschrijving

AdverseEvent.detected

Datatype

datetime

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C4319718
UMLS CUI [1,3]
C0808070
UMLS CUI [1,4]
C0750572
UMLS CUI [2,1]
C0877248
UMLS CUI [2,2]
C4319718
UMLS CUI [2,3]
C0808070
UMLS CUI [2,4]
C0237400
Includes information about the reaction that occurred as a result of exposure to a substance
Beschrijving

For example, a drug or a chemical

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1314792
UMLS CUI [1,3]
C0332157
UMLS CUI [1,4]
C0439861
The information about where the adverse event occurred.
Beschrijving

AdverseEvent.location

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0450429
Assessment whether this event was of real importance.
Beschrijving

AdverseEvent.seriousness

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1516048
UMLS CUI [1,3]
C1710056
Describes the severity of the adverse event, in relation to the subject.
Beschrijving

Contrast to AdverseEvent.seriousness - a severe rash might not be serious, but a mild heart problem is.

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1710066
Describes the type of outcome from the adverse event.
Beschrijving

AdverseEvent.outcome

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1705586
UMLS CUI [1,3]
C0332307
Identifies the actual instance of what caused the adverse event.
Beschrijving

May be a substance, medication, medication administration, medication statement or a device.

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1314792
Information on the possible cause of the event.
Beschrijving

AdverseEvent.suspectEntity.causality.assessment

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0332149
UMLS CUI [1,3]
C1314792
UMLS CUI [1,4]
C1516048
AdverseEvent.suspectEntity.causalityProductRelatedness.
Beschrijving

AdverseEvent.suspectEntity.causality.productRelatedness

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0332149
UMLS CUI [1,3]
C0085978
UMLS CUI [1,4]
C1514468
UMLS CUI [1,5]
C0680206
AdverseEvent.subjectMedicalHistory
Beschrijving

AdverseEvent.subjectMedicalHistory

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0262926
AdverseEvent.study.
Beschrijving

AdverseEvent.study

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C2603343
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Similar models

Resource Adverse Event (0)

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
AdverseEvent
C0877248 (UMLS CUI-1)
AdverseEvent.actuality
Item
Whether the event actually happened, or just had the potential to.
text
C0877248 (UMLS CUI [1,1])
C0237400 (UMLS CUI [1,2])
C1709305 (UMLS CUI [1,3])
C0877248 (UMLS CUI [2,1])
C3245505 (UMLS CUI [2,2])
C1709305 (UMLS CUI [2,3])
AdverseEvent.category
Item
The overall type of event, intended for search and filtering purposes.
text
C0877248 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
AdverseEvent.event
Item
This element defines the specific type of event that occurred or that was prevented from occurring.
text
C0877248 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C1709305 (UMLS CUI [1,4])
C0877248 (UMLS CUI [2,1])
C0332307 (UMLS CUI [2,2])
C1521902 (UMLS CUI [2,3])
C1292733 (UMLS CUI [2,4])
AdverseEvent.subject
Item
This subject or group impacted by the event.
text
C0877248 (UMLS CUI [1,1])
C0681850 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C1705429 (UMLS CUI [2,2])
AdverseEvent.date
Item
The date (and perhaps time) when the adverse event occurred.
datetime
C0877248 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
AdverseEvent.detected
Item
Estimated or actual date the AdverseEvent began, in the opinion of the reporter.
datetime
C0877248 (UMLS CUI [1,1])
C4319718 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0750572 (UMLS CUI [1,4])
C0877248 (UMLS CUI [2,1])
C4319718 (UMLS CUI [2,2])
C0808070 (UMLS CUI [2,3])
C0237400 (UMLS CUI [2,4])
AdverseEvent.resultingCondition
Item
Includes information about the reaction that occurred as a result of exposure to a substance
text
C0877248 (UMLS CUI [1,1])
C1314792 (UMLS CUI [1,2])
C0332157 (UMLS CUI [1,3])
C0439861 (UMLS CUI [1,4])
AdverseEvent.location
Item
The information about where the adverse event occurred.
text
C0877248 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
AdverseEvent.seriousness
Item
Assessment whether this event was of real importance.
text
C0877248 (UMLS CUI [1,1])
C1516048 (UMLS CUI [1,2])
C1710056 (UMLS CUI [1,3])
AdverseEvent.severity
Item
Describes the severity of the adverse event, in relation to the subject.
text
C0877248 (UMLS CUI [1,1])
C1710066 (UMLS CUI [1,2])
AdverseEvent.outcome
Item
Describes the type of outcome from the adverse event.
text
C0877248 (UMLS CUI [1,1])
C1705586 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
AdverseEvent.suspectEntity.instance
Item
Identifies the actual instance of what caused the adverse event.
text
C0877248 (UMLS CUI [1,1])
C1314792 (UMLS CUI [1,2])
AdverseEvent.suspectEntity.causality.assessment
Item
Information on the possible cause of the event.
text
C0877248 (UMLS CUI [1,1])
C0332149 (UMLS CUI [1,2])
C1314792 (UMLS CUI [1,3])
C1516048 (UMLS CUI [1,4])
AdverseEvent.suspectEntity.causality.productRelatedness
Item
AdverseEvent.suspectEntity.causalityProductRelatedness.
text
C0877248 (UMLS CUI [1,1])
C0332149 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,3])
C1514468 (UMLS CUI [1,4])
C0680206 (UMLS CUI [1,5])
AdverseEvent.subjectMedicalHistory
Item
AdverseEvent.subjectMedicalHistory
text
C0877248 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
AdverseEvent.study
Item
AdverseEvent.study.
text
C0877248 (UMLS CUI [1,1])
C2603343 (UMLS CUI [1,2])
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