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ERKNet Core Registry: Adverse events

23 forms  
General information
Description

General information

Alias
UMLS CUI [1,1]
C1508263
uid
Description

I.uid_aes

Data type

integer

Alias
UMLS CUI [1,1]
C2603343
UMLS CUI [1,2]
C2348584
ID
Description

I.id_aes

Data type

text

Alias
UMLS CUI [1,1]
C2348585
Center
Description

I.center_aes

Data type

text

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0565990
Creator
Description

I.creator_aes

Data type

text

Alias
UMLS CUI [1,1]
C1707531
Creation date
Description

I.creation_aes

Data type

date

Alias
UMLS CUI [1,1]
C2347859
Editor
Description

I.editor_aes

Data type

text

Alias
UMLS CUI [1,1]
C1707883
Edit date
Description

I.editor_date_aes

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0868955
Adverse events
Description

Adverse events

Alias
UMLS CUI [1,1]
C0877248
Subregistry
Description

I.sub_reg_aes

Data type

text

Alias
UMLS CUI [1,1]
C1521902
UMLS CUI [1,2]
C0034975
Adverse event id
Description

I.ae_id_aes

Data type

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C2826693
Adverse event date
Description

I.ae_date

Data type

date

Alias
UMLS CUI [1,1]
C2985916
If Adverse event id == XX, additional remark
Description

I.ae_remark

Data type

text

Alias
UMLS CUI [1,1]
C0947611
UMLS CUI [1,2]
C0877248
Treatment involved in the adverse event
Description

I.treatment_involved_aes

Data type

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0087111
Treatment discontinuation
Description

I.treatment_discontinuation

Data type

text

Alias
UMLS CUI [1,1]
C1512699
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C0392360
UMLS CUI [1,4]
C0087111
Dose reduction
Description

I.dose_reduction

Data type

text

Alias
UMLS CUI [1,1]
C1707814
If dose reduction = yes, new medication dosage
Description

I.new_dose

Data type

text

Alias
UMLS CUI [1,1]
C1707814
UMLS CUI [1,2]
C0205314
UMLS CUI [1,3]
C3174092
If dose reduction = yes, new medication dosage unit
Description

I.new_dose_unit

Data type

text

Alias
UMLS CUI [1,1]
C1707814
UMLS CUI [1,2]
C0205314
UMLS CUI [1,3]
C3174092
UMLS CUI [1,4]
C0439148
Outcome of the adverse event
Description

I.outcome

Data type

text

Alias
UMLS CUI [1,1]
C1705586
New medication
Description

I.new_medication

Data type

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0205314
UMLS CUI [1,3]
C2169461
UMLS CUI [1,4]
C1512698
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Similar models

ERKNet Core Registry: Adverse events

23 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
General information
C1508263 (UMLS CUI [1,1])
I.uid_aes
Item
uid
integer
C2603343 (UMLS CUI [1,1])
C2348584 (UMLS CUI [1,2])
I.id_aes
Item
ID
text
C2348585 (UMLS CUI [1,1])
I.center_aes
Item
Center
text
C1301943 (UMLS CUI [1,1])
C0565990 (UMLS CUI [1,2])
I.creator_aes
Item
Creator
text
C1707531 (UMLS CUI [1,1])
I.creation_aes
Item
Creation date
date
C2347859 (UMLS CUI [1,1])
I.editor_aes
Item
Editor
text
C1707883 (UMLS CUI [1,1])
I.editor_date_aes
Item
Edit date
date
C0011008 (UMLS CUI [1,1])
C0868955 (UMLS CUI [1,2])
Item Group
Adverse events
C0877248 (UMLS CUI [1,1])
I.sub_reg_aes
Item
Subregistry
text
C1521902 (UMLS CUI [1,1])
C0034975 (UMLS CUI [1,2])
I.ae_id_aes
Item
Adverse event id
integer
C0877248 (UMLS CUI [1,1])
C2826693 (UMLS CUI [1,2])
I.ae_date
Item
Adverse event date
date
C2985916 (UMLS CUI [1,1])
I.ae_remark
Item
If Adverse event id == XX, additional remark
text
C0947611 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
I.treatment_involved_aes
Item
Treatment involved in the adverse event
integer
C0877248 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Item
Treatment discontinuation
text
C1512699 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0087111 (UMLS CUI [1,4])
CL.165
Code List
Treatment discontinuation
CL Item
No (0)
C1298908 (UMLS CUI [1,1])
CL Item
Yes (1)
C1705108 (UMLS CUI [1,1])
CL Item
Unknown (9)
C0439673 (UMLS CUI [1,1])
Item
Dose reduction
text
C1707814 (UMLS CUI [1,1])
CL.26
Code List
Dose reduction
CL Item
No (0)
C1298908 (UMLS CUI [1,1])
CL Item
Yes (1)
C1705108 (UMLS CUI [1,1])
CL Item
Unknown (2)
C0439673 (UMLS CUI [1,1])
I.new_dose
Item
If dose reduction = yes, new medication dosage
text
C1707814 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
Item
If dose reduction = yes, new medication dosage unit
text
C1707814 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
C0439148 (UMLS CUI [1,4])
CL.162
Code List
If dose reduction = yes, new medication dosage unit
CL Item
mg (mg)
C0439210 (UMLS CUI [1,1])
CL Item
µg (ug)
C0439211 (UMLS CUI [1,1])
CL Item
I.U (iu)
C0439453 (UMLS CUI [1,1])
CL Item
Tablet(s)  (ta)
C0039225 (UMLS CUI [1,1])
Item
Outcome of the adverse event
text
C1705586 (UMLS CUI [1,1])
CL.167
Code List
Outcome of the adverse event
CL Item
Recovery (1)
C2004454 (UMLS CUI [1,1])
CL Item
Partial recovery (2)
C0728938 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
CL Item
No recovery (3)
C1298908 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
C1709277 (UMLS CUI [1,3])
CL Item
Unknown (9)
C0439673 (UMLS CUI [1,1])
C1705586 (UMLS CUI [1,2])
Item
New medication
text
C0013227 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
C2169461 (UMLS CUI [1,3])
C1512698 (UMLS CUI [1,4])
CL.165
Code List
New medication
CL Item
No (0)
C1298908 (UMLS CUI [1,1])
CL Item
Yes (1)
C1705108 (UMLS CUI [1,1])
CL Item
Unknown (9)
C0439673 (UMLS CUI [1,1])
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