Protocol required concomitant vaccination, convulsion episode

Administrative data
Beschrijving

Administrative data

Alias
UMLS CUI-1
C1320722
Subject number
Beschrijving

Subject number

Datatype

text

Alias
UMLS CUI [1]
C2348585
Visit number
Beschrijving

Visit number

Datatype

integer

Alias
UMLS CUI [1]
C1549755
Date of Visit
Beschrijving

Date of Visit

Datatype

date

Alias
UMLS CUI [1]
C1320303
Workbook number
Beschrijving

Workbook number

Datatype

integer

Alias
UMLS CUI [1]
C2986015
PROTOCOL REQUIRED CONCOMITANT VACCINATION
Beschrijving

PROTOCOL REQUIRED CONCOMITANT VACCINATION

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C0042196
UMLS CUI-3
C1708545
Have the following protocol required concomitant vaccines been administered?
Beschrijving

If Yes is ticked, the applicable vaccine is not to be reported again in the Concomitant Vaccination section at the end of the CRF. Any other vaccines administered during the study period are to be recorded in the Concomitant Vaccination section at the end of the CRF. Reminder: Any vaccine should be administered at least 30 days before the date of study vaccine administration.

Datatype

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0042196
UMLS CUI [1,3]
C1708545
UMLS CUI [1,4]
C2368628
Vaccines
Beschrijving

In visit 8 only HAV vaccine

Datatype

integer

Alias
UMLS CUI [1]
C0042210
Date if different from visit date
Beschrijving

Vaccine administration, Date

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C2368628
CONVULSION EPISODE
Beschrijving

CONVULSION EPISODE

Alias
UMLS CUI-1
C0332189
UMLS CUI-2
C4048158
Has the subject experienced any CONVULSION EPISODE occurring within 30 days after booster vaccination?
Beschrijving

If yes please complete the CONVULSION EPISODE section

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332189
UMLS CUI [1,2]
C4048158
UMLS CUI [1,3]
C0332282
UMLS CUI [1,4]
C0042196
UMLS CUI [1,5]
C3259236

Similar models

Protocol required concomitant vaccination, convulsion episode

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Item
Visit number
integer
C1549755 (UMLS CUI [1])
Code List
Visit number
CL Item
Visit 2 (2)
CL Item
Visit 3 (3)
CL Item
Visit 4 (4)
CL Item
Visit 5 (5)
CL Item
Visit 6 (6)
CL Item
Visit 7 (7)
CL Item
Visit 8 (8)
CL Item
Visit 9 (9)
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Item
Workbook number
integer
C2986015 (UMLS CUI [1])
Code List
Workbook number
CL Item
workbook 1 (1)
CL Item
workbook 2 (2)
CL Item
workbook 3 (3)
Item Group
PROTOCOL REQUIRED CONCOMITANT VACCINATION
C2347852 (UMLS CUI-1)
C0042196 (UMLS CUI-2)
C1708545 (UMLS CUI-3)
Administration of protocol required concomitant vaccines
Item
Have the following protocol required concomitant vaccines been administered?
boolean
C2347852 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C1708545 (UMLS CUI [1,3])
C2368628 (UMLS CUI [1,4])
Item
Vaccines
integer
C0042210 (UMLS CUI [1])
Code List
Vaccines
CL Item
HAV vaccine (1)
CL Item
MMR vaccine (2)
CL Item
Meningococcal C conjugated vaccine (3)
Vaccine administration, Date
Item
Date if different from visit date
date
C0011008 (UMLS CUI [1,1])
C2368628 (UMLS CUI [1,2])
Item Group
CONVULSION EPISODE
C0332189 (UMLS CUI-1)
C4048158 (UMLS CUI-2)
Convulsion episode following booster vaccination
Item
Has the subject experienced any CONVULSION EPISODE occurring within 30 days after booster vaccination?
boolean
C0332189 (UMLS CUI [1,1])
C4048158 (UMLS CUI [1,2])
C0332282 (UMLS CUI [1,3])
C0042196 (UMLS CUI [1,4])
C3259236 (UMLS CUI [1,5])