English

Dose 3 - Solicited Adverse Events - Local Symptoms; Visit 5 - Laboratory Tests

1 forms  
Administration
Description

Administration

Alias
UMLS CUI-1
C1320722
Subject number
Description

Subject number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Solicited Adverse Events - Local Symptoms
Description

Solicited Adverse Events - Local Symptoms

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
Has the subject experienced any of the following local (at administration site) signs/symptoms during the solicited period?
Description

If yes, please check a No/Yes box for each symptom. If Yes is checked, please fill in the complete line.

Data type

text

Alias
UMLS CUI [1,1]
C0037088
UMLS CUI [1,2]
C0205276
UMLS CUI [1,3]
C1515974
UMLS CUI [1,4]
C0013153
Solicited Adverse Events - Local Symptoms (Engerix Vaccine)
Description

Solicited Adverse Events - Local Symptoms (Engerix Vaccine)

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
UMLS CUI-5
C0116078
Redness
Description

Redness

Data type

boolean

Alias
UMLS CUI [1]
C0332575
Redness size Day 0
Description

Redness size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 1
Description

Redness size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 2
Description

Redness size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 3
Description

Redness size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness Ongoing after Day 3?
Description

Redness Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0332575
UMLS CUI [1,2]
C3174772
If Redness is ongoing, record date of last Day of Symptoms
Description

If Redness is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0332575
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Swelling
Description

Swelling

Data type

boolean

Alias
UMLS CUI [1]
C0038999
Swelling Size Day 0
Description

Swelling Size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 1
Description

Swelling Size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 2
Description

Swelling Size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 3
Description

Swelling Size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Ongoing after Day 3? +
Description

Swelling Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C3174772
If Swelling is ongoing, record date of last Day of Symptoms
Description

If Swelling is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0038999
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Pain
Description

Pain

Data type

boolean

Alias
UMLS CUI [1]
C0030193
Pain intensity Day 0
Description

Pain intensity Day 0

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 1
Description

Pain intensity Day 1

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 2
Description

Pain intensity Day 2

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 3
Description

Pain intensity Day 3

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain Ongoing after Day 3?
Description

Pain Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C3174772
If Pain is ongoing, record date of last Day of Symptoms
Description

If Pain is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0030193
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Solicited Adverse Events - Local Symptoms (Infanrix Vaccine)
Description

Solicited Adverse Events - Local Symptoms (Infanrix Vaccine)

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
UMLS CUI-4
C1964896
Redness
Description

Redness

Data type

boolean

Alias
UMLS CUI [1]
C0332575
Redness size Day 0
Description

Redness size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 1
Description

Redness size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 2
Description

Redness size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 3
Description

Redness size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness Ongoing after Day 3?
Description

Redness Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0332575
UMLS CUI [1,2]
C3174772
If Redness is ongoing, record date of last Day of Symptoms
Description

If Redness is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0332575
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Swelling
Description

Swelling

Data type

boolean

Alias
UMLS CUI [1]
C0038999
Swelling Size Day 0
Description

Swelling Size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 1
Description

Swelling Size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 2
Description

Swelling Size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 3
Description

Swelling Size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Ongoing after Day 3?
Description

Swelling Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C3174772
If Swelling is ongoing, record date of last Day of Symptoms
Description

If Swelling is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0038999
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Pain
Description

Pain

Data type

boolean

Alias
UMLS CUI [1]
C0030193
Pain intensity Day 0
Description

Pain intensity Day 0

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 1
Description

Pain intensity Day 1

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 2
Description

Pain intensity Day 2

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 3
Description

Pain intensity Day 3

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain Ongoing after Day 3?
Description

Pain Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C3174772
If Pain is ongoing, record date of last Day of Symptoms
Description

If Pain is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0030193
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Solicited Adverse Events - Local Symptoms (Prevnar Vaccine)
Description

Solicited Adverse Events - Local Symptoms (Prevnar Vaccine)

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
UMLS CUI-4
C0876134
Redness
Description

Redness

Data type

boolean

Alias
UMLS CUI [1]
C0332575
Redness size Day 0
Description

Redness size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 1
Description

Redness size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 2
Description

Redness size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 3
Description

Redness size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness Ongoing after Day 3?
Description

Redness Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0332575
UMLS CUI [1,2]
C3174772
If Redness is ongoing, record date of last Day of Symptoms
Description

If Redness is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0332575
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Swelling
Description

Swelling

Data type

boolean

Alias
UMLS CUI [1]
C0038999
Swelling Size Day 0
Description

Swelling Size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 1
Description

Swelling Size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 2
Description

Swelling Size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 3
Description

Swelling Size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Ongoing after Day 3?
Description

Swelling Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C3174772
If Swelling is ongoing, record date of last Day of Symptoms
Description

If Swelling is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0038999
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Pain
Description

Pain

Data type

boolean

Alias
UMLS CUI [1]
C0030193
Pain intensity Day 0
Description

Pain intensity Day 0

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 1
Description

Pain intensity Day 1

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 2
Description

Pain intensity Day 2

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 3
Description

Pain intensity Day 3

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain Ongoing after Day 3?
Description

Pain Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C3174772
If Pain is ongoing, record date of last Day of Symptoms
Description

If Pain is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0030193
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Solicited Adverse Events - Local Symptoms (HibTITER® Vaccine)
Description

Solicited Adverse Events - Local Symptoms (HibTITER® Vaccine)

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
UMLS CUI-4
C1524027
Redness
Description

Redness

Data type

boolean

Alias
UMLS CUI [1]
C0332575
Redness size Day 0
Description

Redness size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 1
Description

Redness size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 2
Description

Redness size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 3
Description

Redness size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness Ongoing after Day 3?
Description

Redness Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0332575
UMLS CUI [1,2]
C3174772
If Redness is ongoing, record date of last Day of Symptoms
Description

If Redness is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0332575
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Swelling
Description

Swelling

Data type

boolean

Alias
UMLS CUI [1]
C0038999
Swelling Size Day 0
Description

Swelling Size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 1
Description

Swelling Size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 2
Description

Swelling Size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 3
Description

Swelling Size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Ongoing after Day 3?
Description

Swelling Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C3174772
If Swelling is ongoing, record date of last Day of Symptoms
Description

If Swelling is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0038999
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Pain
Description

Pain

Data type

boolean

Alias
UMLS CUI [1]
C0030193
Pain intensity Day 0
Description

Pain intensity Day 0

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 1
Description

Pain intensity Day 1

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 2
Description

Pain intensity Day 2

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 3
Description

Pain intensity Day 3

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain Ongoing after Day 3?
Description

Pain Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C3174772
If Pain is ongoing, record date of last Day of Symptoms
Description

If Pain is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0030193
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Solicited Adverse Events - Local Symptoms (ActHib Vaccine)
Description

Solicited Adverse Events - Local Symptoms (ActHib Vaccine)

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
UMLS CUI-4
C0042196
Redness
Description

Redness

Data type

boolean

Alias
UMLS CUI [1]
C0332575
Redness size Day 0
Description

Redness size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 1
Description

Redness size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 2
Description

Redness size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 3
Description

Redness size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness Ongoing after Day 3?
Description

Redness Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0332575
UMLS CUI [1,2]
C3174772
If Redness is ongoing, record date of last Day of Symptoms
Description

If Redness is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0332575
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Swelling
Description

Swelling

Data type

boolean

Alias
UMLS CUI [1]
C0038999
Swelling Size Day 0
Description

Swelling Size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 1
Description

Swelling Size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 2
Description

Swelling Size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 3
Description

Swelling Size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Ongoing after Day 3?
Description

Swelling Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C3174772
If Swelling is ongoing, record date of last Day of Symptoms
Description

If Swelling is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0038999
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Pain
Description

Pain

Data type

boolean

Alias
UMLS CUI [1]
C0030193
Pain intensity Day 0
Description

Pain intensity Day 0

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 1
Description

Pain intensity Day 1

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 2
Description

Pain intensity Day 2

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 3
Description

Pain intensity Day 3

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain Ongoing after Day 3?
Description

Pain Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C3174772
If Pain is ongoing, record date of last Day of Symptoms
Description

If Pain is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0030193
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Solicited Adverse Events - Local Symptoms (Comvax Vaccine)
Description

Solicited Adverse Events - Local Symptoms (Comvax Vaccine)

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C1457887
UMLS CUI-3
C0205276
UMLS CUI-4
C0535643
Redness
Description

Redness

Data type

boolean

Alias
UMLS CUI [1]
C0332575
Redness size Day 0
Description

Redness size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 1
Description

Redness size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 2
Description

Redness size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness size Day 3
Description

Redness size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0456389
UMLS CUI [1,2]
C0332575
mm
Redness Ongoing after Day 3?
Description

Redness Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0332575
UMLS CUI [1,2]
C3174772
If Redness is ongoing, record date of last Day of Symptoms
Description

If Redness is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0332575
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Swelling
Description

Swelling

Data type

boolean

Alias
UMLS CUI [1]
C0038999
Swelling Size Day 0
Description

Swelling Size Day 0

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 1
Description

Swelling Size Day 1

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 2
Description

Swelling Size Day 2

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Size Day 3
Description

Swelling Size Day 3

Data type

integer

Measurement units
  • mm
Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C0456389
mm
Swelling Ongoing after Day 3?
Description

Swelling Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0038999
UMLS CUI [1,2]
C3174772
If Swelling is ongoing, record date of last Day of Symptoms
Description

If Swelling is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0038999
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Pain
Description

Pain

Data type

boolean

Alias
UMLS CUI [1]
C0030193
Pain intensity Day 0
Description

Pain intensity Day 0

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 1
Description

Pain intensity Day 1

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 2
Description

Pain intensity Day 2

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain intensity Day 3
Description

Pain intensity Day 3

Data type

integer

Alias
UMLS CUI [1]
C1320357
Pain Ongoing after Day 3?
Description

Pain Ongoing after Day 3?

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C3174772
If Pain is ongoing, record date of last Day of Symptoms
Description

If Pain is ongoing, record date of last Day of Symptoms

Data type

date

Alias
UMLS CUI [1]
C0030193
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1517741
UMLS CUI [2,3]
C1457887
Laboratory Tests
Description

Laboratory Tests

Alias
UMLS CUI-1
C0022885
Has a blood sample been taken?
Description

Has a blood sample been taken?

Data type

boolean

Alias
UMLS CUI [1]
C0005834
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Similar models

Dose 3 - Solicited Adverse Events - Local Symptoms; Visit 5 - Laboratory Tests

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administration
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Item Group
Solicited Adverse Events - Local Symptoms
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
Item
Has the subject experienced any of the following local (at administration site) signs/symptoms during the solicited period?
text
C0037088 (UMLS CUI [1,1])
C0205276 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0013153 (UMLS CUI [1,4])
Has the subject experienced any of the following local (at administration site) signs/symptoms during the solicited period? Has the subject experienced any of the following local (at administration site) signs/symptoms during the solicited period?
Code List
Has the subject experienced any of the following local (at administration site) signs/symptoms during the solicited period?
CL Item
Unknown  (U)
CL Item
No  (N)
CL Item
Yes (Y)
Item Group
Solicited Adverse Events - Local Symptoms (Engerix Vaccine)
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0116078 (UMLS CUI-5)
Redness
Item
Redness
boolean
C0332575 (UMLS CUI [1])
Redness size Day 0
Item
Redness size Day 0
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 1
Item
Redness size Day 1
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 2
Item
Redness size Day 2
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 3
Item
Redness size Day 3
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness Ongoing after Day 3?
Item
Redness Ongoing after Day 3?
boolean
C0332575 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Redness is ongoing, record date of last Day of Symptoms
Item
If Redness is ongoing, record date of last Day of Symptoms
date
C0332575 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Swelling
Item
Swelling
boolean
C0038999 (UMLS CUI [1])
Swelling Size Day 0
Item
Swelling Size Day 0
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 1
Item
Swelling Size Day 1
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 2
Item
Swelling Size Day 2
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 3
Item
Swelling Size Day 3
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Ongoing after Day 3?
Item
Swelling Ongoing after Day 3? +
boolean
C0038999 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Swelling is ongoing, record date of last Day of Symptoms
Item
If Swelling is ongoing, record date of last Day of Symptoms
date
C0038999 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Pain
Item
Pain
boolean
C0030193 (UMLS CUI [1])
Item
Pain intensity Day 0
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 0
Code List
Pain intensity Day 0
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
Item
Pain intensity Day 1
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 1
Code List
Pain intensity Day 1
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
Item
Pain intensity Day 2
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 2
Code List
Pain intensity Day 2
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
Item
Pain intensity Day 3
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 3
Code List
Pain intensity Day 3
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
Pain Ongoing after Day 3?
Item
Pain Ongoing after Day 3?
boolean
C0030193 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Pain is ongoing, record date of last Day of Symptoms
Item
If Pain is ongoing, record date of last Day of Symptoms
date
C0030193 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Item Group
Solicited Adverse Events - Local Symptoms (Infanrix Vaccine)
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C1964896 (UMLS CUI-4)
Redness
Item
Redness
boolean
C0332575 (UMLS CUI [1])
Redness size Day 0
Item
Redness size Day 0
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 1
Item
Redness size Day 1
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 2
Item
Redness size Day 2
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 3
Item
Redness size Day 3
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness Ongoing after Day 3?
Item
Redness Ongoing after Day 3?
boolean
C0332575 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Redness is ongoing, record date of last Day of Symptoms
Item
If Redness is ongoing, record date of last Day of Symptoms
date
C0332575 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Swelling
Item
Swelling
boolean
C0038999 (UMLS CUI [1])
Swelling Size Day 0
Item
Swelling Size Day 0
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 1
Item
Swelling Size Day 1
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 2
Item
Swelling Size Day 2
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 3
Item
Swelling Size Day 3
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Ongoing after Day 3?
Item
Swelling Ongoing after Day 3?
boolean
C0038999 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Swelling is ongoing, record date of last Day of Symptoms
Item
If Swelling is ongoing, record date of last Day of Symptoms
date
C0038999 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Pain
Item
Pain
boolean
C0030193 (UMLS CUI [1])
Item
Pain intensity Day 0
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 0
Code List
Pain intensity Day 0
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 1
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 1
Code List
Pain intensity Day 1
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 2
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 2
Code List
Pain intensity Day 2
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 3
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 3
Code List
Pain intensity Day 3
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Pain Ongoing after Day 3?
Item
Pain Ongoing after Day 3?
boolean
C0030193 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Pain is ongoing, record date of last Day of Symptoms
Item
If Pain is ongoing, record date of last Day of Symptoms
date
C0030193 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Item Group
Solicited Adverse Events - Local Symptoms (Prevnar Vaccine)
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0876134 (UMLS CUI-4)
Redness
Item
Redness
boolean
C0332575 (UMLS CUI [1])
Redness size Day 0
Item
Redness size Day 0
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 1
Item
Redness size Day 1
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 2
Item
Redness size Day 2
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 3
Item
Redness size Day 3
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness Ongoing after Day 3?
Item
Redness Ongoing after Day 3?
boolean
C0332575 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Redness is ongoing, record date of last Day of Symptoms
Item
If Redness is ongoing, record date of last Day of Symptoms
date
C0332575 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Swelling
Item
Swelling
boolean
C0038999 (UMLS CUI [1])
Swelling Size Day 0
Item
Swelling Size Day 0
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 1
Item
Swelling Size Day 1
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 2
Item
Swelling Size Day 2
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 3
Item
Swelling Size Day 3
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Ongoing after Day 3?
Item
Swelling Ongoing after Day 3?
boolean
C0038999 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Swelling is ongoing, record date of last Day of Symptoms
Item
If Swelling is ongoing, record date of last Day of Symptoms
date
C0038999 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Pain
Item
Pain
boolean
C0030193 (UMLS CUI [1])
Item
Pain intensity Day 0
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 0
Code List
Pain intensity Day 0
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 1
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 1
Code List
Pain intensity Day 1
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 2
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 2
Code List
Pain intensity Day 2
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 3
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 3
Code List
Pain intensity Day 3
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Pain Ongoing after Day 3?
Item
Pain Ongoing after Day 3?
boolean
C0030193 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Pain is ongoing, record date of last Day of Symptoms
Item
If Pain is ongoing, record date of last Day of Symptoms
date
C0030193 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Item Group
Solicited Adverse Events - Local Symptoms (HibTITER® Vaccine)
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C1524027 (UMLS CUI-4)
Redness
Item
Redness
boolean
C0332575 (UMLS CUI [1])
Redness size Day 0
Item
Redness size Day 0
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 1
Item
Redness size Day 1
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 2
Item
Redness size Day 2
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 3
Item
Redness size Day 3
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness Ongoing after Day 3?
Item
Redness Ongoing after Day 3?
boolean
C0332575 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Redness is ongoing, record date of last Day of Symptoms
Item
If Redness is ongoing, record date of last Day of Symptoms
date
C0332575 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Swelling
Item
Swelling
boolean
C0038999 (UMLS CUI [1])
Swelling Size Day 0
Item
Swelling Size Day 0
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 1
Item
Swelling Size Day 1
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 2
Item
Swelling Size Day 2
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 3
Item
Swelling Size Day 3
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Ongoing after Day 3?
Item
Swelling Ongoing after Day 3?
boolean
C0038999 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Swelling is ongoing, record date of last Day of Symptoms
Item
If Swelling is ongoing, record date of last Day of Symptoms
date
C0038999 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Pain
Item
Pain
boolean
C0030193 (UMLS CUI [1])
Item
Pain intensity Day 0
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 0
Code List
Pain intensity Day 0
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 1
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 1
Code List
Pain intensity Day 1
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 2
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 2
Code List
Pain intensity Day 2
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 3
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 3
Code List
Pain intensity Day 3
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Pain Ongoing after Day 3?
Item
Pain Ongoing after Day 3?
boolean
C0030193 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Pain is ongoing, record date of last Day of Symptoms
Item
If Pain is ongoing, record date of last Day of Symptoms
date
C0030193 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Item Group
Solicited Adverse Events - Local Symptoms (ActHib Vaccine)
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0042196 (UMLS CUI-4)
Redness
Item
Redness
boolean
C0332575 (UMLS CUI [1])
Redness size Day 0
Item
Redness size Day 0
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 1
Item
Redness size Day 1
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 2
Item
Redness size Day 2
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 3
Item
Redness size Day 3
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness Ongoing after Day 3?
Item
Redness Ongoing after Day 3?
boolean
C0332575 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Redness is ongoing, record date of last Day of Symptoms
Item
If Redness is ongoing, record date of last Day of Symptoms
date
C0332575 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Swelling
Item
Swelling
boolean
C0038999 (UMLS CUI [1])
Swelling Size Day 0
Item
Swelling Size Day 0
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 1
Item
Swelling Size Day 1
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 2
Item
Swelling Size Day 2
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 3
Item
Swelling Size Day 3
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Ongoing after Day 3?
Item
Swelling Ongoing after Day 3?
boolean
C0038999 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Swelling is ongoing, record date of last Day of Symptoms
Item
If Swelling is ongoing, record date of last Day of Symptoms
date
C0038999 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Pain
Item
Pain
boolean
C0030193 (UMLS CUI [1])
Item
Pain intensity Day 0
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 0
Code List
Pain intensity Day 0
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 1
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 1
Code List
Pain intensity Day 1
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 2
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 2
Code List
Pain intensity Day 2
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 3
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 3
Code List
Pain intensity Day 3
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Pain Ongoing after Day 3?
Item
Pain Ongoing after Day 3?
boolean
C0030193 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Pain is ongoing, record date of last Day of Symptoms
Item
If Pain is ongoing, record date of last Day of Symptoms
date
C0030193 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Item Group
Solicited Adverse Events - Local Symptoms (Comvax Vaccine)
C0877248 (UMLS CUI-1)
C1457887 (UMLS CUI-2)
C0205276 (UMLS CUI-3)
C0535643 (UMLS CUI-4)
Redness
Item
Redness
boolean
C0332575 (UMLS CUI [1])
Redness size Day 0
Item
Redness size Day 0
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 1
Item
Redness size Day 1
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 2
Item
Redness size Day 2
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness size Day 3
Item
Redness size Day 3
integer
C0456389 (UMLS CUI [1,1])
C0332575 (UMLS CUI [1,2])
Redness Ongoing after Day 3?
Item
Redness Ongoing after Day 3?
boolean
C0332575 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Redness is ongoing, record date of last Day of Symptoms
Item
If Redness is ongoing, record date of last Day of Symptoms
date
C0332575 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Swelling
Item
Swelling
boolean
C0038999 (UMLS CUI [1])
Swelling Size Day 0
Item
Swelling Size Day 0
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 1
Item
Swelling Size Day 1
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 2
Item
Swelling Size Day 2
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Size Day 3
Item
Swelling Size Day 3
integer
C0038999 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
Swelling Ongoing after Day 3?
Item
Swelling Ongoing after Day 3?
boolean
C0038999 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Swelling is ongoing, record date of last Day of Symptoms
Item
If Swelling is ongoing, record date of last Day of Symptoms
date
C0038999 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Pain
Item
Pain
boolean
C0030193 (UMLS CUI [1])
Item
Pain intensity Day 0
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 0
Code List
Pain intensity Day 0
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 1
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 1
Code List
Pain intensity Day 1
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 2
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 2
Code List
Pain intensity Day 2
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Item
Pain intensity Day 3
integer
C1320357 (UMLS CUI [1])
Pain intensity Day 3
Code List
Pain intensity Day 3
CL Item
0  (1)
CL Item
1  (2)
CL Item
2  (3)
CL Item
3 (4)
Pain Ongoing after Day 3?
Item
Pain Ongoing after Day 3?
boolean
C0030193 (UMLS CUI [1,1])
C3174772 (UMLS CUI [1,2])
If Pain is ongoing, record date of last Day of Symptoms
Item
If Pain is ongoing, record date of last Day of Symptoms
date
C0030193 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1517741 (UMLS CUI [2,2])
C1457887 (UMLS CUI [2,3])
Item Group
Laboratory Tests
C0022885 (UMLS CUI-1)
Has a blood sample been taken?
Item
Has a blood sample been taken?
boolean
C0005834 (UMLS CUI [1])
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