Date of Visit
Item
Date of Visit
date
C0545082 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
blood sample
Item
Has a blood sample been taken?
boolean
C0005834 (UMLS CUI [1])
Date sample taken
Item
Date sample taken
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Hepatitis B vaccine
Item
Did the subject receive a dose of Hepatitis B vaccine since the last visit
boolean
C2240392 (UMLS CUI [1])
hepatitis B
Item
Did the subject develop clinical signs possibly related to hepatitis B since last visit or suffered from hepatitis B?
boolean
C0019163 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0267797 (UMLS CUI [2])
hepatitis B
Item
If Yes, please specify
text
C0019163 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0267797 (UMLS CUI [2])
follow-up study
Item
Would the subject be willing to participate in a follow-up study?
boolean
C0016441 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
Item
Please specify the most appropriate reason
integer
C0016441 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
Code List
Please specify the most appropriate reason
CL Item
Adverse Events, or Serious Adverse Events (1)
reason
Item
Please specify if Adverse Events, or Serious Adverse Events
text
C0016441 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
reason
Item
Please specify if Other
text
C0016441 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
Investigators signature
Item
Investigators signature
text
C2346576 (UMLS CUI [1])