Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Center number
Item
Center number
text
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Informed Consent Date
Item
Informed Consent Date
time
C0021430 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Gender
text
C0079399 (UMLS CUI [1])
Item
Race
text
C0034510 (UMLS CUI [1])
Race
Item
Race, if other please specify
text
C0034510 (UMLS CUI [1])
blood sample
Item
Has a blood sample been taken?
boolean
C0005834 (UMLS CUI [1])
Hepatitis A immunoglobulins
Item
Has the subject received a dose of Hepatitis A immunoglobulins within 6 months prior to bleeding ?
boolean
C3652495 (UMLS CUI [1,1])
C0019080 (UMLS CUI [1,2])
Hepatitis A vaccine
Item
Has the subject received a dose of monovalent or combined Hepatitis A vaccine outside the study ?
boolean
C0170300 (UMLS CUI [1])
Item
Has the subject received a dose of monovalent or combined Hepatitis A vaccine outside the study ? If Yes, please specify
integer
C0170300 (UMLS CUI [1,1])
C3543421 (UMLS CUI [1,2])
Code List
Has the subject received a dose of monovalent or combined Hepatitis A vaccine outside the study ? If Yes, please specify
CL Item
Hepatitis A vaccine (1)
CL Item
Combined Hepatitis A (or other) vaccine (2)
Hepatitis A
Item
Did the subject suffer from Hepatitis A since last visit?
boolean
C0019159 (UMLS CUI [1])