Concomitant vaccination during during study protocol period | except for study vaccination
Item
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the protocol?
text
C0042196 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C1948053 (UMLS CUI [1,4])
C2348563 (UMLS CUI [1,5])
C1705847 (UMLS CUI [2,1])
C0042196 (UMLS CUI [2,2])
C3854006 (UMLS CUI [2,3])
Trade name | generic name concomitant vaccination
Item
Please record the trade name and/or generic name of the concomitant vaccination.
text
C2360065 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,3])
C0592502 (UMLS CUI [2,1])
C0042196 (UMLS CUI [2,2])
C2347852 (UMLS CUI [2,3])
Item
Please record the route of administration of the concomitant vaccination.
text
C0013153 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,3])
Code List
Please record the route of administration of the concomitant vaccination.
CL Item
Intramuscular (IM)
CL Item
Subcutaneous (SC)
Date of administration concomitant vaccination
Item
Please record the vaccine administration date of the concomitant vaccination.
date
C0011008 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,3])
Clinical study sponsor comment
Item
For GSK
text
C2347796 (UMLS CUI [1,1])
C0947611 (UMLS CUI [1,2])