Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
non-serious adverse events
Item
Has any non-serious adverse events occurred within one month (minimum 30 days) post-vaccination, excluding those recorded on the Solicited Adverse Events pages?
boolean
C1518404 (UMLS CUI [1])
Description Non- Serious Adverse Events
Item
Description
text
C0678257 (UMLS CUI [1,1])
C1518404 (UMLS CUI [1,2])
Item
Administration sites
integer
C1515974 (UMLS CUI [1,1])
C0042210 (UMLS CUI [1,2])
Code List
Administration sites
CL Item
Hib-MenCY OR Hib-MenC vaccine [ 9 0 1 ] (1)
CL Item
MenC vaccine [ 9 0 2 ] (2)
CL Item
DTPa-HBV-IPV vaccine [ 1 4 ] (3)
CL Item
DTPa-HBV-IPV/Hib vaccine [ 3 8 ] (4)
site vaccines
Item
Non-administration site
boolean
C1515974 (UMLS CUI [1,1])
C0042210 (UMLS CUI [1,2])
Date Started
Item
Date Started
date
C0808070 (UMLS CUI [1])
Date Started
Item
Date Started-during immediate post-vaccination period (at least 30 minutes)
boolean
C0808070 (UMLS CUI [1])
Date Stopped
Item
Date Stopped
date
C0806020 (UMLS CUI [1])
Item
Intensity
text
C1710066 (UMLS CUI [1])
CL Item
Moderate (Moderate)
adverse event drug study
Item
Relationship to investigational products: Is there a reasonable possibility that the AE may have been caused by the investigational product?
boolean
C0877248 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
Item
Outcome
integer
C1705586 (UMLS CUI [1])
CL Item
Recovered / Resolved (1)
CL Item
Recovering / resolving (2)
CL Item
Not recovered / not resolved (3)
CL Item
Recovered with sequelae /Resolved with sequelae (4)
medical advice
Item
Did the subject seek medical advice?
boolean
C1386497 (UMLS CUI [1])
Item
If yes please specify type:
integer
C1386497 (UMLS CUI [1])
Code List
If yes please specify type:
CL Item
HO: Hospitalisation (1)
CL Item
ER: Emergency room (2)
CL Item
MD: Medical doctor (3)