Information:
Error:
NON-SERIOUS ADVERSE EVENT
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
DEFINITION OF A NON-SERIOUS ADVERSE EVENT
Item
DEFINITION OF A NON-SERIOUS ADVERSE EVENT
text
C1518404 (UMLS CUI [1])
Item
INSTRUCTIONS FOR COMPLETING NON-SERIOUS ADVERSE EVENTS
text
Code List
INSTRUCTIONS FOR COMPLETING NON-SERIOUS ADVERSE EVENTS
CL Item
Diagnosis (Diagnosis)
C0011900 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Start Date (Start Date)
C0808070 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Start Time (Start Time)
C1301880 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Outcome (Outcome)
C1705586 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
End Date (End Date)
C0806020 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
End Time (End Time)
C1522314 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Maximum Intensity (Maximum Intensity)
C1710066 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Withdrawal (Withdrawal)
C2349954 (UMLS CUI-1)
C1519255 (UMLS CUI-2)
(Comment:en)
C1519255 (UMLS CUI-2)
(Comment:en)
NON-SERIOUS ADVERSE EVENTS
Item
NON-SERIOUS ADVERSE EVENTS
text
C1518404 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Start Time
Item
Start Time
time
C1301880 (UMLS CUI [1])
Outcome
Item
Outcome
text
C1705586 (UMLS CUI [1])
End Date
Item
End Date
text
C0806020 (UMLS CUI [1])
End time
Item
End time
time
C1522314 (UMLS CUI [1])
Maximum Intensity
Item
Maximum Intensity
text
C1710066 (UMLS CUI [1])
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
Item
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
text
C1704758 (UMLS CUI [1,1])
C1518404 (UMLS CUI [1,2])
C1518404 (UMLS CUI [1,2])
Withdrawal
Item
Withdrawal
text
C2349954 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
Relationship to lnvestigational Product(s)
Item
Relationship to lnvestigational Product(s)
text
C0304229 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
C1522508 (UMLS CUI [1,2])
Did the subject experience any non-serious adverse events during the study?
Item
Did the subject experience any non-serious adverse events during the study?
boolean
C1518404 (UMLS CUI [1])