Dosing Details

  1. StudyEvent: ODM
    1. Dosing Details
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Item
Study Week
integer
C0008972 (UMLS CUI [1,1])
C0439230 (UMLS CUI [1,2])
Code List
Study Week
CL Item
Week 1 (1)
CL Item
Week 2 (2)
CL Item
Week 3 (3)
Item Group
Dosing Details
C0013227 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C1522508 (UMLS CUI-3)
Study Day
Item
Study Day
integer
C2826182 (UMLS CUI [1])
Date
Item
Date
date
C0011008 (UMLS CUI [1])
Dosing time
Item
Dosing time
time
C0040223 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Investigator's name
Item
Dose checked and administered by:
text
C2826892 (UMLS CUI [1])

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