Patient ID (derived)
Item
Patient ID (derived)
text
C2348585 (UMLS CUI [1])
Trial medication end date
Item
Discont. of Trial Medication: Date
date
C1521826 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
Discont. of Trial Medication: Date Status
text
C1521826 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
Code List
Discont. of Trial Medication: Date Status
Code List
Reason (Inv. considers...)
CL Item
Inv. considers it would be in the best interests of the patient (1)
Code List
Reason (Unacceptable toxicity...)
CL Item
Unacceptable toxicity of the study drug (1)
Code List
Reason (HIV infection)
CL Item
HIV infection (1)
Code List
Reason (Patient requests discontinuation)
CL Item
Patient requests discontinuation (1)
Code List
Reason (Patient unable or unwilling to comply...)
CL Item
Pat. is unable or unwilling to comply with planned study safety monitoring (1)
Code List
Reason (Other reason)
Discontinuation reason
Item
Discont. of Trial Medication: Reason Text
text
C0457454 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Date of Signature
Item
Discont. of Trial Medication: Date of Signature
date
C1519316 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Code List
Discont. of Trial Medication: Date of Sig. Status
Code List
Discont. of Trial Medication: Signature yes/no
Comment Discont. Trial Med.
Item
text