Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
patient's initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
patient number
Item
Patient No.
integer
C1830427 (UMLS CUI [1])
Item Group
1- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
4- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
12- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
24- HOUR POST-DOSE QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
QUERY FOR ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Item
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
integer
C0877248 (UMLS CUI [1])
Code List
Have there been any adverse events observed or elicited by the following direct question to the patient: "Have you felt different in any way since starting the new treatment?"
Item Group
ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Item
Has the patient had any new and/or continuing adverse events?
integer
C0877248 (UMLS CUI [1])
Code List
Has the patient had any new and/or continuing adverse events?
Item Group
ADVERSE EVENT
C0877248 (UMLS CUI-1)
Item
Severity of Adverse Events
text
C1710066 (UMLS CUI [1])
Code List
Severity of Adverse Events
CL Item
Serious (Serious)
start date and time of adverse event
Item
START DATE and TIME
datetime
C2697888 (UMLS CUI [1])
C2697889 (UMLS CUI [2])
stop date and time of adverse event
Item
STOP DATE and TIME
datetime
C2697886 (UMLS CUI [1])
C0877248 (UMLS CUI [2,1])
C1522314 (UMLS CUI [2,2])
Item
INTENSITY
integer
C1710066 (UMLS CUI [1])
Item
RELATIONSHIP TO DRUG
integer
C0277579 (UMLS CUI [1])
Code List
RELATIONSHIP TO DRUG
CL Item
SUSPECTED (reasonable possibility) (3)
Item
ACTION TAKEN WITH TEST DRUG
integer
C0580105 (UMLS CUI [1])
Code List
ACTION TAKEN WITH TEST DRUG
CL Item
DOSE INCREASED (3)
CL Item
DRUG INTERRUPTED/RESTARTED (4)
Item
CORRECTIVE THERAPY
integer
C0877248 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Code List
CORRECTIVE THERAPY
Item
EVENT COURSE
integer
C0877248 (UMLS CUI [1,1])
C0750729 (UMLS CUI [1,2])
Item
OUTCOME
integer
C1705586 (UMLS CUI [1])