Study Site; Numbers
Item
Site number
text
C2825164 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Person Initials
Item
Patient's initials
text
C2986440 (UMLS CUI [1])
Clinical Trial Subject Unique Identifier
Item
Patient's trial number
text
C2348585 (UMLS CUI [1])
Pharmaceutical Preparations; Additional Therapy; Taken; Clinical Trials; During
Item
Were any additional medications other than antiepileptic drugs taken during the study? (If yes, record below.)
boolean
C0013227 (UMLS CUI [1,1])
C1706712 (UMLS CUI [1,2])
C1883727 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
C0347984 (UMLS CUI [1,5])
Date in time; Pharmaceutical Preparations; Taken
Item
Date medication first taken during study
date
C0011008 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C1883727 (UMLS CUI [1,3])
Medication name | Generic drug name
Item
Name of drug/ Generic
text
C2360065 (UMLS CUI [1])
C0592502 (UMLS CUI [2])
Antiepileptic Agents; Medication name
Item
Name of antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antiepileptic Agents; Start Date
Item
Start date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Antiepileptic Agents; End date
Item
Stop date antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Time
Item
Time of dose 1
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 1
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 2
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 2
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 3
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 3
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 4
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 4
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 5
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 5
float
C0178602 (UMLS CUI [1])
Antiepileptic Agents; Medication name
Item
Name of antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antiepileptic Agents; Start Date
Item
Start date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Antiepileptic Agents; End date
Item
Stop date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Time
Item
Time of dose 1
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 1
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 2
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 2
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 3
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 3
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 4
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 4
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 5
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 5
float
C0178602 (UMLS CUI [1])
Antiepileptic Agents; Medication name
Item
Name of antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antiepileptic Agents; Start Date
Item
Start date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Antiepileptic Agents; End date
Item
Stop date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Time
Item
Time of dose 1
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 1
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 2
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 2
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 3
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 3
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 4
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 4
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 5
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 5
float
C0178602 (UMLS CUI [1])
Experimental drug; Start Date
Item
Study Medication Start date
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Experimental drug; End Date
Item
Study Medication Stop Date
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Schedule (document type); Study Protocol; Requirement
Item
Protocol required scheduled dose
float
C0178602 (UMLS CUI [1,1])
C0086960 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C1514873 (UMLS CUI [1,4])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Medication dose; Calculated
Item
Calculated dose
text
C3174092 (UMLS CUI [1,1])
C0444686 (UMLS CUI [1,2])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Time; a.m.
Item
Investigator actual prescribed dose - A.M. dose - Time
time
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C4331833 (UMLS CUI [2,3])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Dosage; a.m.
Item
Investigator actual prescribed dose - A.M. dose - Amount
float
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C4331833 (UMLS CUI [2,3])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Time; post meridiem
Item
Investigator actual prescribed dose - P.M. dose - Time
time
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C1509133 (UMLS CUI [2,3])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Dosage; post meridiem
Item
Investigator actual prescribed dose - P.M. dose - Amount
float
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C1509133 (UMLS CUI [2,3])
Experimental drug; Start Date
Item
Study Medication Start date
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Experimental drug; End Date
Item
Study Medication Stop Date
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Experimental drug; Dosage; a.m.
Item
A.M. dose - Amount of dose
float
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C4331833 (UMLS CUI [1,3])
Experimental drug; Time; a.m.
Item
A.M. dose - Time
time
C0304229 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C4331833 (UMLS CUI [1,3])
Experimental drug; Dosage; post meridiem
Item
P.M. dose - Amount of dose
float
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1509133 (UMLS CUI [1,3])
Experimental drug; Time; post meridiem
Item
P.M. dose - Time
time
C0304229 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C1509133 (UMLS CUI [1,3])