ID
35262
Description
Study ID: 102970 Clinical Study ID: 102970 Study Title: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01017952 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: GW642444 Inhalation Powder; FF/GW642444 Inhalation Powder Trade Name: Fluticasone Furoate;Fluticasone Propionate;Fluticasone Propionate/Salmeterol;Salmeterol;Vilanterol Study Indication: Pulmonary Disease, Chronic Obstructive
Keywords
Versions (2)
- 2/25/19 2/25/19 -
- 5/28/19 5/28/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
February 25, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Effect of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on Annual Rate of Exacerbations in Subjects with COPD 102970
LOGS
- StudyEvent: ODM
Description
Non-Serious Adverse Event
Alias
- UMLS CUI-1
- C1518404
Description
Non-serious Adverse Event
Data type
text
Alias
- UMLS CUI [1]
- C1518404
Description
Non-serious Adverse Event, Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
Description
Non-serious Adverse Event, Adverse Event Outcome
Data type
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Description
Non-serious Adverse Event, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Description
Non-serious Adverse Event, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Description
Non-serious Adverse Event, Frequencies
Data type
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Description
Non-serious Adverse Event, Severity of Adverse Event
Data type
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Description
Non-serious Adverse Event, Action Taken with Study Treatment
Data type
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Description
Non-serious Adverse Event, Withdrawal by Subject
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710677
Description
Non-serious Adverse Event, Investigational New Drugs, Relationships
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Description
Serious Adverse Events
Alias
- UMLS CUI-1
- C1519255
Description
Serious Adverse Event, Experimental drug, Initiation
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C1704686
Description
Serious Adverse Event
Data type
text
Alias
- UMLS CUI [1]
- C1519255
Description
Serious Adverse Event, Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
Description
Serious Adverse Event, Adverse Event Outcome
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Description
Serious Adverse Event, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Description
Serious Adverse Event, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Description
Serious Adverse Event, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Description
Serious Adverse Event, Severity of Adverse Event
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710066
Description
Serious Adverse Event, Action Taken with Study Treatment
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1704758
Description
Serious Adverse Event, Withdrawal by Subject
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710677
Description
Serious Adverse Event, Investigational New Drugs, Relationships
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Description
Serious Adverse Event, Subject Study Participation Status, Relationships
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0439849
Description
Serious Adverse Event, Start Date, Start time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Description
Serious Adverse Event, Symptom intensity
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
Description
Serious Adverse Event, Adverse Event Grade Code
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2985911
Description
Serious Adverse Event, Symptom intensity, Adverse Event Grade Code
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C2985911
Description
Serious Adverse Event, Seriousness of Adverse Event
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710056
Description
Serious Adverse Event, Concomitant Agent, Medication name
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C2360065
Description
Serious Adverse Event, Concomitant Agent, Dosage
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0178602
Description
Serious Adverse Event, Concomitant Agent, Unit
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0439148
Description
Serious Adverse Event, Concomitant Agent, Frequencies
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0439603
Description
Serious Adverse Event, Concomitant Agent, Drug Administration Routes
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0013153
Description
Serious Adverse Event, Concomitant Medication Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826734
Description
Serious Adverse Event, Concomitant Medication Ongoing
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826666
Description
Serious Adverse Event, Concomitant Medication End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826744
Description
Serious Adverse Event, Concomitant Agent, Indication
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0392360
Description
Serious Adverse Event, Concomitant Agent, Type
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0332307
Description
COPD Exacerbations
Alias
- UMLS CUI-1
- C0740304
Description
COPD exacerbation, Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0808070
Description
COPD exacerbation, Patient Outcome
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C1547647
Description
COPD exacerbation, Recovered or Resolved, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0806020
Description
COPD exacerbation, Fatal, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C0806020
Description
COPD exaverbation, Severities
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0439793
Description
COPD exacerbation, Withdraw
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C2349954
Description
COPD exacerbation, Causations
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0085978
Description
COPD exacerbation, Adrenal Cortex Hormones
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0001617
Description
COPD exacerbation, Antibiotics
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0003232
Description
COPD exacerbation, Hospitalization
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0019993
Description
COPD exacerbation, Rescue remedy, Changed status
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0884980
- UMLS CUI [1,3]
- C0443172
Description
COPD exacerbation, Plain chest X-ray
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0039985
Description
COPD exacerbation, Home care of patient, Count of entities
Data type
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0204977
- UMLS CUI [1,3]
- C0449788
Description
COPD exacerbation, Physicisn, Visit, Count of entities
Data type
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0031831
- UMLS CUI [1,3]
- C0545082
- UMLS CUI [1,4]
- C0449788
Description
COPD exacerbation, Clinic Visit, Outpatient, Count of entities
Data type
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0008952
- UMLS CUI [1,3]
- C0545084
- UMLS CUI [1,4]
- C0449788
Description
COPD exacerbation, Emergency Room admission, Count of entities
Data type
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0583237
- UMLS CUI [1,3]
- C0449788
Description
COPD exacerbation, Hospitalization length of stay
Data type
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C3694481
Description
COPD exacerbation, Pharmaceutical Preparations, Medication name
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C2360065
Description
COPD exacerbation, Pharmaceutical Preparations, Dosage
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0178602
Description
COPD exacerbation, Pharmaceutical Preparations, Unit
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439148
Description
COPD exacerbation, Pharmaceutical Preparations, Frequencies
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439603
Description
COPD exacerbation, Pharmaceutical Preparations, Drug Administration Routes
Data type
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0013153
Description
COPD exacerbation, Pharmaceutical Preparations, Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0808070
Description
COPD exacerbation, Pharmaceutical Preparations, Previous
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0205156
Description
COPD exacerbation, Pharmaceutical Preparations, Continuous
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0549178
Description
COPD exacerbation, Pharmaceutical Preparations, End Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0806020
Description
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Description
Concomitant Agent, Medication name
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Description
Concomitant Agent, Dosage
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0178602
Description
Concomitant Agent, Unit
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439148
Description
Concomitant Agent, Frequencies
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439603
Description
Concomitant Agent, Drug Administration Routes
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0013153
Description
Concomitant Agent, Indication
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C3146298
Description
Concomitant Medication Start Date
Data type
date
Alias
- UMLS CUI [1]
- C2826734
Description
Concomitant Medication Previous Occurrence
Data type
boolean
Alias
- UMLS CUI [1]
- C2826667
Description
Concomitant Medication Ongoing
Data type
boolean
Alias
- UMLS CUI [1]
- C2826666
Description
Concomitant Medication End Date
Data type
date
Alias
- UMLS CUI [1]
- C2826744
Description
Concomitant Agent, Rescue remedy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0884980
Description
Concomitant Agent, Type
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332307
Description
Date of Visit/Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Description
Fracture
Alias
- UMLS CUI-1
- C0016658
Description
Fracture, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0016658
- UMLS CUI [1,2]
- C0011008
Description
Fracture, Anatomic Site, Code
Data type
text
Alias
- UMLS CUI [1,1]
- C0016658
- UMLS CUI [1,2]
- C1515974
- UMLS CUI [1,3]
- C0805701
Description
Fracture, Type
Data type
text
Alias
- UMLS CUI [1,1]
- C0016658
- UMLS CUI [1,2]
- C0332307
Description
Pharmacogenetic (PGx) Research Consent / Sample Collection
Alias
- UMLS CUI-1
- C0031325
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C0870078
Description
Pharmacogenetics, Informed Consent
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0021430
Description
Pharmacogenetics, Informed Consent, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0011008
Description
Pharmacogenetics, Sampling
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0870078
Description
Pharmacogenetics, Sampling, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
Description
Pharmacogenetics, Sampling, Reason
Data type
text
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0566251
Description
Double Blind Investigational Product Compliance
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Description
Experimental drug; Containers; Identifier
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0600091
Description
Experimental drug, Dispensed, Visit
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0545082
Description
Experimental drug, Dispensed, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0011008
Description
Dosage, Count, Start
Data type
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0750480
- UMLS CUI [1,3]
- C0452588
Description
Experimental drug, Return, Visit
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0545082
Description
Experimental drug, Return, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0011008
Description
Drug Dose, Stop
Data type
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C2746065
Description
Open Label Diskus Taken During Run-in
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Description
Experimental drug; Containers; Identifier
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0600091
Description
Experimental drug, Dispensed, Visit
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0545082
Description
Experimental drug, Dispensed, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0011008
Description
Dosage, Count, Start
Data type
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0750480
- UMLS CUI [1,3]
- C0452588
Description
Experimental drug, Return, Visit
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0545082
Description
Experimental drug, Return, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0011008
Description
Drug Dose, Stop
Data type
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C2746065
Description
IP Device Malfunction
Alias
- UMLS CUI-1
- C3898691
- UMLS CUI-2
- C0086138
Description
Investigational Medicinal Product Documentation, Identifier
Data type
integer
Alias
- UMLS CUI [1,1]
- C3898691
- UMLS CUI [1,2]
- C0600091
Description
Medical Device Failure or Malfunction; Indication of (contextual qualifier)
Data type
text
Alias
- UMLS CUI [1,1]
- C1881681
- UMLS CUI [1,2]
- C0392360
Description
Chest X-Ray
Alias
- UMLS CUI-1
- C0039985
Description
Plain chest X-ray, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0011008
Description
x-ray of chest: pulmonary infiltrate
Data type
text
Alias
- UMLS CUI [1]
- C2073654
Description
Plain chest X-ray, Pulmonary infiltrate, Bilateral, Unilateral
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C0238767
- UMLS CUI [1,4]
- C0205092
Description
Plain chest X-ray, Pulmonary infiltrate, Characterization
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1880022
Description
Plain chest X-ray, Pulmonary infiltrate, Structure of right upper lobe of lung
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261074
Description
Plain chest X-ray, Pulmonary infiltrate, Structure of middle lobe of lung
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C0225757
Description
Plain chest X-ray, Pulmonary infiltrate, Structure of right lower lobe of lung
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261075
Description
Plain chest X-ray, Pulmonary infiltrate, Structure of left upper lobe of lung
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261076
Description
Plain chest X-ray, Pulmonary infiltrate, Lingula of left lung
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C0225740
Description
Plain chest X-ray, Pulmonary infiltrate, Structure of left lower lobe of lung
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261077
Description
Plain chest X-ray, Pleural effusion disorder
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0032227
- UMLS CUI [1,3]
- C0450429
Description
Plain chest X-ray, Pleural effusion disorder, Location
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0032227
- UMLS CUI [1,3]
- C0450429
Description
Plain chest X-ray, Atelectasis
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0004144
Description
Plain chest X-ray, Lung mass
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0149726
Description
Plain chest X-ray, Cardiomegaly
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0018800
Description
Plain chest X-ray, Pulmonary Edema
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0034063
Description
Plain chest X-ray, Comment
Data type
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0947611
Description
Pneumonia Assessment
Alias
- UMLS CUI-1
- C0032285
- UMLS CUI-2
- C0220825
Description
Pneumonia, Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0808070
Description
Pneumonia, Coughing, Level
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0010200
- UMLS CUI [1,3]
- C2946261
Description
Pneumonia, Purulent sputum
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0241235
Description
Pneumonia, Chest auscultation finding
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0577960
Description
Pneumonia, Dyspnea
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0013404
Description
Pneumonia, Blood culture
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0200949
Description
Pneumonia, Blood culture, Pathogenic organism
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0200949
- UMLS CUI [1,3]
- C0450254
Description
Pneumonia, Pleural effusion disorder, Location
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0032227
- UMLS CUI [1,3]
- C0450429
Description
Body Temperature
Data type
float
Measurement units
- °C
Alias
- UMLS CUI [1]
- C0005903
Description
Respiratory rate
Data type
integer
Measurement units
- breaths/min
Alias
- UMLS CUI [1]
- C0231832
Description
Heart rate
Data type
integer
Measurement units
- bpm
Alias
- UMLS CUI [1]
- C0018810
Description
Systolic Pressure
Data type
integer
Measurement units
- mmHg
Alias
- UMLS CUI [1,1]
- C0871470
- UMLS CUI [1,2]
- C0522019
Description
Diastolic blood pressure
Data type
integer
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
Pneumonia, Hypoxemia
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0700292
Description
Pneumonia, White blood cell count procedure
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0023508
Description
Pneumonia, Inpatient
Data type
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0021562
Description
Pneumonia, X-Ray confirmed
Data type
boolean
Alias
- UMLS CUI [1]
- C3843750
Description
Pneumonia, Hospitalization
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0019993
Description
Pneumonia, Cessation of life
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0011065
Description
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Description
Concomitant Agent, During, Clinical Trials
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008976
Description
Non-serious Adverse Event
Data type
boolean
Alias
- UMLS CUI [1]
- C1518404
Description
COPD exacerbation
Data type
boolean
Alias
- UMLS CUI [1]
- C0740304
Description
Pneumonia
Data type
boolean
Alias
- UMLS CUI [1]
- C0032285
Description
Fracture
Data type
boolean
Alias
- UMLS CUI [1]
- C0016658
Description
Dry Powder Inhaler Device, Device Failure
Data type
text
Alias
- UMLS CUI [1,1]
- C1967611
- UMLS CUI [1,2]
- C0086138
Description
SAE Status
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0449438
Description
Subject Status
Alias
- UMLS CUI-1
- C2348568
Similar models
LOGS
- StudyEvent: ODM
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C1710066 (UMLS CUI [1,2])
C1704758 (UMLS CUI [1,2])
C1710677 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C1704686 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1710066 (UMLS CUI [1,2])
C1704758 (UMLS CUI [1,2])
C1710677 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,2])
C2985911 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C2985911 (UMLS CUI [1,3])
C1710056 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C2826734 (UMLS CUI [1,2])
C2826666 (UMLS CUI [1,2])
C2826744 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1547647 (UMLS CUI [1,2])
C1709863 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0439793 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,2])
C0001617 (UMLS CUI [1,2])
C0003232 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0884980 (UMLS CUI [1,2])
C0443172 (UMLS CUI [1,3])
C0039985 (UMLS CUI [1,2])
C0204977 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,3])
C0031831 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0449788 (UMLS CUI [1,4])
C0008952 (UMLS CUI [1,2])
C0545084 (UMLS CUI [1,3])
C0449788 (UMLS CUI [1,4])
C0583237 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,3])
C3694481 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C2360065 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
C0884980 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0021430 (UMLS CUI-2)
C0870078 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1321605 (UMLS CUI-2)
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0750480 (UMLS CUI [1,2])
C0452588 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2746065 (UMLS CUI [1,2])
C1321605 (UMLS CUI-2)
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0750480 (UMLS CUI [1,2])
C0452588 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2746065 (UMLS CUI [1,2])
C0086138 (UMLS CUI-2)
C0600091 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0235896 (UMLS CUI [1,2])
C0238767 (UMLS CUI [1,3])
C0205092 (UMLS CUI [1,4])
C0235896 (UMLS CUI [1,2])
C1880022 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261074 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C0225757 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261075 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261076 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C0225740 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261077 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C0004144 (UMLS CUI [1,2])
C0149726 (UMLS CUI [1,2])
C0018800 (UMLS CUI [1,2])
C0034063 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0010200 (UMLS CUI [1,2])
C2946261 (UMLS CUI [1,3])
C0241235 (UMLS CUI [1,2])
C0577960 (UMLS CUI [1,2])
C0200949 (UMLS CUI [1,2])
C0200949 (UMLS CUI [1,2])
C0450254 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C0522019 (UMLS CUI [1,2])
C0700292 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,2])
C0021562 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0086138 (UMLS CUI [1,2])