ID
42545
Description
Study ID: 110921 Clinical Study ID: 110921 Study Title: A Phase II Trial of Ofatumumab in Subjects with Waldenstrom's Macroglobulinemia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00811733 Clinicaltrials.gov Link: https://clinicaltrials.gov/ct2/show/NCT00811733 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Ofatumumab Trade Name: N/A Study Indication: Waldenstrom Macroglobulinaemia The primary objective of this open-label, multi-center, Phase II study was to evaluate the safety and efficacy of Ofatumumab in subjects diagnosed with Waldenstrom Macroglobulinaemia. For the study, eligible subjects were enrolled to receive up to 3 cycles of treatment with Ofatumumab. The first cycle consisted of a single dose of 300 mg followed by 3 weekly doses of 1000 mg (Treatment Group A) or 4 weekly doses of 2000 mg (Treatment Group B) of Ofatumumab, with response assessment beginning at Week 12. Based on the Week 12-16 response, eligible subjects could receive up to 2 additional cycles of treatment. This form has to be filled out whenever/if a serious adverse event occurred during study.
Lien
https://clinicaltrials.gov/ct2/show/NCT00811733
Mots-clés
Versions (1)
- 25/08/2021 25/08/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
25 août 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 4.0
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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733
Serious Adverse event
- StudyEvent: ODM
Description
Type of Report
Alias
- UMLS CUI-1
- C0585733
Description
Randomisation
Alias
- UMLS CUI-1
- C0034656
Description
Serious Adverse Event Entry
Alias
- UMLS CUI-1
- C1519255
Description
[hidden] Use this itemgroup to enter details of the SAE. For additional SAEs that are clinically or temporally related (e.g., SAEs that occur during the same hospitalization) fill out the items of this itemgroup for entry of the addition.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Description
Diagnosis Only (if known) Otherwise Sign/Symptom. Include ONE event term only.
Type de données
text
Alias
- UMLS CUI [1]
- C1519255
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C2826798
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C1140263
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C3898442
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Description
Serious adverse event start date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
Description
AE start time is required for all events starting on ofatumumab treatment days
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1301880
Description
AE end time is required for all events starting on ofatumumab treatment days.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Description
Serious adverse event, recovered/resolved, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0806020
Description
AE end time is required for all events starting on ofatumumab treatment days
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C1522314
Description
Serious adverse event, recovered/resolved with sequelae, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0243088
- UMLS CUI [1,4]
- C0806020
Description
AE end time is required for all events starting on ofatumumab treatment days
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0243088
- UMLS CUI [1,4]
- C1522314
Description
Serious adverse event, fatal, Date of Death
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C1148348
Description
AE end time is required for all events starting on ofatumumab treatment days
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C1301931
Description
Record maximum intensity throughout duration of event. This item may be hidden if either the Maximum Grade or Maximum Grade or Intensity item has been used.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Description
Record intensity at the onset of the event [hidden] Conditional on the use of the Intensity change section. If the section is not used then the item must be hidden. This item may be hidden if either the Grade/Grade or Intensity at onset of event item has been used.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0574845
Description
Record maximum grade throughout duration of event. This item may be hidden if either the Maximum Intensity or Maximum Grade or Intensity item has been used. Grade 5 is optional.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Description
Record grade at the onset of the event. [hidden] Conditional on using the Intensity change section. If the section is not used the item must be hidden. This item may be hidden if either the Intensity/Grade or Intensity at onset of event item has been used. Grade 5 is optional
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0332162
Description
Record maximum grade or intensity throughout duration of event. [hidden] This item may be hidden if either the Maximum Intensity or Maximum Grade item has been used. Grade 5 is optional.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0806909
- UMLS CUI [2,3]
- C0518690
Description
Record grade or intensity at the onset of the event [hidden] Conditional on the use of the Intensity change section. If the section is not used then the item must be hidden. This item may be hidden if either the Intensity or Grade at onset of event item has been used. Grade 5 is optional
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332162
- UMLS CUI [1,3]
- C0441800
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0332162
- UMLS CUI [2,3]
- C0518690
Description
Action Taken with Investigational Product(s) as a Result of the AE
Type de données
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1519255
Description
Subject withdrawal from study as result of AE
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0422727
Description
Use best judgment at initial entry. May be amended when additional information becomes available. If the study has multiple IP then remove Yes and keep Yes, select appropriate investigational product(s)' and set selection value to Y. Otherwise remove Yes, select appropriate investigational product(s) and keep Yes.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0332149
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C0085978
- UMLS CUI [1,4]
- C1519255
Description
[hidden]
Type de données
integer
Unités de mesure
- hours
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449238
Description
[hidden]
Type de données
integer
Unités de mesure
- minutes
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449238
Description
[hidden]
Type de données
integer
Unités de mesure
- hours
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332162
- UMLS CUI [1,3]
- C1272706
- UMLS CUI [1,4]
- C0304229
- UMLS CUI [1,5]
- C3174092
- UMLS CUI [1,6]
- C1517741
Description
[hidden]
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332162
- UMLS CUI [1,3]
- C1272706
- UMLS CUI [1,4]
- C0304229
- UMLS CUI [1,5]
- C3174092
- UMLS CUI [1,6]
- C1517741
Description
[hidden]
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0085978
- UMLS CUI [1,3]
- C2348568
- UMLS CUI [1,4]
- C0332300
- UMLS CUI [1,5]
- C0304229
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0085978
- UMLS CUI [2,3]
- C0199171
- UMLS CUI [3,1]
- C1519255
- UMLS CUI [3,2]
- C0085978
- UMLS CUI [3,3]
- C0005834
- UMLS CUI [4,1]
- C1519255
- UMLS CUI [4,2]
- C0085978
- UMLS CUI [4,3]
- C1710661
Description
[hidden]
Type de données
boolean
Alias
- UMLS CUI [1]
- C1710056
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C1519255
Description
Intensity Changes Entry
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C0392747
- UMLS CUI-4
- C0920316
Description
Diagnosis Only (if known) Otherwise Sign/Symptom Include ONE event term only
Type de données
text
Alias
- UMLS CUI [1]
- C1519255
Description
Serious adverse event, start date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0808070
Description
Hr:Min (00:00-23:59) If the decision has been made to record every change in intensity, time must be collected to differentiate between, and to indicate the order of, changes that occur within a single day.
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C1301880
Description
This item may be hidden if either the Grade of event segment or Grade or Intensity of event segment item has been used and item not included in the section.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0518690
Description
This item may be hidden if either the Intensity of event segment or Grade or intensity of event segment item has been used and item not included in the section. Grade 5 is optional.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0441800
Description
This item may be hidden if either the Grade of event segment or Grade or Intensity of event segment item has been used and item not included in the section. Grade 5 is optional.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0441800
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0449719
- UMLS CUI [2,3]
- C0518690
Description
Seriousness
Alias
- UMLS CUI-1
- C1710056
Description
Specify the reason for considering this an SAE. Check all that apply.
Type de données
boolean
Alias
- UMLS CUI [1]
- C1320832
Description
Specify the reason for considering this an SAE. Check all that apply.
Type de données
boolean
Alias
- UMLS CUI [1]
- C1517874
Description
Specify the reason for considering this an SAE. Check all that apply.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1514873
- UMLS CUI [1,3]
- C0019993
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0745041
Description
Specify the reason for considering this an SAE. Check all that apply.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0231170
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C3176592
Description
Specify the reason for considering this an SAE. Check all that apply.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0000768
Description
Specify the reason for considering this an SAE. Check all that apply.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1274040
Description
Specify the reason for considering this an SAE. Check all that apply. [Enter protocol specific definition here]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1274040
- UMLS CUI [1,4]
- C1521902
Description
Relevant concomitant/Treatment medications Entry
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C2347946
- UMLS CUI-3
- C0920316
Description
Include details of any medication that may help explain the SAE, may have caused the SAE or was used to treat the SAE. [hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C2348184
- UMLS CUI [1,2]
- C2347852
Description
Enter drug name, not description (Generic name preferred. If combination product, enter Trade name).
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C2826819
Description
Concomitant medication, dose
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C3174092
Description
Include details of any medication that may help explain the SAE, may have caused the SAE or was used to treat the SAE.
Type de données
text
Alias
- UMLS CUI [1]
- C2826646
Description
Concomitant medication, Frequency
Type de données
text
Alias
- UMLS CUI [1]
- C2826654
Description
Concomitant medication, route
Type de données
text
Alias
- UMLS CUI [1]
- C2826730
Description
Concomitant medication, start date
Type de données
date
Alias
- UMLS CUI [1]
- C2826734
Description
Concomitant medication, ongoing
Type de données
boolean
Alias
- UMLS CUI [1]
- C2826666
Description
Concomitant medication, ongoing, End date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2826666
- UMLS CUI [1,2]
- C0806020
Description
Enter a medical diagnosis not description.
Type de données
text
Alias
- UMLS CUI [1,1]
- C2826696
- UMLS CUI [1,2]
- C0205225
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C2826819
Description
Concomitante medication, Drug Type
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0457591
Description
Relevant medical conditions/Risk factors entry
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347946
- UMLS CUI-3
- C0262926
- UMLS CUI-4
- C0035648
Description
Use this itemgroup to enter each past or current medical disorder, allergy or surgery that may be RELEVANT to the SAE. Enter a diagnosis, not description. Relevant family or social history should be described in the ‘General Narrative Comments’ at the bottom of this form. [hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C2348184
- UMLS CUI [1,2]
- C0262926
Description
Enter a medical diagnosis not description.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C2348235
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1]
- C2826728
Description
Medical history, date of onset
Type de données
date
Alias
- UMLS CUI [1,1]
- C0574845
- UMLS CUI [1,2]
- C0262926
Description
Medical history, continuing
Type de données
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0549178
Description
Medical history, date of last occurrence
Type de données
date
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C2745955
- UMLS CUI [1,3]
- C0012634
- UMLS CUI [1,4]
- C0011008
Description
Relevant Medical History / Risk Factors not noted above
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347946
- UMLS CUI [1,3]
- C0262926
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C2347946
- UMLS CUI [2,3]
- C0035648
- UMLS CUI [2,4]
- C0205394
Description
Relevant Diagnostic Results Entry
Alias
- UMLS CUI-1
- C2347946
- UMLS CUI-2
- C0430022
- UMLS CUI-3
- C0456984
- UMLS CUI-4
- C1519255
Description
Provide details of any tests or procedures carried out to diagnose the SAE. [hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C2348184
Description
Provide details of any tests or procedures carried out to diagnose the SAE. Only allow site to choose from List of Values.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C2826273
Description
Provide details of any tests or procedures carried out to diagnose the SAE.
Type de données
date
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C2826247
Description
Provide details of any tests or procedures carried out to diagnose the SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C0456984
Description
Provide details of any tests or procedures carried out to diagnose the SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0430022
Description
Provide details of any tests or procedures carried out to diagnose the SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1518030
Description
Provide details of any tests or procedures carried out to diagnose the SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1519815
Description
Provide details of any tests or procedures carried out to diagnose the SAE.
Type de données
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1274040
- UMLS CUI [1,3]
- C2347946
- UMLS CUI [1,4]
- C0205394
Description
Rechallenge
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347900
Description
Serious adverse event recurrence after investigational products restarted
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0034897
- UMLS CUI [1,3]
- C0085978
- UMLS CUI [1,4]
- C0304229
- UMLS CUI [1,5]
- C2347900
Description
Investigational Product Entry
Alias
- UMLS CUI-1
- C0304229
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
text
Alias
- UMLS CUI [1]
- C0304229
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Description
Investigational Product Entry
Alias
- UMLS CUI-1
- C0304229
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Description
Investigational Product Entry
Alias
- UMLS CUI-1
- C0304229
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
text
Alias
- UMLS CUI [1]
- C0304229
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Type de données
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0678766
Description
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies). This item is conditional
Type de données
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2986497
Description
General Narrative Comments
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0947611
Description
Provide a brief narrative description of SAE, possible other causes of the event (e.g. lack of efficacy, withdrawal of investigational product, the disease under study or other medical conditions) and details of the treatment.
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0947611
Description
Non Clinical
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0205210
- UMLS CUI-3
- C1298908
Description
[hidden]
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0036043
- UMLS CUI [1,3]
- C1511726
- UMLS CUI [1,4]
- C0205257
Description
[hidden]
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2985846
Description
[hidden]
Type de données
boolean
Alias
- UMLS CUI [1]
- C1710056
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0333052
- UMLS CUI [1,3]
- C0237753
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1698493
- UMLS CUI [1,3]
- C0600091
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0034656
- UMLS CUI [1,3]
- C0237753
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0805701
Description
[hidden]
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013849
Similar models
Serious Adverse event
- StudyEvent: ODM
C0011008 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,2])
C1704686 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,4])
C2348184 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C1709863 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C1709863 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
C1709863 (UMLS CUI [1,2])
C0243088 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,4])
C1709863 (UMLS CUI [1,2])
C0243088 (UMLS CUI [1,3])
C1522314 (UMLS CUI [1,4])
C1302234 (UMLS CUI [1,2])
C1148348 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,2])
C1301931 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,2])
C0574845 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0332162 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0806909 (UMLS CUI [2,2])
C0518690 (UMLS CUI [2,3])
C0332162 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0332162 (UMLS CUI [2,2])
C0518690 (UMLS CUI [2,3])
C1519255 (UMLS CUI [1,2])
C0422727 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,4])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0332162 (UMLS CUI [1,2])
C1272706 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,4])
C3174092 (UMLS CUI [1,5])
C1517741 (UMLS CUI [1,6])
C0332162 (UMLS CUI [1,2])
C1272706 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,4])
C3174092 (UMLS CUI [1,5])
C1517741 (UMLS CUI [1,6])
C0085978 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0332300 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,5])
C1519255 (UMLS CUI [2,1])
C0085978 (UMLS CUI [2,2])
C0199171 (UMLS CUI [2,3])
C1519255 (UMLS CUI [3,1])
C0085978 (UMLS CUI [3,2])
C0005834 (UMLS CUI [3,3])
C1519255 (UMLS CUI [4,1])
C0085978 (UMLS CUI [4,2])
C1710661 (UMLS CUI [4,3])
C0439849 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C0518690 (UMLS CUI-2)
C0392747 (UMLS CUI-3)
C0920316 (UMLS CUI-4)
C0449719 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0449719 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C0449719 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,3])
C0449719 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C0449719 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0449719 (UMLS CUI [2,2])
C0518690 (UMLS CUI [2,3])
C1514873 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0745041 (UMLS CUI [2,2])
C0231170 (UMLS CUI [1,2])
C1519255 (UMLS CUI [2,1])
C3176592 (UMLS CUI [2,2])
C0000768 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C2347946 (UMLS CUI-2)
C0920316 (UMLS CUI-3)
C2347852 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,2])
C0457591 (UMLS CUI [1,2])
C2347946 (UMLS CUI-2)
C0262926 (UMLS CUI-3)
C0035648 (UMLS CUI-4)
C0262926 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0262926 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C2745955 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C2347946 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C0035648 (UMLS CUI [2,3])
C0205394 (UMLS CUI [2,4])
C0430022 (UMLS CUI-2)
C0456984 (UMLS CUI-3)
C1519255 (UMLS CUI-4)
C2348184 (UMLS CUI [1,2])
C2826247 (UMLS CUI [1,2])
C0456984 (UMLS CUI [1,2])
C0430022 (UMLS CUI [1,2])
C1518030 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C2347900 (UMLS CUI-2)
C0034897 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,4])
C2347900 (UMLS CUI [1,5])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0678766 (UMLS CUI [1,2])
C2986497 (UMLS CUI [1,2])
C0947611 (UMLS CUI-2)
C0947611 (UMLS CUI [1,2])
C0205210 (UMLS CUI-2)
C1298908 (UMLS CUI-3)
C0036043 (UMLS CUI [1,2])
C1511726 (UMLS CUI [1,3])
C0205257 (UMLS CUI [1,4])
C2985846 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C0333052 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C1698493 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0034656 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,2])
C0013849 (UMLS CUI [1,2])