ID
42545
Beschreibung
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.
Link
https://clinicaltrials.gov/ct2/show/NCT00811733
Stichworte
Versionen (1)
- 25.08.21 25.08.21 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
25. August 2021
DOI
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Lizenz
Creative Commons BY-NC 4.0
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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733
Serious Adverse event
- StudyEvent: ODM
Beschreibung
Type of Report
Alias
- UMLS CUI-1
- C0585733
Beschreibung
Randomisation
Alias
- UMLS CUI-1
- C0034656
Beschreibung
Serious Adverse Event Entry
Alias
- UMLS CUI-1
- C1519255
Beschreibung
[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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Beschreibung
Diagnosis Only (if known) Otherwise Sign/Symptom. Include ONE event term only.
Datentyp
text
Alias
- UMLS CUI [1]
- C1519255
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C2826798
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C1140263
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C3898442
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Beschreibung
Serious adverse event start date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
Beschreibung
AE start time is required for all events starting on ofatumumab treatment days
Datentyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1301880
Beschreibung
AE end time is required for all events starting on ofatumumab treatment days.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Beschreibung
Serious adverse event, recovered/resolved, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0806020
Beschreibung
AE end time is required for all events starting on ofatumumab treatment days
Datentyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C1522314
Beschreibung
Serious adverse event, recovered/resolved with sequelae, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0243088
- UMLS CUI [1,4]
- C0806020
Beschreibung
AE end time is required for all events starting on ofatumumab treatment days
Datentyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0243088
- UMLS CUI [1,4]
- C1522314
Beschreibung
Serious adverse event, fatal, Date of Death
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C1148348
Beschreibung
AE end time is required for all events starting on ofatumumab treatment days
Datentyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C1301931
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0574845
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Beschreibung
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
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0332162
Beschreibung
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.
Datentyp
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
Beschreibung
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
Datentyp
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
Beschreibung
Action Taken with Investigational Product(s) as a Result of the AE
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1519255
Beschreibung
Subject withdrawal from study as result of AE
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0422727
Beschreibung
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.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0332149
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C0085978
- UMLS CUI [1,4]
- C1519255
Beschreibung
[hidden]
Datentyp
integer
Maßeinheiten
- hours
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449238
Beschreibung
[hidden]
Datentyp
integer
Maßeinheiten
- minutes
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449238
Beschreibung
[hidden]
Datentyp
integer
Maßeinheiten
- 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
Beschreibung
[hidden]
Datentyp
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
Beschreibung
[hidden]
Datentyp
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
Beschreibung
[hidden]
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1710056
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C1519255
Beschreibung
Intensity Changes Entry
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C0392747
- UMLS CUI-4
- C0920316
Beschreibung
Diagnosis Only (if known) Otherwise Sign/Symptom Include ONE event term only
Datentyp
text
Alias
- UMLS CUI [1]
- C1519255
Beschreibung
Serious adverse event, start date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0808070
Beschreibung
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.
Datentyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C1301880
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0518690
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0441800
Beschreibung
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.
Datentyp
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
Beschreibung
Seriousness
Alias
- UMLS CUI-1
- C1710056
Beschreibung
Specify the reason for considering this an SAE. Check all that apply.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1320832
Beschreibung
Specify the reason for considering this an SAE. Check all that apply.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1517874
Beschreibung
Specify the reason for considering this an SAE. Check all that apply.
Datentyp
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
Beschreibung
Specify the reason for considering this an SAE. Check all that apply.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0231170
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C3176592
Beschreibung
Specify the reason for considering this an SAE. Check all that apply.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0000768
Beschreibung
Specify the reason for considering this an SAE. Check all that apply.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1274040
Beschreibung
Specify the reason for considering this an SAE. Check all that apply. [Enter protocol specific definition here]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1274040
- UMLS CUI [1,4]
- C1521902
Beschreibung
Relevant concomitant/Treatment medications Entry
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C2347946
- UMLS CUI-3
- C0920316
Beschreibung
Include details of any medication that may help explain the SAE, may have caused the SAE or was used to treat the SAE. [hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2348184
- UMLS CUI [1,2]
- C2347852
Beschreibung
Enter drug name, not description (Generic name preferred. If combination product, enter Trade name).
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C2826819
Beschreibung
Concomitant medication, dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C3174092
Beschreibung
Include details of any medication that may help explain the SAE, may have caused the SAE or was used to treat the SAE.
Datentyp
text
Alias
- UMLS CUI [1]
- C2826646
Beschreibung
Concomitant medication, Frequency
Datentyp
text
Alias
- UMLS CUI [1]
- C2826654
Beschreibung
Concomitant medication, route
Datentyp
text
Alias
- UMLS CUI [1]
- C2826730
Beschreibung
Concomitant medication, start date
Datentyp
date
Alias
- UMLS CUI [1]
- C2826734
Beschreibung
Concomitant medication, ongoing
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Beschreibung
Concomitant medication, ongoing, End date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2826666
- UMLS CUI [1,2]
- C0806020
Beschreibung
Enter a medical diagnosis not description.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2826696
- UMLS CUI [1,2]
- C0205225
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C2826819
Beschreibung
Concomitante medication, Drug Type
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0457591
Beschreibung
Relevant medical conditions/Risk factors entry
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347946
- UMLS CUI-3
- C0262926
- UMLS CUI-4
- C0035648
Beschreibung
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]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2348184
- UMLS CUI [1,2]
- C0262926
Beschreibung
Enter a medical diagnosis not description.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C2348235
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1]
- C2826728
Beschreibung
Medical history, date of onset
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0574845
- UMLS CUI [1,2]
- C0262926
Beschreibung
Medical history, continuing
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0549178
Beschreibung
Medical history, date of last occurrence
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C2745955
- UMLS CUI [1,3]
- C0012634
- UMLS CUI [1,4]
- C0011008
Beschreibung
Relevant Medical History / Risk Factors not noted above
Datentyp
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
Beschreibung
Relevant Diagnostic Results Entry
Alias
- UMLS CUI-1
- C2347946
- UMLS CUI-2
- C0430022
- UMLS CUI-3
- C0456984
- UMLS CUI-4
- C1519255
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE. [hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C2348184
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE. Only allow site to choose from List of Values.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C2826273
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C2826247
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C0456984
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0430022
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1518030
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1519815
Beschreibung
Provide details of any tests or procedures carried out to diagnose the SAE.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0430022
- UMLS CUI [1,2]
- C1274040
- UMLS CUI [1,3]
- C2347946
- UMLS CUI [1,4]
- C0205394
Beschreibung
Rechallenge
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347900
Beschreibung
Serious adverse event recurrence after investigational products restarted
Datentyp
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
Beschreibung
Investigational Product Entry
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
text
Alias
- UMLS CUI [1]
- C0304229
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Beschreibung
Investigational Product Entry
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Beschreibung
Investigational Product Entry
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
text
Alias
- UMLS CUI [1]
- C0304229
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Beschreibung
Monotherapy use one row only. Multiple study drug regimens, use multiple rows as appropriate. (this will apply to any multi phase studies).
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0678766
Beschreibung
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
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2986497
Beschreibung
General Narrative Comments
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0947611
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0947611
Beschreibung
Non Clinical
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0205210
- UMLS CUI-3
- C1298908
Beschreibung
[hidden]
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0036043
- UMLS CUI [1,3]
- C1511726
- UMLS CUI [1,4]
- C0205257
Beschreibung
[hidden]
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2985846
Beschreibung
[hidden]
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1710056
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0333052
- UMLS CUI [1,3]
- C0237753
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1698493
- UMLS CUI [1,3]
- C0600091
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0034656
- UMLS CUI [1,3]
- C0237753
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0805701
Beschreibung
[hidden]
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013849
Ähnliche Modelle
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])