ID
42876
Description
Formblatt für die Meldung von schwerwiegenden unerwünschten Ereignissen (SAE) im Rahmen einer klinischen Prüfung oder Leistungsbewertungsprüfung durch Sponsoren nach § 3 Abs. 5 der MPSV Die Vorlage dieser Meldung stellt an sich keine Schlussfolgerung des Herstellers und / oder seines Bevollmächtigten bzw. der zuständigen Behörde dar, dass der Inhalt dieser Meldung vollständig oder zutreffend ist, dass das (die) aufgeführte(n) Medizinprodukt(e) in irgendeiner Weise versagt und/oder zum angegebenen Tod bzw. zur angegebenen Verschlechterung des Gesundheitszustandes einer Person geführt oder beigetragen hat (haben). Report form for reporting of serious adverse events (SAE) in clinical trials or performance evaluations for use by sponsors according to section 3 (5) of the Ordinance on the Medical Device Safety Plan Submission of this report does not, in itself, represent a conclusion by the manufacturer and/or authorised representative or the National Competent Authority that the content of this report is complete or accurate, that the medical device(s) listed failed in any manner and/or that the medical device(s) caused or contributed to the alleged death or deterioration in the state of the health of any person
Keywords
Versions (2)
- 7/20/19 7/20/19 -
- 9/17/21 9/17/21 -
Copyright Holder
Bundesinstitut für Arzneimittel und Medizinprodukte
Uploaded on
September 17, 2021
DOI
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License
Creative Commons BY-NC 3.0
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Bfarm SAE
Serious Adverse Event Report Form
- StudyEvent: ODM
Description
Report submitted by
Alias
- UMLS CUI-1
- C3897642
- UMLS CUI-2
- C1710230
Description
Name
Data type
text
Alias
- UMLS CUI [1]
- C0027365
Description
Contact Person
Data type
text
Alias
- UMLS CUI [1]
- C0337611
Description
Street, house number
Data type
text
Alias
- UMLS CUI [1]
- C1301826
Description
Postal Code
Data type
float
Alias
- UMLS CUI [1]
- C1514254
Description
City
Data type
text
Alias
- UMLS CUI [1]
- C0008848
Description
Country
Data type
text
Alias
- UMLS CUI [1]
- C0454664
Description
Telephone
Data type
float
Alias
- UMLS CUI [1]
- C1515258
Description
Fax
Data type
float
Alias
- UMLS CUI [1]
- C1549619
Description
Data type
text
Alias
- UMLS CUI [1]
- C1705961
Description
Investigator
Alias
- UMLS CUI-1
- C0008961
Description
Name
Data type
text
Alias
- UMLS CUI [1]
- C0027365
Description
Contact Person
Data type
text
Alias
- UMLS CUI [1]
- C0337611
Description
Street, house number
Data type
text
Alias
- UMLS CUI [1]
- C1301826
Description
Postal Code
Data type
float
Alias
- UMLS CUI [1]
- C1514254
Description
City
Data type
text
Alias
- UMLS CUI [1]
- C0008848
Description
Country
Data type
text
Alias
- UMLS CUI [1]
- C0454664
Description
Telephone
Data type
float
Alias
- UMLS CUI [1]
- C1515258
Description
Fax
Data type
float
Alias
- UMLS CUI [1]
- C1549619
Description
Data type
text
Alias
- UMLS CUI [1]
- C1705961
Description
Medical Device Information
Alias
- UMLS CUI-1
- C1533716
- UMLS CUI-2
- C0025080
Description
Device Name
Data type
text
Alias
- UMLS CUI [1]
- C3242369
Description
if applicable
Data type
text
Alias
- UMLS CUI [1]
- C3274659
Description
for implants only
Data type
date
Alias
- UMLS CUI [1,1]
- C0561946
- UMLS CUI [1,2]
- C0011008
Description
For implants only. To be filled out if the exact implant and explant dates are unknown
Data type
time
Alias
- UMLS CUI [1,1]
- C0021107
- UMLS CUI [1,2]
- C0449238
Description
if applicable
Data type
text
Alias
- UMLS CUI [1,1]
- C2963249
- UMLS CUI [1,2]
- C0025080
- UMLS CUI [2,1]
- C0699733
- UMLS CUI [2,2]
- C0332281
- UMLS CUI [2,3]
- C0025080
Description
Product identifier in the clinical investigation
Data type
text
Alias
- UMLS CUI [1,1]
- C3272556
- UMLS CUI [1,2]
- C4553154
Description
Person(s) affected
Alias
- UMLS CUI-1
- C0522476
Description
Subject
Data type
boolean
Alias
- UMLS CUI [1]
- C0681850
Description
User
Data type
boolean
Alias
- UMLS CUI [1]
- C1706077
Description
Other Person
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0027361
- UMLS CUI [1,2]
- C0205394
Description
Other Person Further Information
Data type
text
Alias
- UMLS CUI [1,1]
- C0027361
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1517331
- UMLS CUI [1,4]
- C1533716
Description
Information on sex, year of birth and weight to be provided if necessary for the assessment of the SAE
Data type
integer
Alias
- UMLS CUI [1]
- C0079399
Description
Information on sex, year of birth and weight to be provided if necessary for the assessment of the SAE
Data type
partialDate
Alias
- UMLS CUI [1]
- C2826771
Description
Information on sex, year of birth and weight to be provided if necessary for the assessment of the SAE
Data type
float
Measurement units
- kg
Alias
- UMLS CUI [1]
- C0005910
Description
Subject ID according to investigation protocol
Data type
text
Alias
- UMLS CUI [1,1]
- C2826694
- UMLS CUI [1,2]
- C2348563
Description
Serious adverse event
Alias
- UMLS CUI-1
- C1519255
Description
Date of the study procedure
Data type
date
Alias
- UMLS CUI [1,1]
- C0008972
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0011008
Description
Date of event
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0441471
Description
Doctor / Investigation site awareness date
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0031831
- UMLS CUI [1,3]
- C1522154
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C2347790
- UMLS CUI [2,3]
- C1522154
Description
Date the report was received by the sponsor
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C3897642
- UMLS CUI [1,3]
- C1709850
- UMLS CUI [1,4]
- C1711305
Description
actual or possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C1306577
Description
actual or possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C3846017
- UMLS CUI [2,1]
- C1274040
- UMLS CUI [2,2]
- C2826244
- UMLS CUI [2,3]
- C3263722
Description
actual or possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0221099
- UMLS CUI [1,3]
- C0205355
- UMLS CUI [1,4]
- C1268086
- UMLS CUI [2,1]
- C1274040
- UMLS CUI [2,2]
- C0221099
- UMLS CUI [2,3]
- C0205355
- UMLS CUI [2,4]
- C0242821
- UMLS CUI [2,5]
- C0542341
Description
actual or possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0019993
- UMLS CUI [2,1]
- C1274040
- UMLS CUI [2,2]
- C0019993
- UMLS CUI [2,3]
- C0439590
Description
actual or possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0221099
- UMLS CUI [1,4]
- C0205355
- UMLS CUI [1,5]
- C1268086
- UMLS CUI [2,1]
- C1274040
- UMLS CUI [2,2]
- C0549433
- UMLS CUI [2,3]
- C0221099
- UMLS CUI [2,4]
- C0205355
- UMLS CUI [2,5]
- C1268086
- UMLS CUI [3,1]
- C1274040
- UMLS CUI [3,2]
- C0184661
- UMLS CUI [3,3]
- C0221099
- UMLS CUI [3,4]
- C0205355
- UMLS CUI [3,5]
- C0242821
- UMLS CUI [3,6]
- C0542341
- UMLS CUI [4,1]
- C1274040
- UMLS CUI [4,2]
- C0549433
- UMLS CUI [4,3]
- C0221099
- UMLS CUI [4,4]
- C0205355
- UMLS CUI [4,5]
- C0242821
- UMLS CUI [4,6]
- C0542341
Description
actual or possible
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0015930
- UMLS CUI [2,1]
- C1274040
- UMLS CUI [2,2]
- C0015927
- UMLS CUI [3,1]
- C1274040
- UMLS CUI [3,2]
- C0000768
- UMLS CUI [4,1]
- C1274040
- UMLS CUI [4,2]
- C2112165
Description
Detailed description of the event by the investigation site
Data type
text
Alias
- UMLS CUI [1,1]
- C2348319
- UMLS CUI [1,2]
- C0441471
- UMLS CUI [1,3]
- C2825164
Description
Additional description by the sponsor
Data type
text
Alias
- UMLS CUI [1,1]
- C1524062
- UMLS CUI [1,2]
- C0678257
- UMLS CUI [1,3]
- C2347796
Description
Remedial action taken by the investigation site relevant to the care of the subject
Data type
text
Alias
- UMLS CUI [1,1]
- C1709895
- UMLS CUI [1,2]
- C2825164
- UMLS CUI [1,3]
- C1947933
- UMLS CUI [1,4]
- C0681850
Description
expected = addressed in the risk analysis of the sponsor or mentioned in the Investigators Brochure
Data type
integer
Alias
- UMLS CUI [1,1]
- C0679138
- UMLS CUI [1,2]
- C0441471
Description
Rationale for the classification as expected or unexpected
Data type
text
Alias
- UMLS CUI [1,1]
- C2699007
- UMLS CUI [1,2]
- C0008902
- UMLS CUI [1,3]
- C1517001
- UMLS CUI [2,1]
- C2699007
- UMLS CUI [2,2]
- C0008902
- UMLS CUI [2,3]
- C4055646
Description
Initial actions taken by the sponsor
Data type
text
Alias
- UMLS CUI [1,1]
- C0205265
- UMLS CUI [1,2]
- C3266814
- UMLS CUI [1,3]
- C1711305
Description
Related to investigation
Alias
- UMLS CUI-1
- C0869014
- UMLS CUI-2
- C0220825
Description
Relation to investigation Medical procedure
Data type
integer
Alias
- UMLS CUI [1,1]
- C0869014
- UMLS CUI [1,2]
- C0220825
- UMLS CUI [1,3]
- C0199171
Description
Relation to investigation Medical device
Data type
integer
Alias
- UMLS CUI [1,1]
- C0869014
- UMLS CUI [1,2]
- C0220825
- UMLS CUI [1,3]
- C0025080
Description
No relation
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0869014
- UMLS CUI [1,2]
- C1705492
Description
in case of changes in rating the relation compared to initial or follow-up reports please provide a rationale
Data type
text
Alias
- UMLS CUI [1,1]
- C2699007
- UMLS CUI [1,2]
- C0871208
- UMLS CUI [1,3]
- C0869014
Description
Number of patients currently enrolled At the investigation site
Data type
float
Alias
- UMLS CUI [1,1]
- C2360800
- UMLS CUI [1,2]
- C4727055
- UMLS CUI [1,3]
- C2825164
Description
Number of patients currently enrolled All investigation sites
Data type
float
Alias
- UMLS CUI [1,1]
- C2360800
- UMLS CUI [1,2]
- C4727055
- UMLS CUI [1,3]
- C2825164
- UMLS CUI [1,4]
- C0444868
Description
Final report by the sponsor
Alias
- UMLS CUI-1
- C0460114
- UMLS CUI-2
- C2347796
Description
Root cause of the SAE is
Data type
text
Alias
- UMLS CUI [1,1]
- C3179036
- UMLS CUI [1,2]
- C1519255
Description
Please provide information if other was picked on the previous item
Data type
text
Alias
- UMLS CUI [1,1]
- C3179036
- UMLS CUI [1,2]
- C1519255
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C1517331
- UMLS CUI [1,5]
- C1533716
Description
including a final risk-benefit assessment of the clinical investigation taking all SAEs into consideration
Data type
text
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0220825
- UMLS CUI [2,1]
- C2699007
- UMLS CUI [2,2]
- C3179036
- UMLS CUI [2,3]
- C0008902
Description
Corrective action taken or planned including time schedule:
Data type
text
Alias
- UMLS CUI [1,1]
- C0719519
- UMLS CUI [1,2]
- C3266814
- UMLS CUI [1,3]
- C1301732
- UMLS CUI [1,4]
- C1549502
- UMLS CUI [2,1]
- C0719519
- UMLS CUI [2,2]
- C3266814
- UMLS CUI [2,3]
- C1272695
- UMLS CUI [2,4]
- C1549502
Similar models
Serious Adverse Event Report Form
- StudyEvent: ODM
C1273803 (UMLS CUI [1,2])
C0681788 (UMLS CUI [1,3])
C4553154 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C3897642 (UMLS CUI [1,2])
C0586393 (UMLS CUI [1,2])
C2347796 (UMLS CUI [1,3])
C1273803 (UMLS CUI [1,2])
C0681788 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
C0586393 (UMLS CUI [1,5])
C1273803 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C3897642 (UMLS CUI [1,4])
C1515023 (UMLS CUI [1,5])
C1550543 (UMLS CUI [1,2])
C1301860 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C4724350 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0025080 (UMLS CUI [1,2])
C0699733 (UMLS CUI [2,1])
C0332281 (UMLS CUI [2,2])
C0025080 (UMLS CUI [2,3])
C4553154 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C1517331 (UMLS CUI [1,3])
C1533716 (UMLS CUI [1,4])
C2348563 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0441471 (UMLS CUI [1,2])
C0031831 (UMLS CUI [1,2])
C1522154 (UMLS CUI [1,3])
C0011008 (UMLS CUI [2,1])
C2347790 (UMLS CUI [2,2])
C1522154 (UMLS CUI [2,3])
C3897642 (UMLS CUI [1,2])
C1709850 (UMLS CUI [1,3])
C1711305 (UMLS CUI [1,4])
C1306577 (UMLS CUI [1,2])
C3846017 (UMLS CUI [1,2])
C1274040 (UMLS CUI [2,1])
C2826244 (UMLS CUI [2,2])
C3263722 (UMLS CUI [2,3])
C0221099 (UMLS CUI [1,2])
C0205355 (UMLS CUI [1,3])
C1268086 (UMLS CUI [1,4])
C1274040 (UMLS CUI [2,1])
C0221099 (UMLS CUI [2,2])
C0205355 (UMLS CUI [2,3])
C0242821 (UMLS CUI [2,4])
C0542341 (UMLS CUI [2,5])
C0019993 (UMLS CUI [1,2])
C1274040 (UMLS CUI [2,1])
C0019993 (UMLS CUI [2,2])
C0439590 (UMLS CUI [2,3])
C0184661 (UMLS CUI [1,2])
C0221099 (UMLS CUI [1,3])
C0205355 (UMLS CUI [1,4])
C1268086 (UMLS CUI [1,5])
C1274040 (UMLS CUI [2,1])
C0549433 (UMLS CUI [2,2])
C0221099 (UMLS CUI [2,3])
C0205355 (UMLS CUI [2,4])
C1268086 (UMLS CUI [2,5])
C1274040 (UMLS CUI [3,1])
C0184661 (UMLS CUI [3,2])
C0221099 (UMLS CUI [3,3])
C0205355 (UMLS CUI [3,4])
C0242821 (UMLS CUI [3,5])
C0542341 (UMLS CUI [3,6])
C1274040 (UMLS CUI [4,1])
C0549433 (UMLS CUI [4,2])
C0221099 (UMLS CUI [4,3])
C0205355 (UMLS CUI [4,4])
C0242821 (UMLS CUI [4,5])
C0542341 (UMLS CUI [4,6])
C0015930 (UMLS CUI [1,2])
C1274040 (UMLS CUI [2,1])
C0015927 (UMLS CUI [2,2])
C1274040 (UMLS CUI [3,1])
C0000768 (UMLS CUI [3,2])
C1274040 (UMLS CUI [4,1])
C2112165 (UMLS CUI [4,2])
C0441471 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])
C0678257 (UMLS CUI [1,2])
C2347796 (UMLS CUI [1,3])
C2825164 (UMLS CUI [1,2])
C1947933 (UMLS CUI [1,3])
C0681850 (UMLS CUI [1,4])
C0008902 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,3])
C2699007 (UMLS CUI [2,1])
C0008902 (UMLS CUI [2,2])
C4055646 (UMLS CUI [2,3])
C3266814 (UMLS CUI [1,2])
C1711305 (UMLS CUI [1,3])
C0220825 (UMLS CUI-2)
C0220825 (UMLS CUI [1,2])
C0199171 (UMLS CUI [1,3])
C0220825 (UMLS CUI [1,2])
C0025080 (UMLS CUI [1,3])
C1705492 (UMLS CUI [1,2])
C0871208 (UMLS CUI [1,2])
C0869014 (UMLS CUI [1,3])
C4727055 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])
C4727055 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])
C0444868 (UMLS CUI [1,4])
C2347796 (UMLS CUI-2)
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C1517331 (UMLS CUI [1,4])
C1533716 (UMLS CUI [1,5])
C0220825 (UMLS CUI [1,2])
C2699007 (UMLS CUI [2,1])
C3179036 (UMLS CUI [2,2])
C0008902 (UMLS CUI [2,3])
C3266814 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C1549502 (UMLS CUI [1,4])
C0719519 (UMLS CUI [2,1])
C3266814 (UMLS CUI [2,2])
C1272695 (UMLS CUI [2,3])
C1549502 (UMLS CUI [2,4])