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ID
42030
Descrizione
HIS systemic therapy - form prostate cancer
Keywords
versioni (2)
- 15/05/13 15/05/13 -
- 15/03/21 15/03/21 - Dr. rer. medic Philipp Neuhaus
Caricato su
15 marzo 2021
DOI
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Licenza
Creative Commons BY-NC 3.0 Legacy
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HIS systemic therapy - form prostate cancer
Similar models
HIS
- StudyEvent: HIS
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Name
Item
Patient surname
string
C0421448 (UMLS CUI-1)
184096005 (SNOMED CT-1)
184096005 (SNOMED CT-1)
Vorname
Item
Patient forename
string
C0421447 (UMLS CUI-1)
184095009 (SNOMED CT-1)
184095009 (SNOMED CT-1)
Titel
Item
Patient title
string
Patient title (observable entity) (Code-1)
C0421450 (UMLS CUI-1)
184098006 (SNOMED CT-1)
C0421450 (UMLS CUI-1)
184098006 (SNOMED CT-1)
früherer Name
Item
former Patient name
string
Previous (Code-1)
C0205156 (UMLS CUI-1)
9130008 (SNOMED CT-1)
Patient name (observable entity) (Code-2)
C1299487 (UMLS CUI-2)
371484003 (SNOMED CT-2)
C0205156 (UMLS CUI-1)
9130008 (SNOMED CT-1)
Patient name (observable entity) (Code-2)
C1299487 (UMLS CUI-2)
371484003 (SNOMED CT-2)
Geburtsdatum
Item
Patient date of birth
date
C0421451 (UMLS CUI-1)
184099003 (SNOMED CT-1)
184099003 (SNOMED CT-1)
Alter
Item
patient age
integer
patient age (Code-1)
CL386174 (UMLS CUI-1)
CL386174 (UMLS CUI-1)
Nationalität
Item
Ethnicity / related nationality data
string
C0438960 (UMLS CUI-1)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
186034007 (SNOMED CT-1)
Patients (Code-2)
C0030705 (UMLS CUI-2)
116154003 (SNOMED CT-2)
Adresse
Item
Street Address
string
C1301826 (UMLS CUI-1)
398099009 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
398099009 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
PLZ
Item
Patient postal code
integer
C0421454 (UMLS CUI-1)
184102003 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
184102003 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Stadt
Item
City of residence
string
C2316883 (UMLS CUI-1)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
433178008 (SNOMED CT-1)
Patient address (Code-2)
C0421449 (UMLS CUI-2)
184097001 (SNOMED CT-2)
Fallnummer
Item
Case Identifier
integer
Case - situation (qualifier value) (Code-1)
C0868928 (UMLS CUI-1)
398241000 (SNOMED CT-1)
Identifier (Code-2)
C0600091 (UMLS CUI-2)
118522005 (SNOMED CT-2)
C0868928 (UMLS CUI-1)
398241000 (SNOMED CT-1)
Identifier (Code-2)
C0600091 (UMLS CUI-2)
118522005 (SNOMED CT-2)
Tumordiagnose (ICD-10)
Item
Cancer Diagnosis
string
Tumor finding (finding) (Code-1)
C1274082 (UMLS CUI-1)
395557000 (SNOMED CT-1)
Diagnosis ICD code (Code-2)
C2598420 (UMLS CUI-2)
C1274082 (UMLS CUI-1)
395557000 (SNOMED CT-1)
Diagnosis ICD code (Code-2)
C2598420 (UMLS CUI-2)
Diagnose-Datum
Item
Date of diagnosis
date
C2316983 (UMLS CUI-1)
432213005 (SNOMED CT-1)
Tumor finding (finding) (Code-2)
C1274082 (UMLS CUI-2)
395557000 (SNOMED CT-2)
432213005 (SNOMED CT-1)
Tumor finding (finding) (Code-2)
C1274082 (UMLS CUI-2)
395557000 (SNOMED CT-2)
Systemische Therapie befolgt die Leitlinien:
Item
Guideline Adherence
boolean
must_have (Item-Info)
C0525059 (UMLS CUI-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
C0525059 (UMLS CUI-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
falls nein, Grund
Item
Reason for Guidelines Adherence
string
Indication of (contextual qualifier) (Code-1)
C0392360 (UMLS CUI-1)
410666004 (SNOMED CT-1)
MTHU008862 (LOINC-1)
Guideline Adherence (Code-2)
C0525059 (UMLS CUI-2)
C0392360 (UMLS CUI-1)
410666004 (SNOMED CT-1)
MTHU008862 (LOINC-1)
Guideline Adherence (Code-2)
C0525059 (UMLS CUI-2)
Therapieart
Item
Therapeutic procedure
boolean
must_have (Item-Info)
for_compare (Code-Info)
C0087111 (UMLS CUI-1)
277132007 (SNOMED CT-1)
10053757 (MedDRA-1)
MTHU008880 (LOINC-1)
for_compare (Code-Info)
C0087111 (UMLS CUI-1)
277132007 (SNOMED CT-1)
10053757 (MedDRA-1)
MTHU008880 (LOINC-1)
Chemotherapie
Item
Chemotherapy Regimen
boolean
C0392920 (UMLS CUI-1)
69960004 (SNOMED CT-1)
10061758 (MedDRA-1)
69960004 (SNOMED CT-1)
10061758 (MedDRA-1)
Hormontherapie
Item
Endocrine Therapy
boolean
C0279025 (UMLS CUI-1)
169413002 (SNOMED CT-1)
10065646 (MedDRA-1)
169413002 (SNOMED CT-1)
10065646 (MedDRA-1)
Immuntherapie
Item
Immunotherapy
boolean
C0021083 (UMLS CUI-1)
76334006 (SNOMED CT-1)
76334006 (SNOMED CT-1)
Antikörper / Tyrosinkinase-Inhibitör
Item
Antibody Therapy
boolean
C0281176 (UMLS CUI-1)
Item
Admission status
integer
Admission statuses (finding) (Code-1)
C0586002 (UMLS CUI-1)
308277006 (SNOMED CT-1)
C0586002 (UMLS CUI-1)
308277006 (SNOMED CT-1)
CL Item
not_coded (teilstationär)
Intention
Item
Intent
boolean
must_have (Item-Info)
changed_datatype (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
changed_datatype (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Item
Intent - chemotherapy
integer
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
367565008 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
CL Item
Curative - procedure intent (kurativ)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent (palliativ)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent (neoadjuvant)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Kombination Radio/Chemo
Item
Chemoradiotherapy
boolean
C0436307 (UMLS CUI-1)
Item
Intent - endocrine therapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
10065646 (MedDRA-2)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
10065646 (MedDRA-2)
CL Item
Curative - procedure intent (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Intent - immunotherapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
CL Item
Curative - procedure intent (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Item
Intent - antibody therapy
integer
extended_coding (Code-Info)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Antibody Therapy (Code-2)
C0281176 (UMLS CUI-2)
C1283828 (UMLS CUI-1)
367565008 (SNOMED CT-1)
Antibody Therapy (Code-2)
C0281176 (UMLS CUI-2)
CL Item
Curative - procedure intent (kurativ)
extended_coding (Code-Info)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
Curative - procedure intent (qualifier value) (Code-1)
C1276305 (UMLS CUI-1)
373808002 (SNOMED CT-1)
CL Item
Palliative - procedure intent (palliativ)
extended_coding (Code-Info)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
Palliative - procedure intent (qualifier value) (Code-1)
C1285530 (UMLS CUI-1)
363676003 (SNOMED CT-1)
CL Item
Adjuvant - intent (adjuvant)
extended_coding (Code-Info)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
Adjuvant - intent (qualifier value) (Code-1)
C1298675 (UMLS CUI-1)
373846009 (SNOMED CT-1)
CL Item
Neo-adjuvant - intent (neoadjuvant)
extended_coding (Code-Info)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Neo-adjuvant - intent (qualifier value) (Code-1)
C1298676 (UMLS CUI-1)
373847000 (SNOMED CT-1)
Unterbrechung
Item
Interruption
boolean
normalized_coding (Code-Info)
Interruption (Code-1)
C1512900 (UMLS CUI-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
Interruption (Code-1)
C1512900 (UMLS CUI-1)
Therapeutic procedure (Code-2)
C0087111 (UMLS CUI-2)
277132007 (SNOMED CT-2)
10053757 (MedDRA-2)
MTHU008880 (LOINC-2)
von
Item
interruption from
date
Date treatment stopped (observable entity) (Code-1)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Interruption (Code-2)
C1512900 (UMLS CUI-2)
C1531784 (UMLS CUI-1)
413947000 (SNOMED CT-1)
Interruption (Code-2)
C1512900 (UMLS CUI-2)
bis
Item
interruption until
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Post (Code-2)
C0231290 (UMLS CUI-2)
237679004 (SNOMED CT-2)
Interruption (Code-3)
C1512900 (UMLS CUI-3)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Post (Code-2)
C0231290 (UMLS CUI-2)
237679004 (SNOMED CT-2)
Interruption (Code-3)
C1512900 (UMLS CUI-3)
Grund
Item
Reason for Treatment Interruption
string
CL436968 (UMLS CUI-1)
Protokoll
Item
Chemotherapy Protocols, Antineoplastic
string
must_have (Item-Info)
C0949219 (UMLS CUI-1)
C0949219 (UMLS CUI-1)
Zyklen
Item
Chemotherapy cycle (procedure)
boolean
must_have (Item-Info)
for_compare (Code-Info)
C1302181 (UMLS CUI-1)
399042005 (SNOMED CT-1)
for_compare (Code-Info)
C1302181 (UMLS CUI-1)
399042005 (SNOMED CT-1)
geplante Zyklen
Item
planned cycles
string
Plan (Code-1)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
C1301732 (UMLS CUI-1)
397943006 (SNOMED CT-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
aktueller Zyklus
Item
current cycle
string
Current Therapy (Code-1)
C2827774 (UMLS CUI-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
C2827774 (UMLS CUI-1)
Chemotherapy cycle (procedure) (Code-2)
C1302181 (UMLS CUI-2)
399042005 (SNOMED CT-2)
Beginn - Chemotherapie
Item
Date treatment started - chemotherapy
date
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Chemotherapy Regimen (Code-2)
C0392920 (UMLS CUI-2)
69960004 (SNOMED CT-2)
10061758 (MedDRA-2)
Beginn - endokrine Therapie
Item
Date treatment started - endocrine therapy
date
extended_coding (Code-Info)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Endocrine Therapy (Code-2)
C0279025 (UMLS CUI-2)
169413002 (SNOMED CT-2)
Beginn - Immuntherapie
Item
Date treatment started - immunotherapy
date
extended_coding (Code-Info)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
Date treatment started (observable entity) (Code-1)
C3173309 (UMLS CUI-1)
413946009 (SNOMED CT-1)
Immunotherapy (Code-2)
C0021083 (UMLS CUI-2)
76334006 (SNOMED CT-2)
voraussichtlich bis
Item
Estimated date of completion
date
C0806067 (UMLS CUI-1)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Systemic Therapy (Code-2)
C1515119 (UMLS CUI-2)
Substanz 1
Item
Chemotherapeutic agent
string
Chemotherapeutic agent (product) (Code-1)
C0729502 (UMLS CUI-1)
312059006 (SNOMED CT-1)
C0729502 (UMLS CUI-1)
312059006 (SNOMED CT-1)
Dosisreduktion
Item
Chemotherapeutic drug level decreased
boolean
C0861114 (UMLS CUI-1)
Einzeldosis
Item
Single dose characteristic
string
Single dose characteristic (observable entity) (Code-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
C1960417 (UMLS CUI-1)
426146003 (SNOMED CT-1)
Menge der Absolutdosis
Item
Cumulative Dose
string
C2986497 (UMLS CUI-1)
Einheit
Item
Unit type (qualifier value)
string
C0565912 (UMLS CUI-1)
288462000 (SNOMED CT-1)
288462000 (SNOMED CT-1)
Begleitmedikation
Item
Concomitant Agent
boolean
normalized_coding (Code-Info)
C2347852 (UMLS CUI-1)
C2347852 (UMLS CUI-1)
CL Item
Cyproterone/Luteinizing Hormone-Releasing Factor (LHRH)
C0678022 (UMLS CUI-1)
Orchiektomie
Item
Orchiectomy
boolean
changed_datatype (Code-Info)
C0029189 (UMLS CUI-1)
120001005 (SNOMED CT-1)
10031060 (MedDRA-1)
C0029189 (UMLS CUI-1)
120001005 (SNOMED CT-1)
10031060 (MedDRA-1)
periphere Hormonblockade
Item
Antiandrogen Therapy
boolean
changed_datatype (Code-Info)
C0279492 (UMLS CUI-1)
10002730 (MedDRA-1)
C0279492 (UMLS CUI-1)
10002730 (MedDRA-1)
CL Item
zoledronic acid (Zometa)
C0257685 (UMLS CUI-1)
420124002 (SNOMED CT-1)
420124002 (SNOMED CT-1)
CL Item
Prednisone (Prednison)
C0032952 (UMLS CUI-1)
116602009 (SNOMED CT-1)
116602009 (SNOMED CT-1)
CL Item
Estramustine (Estramustin)
C0014921 (UMLS CUI-1)
386909008 (SNOMED CT-1)
386909008 (SNOMED CT-1)
CL Item
Other (andere)
C0205394 (UMLS CUI-1)
74964007 (SNOMED CT-1)
Supportive Care (Code-2)
C0344211 (UMLS CUI-2)
243114000 (SNOMED CT-2)
74964007 (SNOMED CT-1)
Supportive Care (Code-2)
C0344211 (UMLS CUI-2)
243114000 (SNOMED CT-2)
andere
Item
Other
string
C0205395 (UMLS CUI-1)
74964008 (SNOMED CT-1)
Supportive Care (Code-2)
C0344212 (UMLS CUI-2)
243114001 (SNOMED CT-2)
Free Text Format (Code-3)
C2348713 (UMLS CUI-3)
74964008 (SNOMED CT-1)
Supportive Care (Code-2)
C0344212 (UMLS CUI-2)
243114001 (SNOMED CT-2)
Free Text Format (Code-3)
C2348713 (UMLS CUI-3)
Nebenwirkungen
Item
Adverse event
boolean
Item
Leukocytes
integer
Leukocytes Adverse Event (Code-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
C1560219 (UMLS CUI-1)
MTHU117099 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Hemoglobin
integer
Hemoglobin Adverse Event (Code-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
C2239101 (UMLS CUI-1)
MTHU116997 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
neutrophil
integer
Neutrophils and Granulocytes Adverse Event (Code-1)
C1560233 (UMLS CUI-1)
MTHU117202 (CTCAE-1)
C1560233 (UMLS CUI-1)
MTHU117202 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Blood Platelets
integer
Platelets Adverse Event (Code-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
C1963076 (UMLS CUI-1)
MTHU117353 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Creatinine
integer
Creatinine Adverse Event (Code-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
C1561535 (UMLS CUI-1)
MTHU116842 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Proteinuria
integer
Proteinuria Adverse Event (Code-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
C1962972 (UMLS CUI-1)
MTHU117382 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Urea
integer
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
bilirubin
integer
Hyperbilirubinemia Adverse Event (Code-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
C1557209 (UMLS CUI-1)
MTHU117008 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Alkaline Phosphatase
integer
Alkaline Phosphatase Adverse Event (Code-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
C1561546 (UMLS CUI-1)
MTHU112158 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Alanine Transaminase
integer
Serum Glutamic Pyruvic Transaminase Adverse Event (Code-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
C1557189 (UMLS CUI-1)
MTHU117450 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
CL Item
only_in_connection with GOT (only_in_connection with GOT)
Item
Aspartate Transaminase
integer
Serum Glutamic Oxaloacetic Transaminase Adverse Event (Code-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
C1557198 (UMLS CUI-1)
MTHU117449 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
CL Item
only_in_connection with GPT (only_in_connection with GPT)
Item
Nausea
integer
Nausea Adverse Event (Code-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
C1963179 (UMLS CUI-1)
MTHU117189 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Diarrhea
integer
Diarrhea Adverse Event (Code-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
C0232708 (UMLS CUI-1)
MTHU116856 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Mucous Membrane
integer
Mucositis and Stomatitis Adverse Event by Functional and Symptomatic Classification (Code-1)
C1556411 (UMLS CUI-1)
MTHU117173 (CTCAE-1)
C1556411 (UMLS CUI-1)
MTHU117173 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Erbrechen
integer
Vomiting Adverse Event (Code-1)
C1963281 (UMLS CUI-1)
MTHU117700 (CTCAE-1)
C1963281 (UMLS CUI-1)
MTHU117700 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Obstipation
integer
Constipation Adverse Event (Code-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
C1963087 (UMLS CUI-1)
MTHU116803 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Peripheral Nerves
integer
Neuralgia and Peripheral Nerve Pain Adverse Event (Code-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
C1557517 (UMLS CUI-1)
MTHU117196 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Conscious
integer
Somnolence and Depressed Level of Consciousness Adverse Event (Code-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
C1557290 (UMLS CUI-1)
MTHU117503 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Dyspnea
integer
Dyspnea Adverse Event (Code-1)
C1963100 (UMLS CUI-1)
MTHU116873 (CTCAE-1)
C1963100 (UMLS CUI-1)
MTHU116873 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Infection
integer
Adverse Event Associated with Infection (Code-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
C1556682 (UMLS CUI-1)
MTHU112135 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Heart Rhythm
integer
Adverse Event Associated with Cardiac Arrhythmia (Code-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
C1560249 (UMLS CUI-1)
MTHU112127 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Cardiac function
integer
Adverse Event Associated with the Heart in General (Code-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
C1556247 (UMLS CUI-1)
MTHU112147 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Pericarditis
integer
Pericarditis Adverse Event (Code-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
C1963211 (UMLS CUI-1)
MTHU117310 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Fever
integer
Fever Without Neutropenia Adverse Event (Code-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
C1556366 (UMLS CUI-1)
MTHU116933 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Allergic Reaction
integer
Adverse Event Associated with Allergy and Immunology (Code-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
C1560126 (UMLS CUI-1)
MTHU112125 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Pain
integer
Other Pain Adverse Event (Code-1)
C1557623 (UMLS CUI-1)
MTHU117260 (CTCAE-1)
C1557623 (UMLS CUI-1)
MTHU117260 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Skin
integer
Other Dermatology or Skin Adverse Event (Code-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
C1559104 (UMLS CUI-1)
MTHU117246 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Cystitis
integer
Cystitis Adverse Event (Code-1)
C1963088 (UMLS CUI-1)
MTHU116844 (CTCAE-1)
C1963088 (UMLS CUI-1)
MTHU116844 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)
Item
Hematuria
integer
Hematuria (Code-1)
C0018965 (UMLS CUI-1)
34436003 (SNOMED CT-1)
10018867 (MedDRA-1)
R31.9 (ICD-10-CM-1)
599.7 (ICD-9-CM-1)
E13000 (CTCAE-1)
C0018965 (UMLS CUI-1)
34436003 (SNOMED CT-1)
10018867 (MedDRA-1)
R31.9 (ICD-10-CM-1)
599.7 (ICD-9-CM-1)
E13000 (CTCAE-1)
CL Item
no adverse event (0 = keine Nebenwirkungen)
Absent Adverse Event (Code-1)
C2699517 (UMLS CUI-1)
C2699517 (UMLS CUI-1)
CL Item
mild adverse event (1 = milde Nebenwirkungen)
Mild Adverse Event (Code-1)
C1513302 (UMLS CUI-1)
C1513302 (UMLS CUI-1)
CL Item
moderate adverse event (2 = moderate Nebenwirkungen)
Moderate Adverse Event (Code-1)
C1513374 (UMLS CUI-1)
C1513374 (UMLS CUI-1)
CL Item
strong adverse event (3 = schwere Nebenwirkungen)
Severe Adverse Event (Code-1)
C1519275 (UMLS CUI-1)
C1519275 (UMLS CUI-1)
CL Item
Life Threatening adverse event (4 = Lebensbedrohliche Nebenwirkungen)
Life Threatening Adverse Event (Code-1)
C1517874 (UMLS CUI-1)
C1517874 (UMLS CUI-1)
CL Item
unknown adverse event (X = Nebenwirkung unbekannt)
Unknown (Code-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
C0439673 (UMLS CUI-1)
261665006 (SNOMED CT-1)
CL Item
Death Related to Adverse Event (S = Tod)
Death Related to Adverse Event (Code-1)
C1705232 (UMLS CUI-1)
C1705232 (UMLS CUI-1)