ID
44688
Beschrijving
ODM derived from http://clinicaltrials.gov/show/NCT01234311
Link
http://clinicaltrials.gov/show/NCT01234311
Trefwoorden
Versies (3)
- 12-02-13 12-02-13 - Martin Dugas
- 19-04-14 19-04-14 - Julian Varghese
- 27-09-21 27-09-21 -
Geüploaded op
27 september 2021
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility DRKS00006523 NCT01234311 Prostate Cancer
Eligibility
- StudyEvent: Eligibility
Beschrijving
Ausschlusskriterien
Beschrijving
Prior cytotoxic chemotherapy for the treatment of prostate ca within 2 years or within 4 weeks for Estracyt (estramustine) prior to study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C0677881
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0600139
- SNOMED CT 2011_0131
- 254900004
- MedDRA 14.1
- 10036921
- UMLS CUI 2011AA
- C0014922
- SNOMED CT 2011_0131
- 108769008
- UMLS CUI 2011AA
- C0014921
- SNOMED CT 2011_0131
- 108768000
Beschrijving
Previous anticancer therapy using radiation, biologics or vaccines, including abiraterone, TAK-700 (Orteronel), or MDV3100 within 4 weeks prior or sipuleucel-T (Provenge) within 2 weeks prior to the start of study treatment. If radiation therapy is applied after baseline scan, a new baseline scan needs to be done at least 4 weeks after the radiation therapy.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- C0920425
- UMLS CUI 2011AA
- C0034619
- UMLS CUI 2011AA
- C0005515
- UMLS CUI 2011AA
- C0042210
- SNOMED CT 2011_0131
- 71181003
- LOINC Version 232
- MTHU014526
- UMLS CUI 2011AA
- C0754011
- UMLS CUI 2011AA
- CL383463
- UMLS CUI 2011AA
- C2348174
- UMLS CUI 2011AA
- C1706668
Beschrijving
Previous therapy with antiandrogens within 4 weeks (within 6 weeks for bicalutamide eg, Casodex) prior to study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C1514463
- UMLS CUI 2011AA
- C0002842
- SNOMED CT 2011_0131
- 346324007
- UMLS CUI 2011AA
- C0285590
- SNOMED CT 2011_0131
- 108766001
Beschrijving
Concurrent use of other anticancer agents or treatments, with the following exceptions:
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205420
- SNOMED CT 2011_0131
- 68405009
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0003392
- SNOMED CT 2011_0131
- 372688009
- UMLS CUI 2011AA
- C0920425
- UMLS CUI 2011AA
- C0332282
- SNOMED CT 2011_0131
- 255260001
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
Beschrijving
Ongoing treatment with luteinizing hormone-releasing hormone agonists or antagonists, denosumab (Prolia) or bisphosphonate (eg, zoledronic acid) is allowed. Ongoing treatment should be kept at a stable schedule; however, if medically required, a change of dose, compound, or both is allowed.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0549178
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C1518041
- UMLS CUI 2011AA
- C1276926
- SNOMED CT 2011_0131
- 326082006
- UMLS CUI 2011AA
- C1524004
- UMLS CUI 2011AA
- C1690432
- SNOMED CT 2011_0131
- 446457007
- UMLS CUI 2011AA
- C0012544
- SNOMED CT 2011_0131
- 372907000
- UMLS CUI 2011AA
- C0257685
- SNOMED CT 2011_0131
- 395926009
Beschrijving
Any treatment modalities involving major surgery within 4 weeks prior to the start of study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0695347
- LOINC Version 232
- MTHU010422
- UMLS CUI 2011AA
- C1314939
- SNOMED CT 2011_0131
- 248448006
- UMLS CUI 2011AA
- C0679637
Beschrijving
Prostate ca pain that requires ongoing treatment with narcotic analgesics or warrants the initiation of radio- or chemotherapy.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0600139
- SNOMED CT 2011_0131
- 254900004
- MedDRA 14.1
- 10036921
- UMLS CUI 2011AA
- C0030193
- SNOMED CT 2011_0131
- 22253000
- MedDRA 14.1
- 10033371
- LOINC Version 232
- MTHU029813
- ICD-10-CM Version 2010
- R52
- ICD-9-CM Version 2011
- 338-338.9
- CTCAE 1105E
- E11167
- UMLS CUI 2011AA
- C1514873
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0027409
- SNOMED CT 2011_0131
- 360204007
- UMLS CUI 2011AA
- C1552821
- HL7 V3 2006_05
- justify
- UMLS CUI 2011AA
- C1704686
- UMLS CUI 2011AA
- C0034619
- UMLS CUI 2011AA
- C0392920
- SNOMED CT 2011_0131
- 150415003
Beschrijving
Ongoing treatment with warfarin unless the international normalized ratio (INR) is well controlled and below 4 (Section 4.6.8.1).
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0549178
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0043031
- SNOMED CT 2011_0131
- 48603004
- LOINC Version 232
- MTHU003212
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
- UMLS CUI 2011AA
- C0525032
- SNOMED CT 2011_0131
- 165581004
- MedDRA 14.1
- 10022400
Beschrijving
Maintenance treatment with corticosteroids corresponding to a prednisolone or prednisone dose above 10 mg/day. The dose must have been stable for at least 5 days.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0677908
- SNOMED CT 2011_0131
- 314122007
- UMLS CUI 2011AA
- C0001617
- SNOMED CT 2011_0131
- 79440004
- UMLS CUI 2011AA
- CL415123
- UMLS CUI 2011AA
- C0032950
- SNOMED CT 2011_0131
- 116601002
- LOINC Version 232
- MTHU003522
- UMLS CUI 2011AA
- C0032952
- SNOMED CT 2011_0131
- 116602009
- LOINC Version 232
- MTHU003245
- UMLS CUI 2011AA
- C0178602
- SNOMED CT 2011_0131
- 260911001
Beschrijving
Systemic exposure to ketoconazole or other strong cytochrome P450 (CYP) 3A4 isozyme inhibitors or inducers within 14 days prior to the start of study treatment. Systemic exposure to amiodarone is not allowed within 1 year prior to the start of study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205373
- SNOMED CT 2011_0131
- 31099001
- UMLS CUI 2011AA
- C0332157
- SNOMED CT 2011_0131
- 24932003
- UMLS CUI 2011AA
- C0022625
- SNOMED CT 2011_0131
- 387216007
- LOINC Version 232
- MTHU002299
- UMLS CUI 2011AA
- C2962753
- UMLS CUI 2011AA
- C0002598
- SNOMED CT 2011_0131
- 372821002
- LOINC Version 232
- MTHU004841
Beschrijving
Ongoing treatment with sensitive CYP1A2 substrate or CYP1A2 substrate with narrow therapeutic range at the start of study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0549178
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0332324
- SNOMED CT 2011_0131
- 83185005
- UMLS CUI 2011AA
- C0207509
- SNOMED CT 2011_0131
- 424020001
- UMLS CUI 2011AA
- C0178623
Beschrijving
Ongoing treatment with CYP3A4 substrate with narrow therapeutic range at the start of study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0549178
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C1142644
- SNOMED CT 2011_0131
- 422741004
- UMLS CUI 2011AA
- C0178623
- UMLS CUI 2011AA
- CL407604
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C1514721
Beschrijving
Simultaneous participation in any other study involving treatment with investigational drugs or having received treatment with investigational drugs < 4 weeks prior to the start of study treatment.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0521115
- SNOMED CT 2011_0131
- 79970003
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C0039798
- UMLS CUI 2011AA
- C0013230
Beschrijving
Myocardial infarction, percutaneous coronary intervention, acute coronary syndrome, coronary artery bypass graft, class III/IV congestive heart failure, cerebrovascular accident, transient ischemic attack, or limb claudication at rest, within 6 months prior to start of study treatment and ongoing symptomatic dysrhythmias, unstable angina, uncontrolled hypertension, and uncontrolled atrial or ventricular arrhythmias.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0027051
- SNOMED CT 2011_0131
- 22298006
- MedDRA 14.1
- 10028596
- LOINC Version 232
- MTHU035551
- ICD-10-CM Version 2010
- I21-I22
- ICD-9-CM Version 2011
- 410
- CTCAE 1105E
- E10152
- UMLS CUI 2011AA
- C1532338
- SNOMED CT 2011_0131
- 415070008
- MedDRA 14.1
- 10065608
- UMLS CUI 2011AA
- C0948089
- SNOMED CT 2011_0131
- 394659003
- MedDRA 14.1
- 10051592
- CTCAE 1105E
- E10066
- UMLS CUI 2011AA
- C0010055
- SNOMED CT 2011_0131
- 232717009
- MedDRA 14.1
- 10011077
- ICD-9-CM Version 2011
- 36.10
- UMLS CUI 2011AA
- C0018802
- SNOMED CT 2011_0131
- 42343007
- MedDRA 14.1
- 10007559
- LOINC Version 232
- MTHU020787
- ICD-10-CM Version 2010
- I50.9
- ICD-9-CM Version 2011
- 428.0
- UMLS CUI 2011AA
- C1319795
- SNOMED CT 2011_0131
- 420913000
- MedDRA 14.1
- 10064081
- UMLS CUI 2011AA
- C1319796
- SNOMED CT 2011_0131
- 422293003
- MedDRA 14.1
- 10064082
- UMLS CUI 2011AA
- C0038454
- SNOMED CT 2011_0131
- 230690007
- MedDRA 14.1
- 10042244
- ICD-10-CM Version 2010
- I63.9
- CTCAE 1105E
- E12826
- UMLS CUI 2011AA
- C0007787
- SNOMED CT 2011_0131
- 266257000
- MedDRA 14.1
- 10044390
- LOINC Version 232
- MTHU020810
- ICD-10-CM Version 2010
- G45.9
- ICD-9-CM Version 2011
- 435.9
- CTCAE 1105E
- E12834
- UMLS CUI 2011AA
- C0015385
- SNOMED CT 2011_0131
- 66019005
- LOINC Version 232
- MTHU001429
- UMLS CUI 2011AA
- C0311395
- SNOMED CT 2011_0131
- 275520000
- MedDRA 14.1
- 10009240
- UMLS CUI 2011AA
- C0443144
- SNOMED CT 2011_0131
- 263678003
- UMLS CUI 2011AA
- C0003811
- SNOMED CT 2011_0131
- 44808001
- MedDRA 14.1
- 10003119
- ICD-9-CM Version 2011
- 427.9
- UMLS CUI 2011AA
- C0002965
- SNOMED CT 2011_0131
- 4557003
- MedDRA 14.1
- 10002388
- ICD-10-CM Version 2010
- I20.0
- ICD-9-CM Version 2011
- 411.1
- UMLS CUI 2011AA
- C1868885
- MedDRA 14.1
- 10066860
- UMLS CUI 2011AA
- C0205318
- SNOMED CT 2011_0131
- 19032002
- UMLS CUI 2011AA
- C0085611
- SNOMED CT 2011_0131
- 17366009
- MedDRA 14.1
- 10003656
- UMLS CUI 2011AA
- C0085612
- SNOMED CT 2011_0131
- 44103008
- MedDRA 14.1
- 10047281
- ICD-10-CM Version 2010
- I49.01
- CTCAE 1105E
- E10230
Beschrijving
History of pancreatitis.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0030305
- SNOMED CT 2011_0131
- 75694006
- MedDRA 14.1
- 10033645
- ICD-10-CM Version 2010
- K85.9
- ICD-9-CM Version 2011
- 577.0
- CTCAE 1105E
- E10930
Beschrijving
Known brain or epidural metastases.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0220650
- MedDRA 14.1
- 10006128
- UMLS CUI 2011AA
- CL337434
- UMLS CUI 2011AA
- C0027627
- SNOMED CT 2011_0131
- 128462008
- MedDRA 14.1
- 10027449
Beschrijving
Known positive serology for HIV (patients with known history of HIV will be excluded because of potential for unforeseen toxicity and morbidity in an immunocompromised host).
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0019699
- SNOMED CT 2011_0131
- 165816005
- MedDRA 14.1
- 10020188
- ICD-10-CM Version 2010
- Z21
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0019682
- SNOMED CT 2011_0131
- 19030005
- UMLS CUI 2011AA
- C0237399
- UMLS CUI 2011AA
- C0040539
- UMLS CUI 2011AA
- C0220880
- UMLS CUI 2011AA
- C0085393
- SNOMED CT 2011_0131
- 370388006
Beschrijving
Chronic hepatitis with advanced, decompensated hepatic disease or cirrhosis of the liver or history of a chronic viral hepatitis or known viral hepatitis carrier (patients who have recovered from hepatitis will be allowed to enter the study).
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0019189
- SNOMED CT 2011_0131
- 76783007
- MedDRA 14.1
- 10008909
- ICD-10-CM Version 2010
- K73.9
- ICD-9-CM Version 2011
- 571.40
- UMLS CUI 2011AA
- C0205179
- SNOMED CT 2011_0131
- 86005002
- UMLS CUI 2011AA
- C0745744
- MedDRA 14.1
- 10050060
- UMLS CUI 2011AA
- C0023890
- SNOMED CT 2011_0131
- 19943007
- MedDRA 14.1
- 10019641
- ICD-10-CM Version 2010
- K74.60
- UMLS CUI 2011AA
- C0276623
- SNOMED CT 2011_0131
- 10295004
- ICD-10-CM Version 2010
- B18
- UMLS CUI 2011AA
- C0733680
- SNOMED CT 2011_0131
- 170489004
- MedDRA 14.1
- 10047458
Beschrijving
Patients with active tuberculosis (TB), or with known, untreated latent TB. (Country-specific TB therapy should have been given for at least 30 days prior to the start of study treatment and the patient should intend to complete the entire course of that therapy.)
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0151332
- SNOMED CT 2011_0131
- 427099000
- MedDRA 14.1
- 10071157
- UMLS CUI 2011AA
- C1518422
- UMLS CUI 2011AA
- CL415147
- UMLS CUI 2011AA
- C1609538
- MedDRA 14.1
- 10065048
Beschrijving
Any condition, including other active or latent infections, medical or psychiatric conditions, or the presence of laboratory abnormalities, which could confound the ability to interpret data from the study or places the patient at unacceptable risk if he participates in the study.
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0348080
- SNOMED CT 2011_0131
- 260905004
- HL7 V3 2006_05
- COND
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0009450
- SNOMED CT 2011_0131
- 257551009
- MedDRA 14.1
- 10021789
- UMLS CUI 2011AA
- C1699700
- HL7 V3 2006_05
- MEDCCAT
- UMLS CUI 2011AA
- C0278060
- SNOMED CT 2011_0131
- 36456004
- LOINC Version 232
- MTHU001424
- CTCAE 1105E
- MTHU117157
- UMLS CUI 2011AA
- C0438215
- SNOMED CT 2011_0131
- 165346000
- MedDRA 14.1
- 10023547
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C0085732
- SNOMED CT 2011_0131
- 371150009
- UMLS CUI 2011AA
- C0459471
- SNOMED CT 2011_0131
- 280452008
- LOINC Version 232
- MTHU003869
- UMLS CUI 2011AA
- C0681873
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C1883420
- UMLS CUI 2011AA
- C0035647
- SNOMED CT 2011_0131
- 30207005
- HL7 V3 2006_05
- RSK
Beschrijving
Any patient who in the opinion of the investigator should not participate
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0022423
- SNOMED CT 2011_0131
- 61254005
- UMLS CUI 2011AA
- CL102947
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C1518422
- UMLS CUI 2011AA
- C0034866
- LOINC Version 232
- MTHU036724
- HL7 V3 2006_05
- RMD
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116154003 (SNOMED CT 2011_0131)
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C0039798 (UMLS CUI 2011AA)
C0600139 (UMLS CUI 2011AA)
254900004 (SNOMED CT 2011_0131)
10036921 (MedDRA 14.1)
C0014922 (UMLS CUI 2011AA)
108769008 (SNOMED CT 2011_0131)
C0014921 (UMLS CUI 2011AA)
108768000 (SNOMED CT 2011_0131)
9130008 (SNOMED CT 2011_0131)
C0920425 (UMLS CUI 2011AA)
C0034619 (UMLS CUI 2011AA)
C0005515 (UMLS CUI 2011AA)
C0042210 (UMLS CUI 2011AA)
71181003 (SNOMED CT 2011_0131)
MTHU014526 (LOINC Version 232)
C0754011 (UMLS CUI 2011AA)
CL383463 (UMLS CUI 2011AA)
C2348174 (UMLS CUI 2011AA)
C1706668 (UMLS CUI 2011AA)
C0002842 (UMLS CUI 2011AA)
346324007 (SNOMED CT 2011_0131)
C0285590 (UMLS CUI 2011AA)
108766001 (SNOMED CT 2011_0131)
68405009 (SNOMED CT 2011_0131)
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0003392 (UMLS CUI 2011AA)
372688009 (SNOMED CT 2011_0131)
C0920425 (UMLS CUI 2011AA)
C0332282 (UMLS CUI 2011AA)
255260001 (SNOMED CT 2011_0131)
C1554961 (UMLS CUI 2011AA)
E (HL7 V3 2006_05)
C0039798 (UMLS CUI 2011AA)
C1518041 (UMLS CUI 2011AA)
C1276926 (UMLS CUI 2011AA)
326082006 (SNOMED CT 2011_0131)
C1524004 (UMLS CUI 2011AA)
C1690432 (UMLS CUI 2011AA)
446457007 (SNOMED CT 2011_0131)
C0012544 (UMLS CUI 2011AA)
372907000 (SNOMED CT 2011_0131)
C0257685 (UMLS CUI 2011AA)
395926009 (SNOMED CT 2011_0131)
C0695347 (UMLS CUI 2011AA)
MTHU010422 (LOINC Version 232)
C1314939 (UMLS CUI 2011AA)
248448006 (SNOMED CT 2011_0131)
C0679637 (UMLS CUI 2011AA)
254900004 (SNOMED CT 2011_0131)
10036921 (MedDRA 14.1)
C0030193 (UMLS CUI 2011AA)
22253000 (SNOMED CT 2011_0131)
10033371 (MedDRA 14.1)
MTHU029813 (LOINC Version 232)
R52 (ICD-10-CM Version 2010)
338-338.9 (ICD-9-CM Version 2011)
E11167 (CTCAE 1105E)
C1514873 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
C0027409 (UMLS CUI 2011AA)
360204007 (SNOMED CT 2011_0131)
C1552821 (UMLS CUI 2011AA)
justify (HL7 V3 2006_05)
C1704686 (UMLS CUI 2011AA)
C0034619 (UMLS CUI 2011AA)
C0392920 (UMLS CUI 2011AA)
150415003 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0043031 (UMLS CUI 2011AA)
48603004 (SNOMED CT 2011_0131)
MTHU003212 (LOINC Version 232)
C1554961 (UMLS CUI 2011AA)
E (HL7 V3 2006_05)
C0525032 (UMLS CUI 2011AA)
165581004 (SNOMED CT 2011_0131)
10022400 (MedDRA 14.1)
314122007 (SNOMED CT 2011_0131)
C0001617 (UMLS CUI 2011AA)
79440004 (SNOMED CT 2011_0131)
CL415123 (UMLS CUI 2011AA)
C0032950 (UMLS CUI 2011AA)
116601002 (SNOMED CT 2011_0131)
MTHU003522 (LOINC Version 232)
C0032952 (UMLS CUI 2011AA)
116602009 (SNOMED CT 2011_0131)
MTHU003245 (LOINC Version 232)
C0178602 (UMLS CUI 2011AA)
260911001 (SNOMED CT 2011_0131)
31099001 (SNOMED CT 2011_0131)
C0332157 (UMLS CUI 2011AA)
24932003 (SNOMED CT 2011_0131)
C0022625 (UMLS CUI 2011AA)
387216007 (SNOMED CT 2011_0131)
MTHU002299 (LOINC Version 232)
C2962753 (UMLS CUI 2011AA)
C0002598 (UMLS CUI 2011AA)
372821002 (SNOMED CT 2011_0131)
MTHU004841 (LOINC Version 232)
C0039798 (UMLS CUI 2011AA)
C0332324 (UMLS CUI 2011AA)
83185005 (SNOMED CT 2011_0131)
C0207509 (UMLS CUI 2011AA)
424020001 (SNOMED CT 2011_0131)
C0178623 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
C1142644 (UMLS CUI 2011AA)
422741004 (SNOMED CT 2011_0131)
C0178623 (UMLS CUI 2011AA)
CL407604 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
C1514721 (UMLS CUI 2011AA)
79970003 (SNOMED CT 2011_0131)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0013230 (UMLS CUI 2011AA)
22298006 (SNOMED CT 2011_0131)
10028596 (MedDRA 14.1)
MTHU035551 (LOINC Version 232)
I21-I22 (ICD-10-CM Version 2010)
410 (ICD-9-CM Version 2011)
E10152 (CTCAE 1105E)
C1532338 (UMLS CUI 2011AA)
415070008 (SNOMED CT 2011_0131)
10065608 (MedDRA 14.1)
C0948089 (UMLS CUI 2011AA)
394659003 (SNOMED CT 2011_0131)
10051592 (MedDRA 14.1)
E10066 (CTCAE 1105E)
C0010055 (UMLS CUI 2011AA)
232717009 (SNOMED CT 2011_0131)
10011077 (MedDRA 14.1)
36.10 (ICD-9-CM Version 2011)
C0018802 (UMLS CUI 2011AA)
42343007 (SNOMED CT 2011_0131)
10007559 (MedDRA 14.1)
MTHU020787 (LOINC Version 232)
I50.9 (ICD-10-CM Version 2010)
428.0 (ICD-9-CM Version 2011)
C1319795 (UMLS CUI 2011AA)
420913000 (SNOMED CT 2011_0131)
10064081 (MedDRA 14.1)
C1319796 (UMLS CUI 2011AA)
422293003 (SNOMED CT 2011_0131)
10064082 (MedDRA 14.1)
C0038454 (UMLS CUI 2011AA)
230690007 (SNOMED CT 2011_0131)
10042244 (MedDRA 14.1)
I63.9 (ICD-10-CM Version 2010)
E12826 (CTCAE 1105E)
C0007787 (UMLS CUI 2011AA)
266257000 (SNOMED CT 2011_0131)
10044390 (MedDRA 14.1)
MTHU020810 (LOINC Version 232)
G45.9 (ICD-10-CM Version 2010)
435.9 (ICD-9-CM Version 2011)
E12834 (CTCAE 1105E)
C0015385 (UMLS CUI 2011AA)
66019005 (SNOMED CT 2011_0131)
MTHU001429 (LOINC Version 232)
C0311395 (UMLS CUI 2011AA)
275520000 (SNOMED CT 2011_0131)
10009240 (MedDRA 14.1)
C0443144 (UMLS CUI 2011AA)
263678003 (SNOMED CT 2011_0131)
C0003811 (UMLS CUI 2011AA)
44808001 (SNOMED CT 2011_0131)
10003119 (MedDRA 14.1)
427.9 (ICD-9-CM Version 2011)
C0002965 (UMLS CUI 2011AA)
4557003 (SNOMED CT 2011_0131)
10002388 (MedDRA 14.1)
I20.0 (ICD-10-CM Version 2010)
411.1 (ICD-9-CM Version 2011)
C1868885 (UMLS CUI 2011AA)
10066860 (MedDRA 14.1)
C0205318 (UMLS CUI 2011AA)
19032002 (SNOMED CT 2011_0131)
C0085611 (UMLS CUI 2011AA)
17366009 (SNOMED CT 2011_0131)
10003656 (MedDRA 14.1)
C0085612 (UMLS CUI 2011AA)
44103008 (SNOMED CT 2011_0131)
10047281 (MedDRA 14.1)
I49.01 (ICD-10-CM Version 2010)
E10230 (CTCAE 1105E)
392521001 (SNOMED CT 2011_0131)
C0030305 (UMLS CUI 2011AA)
75694006 (SNOMED CT 2011_0131)
10033645 (MedDRA 14.1)
K85.9 (ICD-10-CM Version 2010)
577.0 (ICD-9-CM Version 2011)
E10930 (CTCAE 1105E)
10006128 (MedDRA 14.1)
CL337434 (UMLS CUI 2011AA)
C0027627 (UMLS CUI 2011AA)
128462008 (SNOMED CT 2011_0131)
10027449 (MedDRA 14.1)
165816005 (SNOMED CT 2011_0131)
10020188 (MedDRA 14.1)
Z21 (ICD-10-CM Version 2010)
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0019682 (UMLS CUI 2011AA)
19030005 (SNOMED CT 2011_0131)
C0237399 (UMLS CUI 2011AA)
C0040539 (UMLS CUI 2011AA)
C0220880 (UMLS CUI 2011AA)
C0085393 (UMLS CUI 2011AA)
370388006 (SNOMED CT 2011_0131)
76783007 (SNOMED CT 2011_0131)
10008909 (MedDRA 14.1)
K73.9 (ICD-10-CM Version 2010)
571.40 (ICD-9-CM Version 2011)
C0205179 (UMLS CUI 2011AA)
86005002 (SNOMED CT 2011_0131)
C0745744 (UMLS CUI 2011AA)
10050060 (MedDRA 14.1)
C0023890 (UMLS CUI 2011AA)
19943007 (SNOMED CT 2011_0131)
10019641 (MedDRA 14.1)
K74.60 (ICD-10-CM Version 2010)
C0276623 (UMLS CUI 2011AA)
10295004 (SNOMED CT 2011_0131)
B18 (ICD-10-CM Version 2010)
C0733680 (UMLS CUI 2011AA)
170489004 (SNOMED CT 2011_0131)
10047458 (MedDRA 14.1)
427099000 (SNOMED CT 2011_0131)
10071157 (MedDRA 14.1)
C1518422 (UMLS CUI 2011AA)
CL415147 (UMLS CUI 2011AA)
C1609538 (UMLS CUI 2011AA)
10065048 (MedDRA 14.1)
260905004 (SNOMED CT 2011_0131)
COND (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0009450 (UMLS CUI 2011AA)
257551009 (SNOMED CT 2011_0131)
10021789 (MedDRA 14.1)
C1699700 (UMLS CUI 2011AA)
MEDCCAT (HL7 V3 2006_05)
C0278060 (UMLS CUI 2011AA)
36456004 (SNOMED CT 2011_0131)
MTHU001424 (LOINC Version 232)
MTHU117157 (CTCAE 1105E)
C0438215 (UMLS CUI 2011AA)
165346000 (SNOMED CT 2011_0131)
10023547 (MedDRA 14.1)
C0521102 (UMLS CUI 2011AA)
78235001 (SNOMED CT 2011_0131)
C0085732 (UMLS CUI 2011AA)
371150009 (SNOMED CT 2011_0131)
C0459471 (UMLS CUI 2011AA)
280452008 (SNOMED CT 2011_0131)
MTHU003869 (LOINC Version 232)
C0681873 (UMLS CUI 2011AA)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C1883420 (UMLS CUI 2011AA)
C0035647 (UMLS CUI 2011AA)
30207005 (SNOMED CT 2011_0131)
RSK (HL7 V3 2006_05)
61254005 (SNOMED CT 2011_0131)
CL102947 (UMLS CUI 2011AA)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C1518422 (UMLS CUI 2011AA)
C0034866 (UMLS CUI 2011AA)
MTHU036724 (LOINC Version 232)
RMD (HL7 V3 2006_05)