Informed Consent
Item
provision of subject informed consent.
boolean
C0021430 (UMLS CUI [1])
Age
Item
female and/or male, aged > 21 years.
boolean
C0001779 (UMLS CUI [1])
Rheumatoid Arthritis | Osteoarthritis | Ankylosing spondylitis
Item
patients diagnosis with ra (acr 1987 or acr/eular 2010 criteria), oa (acr 1986, 1990 and 1991 criteria) or as (new york 1984 criteria or essg 2002 criteria) (documented in the medical record).
boolean
C0003873 (UMLS CUI [1])
C0029408 (UMLS CUI [2])
C0038013 (UMLS CUI [3])
NSAIDs Dose Quantity
Item
patients receiving at least one dose of nsaids.
boolean
C0003211 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Study Subject Participation Status | Interventional Study Involving Investigational New Drugs
Item
participation in any interventional study involving investigational drugs.
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0013230 (UMLS CUI [2,3])
Clinical Trial Subject Questionnaire Completion Refused
Item
patient refuses to fill in the study questionnaires.
boolean
C3890411 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Neoplastic disease | Exception Basal cell carcinoma
Item
patients with active neoplastic disease in the last 5 years, except basal-cell carcinoma.
boolean
C1882062 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])