ID.1
Item
patient completed a previous efficacy study of thermoprofen.
boolean
C0008976 (UMLS CUI [1])
ID.2
Item
patient has a known allergy to nonsteroidal anti-inflammatory drugs (nsaids) (including aspirin).
boolean
C0020517 (UMLS CUI [1,1])
C0746949 (UMLS CUI [1,2])
ID.3
Item
patient has a suspected hypersensitivity, allergy, or other contraindication to any compound present in the study medication or has a known sensitivity to adhesive components similar to those used in thermoprofen (such as that found in adhesive bandages, e.g. band-aid®).
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
ID.4
Item
patient has asthma that has been induced or made worse by the use of aspirin or any other nsaid.
boolean
C0004096 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C0003211 (UMLS CUI [1,3])
ID.5
Item
patient has a relevant history of serious gastrointestinal disease.
boolean
C0017178 (UMLS CUI [1])
ID.6
Item
patient has a defect, injury, or dermatologic disease or condition on the skin area where the study patch will be applied that may interfere with tolerability or post-application evaluations.
boolean
C0037274 (UMLS CUI [1])
ID.7
Item
patient has neurological or psychiatric disease sufficient to compromise data collection or integrity.
boolean
C0027765 (UMLS CUI [1,1])
C0004936 (UMLS CUI [1,2])
ID.8
Item
patient is taking warfarin, heparin, or low molecular weight heparin.
boolean
C0043031 (UMLS CUI [1,1])
C0019134 (UMLS CUI [1,2])
C0019139 (UMLS CUI [1,3])
ID.9
Item
patient, if female, is pregnant or breastfeeding or is of childbearing potential and not practicing adequate birth control.
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0009862 (UMLS CUI [1,3])