signed informed consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
hcv- infected patients
Item
hcv- infected patients confirmed by pcr or branched dna (b-dna)
boolean
C3844790 (UMLS CUI [1])
scheduled to commence combination rbv/ifn or rbv/peg-ifn therapy on day 1
Item
scheduled to commence combination rbv/ifn or rbv/peg-ifn therapy on day 1
boolean
C0205539 (UMLS CUI [1,1])
C1971490 (UMLS CUI [1,2])
C0205539 (UMLS CUI [2,1])
C0035525 (UMLS CUI [2,2])
C0279030 (UMLS CUI [2,3])
normal serum creatinine
Item
normal serum creatinine
boolean
C0201976 (UMLS CUI [1])
life expectancy > 6 months
Item
life expectancy > 6 months
boolean
C0023671 (UMLS CUI [1])
hiv-infected patients
Item
hiv-infected patients
boolean
C0019699 (UMLS CUI [1])
history of any primary hematologic disease
Item
history of any primary hematologic disease
boolean
C0018939 (UMLS CUI [1,1])
C0277554 (UMLS CUI [1,2])
attributable anemia
Item
anemia attributable to factors such as iron or folate deficiency, pre-treatment
boolean
C0162316 (UMLS CUI [1])
C0497165 (UMLS CUI [2])
hemolysis or gastrointestinal bleeding
Item
hemolysis or gastrointestinal bleeding
boolean
C0019054 (UMLS CUI [1])
C0017181 (UMLS CUI [2])
other hepatic disease
Item
has suspected or confirmed significant hepatic disease from an etiology other than
boolean
C0023895 (UMLS CUI [1])
hcv
Item
hcv (e.g. alcohol, hbv, autoimmune disease etc)
boolean
C0220847 (UMLS CUI [1])
active substance use disorder
Item
current, active substance abuser
boolean
C0038586 (UMLS CUI [1])
pregnant or breast feeding
Item
pregnant or breast feeding
boolean
C0549206 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
birth control measures
Item
women of childbearing potential not taking adequate birth control measures
boolean
C0700589 (UMLS CUI [1])
epoetin alfa
Item
exposure to epoetin alfa within three (3) months prior to study enrollment or during study
boolean
C0357126 (UMLS CUI [1])
recent transfusions
Item
transfusion within three (3) months prior to study entry
boolean
C0005841 (UMLS CUI [1])