Non-interventional post-authorization cohort safety study evaluating the effectiveness of the additional risk minimization measures for filgotinib (Jyseleca®) use in patients with moderate to severe active rheumatoid arthritis within European registries

29/06/2022
10/03/2025
EU PAS number:
EUPAS46852
Study
Ongoing

ENCePP Code of conduct

No
Data sources

Data source(s)

Data source(s), other

ARTIS Sweden, BIOBADASER Spain, DANBIO Denmark

Data sources (types)

Disease registry
Other

Data sources (types), other

Exposure registry
Use of a Common Data Model (CDM)

CDM mapping

No
Data quality specifications

Check conformance

Unknown

Check completeness

Unknown

Check stability

Unknown

Check logical consistency

Unknown
Data characterisation

Data characterisation conducted

No