Post-Authorisation Safety Study (PASS) on Flupirtine-containing Medicinal Products - A retrospective, multicentre, non-interventional study to evaluate the effectiveness of the risk minimisation activities for flupirtine-containing medicinal products

12/11/2015
31/03/2024
EU PAS number:
EUPAS11571
Study
Finalised

ENCePP Code of conduct

No
Data sources

Data sources (types)

Other

Data sources (types), other

Data of this PASS derived from the patients’ medical records and were collected by using a case report form (CRF) specified to the study purpose.
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

Unknown