An Observational Post-Authorization Safety Specialist Cohort Event Monitoring Study (SCEM) to Monitor the Safety and Utilization of Rivaroxaban (Xarelto®) for the Prevention of Stroke in Patients with AF, Treatment of DVT and PE, and the Prevention of Recurrent DVT and PE in the Secondary Care Hospital Setting in England and Wales (ROSE)

22/05/2013
01/04/2024
EU PAS number:
EUPAS3979
Study
Finalised
Documents
Study protocol
Initial protocol
English (1.25 MB - PDF) View document
Study results
Study results
English (458.46 KB - PDF) View document
Study report
Study report
English (6.13 MB - PDF) View document
Other information