An observational post-authorization Modified Prescription-Event Monitoring safety study to monitor the safety and utilization of rivaroxaban (XARELTO®) for the prevention of stroke in patients with AF, treatment of DVT and PE, and prevention of recurrent DVT and PE following an acute DVT in the primary care setting in England, extended to include Acute Coronary Syndrome Patients (Rivaroxaban MPEM)

25/10/2016
01/04/2024
EU PAS number:
EUPAS15961
Study
Finalised
Documents
Study protocol
Initial protocol
English (1.55 MB - PDF) View document
Updated protocol
English (1.46 MB - PDF) View document
Study results
Study results
English (134.43 KB - PDF) View document
Study report
Other information