AN OBSERVATIONAL POST-AUTHORIZATION MODIFIED PRESCRIPTION-EVENT MONITORING SAFETY STUDY TO MONITOR THE SAFETY AND UTILIZATION OF EXENATIDE ONCE WEEKLY (BYDUREON®) IN THE PRIMARY CARE SETTING IN ENGLAND

21/01/2014
16/02/2024
EU PAS number:
EUPAS5599
Study
Finalised
Documents
Study protocol
Initial protocol
English (722.7 KB - PDF) View document
Study results
Study results
English (4.2 MB - PDF) View document
Study report
Other information