Thromboembolic events reported in association with idarucizumab and andexanet alfa: disproportionality analysis of the Food and Drugs Administration Adverse Eventr Resporting System (FAERS) database (Idarucizumab/andexanet alfa & thromboembolism)

24/10/2023
02/04/2024
EU PAS number:
EUPAS107330
Study
Ongoing
Documents
Study protocol
Initial protocol
English (937.54 KB - PDF) View document
Updated protocol
English (940.16 KB - PDF) View document
Study results
Study report
Other information