The WMDA has set up a central global reporting system for WMDA member organisations to report Serious (Product) Events and Adverse Reactions – S(P)EARs – to the WMDA.
Aim
Purpose
To collect and analyze information on recipient and donor serious adverse events (SAE) and reactions which affect donors and/or products from all WMDA stem cell
donor registries and cord blood banks.
To follow a rapid alert system for disseminating information on SAE/R to all members of the international community in contact with allogeneic donors and patients.
Quick links
See for more graphs the S(P)EAR Annual Report of 2018 |