Important note!
The S(P)EAR Committee reviews all reported incidents once a week. If you have a rapid alert that needs to be shared with the community quickly, we urge you to send a separate e-mail to the WMDA office (sear-spear@wmda.info) or call us on: +31 88 505 7900.
Serious (Product) Events and Adverse Reactions: S(P)EAR
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
- To gain insight in the occurrence of serious events and adverse effects in relation to blood stem cell donation by unrelated donors and blood stem cell collection/processing from unrelated donors.
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.
*See for more graphs the Annual Report of 2018