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.
To access the reporting system, you login with your email address and password. If you do not have a password yet, please check with the WMDA office whether you are registered S(P)EAR reporter.
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 analyse 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 the Annual Report of 2019 for more graphs and details