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Serious (Product) Events and Adverse Reactions: S(P)EAR

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 as a 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.



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.


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