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WMDA has set up a central global reporting system

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, contact the WMDA office. 

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.

In case of recall or big risks for future donations or transfusions a report can be submitted as a rapid alert. This includes, but is not limited to:

• any prohibition or restriction imposed by the competent authority/health authorities of any country in which the stem cell product is provided or transplanted;
• donor death;