Joom!Fish config error: Default language is inactive!
 
Please check configuration, try to use first active language

Case Study O5 - Discussion Part 5 - Answer (Question 1)
 

TraQ Program of the BC PBCO

Home Case Studies O-Level Case Study O5: Adverse event following plasma transfusion Case Study O5 - Discussion Part 5 - Answer (Question 1)
Tuesday, 21 November 2017

Case Study O5 - Discussion Part 5 - Answer (Question 1)

In Canada which three general categories of transfusion-related adverse events must be reported to the blood supplier or government regulator?

The three general categories that must be reported are

  1. serious adverse events (report to transfusion service)
  2. adverse reactions that can be attributed to the quality of the blood (report to blood supplier)
  3. fatalities (report to blood supplier for reporting to Health Canada)
Last modified on Friday, 08 April 2011 08:49