Month: May 2017
May 8, 2017
No “clear and consistent evidence” of difference in inhibitor risk
There is no clear and consistent evidence of a difference in the incidence of inhibitor development between factor VIII products derived from plasma and those made by recombinant DNA technology. The Pharmacovigilance Risk Assessment Committee (PRAC) of the European Medicines Agency has now completed its review of factor VIII medicines to evaluate the risk of …
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