ReFacto AF (moroctocog alfa) Prescribing Information for Great Britain click here. ReFacto AF (moroctocog alfa) Prescribing Information for Northern Ireland click here.
Adverse event reporting information can be found at the bottom of the page.
ReFacto AF® (moroctocog alfa) is indicated for the treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency). ReFacto AF® is appropriate for use in adults and children of all ages, including newborns. ReFacto AF® does not contain von Willebrand factor, and hence is not indicated in von Willebrand's disease.1
The original ReFacto® (moroctocog alfa) was approved in 1999 - the first recombinant factor VIII product licensed for patients with haemophilia A.1
Pfizer continue to invest in the research and development of haemophilia treatment.
ReFacto AF® (moroctocog alfa) contains recombinant coagulation factor VIII, which has functional characteristics comparable to those of endogenous factor VIII.1
The ReFacto AF® manufacturing process is completely albumin-free from cell culture to the end product.10
ReFacto AF® has a well-documented safety profile in adult patients. Paediatric safety profile is comparable to that of adults.1
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PP-PFE-GBR-3863. November 2021
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