Evolution of recombinant factor VIII safety: KOGENATE® and Kogenate® FS/Bayer
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12185-009-0435-x.pdf
Reference45 articles.
1. Ludlam CA, Powderly WG, Bozzette S, Diamond M, Koerper MA, Kulkarni R, et al. Clinical perspectives of emerging pathogens in bleeding disorders. Lancet. 2006;367:252–61.
2. Hay CR. The epidemiology of factor VIII inhibitors. Haemophilia. 2006;12:23–8.
3. Neugebauer B, Drai C, Haase M, Hilger A, Keller-Stanislawski B, Laitinen-Parkkonen P, et al. Factor VIII products and inhibitor development: concepts for revision of European regulatory guidelines. Haemophilia. 2008;14:142–4.
4. Peerlinck K, Hermans C. Epidemiology of inhibitor formation with recombinant factor VIII replacement therapy. Haemophilia. 2006;12:579–90.
5. Peerlinck K, Arnout J, Di Giambattista M, Gilles JG, Laub R, Jacquemin M, et al. Factor VIII inhibitors in previously treated haemophilia A patients with a double virus-inactivated plasma derived factor VIII concentrate. Thromb Haemost. 1997;77:80–6.
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