This manuscript is based on the data submitted in abstract format and presented as posters at the XXIII Congress of the International Society on Thrombosis and Haemostasis in 2011, the National Hemophilia Foundation's 63rd Annual Meeting in 2011, and the 53rd Annual Meeting and Exposition of the American Society of Hematology in 2011.
Safety of recombinant activated factor VII (rFVIIa) in patients with congenital haemophilia with inhibitors: overall rFVIIa exposure and intervals following high (>240 μg kg−1) rFVIIa doses across clinical trials and registries
Article first published online: 20 DEC 2013
© 2013 John Wiley & Sons Ltd
Volume 20, Issue 1, pages e23–e31, January 2014
How to Cite
Shapiro, A. D., Neufeld, E. J., Blanchette, V., Salaj, P., Gut, R. Z. and Cooper, D. L. (2014), Safety of recombinant activated factor VII (rFVIIa) in patients with congenital haemophilia with inhibitors: overall rFVIIa exposure and intervals following high (>240 μg kg−1) rFVIIa doses across clinical trials and registries. Haemophilia, 20: e23–e31. doi: 10.1111/hae.12329
- Issue published online: 20 DEC 2013
- Article first published online: 20 DEC 2013
- Manuscript Accepted: 21 OCT 2013
- Novo Nordisk Inc
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