BeneFIX (nonacog alfa) Prescribing Information for Great Britain click here. BeneFIX (nonacog alfa) Prescribing Information for Northern Ireland click here.
Adverse event reporting can be found at the bottom of this page.
BeneFIX® (nonacog alfa) is recombinant coagulation factor IX indicated for the treatment and prophylaxis of bleeding in patients with haemophilia B (congenital factor IX deficiency). BeneFIX® can be used for all age groups.1
Dose based on bodyweight may require adjustment in underweight or overweight patients. Individual patients may vary in their response to factor IX, demonstrating different half-lives and recoveries.1 |
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In the case of major surgical interventions in particular, precise monitoring of the substitution therapy by means of coagulation analysis (plasma factor IX activity) is indispensable.1 |
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When using an in vitro thromboplastin time (aPTT)-based one stage clotting assay for determining factor IX activity in patients' blood samples, plasma factor IX activity results can be significantly affected by both the type of aPTT reagent and the reference standard used in the assay. This is of importance particularly when changing the laboratory and/or reagents used in the assay.1 |
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The R2 device is used for reconstitution of BeneFIX® by injection.
No two days are the same. No two patients are the same. BeneFIX® offers frequent, flexible dosing so your patients are covered for everyday life.1–3
rFIX products like BeneFIX® are effective at preventing bleeds in everyday settings.4
** This is an optional area where footnotes can live.
Contact a member of the Pfizer haemophilia team.
** This is an optional area where footnotes can live.
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PP-PFE-GBR-3863. November 2021
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