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1 ies for off-label utilization of recombinant activated factor VII.
3 for hemorrhage control, such as recombinant activated factor VII and hemostatic bandages, are in dev
4 binding constants of prothrombin, factor X, activated factor VII, and activated protein C to seven d
5 s (e.g., fresh-frozen plasma and recombinant-activated factor VII) are poorly aligned with recommende
6 drotrecogin alpha (activated protein C) and activated factor VII concentrate (NovoSeven), have been
11 Intravenous infusion of recombinant human activated Factor VII (FVIIa) has been used for over a de
15 c tenase complexes of tissue factor (TF) and activated factor VII (FVIIa), and trigger blood coagulat
17 arize the safety and efficacy of recombinant activated factor VII in diverse clinical settings based
18 zed control trials investigating recombinant activated factor VII in non-hemophiliacs have been publi
19 ed the role of the tissue factor (TF)-FVIIa (activated factor VII)-integrin B1-PAR2 (protease-activat
20 Case reports would suggest that recombinant activated factor VII is an efficacious and safe "univers
23 tion of thrombin generation with recombinant activated factor VII or activated prothrombin complex co
24 with soluble tissue factor and phospholipid, activated factor VII-Q10E32 displayed increased activati
25 trials have reported the use of recombinant-activated factor VII (rFVIIa) as an adjunct for reversal
27 We sought to determine whether recombinant activated factor VII (rFVIIa) can reduce hematoma growth
29 onfirm a previous study in which recombinant activated factor VII (rFVIIa) reduced growth of the hema
30 alysis of safety and efficacy of recombinant activated factor VII (rFVIIa) used as the last resort fo
35 ctivity of recombinant human TF complexed to activated factor VII was inhibited by PAEC and HAEC-asso