Примери за използване на Andexanet alfa на Английски и техните преводи на Български
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Each vial contains 200 mg of andexanet alfa.
The interaction between andexanet alfa and TFPI has not been fully characterized.
Animal reproductive and developmental studies have not been conducted with andexanet alfa.
After reconstitution, each mL of solution contains 10 mg of andexanet alfa.
Use andexanet alfa within eight hours after reconstitution when stored at room temperature.
Andexanet alfa will not reverse the effects of non-FXa inhibitors(see section 5.1).
Renal impairment: The effect of renal impairment on andexanet alfa exposure levels has not been evaluated.
No trials have been conducted to investigate the pharmacokinetics of andexanet alfa in renally impaired patients.
Andexanet alfa binds direct FXa inhibitors with high affinity,
No trials have been conducted to investigate the pharmacokinetics of andexanet alfa in patients with hepatic impairment.
Andexanet alfa does not need to be brought to room temperature before reconstitution or administration to the patient.
Table 4 provides the list of adverse reactions from clinical studies of healthy subjects treated with andexanet alfa.
Andexanet alfa reverses the anticoagulant effect of direct factor Xa(FXa)
Andexanet alfa is a recombinant form of human FXa protein that has been modified to lack FXa enzymatic activity.
Package Leaflet: Information for the patient and user Ondexxya 200 mg powder for solution for infusion andexanet alfa.
When Ondexxya is given, the anticoagulants attach to andexanet alfa instead, and they are no longer available to block factor Xa.
unfractionated heparin) with andexanet alfa has not been studied in humans.
Andexanet alfa, the active substance in Ondexxya, acts as a decoy target for
then receiving andexanet alfa, no serious or severe adverse reactions were reported.