Examples of using Refacto in English and their translations into Finnish
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Medicine
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Colloquial
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Official
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Financial
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Ecclesiastic
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Official/political
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Computer
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Programming
The name of the medicine was also changed from ReFacto to ReFacto AF.
The specific activity of ReFacto AF is 7,600-13,800 IU/ mg protein.
ReFacto AF contains B-domain deleted recombinant coagulation factor VIII moroctocog alfa.
ReFacto AF has functional characteristics comparable to those of endogenous factor VIII.
ReFacto AF is given by injection into a vein lasting several minutes.
This indicates no time-dependent changes in the pharmacokinetic properties of ReFacto AF.
Your doctor will decide the dose of ReFacto AF you will receive.
ReFacto AF is given by injection into a vein lasting several minutes.
That after switching to ReFacto AF, patients should remain on ReFacto AF
Specific instructions regarding the proper identification, dosing and monitoring of ReFacto AF.
Trace amounts of hamster protein may be present in ReFacto AF.
ReFacto AF contains the active substance moroctocog alfa,
The reconstituted ReFacto AF product should be injected intravenously over several minutes.
ReFacto AF can be used in patients of all ages, including newborns.
The name of the medicine was changed to ReFacto AF on 18 December 2008.
There are no clinical data on previously untreated patients(PUPs) with ReFacto AF.
Your doctor or other healthcare professional should teach you how to infuse ReFacto AF.
The procedures below are provided as guidelines for the reconstitution and administration of ReFacto AF.
Once reconstituted, ReFacto AF should be inspected for particulate matter and discolouration prior to administration.
The ReFacto AF laboratory standard can be used to correct for this discrepancy see section 5.2.