Examples of using Refacto in English and their translations into French
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Colloquial
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Official
It also carried out two main studies looking at the effectiveness of ReFacto AF: the first looked at the prevention and treatment of bleeding
The dose and the frequency of treatment depend on whether ReFacto AF is used to treat
It is strongly recommended that every time ReFacto AF is administered to a patient,
ReFacto obtained its Notice of Compliance in June 2002.
Allergic type hypersensitivity reactions have been observed with ReFacto AF.
Trace amounts of hamster protein may be present in ReFacto AF.
ReFacto AF has functional characteristics comparable to those of endogenous factor VIII.
ReFacto AF must be used within 3 hours of reconstitution.
ReFacto AF is given by injection into a vein over several minutes.
ReFacto AF is administered by intravenous(IV) infusion after reconstitution.
Your doctor will decide the dose of ReFacto AF you will receive.
ReFacto AF has no influence on the ability to drive
ReFacto AF is given by injection into a vein lasting several minutes.
The name of the medicine was also changed from ReFacto to ReFacto AF.
Clinical trials are ongoing in previously untreated patients(PUPs) with ReFacto AF.
In PUPs, pharmacokinetic parameters of ReFacto were evaluated using the chromogenic assay.
Patients may also develop antibodies against factor VIII medicines such as Refacto AF.
other healthcare professional should teach you how to infuse ReFacto AF.
ReFacto AF has no influence on the ability to drive or use machines.
ReFacto AF contains 1.23 mmol(or 29 mg)