Примери за използване на To atazanavir на Английски и техните преводи на Български
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When compared to atazanavir 300 mg/ritonavir 100 mg q.d.
There was an increase in the maximum PR interval compared to atazanavir alone.
When compared to atazanavir 300 mg QD with ritonavir 100 mg QD.
There was an increase in the maximum PR interval compared to atazanavir alone.
When compared to atazanavir 300 mg and ritonavir 100 mg without nevirapine.
Хората също превеждат
Limited data are available on the development of resistance to atazanavir boosted with cobicistat.
When compared to atazanavir 300 mg once daily with ritonavir 100 mg once daily.
There is a risk of loss of therapeutic effect anddevelopment of resistance to atazanavir(see section 4.3).
When compared to Atazanavir 300 mg/ritonavir 100 mg once daily in the evening without efavirenz.
This may result in loss of therapeutic effect of EVOTAZ anddevelopment of resistance to atazanavir(see section 4.4).
When compared to Atazanavir 300 mg/ritonavir 100 mg once daily in the evening without efavirenz.
The medicine is for use only in patients whose infection is not expected to be resistant to atazanavir.
Viruses were known to be susceptible to atazanavir, emtricitabine and tenofovir DF at baseline.
Concomitant administration of boceprevir andatazanavir/ritonavir resulted in reduced exposures to atazanavir and ritonavir.
(CYP3A4 induction)* When compared to atazanavir 300 mg/ritonavir 100 mg once daily in the evening without efavirenz.
Co-administration of EVOTAZ and nevirapine is not recommended and may result in a loss of therapeutic effect of EVOTAZ anddevelopment of resistance to atazanavir.
The activity of cobicistat as a pharmacokinetic enhancer to atazanavir has been demonstrated in pharmacokinetic trials.
Resistance levels to atazanavir ranged from 3.5- to 29-fold without evidence of phenotypic cross resistance to other PIs.
In an ex vivo rabbit pharmacology study,isolated hearts were exposed to atazanavir, cobicistat, or atazanavir and cobicistat in combination.
When compared to atazanavir 300 mg once daily with ritonavir 100 mg once daily and tenofovir disoproxil fumarate 300 mg all as a single dose with food.
In vitro, there was a clear trend toward decreased susceptibility to atazanavir as isolates exhibited high resistance levels to. .
EVOTAZ is not recommended for co-administration with etravirine because it may result in the loss of therapeutic effect anddevelopment of resistance to atazanavir.
Viruses were known to be susceptible to atazanavir, emtricitabine and tenofovir disoproxil fumarate at baseline.
Rifampicin substantially decreases plasma concentrations of atazanavir, which may result in loss of therapeutic effect of EVOTAZ anddevelopment of resistance to atazanavir.
Do not take REYATAZ if you are allergic to atazanavir or any of the other ingredients of this medicine(listed in section 6) if you have moderate to severe liver problems.
There was no evidence of cross-resistance between atazanavir and amprenavir, with the presence of the I50L andI50V substitutions yielding selective resistance to atazanavir and amprenavir, respectively.
If you are allergic(hypersensitive) to atazanavir or any of the other ingredients of REYATAZ if you have moderate to severe liver problems.
Systemic exposure to atazanavir at doses that resulted in maternal toxicity was at least equal to or slightly greater than that observed in humans given 400 mg once daily.
Reyataz should not be used in people who may be hypersensitive(allergic) to atazanavir or any of the other ingredients, or who have moderate to severe problems with their liver.
Systemic exposure to atazanavir at doses that resulted in maternal toxicity was at least equal to or slightly greater than that observed in humans given 400 mg once daily.