Примери за използване на Mean plasma на Английски и техните преводи на Български
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Mean plasma AUC of sitagliptin was 8.52M•hr and Cmax was 950 nM.
Following intravenous administration, the mean plasma clearance is approximately 9 l/h.
The mean plasma half-life of hydrochlorothiazide reportedly ranges from 5-15 hours.
Boceprevir is eliminated with a mean plasma half-life(t½) of approximately 3.4 hours.
Mean plasma elimination half-life(t1/2) was 2.75 hours for the two dose groups.
Fifteen days after the last administration, the mean plasma concentration is about 6.5 µg/l.
Mean plasma elimination half-life of atorvastatin in humans is approximately 14 hours.
Following intravenous administration of a 2 mg dose of cobimetinib, the mean plasma clearance(CL) was 10.7 L/hr.
The mean plasma half-life in healthy subjects is 4-6 hours and in patients is 9-12 hours.
CYP2D6 genetic polymorphism has minimal impact on the mean plasma exposure to mirabegron(see section 5.2).
Mirtazapine, the mean plasma concentration of mirtazapin may increase more than 50%.
Following dosing of dasabuvir with ombitasvir/ paritaprevir/ritonavir, mean plasma half-life of dasabuvir was approximately 6 hours.
Mean plasma elimination half-life is 5 hours with high inter-subject variability.
However, after adjusting for creatinine clearance and body weight, gender andage were not significant factors for mean plasma clearance.
The mean plasma elimination half-life(%CV) of avatrombopag is approximately 19 hours(19%).
Following administration of multiple doses of 50 mg and100 mg of topiramate twice a day, the mean plasma elimination half-life was approximately 21 hours.
Measured mean plasma concentrations were 44.4(± 14.7) ng/ml and 165(±90) ng/ml respectively.
The potent CYP3A4 inhibitors ketoconazole(200 mg once daily) and josamycin(1 g twice daily)increased ivabradine mean plasma exposure by 7 to 8 fold.
Mean plasma ara-G Cmax and AUCinf values were 115 µM(16%) and 571 µM. h(30%), respectively.
When cimetidine(weak inhibitor of CYP1A2, CYP2D6 and CYP3A4)is administered with mirtazapine, the mean plasma concentration of mirtazapin may increase more than 50%.
Mean plasma fentanyl concentrations following single doses of PecFent and OTFC in healthy subjects.
Data from these studies revealed minimal differences in mean plasma aztreonam concentrations between age groups in patients receiving Cayston 3 times a day.
The mean plasma half-lives of imipenem and cilastatin were 91± 7.0 minutes and 69± 15 minutes, respectively.
Approximately 10 weeks after discontinuation of prolonged-release exenatide therapy, mean plasma exenatide concentrations fell below minimal detectable concentrations.
The mean plasma loxapine concentrations following administration of ADASUVE were linear over the clinical dose range.
Following subcutaneous administration, meloxicam is completely bioavailable and maximal mean plasma concentrations of 1.1 µg/ml were reached approximately 1.5 hours post administration.
Mean plasma half-life: the plasma elimination half-life of fenofibric acid is approximately 20 hours.
During celecoxib treatment, the mean plasma concentrations of the CYP2D6 substrate dextromethorphan were increased by 136%.
Mean plasma concentrations increased in a dose-related manner and by successive doses as observed in healthy volunteers.
These free-floating particles mean plasma carries electric and magnetic fields, and changes in the plasma often make marks on those fields.