Examples of using Steady-state in English and their translations into Polish
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Medicine
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Steady-state asenapine pharmacokinetics are similar to single-dose pharmacokinetics.
Steady-state exposures are achieved following 3-5 weeks of once-weekly administration.
Steady-state plasma concentrations are achieved in approximately 2 weeks.
The steady-state volume of distribution following intravenous microdose administration is 46 L.
Moreover, steady-state, near-infrared spectroscopy is a very significant tool in pharmaceutical analysis.
In steady-state EIS, a constant perturbation is imposed on the system.
Varenicline did not alter the steady-state pharmacokinetics of bupropion.
Furthermore, the effect of CYP3A inhibitors on steady-state crizotinib exposure has not been established.
Table 5: Rilonacept steady-state pharmacokinetic properties1.
The volume of distribution for venlafaxine at steady-state is 4.4±1.6 I/ kg following intravenous administration.
At steady-state, brinzolamide and its metabolite RBC concentrations ranged from 22.0 to 46.1
At steady-state, predicted AUC
The volume of distribution at steady-state(Vss) determined after intravenous administration was 11 I/ kg.
Co-administration of darifenacin 7.5 mg with the potent CYP3A4 inhibitor ketoconazole 400 mg resulted in a 5-fold increase in steady-state darifenacin AUC.
Steady-state plasma concentrations of ramiprilat after once daily dosing with the usual doses of ramipril are reached by about the fourth day of treatment.
At steady-state, the exposure ratio for the two diastereomers is approximately 2:1,
Doubling the darifenacin dose from 7.5 mg to 15 mg result in a 150% increase in steady-state exposure.
Owing to the slow elimination, steady-state concentrations in serum are reached in 4 to 6 weeks.
Due to lack of steady-state data, control of warfarin pharmacodynamic markers(INR or PT)
The mean volume of distribution of vildagliptin at steady-state after intravenous administration(V ss)