Examples of using Multiple-dose in English and their translations into Romanian
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No accumulation occurs after multiple-dose administration.
Multiple-dose study: data are restricted to one study.
No accumulation occurs after multiple-dose administration.
Mean(% CV) multiple-dose pharmacokinetic parameters for interferon alfa-2b and.
Steady-state is attained following 7 to 10 days of multiple-dose administration.
In multiple-dose patient studies, drug clearance was slightly faster(approximately 22%) in men.
Otherwise, the use of a multiple-dose syringe is recommended.
No accumulation in plasma, either of parent compound or active metabolite,occurred after multiple-dose administration.
Ed-Renal impairment In a multiple-dose study, 36 subjects with varying degrees of renal impairment.
The pharmacokinetics of opicapone was evaluated in elderly subjects(aged 65-78 years old)after 7- day multiple-dose administration of 30 mg.
Multiple-dose pharmacokinetics were studied in a small number of children enrolled in a clinical efficacy study.
Food had no effect on darifenacin pharmacokinetics during multiple-dose administration of prolonged-release tablets.
After multiple-dose administration, steady state conditions of selexipag and the active metabolite were reached within 3 days.
Upon multiple dosing, ribavirin accumulates extensively in plasma with a six-fold ratio of multiple-dose to single-dose AUC12hr.
The single- and multiple-dose pharmacokinetics of telbivudine were evaluated in healthy subjects and in patients with chronic hepatitis B.
Consequently, no meaningful change in AUC of methylnaltrexone, in addition to Cmax,was observed before and after multiple-dose administration of cimetidine.
Following multiple-dose administration of 5, 10, and 25 mg once daily for 14 days, systemic exposures of obeticholic acid increase dose proportionally.
The pharmacokinetics(PK) of nintedanib can be considered linear with respect to time(i.e. single- dose data can be extrapolated to multiple-dose data).
Mean(% CV) multiple-dose pharmacokinetic parameters for interferon alfa-2b and ribavirin when administered to paediatric patients with chronic hepatitis C.
The potential interaction of peginterferon alfa-2b(PegIntron) on substrates of metabolic enzymes was evaluated in 3 multiple-dose clinical pharmacology studies.
Multiple-dose administration of elbasvir or grazoprevir is unlikely to induce the metabolism of medicinal products metabolised by CYP isoforms based on in vitro data.
Co-administration of single-dose bedaquiline and multiple-dose nevirapine did not result in clinically relevant changes in the exposure to bedaquiline.
In healthy subjects, the opicapone elimination half-life(t1/2)was 0.7 h to 3.2 h following once-daily multiple-dose administration up to 50 mg opicapone.
Following multiple-dose administration of daclatasvir in HCV-infected patients, the terminal elimination half-life of daclatasvir ranged from 12 to 15 hours.
In an interaction study of single-dose bedaquiline and multiple-dose lopinavir/ritonavir, exposure(AUC) to bedaquiline was increased by 22%[90% CI(11; 34)].
Mean(% CV) multiple-dose pharmacokinetic parameters for interferon alfa-2b and Rebetol capsules when administered to children or adolescents with chronic hepatitis C.
Systemic absorption of all active substances was determined in multiple-dose studies after placing the veterinary medicinal product into both ear canals of healthy mixed breed dogs.
In a multiple-dose pharmacokinetic study conducted with the tablet formulation in healthy adult subjects, four subjects were found to be poor metabolisers of desloratadine.
No inhibitory effect of 40 mg single-dose omeprazole(CYP2C19 inhibitor)was observed on the multiple-dose pharmacokinetics of vortioxetine in healthy subjects.
Table 9 Mean(% CV) multiple-dose pharmacokinetic parameters for interferon alfa-2b and Ribavirin when administered to children or adolescents with chronic hepatitis C.