Examples of using Multiple-dose in English and their translations into Italian
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Medicine
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Multiple-dose study: data are restricted to one study.
No accumulation occurs after multiple-dose administration.
In multiple-dose patient studies, drug clearance was slightly
Food had no effect on darifenacin pharmacokinetics during multiple-dose administration of prolonged-release tablets.
Multiple-dose pharmacokinetics were studied in a small number
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No accumulation in plasma, either of parent compound or active metabolite, occurred after multiple-dose administration.
For radiopharmaceuticals prepared in multiple-dose vials, the stability following removal of successive doses should be discussed.
which is of relevance for the serum concentrations under multiple-dose conditions, is about 5 to 8 hours.
The single- and multiple-dose pharmacokinetics of telbivudine were evaluated in healthy subjects
The renal clearance of methylnaltrexone was reduced following multiple-dose administration of cimetidine from 31 l/ h
After multiple-dose administration, steady state conditions of selexipag
The apparent elimination half-life estimated from the multiple-dose pharmacokinetics with daily dosing was approximately 17 hours.
day multiple-dose administration of 30 mg.
In an open-label, ascending multiple-dose study, 39 children aged 8
with maximal induction occurring within 2-4 weeks of initiating multiple-dose therapy.
Mean(% CV) multiple-dose pharmacokinetic parameters for Viraferon
on substrates of metabolic enzymes was evaluated in 3 multiple-dose clinical pharmacology studies.
In multiple-dose studies, serum concentrations
In an interaction study of single-dose bedaquiline and multiple-dose lopinavir/ritonavir, exposure(AUC)
Multiple-dose administration of elbasvir or grazoprevir is unlikely to
was observed on the multiple-dose pharmacokinetics of vortioxetine in healthy subjects.
Table 15 Mean(% CV) multiple-dose pharmacokinetic parameters for interferon alfa-2b
was 0.7 h to 3.2 h following once-daily multiple-dose administration up to 50 mg opicapone.
Mean(% CV) multiple-dose pharmacokinetic parameters for interferon alfa-2b and ribavirin
h to 2.5 h following once-daily multiple-dose administration up to 50 mg opicapone.
A multiple-dose, open-label study was conducted to evaluate the pharmacokinetics of linagliptin(5 mg dose) in patients
was observed before and after multiple-dose administration of cimetidine.
In Phase I multiple-dose studies, there were no dose-related clinical adverse
Multiple-dose toxicity studies in rats and dogs confirmed these above-mentioned observations, but the