Examples of using Multiple-dose in English and their translations into Greek
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Preserve in single-dose or multiple-dose containers.
In multiple-dose patient studies, drug clearance was slightly faster(approximately 22%) in men.
Otherwise, the use of a multiple-dose syringe is recommended.
In addition, Aerius orodispersible tablets were well tolerated in a multiple-dose trial.
In acute and multiple-dose studies, the combination of loratadine/ pseudoephedrine sulfate exhibited a low order of toxicity.
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Steady-state is attained following 7 to 10 days of multiple-dose administration.
Single-dose and multiple-dose pharmacokinetic studies have been conducted in adult patients undergoing kidney transplantation.
If more injections than that are needed, the use of a multiple-dose syringe is recommended.
In a multiple-dose pharmacokinetic study in healthy volunteers, steady state was reached by day 5 of dosing.
No accumulation in plasma, either of parent compound or active metabolite,occurred after multiple-dose administration.
After multiple-dose administration, steady state conditions of selexipag and the active metabolite were reached within 3 days.
Food had no effect on darifenacin pharmacokinetics during multiple-dose administration of prolonged-release tablets.
Multiple-dose administration of rifampin(a UGT and CYP inducer) decreases ertugliflozin AUC and Cmax by 39% and 15%, respectively.
The renal clearance of methylnaltrexone was reduced following multiple-dose administration of cimetidine(from 31 l/ h to 18 L/ h).
Nevirapine is an inducer of CYP3A andpotentially CYP2B6, with maximal induction occurring within 2-4 weeks of initiating multiple-dose therapy.
Co-administration of single-dose bedaquiline and multiple-dose nevirapine did not result in clinically relevant changes in the exposure to bedaquiline.
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.
The combination of loratadine/ pseudoephedrine sulphate used in acute and multiple-dose studies, exhibited a low order of toxicity.
Single- and multiple-dose pharmacokinetics(PK) of nusinersen, administered via intrathecal injection, were determined in paediatric patients diagnosed with SMA.
No clinically relevant changes in desloratadine plasma concentrations were observed in multiple-dose ketoconazole and erythromycin interaction trials.
Following multiple-dose administration of 5, 10, and 25 mg once daily for 14 days, systemic exposures of obeticholic acid increase dose proportionally.
No clinically relevant changes in desloratadine plasma concentrations were observed in multiple-dose, ketoconazole and erythromycin interaction trials.
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.
The potential interaction of peginterferon alfa-2b(PegIntron) on substrates of metabolic enzymes was evaluated in 3 multiple-dose clinical pharmacology studies.
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)].
In summary, NSI-189 looks promising as a potential treatment for MDD in a Phase 1B, double-blind, randomized,placebo-controlled, multiple-dose study with three ascending cohorts.
In a multiple-dose clinical trial, in which up to 20 mg of desloratadine was administered daily for 14 days, no statistically or clinically relevant cardiovascular effect was observed.
No inhibitory effect of 40 mg single-dose omeprazole(CYP2C19 inhibitor)was observed on the multiple-dose pharmacokinetics of vortioxetine in healthy subjects.
In short-term, multiple-dose clinical studies of post-orthopaedic surgical pain and pain from primary dysmenorrhea, lumiracoxib 400 mg once daily was effective in relieving pain.