Examples of using Multiple dosing in English and their translations into Slovenian
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Financial
-
Computer
-
Official/political
-
Programming
Pharmacokinetics do not change with multiple dosing.
Multiple dosing does not cause marked medicinal product accumulation.
The pharmacokinetics are linear following single and multiple dosing.
Multiple dosing does not result in plasma accumulation of prednisolone.
This indicates no time-dependency in the kinetics of alogliptin after multiple dosing.
Multiple dosing of 7,200 mg/ day was associated with no major signs or symptoms.
Similar inhibition was seen following single and multiple dosing.
Toxicity after a single dose and multiple dosing has been investigated in mice, rats and dogs.
Multiple dosing of mycophenolate mofetil in patients with severe chronic renal impairment has not been studied.
The estimated apparent half-life is 50 to 60 hours,which is in line with the accumulation observed after multiple dosing.
After multiple dosing, less than 3% of the lopinavir dose is excreted unchanged in the urine.
The pharmacokinetics of single and multiple doses of simvastatin showed that no accumulation of medicinal product occurred after multiple dosing.
On multiple dosing there is no marked accumulation, with steady state exposures achieved within~3 to 4 days.
At a dose of 10 mg/kg, mean Vss averaged between 133(SD 24)ml/kg after multiple dosing, corresponding to a value of approximately 10 l for a 75 kg person.
Upon multiple dosing, plasma concentrations of bosentan decrease gradually to 50%- 65% of those seen after single dose administration.
A greater than dose-proportional increase in nelfinavir plasmaconcentrations was observed after single doses; however, this was not observed after multiple dosing.
Multiple dosing of 800/200 mg Kaletra once daily for 2 weeks without meal restriction(n=16) produced a mean± SD.
Posaconazole tablets are absorbed with a median Tmax of 4 to 5 hours andexhibits dose proportional pharmacokinetics after single and multiple dosing up to 300 mg.
Upon multiple dosing, ribavirin accumulates extensively in plasma with a six-fold ratio of multiple-dose to single-dose AUC12hr.
Suggesting that meal content has less effect on nelfinavir exposures during multiple dosing than would be anticipated based on data from single dose studies.
Upon multiple dosing, there is an accumulation of immunoreactive interferons. There is, however, only a modest increase in biologic activity as measured by a bioassay.
Without the loading dose, accumulation occurs during twice daily multiple dosing with steady- state plasma voriconazole concentrations being achieved by day 6 in the majority of subjects.
Upon multiple dosing, ritonavir accumulation is slightly less than predicted from a single dose due to a time and dose-related increase in apparent clearance(Cl/F).
Table 8: Mean(% CV) AUC,Cmax and Cmin of saquinavir in patients following multiple dosing of Invirase, saquinavir soft capsules, Invirase/ritonavir, and saquinavir soft capsules/ritonavir.
Multiple dosing of perampanel 12 mg/day increased levels of anger, confusion, and depression as assessed using the Profile of Mood State 5-point rating scale(see section 5.1).
The pentavalent metabolites, MMAV and DMAV, are slow to appear in plasma(approximately 10-24 hours after first administration of arsenic trioxide),but due to their longer half-life, accumulate more upon multiple dosing than does AsIII.
After multiple dosing with 750 mg every 8 hours for 28 days(steady-state), peak plasma concentrations(Cmax) averaged 3-4 µg/ml and plasma concentrations prior to the next dose(trough) were 1-3 µg/ml.
The exposure camparison across species indicates that exposures that did not elicit adverse effects in the 6- and 9-month toxicity studies in rats and dogs, respectively,were similar to or slightly exceeding the exposure in humans after multiple dosing of 500 mg.
Absorption Multiple dosing with 400/100 mg Kaletra twice daily for 2 weeks and without meal restriction produced a mean± SD lopinavir peak plasma concentration(Cmax) of 12.3± 5.4 g/ml, occurring approximately 4 hours after administration.
Because nevirapine induces its own metabolism with multiple dosing, this single dose study may not reflect the impact of hepatic impairment on multiple dose pharmacokinetics(see section 4.4).