Примери за използване на Peak concentration на Английски и техните преводи на Български
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The peak concentration of this drug in the blood is recorded after 7 hours.
Following subcutaneous administration of peginterferon beta-1a in multiple sclerosis patients, the peak concentration was reached between 1 to 1.5 days post-dose.
The peak concentration of digoxin is increased when co-administered with Tybost.
Not surprisingly, the antibody peak concentration was higher after the second exposure.
Its peak concentration is achieved after 120 minutes, and the bioavailability is 65-85%.
Хората също превеждат
Antibodies to OP-1 and bovine bone collagen type 1 werefound after both exposures; the antibody peak concentration was higher after the second implantation.
The peak concentration of digoxin is increased when co-administered with cobicistat.
Epilim Chrono is a prolonged release formulation of Epilim which reduces peak concentration and ensures more even plasma concentrations throughout the day.
Time to peak concentration was also delayed in the presence of a high-fat meal.
Abbreviations: AUC∞= area under the plasma concentration-time curve from time zero to infinity;Cmax= peak concentration; t1/2= plasma elimination half-life; CL= clearance; SD= standard deviation.
The mean time to peak concentration was 1 hour and the mean peak concentration 195 μg/ml.
In response to subcutaneous doses of Preotact(100 micrograms parathyroid hormone),serum total calcium levels increase gradually and reach peak concentrationmean increase in 129 patients.
The mean time to peak concentration is 1.35 hour and the mean peak concentration 218 µg/ ml.
Following co-administration of canagliflozin with rifampicin(an inducer of various active transporters and drug-metabolising enzymes), 51% and28% decreases in canagliflozin systemic exposure(AUC) and peak concentration(Cmax) were observed.
The peak concentration in the blood is achieved at roughly the same time, whether the drug is injected or ingested.
Concurrent administration of probenecid significantly increases the peak concentration, area under the serum concentration time curve and elimination half-life of cefuroxime.
The peak concentration in the blood is reached 10 minutes after smoking a cigarette and is reduced in half in half an hour.
Administration of high-fat food increases the total exposure(AUC)by 30% and the peak concentration(Cmax) by 50%; the time to peak concentration(tmax) is delayed by 30 min(tmax is 1.5 hours).
The peak concentration of the active part in the plasma after taking one tablet occurs after 20-30 minutes and lasts for 2-3 hours.
Pharmacokinetic profiles in healthy volunteers and diabetes patients(type 1 or 2)demonstrated that absorption of insulin glulisine was about twice as fast with a peak concentration approximately twice as high as compared to regular human insulin.
This decrease in peak concentration is not clinically significant, and therefore ambrisentan can be taken with or without food.
In response to subcutaneous doses of Preotact(100 micrograms parathyroid hormone),serum total calcium levels increase gradually and reach peak concentration(mean increase in 129 patients, 0.15 mmol/l) at approximately 6 to 8 hours after dosing.
Total exposure and peak concentration of insulin aspart were higher in children than in adults and were similar for adolescents and adults.
Food delays the time to reach the peak concentration from 6 to 10 hours and it marginally decreases the extent of absorption(approximately 11%).
Peak concentration(Cmax) and plasma AUC of rufinamide increase less than proportionally with doses in both fasted and fed healthy subjects and in patients, probably due to dose-limited absorption behaviour.
Food delays the time to reach the peak concentration from 6 to 10 hours and it marginally decreases the extent of absorption(approximately 11%).
The mean time to peak concentration is 3.74 and 3.43 hours, respectively, and the mean peak concentration is 48.5 and 68.5 µg/ ml, respectively.
Zaleplon was rapidly absorbed with a time to peak concentration(tmax) of approximately 1 hour and a terminal-phase elimination half-life(t1/2) of approximately 1 hour.
Elimination After reaching peak concentration, plasma disposition of telbivudine declined in an bi-exponential manner with a terminal elimination half-life(t1/ 2) of 41.8± 11.8 hours.
Exposure to pembrolizumab as expressed by peak concentration(Cmax) or area under the plasma concentration time curve(AUC) increased dose proportionally within the dose range for efficacy.