Examples of using Systemic exposure in English and their translations into Polish
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Medicine
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
The systemic exposure at the lowest dose was below or comparable to that observed in humans(based on AUC0-∞) at the recommended human dose.
Alogliptin was not teratogenic in rats or rabbits with a systemic exposure at the NOAELs far above the human exposure at the recommended dose.
While the terminal elimination half-life and mean systemic exposure of palonosetron is increased in the subjects with severe hepatic impairment, this does not warrant dose reduction.
These occurred at dosages which provided> 17-fold the systemic exposure seen at the clinical dosage.
Considering the type of product, systemic exposure of the suckling infant is not expected, however a risk to the newborn/infant cannot be excluded.
Prolonged systemic exposure to intense immunosuppression in transplant patients following systemic administration of calcineurin inhibitors has been associated with an increased risk of developing lymphomas
However, it should be noted that systemic exposure in rodents was similar
Effect of food on absorption The systemic exposure(AUC) to etravirine was decreased by about 50% when INTELENCE was administered under fasting conditions, as compared to administration following a meal.
Dose-normalised fluticasone furoate systemic exposure was similar in subjects with moderate and severe hepatic impairment Child-Pugh B or C.
It should be noted that systemic exposure in male rats was lower than the therapeutic exposure in humans at 40 mg.
Although clinical data have shown that systemic exposure from application of tacrolimus ointment is low,
BPD-DA is also a photosensitiser but its systemic exposure is low 5-10% of the verteporfin exposure,
Dosing of lapatinib one hour after a meal results in approximately 2-3 times higher systemic exposure, compared to dosing one hour before a meal see sections 4.5 and 5.2.
The systemic exposure at this dose represents 2- 3 times the clinical exposure at the recommended clinical dose of 2 g/day.
Patients showed a higher degree of variability with respect to systemic exposure as compared to healthy subjects.
Daily systemic exposure to nilotinib with 400 mg twice-daily dosing at steady state was 35% higher than with 800 mg once-daily dosing.
Genetic differences in N-acetyl transferase enzymes can account for the variable systemic exposure of amifampridine see sections 4.4 and 5.2.
Maximum plasma concentration and overall systemic exposure increase with age but no dose adjustment is required in elderly patients.
The systemic exposure at this dose was approximately 0.5 times the clinical exposure at the recommended clinical dose of 2 g/day.
BPD-DA is also a photosensitiser but its systemic exposure is low 5-10% of the verteporfin exposure, suggesting that most of the drug is eliminated unchanged.