Примери за използване на Pharmacokinetic differences на Английски и техните преводи на Български
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These pharmacokinetic differences were not considered clinically relevant.
This analysis did not show gender or age-related pharmacokinetic differences.
These pharmacokinetic differences were not considered clinically relevant.
There were no clinically important pharmacokinetic differences based on age or gender.
Race- Pharmacokinetic differences due to race have not been studied prospectively.
Elderly patients: no clinically relevant age-related pharmacokinetic differences have been observed in these patients.
Race No pharmacokinetic differences based on ethnic group were observed.
Gender, Race andBMI There were no clinically important pharmacokinetic differences due to gender, race or body mass index(BMI).
No major pharmacokinetic differences have been observed based on gender or age.
There were no clinically important pharmacokinetic differences due to gender, race or body mass index(BMI) for.
Race No pharmacokinetic differences were observed between Japanese and Caucasian healthy volunteers.
There were no clinically important pharmacokinetic differences between patients with severe renal insufficiency.
Race No pharmacokinetic differences were observed between Japanese and Caucasian healthy volunteers.
No body weight, gender, age, or race-related pharmacokinetic differences have been observed in adult patients studied.
Gender: pharmacokinetic differences have been identified between males and females(apparent plasma clearance is approximatively 50% lower in females).
Based upon the overlap in the range of clearance, gender-based pharmacokinetic differences do not justify the recommendation for using a lower dose for female patients.
Gender: Pharmacokinetic differences have been identified between males and females(apparent plasma clearance is approximately 50% lower in females).
Based upon the overlap in the range of clearance, gender-based pharmacokinetic differences do not justify the recommendation for using a lower dose for female patients.
The observed pharmacokinetic differences between elderly and young patients with ET(see section 5.2) do not warrant using a different starting regimen or different dose titration step to achieve an individual patient-optimised anagrelide regimen.
No information is available regarding pharmacokinetic differences due to age(except paediatric patients), gender or race.
No significant pharmacokinetic differences were observed between subjects with normal renal function and subjects with renal impairment.
Nalmefene does not exhibit any substantial pharmacokinetic differences between sexes, between young and elderly, or between ethnic groups.
No significant pharmacokinetic differences have been observed between males and females.
In adults, there were no clinically important pharmacokinetic differences between patients with moderate hepatic insufficiency and healthy subjects.
Elderly: no pharmacokinetic differences(AUC and Cmax) have been observed between elderly≥.
In patients with type 2 diabetes over a wide range of renal function the pharmacokinetic differences between insulin lispro and soluble human insulin were generally maintained and shown to be independent of renal function.
No clinically relevant pharmacokinetic differences have been identified between men and women for doravirine.
Gender No significant pharmacokinetic differences have been observed between men and women.
There are no significant pharmacokinetic differences between intramuscular and subcutaneous administration of Puregon.
There were no apparent pharmacokinetic differences between male and female patients with type 1 Gaucher disease.