Examples of using Clinically relevant differences in English and their translations into Bulgarian
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
There were no clinically relevant differences in Cmax compared to healthy volunteers.
In a population pharmacokinetic analysis of ceftolozane/tazobactam, no clinically relevant differences in exposure were observed with regard to age.
There were no clinically relevant differences in the clearance of tigecycline between men and women.
In healthy female and male subjects following single andmultiple-doses of tadalafil, no clinically relevant differences in exposure were observed.
There are no clinically relevant differences in pharmacokinetics between Caucasian and Asian subjects.
In a population pharmacokinetic analysis of eravacycline, no clinically relevant differences in AUC by gender were observed for eravacycline.
There are no clinically relevant differences between genders in pharmacokinetic properties of Levemir.
In a population pharmacokinetic analysis of ceftolozane/tazobactam, no clinically relevant differences in AUC were observed for ceftolozane and tazobactam.
No clinically relevant differences in pharmacokinetics of rilpivirine have been observed between men and women.
Based on pharmacokinetic data from studies in Japanese and Chinese patients with prostate cancer,there were no clinically relevant differences in exposure among the populations.
Elderly There are no clinically relevant differences due to age in the pharmacokinetics of cinacalcet.
There were no clinically relevant differences in pharmacokinetic properties between young children, children, adolescents and adults.
In a population pharmacokinetic analysis of ceftolozane/tazobactam, no clinically relevant differences in ceftolozane/tazobactam AUC were observed in Caucasians compared to other ethnicities.
No clinically relevant differences in adverse reactions were observed between the overall dataset and the approved indications.
The results demonstrated no clinically relevant differences between sildenafil and placebo in time to limiting angina.
No clinically relevant differences in ledipasvir pharmacokinetics were observed between healthy subjects and patients with severe renal impairment.
Gender There are no clinically relevant differences in the pharmacokinetics of brivaracetam by gender.
There were no clinically relevant differences in the pharmacokinetics of lurasidone in a population pharmacokinetic analysis in patients with schizophrenia.
There were no clinically relevant differences observed in saxagliptin pharmacokinetics between males and females.
There were no clinically relevant differences in systemic exposures between White, Black or Asian races.
There were no clinically relevant differences in safety between males(N=382) and females(N=139) in the FLAGS study.
There were no clinically relevant differences observed for the safety profile of ALIMTA within the histology subgroups.
There were no clinically relevant differences observed for the safety profile of pemetrexed within the histology subgroups.
There were no clinically relevant differences observed for the safety profile of ALIMTA plus cisplatin within the histology subgroups.
There were no clinically relevant differences in empagliflozin pharmacokinetics between healthy volunteers and patients with type 2 diabetes.
There are no clinically relevant differences in serum insulin or glucose levels after abdominal, deltoid or thigh administration of Semglee.
No clinically relevant differences in tenofovir alafenamide or tenofovir pharmacokinetics were observed between adolescent and adult HIV-1 infected subjects.
No clinically relevant differences in elvitegravir or cobicistat pharmacokinetics were observed between subjects with moderate impairment and healthy subjects.
No clinically relevant differences were seen in the pharmacokinetics of repaglinide, when repaglinide was administered 0, 15 or 30 minutes before a meal or in fasting state.
No clinically relevant differences requiring dose adjustment based on race, gender or weight were observed in fluticasone furoate, umeclidinium or vilanterol systemic exposure.