Examples of using Clinically relevant differences in English and their translations into Croatian
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There were no clinically relevant differences in Cmax compared to healthy volunteers.
The analysis of the impact of NSCLC histology on overall survival demonstrated clinically relevant differences in survival according to histology, see table below.
There are no clinically relevant differences in the pharmacokinetics of brivaracetam by gender.
Based on pharmacokinetic data from a study in Japanese patients with prostate cancer,there were no clinically relevant differences in exposure between Japanese and Caucasians.
Elderly: There are no clinically relevant differences due to age in the pharmacokinetics of cinacalcet.
A population PK analysis did not identify clinically relevant differences in PK of cabozantinib based on race.
No clinically relevant differences in aprepitant pharmacokinetics is expected due to age and gender.
Dapagliflozin: There were no clinically relevant differences in systemic exposures between White, Black or Asian races.
No clinically relevant differences in the pharmacokinetics of rilpivirine have been observed between men and women.
There were no clinically relevant differences in the clearance of tigecycline between men and women.
There are no clinically relevant differences between genders in pharmacokinetic properties of Levemir.
There were no clinically relevant differences in systemic exposures between White, Black or Asian races.
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 observed for the safety profile of pemetrexed within the histology subgroups.
There were no clinically relevant differences in pharmacokinetics and pharmacodynamics between male and female patients.
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 in pharmacokinetic properties between young children, children, adolescents and adults.
There are no clinically relevant differences in the rate of absorption when lixisenatide is administered subcutaneously in the abdomen, thigh, or arm.
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 were no clinically relevant differences observed for the safety profile of pemetrexed plus cisplatin within the histology subgroups.
There are no clinically relevant differences in serum insulin or glucose levels after abdominal, deltoid or thigh administration of Lantus.
There were no clinically relevant differences between genders in the pharmacokinetics of lurasidone in a population pharmacokinetic analysis in patients with schizophrenia.
There were no clinically relevant differences in incidence or severity of hypoglycaemia with exenatide compared to placebo, in combination with a thiazolidinedione, with or without metformin.
There are no clinically relevant differences in the pharmacokinetics of Ryzodeg between elderly and younger adult patients, between races or between healthy subjects and patients with renal or hepatic impairment.
There were no clinically relevant differences between naloxegol 12.5 mg, 25 mg, and placebo in average pain intensity, daily opioid dose or in opioid withdrawal scores over the 12-week study.
There were no other clinically relevant differences between two concurrent injections of Xiapex in the same hand and up to three single injections of Xiapex in the types of adverse events reported ie, most adverse events were local to the treated extremity and of mild or moderate intensity.
There was no clinically relevant difference in pharmacokinetics of Levemir between older and young subjects.