Examples of using Clinically relevant differences in English and their translations into Hungarian
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Programming
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Official/political
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Computer
There were no clinically relevant differences in Cmax compared to healthy volunteers.
The analysis of the impact ofNSCLC 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.
The analysis of the impact ofNSCLC histology on overall survival demonstrated clinically relevant differences in survival according to histology, see table below.
No clinically relevant differences in aprepitant pharmacokinetics is expected due to age and gender.
In a population pharmacokinetic analysis of ceftolozane/tazobactam, no clinically relevant differences in ceftolozane/tazobactam AUC were observed in Caucasians(n= 156) compared to all other ethnicities combined(n= 30).
No clinically relevant differences in adverse reactions were observed between the overall dataset and the approved indications.
In a population pharmacokinetic analysis of ceftolozane/tazobactam, no clinically relevant differences in AUC were observed for ceftolozane(116 males compared to 70 females) and tazobactam(80 males compared to 50 females).
No clinically relevant differences in ledipasvir pharmacokinetics were observed between healthy subjects and patients with severe renal impairment.
There were no clinically relevant differences in the clearance of tigecycline between men and women.
No clinically relevant differences in cobicistat pharmacokinetics were observed between subjects with moderate impairment and healthy subjects.
There are no clinically relevant differences in pharmacokinetics between Caucasian and Asian subjects.
No clinically relevant differences in tenofovir alafenamide, or tenofovir pharmacokinetics were observed between healthy subjects and subjects with severe renal impairment(estimated CrCl from 15 to< 30 mL/min) in studies of cobicistat-boosted elvitegravir or of tenofovir alafenamide.
There are no clinically relevant differences between genders in pharmacokinetic properties of insulin detemir.
There were no clinically relevant differences in systemic exposures between White, Black or Asian races.
Gender There were no clinically relevant differences in the clearance of tigecycline between men and women.
There were no clinically relevant differences observed in saxagliptin pharmacokinetics between males and females.
There were no clinically relevant differences in safety between males(N=382) and females(N=139) in the FLAGS study.
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 between genders in the pharmacokinetics of lurasidone in a population pharmacokinetic analysis in patients with schizophrenia.
There were no clinically relevant differences in the safety population of the elderly subjects who received oseltamivir or placebo compared with the adult population aged up to 65 years.
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 were neither statistically significant nor clinically relevant differences in bevacizumab clearance in patients receiving Avastin monotherapy compared to patients receiving Avastin in combination with interferon alfa-2a, erlotinib or chemotherapies(IFL, 5-FU/LV, carboplatin/paclitaxel, capecitabine, doxorubicin or cisplatin/gemcitabine).
Overall, no clinically relevant difference between genders was observed.
However, this is not considered to be a clinically relevant difference.
Population pharmacokinetic analysis of decitabine did not show any clinically relevant difference between men and women.
Clinically relevant difference in lacosamide exposure was observed comparing its pharmacokinetics in extensive metabolisers(EMs, with a functional CYP2C19) and poor metabolisers(PMs, lacking a functional CYP2C19).
No clinically relevant difference in ulcer prevention between the 15 and 30 mg dose of lansoprazole could be demonstrated.