Examples of using Relevant differences in English and their translations into Hungarian
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Medicine
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Ecclesiastic
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Computer
The relevant differences are displayed in Table 5.20.
In this respect it is necessary to clarify the relevant differences between types or modalities of crisis.
No clinically relevant differences in adverse reactions were observed between the overall dataset and the approved indications.
The analysis of the impact of NSCLChistology on overall survival demonstrated clinically relevant differences in survival according to histology, see table below.
There were no clinically relevant differences in safety between males(N=382) and females(N=139) in the FLAGS study.
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The other large part is the comparing function, which is looking for the differences between the answers given by the systems-but only reporting the relevant differences.
Pharmacokinetic data reveal no relevant differences due to weight in the exposure to riociguat.
No clinically relevant differences in ledipasvir pharmacokinetics were observed between healthy subjects and patients with severe renal impairment.
The analysis of the impact of NSCLChistology on overall survival demonstrated clinically relevant differences in survival according to histology, see table below.
In clinical studies, no relevant differences in exposure, safety or efficacy were observed between male and female patients.
When aclidinium and formoterol were administered in combination by the inhaled route,the pharmacokinetics of each component showed no relevant differences from those observed when the medicinal products were administered separately.
In clinical studies, no relevant differences in exposure or efficacy were observed between patients of different ethnic groups.
They also arguethat, despite the genetic similarities between chimps and humans, they have relevant differences in, for instance, immune-response genes9, and that differences in gene expression make chimps weak as a biological model.
There were no relevant differences between Nivestim and the reference product with regard to duration of severe neutropenia and incidence of febrile neutropenia.
Gender 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.
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).
There were no relevant differences in the distribution of demographics, disease characteristics, or the use of post-study systemic therapy between the subset of patients with detectable EGFR protein expression and the ITT population.
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 elvitegravir, cobicistat, tenofovir alafenamide, or tenofovir pharmacokinetics were observed between healthy subjects and patients with severe renal impairment(estimated CrCl> 15 but< 30 mL/min) in studies of cobicistat-boosted elvitegravir or of tenofovir alafenamide.
Based on studies in healthy subjects, no relevant differences in ruxolitinib pharmacokinetics were observed with regard to gender and race.
There were no relevant differences between Tevagrastim and the reference product with regard to duration of severe neutropenia and incidence of febrile neutropenia.
Although they could lead to substantial benefits by effectively removing all the relevant differences between national laws and by ensuring the same tax treatment across the EU, these options would be technically challenging and politically unacceptable to Member States, not least due to the political sensitivity of tax issues.
There were no clinically relevant differences between genders in the pharmacokinetics of lurasidone in a population pharmacokinetic analysis in patients with schizophrenia.
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 in the safety population of the elderly subjects who received oseltamivir or placebo compared with the adult population aged up to 65 years.
No clinically relevant differences in elvitegravir or cobicistat pharmacokinetics were observed between subjects with severe renal impairment and healthy subjects.
In clinical studies, no relevant differences in exposure, safety or efficacy were observed between elderly(aged 65 years and above) and younger patients(see also section 5.2).
In clinical studies, no relevant differences in exposure, safety or efficacy were observed between patients with mild hepatic impairment(Child-Pugh A) and normal hepatic function.
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).