Examples of using Clinically significant differences in English and their translations into Romanian
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Medicine
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No clinically significant differences were observed between men and women.
Data on Cushing's disease patients older than 65years are limited but do not suggest any clinically significant differences in safety and efficacy in relation to younger patients.
There were no clinically significant differences in safety parameters or in pharmacodynamics.
In a study of patients with varying degrees of stable chronic liver impairment(mild,moderate and severe), no clinically significant differences in pharmacokinetic parameters were found, and no dose adjustment is recommended.
No clinically significant differences in AUC or Cmax were noted between males and females.
Patient pharmacokinetic data indicated that no clinically significant differences in the pharmacokinetics of caspofungin were seen among Caucasians, Blacks, Hispanics, and Mestizos.
No clinically significant differences were seen when the safety data were analysed by age, race, or gender.
In the clinical studies of eltrombopag, overall no clinically significant differences in safety of eltrombopag were observed between subjects aged at least 65 years and younger subjects.
No clinically significant differences were seen when the safety data were analysed by gender or race.
In the RCC studies of pazopanib, overall no clinically significant differences in safety of pazopanib were observed between subjects aged at least 65 years and younger subjects.
No clinically significant differences were found in pharmacokinetic parameters of celecoxib between African-Americans and Caucasians.
After accounting for body weight differences, no clinically significant differences in the pharmacokinetic properties of canakinumab were observed between CAPS and SJIA patients.
No clinically significant differences in pharmacokinetics of telavancin were observed between healthy elderly and healthy young subjects.
There were no clinically significant differences in safety parameters or in pharmacodynamics.
No clinically significant differences were observed for QT, PR, QRS, or QTcB measurements between duloxetine- treated and placebo-treated patients.
Gender: No clinically significant differences in nateglinide pharmacokinetics were observed between men and women.
No clinically significant differences in LVMi were observed during the initial 6-month placebo-controlled period.
There are no clinically significant differences in the pharmacokinetics of indinavir in HIV seropositive women compared to HIV seropositive men.
No clinically significant differences in pharmacokinetic parameters were observed between patients with end-stage renal disease(ESRD) and healthy subjects.
There are no clinically significant differences in the pharmacokinetics of rosiglitazone in patients with renal impairment or end stage renal disease on chronic dialysis.
There were no clinically significant differences in the incidence of hypoglycaemic episodes in the immediate-release exenatide compared to the placebo group(25% and 29% respectively).
There are no clinically significant differences in the pharmacokinetics of rosiglitazone in patients with renal impairment or end stage renal disease on chronic dialysis.
There were no clinically significant differences in the percent decrease in serum uric acid concentration in healthy subjects irrespective of their renal function(58% in the normal renal function group and 55% in the severe renal dysfunction group).
No clinically significant differences in exposure to capecitabine or its metabolites, free platinum or total platinum occurred when capecitabine was administered in combination with oxaliplatin or in combination with oxaliplatin and bevacizumab.
No clinically significant gender-related differences in telavancin pharmacokinetics have been observed.
Clinically significant gender-related differences in dalbavancin pharmacokinetics have not been observed in healthy subjects or in patients with infections.
Population pharmacokinetic evaluation has revealed no evidence of clinically significant race-related differences or effects from smoking upon the pharmacokinetics of aripiprazole.