Eksempler på brug af Pharmacokinetic differences på Engelsk og deres oversættelser til Dansk
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Pharmacokinetic differences due to race have not been identified.
There were no clinically important pharmacokinetic differences based on age or gender.
No pharmacokinetic differences(AUC and Cmax) have been observed between elderly≥.
Elderly patients: no clinically relevant age-related pharmacokinetic differences have been observed in these patients.
Similar pharmacokinetic differences between males and females and smokers and nonsmokers were observed in ZYPADHERA clinical trials.
Gender, Race andBMI There were no clinically important pharmacokinetic differences due to gender, race or body mass index BMI.
Pharmacokinetic differences have been identified between males and females apparent plasma clearance is approximatively 50% lower in females.
No information is available regarding pharmacokinetic differences due to age(except paediatric patients), gender or race.
The risk of myopathy with statins appears to be exposure-dependent andtherefore may vary with individual drugs(due to lipophilicity and pharmacokinetic differences), including their dosage and potential for drug interactions.
Gender No significant pharmacokinetic differences have been observed between men and women.
Based upon the overlap in the range of clearance, gender-based pharmacokinetic differences do not justify the recommendation for using a lower dose for female patients.
The gender- related pharmacokinetic differences are not considered to be clinically relevant and dose adjustment is not required.
Based upon the overlap in the range of clearance, gender-based pharmacokinetic differences do not justify the recommendation for using a lower dose for female patients.
No significant age-related pharmacokinetic differences have been observed in adult patients in clinical trials which included over 20% of patients age 65 and older.
No age or gender related pharmacokinetic differences have been observed in adult patients.
There are no significant pharmacokinetic differences between intramuscular and subcutaneous administration of Puregon.
There were no clinically important pharmacokinetic differences between patients with moderate hepatic insufficiency and healthy subjects.
There were no clinically important pharmacokinetic differences between patients with severe renal insufficiency and healthy subjects see section 4.2.
In patients with type 2 diabetes over a wide range of renal function the pharmacokinetic differences between insulin lispro and soluble human insulin were generally maintained and shown to be independent of renal function.
In patients with type 2 diabetes over a wide range of renal function the pharmacokinetic differences between insulin lispro and soluble human insulin were generally maintained and shown to be independent of renal function.
No clinically important pharmacokinetic difference due to race has been identified.
There is no apparent pharmacokinetic difference between males and females.
An analysis in 126 CKD patients showed no pharmacokinetic difference between patients on dialysis and patients not on dialysis.
Limited data does not indicate differences in pharmacokinetic parameters in Black or African Americans.
Given the difference in pharmacokinetic profiles and dosing schedules, Caelyx should not be used interchangeably with other formulations of doxorubicin hydrochloride.