Examples of 'pharmacokinetic parameters' in a sentence

Meaning of "pharmacokinetic parameters"

This phrase pertains to specific measurements or factors used to describe the action and movement of drugs within a living organism. It includes parameters such as absorption, distribution, metabolism, and excretion of the drug. Pharmacokinetic parameters are crucial in determining the dosage, efficacy, and safety of medications

How to use "pharmacokinetic parameters" in a sentence

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pharmacokinetic parameters
The pharmacokinetic parameters obtained in studies comparing.
There are no marked changes in the pharmacokinetic parameters.
Pharmacokinetic parameters are summarised in the table below.
Differences in other pharmacokinetic parameters were not significant.
Pharmacokinetic parameters are comparable to those reported in adults.
Different triptans have varying pharmacokinetic parameters.
Pharmacokinetic parameters were determined using noncompartmental analysis.
And used for calculation of pharmacokinetic parameters.
Summary of pharmacokinetic parameters of the clinical testings.
Gender had no clinically relevant effect on pharmacokinetic parameters.
Other pharmacokinetic parameters may be measured as well.
There were no changes in the pharmacokinetic parameters for nefazodone.
Pharmacokinetic parameters were estimated for all cases.
The calculation of these pharmacokinetic parameters is explained below.
Pharmacokinetic parameters were calculated for each mouse.

See also

There is no gender effect on pharmacokinetic parameters.
The pharmacokinetic parameters were calculated using WinNonlin.
Formulations may also be characterized by their pharmacokinetic parameters.
Estimation of pharmacokinetic parameters was done by using moment analysis.
This was also reflected in the calculation of pharmacokinetic parameters.
The pharmacokinetic parameters in the second study were comparable.
Potency and efficacy are two key pharmacokinetic parameters of glucocorticoids.
Pharmacokinetic parameters of tocilizumab did not change with time.
Additional pulmonary safety and pharmacokinetic parameters were also evaluated.
Pharmacokinetic parameters were not altered by diminishing hepatic function.
Age alone had no clinically relevant effect on pharmacokinetic parameters.
Pharmacokinetic parameters were calculated using the program PCNONLiN.
Release forms may also be characterized by their pharmacokinetic parameters.
The results of the pharmacokinetic parameters analysis are below.
A confirmatory calculation for flux requires further pharmacokinetic parameters.
A summary of pharmacokinetic parameters are shown in the tables below.
The mean plasma concentration was used for calculation of pharmacokinetic parameters.
Pharmacokinetic parameters as well as taste were measured in adult volunteers.
Alternatively and particularly where pharmacokinetic parameters can not demonstrate a.
Pharmacokinetic parameters were summarized by treatment using descriptive statistics.
No apparent differences were noted in pharmacokinetic parameters between males and females.
Pharmacokinetic parameters were calculated from the plasma data.
These concentrations are subsequently used to determine the reported pharmacokinetic parameters.
Determination of the pharmacokinetic parameters after intravenous administration.
There were no consistent gender differences for any of the pharmacokinetic parameters.
Pharmacokinetic parameters after administration are determined.
There was no apparent gender difference for any of the pharmacokinetic parameters.
The main pharmacokinetic parameters are shown in the following table.
Actual time points were used for the calculation of pharmacokinetic parameters.
These pharmacokinetic parameters obtained from the compartmental analysis.
These concentrations were subsequently used to determine the reported pharmacokinetic parameters.
There are no changes in pharmacokinetic parameters following multiple daily doses.
Mild to moderate renal impairment does not significantly affect palonosetron pharmacokinetic parameters.
The variability in pharmacokinetic parameters was higher in sputum as compared to serum.
Descriptive statistics were calculated for fentanyl pharmacokinetic parameters for each treatment.

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