Examples of 'relevant pharmacokinetic' in a sentence
Meaning of "relevant pharmacokinetic"
relates to the study of how drugs are absorbed, distributed, metabolized, and excreted by the body. It emphasizes the importance of understanding how drugs interact with the body and how their pharmacological effects are influenced by factors such as metabolism and elimination
How to use "relevant pharmacokinetic" in a sentence
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relevant pharmacokinetic
No relevant pharmacokinetic interactions have been described.
Interaction studies did not indicate any relevant pharmacokinetic effects on concurrent.
No clinically relevant pharmacokinetic differences due to ethnicity have been identified for cobicistat.
Clinical studies performed with healthy subjects have shown no clinically relevant pharmacokinetic interactions.
No clinically relevant pharmacokinetic differences due to gender have been identified for cobicistat.
R There is no pharmacodynamic or clinically relevant pharmacokinetic interaction with low-dose.
No clinically relevant pharmacokinetic differences due to gender have been identified for boosted.
There were no clinically relevant pharmacokinetic interactions between Abraxane and carboplatin.
The relevant pharmacokinetic data of the developed sublingual tablet are,.
Based on literature data, no clinically relevant pharmacokinetic interaction between paclitaxel and carboplatin is expected.
Clinically relevant pharmacokinetic interaction has been observed between paclitaxel and cisplatin.
Such studies should address relevant pharmacokinetic and pharmacodynamic endpoints and employ suitable statistical analyses.
No clinically relevant pharmacokinetic differences due to ethnicity have been identified for atazanavir or cobicistat.
In these studies, no clinically relevant pharmacokinetic interactions were observed after co-administration with vildagliptin.
No clinically relevant pharmacokinetic differences due to ethnicity have been identified for boosted.
See also
In the table is given relevant pharmacokinetic parameters from the pilot studies see Fig 2.
No clinically relevant pharmacokinetic differences due to gender have been identified for atazanavir or cobicistat.
There is no clinically relevant pharmacokinetic drug-drug interaction between nalmefene and alcohol.
No clinically relevant pharmacokinetic differences have been identified between men and women for doravirine.
Therefore, no relevant pharmacokinetic interactions are expected.
No clinically relevant pharmacokinetic interaction has, however, been seen with lamivudine.
There were no clinically relevant pharmacokinetic interactions between human serum albumin-paclitaxel nanoparticlesand carboplatin.
No clinically relevant pharmacokinetic drug-drug interaction was evidenced either with modafinil or with sodium oxybate.
No clinically relevant pharmacokinetic differences due to gender have been identified for sofosbuvir or GS-331007.
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