Examples of using Cmax in English and their translations into Vietnamese
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Colloquial
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Ecclesiastic
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Computer
increased Cmax and AUC for cilostazol by 18% and 26% respectively,
of 300mg once daily, the mean(CV) steady-state Cmax, Cmin and 24h AUC are 2.0 µg/ml(26%),
the drug Cmax was 24 IU/L,
the extent of exposure(AUC) of the levocetirizine tablet, but Tmax was delayed by about 1.25 hours and Cmax was decreased by about 36% after administration with a high fat meal; therefore, levocetirizine can be administered with or without food.
Cmin and Cmax of tocilizumab were 55500± 14100 mcg∙h per mL, 19.0± 12.0 mcg per mL,
Although food decreases the rate and extent of drug absorption by approximately 25% and 9%, respectively, as assessed by the Cmax and area under curve(AUC), LDL-C reduction is similar whether
150 mg twice daily, mean(CV) steady-state Cmax and Cmin of lamivudine in plasma are 1.2 µg/ml(24%) and 0.09 µg/ml(27%), respectively.
In a single dose clinical pharmacology study using 60 mg dapoxetine, plasma concentrations in poor metabolizers of CYP2D6 were higher than in extensive metabolizers of CYP2D6(approximately 31% higher for Cmax and 36% higher for AUCinf of dapoxetine and 98% higher for Cmax and 161% higher for AUCinf of desmethyldapoxetine).
The post-infusion decline of zoledronic acid concentrations in plasma was consistent with a triphasic process showing a rapid decrease from peak concentrations at end-of-infusion to less than 1% of Cmax 24 hours post infusion with population half-lives of t1/2α 0.24 hour and t1/2β 1.87 hours for the early disposition phases of the drug.
concentration-derived parameters such as AUC(area under the concentration curve) and Cmax(peak level of the concentration curve) of the drug after its administration[citation needed].
The postinfusion decline of zoledronic acid concentrations in plasma was consistent with a triphasic process showing a rapid decrease from peak concentrations at end of infusion to less than 1% of Cmax 24 hours postinfusion with population half-lives of t1/2α 0.24 hours and t1/2β 1.87 hours for the early disposition phases of the drug.
undesirable effects may occur(AUC is the total concentration of the drug in plasma; MHO is the international normalized ratio- the ratio of prothrombin time to standard average prothrombin time; Cmax is the maximum concentration of drug in the blood; T1/ 2- half-life).
Cmax was unchanged.
AUC and Cmax.
For acetaminophen, Cmax was measured as mcg/mL.
Erythromycin: decrease in AUC and Cmax of rosuvastatin;
The time to reach Cmax is about one hour.
Time to reach Cmax is also prolonged by 1 hour.
ª For acetaminophen, Cmax was measured as mcg/mL.
Cmax and AUC increased in proportion to the dose increase.