Examples of 'peak plasma concentrations' in a sentence
Meaning of "peak plasma concentrations"
peak plasma concentrations - the point of time when a drug in the bloodstream reaches its highest level. This phrase is commonly used in medical contexts, especially in pharmacokinetics and drug administration studies
How to use "peak plasma concentrations" in a sentence
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peak plasma concentrations
These reach peak plasma concentrations in.
There is a relationship between the subcutaneous dose of calcitonin and peak plasma concentrations.
Peak plasma concentrations are lower than by intravenous administration.
Concentrations equivalent to peak plasma concentrations investigated for receptor binding.
Peak plasma concentrations are attained within the first hour of administration.
The combinations may be administered to achieve peak plasma concentrations of each active ingredient.
Peak plasma concentrations of sulcardine sulfate increased with increasing dose.
Bolus have been exposed to peak plasma concentrations of almost 1 mM.
Higher peak plasma concentrations for MST were also found for the metabolites.
After subcutaneous administration of efalizumab peak plasma concentrations are reached after 12 days.
Peak plasma concentrations are reached in approximately 1 hour.
When administered with food to healthy subjects, peak plasma concentrations are delayed by 2 hours.
Peak plasma concentrations are achieved 90 minutes after sublingual administration.
Thereafter the drug is rapidly absorbed and peak plasma concentrations are attained after 1 hour.
Peak plasma concentrations are observed about 1 hour after dosing.
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Following subcutaneous administration to patients with type 2 diabetes, exenatide reaches median peak plasma concentrations in 2 h.
Peak plasma concentrations of up to 20 micromolar may be achieved for systemic administration.
ADVATE ® and rFVIIIFc had comparable dose-dependent peak plasma concentrations and recoveries.
Peak plasma concentrations of the unchanged active substance are attained within 24 hours.
Edoxaban is absorbed with peak plasma concentrations within 1 - 2 hours.
However, peak plasma concentrations at levels of those achieved by intravenous administration are preferably avoided.
Celecoxib is well absorbed reaching peak plasma concentrations after approximately 2-3 hours.
Peak plasma concentrations of 6MNA are increased by approximately one third.
It is absorbed in the gastrointestinal tract, reaching peak plasma concentrations within 30 minutes.
Quetiapine achieves peak plasma concentrations at approximately 6 hours after administration Tmax.
Following subcutaneous administration to patients with type 2 diabetes, dulaglutide reaches peak plasma concentrations in 48 hours.
Quetiapine fumarate reaches peak plasma concentrations approximately 6 hours following administration.
Further, peak plasma concentrations for Tiazac are achieved after about 7 hours after dose administration.
Emtricitabine is rapidly absorbed with peak plasma concentrations occurring at 1 to 2 hours post-dose.
Peak plasma concentrations are reached within 30 minutes.
Aripiprazole is well absorbed, with peak plasma concentrations occurring within 3-5 hours after dosing.
Peak plasma concentrations of oseltamivir carboxylate decline with a half-life of 6 to 10 hours in most subjects.
Sofosbuvir was absorbed quickly and the median peak plasma concentrations were observed ~ 1 hour post-dose.
The peak plasma concentrations were observed between 1 hour and 5 hour postdose.
Pharmacokinetic properties Celecoxib is well absorbed reaching peak plasma concentrations after approximately 2-3 hours.
Results, The peak plasma concentrations are lower than the toxic level.
Absorption, entecavir is rapidly absorbed with peak plasma concentrations occurring between 0.5 -.
Peak plasma concentrations ( Cmax ) of lapatinib are achieved approximately 4 hours after administration.
Fluoxetine has a bioavailability of approximately 72 %, and peak plasma concentrations are reached in 6 to 8 hours.
Peak plasma concentrations ( Cmax ) and corresponding peak times ( Tmax ) were determined.
Intramuscular injection produces mean peak plasma concentrations of 20 mg / l within 30 minutes following a 1 g dose.
Peak plasma concentrations were approximately 300 mg / L and were achieved immediately following the end of infusion.
Following sublingual administration, asenapine is rapidly absorbed with peak plasma concentrations occurring within 0.5 to 1.5 hours.
Peak plasma concentrations ( Cmax ) and peak times ( tmax ) were derived directly from the measured values.
Following subcutaneous injection, peak plasma concentrations of volanesorsen are typically reached in 2 to 4 hours.
Peak plasma concentrations are reached at about 4.5 hours.
Following subcutaneous administration, peak plasma concentrations of certolizumab pegol were attained between 54 and 171 hours post-injection.
Peak plasma concentrations of hydrochlorothiazide are reached within 1.5 to 5 hours.
Mean peak plasma concentrations were 60 % higher.
Peak plasma concentrations of haloperidol are attained within 20 to 40 minutes.
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