Examples of 'terminal elimination half-life' in a sentence
Meaning of "terminal elimination half-life"
Terminal elimination half-life: In pharmacology and pharmacokinetics, the terminal elimination half-life refers to the time it takes for the concentration of a drug in the body to decrease by half during the elimination phase
How to use "terminal elimination half-life" in a sentence
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terminal elimination half-life
It has a terminal elimination half-life of seven hours.
Otherwise it will be shorter than the terminal elimination half-life.
The terminal elimination half-life increased approximately two fold.
No differences were observed in the terminal elimination half-life between treatments.
The terminal elimination half-life of gentamicin may be prolonged in elderly patients.
Telmisartan is characterised by biexponential decay pharmacokinetics with a terminal elimination half-life of.
The estimated median terminal elimination half-life of MabThera subcutaneous formulation was.
Urine should be collected over no less than three times the terminal elimination half-life.
The apparent terminal elimination half-life of monomethyl fumarate is about 2 hours.
Data contradicted the earlier data from DiSanto and Wagner as regards terminal elimination half-life.
The terminal elimination half-life of dutasteride is approximately 5 weeks at steady state.
The most important is that the terminal elimination half-life deduced by Peter et al.
Terminal elimination half-life values were generally between one and three hours.
Following subcutaneous administration, terminal elimination half-life is approximately 2 to 5 weeks.
The terminal elimination half-life and the apparent clearance rate were independent of the dose administered.
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The kinetics is linear and the terminal elimination half-life is 24 h.
The terminal elimination half-life of paliperidone is about 23 hours.
The kinetic is linear and the terminal elimination half-life is 24 h.
The terminal elimination half-life of rilpivirine is approximately 45 hours.
Telmisartan is characterised by biexponential decay pharmacokinetics with a terminal elimination half-life of > 20 hours.
The relatively long terminal elimination half-life reflects doxorubicin 's distribution into a deep tissue compartment.
After absorption in the bone, alendronate has an estimated terminal elimination half-life of 10 years.
A prolonged terminal elimination half-life of approximately 15 h is observed.
Amlodipine elimination from plasma is biphasic with a terminal elimination half-life of approximately 30 to 50 hours.
The terminal elimination half-life of carboxy terfenadine is about 20 hours.
In another embodiment, the antibody has a terminal elimination half-life in a rat of at least 8 days.
The terminal elimination half-life of total radioactivity was approximately 80 hours.
Ten percent of patients have a mean terminal elimination half-life greater than 100 hours.
The mean terminal elimination half-life of ceftaroline in healthy adults is approximately 2.5 hours.
A slower terminal elimination phase follows with a dose-independent mean terminal elimination half-life of 2 to 3 h.
Teduglutide has a terminal elimination half-life of approximately 2 hours.
Fampyra is characterized by linear ( dose-proportional ) pharmacokinetics with a terminal elimination half-life of approximately 6 hours.
The apparent terminal elimination half-life in plasma is about 2 days.
The term " half-life " is the apparent terminal elimination half-life.
The terminal elimination half-life is longer than the effective half-life.
Elimination from the plasma is biphasic with a terminal elimination half-life of about 30-50 hours.
The terminal elimination half-life of darunavir was approximately 15 hours when combined with ritonavir.
It is excreted predominantly unchanged in urine and has a terminal elimination half-life of about 60-80 hours.
The apparent mean terminal elimination half-life of carvedilol generally ranges from seven to 10 hours.
The terminal elimination half-life ( t ½ ) was derived from the slope of the log linear terminal phase.
Upadacitinib mean terminal elimination half-life ranged from 9 to 14 hours.
The terminal elimination half-life of Dilaudid following intravenous dose is around 2.3 hours.
The observed terminal elimination half-life was 142 hours in CKD patients not on dialysis.
The terminal elimination half-life of digoxin in patients with normal renal function is 30 to 40 hours.
Apparent plasma terminal elimination half-life differences were 3-4 fold between subjects in the food effect study.
The terminal elimination half-life after ACTIQ administration is about 7 hours.
The median terminal elimination half-life of tenofovir alafenamide was 0.3 hours when administered as Symtuza.
The terminal elimination half-life of ocrelizumab was 26 days.
The terminal elimination half-life of 4.
In contrast, the terminal elimination half-life ( T ½ ) appeared unaffected by dose.
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The half-life was prolonged in these patients
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Each elimination phase determines a half-life
