Примери за използване на Intravenous dose на Английски и техните преводи на Български
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An intravenous dose of 2.3 g/kg was fatal in dogs.
A medical professional will need to give an intravenous dose.
The recommended intravenous dose is 3 to 5 mg/kg/day.
Assessment of bevacizumab metabolism in rabbits following a single intravenous dose of.
After a single intravenous dose of 250 mg, the clearance was 8.2 L/h.
Хората също превеждат
EXJADE tablets is about 70% compared to an intravenous dose.
The plasma clearance after a 25-mg intravenous dose is estimated to be approximately 50 ml/ min.
The first subcutaneous dose should be given at week 8 following the intravenous dose.
Following an intravenous dose of 100 mg/m2 given as a 3 hour infusion to 19 patients with.
The terminal half-life at the maximum tolerated intravenous dose(150 µg/m2) was 15-30 min.
After an intravenous dose, the dabigatran-derived radioactivity was eliminated primarily in the urine(85%).
A volume of distribution(Vss) of about 18 litres was determined after an intravenous dose of 250 mg.
The highest non-lethal single intravenous dose was 10 mg/kg bodyweight in mice and 0.6 mg/kg in rats.
The mean extent of absorption of a subcutaneous dose was 57% relative to an intravenous dose.
Approximately 71% of an intravenous dose of lamivudine is recovered as unchanged medicinal product in the urine.
STELARA treatment is to be initiated with a single intravenous dose based on body weight.
The recommended single intravenous dose of peramivir depends on age and body weight as shown in Table 1.
The first subcutaneous administration of 90 mg STELARA should take place at week 8 after the intravenous dose.
The terminal half-life of aprepitant following a 150 mg intravenous dose of fosaprepitant was approximately 11 hours.
The absolute bioavailability(AUC) of deferasirox(dispersible tablet formulation)is about 70% compared to an intravenous dose.
Alpivab should be administered as a single intravenous dose within 48 hours of the onset of symptoms of influenza.
Absolute bioavailability of a 0.30 mg/kg subcutaneous dose versus a 0.30 mg/kg intravenous dose is 82%.
Elimination Following a single 25 mg intravenous dose of temsirolimus, temsirolimus mean±SD systemic clearance was 11.4± 2.4 l/ h.
In patients on haemodialysis or CAPD,the maximum daily intravenous dose is also 400 mg.
Approximately 70-80% of the intravenous dose of tenofovir is recovered as unchanged medicinal product in the urine within 72 hours of dosing. .
There is limited clinical trial experience with doses higher than the approved intravenous dose of Ocrevus.
In patients with normal renal function,80 to 100% of the intravenous dose was recovered in the urine over 24 hours as unchanged cidofovir.
All occurred in paediatric patients, who received up to five times the recommended intravenous dose of voriconazole.
If patient response to treatment is inadequate, the intravenous dose may be increased by 1 mg/kg steps.
Therefore, the duration of infusion should not be less than the recommended 60 minutes and the intravenous dose of 400 mg once a day should not be exceeded.