INTRAVENSKEM ODMERKU in English translation

• intravenous dose
• IV dose
• intravenous doses

Examples of using Intravenskem odmerku in Slovenian and their translations into English

po enem samem subkutanem ali intravenskem odmerku.
after a single subcutaneous or intravenous dose.

dosežene pri človeku po enem samem intravenskem odmerku vernakalanta.
achieved after a single intravenous dose of vernakalant.

Po intravenskem odmerku 100 mg/ m2, ki ga je s triurno infuzijo dobilo 19 bolnikov, ki imajo z aidsom povezan Kaposijev sarkom, se je največja
Following an intravenous dose of 100 mg/ m2 given as a 3 hour infusion to 19 patients with AIDS- related Kaposi' s sarcoma,

Porazdelitev: Povprečni volumen porazdelitve, ki sledi enkratnemu intravenskemu odmerku.
Distribution: The mean volume of distribution following a single intravenous dose of rasagiline is 243 l.

Intravenski odmerki[mg].
Intravenous Dose[mg].

Očistek in volumen porazdelitve se zmanjšujeta z višanjem intravenskega odmerka in večata s časom.
Clearance and volume of distribution decrease with increased intravenous doses and increase with time.

Povprečni volumen porazdelitve, ki sledi enkratnemu intravenskemu odmerku razagilina, je 243 l.
The mean volume of distribution following a single intravenous dose of rasagiline is 243 l.

Pri anesteziranih psih in opicah vrste Cynomolgus so pri intravenskih odmerkih 15-60 mg/kg opazili zmanjšanje atrijske
In anesthetized dogs and Cynomolgus monkeys, at intravenous doses of 15-60 mg/kg, slowing of atrial

Največji do zdaj preizkušen intravenski odmerek zdravila MabThera pri človeku je 5.000 mg(2.250 mg/m2),
The highest intravenous dose of MabThera tested in humans to date is 5000 mg(2250 mg/m2),

Študije z visokimi intravenskimi odmerki fenilacetata so odkrile nelinearno farmakokinetiko, katere značilnost je nasičena presnova v fenilacetilglutamin.
Studies with high intravenous doses of phenylacetate showed non linear pharmacokinetics characterised by saturable metabolism to phenylacetylglutamine.

Največji ne-letalen enkratni intravenski odmerek je bil 10 mg/kg telesne mase pri miših
The highest non-lethal single intravenous dose was 10 mg/kg body weight in mice

Posamezni intravenski odmerki 10 in 30 mg/kg so povzročili zmerno do hudo z odmerkom povezano hipotenzijo, ki jo je spremljala blaga tahikardija.
Single intravenous doses of 10 and 30 mg/kg produced moderate to severe dose related hypotension accompanied by a slight tachycardia.

Največji neletalni enkratni intravenski odmerek je bil 10 mg/kg telesne mase pri miših
The highest non-lethal single intravenous dose was 10 mg/kg bodyweight in mice

Študije z visokimi intravenskimi odmerki fenilacetata so odkrile nelinearno farmakokinetiko, katere značilnost je presnova v fenilacetilglutamin.
Studies with high intravenous doses of phenylacetate showed non-linear pharmacokinetics characterised by saturable metabolism to phenylacetylglutamine.

Priporočeni intravenski odmerek asparaginaze je 5.000 enot na kvadratni meter(E/m²) telesne površine vsak tretji dan.
The recommended intravenous dose of asparaginase is 5,000 units per square metre(U/m²) body surface area(BSA) given every third day.

Študija embria/zarodka pri kuncih ni pokazala učinkov pri intravenskih odmerkih do 80 mg/kg natrijevega kolistimetata(32 mg kolistina/kg).
An embryo-fetal study in rabbits reported no effects at intravenous doses up to 80 mg/kg colistimethate sodium(32 mg colistin base/kg).

Priporočena shema intravenskih odmerkov za bolnike z očistkom kreatinina>
The recommended intravenous dose regimen for patients with creatinine clearance>

Povprečni volumen porazdelitve je bil pri zdravih osebah 49,3 ml/kg po intravenskih odmerkih 50 in 100 i.e. /kg.
The mean volume of distribution was 49.3 ml/kg after intravenous doses of 50 and 100 IU/kg in healthy subjects.

Preiskovanci so prejeli bodisi enkraten intravenski odmerek 1000 enot bodisi odmerek 1000 enot,
The subjects received either a single intravenous dose of 1000 Units

Farmakokinetiko rituksimaba so ocenili po dveh 500 mg in 1.000 mg intravenskih odmerkih pri ponovnem zdravljenju v drugem ciklu.
The pharmacokinetics of rituximab were assessed following two intravenous doses of 500 mg and 1,000 mg upon re-treatment in the second course.