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drotrecogin alfa
- alfa drotrekogīns (aktivētais) ir dabiskas olbaltumvielas, kas ir asinīs un ko sauc par c proteīnu
Ultimo aggiornamento 2011-10-23
Frequenza di utilizzo: 1
Qualità:
Attenzione: Questo allineamento potrebbe essere errato.
Eliminalo se ritieni che sia così.
drotrecogin alfa (activated)
drotrekogīns alfa (aktivēts)
Ultimo aggiornamento 2014-11-21
Frequenza di utilizzo: 1
Qualità:
drotrecogin alfa (activated) [enhance] n=2378
alfa drotrekogīns (aktivētais) [enhance] n=2378
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 1
Qualità:
a vial contains 20 mg of drotrecogin alfa (activated).
flakons satur 20 mg alfa drotrekogīna (aktivētā).
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 6
Qualità:
it contains the active substance drotrecogin alfa (activated).
tas satur aktīvo vielu alfa drotrekogīnu (aktivētu).
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 1
Qualità:
each xigris vial contains 20 mg of drotrecogin alfa (activated).
katrā xigris flakonā ir 20 mg alfa drotrekogīna (aktivētā).
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 8
Qualità:
xigris 20 mg powder for solution for infusion drotrecogin alfa (activated)
xigris 20 mg pulveris infūziju šķīduma pagatavošanai drotrecogin alfa (activated)
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 10
Qualità:
the active substance is 20 mg of drotrecogin alfa (activated) in each vial.
aktīvā viela ir 20 mg alfa drotrekogīna (aktivētā) katrā flakonā.
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 6
Qualità:
slowly withdraw the appropriate amount of reconstituted drotrecogin alfa (activated) solution from the vial.
lēnām atvelciet nepieciešamo atšķaidītā alfa drotrekogīna (aktivētā) šķīduma daudzumu no flakona.
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 3
Qualità:
after reconstitution with 10 ml of water for injection each ml contains 2 mg of drotrecogin alfa (activated).
pēc izšķīdināšanas 10 ml ūdens injekcijām katrs mililitrs satur 2 mg alfa drotrekogīna (aktivētā).
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 6
Qualità:
virtually no measurable activity of drotrecogin alfa (activated) is present 2 hours after obtaining the blood sample.
faktiski 2 stundas pēc asins parauga paņemšanas alfa drotrekogīna (aktivētā) aktivitāte nav nosakāma.
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 3
Qualità:
there have been no clinical trials in severe sepsis specifically studying drotrecogin alfa (activated) re- administration.
specifiski klīniski pētījumi par atkārtotu aktivētā alfa drotrekogīna ievadi smagas sepses gadījumos nav veikti.
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 3
Qualità:
patients received drotrecogin alfa (activated) within 48 hours of onset of the first sepsis- induced organ dysfunction.
pacientiem alfa drotrekogīns (aktivētais) tika ievadīts 48 stundu laikā no pirmo sepses izraisītas orgānu disfunkcijas simptomu novērošanas brīža.
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 3
Qualità:
drotrecogin alfa (activated) is contraindicated in children below the age of 18 years (see section 5.1).
alfa drotrekogīns (aktivētais) kontrindicēts bērniem līdz 18 gadu vecumam (skatīt apakšpunktu 5.1).
Ultimo aggiornamento 2017-04-26
Frequenza di utilizzo: 1
Qualità:
