Examples of using Etexilate in English and their translations into Polish
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Financial
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Official/political
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Programming
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Computer
Dabigatran etexilate can be given as soon as the International Normalized Ratio(INR) is< 2.0.
Dabigatran etexilate was given twice daily over 3 consecutive days,
Food does not affect the bioavailability of dabigatran etexilate but delays the time to peak plasma concentrations by 2 hours.
Concomitant administration of the P-gp substrate dabigatran etexilate may result in increased dabigatran plasma concentrations.
Dabigatran etexilate, a medicine used to treat heart conditions,
It is recommended to continue with the remaining daily doses of dabigatran etexilate at the same time of the next day.
Dabigatran etexilate should be restarted after the invasive procedure
Dabigatran etexilate and dabigatran are not metabolised by the cytochrome P450 system
It is recommended to wait 12 hours after the last dose before switching from dabigatran etexilate to a parenteral anticoagulant see section 4.5.
Patients on dabigatran etexilate who undergo surgery
with possible exposure increases of e.g. dabigatran etexilate, digoxin or aliskiren.
all secondary endpoints showed superiority of dabigatran etexilate over placebo.
A higher anti-FXa/FIIa activity was observed after dabigatran etexilate administration with enoxaparin pre-treatment compared to that after treatment with dabigatran etexilate alone.
LMWH: The concomitant use of LMWHs, such as enoxaparin and dabigatran etexilate has not been specifically investigated.
With chronic use in the RE-LY study, NSAIDs increased the risk of bleeding by approximately 50% on both dabigatran etexilate and warfarin.
indicating that the initial treatment effect of dabigatran etexilate was sustained.
dabigatran etexilate, digoxin, talinolol, and tolvaptan.
With chronic use NSAIDs increased the risk of bleeding by approximately 50% on both dabigatran etexilate and warfarin.
SEE in patients with atrial fibrillation, a total of 12,042 patients were treated with dabigatran etexilate.
This may result in increased sytemic exposure of substrates of these transporters, such as dabigatran etexilate, ciclosporin, rosuvastatin