Examples of using Prasugrel 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
Alternatively, a loading dose of ticagrelor or prasugrel, but not clopidogrel, may be administered up to 30 minutes before the end of the infusion, see section 4.5.
Treatment in combination with other antiplatelet agents, e.g. prasugrel or ticagrelor, has not been studied and is not recommended.
reaction to any medicine used to treat your disease if you are allergic to other thienopyridines such as prasugrel, ticlopidine.
0.3% received prasugrel.
Of these, bleeding was the most common adverse reaction for both drugs leading to study drug discontinuation 2.5% for prasugrel and 1.4% for clopidogrel.
those below 60 kg(N=3022) were randomized to 5 mg prasugrel.
Patients≥ 75 years in whom the benefit with prasugrel was more evident included those with diabetes,
Prasugrel was associated with a 50% reduction in stent thrombosis through the 15 month follow-up period.
dentists that they are taking prasugrel before any surgery is scheduled
Prasugrel should be used with caution in patients≥ 75 years old
Efient should not be used in people who may be hypersensitive(allergic) to prasugrel or any of the other ingredients.
Following a 60 mg loading dose of prasugrel, inhibition of ADP-induced platelet aggregation occurs at 15 minutes with 5 µM ADP and 30 minutes with 20 µM ADP.
Analysis of all cause death did not show any significant difference between prasugrel and clopidogrel in the All ACS population(2.76% vs 2.90%), in the UA/NSTEMI population(2.58% vs 2.41%),
did not change the prasugrel active metabolite' s AUC and Tmax, but decreased the Cmax by 14% and 29%, respectively.
did not affect prasugrel-mediated inhibition of platelet aggregation or the prasugrel active metabolite' s AUC
2.8% for clopidogrel; rates for fatal bleeding were 0.2% for prasugrel and 0.1% for clopidogrel.
In an analysis of patients who survived an ischaemic event, prasugrel was associated with a reduction in the incidence of subsequent primary endpoint events 7.8% for prasugrel vs 11.9% for clopidogrel.
did not significantly change the pharmacokinetics of prasugrel.
did not affect prasugrel-mediated inhibition of platelet aggregation or the prasugrel active metabolite's AUC
did not change the prasugrel active metabolite's AUC and Tmax, but decreased the Cmax by 14% and 29%, respectively.