Examples of using Eltrombopag in English and their translations into Bulgarian
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Colloquial
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
Eltrombopag dose(once daily).
The active substance in Revolade is eltrombopag.
Absorbed eltrombopag is extensively metabolised.
Revolade 12.5 mg film-coated tablets eltrombopag.
Effects of eltrombopag on other medicinal products.
Bleeding following discontinuation of eltrombopag.
Eltrombopag(used for increasing platelet counts).
Effects of other medicinal products on eltrombopag.
Eltrombopag must not be used to normalise platelet counts.
Use lowest dose of eltrombopag to maintain platelet counts.
Eltrombopag should be initiated at a dose of 50 mg once daily.
The plasma elimination half-life of eltrombopag is approximately 21-32 hours.
Eltrombopag is a substrate for BCRP, but is not a substrate for P-glycoprotein or OATP1B1.
Approximately 21% of an eltrombopag dose could undergo oxidative metabolism.
The median time to diagnosis was 3 months from the start of eltrombopag treatment.
In clinical studies with eltrombopag, a dose reduction of statins by 50% was recommended.
The primary endpoint was haematological response assessed after 12 weeks of eltrombopag treatment.
Each sachet contains eltrombopag olamine equivalent to 25 mg of eltrombopag.
In vitro studies suggest that CYP1A2 andCYP2C8 are responsible for oxidative metabolism of eltrombopag.
Eltrombopag treatment delayed and reduced the number of peginterferon dose reductions.
Each film-coated tablet contains eltrombopag olamine equivalent to 12.5 mg eltrombopag.
Eltrombopag dose may need to be increased based on these platelet counts.
Dose adjustment is not required when eltrombopag is co-administered with either telaprevir or boceprevir.
Eltrombopag chelates with polyvalent cations such as iron, calcium, magnesium, aluminium, selenium and zinc.
The co-administration of 600 mg ciclosporin decreased the Cmax and the AUCinf of eltrombopag by 39% and 24%, respectively.
Eltrombopag treatment should be terminated when antiviral therapy is discontinued unless otherwise justified.
Six patients had cytogenetic abnormality at Month 3 of eltrombopag therapy and one patient had cytogenetic abnormality at Month 6.
Eltrombopag does not stimulate platelet production in mice, rats or dogs because of unique TPO receptor specificity.
At baseline, 71% of patients in the eltrombopag group and 69% in the placebo group reported any bleeding(WHO Grades 1-4).
Eltrombopag is primarily metabolised through cleavage, oxidation and conjugation with glucuronic acid, glutathione, or cysteine.