Examples of using An inducer in English and their translations into Swedish
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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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Official/political
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Computer
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Programming
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Political
Aprepitant is also an inducer of CYP2C9.
Forskolin is an inducer that is extensively used in the formation of cAMP.
Afatinib is not an inhibitor or an inducer of CYP enzymes.
Bosentan is an inducer of the cytochrome P450(CYP)
Therefore, laropiprant is not an inducer or inhibitor of CYP3A4.
Bosentan is an inducer of CYP2C9 and CYP3A4
Based upon in vitro data, migalastat is not an inducer of CYP1A2, 2B6, or 3A4.
It is not an inducer of CYP isozymes.
Tipranavir is a substrate, an inducer and an inhibitor of cytochrome P450 CYP3A.
Results from in vitro and in vivo studies show that rosuvastatin is neither an inhibitor nor an inducer of cytochrome P450 isoenzymes.
Conversely, cessation of treatment of an inducer might lead to increased plasma levels of febuxostat.
indicating that A771726 is not an inhibitor or an inducer of CYP2C9.
Similarly, ataluren is not expected in vivo to be an inducer of cytochrome P450 isoenzymes.
Rifampicin, which is an inducer of P-gp, reduced aliskiren bioavailability by approximately 50% in a clinical study.
This indicates that sorafenib is neither an inhibitor nor an inducer of these cytochrome P450 isoenzymes.
Rifampicin, which is an inducer of P-gp, reduced aliskiren bioavailability by approximately 50% in a clinical study.
acts both as an inducer and inhibitor of the metabolism of repaglinide.
Nevirapine is an inducer of CYP3A and potentially CYP2B6,
In vitro data indicate that selexipag could be an inducer of both CYP3A4 and CYP2C9 in the intestine.
Rifampicin an inducer of all three cytochromes involved in the metabolism of agomelatine may decrease the bioavailability of agomelatine.
In vivo, lesinurad is neither an inhibitor nor an inducer of CYP2C9 and 2C8,
Nevirapine is an inducer of CYP3A and potentially CYP2B6,
No data are available that can be used to exclude the risk that lenvatinib could be an inducer of CYP3A4 or P-gp in the gastrointestinal tract.
Entecavir is not a substrate, an inducer or an inhibitor of cytochrome P450(CYP450) enzymes see section 5.2.
indicating that teriflunomide is not an inhibitor or an inducer of CYP2C9.
Co-administration of rosiglitazone with rifampicin(an inducer of CYP2C8) resulted in a 66% decrease in rosiglitazone plasma concentrations.
The interaction potential of dalbavancin on medicinal products metabolised by CYP enzymes is expected to be low since it is neither an inhibitor nor an inducer of CYP enzymes in vitro.
Eluxadoline is not an inducer/inhibitor of major CYP enzymes,
it cannot be excluded that vismodegib upon longer treatment is an inducer of enzymes which metabolise contraceptive steroids.