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Brukinsa · 4.5 · Zanubrutinib is primarily metabolized by cytochrome P450 enzyme 3A (CYP3A).
Eintrag öffnenBrukinsa · 4.5 · Zanubrutinib is primarily metabolized by cytochrome P450 enzyme 3A (CYP3A).
Eintrag öffnenBuccolam · 4.5 · Midazolam is metabolized by CYP3A4. Inhibitors and inducers of CYP3A4 have the potential to respectively incre
Eintrag öffnenCotellic · 4.5 · Cobimetinib is metabolized by CYP3A and cobimetinib AUC increased approximately 7 fold in the presence of a st
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.5 · CYP3A4 inducers Pretomanid is metabolized in part by CYP3A4. In consequence, exposure to pretomanid may be red
Eintrag öffnenEmblaveo · 4.5 · Aztreonam is not metabolized by cytochrome P450 enzymes. In vitro, avibactam showed no significant inhibition
Eintrag öffnenEpclusa · 4.5 · Impact of DAA therapy on medicinal products metabolized by the liver
Eintrag öffnenEpclusa · 4.5 · Impact of DAA therapy on medicinal products metabolized by the liver
Eintrag öffnenEpclusa · 4.5 · The pharmacokinetics of medicinal products that are metabolized by the liver (e.g. immunosuppressive medicinal
Eintrag öffnenEpclusa · 4.5 · The pharmacokinetics of medicinal products that are metabolized by the liver (e.g. immunosuppressive medicinal
Eintrag öffnenHarvoni · 4.5 · 46 Impact of DAA therapy on drugs metabolized by the liver
Eintrag öffnenHarvoni · 4.5 · Impact of DAA therapy on drugs metabolized by the liver
Eintrag öffnenHarvoni · 4.5 · The pharmacokinetics of drugs that are metabolized by the liver (e.g. immunosuppressive agents such as calcine
Eintrag öffnenHarvoni · 4.5 · The pharmacokinetics of drugs that are metabolized by the liver (e.g. immunosuppressive agents such as calcine
Eintrag öffnenIclusig · 4.5 · CYP3A inhibitors Ponatinib is metabolized by CYP3A4. Co-administration of a single 15 mg oral dose of Iclusig
Eintrag öffnenIclusig · 4.5 · CYP3A inhibitors Ponatinib is metabolized by CYP3A4. Co-administration of a single 15 mg oral dose of Iclusig
Eintrag öffnenOgsiveo · 4.5 · Nirogacestat is primarily metabolized by CYP3A4 and is a substrate of P‑glycoprotein (P-gp).
Eintrag öffnenOntozry · 4.5 · CYP2B6 Substrates ↓ CYP2B6 substrates plasma An increase in the dose of concentrations medicines metabolized b
Eintrag öffnenOntozry · 4.5 · CYP2C19 Substrates ↑ CYP2C19 substrates plasma A dose reduction of medicines concentrations metabolized by CYP
Eintrag öffnenOntozry · 4.5 · CYP3A4 substrates An increase in the dose of ↓ CYP3A4 substrates plasma medicines metabolized by concentration
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