Examples of using Substrate of p-gp in English and their translations into Swedish
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Official/political
-
Computer
-
Programming
-
Political
Fidaxomicin is a substrate of P-gp.
In vitro experiments with human Caco-2 cells indicated that simeprevir is a substrate of P-gp.
Nintedanib is a substrate of P-gp.
Lurasidone is a substrate of P-gp and BCRP in vitro
in vivo studies showed that daclatasvir is a substrate of P-gp.
Cobimetinib is a substrate of P-gp in vitro.
digoxin(substrate of P-gp) or atorvastatin substrate of CYP3A4 and P-gp. .
Nintedanib is a substrate of P-gp see section 5.2.
In vitro studies have demonstrated that afatinib is a substrate of P-gp and BCRP.
In vitro, lenalidomide is a substrate of P-gp, but is not a P-gp inhibitor.
Dasabuvir is a substrate of P-gp and BCRP and its major metabolite M1 is a substrate of OCT1 in vitro.
In vitro studies indicated that ibrutinib is not a substrate of P-gp, nor other major transporters, except OCT2.
Tigecycline is a substrate of P-gp based on an in vitro study using a cell line overexpressing P-gp. .
digoxin(substrate of P-gp), atorvastatin(substrate of CYP3A4
In vitro: Cysteamine bitartrate is a substrate of P-gp and OCT2, but not a substrate of BCRP,
Based on in vitro data, sonidegib is not a substrate of P-gp, BCRP or multi-resistance protein 2 MRP2.
Idelalisib and GS-563117 are substrates of P-gp and BCRP.
M-5 are weak substrates of P-gp.
Bedaquiline and M2 were not substrates of P-gp in vitro.
Therefore, cabozantinib may have the potential to increase plasma concentrations of co-administered substrates of P-gp.
Fidaxomicin and the metabolite OP-1118 are substrates of P-gp.
Co-administration with medicinal products that are substrates of P-gp, BCRP, OATP1B1
See Table 3 for examples of interactions with sensitive substrates of P-gp(digoxin), BCRP(rosuvastatin),
Therefore, crizotinib may have the potential to increase plasma concentrations of coadministered medicinal products that are substrates of P-gp see section 4.5.
Therefore, administration of crizotinib with medicinal products that are substrates of P-gp(e.g., digoxin,
Administration of Daklinza may increase systemic exposure to medicinal products that are substrates of P-gp, OATP 1B1,
Therefore, ponatinib may have the potential to increase plasma concentrations of co-administered substrates of P-gp(e.g., digoxin,
or are substrates of P-gp, BCRP, OATP1B1
Cobimetinib is a substrate of P-glycoprotein P-gp.
Methylthioninium chloride is a substrate of P-glycoprotein P-gp.