Examples of using Sofosbuvir in English and their translations into Polish
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Financial
-
Official/political
-
Programming
-
Computer
Sofosbuvir(400 mg once daily)/.
The active substance is sofosbuvir.
Sofosbuvir is a nucleotide prodrug.
Use with ledipasvir and sofosbuvir.
Sofosbuvir was administered at a dose of 400 mg once daily.
The predominant circulating metabolite of sofosbuvir.
Sofosbuvir is a nucleotide prodrug that is extensively metabolised.
See also under Use with ledipasvir and sofosbuvir below.
It is not known whether sofosbuvir, the active substance of Sovaldi, passes into human breast milk.
This medicine is taken with another antiviral drug named sofosbuvir.
In particular, interaction between sofosbuvir+ simeprevir and amiodarone has also been identified.
Data generated from simultaneous dosing with ledipasvir/sofosbuvir.
Sofosbuvir and GS-331007 are not inhibitors of drug transporters P-gp, BCRP, MRP2, BSEP, OATP1B1, OATP1B3 and OCT1.
In clinical pharmacology studies, both sofosbuvir and GS-331007 were monitored for purposes of pharmacokinetic analyses.
It is also important to tell your doctor if you are taking ledipasvir/sofosbuvir to treat hepatitis C infection.
Sofosbuvir is a pan-genotypic inhibitor of the HCV NS5B RNA-dependent RNA polymerase, which is essential for viral replication.
GS-331007 in these studies was up to 30 times(mouse) and 15 times(rat)higher than the clinical exposure at 400 mg sofosbuvir.
Sofosbuvir is extensively metabolised in the liver to form the pharmacologically active nucleoside analog triphosphate GS-461203.
In the ELECTRON study(N 11), the duration of peginterferon alfa ranged from 4-12 weeks in combination with sofosbuvir+ ribavirin.
Sofosbuvir and GS-331007 are not substrates or inhibitors of UGT1A1 or CYP3A4, CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, and CYP2D6 enzymes.
Co-administration will significantly decrease sofosbuvir plasma concentration and could result in loss of efficacy of Sovaldi see section 4.5.
Sofosbuvir had no effects on embryo-foetal viability or on fertility in rat and was not teratogenic in rat and rabbit development studies.
Since the existing wording restricted the warning only to the use of sofosbuvir+ daclatasvir and amiodarone, it became outdated and had to be modified.
Sofosbuvir is not a substrate for hepatic uptake transporters, organic anion-transporting polypeptide(OATP) 1B1 or 1B3, and organic cation transporter(OCT) 1.
Patients receiving Stribild concomitantly with ledipasvir/sofosbuvir should be monitored for adverse reactions related to tenofovir disoproxil fumarate.
Sofosbuvir and GS-331007 are not inhibitors of P-gp and BCRP and thus are not expected to increase exposures of medicinal products that are substrates of these transporters.
The safety of tenofovir disoproxil fumarate when used with ledipasvir/sofosbuvir and a pharmacokinetic enhancer(e.g. ritonavir or cobicistat) has not been established.
Subjects received 400 mg sofosbuvir and weight-based ribavirin 1,000 mg for subjects weighing< 75 kg or 1,200 mg for subjects weighing≥75 kg.
Medicinal products that are moderate P-gp inducers in the intestine(e.g. oxcarbazepine and modafinil)may decrease sofosbuvir plasma concentration leading to reduced therapeutic effect of Sovaldi.
However, if ribavirin is co-administered with sofosbuvir, the contraindications regarding use of ribavirin during pregnancy apply see also the Summary of Product Characteristics for ribavirin.