Приклади вживання Protease inhibitors Англійська мовою та їх переклад на Українською
{-}
-
Colloquial
-
Ecclesiastic
-
Computer
Protease inhibitors.
Next Patent: HCV NS3 protease inhibitors.
Protease inhibitors.
Rifampicin reduces the activity of most protease inhibitors by about 90%.
Drugs called protease inhibitors interfere with this step of the viral life cycle.
Insufficient information is available on interactions with other protease inhibitors.
On reacting paclitaxel with other protease inhibitors is insufficient information.
Insufficient information is available on interactions with other protease inhibitors.
Mathematical modelling of enfuvirtide and protease inhibitors as combination therapy for HIV.
Patients taking protease inhibitors are also advised to take no more than 25 mg of the drug and no more than once every 48 hours.
Varying degrees of cross-resistance among protease inhibitors have been observed.
It is composed of several endopeptidases and compounds like phosphatase, glucosidase, peroxidase, cellulase,escharase and protease inhibitors.
After several years of laboratory testing, protease inhibitors were first given to patients in the United States in 1994.
However, full induction by bosentan might not have been reached anda further decrease of protease inhibitors cannot be excluded.
Today, AIDS patients take protease inhibitors in combination with two other drugs called reverse transcriptase inhibitors. .
Do not concomitantly take the drug with HIV protease inhibitors, cyclosporine.
Protease inhibitors: No formal study data are available; however, since ritonavir is a strong CYP3A4 inhibitor and a weak CYP2D6 inhibitor, ritonavir and ritonavir-boosted protease inhibitors potentially raise concentrations of the risperidone active antipsychotic fraction.
Although cell extracts maintain a pH at which such enzymes are inactive,they also preferably use chemical protease inhibitors such as PMSF.
The drug should not be used by HIV-infected patients, patients taking protease inhibitors and indinavir, as well as patients with increased photosensitivity.
Similarly, pharmacokinetic interactions with CYP 3A4 inhibitors such as azole antimycotics, cimetidine,erythromycin and protease inhibitors are unlikely, although some have been reported.
Rifapentin is the inducer of cytochrome P450 isoenzymes, so when used concomitantly with drugsmetabolized by this enzyme system, such as protease inhibitors, reverse transcriptase inhibitors, can cause a significant decrease in the concentration of these drugs in the blood plasma and the loss of their therapeutic effect.
In those patients who discontinued protease inhibitor therapy, hyperglycemia persisted in some cases.
The causal relationship between protease inhibitor therapy and these cases has not been established.
In the case of a high risk of infection, a drug from the protease inhibitor group should be included in the regimen of antiretroviral therapy.
Other researchers are using the glowing bacteria to develop a protease inhibitor to treat HIV and other diseases.
The concomitant administration of the protease inhibitor ritonavir substantially increases serum concentrations of sildenafil(11-fold increase in AUC).
HIV protease inhibitor(lopinavir plus ritonavir) Use with caution and lowest dose necessary.
People who take the protease inhibitor indinavir, a drug used to treat HIV infection, are at risk of developing kidney stones.
Because these events have been reported voluntarily during clinical practice,estimates of frequency cannot be made and a causal relationship between protease inhibitor therapy and these events has not been established.
Co-administration of the HIV protease inhibitor saquinavir, also a CYP3A4 inhibitor, at steady state(1200 mg tid) with Viagra(100 mg single dose) resulted in a 140% increase in sildenafil C maxmax and a 210% increase in sildenafil AUC.