Examples of using Indinavir in English and their translations into German
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CRIXIVAN contains a substance called indinavir.
When indinavir is administered as monotherapy resistant viruses rapidly emerge see section 5.1.
Overdose If you thin that overdosed Indinavir seek urgent medical help.
Indinavir and didanosine formulations containing buffer should be administered at least one hour apart on an empty stomach.
Interaction not studied↑ dexamethasone exposure expected(CYP3A inhibition).↓ indinavir plasma concentrations may be expected CYP3A induction.
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The geometric mean Cmin for indinavir(0.33 mg/l) when given with ritonavir and efavirenz was higher than the mean historical Cmin(0.15 mg/l) when indinavir was given alone at 800 mg q8h.
At least eleven amino acidsites in the protease have been associated with indinavir resistance: L10, K20, L24, M46, I54, L63, I64, A71, V82, I84, and L90.
In addition, indinavir with ritonavir should not be administered with alfuzosin, meperidine, piroxicam, propoxyphene, bepridil, encainide, flecanide, propafenone, quinidine, fusidic acid, clozapine, clorazepate, diazepam, estazolam and flurazepam.
In the studies of Invirase in combination with ritonavir,Invirase led to similar rates of treatment failure to indinavir, but higher rates than lopinavir.
It is used to reduce the body's natural immu… zł 3.36 Per pill Indinavir Indinavir is an HIV protease inhibitor used in combination with other medicines to manage human immunodeficiency virus… zł 13.78 Per pill.
It is contraindicated to take Levitra Super Active if you have sensitivity to itsingredients, if you had organic nitrates treatment or took HIV protease inhibitors such as indinavir and ritonavir, if you are less than 16 years old.
Zł 23.98 Per pill Indinavir Indinavir is an HIV protease inhibitor used in combination with other medicines to manage human immunodeficiency virus… zł 13.78 Per pill Keppra Keppra(levetiracetam) is an anti-epileptic drug, also called an anticonvulsant.
Rifampicin is a strong CYP3A4 inducer andhas been shown to cause a 92% decrease in indinavir AUC which can result in virological failure and resistance development.
In zidovudine experienced patients, indinavir, zidovudine and lamivudine in combination compared with lamivudine added to zidovudine reduced the probability of AIDS defining illness or death(ADID) at 48 weeks from 13% to 7.
The combination of Invirase with ritonavir was assessed in656 patients in two studies that compared Invirase with indinavir and with lopinavir(other antiviral medicines), both in combination with ritonavir and other antiviral medicines.
Similarly, in antiretroviral naive patients, indinavir with and without zidovudine compared with zidovudine alone reduced the probability of ADID at 48 weeks from 15% with zidovudine alone to approximately 6% with indinavir alone or in combination with zidovudine.
Nevirapine exhibited additive to synergistic anti-HIV-1 activity in combination with the protease inhibitorsamprenavir, atazanavir, indinavir, lopinavir, saquinavir and tipranavir, and the NRTIs abacavir, didanosine, emtricitabine, lamivudine, stavudine, tenofovir and zidovudine.
Interactions between indinavir and other medicinal products are listed in the tables below increase is indicated as“↑”, decrease as“↓”, no change(≤+/- 20%) as“↔”, single dose as“ SD”, once daily as“ QD”, twice daily as“ BID”, three times daily as“ TID”, and four times as"QID.
Pharmacokinetic analysis in one study was performed on nineteen of the patients, with a median(range) indinavir AUC 0-12hr, Cmax, and Cmin of 25421 nM*h(21489-36236 nM*h), 5758 nM(5056-6742 nM) and 239(169-421 nM), respectively.
They include, but are not limited to, atazanavir, clarithromycin, indinavir, itraconazole, ketoconazole, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, amprenavir, aprepitant, diltiazem, erythromycin, fluconazole, fosamprenavir, grapefruit juice, and verapamil.
Given that substantially lower antepartum exposures have been observed in a small study of HIV-infected pregnant patients andthe limited data in this patient population, indinavir use is not recommended in HIV-infected pregnant patients see section 5.2.
These are medicines such as ketoconazole and itraconazole(used to treat fungal infections),atazanavir, indinavir, nelfinavir, ritonavir and saquinavir(medicines used in HIV-positive patients), clarithromycin and telithromycin(antibiotics), and nefazodone used to treat depression.
Overall, the in vitro characterisation of phenotypic cross-resistance between lopinavir and other protease inhibitors suggestthat decreased susceptibility to lopinavir correlated closely with decreased susceptibility to ritonavir and indinavir, but did not correlate closely with decreased susceptibility to amprenavir, saquinavir, and nelfinavir.
Kaletra(400/ 100 mg twice daily)has been studied in combination with reduced doses of amprenavir, indinavir, nelfinavir and saquinavir in steady-state controlled healthy volunteer studies relative to clinical doses of each HIV protease inhibitor in the absence of ritonavir.
Cross-resistance Darunavir has a< 10-fold decreased susceptibility against 90% of 3,309 clinical isolates resistant to amprenavir,atazanavir, indinavir, lopinavir, nelfinavir, ritonavir, saquinavir and/or tipranavir showing that viruses resistant to most PIs remain susceptible to darunavir.
Combinations of atazanavir with stavudine, didanosine, lamivudine, zidovudine,nelfinavir, indinavir, ritonavir, saquinavir, amprenavir, did not result in antagonistic anti-HIV activity or enhanced cytotoxic effects at the highest concentrations used for antiviral evaluation.
Darunavir showed synergistic antiviral activity when studied in combination with the protease inhibitors ritonavir, nelfinavir, or amprenavir andadditive antiviral activity when studied in combination with the protease inhibitors indinavir, saquinavir, lopinavir, atazanavir, or tipranavir, the N(t)RTIs zidovudine, lamivudine, zalcitabine, didanosine, stavudine, abacavir, emtricitabine, or tenofovir, the NNRTIs nevirapine, delavirdine, or efavirenz and the fusion inhibitor enfuvirtide.
The concomitant use of bosutinib with strong CYP3A inhibitors( including, but not limited to itraconazole, ketoconazole, posaconazole, voriconazole, clarithromycin, telithromycin, nefazodone,mibefradil, indinavir, lopinavir/ ritonavir, nelfinavir, ritonavir, saquinavir, boceprevir, telaprevir, grapefruit products including grapefruit juice) or moderate CYP3A inhibitors( including, but not limited to fluconazole, ciprofloxacin, erythromycin, diltiazem, verapamil, amprenavir, atazanavir, darunavir/ ritonavir, fosamprenavir, aprepitant, crizotinib, imatinib) should be avoided, as an increase in bosutinib plasma concentration will occur.
Analysis of long-term data from study 006(median follow-up 180 weeks, 102 weeks, and 76 weeks for patients treated with efavirenz+ zidovudine+ lamivudine, efavirenz+ indinavir, and indinavir+ zidovudine+ lamivudine, respectively) showed that, beyond 24 weeks of therapy, the incidences of new-onset nervous system symptoms among efavirenz-treated patients were generally similar to those in the control arm.