Sexual Health

Tenvir EM 300/200mg vs Other Antiretroviral Therapies

Tenvir EM 300/200mg vs. Other Antiretroviral Therapies: Which is Right for You?

The nucleotide correspondent tenofovir is used to treat mutually HIV and hepatitis B and HIV pre-exposure prophylaxis. The original tenofovir disoproxil fumarate (TDF) type was developed at a dose of 300 mg once regular. A subsequent pro-drug formulation, tenofovir alafenamide (TAF), has newly been launched in North America and Europe at quantities of 10 or 25 mg once daily. The pharmacokinetics of TAF lead to a 6.5-times advanced intracellularly.

The dose of TAF is conversant from 25 mg to 10 mg daily in the company of the pharmacokinetic sauces ritonavir (RTV) or cobicistat (COBI) to version for their improving effects. Pharmacokinetic boosters also yield higher serum tenofovir levels when co-administered finished TDF: the area under the bend (AUC) is 23% higher once TDF and COBI are co-administered, too 37% developed with atazanavir/RTV. But, alterations to the 300-mg dosing of TDF are not completed. There could be other antiretrovirals producing changes in fashionable tenofovir exposure, such in place of rilpivirine, but doses of TDF again expended have not been adjusted to reimburse.

When it comes to managing HIV infection, several antiretroviral therapies (ART) are available, each with its unique characteristics and considerations. One commonly prescribed combination therapy is Tenvir EM, which consists of two active ingredients, tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC). Tenvir EM is primarily used to treat HIV-1 infection in adults and adolescents. However, it is essential to consult with a healthcare professional to determine the most suitable ART regimen for an individual based on their specific needs and circumstances.

Comparing Tenvir EM 300/200mg to other antiretroviral therapies involves evaluating factors such as efficacy, side effects, drug interactions, dosing regimens, and individual patient factors. This article aims to provide an overview of Tenvir EM 300/200mg and highlight some important considerations when selecting the right antiretroviral therapy for managing HIV infection. It is crucial to note that this information is not intended to replace medical advice, and healthcare professionals should be consulted for personalized recommendations.

TDF was first advanced in clinical trials without RTV or COBI. In these court-martials the additional risks of bone or renal adverse events were trivial or non-significant compared with other nucleoside analogs. For the sample, there were no terminations for bone or renal adverse events after long-term follow-up in the Gilead 903 schoolwork of the fixed-dose combination of TDF, lamivudine (3TC), and efavirenz (EFV). There were minor changes in inert bone density in the first 48.

Most newly published randomized trials of TAF versus TDF have encompassed RTV or COBI (e.g., with elvitegravir/COBI or darunavir/RTV). However, the most common use of TDF worldwide is unboosted, mutual with either FTC or 3TC and EFV or dolutegravir.


 Showed a meta-analysis of TAF against TDF in treating HIV-1 and chronic hepatitis B in randomized head-to-head medical court-martials. PubMed, and Embase, besides databases, were rifled on 17 July 2017—the search footings for the intervention concepts agreed with the Cochrane guidance on examination terms. Studies qualifying for addition had randomized controlled designs through at least 24 weeks of randomized treatment. Observational besides dose-ranging training were omitted.

Data were mined on two measures of efficacy: patients through HIV RNA <50 copies/mL and treatment-emergent primary genotypic battle. The efficacy results were analyzed for the studies of either TAF or TDF in individuals living with HIV. The safety analyses were conducted with studies of TAF versus TDF in either HIV or hepatitis B contamination.

Higher plasma tenofovir concentrations are associated with higher risks of renal besides bone adverse events. The pharmacokinetic boosters ritonavir (RTV) and cobicistat (COBI) significantly increase plasma extent under the curve (AUC) concentrations of tenofovir disoproxil fumarate (TDF) by 25–37%. When combined with RTV or COBI, the dose of tenofovir alafenamide (TAF) is sank from 25 mg to 10 mg daily, but the TDF dose is preserved at 300 mg daily.


To assess the differences in safety and efficacy between tenofovir alafenamide (TAF) and tenofovir disoproxil fumarate (TDF) in regimens with and without the pharmacokinetic boosters RTV and COBI.

Tenvir EM 300/200mg vs. Other Antiretroviral Therapies: Which is Right for You?
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A PubMed/Embase search wide-ranging dates up to 17 July 2017 known 11 randomized head-to-head court-martials (8111 patients) of TDF against TAF. The Mantel–Haenszel method stood used to calculate pooled risk alterations and 95% confidence intervals using random-effects mockups. A pre-defined sub-group analysis compared TAF with TDF, either once boosted with RTV or COBI or once unboosted.


Nine clinical trials compared TAF and TDF for the treatment of HIV-1, and two remained for hepatitis B treatment. The eleven medical trials documented 4574 patients with boosting RTV or COBI in both arms, casing 7198 patient-years of follow-up. Some 3537 affected roles received unboosted regimens, totaling 3595 patient-years of follow-up. Improved TDF-treated patients showed borderline lower HIV RNA suppression <50 copies/mL (P=0.05), more bone breaks (P=0.04), more significant decreases in bone inanimate density (P<0.001), and more discontinuations for mandible (P=0.03) or renal (P=0.002) contrary events. By contrast, there were no noteworthy differences in HIV RNA suppression rates or clinical safety endpoints among unboosted TAF and unboosted TDF.


TDF boosted through RTV or COBI was associated with higher risks of jaw and renal adverse events, and lesser HIV RNA suppression rates, compared to TAF. By contrast, when ritonavir and cobicistat stood not used, there were no efficacy alterations between TAF and TDF and marginal alterations in safety. The health-economic value of TAF versus low-cost generic TDF may be imperfect when these drugs are used short of cobicistat or ritonavir.

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