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This is NOT insurance. In HIV-1 infected patients with renal risk factors, the co-administration of tenofovir disoproxil with a boosted protease inhibitor should be carefully evaluated.Emtricitabine/tenofovir disoproxil should not be administered concomitantly with other medicinal products containing emtricitabine, tenofovir disoproxil, tenofovir alafenamide, or other cytidine analogues, such as lamivudine (see section 4.5).

Ships Worldwide Except Canada from Canada, India, UK Tenofovir disoproxil should be avoided in patients with HIV-1 harbouring the K65R mutation.

The time to onset of protection after commencing emtricitabine/tenofovir disoproxil is unknown.Emtricitabine/tenofovir disoproxil should only be used for pre-exposure prophylaxis as part of an overall HIV-1 infection prevention strategy including the use of other HIV-1 prevention measures (e.g. Free Shipping. A subgroup of patients with baseline creatinine clearance between 50 and 60 mL/min, receiving once daily dosing, had a 2-4-fold increase in tenofovir exposure and worsening renal function. By continuing to browse the site you are agreeing to our policy on the use of cookies. consistent and correct condom use, knowledge of HIV-1 status, regular testing for other sexually transmitted infections).Emtricitabine/tenofovir disoproxil should only be used to reduce the risk of acquiring HIV-1 in individuals confirmed to be HIV negative (see section 4.3).

Ships Worldwide Except Canada from Canada, India, UK

The mean (%CV) tenofovir drug exposure increased from 2,185 (12%) ng•h/mL in subjects with normal renal function, to 3,064 (30%) ng•h/mL, 6,009 (42%) ng•h/mL and 15,985 (45%) ng•h/mL, in subjects with mild, moderate and severe renal impairment, respectively. at least every 3 months) using a combined antigen/antibody test while taking emtricitabine/tenofovir disoproxil for pre-exposure prophylaxis.Emtricitabine/tenofovir disoproxil alone does not constitute a complete regimen for the treatment of HIV-1 and HIV-1 resistance mutations have emerged in individuals with undetected HIV-1 infection who are only taking emtricitabine/tenofovir disoproxil.If clinical symptoms consistent with acute viral infection are present and recent (< 1 month) exposures to HIV-1 are suspected, use of emtricitabine/tenofovir disoproxil should be delayed for at least one month and HIV-1 status reconfirmed before starting emtricitabine/tenofovir disoproxil for pre-exposure prophylaxis.The effectiveness of Emtricitabine/tenofovir disoproxil in reducing the risk of acquiring HIV-1 is strongly correlated with adherence as demonstrated by measurable drug levels in blood (see section 5.1). Ships Worldwide from Canada Ships Worldwide Except Canada from India Store in the original package in order to protect from moisture.HDPE bottle with white opaque polypropylene screw cap or white opaque polypropylene child resistant closure with wad containing aluminium induction sealing liner and dessicant labelled 'DO NOT EAT'pack containing 30 film-coated tablets and mutlipacks containing 90 (3 packs of 30) film-coated tabletsCold form blister laminated with embedded desiccant layer on one side and hard tampered aluminium foil on the other pack containing 30 film-coated tabletsCold form unit dose blister pack containing 30 x 1, 90 x 1, 100 x 1 film-coated tabletsAny unused medicinal product or waste material should be disposed of in accordance with local requirements.Building 4, Trident Place, Mosquito Way, Hatfield, Hertfordshire, AL10 9ULTo bookmark a medicine you must sign up and log in.To view the changes to a medicine you must sign up and log in.

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