TENOFOVIR DISOPROXIL FUMARATE tablet, film coated USA - engelsk - NLM (National Library of Medicine)

tenofovir disoproxil fumarate tablet, film coated

aurobindo pharma limited - tenofovir disoproxil fumarate (unii: ott9j7900i) (tenofovir anhydrous - unii:w4hfe001u5) - tenofovir disoproxil fumarate 150 mg - tenofovir disoproxil fumarate tablets are indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults and pediatric patients 2 years of age and older weighing at least 10 kg. tenofovir disoproxil fumarate tablets are indicated for the treatment of chronic hepatitis b virus (hbv) in adults and pediatric patients 2 years of age and older weighing at least 10 kg. none. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to tenofovir disoproxil fumarate during pregnancy. healthcare providers are encouraged to register patients by calling the antiretroviral pregnancy registry (apr) at 1-800-258-4263. risk summary available data from the apr show no increase in the overall risk of major birth defects with first trimester exposure for tenofovir disoproxil fumarate (tdf) (2.1%) compared with the background rate for major birth defects of 2.7% in a u.s. reference popul

TENOFOVIR DISOPROXIL FUMARATE tablet USA - engelsk - NLM (National Library of Medicine)

tenofovir disoproxil fumarate tablet

remedyrepack inc. - tenofovir disoproxil fumarate (unii: ott9j7900i) (tenofovir anhydrous - unii:w4hfe001u5) - tenofovir disoproxil fumarate 300 mg - tenofovir disoproxil fumarate is indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults and pediatric patients 2 years of age and older weighing at least 10 kg. tenofovir disoproxil fumarate is indicated for the treatment of chronic hepatitis b virus (hbv) in adults and pediatric patients 12 years of age and older pediatric use information is approved for gilead sciences, inc.'s viread® (tenofovir disoproxil fumarate) tablets. however, due to gilead sciences, inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. none. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to tenofovir disoproxil fumarate during pregnancy. healthcare providers are encouraged to register patients by calling the antiretroviral pregnancy registry (apr) at 1-800-258-4263. risk summary available data from the apr show no increase in the

TENOFOVIR DISOPROXIL FUMARATE tablet USA - engelsk - NLM (National Library of Medicine)

tenofovir disoproxil fumarate tablet

strides pharma science limited - tenofovir disoproxil fumarate (unii: ott9j7900i) (tenofovir anhydrous - unii:w4hfe001u5) - tenofovir disoproxil fumarate 300 mg - tenofovir disoproxil fumarate is indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults and pediatric patients 2 years of age and older weighing at least 10 kg. tenofovir disoproxil fumarate is indicated for the treatment of chronic hepatitis b virus (hbv) in adults and pediatric patients 12 years of age and older pediatric use information is approved for gilead sciences, inc.'s viread® (tenofovir disoproxil fumarate) tablets. however, due to gilead sciences, inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. none. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to tenofovir disoproxil fumarate during pregnancy. healthcare providers are encouraged to register patients by calling the antiretroviral pregnancy registry (apr) at 1-800-258-4263. risk summary available data from the apr show no increase in the

RIVA-EFAVIRENZ/EMTRICITABINE/TENOFOVIR TABLET Canada - engelsk - Health Canada

riva-efavirenz/emtricitabine/tenofovir tablet

laboratoire riva inc. - efavirenz; emtricitabine; tenofovir disoproxil fumarate - tablet - 600mg; 200mg; 300mg - efavirenz 600mg; emtricitabine 200mg; tenofovir disoproxil fumarate 300mg - nonnucleoside reverse transcriptase inhibitors

Tenofovir Disoproxil Fumarate/Efavirenz/Emtricitabine Tablets Tenofovir Disoproxil Fumarate / Efavirenz/ Emtricitabine 300 Mg/600 Mg And 200 Mg Tanzania - engelsk - Tanzania Medicinces & Medical Devices Authority

tenofovir disoproxil fumarate/efavirenz/emtricitabine tablets tenofovir disoproxil fumarate / efavirenz/ emtricitabine 300 mg/600 mg and 200 mg

mylan laboratories limited, india - emtricitabine, tenofovir disoproxil , efavirenz - tablets - tenofovir disoproxil fumarate / efavirenz/ emtricitabine 300 mg/600 mg and 200 mg

TENOFOVIR DISOPROXIL FUMARATE- tenofovir disoproxil fumarate tablets tablet, film coated USA - engelsk - NLM (National Library of Medicine)

tenofovir disoproxil fumarate- tenofovir disoproxil fumarate tablets tablet, film coated

chartwell rx, llc. - tenofovir disoproxil fumarate (unii: ott9j7900i) (tenofovir anhydrous - unii:w4hfe001u5) - tenofovir disoproxil fumarate tablets are indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults and pediatric patients 2 years of age and older weighing at least 10 kg. tenofovir disoproxil fumarate tablets are indicated for the treatment of chronic hepatitis b virus (hbv) in adults and pediatric patients 2 years of age and older weighing at least 10 kg. none. p r eg n an cy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to tenofovir disoproxil fumarate during pregnancy. healthcare providers are encouraged to register patients by calling the  antiretroviral pregnancy registry (apr) at 1-800-258-4263. risk summary available data from the apr show no increase in the overall risk of major birth defects with first trimester exposure for tenofovir disoproxil fumarate (tdf) (2.1%) compared with the background rate for major birth defects of 2.7% in a u.s. refe

Emtricitabine 200mG & Tenofovir Disoproxil Film-Coated Tablet Kenya - engelsk - Pharmacy and Poisons Board

emtricitabine 200mg & tenofovir disoproxil film-coated tablet

strides pharma science limited no 36/7, suragajakkanahalli, lndlavadi cross, - emtricitabine tenofovir disoproxil fumarate - film-coated tablet - emtricitabine 200 mg tenofovir disoproxil… - tenofovir disoproxil and emtricitabine

Tenofovir Disoproxil Viatris New Zealand - engelsk - Medsafe (Medicines Safety Authority)

tenofovir disoproxil viatris

viatris limited - tenofovir disoproxil maleate 300mg equivalent to tenofovir disoproxil 245mg - film coated tablet - 300 mg - active: tenofovir disoproxil maleate 300mg equivalent to tenofovir disoproxil 245mg excipient: colloidal silicon dioxide hyprolose lactose monohydrate magnesium stearate microcrystalline cellulose opadry blue 32k505018 - tenofovir disoproxil mylan is indicated for the treatment of chronic hepatitis b in adults and paediatric patients 12 years of age and older.

Efavirenz/ Emtricitabine/ Tenofovir disoproxil DEXTREG Tablet, film coated 600mg/200mg/245mg, Malta - engelsk - Malta Medicines Authority

efavirenz/ emtricitabine/ tenofovir disoproxil dextreg tablet, film coated 600mg/200mg/245mg,

pharos – pharmaceutical oriented services limited lesvou str. (end), thesi loggos, industrial zone, 144 52 metamorfossi attikis,, greece - efavirenz, emtricitabine, tenofovir disoproxil - film-coated tablet - efavirenz 600 mg emtricitabine 200 mg tenofovir disoproxil 245 mg - antivirals for systemic use

TENOFOVIR / EMTRICITABINE SANDOZ 301/200 tenofovir disoproxil succinate / emtricitabine 301/200 mg film-coated tablet bottle Australien - engelsk - Department of Health (Therapeutic Goods Administration)

tenofovir / emtricitabine sandoz 301/200 tenofovir disoproxil succinate / emtricitabine 301/200 mg film-coated tablet bottle

sandoz pty ltd - emtricitabine, quantity: 200 mg; tenofovir disoproxil succinate, quantity: 300.6 mg - tablet, film coated - excipient ingredients: macrogol 3350; indigo carmine aluminium lake; magnesium stearate; isopropyl alcohol; polyvinyl alcohol; microcrystalline cellulose; titanium dioxide; lactose monohydrate; purified talc; croscarmellose sodium; purified water; pregelatinised maize starch - treatment of hiv-1 infection,tenofovir/emtricitabine sandoz is indicated for the treatment of hiv infected adults over the age of 18 years, in combination with other antiretroviral agents.,pre-exposure prophylaxis,tenofovir/emtricitabine sandoz is indicated in combination with safer sex practices for pre-exposure prophylaxis (prep) to reduce the risk of sexually acquired hiv-1 in adults at high risk. this indication is based on clinical trials in men who have sex with men (msm) at high risk for hiv-1 infection and in heterosexual serodiscordant couples (see section 5.1 pharmacodynamic properties, clinical trials).