Ribavirin Teva Pharma B.V. Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ribavirin teva pharma b.v.

teva b.v. - ribavirin - epatite Ċ, kronika - antivirali għal użu sistemiku - ribavirin teva pharma b. is indicated in combination with other medicinal products for the treatment ofchronic hepatitis c (chc) in adults (see sections 4. 2, 4. 4, u 5. ribavirin teva pharma b. is indicated in combination with other medicinal products for the treatment ofchronic hepatitis c (chc) for paediatric patients (children 3 years of age and older and adolescents) notpreviously treated and without liver decompensation (see sections 4. 2, 4. 4 u 5.

Lamivudine Teva Pharma B.V. Unjoni Ewropea - Malti - EMA (European Medicines Agency)

lamivudine teva pharma b.v.

teva b.v.  - lamivudine - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - lamivudine teva pharma b. huwa indikat bħala parti ta ' terapija ta ' kombinazzjoni ta ' antiretroviral għat-trattament tal-bniedem-immunodefiċjenza-virus (hiv)-infettati adulti u tfal.

Truvada Unjoni Ewropea - Malti - EMA (European Medicines Agency)

truvada

gilead sciences ireland uc - emtricitabine, tenofovir disoproxil fumarate - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - treatment of hiv-1 infection: , truvada is indicated in antiretroviral combination therapy for the treatment of hiv-1 infected adults. , truvada huwa wkoll indikat għall-kura ta ' l-hiv-1 infettati fl-adolexxenti, b'reżistenza għal nrti li dehret jew tossiċitajiet li teskludi l-użu tal-ewwel linja ta'l-aġenti, l-età bejn 12 u < 18-il sena. , pre-exposure prophylaxis (prep): , truvada is indicated in combination with safer sex practices for pre-exposure prophylaxis to reduce the risk of sexually acquired hiv-1 infection in adults at high risk.

Tecovirimat SIGA Unjoni Ewropea - Malti - EMA (European Medicines Agency)

tecovirimat siga

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - antivirali għal użu sistemiku - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 u 5. tecovirimat siga should be used in accordance with official recommendations.

Combivir Unjoni Ewropea - Malti - EMA (European Medicines Agency)

combivir

viiv healthcare bv - lamivudine, zidovudine - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - combivir is indicated in antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infection.

Isentress Unjoni Ewropea - Malti - EMA (European Medicines Agency)

isentress

merck sharp & dohme b.v. - raltegravir - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - isentress huwa indikata f'kumbinazzjoni ma ' anti-retrovirali-prodotti mediċinali għall-kura tal-vajrus tal-immunodefiċjenza umana (hiv 1) l-infezzjoni.

Vemlidy Unjoni Ewropea - Malti - EMA (European Medicines Agency)

vemlidy

gilead sciences ireland uc - tenofovir alafenamide fumarate - epatite b - antivirali għal użu sistemiku - vemlidy is indicated for the treatment of chronic hepatitis b (chb) in adults and paediatric patients 6 years of age and older weighing at least 25 kg (see section 5.

Emtricitabine/Tenofovir disoproxil Zentiva Unjoni Ewropea - Malti - EMA (European Medicines Agency)

emtricitabine/tenofovir disoproxil zentiva

zentiva k.s. - emtricitabine, tenofovir disoproxil phosphate - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - it-trattament ta 'l-hiv-1 infectionemtricitabine/tenofovir disoproxil zentiva hu indikat għal terapija antiretrovirali kombinata għall-kura ta' l-hiv-1 adulti infettati. emtricitabine/tenofovir disoproxil zentiva huwa wkoll indikat għall-kura ta ' l-hiv-1 infettati fl-adolexxenti, b'reżistenza għal nrti li dehret jew tossiċitajiet li teskludi l-użu tal-ewwel linja aġenti. espożizzjoni minn qabel profilassi (j)ta ' emtricitabine/tenofovir disoproxil zentiva hu indikat flimkien mal-prattiċi ta'sess aktar għall-espożizzjoni minn qabel l-profilassi biex jitnaqqas ir-riskju ta sesswalment miksuba bl-hiv-1-infezzjoni fl-adulti u fl-adoloxxenti f'riskju għoli.

Evotaz Unjoni Ewropea - Malti - EMA (European Medicines Agency)

evotaz

bristol-myers squibb pharma eeig - cobicistat, atazanavir - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - evotaz is indicated in combination with other antiretroviral medicinal products for the treatment of hiv-1 infected adults and adolescents (aged 12 years and older weighing at least 35 kg) without known mutations associated with resistance to atazanavir (see sections 4. 4 u 5.

Exviera Unjoni Ewropea - Malti - EMA (European Medicines Agency)

exviera

abbvie ltd - dasabuvir sodium - epatite Ċ, kronika - antivirali għal użu sistemiku - exviera huwa indikat flimkien ma 'prodotti mediċinali oħra għall-kura ta' l-epatite Ċ kronika (chc) fl-adulti. għall-vajrus tal-epatite Ċ (hcv) ġenotip attività speċifika.