Emtricitabine/Tenofovir disoproxil Krka d.d. Union européenne - espagnol - EMA (European Medicines Agency)

emtricitabine/tenofovir disoproxil krka d.d.

krka, d.d., novo mesto - emtricitabina, tenofovir disoproxil succinato - infecciones por vih - antivirales para uso sistémico - emtricitabina / tenofovir disoproxil krka d. está indicado en la terapia de combinación antirretroviral para el tratamiento de adultos infectados con vih-1. emtricitabina / tenofovir disoproxil krka d. también está indicado para el tratamiento de los infectados por vih-1 a los adolescentes, con intr resistencia o toxicidad impide el uso de agentes de primera línea, con edades de 12 a < 18 años.

Biktarvy Union européenne - espagnol - EMA (European Medicines Agency)

biktarvy

gilead sciences ireland uc - bictegravir, emtricitabina, tenofovir alafenamide, fumarate - infecciones por vih - antivirales para uso sistémico - biktarvy is indicated for the treatment of human immunodeficiency virus 1 (hiv 1) infection in adults and paediatric patients at least 2 years of age and weighing at least 14 kg i without present or past evidence of viral resistance to the integrase inhibitor class, emtricitabine or tenofovir. (ver la sección 5.

Juluca Union européenne - espagnol - EMA (European Medicines Agency)

juluca

viiv healthcare b.v. - dolutegravir de sodio, rilpivirina hidrocloruro - infecciones por vih - antivirales para uso sistémico - juluca está indicado para el tratamiento del virus de inmunodeficiencia humana tipo 1 (vih-1) en adultos que son virológicamente-suprimida (arn del vih-1.

Dovato Union européenne - espagnol - EMA (European Medicines Agency)

dovato

viiv healthcare b.v. - dolutegravir de sodio, lamivudina - infecciones por vih - antivirales para uso sistémico - dovato está indicado para el tratamiento del virus de inmunodeficiencia humana tipo 1 (vih-1) en adultos y adolescentes mayores de 12 años de edad de un peso mínimo de 40 kg, con la que no se conoce o se sospecha resistencia al inhibidor de la integrasa clase, o lamivudina.

Rukobia Union européenne - espagnol - EMA (European Medicines Agency)

rukobia

viiv healthcare b.v. - fostemsavir trometamol - infecciones por vih - antivirales para uso sistémico - rukobia, in combination with other antiretrovirals, is indicated for the treatment of adults with multidrug resistant hiv-1 infection for whom it is otherwise not possible to construct a suppressive anti-viral regimen.

FAMCICLOVIR ACTAVIS 750 mg COMPRIMIDOS RECUBIERTOS CON PELICULA EFG Espagne - espagnol - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

famciclovir actavis 750 mg comprimidos recubiertos con pelicula efg

actavis group ptc ehf - famciclovir - excipientes: almidon pregelatinizado,laurilsulfato de sodio,croscarmelosa sodica - antivirales de acciÓn directa - nucleosidos y nucleotidos, excluyendo inhibidores de la transcriptasa inversa - famciclovir

FAMCICLOVIR MYLAN 750 mg COMPRIMIDOS RECUBIERTOS CON PELICULA EFG Espagne - espagnol - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

famciclovir mylan 750 mg comprimidos recubiertos con pelicula efg

mylan pharmaceuticals, s.l. - famciclovir - excipientes: almidon pregelatinizado,laurilsulfato de sodio,croscarmelosa sodica - antivirales de acciÓn directa - nucleosidos y nucleotidos, excluyendo inhibidores de la transcriptasa inversa - famciclovir

Harvoni Union européenne - espagnol - EMA (European Medicines Agency)

harvoni

gilead sciences ireland uc - ledipasvir, sofosbuvir - hepatitis c, crónica - antivirales para uso sistémico - harvoni is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 y 5. para el virus de la hepatitis c (vhc) de genotipo específico de la actividad véanse las secciones 4. 4 y 5.

Prezista Union européenne - espagnol - EMA (European Medicines Agency)

prezista

janssen-cilag international nv - darunavir - infecciones por vih - antivirales para uso sistémico - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

Viekirax Union européenne - espagnol - EMA (European Medicines Agency)

viekirax

abbvie deutschland gmbh co. kg - ombitasvir, paritaprevir, ritonavir - hepatitis c, crónica - antivirales para uso sistémico - viekirax está indicado en combinación con otros medicamentos para el tratamiento de la hepatitis c crónica (chc) en adultos. para el virus de la hepatitis c (vhc) de genotipo específico de la actividad.