Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

actavis group ptc ehf. - nevirapina - comprimido - 200 mg - nevirapina 200 mg - nevirapina

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

laboratorios aurobindo s.l.u. - nevirapina - comprimido - 200 mg - nevirapina 200 mg - nevirapina

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

helm iberica s.a. - nevirapina - excipientes: lactosa monohidrato,carboximetilalmidon sodico - antivirales de acciÓn directa - inhibidores no nucleosidicos de la transcriptasa inversa - nevirapina

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

mylan pharmaceuticals, s.l. - nevirapina - comprimido - 200 mg - nevirapina 200 mg - inhibidores no nucleosidicos de la transcriptasa inversa

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

laboratorios normon s.a. - nevirapina - comprimido - 200 mg - nevirapina 200 mg - nevirapina

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

aurovitas spain, s.a.u. - efavirenz - comprimido recubierto con pelÍcula - 600 mg - efavirenz 600 mg - efavirenz

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

mylan pharmaceuticals, s.l. - efavirenz - comprimido recubierto con pelÍcula - 600 mg - efavirenz 600 mg - efavirenz

Spānija - spāņu - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

sandoz farmaceutica s.a. - efavirenz - comprimido recubierto con pelÍcula - 600 mg - efavirenz 600 mg - efavirenz

Eiropas Savienība - spāņu - EMA (European Medicines Agency)

teva b.v. - efavirenz - infecciones por vih - antivirales para uso sistémico - efavirenz está indicado en el tratamiento combinado antiviral de adultos, adolescentes y niños infectados con el virus de la inmunodeficiencia humana-1 (vih-1) de 3 años de edad y mayores. efavirenz no ha sido adecuadamente estudiado en pacientes con enfermedad avanzada por vih, es decir, en pacientes con recuentos de cd4 < 50 células/mm3, o después de un fallo de inhibidor de la proteasa (pi)-los regímenes que contienen. aunque la resistencia cruzada de efavirenz con inhibidores de la proteasa (pis) no se ha documentado, en la actualidad hay datos suficientes sobre la eficacia de la utilización posterior de pi basado en la combinación de la terapia después del fracaso de los regímenes que contienen efavirenz.

Eiropas Savienība - spāņu - EMA (European Medicines Agency)

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.