Argentina - español - SANI (Asociación de Cooperativas Argentinas)

vabriela - sistema nervioso - bovinos; caninos; caprinos; felinos; ovinos;

Argentina - español - SANI (Asociación de Cooperativas Argentinas)

vabriela - sistema nervioso - caninos; felinos;

Unión Europea - español - 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.

Unión Europea - español - EMA (European Medicines Agency)

vetcare oy - medetomidine hydrochloride, vatinoxan hydrochloride - psicolépticos, hipnóticos y sedantes - perros - to provide restraint, sedation and analgesia during conduct of non-invasive, non-painful or mildly painful procedures and examinations intended to last no more than 30 minutes.

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

dsm sinochem pharmaceuticals netherlands b.v. - amoxicilina, clavulanico acido - excipientes: aspartamo - antibacterianos betalactÁmicos, penicilinas - combinaciones de penicilinas, incluyendo inhibidores de la betalactamasa - amoxicilina e inhibidores de la enzima

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

dsm sinochem pharmaceuticals netherlands b.v. - amoxicilina, clavulanico acido - excipientes: aspartamo - antibacterianos betalactÁmicos, penicilinas - combinaciones de penicilinas, incluyendo inhibidores de la betalactamasa - amoxicilina e inhibidores de la enzima

Unión Europea - español - EMA (European Medicines Agency)

pierre fabre medicament - vinflunine - carcinoma, transitional cell; urologic neoplasms - agentes antineoplásicos - javlor está indicado en monoterapia para el tratamiento de pacientes adultos con carcinoma de células de transición avanzado o metastásico del tracto urotelial después del fracaso de un régimen anterior que contiene platino. eficacia y seguridad de vinflunine no han sido estudiados en pacientes con estado de funcionamiento ≥ 2.

Unión Europea - español - EMA (European Medicines Agency)

pharmaand gmbh - panobinostat lactato anhidro - mieloma múltiple - agentes antineoplásicos - farydak, en combinación con bortezomib y dexametasona, está indicado para el tratamiento de pacientes adultos con mieloma múltiple recidivante o refractario que han recibido al menos dos regímenes anteriores de bortezomib como agente inmunomodulador. farydak, en combinación con bortezomib y dexametasona, está indicado para el tratamiento de pacientes adultos con mieloma múltiple recidivante o refractario que han recibido al menos dos regímenes anteriores de bortezomib como agente inmunomodulador.

Unión Europea - español - EMA (European Medicines Agency)

bial portela & companhia s.a. - opicapone - mal de parkinson - medicamentos contra el parkinson - ontilyv is indicated as adjunctive therapy to preparations of levodopa/ dopa decarboxylase inhibitors (ddci) in adult patients with parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

leo pharma a/s - alfacalcidol - excipientes: aceite de sesamo,glicerol,sorbato potasico - vitaminas a y d, incluyendo combinaciones de las dos - vitamina d y análogos - alfacalcidol