efectin er tvrdá tobolka s prodlouženým uvolňováním 375mg - Zoekresultaten

Europese Unie - Spaans - EMA (European Medicines Agency)

tadalafil mylan

mylan pharmaceuticals limited - tadalafil - disfuncion erectil - urológicos - tratamiento de la disfunción eréctil en hombres adultos. para que tadalafil sea efectivo, se requiere estimulación sexual. tadalafil mylan no está indicado para su uso por las mujeres.

Europese Unie - Spaans - EMA (European Medicines Agency)

vitekta

gilead sciences international ltd - elvitegravir - infecciones por vih - antivirales para uso sistémico - vitekta co administrado con un inhibidor de la proteasa impulsado por ritonavir y con otros agentes antirretrovirales, está indicado para el tratamiento de la infección de humanos-inmunodeficiencia-virus-1 (vih-1) en adultos infectados con vih-1 sin mutaciones conocidas asociados con la resistencia de elvitegravir.

Europese Unie - Spaans - EMA (European Medicines Agency)

xeljanz

pfizer europe ma eeig - tofacitinib - artritis, reumatoide - inmunosupresores - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 y 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) in adult patients who have had an inadequate response or who have been intolerant to a prior disease modifying antirheumatic drug (dmard) therapy (see section 5. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.

Europese Unie - Spaans - EMA (European Medicines Agency)

yondelis

pharma mar s.a. - trabectedin - ovarian neoplasms; sarcoma - agentes antineoplásicos - yondelis está indicado para el tratamiento de pacientes con sarcoma de tejidos blandos avanzado, después del fracaso de las antraciclinas y la ifosfamida, o que no son aptos para recibir estos agentes. los datos de eficacia se basan principalmente en pacientes con liposarcoma y leiomiosarcoma. yondelis ® en combinación con doxorubicina liposomal pegilada (pld) está indicado para el tratamiento de los pacientes con recaída platino-sensible cáncer de ovario.

Europese Unie - Spaans - EMA (European Medicines Agency)

carmustine medac (previously carmustine obvius)

medac gesellschaft für klinische spezialpräparate mbh - la carmustina - hodgkin disease; lymphoma, non-hodgkin - agentes antineoplásicos - carmustine is indicated n adults in the following malignant neoplasms as a single agent or in combination with other antineoplastic agents and/or other therapeutic measures (radiotherapy, surgery): , brain tumours (glioblastoma, brain-stem gliomas, medulloblastoma, astrocytoma and ependymoma), brain metastases, secondary therapy in non-hodgkin’s lymphoma and hodgkin’s disease, as conditioning treatment prior to autologous haematopoietic progenitor cell transplantation (hpct) in malignant haematological diseases (hodgkin’s disease / non-hodgkin’s lymphoma).