Ngenla Европейский союз - португальский - EMA (European Medicines Agency)

ngenla

pfizer europe ma eeig - somatrogon - growth and development - hipÓfise e hipotÁlamo hormÔnios e anÁlogos - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Apexxnar Европейский союз - португальский - EMA (European Medicines Agency)

apexxnar

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infecções pneumocócicas - vacinas - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. veja as seções 4. 4 e 5. 1 para informações sobre proteção contra serotipos pneumocócicos específicos. apexxnar should be used in accordance with official recommendations. .

Abrysvo Европейский союз - португальский - EMA (European Medicines Agency)

abrysvo

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - infecções respiratórias do vírus sincitial - vacinas - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. veja as seções 4. 2 e 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. o uso desta vacina deve ser de acordo com as recomendações oficiais.

Champix Европейский союз - португальский - EMA (European Medicines Agency)

champix

pfizer europe ma eeig - vareniclina - cessação do uso do tabaco - outros medicamentos do sistema nervoso - champix é indicado para a cessação do tabagismo em adultos.

Xalkori Европейский союз - португальский - EMA (European Medicines Agency)

xalkori

pfizer europe ma eeig - crizotinib - carcinoma, pulmão de células não pequenas - agentes antineoplásicos - xalkori as monotherapy is indicated for:the first‑line treatment of adults with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with previously treated anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with ros1‑positive advanced non‑small cell lung cancer (nsclc)the treatment of paediatric patients (age ≥6 to.

Vfend Европейский союз - португальский - EMA (European Medicines Agency)

vfend

pfizer europe ma eeig - voriconazol - candidiasis; mycoses; aspergillosis - antimicóticos para uso sistêmico - voriconazol, é um amplo espectro, triazole agente antifúngico e é indicado em adultos e crianças de 2 anos de idade e acima, como segue:o tratamento de aspergilose invasiva;tratamento de candidaemianon-neutropénicos de pacientes;tratamento de fluconazol resistente a sério invasivas de infecções por candida (incluindo c. krusei);tratamento de graves infecções fúngicas causadas por scedosporium spp. e fusarium spp. vfend deve ser administrado principalmente a pacientes com progressiva, possivelmente, ameaçam a vida, infecções. profilaxia de infecções fúngicas invasivas em alto risco de hematopoiéticas alogênico de transplante de células-tronco (hsct) destinatários.

Xeljanz Европейский союз - португальский - EMA (European Medicines Agency)

xeljanz

pfizer europe ma eeig - tofacitinib - artrite, reumatóide - imunossupressores - 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 e 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.