Brésil - portugais - ANVISA (Agência Nacional de Vigilância Sanitária)

infan industria quimica farmaceutica nacional s/a - misoprostol - outros produtos para uso em ginecologia e obstetricia

Brésil - portugais - ANVISA (Agência Nacional de Vigilância Sanitária)

ems sigma pharma ltda - citrato de zinco, Ácido ascÓrbico - vitaminas e suplementos minerais

Brésil - portugais - ANVISA (Agência Nacional de Vigilância Sanitária)

zambon laboratÓrios farmacÊuticos ltda. - Ácido ursodesoxicÓlico - colagogos, colereticos e hepatoprotetores

Brésil - portugais - ANVISA (Agência Nacional de Vigilância Sanitária)

sun farmacÊutica do brasil ltda - Ácido ursodesoxicÓlico - colagogos, colereticos e hepatoprotetores

Brésil - portugais - ANVISA (Agência Nacional de Vigilância Sanitária)

ems s/a - Ácido ursodesoxicÓlico - colagogos, colereticos e hepatoprotetores

Union européenne - portugais - EMA (European Medicines Agency)

janssen-cilag international n.v. - daratumumab - mieloma múltiplo - monoclonal antibodies and antibody drug conjugates, antineoplastic agents - multiple myelomadarzalex is indicated: in combination with lenalidomide and dexamethasone or with bortezomib, melphalan and prednisone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant. em combinação com o bortezomib, talidomida e dexametasona para o tratamento de pacientes adultos diagnosticados com mieloma múltiplo que são elegíveis para transplante de células-tronco autólogas. em combinação com a lenalidomida e dexametasona, ou o bortezomib e dexametasona para o tratamento de pacientes adultos com mieloma múltiplo que tenham recebido pelo menos uma terapêutica prévia. in combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one prior therapy containing a proteasome inhibitor and lenalidomide and were lenalidomide refractory, or who have received at least two prior therapies that included lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or after the last therapy (see section 5. como monoterapia para o tratamento de pacientes adultos com uma recaída e refratários mieloma múltiplo, cuja terapêutica prévia incluído um inibidor de proteassoma e um agente imunomodulador e que tenham demonstrado a progressão da doença no último terapia. al amyloidosisdarzalex is indicated in combination with cyclophosphamide, bortezomib and dexamethasone for the treatment of adult patients with newly diagnosed systemic light chain (al) amyloidosis.

Union européenne - portugais - EMA (European Medicines Agency)

merial - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain) - imunológicos para felidae, - gatos - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs and excretion;against chlamydophila felis infection to reduce clinical signs. os começos de imunidade foram demonstrados 1 semana após o curso de vacinação primária para componentes de rinotraqueíte, calicivírus e chlamydophila felis. a duração da imunidade é de 1 ano após a última (re) vacinação.

Union européenne - portugais - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - imunológicos para felidae, - gatos - active immunisation of cats aged eight weeks and older:• against feline viral rhinotracheitis to reduce clinical signs;• against calicivirus infection to reduce clinical signs;• against chlamydophila felis infection to reduce clinical signs;• against feline panleucopenia to prevent mortality and clinical signs. os começos de imunidade foram demonstrados uma semana após o curso de vacinação primária para rinotraqueíte, calicivírus, chlamydophila felis e componentes de panleucopenia. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Union européenne - portugais - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97), attenuated chlamydophila felis (905 strain) - imunológicos para felidae, - gatos - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against chlamydophila felis infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus, chlamydophila felis and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the chlamydiosis and feline leukaemia components, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Union européenne - portugais - EMA (European Medicines Agency)

sanquin plasma products b.v. - fator ix de coagulação humana - hemofilia b - anti-hemorrágicos - tratamento e profilaxia do sangramento em pacientes com hemofilia b (deficiência congênita de factor ix).