Nicorette Icemint 2 mg imeskelytabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

nicorette icemint 2 mg imeskelytabletti

mcneil / jntl consumer health (finland) oy - nicotine resinate - imeskelytabletti - 2 mg - nikotiini

Nicorette Icemint 4 mg imeskelytabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

nicorette icemint 4 mg imeskelytabletti

mcneil / jntl consumer health (finland) oy - nicotine resinate - imeskelytabletti - 4 mg - nikotiini

Nicorette Fruit 2 mg imeskelytabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

nicorette fruit 2 mg imeskelytabletti

mcneil / jntl consumer health (finland) oy - nicotine resinate - imeskelytabletti - 2 mg - nikotiini

Nicorette Fruit 4 mg imeskelytabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

nicorette fruit 4 mg imeskelytabletti

mcneil / jntl consumer health (finland) oy - nicotine resinate - imeskelytabletti - 4 mg - nikotiini

Optimark Euroopan unioni - suomi - EMA (European Medicines Agency)

optimark

mallinckrodt deutschland gmbh - gadoversetamidi - magneettikuvaus - kontrastimediat - tämä lääkevalmiste on tarkoitettu vain diagnostiseen käyttöön. optimark on tarkoitettu käytettäväksi magneettikuvaus (mri) keskushermostoon (cns) ja maksan. se tarjoaa varjoainetta ja helpottaa visualisointia ja auttaa luonnehdinta fokaalimuutosten ja poikkeavien rakenteiden keskushermoston ja maksan potilailla, joilla tiedetään tai vahvasti epäillään patologian.

IsoFlo vet 100 w/w% inhalaatiohöyry, neste Suomi - suomi - Fimea (Suomen lääkevirasto)

isoflo vet 100 w/w% inhalaatiohöyry, neste

zoetis animal health aps - isoflurane - inhalaatiohöyry, neste - 100 w/w% - isofluraani

NORFLOXACIN SANDOZ 400 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

norfloxacin sandoz 400 mg tabletti, kalvopäällysteinen

sandoz gmbh - norfloxacinum - tabletti, kalvopäällysteinen - 400 mg - norfloksasiini

Amgevita Euroopan unioni - suomi - EMA (European Medicines Agency)

amgevita

amgen europe b.v. - adalimumabi - arthritis, psoriatic; colitis, ulcerative; arthritis, juvenile rheumatoid; spondylitis, ankylosing; psoriasis; crohn disease; arthritis, rheumatoid - immunosuppressantit - rheumatoid arthritis  amgevita in combination with methotrexate, is indicated for: , the treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate. hoitoon vaikean, aktiivisen ja progressiivisen nivelreuman hoitoon aikuisilla, joita ei aiemmin ole hoidettu metotreksaatilla. ,  amgevita can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. amgevita vähentää määrä etenemistä nivelvaurioita mitattuna x-ray ja parantaa fyysistä toimintakykyä, kun sitä annetaan yhdessä metotreksaatin kanssa. juvenile idiopathic arthritis polyarticular juvenile idiopathic arthritis amgevita in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis, in patients from the age of 2 years who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (dmards). amgevita voidaan antaa monoterapiana, jos potilas ei siedä metotreksaattia tai metotreksaattihoidon jatkaminen ei ole tarkoituksenmukaista (tehoa monoterapiana ks. kohta 5. humiraa ei ole tutkittu potilailla, joiden ikä on alle 2 vuotta. enthesitis-related arthritis amgevita is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy (see section 5. axial spondyloarthritis ankylosing spondylitis (as) amgevita is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. axial spondyloarthritis without radiographic evidence of as amgevita is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of as but with objective signs of inflammation by elevated crp and/or mri, who have had an inadequate response to, or are intolerant to non-steroidal anti-inflammatory drugs. psoriatic arthritis amgevita is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. amgevita vähentää määrä etenemistä perifeeristen nivelvaurioiden mitattuna x-ray potilailla, joilla idiopaattisen symmetrinen alatyypit sairauden (ks. kohta 5. 1) ja parantaa fyysistä toimintakykyä. psoriasis amgevita is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy. paediatric plaque psoriasis amgevita is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies. hidradenitis suppurativa (hs) amgevita is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adults and adolescents from 12 years of age with an inadequate response to conventional systemic hs therapy (see sections 5. 1 ja 5. crohn’s disease amgevita is indicated for treatment of moderately to severely active crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies. paediatric crohn's disease amgevita is indicated for the treatment of moderately to severely active crohn's disease in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and/or an immunomodulator, or who are intolerant to or have contraindications for such therapies. ulcerative colitis amgevita is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. uveitis amgevita is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate. paediatric uveitis amgevita is indicated for the treatment of paediatric chronic non-infectious anterior uveitis in patients from 2 years of age who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

Sedator vet 1.0 mg/ml injektioneste, liuos Suomi - suomi - Fimea (Suomen lääkevirasto)

sedator vet 1.0 mg/ml injektioneste, liuos

eurovet animal health b.v. - medetomidine hydrochloride - injektioneste, liuos - 1.0 mg/ml - medetomidiini

PETSEDAN VET 1 mg/ml injektioneste, liuos Suomi - suomi - Fimea (Suomen lääkevirasto)

petsedan vet 1 mg/ml injektioneste, liuos

provivo oy provivo oy - medetomidini hydrochloridum - injektioneste, liuos - 1 mg/ml - medetomidiini