Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

zoetis animal health aps - erysipelothrix rhusiopathiae, inactivated, strain b-7, serotype 2, porcine parvovirus, inactivated, strain s-80 - injektioneste, emulsio - inaktivoitu sian parvovirus -rokote + inaktivoitu erysipelothrix rokote

Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

eurovet animal health b.v. - methadone hydrochloride - injektioneste, liuos - 10 mg/ml - metadoni

Umoja wa Ulaya - Kifinlandi - EMA (European Medicines Agency)

ceva santé animale - heikennetty elävä raivotautirokotusvirus, kanta spbn gasgas - immunologisia valmisteita varten canidae, elävät virusrokotteet - red foxes (vulpes vulpes); raccoon dogs (nyctereutes procyonoides) - kettujen ja supikoirien aktiiviseen immunisointiin raivotautia vastaan ​​tartunnan ja kuolleisuuden estämiseksi.

Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

rotop pharmaka gmbh - tetrofosmin - valmisteyhdistelmä radioaktiivista lääkettä varten - 0.23 mg - teknetium(99mtc)tetrofosmiini

Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

vetviva richter gmbh - methadone hydrochloride - injektioneste, liuos - 10 mg/ml - metadoni

Umoja wa Ulaya - Kifinlandi - EMA (European Medicines Agency)

sanofi pasteur - chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated) - dengue - - rokotteet - dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 ja 4. käyttö dengvaxia pitäisi olla virallisten suositusten mukaisesti.

Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

ceva-phylaxia co. ltd. - ibd elävä heikennetty virus, serotyyppi 1, kanta syza26 - injektiokonsentraatti ja liuotin, suspensiota varten - gumboron tauti -rokote

Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

dechra regulatory b.v. - equine herpesvirus, type 1, inactived - injektioneste, emulsio - hevosen rinopneumoniittivirus -rokote

Umoja wa Ulaya - Kifinlandi - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - niveltulehdus, nivelreuma - immunosuppressantit - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Ufini - Kifinlandi - Fimea (Suomen lääkevirasto)

bioveta a.s. - rabies-virus live - oraalisuspensio