VIAROX NASAL 50 mikrog/annos nenäaerosoli Finlande - finnois - Fimea (Suomen lääkevirasto)

viarox nasal 50 mikrog/annos nenäaerosoli

schering-plough labo n.v. - beclometasoni dipropionas - nenäaerosoli - 50 mikrog/annos - beklometasoni

PROVIRON 10 mg tabletti Finlande - finnois - Fimea (Suomen lääkevirasto)

proviron 10 mg tabletti

schering oy - mesterolonum - tabletti - 10 mg - mesteroloni

PROVIRON 25 mg tabletti Finlande - finnois - Fimea (Suomen lääkevirasto)

proviron 25 mg tabletti

schering oy - mesterolonum - tabletti - 25 mg - mesteroloni

Iqymune 100 mg/ml infuusioneste, liuos Finlande - finnois - Fimea (Suomen lääkevirasto)

iqymune 100 mg/ml infuusioneste, liuos

laboratoire francais du fractionnement et des biotechnologies - human normal immunoglobulin - infuusioneste, liuos - 100 mg/ml - ihmisen normaali immunoglobuliini intravaskulaariseen käyttöön

Fibclot 1.5 g injektio/infuusiokuiva-aine ja liuotin, liuosta varten Finlande - finnois - Fimea (Suomen lääkevirasto)

fibclot 1.5 g injektio/infuusiokuiva-aine ja liuotin, liuosta varten

laboratoire francais du fractionnement et des biotechnologies - human fibrinogen - injektio/infuusiokuiva-aine ja liuotin, liuosta varten - 1.5 g - fibrinogeeni

Purevax RCP FeLV Union européenne - finnois - EMA (European Medicines Agency)

purevax rcp felv

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) - immunologisia valmisteita varten felidae, - kissat - 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 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 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 feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Purevax RCPCh Union européenne - finnois - EMA (European Medicines Agency)

purevax rcpch

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) - immunologisia valmisteita varten felidae, - kissat - 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. immuniteettia on osoitettu viikon kuluttua rhinotracheiitin, kalikiviruksen, chlamydophila felisin ja panleukopenia -komponenttien ensisijaisesta rokotuskurssista. 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.

Purevax RCPCh FeLV Union européenne - finnois - EMA (European Medicines Agency)

purevax rcpch felv

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) - immunologisia valmisteita varten felidae, - kissat - 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.

Spikevax (previously COVID-19 Vaccine Moderna) Union européenne - finnois - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - rokotteet - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

MIBG (123 I) 52 MBq/ml injektioneste Finlande - finnois - Fimea (Suomen lääkevirasto)

mibg (123 i) 52 mbq/ml injektioneste

map medical technologies oy - iobenguani sulfas,natrii iodidum (123i) - injektioneste - 52 mbq/ml - jodi(123i)jobenguani