MICROLUTON 30 mikrog tabletti, päällystetty Suomi - suomi - Fimea (Suomen lääkevirasto)

microluton 30 mikrog tabletti, päällystetty

bayer oy - levonorgestrelum - tabletti, päällystetty - 30 mikrog - levonorgestreeli

MICROLUTON 30 mikrog tabletti, päällystetty Suomi - suomi - Fimea (Suomen lääkevirasto)

microluton 30 mikrog tabletti, päällystetty

orifarm oy - levonorgestrelum - tabletti, päällystetty - 30 mikrog - levonorgestreeli

MICROLUTON 30 mikrog tabletti, päällystetty Suomi - suomi - Fimea (Suomen lääkevirasto)

microluton 30 mikrog tabletti, päällystetty

paranova oy - levonorgestrelum - tabletti, päällystetty - 30 mikrog - levonorgestreeli

MICROLUTON 30 mikrog tabletti, päällystetty Suomi - suomi - Fimea (Suomen lääkevirasto)

microluton 30 mikrog tabletti, päällystetty

orifarm oy - levonorgestrelum - tabletti, päällystetty - 30 mikrog - levonorgestreeli

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

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna 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 - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. käyttö tämä rokote tulee virallisten suositusten mukaisesti.

Spikevax (previously COVID-19 Vaccine Moderna) Euroopan unioni - suomi - 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.

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

nuvaxovid

novavax cz, a.s. - sars cov-2 (original) recombinant spike protein, sars-cov-2 (omicron xbb.1.5) recombinant spike protein - covid-19 virus infection - covid-19 vaccines - nuvaxovid is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. käyttö tämä rokote tulee virallisten suositusten mukaisesti. nuvaxovid xbb. 5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. käyttö tämä rokote tulee virallisten suositusten mukaisesti.

Versican Plus DHPPi/L4 Euroopan unioni - suomi - EMA (European Medicines Agency)

versican plus dhppi/l4

zoetis belgium sa - koiran penikkatautivirus, kanta cdv bio 11/a koiran adenovirus tyyppi 2, kanta cav-2 bio 13, koiran parvovirus tyyppi 2b, kanta cpv-2b-bio 12/b, koiran parainfluenssa 2-tyypin virus, kanta cpiv-2 bio 15 (kaikki eläviä, heikennettyjä), leptospira interrogansin seroryhmä australis serovariantti bratislava, kanta mslb 1088, l. interrogansin seroryhmä icterohaemorrhagiae serovariantti icterohaemorrhagiae, kanta mslb 1089, l. interrogansin seroryhmä canicola serovariantti canicola, kanta mslb 1090, l. kirschneri seroryhmä grippotyphosa serovariantti grippotyphosa, kanta mslb 1091... - elää koiran penikkatauti-virus, + live koiran adenovirus + live koiran parainfluenssa-virus, + live koiran parvoviruksen + inaktivoidut leptospira, immunologisia valmisteita varten canidae - koirat - aktiivinen immunisointi koirien 6 viikon iässä:ehkäisemään kuolleisuutta ja kliinisiä oireita aiheuttanut koiran penikkatauti-virus,ehkäisemään kuolleisuutta ja kliinisiä oireita aiheuttanut koiran adenovirus tyyppi 1,estää kliinisiä oireita ja vähentää viruksen erittymistä aiheuttama koiran adenovirus tyyppi 2,estää kliinisiä merkkejä, leukopenia ja viruksen erittyminen aiheuttama koiran parvovirus,estää kliinisiä oireita (nenän ja silmien vastuuvapauden), ja vähentää viruksen erittymistä aiheuttama koiran parainfluenssa-virus,estää kliinisten oireiden, infektion ja virtsaan aiheuttama l. interrogansin seroryhmä australis serovariantti bratislava,estää kliiniset oireet ja virtsan erittymistä ja vähentää infektion aiheuttama l. interrogans seroryhmä canicola serovar canicola ja l. interrogans serogroup icterohaemorrhagiae serovar icterohaemorrhagiae ja estää kliinisiä oireita ja vähentää infektioita ja virtsan erittymistä aiheuttama l. interrogans serogroup grippotyphosa serovar grippotyphosa.