CIPRALEX 10 mg tabletti, suussa hajoava Suomi - suomi - Fimea (Suomen lääkevirasto)

cipralex 10 mg tabletti, suussa hajoava

h. lundbeck a/s h. lundbeck a/s - escitalopramum - tabletti, suussa hajoava - 10 mg - essitalopraami

CIPRALEX 20 mg tabletti, suussa hajoava Suomi - suomi - Fimea (Suomen lääkevirasto)

cipralex 20 mg tabletti, suussa hajoava

h. lundbeck a/s h. lundbeck a/s - escitalopramum - tabletti, suussa hajoava - 20 mg - essitalopraami

Losartan Medical Valley 12.5 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

losartan medical valley 12.5 mg tabletti, kalvopäällysteinen

medical valley invest ab - losartan potassium - tabletti, kalvopäällysteinen - 12.5 mg - losartaani

Losartan Medical Valley 50 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

losartan medical valley 50 mg tabletti, kalvopäällysteinen

medical valley invest ab - losartan potassium - tabletti, kalvopäällysteinen - 50 mg - losartaani

Losartan Medical Valley 100 mg tabletti, kalvopäällysteinen Suomi - suomi - Fimea (Suomen lääkevirasto)

losartan medical valley 100 mg tabletti, kalvopäällysteinen

medical valley invest ab - losartan potassium - tabletti, kalvopäällysteinen - 100 mg - losartaani

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

eperzan

glaxosmithkline trading services limited - albiglutide - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - eperzan on tarkoitettu hoitoon tyypin 2 diabetesta sairastaville aikuisille parantamaan glukoositasapainoa:monotherapywhen ruokavalio ja liikunta eivät yksin tarjoa riittävää glukoositasapainoa potilaille, joille metformiinin käyttöä ei pidetä riittävänä, koska vasta tai intoleranssi. add-on yhdistelmä therapyin yhdessä muiden verensokeria alentavien lääkevalmisteiden kanssa, mukaan lukien basal insuliinia, kun nämä, yhdessä ruokavalion ja liikunnan kanssa, eivät tarjoa riittävää glukoositasapainoa (ks. kohta 4. 4 ja 5. 1 käytettävissä olevista tiedoista eri yhdistelmistä).

Fucidin-Hydrocortison emulsiovoide Suomi - suomi - Fimea (Suomen lääkevirasto)

fucidin-hydrocortison emulsiovoide

leo pharma a/s - hydrocortisone acetate, fusidic acid - emulsiovoide - hydrokortisoni ja antibiootit

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.