Den europeiske union -
latvisk -
EMA (European Medicines Agency)
mysimba
orexigen therapeutics ireland limited - bupropions hidrohlorīds, naltreksons hidrohlorīds - obesity; overweight - pretiekaisuma līdzekļi, izņemot diētas produkti - mysimba ir norādīts, kā palīglīdzekli, lai samazinātu kaloriju diētu un palielināt fiziskās aktivitātes, vadības svars pieaugušiem pacientiem (≥18 gadi) ar sākotnējās Ķermeņa masas indekss (Ķmi) ir≥ 30 kg/m2 (aptaukošanās) vai≥ 27 kg/m2 līdz < 30 kg/m2 (liekais svars), ka produktā ir viens vai vairāk svara, kas saistīti co saistīti ar blakus saslimšanām (e. , 2. tipa cukura diabētu, dyslipidaemia, vai kontrolētu hipertensiju)apstrāde ar mysimba būtu jāpārtrauc pēc 16 nedēļas, ja pacients nav zaudējuši vismaz 5% no to sākotnējās ķermeņa masas.
Den europeiske union -
finsk -
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.
Finland -
finsk -
Fimea (Suomen lääkevirasto)
fostimon 75 iu/ml injektiokuiva-aine ja liuotin, liuosta varten
ibsa farmaceutici italia s.r.l - urofollitropin - injektiokuiva-aine ja liuotin, liuosta varten - 75 iu/ml - urofollitropiini
Finland -
finsk -
Fimea (Suomen lääkevirasto)
fostimon 150 iu/ml injektiokuiva-aine ja liuotin, liuosta varten
ibsa farmaceutici italia s.r.l - urofollitropin - injektiokuiva-aine ja liuotin, liuosta varten - 150 iu/ml - urofollitropiini
Finland -
finsk -
Fimea (Suomen lääkevirasto)
fostimon set 75 iu/ml injektiokuiva-aine ja liuotin, liuosta varten
ibsa farmaceutici italia s.r.l - urofollitropin - injektiokuiva-aine ja liuotin, liuosta varten - 75 iu/ml - urofollitropiini
Finland -
finsk -
Fimea (Suomen lääkevirasto)
fostimon set 150 iu/ml injektiokuiva-aine ja liuotin, liuosta varten
ibsa farmaceutici italia s.r.l - urofollitropin - injektiokuiva-aine ja liuotin, liuosta varten - 150 iu/ml - urofollitropiini
Finland -
finsk -
Fimea (Suomen lääkevirasto)
fostimon set 225 iu injektiokuiva-aine ja liuotin, liuosta varten
ibsa farmaceutici italia s.r.l - urofollitropin - injektiokuiva-aine ja liuotin, liuosta varten - 225 iu - urofollitropiini
Finland -
finsk -
Fimea (Suomen lääkevirasto)
fostimon set 300 iu injektiokuiva-aine ja liuotin, liuosta varten
ibsa farmaceutici italia s.r.l - urofollitropin - injektiokuiva-aine ja liuotin, liuosta varten - 300 iu - urofollitropiini