Tecovirimat SIGA האיחוד האירופי - פינית - EMA (European Medicines Agency)

tecovirimat siga

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - antiviraalit systeemiseen käyttöön - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 ja 5. tecovirimat siga should be used in accordance with official recommendations.

Trogarzo האיחוד האירופי - פינית - EMA (European Medicines Agency)

trogarzo

theratechnologies europe limited - ibalizumab - hiv-infektiot - antiviraalit systeemiseen käyttöön - trogarzo, yhdessä muiden antiretroviraalisten(s), on tarkoitettu hoitoon aikuisille tartunnan kanssa useita resistenttejä hiv-1-infektio, joille se ei muuten ole mahdollista rakentaa tukahduttava antiviraalinen hoito.

Comirnaty האיחוד האירופי - פינית - 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.

VIAROX 50 mikrog/annos inhalaatioaerosoli פינלנד - פינית - Fimea (Suomen lääkevirasto)

viarox 50 mikrog/annos inhalaatioaerosoli

orion oyj - beclometasoni dipropionas - inhalaatioaerosoli - 50 mikrog/annos - beklometasoni

VIAROX COMBI 50 mikrog/annos inhalaatioaerosoli פינלנד - פינית - Fimea (Suomen lääkevirasto)

viarox combi 50 mikrog/annos inhalaatioaerosoli

orion oyj - beclometasoni dipropionas - inhalaatioaerosoli - 50 mikrog/annos - beklometasoni

VIAROX 50 mikrog/annos inhalaatioaerosoli פינלנד - פינית - Fimea (Suomen lääkevirasto)

viarox 50 mikrog/annos inhalaatioaerosoli

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

VIAROX NASAL 50 mikrog/annos nenäaerosoli פינלנד - פינית - 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 פינלנד - פינית - Fimea (Suomen lääkevirasto)

proviron 10 mg tabletti

schering oy - mesterolonum - tabletti - 10 mg - mesteroloni

PROVIRON 25 mg tabletti פינלנד - פינית - Fimea (Suomen lääkevirasto)

proviron 25 mg tabletti

schering oy - mesterolonum - tabletti - 25 mg - mesteroloni

Fludeomap 250 MBq/ml injektioneste, liuos פינלנד - פינית - Fimea (Suomen lääkevirasto)

fludeomap 250 mbq/ml injektioneste, liuos

map medical technologies oy - fludeoxyglucose (18f) - injektioneste, liuos - 250 mbq/ml - fluori(18f)deoksiglukoosi