rhophylac 1000 iu injektioneste, liuos, esitäytetty ruisku
csl behring gmbh - human anti-d immunoglobulin - injektioneste, liuos, esitäytetty ruisku - 1000 iu - anti-d-immunoglobuliini
rhophylac 1500 iu injektioneste, liuos, esitäytetty ruisku
csl behring gmbh - human anti-d immunoglobulin - injektioneste, liuos, esitäytetty ruisku - 1500 iu - anti-d-immunoglobuliini
berinert 500 iu injektio/infuusiokuiva-aine ja liuotin, liuosta varten
csl behring gmbh - c1-esteraasin estäjä - injektio/infuusiokuiva-aine ja liuotin, liuosta varten - 500 iu - proteiini-c1-estäjät
riastap 1 g injektio/infuusiokuiva-aine, liuosta varten
csl behring gmbh - human fibrinogen - injektio/infuusiokuiva-aine, liuosta varten - 1 g - fibrinogeeni
berinert 1500 iu injektiokuiva-aine ja liuotin, liuosta varten
csl behring gmbh - c1-esteraasin estäjä - injektiokuiva-aine ja liuotin, liuosta varten - 1500 iu - proteiini-c1-estäjät
albumin behring 200 g/l infuusioneste, liuos
csl behring gmbh - albumin, human - infuusioneste, liuos - 200 g/l - albumiini
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.
dacogen
janssen-cilag international n.v. - decitabine - leukemia, myeloidi - antineoplastiset aineet - uusien diagnosoitujen de novo tai toissijainen akuutti myelooinen leukemia (aml) maailman terveysjärjestön (who)-luokituksen mukaisesti aikuisten potilaille, jotka eivät ole ehdolla standardin induktio solunsalpaajahoitoa.
imprida
novartis europharm ltd - valsartan, amlodipine (as amlodipine besilate) - verenpainetauti - reniini-angiotensiinijärjestelmään vaikuttavat aineet - essentiaalisen hypertension hoito. imprida on tarkoitettu potilaille, joiden verenpaine ei laske riittävästi yksinomaan amlodipiinilla tai valsartaanilla.
revitacam
zoetis belgium sa - meloksikaami - oxicams - koirat - tulehduksen ja kivun lievittäminen sekä akuuteissa että kroonisissa tuki- ja liikuntaelinten sairauksissa koirilla.