CircoMax Myco Euroopan unioni - suomi - EMA (European Medicines Agency)

circomax myco

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - immunologiset suidaeille - siat (lihotus) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Heplisav B Euroopan unioni - suomi - EMA (European Medicines Agency)

heplisav b

dynavax gmbh - hepatiitti b-pinta-antigeeni - b-hepatiitti - rokotteet - heplisav b is indicated for the active immunisation against hepatitis b virus infection (hbv) caused by all known subtypes of hepatitis b virus in adults 18 years of age and older. the use of heplisav b should be in accordance with official recommendations. it can be expected that hepatitis d will also be prevented by immunisation with heplisav b as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection.

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

abrysvo

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - hengitystyön syntiusvirusinfektiot - rokotteet - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. katso kohdat 4. 2 ja 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. käyttö tämä rokote tulee virallisten suositusten mukaisesti.

Joflupaani (123I) Rotop 74 MBq/ml injektioneste, liuos Suomi - suomi - Fimea (Suomen lääkevirasto)

joflupaani (123i) rotop 74 mbq/ml injektioneste, liuos

rotop radiopharmacy gmbh - ioflupane - injektioneste, liuos - 74 mbq/ml - jodi(123i)joflupaani

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

bosulif

pfizer europe ma eeig - bosutinibi (monohydraattina) - leukemia, myeloidi - antineoplastic agents, protein kinase inhibitors - bosulif on tarkoitettu aikuisille potilaille, joilla on:hiljattain diagnosoitu kroonisen vaiheen (cp) philadelphia-kromosomi-positiivinen krooninen myelooinen leukemia (ph+ kml). cp, akseleraatiovaiheen (ap), ja blastikriisivaiheen (bp) ph+ kml on aikaisemmin hoidettu yksi tai useampi tyrosiinikinaasin estäjä(s) [tki(s)] ja joille imatinibin, nilotinibin ja dasatinibin ei katsota asianmukaista hoitoa vaihtoehtoja.

Mavrik Suomi - suomi - Adama

mavrik

adama - tuohyönteisten torjunta

Porcilis Ery vet injektioneste, suspensio Suomi - suomi - Fimea (Suomen lääkevirasto)

porcilis ery vet injektioneste, suspensio

intervet international b.v. - erysipelothrix rhusiopathiae bacterium, serotype 2, inactivated - injektioneste, suspensio - erysipelothrix rokote

Porcilis Ery + Parvo vet. injektioneste, suspensio Suomi - suomi - Fimea (Suomen lääkevirasto)

porcilis ery + parvo vet. injektioneste, suspensio

intervet international b.v. - porcine parvovirus inactivated, strain 014, erysipelothrix rhusiopathiae, inactivated, strain m2, serotype 2 - injektioneste, suspensio - inaktivoitu sian parvovirus -rokote + inaktivoitu erysipelothrix rokote

Aftovaxpur DOE Euroopan unioni - suomi - EMA (European Medicines Agency)

aftovaxpur doe

boehringer ingelheim vetmedica gmbh - enintään kolme seuraavista puhdistettua inaktivoitua suu-ja sorkkataudin virus, kantoja: o1 manisa ≥ 6 pd50*; o1 bfs ≥ 6 pd50*; o taiwan 3/97 ≥ 6 pd50*; a22 irakin ≥ 6 pd50*; a24 cruzeiro ≥ 6 pd50*; kalkkuna 14/98 ≥ 6 pd50*; aasia 1 shamir ≥ 6 pd50*; sat2 saudi-arabia ≥ 6 pd50*; * pd50 – 50% suojaava annos karjaa kuvattu ph. eur. monografia 0063. - immunologian osalta - pigs; cattle; sheep - nautaeläinten, lampaiden ja sikojen aktiivinen immunisointi 2 viikon ikäisiltä suu- ja sorkkatautia vastaan ​​kliinisten oireiden vähentämiseksi.