Baycoxine vet 50 mg/ml oraalisuspensio Finnland - finnska - Fimea (Suomen lääkevirasto)

baycoxine vet 50 mg/ml oraalisuspensio

bayer animal health gmbh - toltrazuril - oraalisuspensio - 50 mg/ml - toltratsuriili

Chanox vet 50 mg/ml oraalisuspensio Finnland - finnska - Fimea (Suomen lääkevirasto)

chanox vet 50 mg/ml oraalisuspensio

chanelle pharmaceuticals manufacturing limited - toltrazuril - oraalisuspensio - 50 mg/ml - toltratsuriili

Thiamacare Vet 10 mg/ml oraaliliuos Finnland - finnska - Fimea (Suomen lääkevirasto)

thiamacare vet 10 mg/ml oraaliliuos

ecuphar nv - thiamazole - oraaliliuos - 10 mg/ml - tiamatsoli

Felithyrol Vet 5 mg/ml oraaliliuos Finnland - finnska - Fimea (Suomen lääkevirasto)

felithyrol vet 5 mg/ml oraaliliuos

cp-pharma handelsgesellschaft mbh - thiamazole - oraaliliuos - 5 mg/ml - tiamatsoli

Atriance Evrópusambandið - finnska - EMA (European Medicines Agency)

atriance

sandoz pharmaceuticals d.d. - nelarabiini - prekursori t-solulymfoblastinen leukemia-lymfooma - antineoplastiset aineet - nelarabiini on tarkoitettu niiden potilaiden hoitoon akuutin t-lymfoblastisen leukemian (t-all) ja t-lymfoblastisen lymfooman (t-lbl), joiden tauti ei ole reagoinut tai on uusiutunut hoidon jälkeen vähintään kaksi solunsalpaajahoito. due to the small patient populations in these disease settings, the information to support these indications is based on limited data.

Fluenz Evrópusambandið - finnska - EMA (European Medicines Agency)

fluenz

medimmune llc - reassortant influenssa virus (elävä heikennetty) seuraavista viruskannoista:a/california/7/2009 (h1n1)pdm09-kaltainen kanta, a/victoria/361/2011 (h3n2) - kaltainen kanta, b/massachusetts/2/2012-kaltainen kanta - influenza, human; immunization - rokotteet - profylaksia influenssan yksilöiden 24 kk alle 18-vuotiaat. fluenz-valmisteen käytön tulisi perustua virallisiin suosituksiin.

Fluenz Tetra Evrópusambandið - finnska - EMA (European Medicines Agency)

fluenz tetra

astrazeneca ab - a/darwin/9/2021 (h3n2) - like strain (a/norway/16606/2021, medi 355293) / a/victoria/2570/2019 (h1n1)pdm09 - like strain (a/victoria/1/2020, medi 340505) / b/austria/1359417/2021 - like strain (b/austria/1359417/2021, medi 355292) / b/phuket/3073/2013 - like strain (b/phuket/3073/2013, medi 306444) - influenssa, ihminen - influenssa influenssa, elävä heikennetty - prophylaxis of influenza in children and adolescents from 24 months to less than 18 years of age. fluenz tetran käytön olisi perustuttava virallisiin suosituksiin.

Revolade Evrópusambandið - finnska - EMA (European Medicines Agency)

revolade

novartis europharm limited - eltrombopag - purpura, trombosytopeeninen, idiopaattinen - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 ja 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 ja 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Fasenra Evrópusambandið - finnska - EMA (European Medicines Agency)

fasenra

astrazeneca ab - benralizumab - astma - obstruktiivisten hengitystiesairauksien lääkkeet, - fasenra on merkitty add huolto hoito aikuisilla potilailla, joilla on vaikea eosinofiilinen astma on riittävästi hallinnassa huolimatta korkea-annos inhaloitavat kortikosteroidit plus pitkävaikutteista β-agonistit.

Hepcludex Evrópusambandið - finnska - EMA (European Medicines Agency)

hepcludex

gilead sciences ireland uc - bulevirtide acetate - hepatitis d, chronic - antiviraalit systeemiseen käyttöön - hepcludex is indicated for the treatment of chronic hepatitis delta virus (hdv) infection in plasma (or serum) hdv-rna positive adult patients with compensated liver disease.