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

evusheld

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

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

tyenne

fresenius kabi deutschland gmbh - tosilitsumabin - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - immunosuppressantit - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

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

tagrisso

astrazeneca ab - osimertinib mesilate - karsinooma, ei-pienisoluinen keuhko - muut antineoplastiset aineet, proteiinikinaasin estäjät - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Celecoxib Sandoz 100 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

celecoxib sandoz 100 mg kapseli, kova

sandoz a/s - celecoxib - kapseli, kova - 100 mg - selekoksibi

Celecoxib Sandoz 200 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

celecoxib sandoz 200 mg kapseli, kova

sandoz a/s - celecoxib - kapseli, kova - 200 mg - selekoksibi

Innovax-ND-IBD Euroopan unioni - suomi - EMA (European Medicines Agency)

innovax-nd-ibd

intervet international b.v. - solu-liittyvät live rekombinantti kalkkunan herpesvirus (kanta hvp360), ilmaista fusion proteiini nd virus ja vp2 proteiini ibd-viruksen - lintuinfluenssan herpes virus (marek ' s disease) + lintuinfluenssan gumboron tautiviruksen (gumboro-tauti) + newcastlen tauti-viruksen/paramyksoviruksen - chicken; embryonated chicken eggs - for active immunisation of one-day-old chicks or 18-19-day-old embryonated chicken eggs:to reduce mortality and clinical signs caused by newcastle disease (nd) virus,to prevent mortality and to reduce clinical signs and lesions caused by infectious bursal disease (ibd) virus,to reduce mortality, clinical signs and lesions caused by marek’s disease (md) virus.

Hepcludex Euroopan unioni - suomi - 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.

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

actraphane

novo nordisk a/s - insulin human - diabetes mellitus - diabeetilla käytettävät lääkkeet - diabetes mellituksen hoito.

Budesonide/Formoterol Teva Euroopan unioni - suomi - EMA (European Medicines Agency)

budesonide/formoterol teva

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - obstruktiivisten hengitystiesairauksien lääkkeet, - budesonide/formoterol teva on tarkoitettu aikuisille 18 vuotta täyttäneille vain. asthmabudesonide/formoterol teva on tarkoitettu säännölliseen astman hoitoon, jossa käytetään yhdistelmää (kortikosteroidi ja pitkävaikutteinen β2 adrenergisten reseptorien agonisti) on tarkoituksenmukaista:potilailla, joilla ei ole riittävästi hallinnassa hengitettävillä kortikosteroideilla ja "tarvittaessa" inhaloitava lyhytvaikutteinen β2 adrenoceptor agonistien. orin potilaat, jotka jo riittävästi hallintaan sekä inhaloitavia kortikosteroideja ja pitkävaikutteista β2 adrenoceptor agonistien. copdsymptomatic hoito potilailla, joilla on vaikea keuhkoahtaumatauti (fev1 < 50% viitearvosta normaali) ja ollut toistuvasti pahenemisvaiheita, jotka ovat merkittäviä oireita, vaikka säännöllinen hoito pitkävaikutteinen keuhkoputkia.