Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - glycopyrronium, formoterol fumarate dihydrate - keuhkosairaus, krooninen obstruktiivinen - formoteroli ja glykopyrroniumbromidi - bevespi aerosphere on merkitty huolto keuhkoputkia hoito lievittää oireita aikuisilla potilailla, joilla on krooninen keuhkoahtaumatauti (copd).

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - andexanet alfa - huumeisiin liittyviä sivuvaikutuksia ja haittavaikutuksia - kaikki muut terapeuttiset tuotteet - aikuisilla potilailla, joilla on suora hyytymistekijä xa: n (fxa) estäjä (apixaban tai rivaroksabaani), kun käänteinen antikoagulaatio tarvitaan, koska henkeä uhkaava tai hallitsematon verenvuoto.

Suomi - suomi - Fimea (Suomen lääkevirasto)

astrazeneca oy - budesonide, formoterol fumarate dihydrate - inhalaatiosumute, suspensio - 80 mikrog / 2.25 mikrog / inhalaatio - formoteroli ja budesonidi

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - formoterol fumarate dihydrate, glycopyrronium bromide, budesonide - keuhkosairaus, krooninen obstruktiivinen - obstruktiivisten hengitystiesairauksien lääkkeet, - trixeo aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long acting beta2 agonist or combination of a long-acting beta2 agonist and a long acting muscarinic antagonist.

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - acalabrutinib - leukemia, lymfosyyttinen, krooninen, b-solu - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - moxetumomab pasudotox - leukemia, karvainen solu - antineoplastiset aineet - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - selumetinib sulfate - neurofibromatosis 1 - antineoplastiset aineet - koselugo as monotherapy is indicated for the treatment of symptomatic, inoperable plexiform neurofibromas (pn) in paediatric patients with neurofibromatosis type 1 (nf1) aged 3 years and above.

Euroopan unioni - suomi - EMA (European Medicines Agency)

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

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - anifrolumab - lupus erythematosus, systemaattinen - immunosuppressantit - saphnelo is indicated as an add-on therapy for the treatment of adult patients with moderate to severe, active autoantibody-positive systemic lupus erythematosus (sle), despite standard therapy.

Euroopan unioni - suomi - EMA (European Medicines Agency)

astrazeneca ab - budesonide, formoterol fumarate dihydrate, glycopyrronium bromide - keuhkosairaus, krooninen obstruktiivinen - obstruktiivisten hengitystiesairauksien lääkkeet, - riltrava aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2 agonist or combination of a long-acting beta2 agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5.