यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

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

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - anifrolumab - lupus erythematosus, systemic - Ónæmisbælandi lyf - 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.

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - budesonide, formoterol fumarate dihydrate, glycopyrronium bromide - lungnasjúkdómur, langvarandi hindrandi - lyf til veikindi öndunarvegi sjúkdómum, - 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.

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - tezepelumab - astma - lyf til veikindi öndunarvegi sjúkdómum, - tezspire is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment.

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - Æxlishemjandi lyf - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - durvalumab - krabbamein, lungnakrabbamein - Æxlishemjandi lyf - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - sjúklingar stutt og long-term, saxagliptin, dapagliflozin - sykursýki, tegund 2 - lyf notuð við sykursýki - qtrilmet er ætlað í fullorðnir 18 ára og eldri með tegund sykursýki 2:til að bæta blóðsykursstjórnun þegar sjúklingar með eða án sulphonylurea (su) og annaðhvort saxagliptin eða dapagliflozin veitir ekki fullnægjandi blóðsykursstjórnun. þegar þegar í meðferð með sjúklingar og saxagliptin og dapagliflozin.

आइसलैंड - आइसलैंडी - LYFJASTOFNUN (Icelandic Medicines Agency)

astrazeneca ab - goserelinum acetat - vefjalyf - 10,8 mg

आइसलैंड - आइसलैंडी - LYFJASTOFNUN (Icelandic Medicines Agency)

astrazeneca ab - goserelinum acetat - vefjalyf - 3,6 mg

यूरोपीय संघ - आइसलैंडी - EMA (European Medicines Agency)

astrazeneca ab - nirsevimab - Ónæmiskerfið sera og mótefni, - beyfortus is indicated for the prevention of respiratory syncytial virus (rsv) lower respiratory tract disease in neonates and infants during their first rsv season. beyfortus should be used in accordance with official recommendations.