Imfinzi Euroopa Liit - islandi - EMA (European Medicines Agency)

imfinzi

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).

Qtrilmet Euroopa Liit - islandi - EMA (European Medicines Agency)

qtrilmet

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.

Beyfortus Euroopa Liit - islandi - EMA (European Medicines Agency)

beyfortus

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.

Logimax forte Forðatafla 10 mg + 100 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

logimax forte forðatafla 10 mg + 100 mg

recordati ireland limited* - metoprololum súkkínat; felodipinum inn - forðatafla - 10 mg + 100 mg

Logimax Forðatafla 5 mg + 50 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

logimax forðatafla 5 mg + 50 mg

recordati ireland limited* - metoprololum súkkínat; felodipinum inn - forðatafla - 5 mg + 50 mg

Seloken ZOC Forðatafla 95 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

seloken zoc forðatafla 95 mg

recordati ireland limited* - metoprololum súkkínat - forðatafla - 95 mg

Seloken ZOC Forðatafla 47,5 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

seloken zoc forðatafla 47,5 mg

recordati ireland limited* - metoprololum súkkínat - forðatafla - 47,5 mg

Seloken ZOC Forðatafla 23,75 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

seloken zoc forðatafla 23,75 mg

recordati ireland limited* - metoprololum súkkínat - forðatafla - 23,75 mg

Seloken ZOC Forðatafla 190 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

seloken zoc forðatafla 190 mg

recordati ireland limited* - metoprololum súkkínat - forðatafla - 190 mg

Symbicort forte Turbuhaler Innöndunarduft 320/9 míkróg/skammt Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

symbicort forte turbuhaler innöndunarduft 320/9 míkróg/skammt

astrazeneca a/s - budesonidum inn; formoterolum fúmarat - innöndunarduft - 320/9 míkróg/skammt