NexoBrid Europäische Union - Isländisch - EMA (European Medicines Agency)

nexobrid

mediwound germany gmbh - proteolytic enzymes enriched in bromelain - debridement - undirbúningur til meðferðar á sár og sár - nexobrid er ætlað til að fjarlægja eschar hjá fullorðnum með djúpum hluta og fullum þykktumbruna.

Combivir Europäische Union - Isländisch - EMA (European Medicines Agency)

combivir

viiv healthcare bv - áhrif, zídóvúdíns - hiv sýkingar - veirueyðandi lyf til almennrar notkunar - combivir is indicated in antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infection.

Cresemba Europäische Union - Isländisch - EMA (European Medicines Agency)

cresemba

basilea pharmaceutica deutschland gmbh - isavuconazol - aspergillosis - cresemba er ætlað í fullorðnir fyrir meðferð:innrásar aspergillosismucormycosis í sjúklingar sem amfótericín b er inappropriateconsideration ætti að opinbera leiðsögn á réttri notkun mikla lyfjum.

Zydelig Europäische Union - Isländisch - EMA (European Medicines Agency)

zydelig

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Tybost Europäische Union - Isländisch - EMA (European Medicines Agency)

tybost

gilead sciences ireland uc - cobicistat - hiv sýkingar - veirueyðandi lyf til almennrar notkunar - tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (hiv-1) infected adults and adolescents aged 12 years and older:weighing at least 35 kg co‑administered with atazanavir orweighing at least 40 kg co‑administered with darunavir.

Paxlovid Europäische Union - Isländisch - EMA (European Medicines Agency)

paxlovid

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Glucos Fresenius Kabi (Glucos 100 mg/ml Fresenius Kabi) Innrennslislyf, lausn 100 mg/ml Island - Isländisch - LYFJASTOFNUN (Icelandic Medicines Agency)

glucos fresenius kabi (glucos 100 mg/ml fresenius kabi) innrennslislyf, lausn 100 mg/ml

fresenius kabi ab - glucosum - innrennslislyf, lausn - 100 mg/ml

Glucos Fresenius Kabi (Glucos 200 mg/ml Fresenius Kabi) Innrennslislyf, lausn 200 mg/ml Island - Isländisch - LYFJASTOFNUN (Icelandic Medicines Agency)

glucos fresenius kabi (glucos 200 mg/ml fresenius kabi) innrennslislyf, lausn 200 mg/ml

fresenius kabi ab - glucosum - innrennslislyf, lausn - 200 mg/ml

Glucos Fresenius Kabi (Glucos 50 mg/ml Fresenius Kabi) Innrennslislyf, lausn 50 mg/ml Island - Isländisch - LYFJASTOFNUN (Icelandic Medicines Agency)

glucos fresenius kabi (glucos 50 mg/ml fresenius kabi) innrennslislyf, lausn 50 mg/ml

fresenius kabi ab - glucosum - innrennslislyf, lausn - 50 mg/ml

Glucos Fresenius Kabi (Glucos 500 mg/ml Fresenius Kabi) Innrennslislyf, lausn 500 mg/ml Island - Isländisch - LYFJASTOFNUN (Icelandic Medicines Agency)

glucos fresenius kabi (glucos 500 mg/ml fresenius kabi) innrennslislyf, lausn 500 mg/ml

fresenius kabi ab - glucosum - innrennslislyf, lausn - 500 mg/ml