Starlix Europeiska unionen - isländska - EMA (European Medicines Agency)

starlix

novartis europharm limited - nateglinide - sykursýki, tegund 2 - lyf notuð við sykursýki - nateglinid er ætlað til samsettrar meðferðar með metformíni hjá sjúklingum með sykursýki af tegund 2 sem eru ófullnægjandi þrátt fyrir hámarksþolinn skammt af metformíni einu sér.

Darunavir Medical Valley Filmuhúðuð tafla 600 mg Island - isländska - LYFJASTOFNUN (Icelandic Medicines Agency)

darunavir medical valley filmuhúðuð tafla 600 mg

medical valley invest ab - darunavir propylene glycolate - filmuhúðuð tafla - 600 mg

Metoprolol Alvogen (Metoprolol ratiopharm) Forðatafla 95 mg Island - isländska - LYFJASTOFNUN (Icelandic Medicines Agency)

metoprolol alvogen (metoprolol ratiopharm) forðatafla 95 mg

alvogen ehf. - metoprololum súkkínat - forðatafla - 95 mg

Metoprolol Alvogen (Metoprolol ratiopharm) Forðatafla 190 mg Island - isländska - LYFJASTOFNUN (Icelandic Medicines Agency)

metoprolol alvogen (metoprolol ratiopharm) forðatafla 190 mg

alvogen ehf. - metoprololum súkkínat - forðatafla - 190 mg

Metoprolol Alvogen (Metoprolol ratiopharm) Forðatafla 23,75 mg Island - isländska - LYFJASTOFNUN (Icelandic Medicines Agency)

metoprolol alvogen (metoprolol ratiopharm) forðatafla 23,75 mg

alvogen ehf. - metoprololum súkkínat - forðatafla - 23,75 mg

Metoprolol Alvogen (Metoprolol ratiopharm) Forðatafla 47,5 mg Island - isländska - LYFJASTOFNUN (Icelandic Medicines Agency)

metoprolol alvogen (metoprolol ratiopharm) forðatafla 47,5 mg

alvogen ehf. - metoprololum súkkínat - forðatafla - 47,5 mg

Zejula Europeiska unionen - isländska - EMA (European Medicines Agency)

zejula

glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - Æxlishemjandi lyf - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. , as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

Artesunate Amivas Europeiska unionen - isländska - EMA (European Medicines Agency)

artesunate amivas

amivas ireland ltd - artesunate - malaría - krabbamein - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. Íhuga ætti að opinbera leiðsögn á réttri notkun malaríulyf lyfjum.