Sogroya Ευρωπαϊκή Ένωση - Ισλανδικά - EMA (European Medicines Agency)

sogroya

novo nordisk a/s - somapacitan - vöxtur - hinsveiflur og heilahimnubólur og hliðstæður - sogroya is indicated for the replacement of endogenous growth hormone (gh) in children  aged 3  years and above, and adolescents with growth failure due to growth hormone deficiency (paediatric ghd), and in adults with growth hormone deficiency (adult ghd).

Brukinsa Ευρωπαϊκή Ένωση - Ισλανδικά - EMA (European Medicines Agency)

brukinsa

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - Æxlishemjandi lyf - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Orgovyx Ευρωπαϊκή Ένωση - Ισλανδικά - EMA (European Medicines Agency)

orgovyx

accord healthcare s.l.u. - relugolix - blöðruhálskirtli - innkirtla meðferð - orgovyx is indicated for the treatment of adult patients with advanced hormone-sensitive prostate cancer.

Quviviq Ευρωπαϊκή Ένωση - Ισλανδικά - EMA (European Medicines Agency)

quviviq

idorsia pharmaceuticals deutschland gmbh - daridorexant hydrochloride - svefntruflun og viðhald - psycholeptics - quviviq is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.

Pyrukynd Ευρωπαϊκή Ένωση - Ισλανδικά - EMA (European Medicines Agency)

pyrukynd

agios netherlands b.v. - mitapivat sulfate - genetic diseases, inborn; anemia, hemolytic - other hematological agents - pyrukynd is indicated for the treatment of pyruvate kinase deficiency (pk deficiency) in adult patients (see section 4.