Zynteglo European Union - Icelandic - EMA (European Medicines Agency)

zynteglo

bluebird bio (netherlands) b.v. - samgena cd34+ klefi inniheldur íbúa sem inniheldur blóðmyndandi stofnfrumur transduced með lentiglobin bb305 lentiviral vektor kóðun beta-a-t87q-glóbín gene - beta-thalassemia - other hematological agents - zynteglo er ætlað fyrir meðferð sjúklinga 12 ára og eldri með blóðgjöf-háð beta thalassaemia (tdt) sem hafa ekki β0/β0 arfgerð, fyrir hvern skurðaðgerðir stafa klefi (hsc) ígræðslu er rétt en hvítra manna antigen (hla)-samsvörun tengjast hsc gjafa er ekki í boði.

Cegfila (previously Pegfilgrastim Mundipharma) European Union - Icelandic - EMA (European Medicines Agency)

cegfila (previously pegfilgrastim mundipharma)

mundipharma corporation (ireland) limited - pegfilgrastim - daufkyrningafæð - Ónæmisörvandi, - lækkun á lengd mæði í tengslum og tíðni hita og mæði í tengslum í fullorðinn sjúklinga með frumudrepandi lyfjameðferð fyrir illkynja (með undantekning langvarandi merg hvítblæði og myelodysplastic heilkennum).

Vazkepa European Union - Icelandic - EMA (European Medicines Agency)

vazkepa

amarin pharmaceuticals ireland limited - icosapent ethyl - dýrarannsóknir - lipid breytandi lyf - indicated to reduce cardiovascular risk as an adjunct to statin therapy.

Bimzelx European Union - Icelandic - EMA (European Medicines Agency)

bimzelx

ucb pharma s.a.   - bimekizumab - psoriasis - Ónæmisbælandi lyf - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Stimufend European Union - Icelandic - EMA (European Medicines Agency)

stimufend

fresenius kabi deutschland gmbh - pegfilgrastim - daufkyrningafæð - Ónæmisörvandi, , nýlendan að örva þáttum - lækkun á lengd mæði í tengslum og tíðni hita og mæði í tengslum í fullorðinn sjúklinga með frumudrepandi lyfjameðferð fyrir illkynja (með undantekning langvarandi merg hvítblæði og myelodysplastic heilkennum).

Vildagliptin/Metformin Krka Filmuhúðuð tafla 50 mg/1000 mg Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

vildagliptin/metformin krka filmuhúðuð tafla 50 mg/1000 mg

krka d.d. novo mesto* - metforminum hýdróklóríð; vildagliptinum inn - filmuhúðuð tafla - 50 mg/1000 mg

Vildagliptin/Metformin Krka Filmuhúðuð tafla 50 mg/850 mg Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

vildagliptin/metformin krka filmuhúðuð tafla 50 mg/850 mg

krka d.d. novo mesto* - vildagliptinum inn; metforminum hýdróklóríð - filmuhúðuð tafla - 50 mg/850 mg