Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
xylocain húðúði, lausn 100 mg/ml
aspen pharma trading limited - lidocainum inn - húðúði, lausn - 100 mg/ml
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
zofran mixtúra, lausn 0,8 mg/ml
sandoz a/s - ondansetronum hýdróklóríð - mixtúra, lausn - 0,8 mg/ml
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
hyftor
plusultra pharma gmbh - sirolimus - angiofibroma; tuberous sclerosis - hyftor is indicated for the treatment of facial angiofibroma associated with tuberous sclerosis complex in adults and paediatric patients aged 6 years and older.
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
repevax stungulyf, dreifa áfyllt sprauta
sanofi pasteur* - tetanus toxoid; diphtheria toxoid; pertussis toxoid; filamentous haemagglutinin; pertussis fimbrial agglutinogens (fim) 2 and 3; pertactin; poliovirus (inactivated) type 1 (mahoney strain); poliovirus (inactivated) type 2 (mef-1 strain); poliovirus (inactivated) type 3 (saukett strain) - stungulyf, dreifa - áfyllt sprauta
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
onpattro
alnylam netherlands b.v. - patisiran járn - amyloidosis, Ættingja - Önnur lyf í taugakerfinu - onpattro er ætlað fyrir meðferð arfgenga transthyretin-miðlað amyloidosis (hattr amyloidosis) í fullorðinn sjúklinga með stigi 1 eða stigi 2 polyneuropathy.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
amvuttra
alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - Önnur lyf í taugakerfinu - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
eylea
bayer ag - aflibercept - wet macular degeneration; macular edema; diabetes complications - augnlækningar - eylea er ætlað fyrir fullorðna fyrir meðferð:neovascular (blautur) aldri-tengjast ský á auga (rÍsa);sjón skert vegna ský bjúg efri að sjónhimnu æð stíflu (útibú rvo eða central rvo);sjón skert vegna sykursýki ský bjúg (dme);sjón skert vegna myopic æðu neovascularisation (myopic cnv).
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
beovu
novartis europharm limited - brolucizumab - wet macular degeneration - augnlækningar - beovu er ætlað í fullorðnir fyrir meðferð neovascular (blautur) aldri-tengjast ský á auga (rÍsa).
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
pemazyre
incyte biosciences distribution b.v. - pemigatinib - cholangiocarcinoma - Æxlishemjandi lyf - pemazyre monotherapy is indicated for the treatment of adults with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
vabysmo
roche registration gmbh - faricimab - wet macular degeneration; macular edema; diabetes complications - augnlækningar - vabysmo is indicated for the treatment of adult patients with:neovascular (wet) age-related macular degeneration (namd),visual impairment due to diabetic macular oedema (dme).