Ephedrine Sintetica Stungulyf, lausn 50 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

ephedrine sintetica stungulyf, lausn 50 mg/ml

sintetica gmbh - ephedrinum hýdróklóríð - stungulyf, lausn - 50 mg/ml

Lusduna Evrópusambandið - íslenska - EMA (European Medicines Agency)

lusduna

merck sharp & dohme b.v. - glargíninsúlín - sykursýki - lyf notuð við sykursýki - meðferð sykursýki hjá fullorðnum, unglingum og börnum 2 ára og eldri.

Zonegran Evrópusambandið - íslenska - EMA (European Medicines Agency)

zonegran

amdipharm limited - zonisamíðs - flogaveiki, partial - antiepileptics, - zonegran er ætlað eins og:sér í meðferð hluta flog, með eða án efri almenn ákvörðun er tekin, í fullorðnir með nýlega greind flogaveiki;venjulega meðferð í meðferð hluta flog, með eða án efri almenn ákvörðun er tekin, í fullorðnir, unglingar, og börn sem eru sex ára og eldri.

Ximluci Evrópusambandið - íslenska - EMA (European Medicines Agency)

ximluci

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - augnlækningar - ximluci is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

Ranivisio Evrópusambandið - íslenska - EMA (European Medicines Agency)

ranivisio

midas pharma gmbh - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - augnlækningar - ranivisio is indicated in adults for:• the treatment of neovascular (wet) age-related macular degeneration (amd)• the treatment of visual impairment due to diabetic macular oedema (dme)• the treatment of proliferative diabetic retinopathy (pdr)• the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)• the treatment of visual impairment due to choroidal neovascularisation (cnv).

Topiramate Alvogen (Topiramate Portfarma) Filmuhúðuð tafla 25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

topiramate alvogen (topiramate portfarma) filmuhúðuð tafla 25 mg

alvogen ehf. - topiramatum inn - filmuhúðuð tafla - 25 mg

Topiramate Alvogen (Topiramate Portfarma) Filmuhúðuð tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

topiramate alvogen (topiramate portfarma) filmuhúðuð tafla 50 mg

alvogen ehf. - topiramatum inn - filmuhúðuð tafla - 50 mg

Valsartan/Hydroklortiazid Jubilant Filmuhúðuð tafla 160 mg/ 12.5 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

valsartan/hydroklortiazid jubilant filmuhúðuð tafla 160 mg/ 12.5 mg

jubilant pharmaceuticals nv - valsartanum inn; hydrochlorothiazidum inn - filmuhúðuð tafla - 160 mg/ 12.5 mg

Yesafili Evrópusambandið - íslenska - EMA (European Medicines Agency)

yesafili

viatris limited - aflibercept - macular edema; retinal vein occlusion; diabetic retinopathy; myopia, degenerative; diabetes complications - augnlækningar - yesafili is indicated for adults for the treatment ofneovascular (wet) age-related macular degeneration (amd) (see section 5. 1),visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo) (see section 5. 1),visual impairment due to diabetic macular oedema (dme) (see section 5. 1),visual impairment due to myopic choroidal neovascularisation (myopic cnv) (see section 5.

Abasaglar (previously Abasria) Evrópusambandið - íslenska - EMA (European Medicines Agency)

abasaglar (previously abasria)

eli lilly nederland b.v. - glargíninsúlín - sykursýki - lyf notuð við sykursýki - meðferð sykursýki hjá fullorðnum, unglingum og börnum 2 ára og eldri.