Zeposia Evrópusambandið - íslenska - EMA (European Medicines Agency)

zeposia

bristol-myers squibb pharma eeig - ozanimod stutt og long-term - multiple sclerosis, relapsing-remitting; colitis, ulcerative - Ónæmisbælandi lyf - multiple sclerosiszeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (rrms) with active disease as defined by clinical or imaging features. ulcerative colitiszeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Abstral Tungurótartafla 800 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 800 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 800 míkróg

Abstral Tungurótartafla 600 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 600 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 600 míkróg

Abstral Tungurótartafla 400 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 400 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 400 míkróg

Abstral Tungurótartafla 300 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 300 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 300 míkróg

Abstral Tungurótartafla 200 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 200 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 200 míkróg

Abstral Tungurótartafla 100 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 100 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 100 míkróg

Modiodal Tafla 100 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

modiodal tafla 100 mg

teva pharma b.v. - modafinilum inn - tafla - 100 mg

Briviact (in Italy: Nubriveo) Evrópusambandið - íslenska - EMA (European Medicines Agency)

briviact (in italy: nubriveo)

ucb pharma sa - brivaracetam - flogaveiki - antiepileptics, - briviact er ætlað sem viðbótarmeðferð við meðhöndlun á flogaveiki með eða án aukakvilla hjá fullorðnum og unglingum frá 16 ára aldri með flogaveiki.

Cometriq Evrópusambandið - íslenska - EMA (European Medicines Agency)

cometriq

ipsen pharma - cabozantinib - skjaldkirtilsæxli - Æxlishemjandi lyf - meðferð hjá fullorðnum sjúklingum með framsækið, óleysanlegt, staðbundið langt gengið eða meinvörpað skjaldkirtilskrabbamein.