Inegy Tafla 10/20 mg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

inegy tafla 10/20 mg

n.v. organon* - simvastatinum inn; ezetimibum inn - tafla - 10/20 mg

Inegy Tafla 10/40 mg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

inegy tafla 10/40 mg

n.v. organon* - simvastatinum inn; ezetimibum inn - tafla - 10/40 mg

Inegy Tafla 10/80 mg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

inegy tafla 10/80 mg

n.v. organon* - simvastatinum inn; ezetimibum inn - tafla - 10/80 mg

Fingolimod Accord Kesatuan Eropah - Iceland - EMA (European Medicines Agency)

fingolimod accord

accord healthcare s.l.u. - fingolimod stutt og long-term - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi, sérhæfður ónæmisbælandi - tilgreindur sem einn sjúkdómur breyta meðferð í mjög virk köstum skil heila-og mænusigg fyrir eftirfarandi tekur af fullorðnum sjúklingum og börn sjúklinga á aldrinum 10 ára og eldri:sjúklingar með mjög virk sjúkdómur þrátt fyrir fullt og fullnægjandi meðferð með að minnsta kosti einn sjúkdómur breyta therapyorpatients með ört vaxandi alvarlega köstum skil heila-og mænusigg skilgreind af 2 eða meira að slökkva köst í eitt ár, og með 1 eða meira skuggaefna efla sár á heilanum segulÓmun eða mikil aukning í t2 sár álag eins og miðað við fyrri undanförnum segulÓmun.

Fingolimod Mylan Kesatuan Eropah - Iceland - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod stutt og long-term - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 og 5. 1)orpatients með ört vaxandi alvarlega köstum skil heila-og mænusigg skilgreind af 2 eða meira að slökkva köst í eitt ár, og með 1 eða meira skuggaefna efla sár á heilanum segulÓmun eða mikil aukning í t2 sár álag eins og miðað við fyrri undanförnum segulÓmun.

Fingolimod Mylan Kesatuan Eropah - Iceland - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod stutt og long-term - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 og 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Abstral Tungurótartafla 800 míkróg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 800 míkróg

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

Abstral Tungurótartafla 600 míkróg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 600 míkróg

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

Abstral Tungurótartafla 400 míkróg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 400 míkróg

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

Abstral Tungurótartafla 300 míkróg Iceland - Iceland - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 300 míkróg

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