Movicol Junior Neutral Mixtúruduft, lausn 6,9 g Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

movicol junior neutral mixtúruduft, lausn 6,9 g

norgine healthcare b.v. - macrogol 3350; sodium hydrogen carbonate; kalii chloridum; sodium chloride - mixtúruduft, lausn - 6,9 g

Movicol Mixtúruduft, lausn 13,8 g Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

movicol mixtúruduft, lausn 13,8 g

norgine healthcare b.v. - macrogol 3350; sodium chloride; sodium hydrogen carbonate; kalii chloridum - mixtúruduft, lausn - 13,8 g

Moviprep Mixtúruduft, lausn Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

moviprep mixtúruduft, lausn

norgine b.v. - macrogol 3350; natrii sulfas; natrii chloridum; kalii chloridum; acidum ascorbicum inn; natrii ascorbas inn - mixtúruduft, lausn

Mekinist Europos Sąjunga - islandų - EMA (European Medicines Agency)

mekinist

novartis europharm limited - trametinib - melanoma - Æxlishemjandi lyf - melanomatrametinib as monotherapy or in combination with dabrafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 og 5. trametinib monotherapy has not demonstrated clinical activity in patients who have progressed on a prior braf inhibitor therapy (see section 5. adjuvant treatment of melanomatrametinib in combination with dabrafenib is indicated for the adjuvant treatment of adult patients with stage iii melanoma with a braf v600 mutation, following complete resection. ekki lítinn klefa lungnakrabbamein (nsclc)trametinib ásamt dabrafenib er ætlað fyrir meðferð fullorðinn sjúklinga með langt ekki lítið klefi lungnakrabbamein með meÐferÐ v600 stökkbreytingu.

Alpha Ject 3000 Stungulyf, fleyti Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

alpha ject 3000 stungulyf, fleyti

pharmaq as* - aeromonas salmonicida subs. salmonicida al 2017; vibrio anguillarum serotype o1 al 112; vibrio anguillarum serotype 02 al 104 - stungulyf, fleyti

ALPHA JECT 5-3 Stungulyf, fleyti Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

alpha ject 5-3 stungulyf, fleyti

pharmaq as* - aeromonas salmonicida subsp. salmonicida; vibrio salmonicida; listonella anguillarum serotype o1; listonella anguillarum serotype o2a; moritella viscosa - stungulyf, fleyti

Onpattro Europos Sąjunga - islandų - 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.

Givlaari Europos Sąjunga - islandų - EMA (European Medicines Agency)

givlaari

alnylam netherlands b.v. - givosiran - porphyrias, lifur - Ýmsum meltingarvegi og efnaskipti vörur - meðferð bráð lifur porfýría (wells fargo) í fullorðnir og unglingar á aldrinum 12 ára og eldri.

Oxlumo Europos Sąjunga - islandų - EMA (European Medicines Agency)

oxlumo

alnylam netherlands b.v. - lumasiran sodium - hyperoxaluria, primary - Önnur meltingarvegi og efnaskipti vörur, - treatment of primary hyperoxaluria type 1 (ph1) in all age groups.

Amvuttra Europos Sąjunga - islandų - 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.