Prometazin Actavis Filmuhúðuð tafla 25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

prometazin actavis filmuhúðuð tafla 25 mg

actavis group ptc ehf. - promethazinum hýdróklóríð - filmuhúðuð tafla - 25 mg

Phenergan Filmuhúðuð tafla 25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

phenergan filmuhúðuð tafla 25 mg

opella healthcare france s.a.s. - promethazinum hýdróklóríð - filmuhúðuð tafla - 25 mg

Lumeblue (previously known as Methylthioninium chloride Cosmo) Evrópusambandið - íslenska - EMA (European Medicines Agency)

lumeblue (previously known as methylthioninium chloride cosmo)

alfasigma s.p.a. - metýlþíóníumklóríð - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Sarclisa Evrópusambandið - íslenska - EMA (European Medicines Agency)

sarclisa

sanofi winthrop industrie - isatuximab - mergæxli - Æxlishemjandi lyf - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Angiox Evrópusambandið - íslenska - EMA (European Medicines Agency)

angiox

the medicines company uk ltd - bivalirudin - bráð kransæðasjúkdómur - blóðþurrðandi lyf - angiox er ætlað sem blóðþynningarlyf hjá fullorðnum sjúklingum sem gangast undir kransæðahimnu (pci), þar með talið sjúklingar með hjartadrep í st-stigi (stemi) sem gangast undir aðal pci. getið í sumum tilkynningum er einnig ætlað til meðferð við fullorðinn sjúklinga með óstöðug hjartslætti / non-l-hluti-hæð kransæðastíflu (ha / nstemi) skipulagt fyrir aðkallandi eða snemma á íhlutun. getið í sumum tilkynningum skal gefa með aspirín og eftir að.

Haldol Depot Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

haldol depot stungulyf, lausn 100 mg/ml

essential pharma limited - haloperidolum dekanóat - stungulyf, lausn - 100 mg/ml

Haldol Tafla 1 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

haldol tafla 1 mg

essential pharma limited - haloperidolum inn - tafla - 1 mg

Haldol Stungulyf, lausn 5 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

haldol stungulyf, lausn 5 mg/ml

essential pharma limited - haloperidolum inn - stungulyf, lausn - 5 mg/ml

Ozawade Evrópusambandið - íslenska - EMA (European Medicines Agency)

ozawade

bioprojet pharma - pitolisant - sleep apnea, obstructive - Önnur lyf í taugakerfinu - ozawade is indicated to improve wakefulness and reduce excessive daytime sleepiness (eds) in adult patients with obstructive sleep apnoea (osa).

Pentocur (Tiopental Abcur) Stungulyfsstofn, lausn 1 g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

pentocur (tiopental abcur) stungulyfsstofn, lausn 1 g

abcur ab - thiopentalum natricum inn - stungulyfsstofn, lausn - 1 g