Movicol Junior Neutral Mixtúruduft, lausn 6,9 g Ísland - íslenska - 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 Ísland - íslenska - 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

Ceplene Evrópusambandið - íslenska - EMA (European Medicines Agency)

ceplene

laboratoires delbert - histamín díhýdróklóríð - kyrningahvítblæði, mergbólga, bráð - Ónæmisörvandi, - ceplene maintenance therapy is indicated for adult patients with acute myeloid leukaemia in first remission concomitantly treated with interleukin-2 (il-2). verkun ceplene hefur ekki verið sýnt að fullu hjá sjúklingum eldri en 60 ára.

Septabene Munnholsúði, lausn 1,5 mg/ml+5 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

septabene munnholsúði, lausn 1,5 mg/ml+5 mg/ml

krka, d.d., novo mesto - benzydaminum hýdróklóríð; cetylpyridinii chloridum - munnholsúði, lausn - 1,5 mg/ml+5 mg/ml

Harmonet Tafla 75 míkróg+ 20 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

harmonet tafla 75 míkróg+ 20 míkróg

pfizer aps (p) - gestodenum inn; ethinylestradiolum inn - tafla - 75 míkróg+ 20 míkróg

Septabene citron og honning Munnsogstafla 3 mg/1 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

septabene citron og honning munnsogstafla 3 mg/1 mg

krka, d.d., novo mesto - benzydaminum hýdróklóríð; cetylpyridinii chloridum - munnsogstafla - 3 mg/1 mg

Comirnaty Evrópusambandið - íslenska - EMA (European Medicines Agency)

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - bóluefni - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. notkun þetta bóluefni ætti að vera í samræmi við opinbera tillögur.

Kabiven Perifer Innrennslislyf, fleyti Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

kabiven perifer innrennslislyf, fleyti

fresenius kabi ab - soya-bean oil refined; glucosum; alaninum inn; arginine; aspartic acid; glutamic acid; glycine; histidinum inn; isoleucinum inn; leucinum inn; lysinum inn; methioninum inn; phenylalaninum inn; proline; serine; threoninum inn; tryptophanum inn; tyrosinum inn; valine; magnesii sulfas; kalii chloridum; sodium acetate trihydrate; natrii glycerophosphas; calcium chloride dihydrate - innrennslislyf, fleyti

Kabiven Innrennslislyf, fleyti Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

kabiven innrennslislyf, fleyti

fresenius kabi ab - soya-bean oil refined; glucosum; alaninum inn; arginine; aspartic acid; glutamic acid; glycine; histidinum inn; isoleucinum inn; leucinum inn; lysinum inn; methioninum inn; phenylalaninum inn; proline; serine; threoninum inn; tryptophanum inn; tyrosinum inn; valine; natrii glycerophosphas; magnesii sulfas; kalii chloridum; sodium acetate trihydrate; calcium chloride dihydrate - innrennslislyf, fleyti

Microgyn Tafla Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

microgyn tafla

bayer ab* - levonorgestrelum inn; ethinylestradiolum inn - tafla