Simdax Innrennslisþykkni, lausn 2,5 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

simdax innrennslisþykkni, lausn 2,5 mg/ml

orion corporation - levosimendanum inn - innrennslisþykkni, lausn - 2,5 mg/ml

Vetmedin vet. (Pimovita) Tuggutafla 1,25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

vetmedin vet. (pimovita) tuggutafla 1,25 mg

boehringer ingelheim vetmedica gmbh* - pimobendanum inn - tuggutafla - 1,25 mg

Vetmedin vet. (Pimovita) Tuggutafla 10 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

vetmedin vet. (pimovita) tuggutafla 10 mg

boehringer ingelheim vetmedica gmbh* - pimobendanum inn - tuggutafla - 10 mg

Vetmedin vet. (Pimovita) Tuggutafla 5 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

vetmedin vet. (pimovita) tuggutafla 5 mg

boehringer ingelheim vetmedica gmbh* - pimobendanum inn - tuggutafla - 5 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.

Baqsimi Evrópusambandið - íslenska - EMA (European Medicines Agency)

baqsimi

eli lilly nederland b.v. - glúkagon - sykursýki - brisi hormón, glycogenolytic hormón - baqsimi er ætlað fyrir meðferð alvarlega blóðsykursfall í fullorðnir, unglingar, og börn sem eru 4 ár og yfir með sykursýki.

Spikevax (previously COVID-19 Vaccine Moderna) Evrópusambandið - íslenska - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) 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 - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Berinert Stungulyfs-/innrennslisstofn og leysir, lausn 500 a.e. Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

berinert stungulyfs-/innrennslisstofn og leysir, lausn 500 a.e.

csl behring gmbh* - c1-hemill - stungulyfs-/innrennslisstofn og leysir, lausn - 500 a.e.