Vaxneuvance Evrópusambandið - íslenska - EMA (European Medicines Agency)

vaxneuvance

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - sýkingar af völdum pneumókokka - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. sjá kafla 4. 4 og 5. 1 til að fá upplýsingar um vernd gegn tilteknum sermigerðum pneumokokkum. the use of vaxneuvance should be in accordance with official recommendations.

Ebvallo Evrópusambandið - íslenska - EMA (European Medicines Agency)

ebvallo

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

Azyter Augndropar, lausn í stakskammtaíláti 15 mg/g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

azyter augndropar, lausn í stakskammtaíláti 15 mg/g

laboratoires thea s.a.s. - azithromycinum díhýdrat - augndropar, lausn í stakskammtaíláti - 15 mg/g

Fibryga Stungulyfs-/innrennslisstofn og leysir, lausn 1 g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fibryga stungulyfs-/innrennslisstofn og leysir, lausn 1 g

octapharma ab - human fibrinogen - stungulyfs-/innrennslisstofn og leysir, lausn - 1 g