Եվրոպական Միություն - ֆիններեն - EMA (European Medicines Agency)

dipharma arzneimittel gmbh - miglustaattia - gaucherin tauti - muut ruoansulatuskanavan ja aineenvaihduntatuotteet - miglustaatti dipharma on tarkoitettu suun hoito aikuisten lievän ja keskivaikean tyypin 1 gaucher ' n tautia. miglustaatti dipharma voidaan käyttää vain potilaille, joille entsyymikorvaushoito ei sovi. miglustaatti dipharma on tarkoitettu hoitoon progressiivinen neurologiset oireet aikuisilla ja lapsilla, joilla oli niemann-pickin tyypin c tautia.

Եվրոպական Միություն - ֆիններեն - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - immunosuppressantit - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Եվրոպական Միություն - ֆիններեն - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - anemia, sickle cell - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Եվրոպական Միություն - ֆիններեն - EMA (European Medicines Agency)

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 - rokotteet - 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. käyttö tämä rokote tulee virallisten suositusten mukaisesti.

Եվրոպական Միություն - ֆիններեն - EMA (European Medicines Agency)

angelini pharma s.p.a - cenobamate - epilepsia - epilepsialääkkeet, - adjunctive treatment of focal-onset seizures with or without secondary generalisation in adult patients with epilepsy who have not been adequately controlled despite a history of treatment with at least 2 anti-epileptic medicinal products.

Եվրոպական Միություն - ֆիններեն - EMA (European Medicines Agency)

biomarin international limited - vosoritide - achondroplasia - lääkkeet luusairauksien hoitoon - voxzogo is indicated for the treatment of achondroplasia in patients 4 months of age and older whose epiphyses are not closed. the diagnosis of achondroplasia should be confirmed by appropriate genetic testing.

Ֆինլանդիա - ֆիններեն - Fimea (Suomen lääkevirasto)

septodont - adrenaline tartrate, articaine hydrochloride - injektioneste, liuos - 40 mg/ml + 5 mikrog/ml - artikaiini

Ֆինլանդիա - ֆիններեն - Fimea (Suomen lääkevirasto)

fresenius kabi deutschland gmbh - calcium folinate - injektio-/infuusioneste, liuos - 10 mg/ml - kalsiumfolinaatti

Ֆինլանդիա - ֆիններեն - Fimea (Suomen lääkevirasto)

b. braun melsungen ag - ondansetron hydrochloride dihydrate - injektioneste, liuos - 2 mg/ml - ondansetroni

Ֆինլանդիա - ֆիններեն - Fimea (Suomen lääkevirasto)

orion corporation - pyrvinium embonate - tabletti, kalvopäällysteinen - 100 mg - pyrviini