Европейски съюз - фински - EMA (European Medicines Agency)

meda ab - tsaleplonia - unihäiriöiden ja ylläpidon häiriöt - psyykenlääkkeiden - zerene on tarkoitettu unettomuuspotilaiden hoitoon, joilla on vaikeuksia nukahtaa. se on osoitettu vain silloin, kun häiriö on vakava, henkilöiden käytöstä poistaminen tai altistaminen äärimmäiselle ahdistukselle.

Европейски съюз - фински - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinuria, paroxysmal - selektiiviset immunosuppressantit - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Европейски съюз - фински - EMA (European Medicines Agency)

evolus pharma b.v. - botuliinitoksiini tyyppi a - ihon vanhenemista - muut lihasrelaksantit, perifeerisesti vaikuttavat aineet - tilapäisesti vuonna ulkonäkö on kohtalainen tai vaikea pystysuoran rivit kulmakarvojen välissä nähnyt korkeintaan paheksua (glabellaariuurteita), kun vakavuus edellä kasvojen juonteita on tärkeä psykologinen vaikutus aikuisilla alle 65-vuotiaille.

Европейски съюз - фински - EMA (European Medicines Agency)

paion deutschland gmbh - remimazolam besilate - tietoinen sedaatio - psyykenlääkkeiden - remimazolam is indicated in adults for procedural sedation. remimazolam 50 mg is indicated in adults for intravenous induction and maintenance of general anaesthesia.

Финландия - фински - Fimea (Suomen lääkevirasto)

agepha pharma s.r.o - aciclovir - silmävoide - 30 mg/g - asikloviiri

Финландия - фински - Fimea (Suomen lääkevirasto)

orion corporation - acetylsalicylic acid, dipyridamole - säädellysti vapauttava kapseli, kova - 200 mg / 25 mg - yhdistelmävalmisteet

Финландия - фински - Fimea (Suomen lääkevirasto)

alfasan nederland b.v. - doxycycline hyclate - oraalisuspensio - 10 mg/ml - doksisykliini

Финландия - фински - Fimea (Suomen lääkevirasto)

zoetis animal health aps - bismuth subnitrate - intramammaarisuspensio - 2.6 g - muut vetimien ja utareiden hoitoon tarkoitetut valmisteet

Финландия - фински - Fimea (Suomen lääkevirasto)

grifols deutschland gmbh - human normal immunoglobulin - infuusioneste, liuos - 100 mg/ml - ihmisen normaali immunoglobuliini intravaskulaariseen käyttöön

Финландия - фински - Fimea (Suomen lääkevirasto)

ceva santÉ animale - amlodipine besylate - purutabletti - 1.25 mg - amlodipiini