Bovigen RCE vet injektioneste, emulsio Finnország - finn - Fimea (Suomen lääkevirasto)

bovigen rce vet injektioneste, emulsio

forte healthcare limited - bovine rotavirus strain tm-91, serotype g6p1, inactivated, inactivated bovine coronavirus, strain c-197, e.coli strain ec/17, inactivated, expressing f5 (k99) adhesin - injektioneste, emulsio

Adrenalin Martindale Pharma 0.1 mg/ml injektioneste, liuos Finnország - finn - Fimea (Suomen lääkevirasto)

adrenalin martindale pharma 0.1 mg/ml injektioneste, liuos

ethypharm - adrenaline tartrate - injektioneste, liuos - 0.1 mg/ml - adrenaliini

Posaconazole Accord Európai Unió - finn - EMA (European Medicines Agency)

posaconazole accord

accord healthcare s.l.u. - posakonatsoli - mykoosit - antimykoottiset aineet systeemiseen käyttöön - posaconazole accord is indicated for use in the treatment of the following fungal infections in adults:invasive aspergillosis;fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. vastareaktioita on määritelty, jos infektio etenee tai epäonnistuminen parantaa jälkeen vähintään 7 päivää ennen terapeuttisia annoksia tehokasta sienilääkitystä. posakonatsolin accord on tarkoitettu myös syvien sieni-infektioiden estoon seuraaville potilaille: potilaat, jotka saavat remissioon tähtäävää-induktio kemoterapiaa akuutti myelooinen leukemia (aml) tai myelodysplastiseen oireyhtymään (mds) odotetaan johtavan pitkittyneeseen neutropeniaan ja joilla on suuri riski kehittää syvä sieni-infektiot;hematopoieettisen kantasolujen siirteen (hsct) saaneilla, jotka ovat parhaillaan suuren annoksen immunosuppressiivinen hoito graft versus host disease, ja joilla on suuri riski kehittää syvä sieni-infektiot.

Lugesteron 300 mg emätinpuikko, kapseli, pehmeä Finnország - finn - Fimea (Suomen lääkevirasto)

lugesteron 300 mg emätinpuikko, kapseli, pehmeä

besins healthcare ireland ltd. - progesterone - emätinpuikko, kapseli, pehmeä - 300 mg - progesteroni

LUGESTERON 400 mg emätinpuikko, kapseli, pehmeä Finnország - finn - Fimea (Suomen lääkevirasto)

lugesteron 400 mg emätinpuikko, kapseli, pehmeä

besins healthcare ireland ltd. besins healthcare ireland ltd. - progesteronum - emätinpuikko, kapseli, pehmeä - 400 mg - progesteroni

Fampridine Accord Európai Unió - finn - EMA (European Medicines Agency)

fampridine accord

accord healthcare s.l.u. - fampridine - multippeliskleroosi - muut hermoston huumeet - fampridine accord is indicated for the improvement of walking in adult patients with multiple sclerosis with walking disability (edss 4-7).

Fintepla Európai Unió - finn - EMA (European Medicines Agency)

fintepla

ucb pharma s.a.   - fenfluramine hydrochloride - epilepsies, myoclonic - epilepsialääkkeet, - treatment of seizures associated with dravet syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older. fintepla is indicated for the treatment of seizures associated with dravet syndrome and lennox-gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older.

Adtralza Európai Unió - finn - EMA (European Medicines Agency)

adtralza

leo pharma a/s - tralokinumab - dermatitis, atopic - muut dermatologiset valmisteet - adtralza is indicated for the treatment of moderate to severe atopic dermatitis in adult and adolescent patients 12 years and older who are candidates for systemic therapy.

Bimzelx Európai Unió - finn - EMA (European Medicines Agency)

bimzelx

ucb pharma s.a.   - bimekizumab - psoriasis - immunosuppressantit - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, 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). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Artesunate Amivas Európai Unió - finn - EMA (European Medicines Agency)

artesunate amivas

amivas ireland ltd - artesunate - malaria - antiprototsooisia - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. on otettava huomioon viralliset ohjeet antibioottien asianmukaisesta käytöstä malarian aineet.