Incruse Ellipta (previously Incruse) Euroopan unioni - suomi - EMA (European Medicines Agency)

incruse ellipta (previously incruse)

glaxosmithkline (ireland) limited - umeklidiniumbromidia - keuhkosairaus, krooninen obstruktiivinen - obstruktiivisten hengitystiesairauksien lääkkeet, - osoitettu hoidon bronkodilataattorikäsittelyksi oireiden lievittämiseksi aikuispotilailla, joilla on krooninen obstruktiivinen keuhkosairaus (copd).

Optimmune vet 2 mg/g silmävoide Suomi - suomi - Fimea (Suomen lääkevirasto)

optimmune vet 2 mg/g silmävoide

intervet international b.v. - ciclosporin - silmävoide - 2 mg/g - siklosporiini

Minjuvi Euroopan unioni - suomi - EMA (European Medicines Agency)

minjuvi

incyte biosciences distribution b.v. - tafasitamab - lymphoma, large b-cell, diffuse - antineoplastiset aineet - minjuvi is indicated in combination with lenalidomide followed by minjuvi monotherapy for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) who are not eligible for autologous stem cell transplant (asct).

Fluenz Euroopan unioni - suomi - EMA (European Medicines Agency)

fluenz

medimmune llc - reassortant influenssa virus (elävä heikennetty) seuraavista viruskannoista:a/california/7/2009 (h1n1)pdm09-kaltainen kanta, a/victoria/361/2011 (h3n2) - kaltainen kanta, b/massachusetts/2/2012-kaltainen kanta - influenza, human; immunization - rokotteet - profylaksia influenssan yksilöiden 24 kk alle 18-vuotiaat. fluenz-valmisteen käytön tulisi perustua virallisiin suosituksiin.

Pandemic influenza vaccine H5N1 AstraZeneca (previously Pandemic influenza vaccine H5N1 Medimmune) Euroopan unioni - suomi - EMA (European Medicines Agency)

pandemic influenza vaccine h5n1 astrazeneca (previously pandemic influenza vaccine h5n1 medimmune)

astrazeneca ab - (live attenuated) reassortant influenza virus (a / vietnam / 1203/2004 (h5n1) -kanta - influenssa, ihminen - rokotteet - influenssan ennaltaehkäisy virallisesti ilmoitetussa pandemiatilanteessa lapsilla ja nuorilla 12 kuukauden ikäisiltä alle 18-vuotiaille. pandemic influenza vaccine h5n1 astrazeneca tulee käyttää virallisen ohjeistuksen mukaisesti.

Opzelura Euroopan unioni - suomi - EMA (European Medicines Agency)

opzelura

incyte biosciences distribution b.v. - ruxolitinib phosphate - vitiligo - muut dermatologiset valmisteet - opzelura is indicated for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age.

Kesimpta Euroopan unioni - suomi - EMA (European Medicines Agency)

kesimpta

novartis ireland ltd - ofatumumab - multippeliskleroosi, relapsoiva-remittoiva - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Salmeson 50 mikrog / 250 mikrog / annos inhalaatiojauhe, annosteltu Suomi - suomi - Fimea (Suomen lääkevirasto)

salmeson 50 mikrog / 250 mikrog / annos inhalaatiojauhe, annosteltu

elpen pharmaceutical co. inc. - salmeterol xinafoate, fluticasone propionate - inhalaatiojauhe, annosteltu - 50 mikrog / 250 mikrog / annos - salmeteroli ja flutikasoni

Salmeson 50 mikrog / 500 mikrog / annos inhalaatiojauhe, annosteltu Suomi - suomi - Fimea (Suomen lääkevirasto)

salmeson 50 mikrog / 500 mikrog / annos inhalaatiojauhe, annosteltu

elpen pharmaceutical co. inc. - salmeterol xinafoate, fluticasone propionate - inhalaatiojauhe, annosteltu - 50 mikrog / 500 mikrog / annos - salmeteroli ja flutikasoni

Jayempi Euroopan unioni - suomi - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - graft hylkääminen - immunosuppressantit - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.