Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

teva pharma b.v.  - budesonide, formoterol fumarate dihydrate - asthma; pulmonary disease, chronic obstructive - obstruktiivisten hengitystiesairauksien lääkkeet, - budesonidi / formoterol teva pharma b. on tarkoitettu aikuisille vain 18-vuotiaille ja vanhemmille. asthmabudesonide/formoterol teva pharma b. on tarkoitettu astman säännölliseen hoitoon, jos käyttää yhdistelmä (kortikosteroidi ja pitkävaikutteinen β2 adrenergisten reseptorien agonisti) on tarkoituksenmukaista:-potilailla, joilla ei ole riittävästi hallinnassa hengitettävillä kortikosteroideilla ja "tarvittaessa" inhaloitava lyhytvaikutteinen β2 adrenoceptor agonistien. tai-potilailla on jo saatu riittävästi hallintaan sekä inhaloitavia kortikosteroideja ja pitkävaikutteista β2 adrenoceptor agonistien. copdsymptomatic hoito potilailla, joilla on copd, jossa uloshengityksen 1 toinen (fev1) .

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

accord healthcare s.l.u. - deferasiroksi - iron overload; beta-thalassemia - muut lääkevalmisteet, rautaa kelatoivia aineita - deferasiroksi accord on indisoitu kroonisen raudan liikavarastoitumisen johtuu usein verensiirtoja (≥7 ml/kg/kuukausi punasoluja) potilailla, joilla on beeta-talassemia major-vuotiaat 6-vuotiaat ja sitä vanhemmat. deferasiroksi accord on tarkoitettu myös kroonisen raudan liikavarastoitumisen verensiirroista silloin, kun deferoksamiinihoito on kontraindikoitu tai riittämätön seuraavissa potilasryhmissä:lapsipotilailla, joilla on beeta-talassemia major ja raudan ylikuormitus johtuu usein verensiirtoja (≥7 ml/kg/kuukausi punasoluja) 2-5-vuotiailla,aikuisilla ja lapsipotilailla, joilla on beeta-talassemia major, joilla on raudan liikavarastoitumista, koska harvoin verensiirrot (.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

dechra regulatory b.v. - mirtatsapiini - psychoanaleptics, antidepressants in combination with psycholeptics - kissat - sillä painonnousua, kissoilla kokee huono ruokahalu ja laihtuminen, jotka johtuvat krooninen sairaus.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

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.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

proveca pharma limited - enalapril (maleate) - sydämen vajaatoiminta - reniini-angiotensiinijärjestelmään vaikuttavat aineet - treatment of heart failure.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

laboratoires delbert - histamiini - leukemia, myeloidi, akuutti - immunostimulantit, - ceplene maintenance therapy is indicated for adult patients with acute myeloid leukaemia in first remission concomitantly treated with interleukin-2 (il-2). ceplenin tehokkuutta ei ole täysin osoitettu yli 60-vuotiailla potilailla.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

novartis europharm limited - vildagliptiini, metformiinihydrokloridia - diabetes mellitus, tyyppi 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

novartis europharm limited - vildagliptiini - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - vildagliptin is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:as monotherapy in patients in whom metformin is inappropriate due to contraindications or intolerance. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

novartis europharm limited - vildagliptiini, metformiinihydrokloridia - diabetes mellitus, tyyppi 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 ja 5. 1 käytettävissä olevista tiedoista eri yhdistelmistä).

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

novartis europharm limited - vildagliptiini - diabetes mellitus, tyyppi 2 - dipeptidyl peptidase 4 (dpp-4) inhibitors, drugs used in diabetes - vildagliptin is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:as monotherapy in patients in whom metformin is inappropriate due to contraindications or intolerance. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 ja 5. 1 käytettävissä olevista tiedoista eri yhdistelmistä).