الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

zoetis belgium sa - dirlotapidi - antiobesity preparations, excl. ruokavalion tuotteita - koirat - apuna ylipainoisuuden ja lihavuuden hallinnassa aikuisille koirille. voidaan käyttää osana yleistä painonhallintaohjelmaa, johon sisältyy myös asianmukaisia ​​ruokavalion muutoksia ja harjoittelua.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - rekombinantti kalkkunan herpesvirus, kanta vhvt013-69, live - immunologisia valmisteita varten aves, kanoja, immunologisia valmisteita - embryonated eggs; chicken - kanojen aktiivinen immunisointi:ehkäisemään kuolleisuutta ja vähentämään kliinisiä oireita ja leesioita gumboron tauti. vähentää kuolleisuutta, kliinisiä oireita ja vaurioita marekin tautia.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

ceva sante animale - dinotefuran, pyriproksifeeni, permetriini - permetriini, yhdistelmiä - koirat - hoito ja ehkäisy kirpputartuntojen (ctenocephalides felis ja ctenocephalides canis). hoito ja ehkäisy rasti tartuntoja (rhipicephalus sanguineus, dermacentor reticulatus, ixodes ricinus). ehkäisy puree hiekkaa lentää (phlebotomus perniciosus), hyttysiä (culex pipiens, aedes aegypti) ja vakaa lentää (stomoxys calcitrans). hoito hyttysen (aedes aegypti) ja vakaa lentää (stomoxys calcitrans) tartuntoja.

الاتحاد الأوروبي - الفنلندية - 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).

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

novo nordisk a/s - insulin human - diabetes mellitus - diabeetilla käytettävät lääkkeet - diabetes mellituksen hoito.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

dompé biotec s.p.a. - darbepoetiini alfa - kidney failure, chronic; anemia; cancer - antianemiset valmisteet - krooniseen munuaisten vajaatoimintaan (crf) liittyvän oireisen anemian hoito aikuisilla ja pediatrisilla potilailla. oireisen anemian hoito solunsalpaajia saavilla aikuisilla syöpäpotilailla, joilla on ei-myeloidinen syöpä.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

mediwound germany gmbh - proteolytic enzymes enriched in bromelain - puhdistus - valmisteet haavojen ja haavaumien hoitoon - nexobrid on tarkoitettu syksyn poistamiseen aikuisilla, joilla on syvä osittainen ja täysipaksuinen lämpöpalovamma.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

merck sharp and dohme b.v - posakonatsoli - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimykoottiset aineet systeemiseen käyttöön - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 ja 5. 1):- invasive aspergillosisnoxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections  4. 2 ja 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- 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. noxafil gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4. 2 ja 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 ja 5. 1):- invasive aspergillosisnoxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adult and paediatric patients from 2 years of age (see sections 4. 2 ja 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- 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. noxafil concentrate for solution for infusion is also indicated for prophylaxis of invasive fungal infections in the following adult and paediatric patients from 2 years of age (see sections 4. 2 ja 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease (gvhd) and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil gastro resistant powder and solvent for oral suspension is indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age (see sections 4. 2 ja 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- 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. noxafil gastro-resistant powder and solvent for oral suspension is indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2  years of age:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high  risk of developing invasive fungal infections;- haematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high  risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil oral suspension is indicated for use in the treatment of the following fungal infections in adults (see section 5. 1):- invasiivinen aspergilloosi potilailla, joiden sairauteen, joka on tulenkestävä amfoterisiini b tai itrakonatsoli eivät tehonneet tai kun potilaat eivät sietäneet näitä lääkkeitä;- epäilty fusarioosi potilailla, joilla on sairaus, joka on tulenkestävä amfoterisiini b: tä tai potilailla, jotka eivät siedä amfoterisiini b;- kromoblastomykoosi ja mysetooman hoidossa potilailla, joilla on sairaus, joka on tulenkestävä itrakonatsoli tai potilailla, jotka eivät siedä itrakonatsoli;- koksidioidomykoosi potilailla, joilla on sairaus, joka on tulenkestävä amfoterisiini b, itrakonatsoli tai flukonatsoli, tai potilailla, jotka eivät siedä näitä lääkkeitä;- suunielun kandidiaasi: ensilinjan lääkkeenä potilaille, joiden sairaus on vakava tai joiden immuunipuolustus on heikentynyt, ja vastaus paikalliseen hoitoon odotetaan olevan heikon. vastareaktioita on määritelty, jos infektio etenee tai epäonnistuminen parantaa jälkeen vähintään 7 päivää ennen terapeuttisia annoksia tehokasta sienilääkitystä. noxafil oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

novartis europharm limited  - vildagliptiini, metformiinihydrokloridia - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - zomarist 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.

الاتحاد الأوروبي - الفنلندية - EMA (European Medicines Agency)

corza medical gmbh - ihmisen fibrinogeeni, ihmisen trombiini - hemostaasi, kirurginen - hemostaatit - tachosil is indicated in adults and children from 1 month of age for supportive treatment in surgery for improvement of haemostasis, to promote tissue sealing and for suture support in vascular surgery where standard techniques are insufficient. tachosil is indicated in adults for supportive sealing of the dura mater to prevent postoperative cerebrospinal leakage following neurological surgery (see section 5.