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

firmagon

ferring pharmaceuticals a/s - degareliksia - prostatiset kasvaimet - endokriinihoito - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Bayvantic vet paikallisvaleluliuos Suomi - suomi - Fimea (Suomen lääkevirasto)

bayvantic vet paikallisvaleluliuos

bayer animal health gmbh - permethrin, imidacloprid - paikallisvaleluliuos - permetriini

Bayvantic vet paikallisvaleluliuos Suomi - suomi - Fimea (Suomen lääkevirasto)

bayvantic vet paikallisvaleluliuos

bayer animal health gmbh - permethrin, imidacloprid - paikallisvaleluliuos - permetriini

Bayvantic vet paikallisvaleluliuos Suomi - suomi - Fimea (Suomen lääkevirasto)

bayvantic vet paikallisvaleluliuos

bayer animal health gmbh - permethrin, imidacloprid - paikallisvaleluliuos - permetriini

Bayvantic vet paikallisvaleluliuos Suomi - suomi - Fimea (Suomen lääkevirasto)

bayvantic vet paikallisvaleluliuos

bayer animal health gmbh - permethrin, imidacloprid - paikallisvaleluliuos - permetriini

Bayvantic vet paikallisvaleluliuos Suomi - suomi - Fimea (Suomen lääkevirasto)

bayvantic vet paikallisvaleluliuos

bayer animal health gmbh - permethrin, imidacloprid - paikallisvaleluliuos - permetriini

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

reblozyl

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - muut anemialääkkeet - reblozyl is indicated for the treatment of adult patients with transfusion-dependent anaemia due to very low, low and intermediate-risk myelodysplastic syndromes (mds) with ring sideroblasts, who had an unsatisfactory response to or are ineligible for erythropoietin-based therapy (see section 5. reblozyl is indicated in adults for the treatment of anaemia associated with transfusion dependent and non transfusion dependent beta thalassaemia (see section 5.

Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Euroopan unioni - suomi - EMA (European Medicines Agency)

lenalidomide krka (previously lenalidomide krka d.d. novo mesto)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - immunosuppressantit - multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) on tarkoitettu aikuisille potilaille, joilla on aiemmin hoitamaton multippeli myelooma, jotka eivät ole oikeutettuja siirto. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 ja 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) on tarkoitettu aikuisille potilaille, joilla on aiemmin hoitamaton multippeli myelooma, jotka eivät ole oikeutettuja siirto. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 ja 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Degarelix Accord Euroopan unioni - suomi - EMA (European Medicines Agency)

degarelix accord

accord healthcare s.l.u. - degarelix acetate - prostatiset kasvaimet - other hormone antagonists and related agents - degarelix accord is a gonadotrophin releasing hormone (gnrh) antagonist indicated:for treatment of adult male patients with advanced hormone-dependent prostate cancer. for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

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

broadline

boehringer ingelheim vetmedica gmbh - eprinomeettiini, fiproniili, pracilikanteli, (s) -metopreeni - antiparasitic products, insecticides and repellents, avermectins, eprinomectin, combinations, - kissat - kissat, joilla on tai jotka ovat vaarassa keskittyä hyönteisten, orgaanisten ja ektoparasiittien aiheuttamien sekaantumisten varalta. eläinlääke on tarkoitettu yksinomaan, kun kaikki kolme ryhmää ovat suunnattu samaan aikaan. ectoparasitestreatment ja ehkäisyyn loistartuntojen kirppujen (ctenocephalides felis). poistaminen kirput 24 tunnin kuluessa. yksi hoitokerta ehkäisee uusia tartuntoja vähintään yksi kuukausi. ehkäisy ympäristön kirppu saastuminen estämällä kehitys kirppu epäkypsä vaiheessa (munat, toukat ja kotelot) yli kuukauden. tuotetta voidaan käyttää osana hoidostrategiaa kirppuallergisen dermatiitin (fad). hoitoon ja ehkäisyyn loistartuntojen, jonka punkkeja (ixodes ricinus). poistaminen punkkeja 48 tunnin kuluessa. yksi hoitokerta ehkäisee uusia tartuntoja jopa 3 viikkoa. hoito notoedric mange (notoedres cati). cestodestreatment tartuntoja kanssa heisimato (dipylidium caninum, taenia taeniaeformis, echinococcus multilocularis, joyeuxiella pasqualei (aikuinen), ja joyeuxiella fuhrmanni (aikuinen)). nematodestreatment tartuntoja ruoansulatuskanavan sukkulamadot (l3 -, l4-toukat ja aikuiset toxocara cati, aikuiset sekä toxascaris leonina, l4-toukat ja aikuiset, ancylostoma tubaeforme-ja ancylostoma ceylanicum, ja aikuiset, ancylostoma brazilienze). hoito tartuntoja kanssa kissan lungworms (l3 toukat, l4-toukat ja aikuiset aelurostrongylus abstrusus, l4-toukat ja aikuiset troglostrongylus brevior). hoito tartuntoja kanssa matoja tai virtsarakon kaulan ahtauma (capillaria plica). ehkäisy sydänmatotartunnan (dirofilaria immitis-loisen toukat) yhden kuukauden.