Venlazid 75 mg Norvège - norvégien - Statens legemiddelverk

venlazid 75 mg

medical valley invest ab - venlafaksinhydroklorid - depottablett - 75 mg

Venlazid 225 mg Norvège - norvégien - Statens legemiddelverk

venlazid 225 mg

medical valley invest ab - venlafaksinhydroklorid - depottablett - 225 mg

Venlix 37.5 mg Norvège - norvégien - Statens legemiddelverk

venlix 37.5 mg

ratiopharm gmbh - venlafaksinhydroklorid - tablett - 37.5 mg

Travoprost/Timolol Medical Valley 40 mikrog/ ml / 5 mg/ ml Norvège - norvégien - Statens legemiddelverk

travoprost/timolol medical valley 40 mikrog/ ml / 5 mg/ ml

medical valley invest ab - travoprost / timololmaleat - Øyedråper, oppløsning - 40 mikrog/ ml / 5 mg/ ml

Travoprost/Timolol Mylan 40 mikrog/ ml / 5 mg/ ml Norvège - norvégien - Statens legemiddelverk

travoprost/timolol mylan 40 mikrog/ ml / 5 mg/ ml

mylan ab - travoprost / timololmaleat - Øyedråper, oppløsning - 40 mikrog/ ml / 5 mg/ ml

Fixopost 50 mikrog/ ml / 5 mg/ ml Norvège - norvégien - Statens legemiddelverk

fixopost 50 mikrog/ ml / 5 mg/ ml

laboratoires thea s.a.s - latanoprost / timololmaleat - Øyedråper, oppløsning i endosebeholder - 50 mikrog/ ml / 5 mg/ ml

Pamorelin 3.75 mg Norvège - norvégien - Statens legemiddelverk

pamorelin 3.75 mg

institut produits synthèse (ipsen) ab - triptorelinembonat - pulver og væske til depotinjeksjonsvæske, suspensjon - 3.75 mg

Buprefarm 15 mikrog/ time Norvège - norvégien - Statens legemiddelverk

buprefarm 15 mikrog/ time

orifarm generics a/s - buprenorfin - depotplaster - 15 mikrog/ time

Abiraterone Accord Union européenne - norvégien - EMA (European Medicines Agency)

abiraterone accord

accord healthcare s.l.u. - abirateronacetat - prostata neoplasmer - endokrin terapi - abiraterone accord is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicatedthe treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Union européenne - norvégien - 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 - immunsuppressive - 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) er indisert for behandling av voksne pasienter med tidligere ubehandlet myelomatose som ikke er kvalifisert for transplantasjon. 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 og 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) er indisert for behandling av voksne pasienter med tidligere ubehandlet myelomatose som ikke er kvalifisert for transplantasjon. 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 og 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).