levetiracetam stada arzneimittel 1000 mg filmom obalené tablety
stada arzneimittel ag, nemecko - levetiracetam - 21 - antiepileptica, anticonvulsiva
levetiracetam stada arzneimittel 500 mg filmom obalené tablety
stada arzneimittel ag, nemecko - levetiracetam - 21 - antiepileptica, anticonvulsiva
levetiracetam stada arzneimittel 250 mg filmom obalené tablety
stada arzneimittel ag, nemecko - levetiracetam - 21 - antiepileptica, anticonvulsiva
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 - imunosupresíva - 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) je indikovaný na liečbu dospelých predtým neliečených pacientov s myelómom je mladších, ktorí nie sú spôsobilí na transplantáciu. 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 a 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) je indikovaný na liečbu dospelých predtým neliečených pacientov s myelómom je mladších, ktorí nie sú spôsobilí na transplantáciu. 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 a 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).
azacitidine stada arzneimittel 25 mg/ml prášok na injekčnú suspenziu
stada arzneimittel ag, nemecko - azacitidín - 44 - cytostatica
losartan stada arzneimittel 50 mg filmom obalené tablety
stada arzneimittel ag, nemecko - losartan - 58 - hypotensiva
losartan/hydrochlorothiazide stada arzneimittel 100 mg/25 mg
stada arzneimittel ag, nemecko - losartan a diuretiká - 58 - hypotensiva
losartan/hydrochlorothiazide stada arzneimittel 50 mg/12,5 mg
stada arzneimittel ag, nemecko - losartan a diuretiká - 58 - hypotensiva
dabigatran-etexilát stada arzneimittel 75 mg tvrdé kapsuly
stada arzneimittel ag, nemecko - dabigatran-etexilát - 16 - anticoagulantia (fibrinolytica, antifibrinol.)
dabigatran-etexilát stada arzneimittel 110 mg tvrdé kapsuly
stada arzneimittel ag, nemecko - dabigatran-etexilát - 16 - anticoagulantia (fibrinolytica, antifibrinol.)