Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka) Europska Unija - hrvatski - EMA (European Medicines Agency)

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

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - imunosupresivi - multiple myelomalenalidomide krka d. novo mesto 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 d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) indiciran za liječenje odraslih bolesnika s ranije нелеченной multiplog mijeloma koji se ne oslanja transplantacije. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto 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 d. novo mesto 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 d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) indiciran za liječenje odraslih bolesnika s ranije нелеченной multiplog mijeloma koji se ne oslanja transplantacije. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Europska Unija - hrvatski - 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 - imunosupresivi - 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) indiciran za liječenje odraslih bolesnika s ranije нелеченной multiplog mijeloma koji se ne oslanja transplantacije. 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 i 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) indiciran za liječenje odraslih bolesnika s ranije нелеченной multiplog mijeloma koji se ne oslanja transplantacije. 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 i 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).

Klaritromicin Krka 250 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

klaritromicin krka 250 mg filmom obložene tablete

krka d.d., novo mesto, Šmarješka cesta 6, novo mesto, slovenija - klaritromicin - filmom obložena tableta - 250 mg - urbroj: svaka filmom obložena tableta sadrži 250 mg klaritromicina

Klaritromicin Krka 500 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

klaritromicin krka 500 mg filmom obložene tablete

krka d.d., novo mesto, Šmarješka cesta 6, novo mesto, slovenija - klaritromicin - filmom obložena tableta - 500 mg - urbroj: svaka filmom obložena tableta sadrži 500 mg klaritromicina

DEXAMETHASON KRKA 4mg/ml Rastvor za injekciju Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

dexamethason krka 4mg/ml rastvor za injekciju

dio stranog druŠtva "krka d.d. novo mesto" slovenija - predstavniŠtvo podgorica - deksametazon - rastvor za injekciju - 4mg/ml

DEXAMETHASON KRKA 0.5mg Tableta Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

dexamethason krka 0.5mg tableta

dio stranog druŠtva "krka d.d. novo mesto" slovenija - predstavniŠtvo podgorica - deksametazon - tableta - 0.5mg

TRAMADOL KRKA 50mg/ml Rastvor za injekciju Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

tramadol krka 50mg/ml rastvor za injekciju

dio stranog druŠtva "krka d.d. novo mesto" slovenija - predstavniŠtvo podgorica - tramadol - rastvor za injekciju - 50mg/ml

TRAMADOL KRKA 100mg/2ml Rastvor za injekciju Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

tramadol krka 100mg/2ml rastvor za injekciju

dio stranog druŠtva "krka d.d. novo mesto" slovenija - predstavniŠtvo podgorica - tramadol - rastvor za injekciju - 100mg/2ml

Atazanavir Krka Europska Unija - hrvatski - EMA (European Medicines Agency)

atazanavir krka

krka, d.d., novo mesto - atazanavir (as sulfate) - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - atazanavir kapsule krka, uvedeni zajedno s malom dozom ritonavir, nije indiciran za liječenje hiv-1 zaraženih odraslih i pedijatrijska bolesnika 6 godina i stariji u kombinaciji s drugim antiretrovirusne lijekove. na osnovu вирусологических i kliničkih podataka kod odraslih pacijenata, nikakvu korist ne očekuje se da će u bolesnika s sojeva rezistentnih na više inhibitori proteaze (≥ 4 mutacije pi). izbor atazanavir krka u liječenju iskusni, odrasli i педиатрические pacijenti moraju se temeljiti na individualnoj virusne rezistencije i povijesti liječenja pacijenta .

Emtricitabine/Tenofovir disoproxil Krka d.d. Europska Unija - hrvatski - EMA (European Medicines Agency)

emtricitabine/tenofovir disoproxil krka d.d.

krka, d.d., novo mesto - эмтрицитабин, Тенофовир дизопроксил sukcinata - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - emtricitabin / tenofovir disoproksil krka d. naznačena je antiretrovirusnom kombinacijskom terapijom za liječenje hiv-1 inficiranih odraslih osoba. emtricitabin / tenofovir disoproksil krka d. također indiciran za liječenje hiv-1-zaražene mlade НИОТ otpor ili toksičnosti, isključuje primjena prvi agenata, u dobi od 12 do < 18 godina.