Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fresenius medical care deutschland gmbh - glukosmonohydrat; kalciumkloriddihydrat; magnesiumkloridhexahydrat; natriumklorid; natriumvätekarbonat - hemodialysvätska/hemofiltrationsvätska - glukosmonohydrat 22 mg aktiv substans; magnesiumkloridhexahydrat 2,033 mg aktiv substans; kalciumkloriddihydrat 4,41 mg aktiv substans; natriumvätekarbonat 3,104 mg aktiv substans; natriumklorid 6,453 mg aktiv substans - hemofiltrationsvätskor

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fresenius medical care deutschland gmbh - glukosmonohydrat; kalciumkloriddihydrat; kaliumklorid; magnesiumkloridhexahydrat; natriumklorid; natriumvätekarbonat - hemodialysvätska/hemofiltrationsvätska - natriumklorid 6,453 mg aktiv substans; natriumvätekarbonat 3,104 mg aktiv substans; magnesiumkloridhexahydrat 2,033 mg aktiv substans; kalciumkloriddihydrat 4,41 mg aktiv substans; kaliumklorid 2,982 mg aktiv substans; glukosmonohydrat 22 mg aktiv substans - hemofiltrationsvätskor

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fresenius medical care deutschland gmbh - glukosmonohydrat; kalciumkloriddihydrat; kaliumklorid; magnesiumkloridhexahydrat; natriumklorid; natriumvätekarbonat - hemodialysvätska/hemofiltrationsvätska - kalciumkloriddihydrat 4,41 mg aktiv substans; glukosmonohydrat 22 mg aktiv substans; magnesiumkloridhexahydrat 2,033 mg aktiv substans; kaliumklorid 4,473 mg aktiv substans; natriumklorid 6,453 mg aktiv substans; natriumvätekarbonat 3,104 mg aktiv substans - hemofiltrationsvätskor

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fresenius medical care deutschland gmbh - glukosmonohydrat; kalciumkloriddihydrat; kaliumklorid; magnesiumkloridhexahydrat; natriumklorid; natriumvätekarbonat - hemodialysvätska/hemofiltrationsvätska - natriumvätekarbonat 3,104 mg aktiv substans; natriumklorid 6,453 mg aktiv substans; magnesiumkloridhexahydrat 2,033 mg aktiv substans; glukosmonohydrat 22 mg aktiv substans; kalciumkloriddihydrat 4,41 mg aktiv substans; kaliumklorid 5,964 mg aktiv substans - hemofiltrationsvätskor

Europeiska unionen - svenska - EMA (European Medicines Agency)

janssen-cilag international n.v. - daratumumab - multipelt myelom - monoclonal antibodies and antibody drug conjugates, antineoplastic agents - multiple myelomadarzalex is indicated: in combination with lenalidomide and dexamethasone or with bortezomib, melphalan and prednisone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant. i kombination med bortezomib, talidomid och dexametason för behandling av vuxna patienter med nyligen fått diagnosen multipelt myelom som är berättigade till autolog stamcellstransplantation. i kombination med lenalidomid och dexametason, eller bortezomib och dexametason, för behandling av vuxna patienter med multipelt myelom som har fått minst en tidigare behandling. in combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one prior therapy containing a proteasome inhibitor and lenalidomide and were lenalidomide refractory, or who have received at least two prior therapies that included lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or after the last therapy (see section 5. som monoterapi för behandling av vuxna patienter med återfall och eldfasta multipelt myelom, vars tidigare behandling ingår en proteasom-hämmare och en immunmodulerande substans avsedd att fungera som agent och som har visat att de försämras i sin sjukdom på den sista terapi. al amyloidosisdarzalex is indicated in combination with cyclophosphamide, bortezomib and dexamethasone for the treatment of adult patients with newly diagnosed systemic light chain (al) amyloidosis.

Europeiska unionen - svenska - EMA (European Medicines Agency)

accord healthcare s.l.u. - lenalidomid - multipelt myelom - immunsuppressiva - multiple myelomalenalidomide accord as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide accord as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) är indicerat för behandling av vuxna patienter med tidigare obehandlat multipelt myelom som inte är berättigade till transplantation. lenalidomid accord i kombination med dexametason är indicerat för behandling av multipelt myelom hos vuxna patienter som har fått minst en tidigare behandling. follicular lymphomalenalidomide accord in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Europeiska unionen - svenska - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ozanimod hydroklorid - multiple sclerosis, relapsing-remitting; colitis, ulcerative - immunsuppressiva - multiple sclerosiszeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (rrms) with active disease as defined by clinical or imaging features. ulcerative colitiszeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Europeiska unionen - svenska - EMA (European Medicines Agency)

mylan ireland limited - lenalidomid - multipelt myelom - immunsuppressiva - multiple myelomalenalidomide mylan as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide mylan as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. lenalidomide mylan 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 mylan in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1-3a).

Europeiska unionen - svenska - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - immunsuppressiva - 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) är indicerat för behandling av vuxna patienter med tidigare obehandlat multipelt myelom som inte är berättigade till transplantation. 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) är indicerat för behandling av vuxna patienter med tidigare obehandlat multipelt myelom som inte är berättigade till transplantation. 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).

Europeiska unionen - svenska - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - immunsuppressiva - 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) är indicerat för behandling av vuxna patienter med tidigare obehandlat multipelt myelom som inte är berättigade till transplantation. 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 och 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) är indicerat för behandling av vuxna patienter med tidigare obehandlat multipelt myelom som inte är berättigade till transplantation. 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 och 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).