Latvija - latviešu - Zāļu valsts aģentūra

lek pharmaceuticals d.d., slovenia - amoxicillinum, skābes clavulanicum - apvalkotā tablete - 875 mg/125 mg

Latvija - latviešu - Zāļu valsts aģentūra

glaxosmithkline latvia, sia, latvija - amoxicillinum, skābes clavulanicum - pulveris iekšķīgi lietojamas suspensijas pagatavošanai - 400 mg/57 mg/5 ml

Latvija - latviešu - Zāļu valsts aģentūra

lek pharmaceuticals d.d., slovenia - amoxicillinum, skābes clavulanicum - apvalkotā tablete - 875 mg/125 mg

Latvija - latviešu - Zāļu valsts aģentūra

lek pharmaceuticals d.d., slovenia - amoxicillinum, skābes clavulanicum - apvalkotā tablete - 875 mg/125 mg

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

janssen-cilag international n.v. - daratumumabs - multiple mieloma - 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. kopā ar bortezomib, talidomīds un deksametazona ārstēšanai pieaugušiem pacientiem, kuriem nesen diagnosticēta multiplā mieloma, kuri ir tiesīgi saņemt autologās cilmes šūnu transplantācijas. kopā ar lenalidomide un deksametazona, vai bortezomib un deksametazona, ārstēšanai pieaugušiem pacientiem ar multiplā mieloma, kuri ir saņēmuši vismaz vienu pirms terapijas. 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. kā monotherapy ārstēšanai pieaugušiem pacientiem ar relapsed un ugunsizturīgo multiplā mieloma, kuru pirms terapijas iekļauts proteasome inhibitoru un imūnmodulējošu līdzekli un kas ir pierādījuši slimības progresēšanu pēdējā terapija. 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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ozanimod hidrohlorīds - multiple sclerosis, relapsing-remitting; colitis, ulcerative - imūnsupresanti - 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.

Latvija - latviešu - Zāļu valsts aģentūra

merz pharmaceuticals gmbh, germany - toxinum botulinicum a sine proteinorum multiplex - pulveris injekciju šķīduma pagatavošanai - 50 vienības

Latvija - latviešu - Zāļu valsts aģentūra

merz pharmaceuticals gmbh, germany - toxinum botulinicum a sine proteinorum multiplex - pulveris injekciju šķīduma pagatavošanai - 100 vienības

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

accord healthcare s.l.u. - temozolomide - glioma; glioblastoma - antineoplastiski līdzekļi - pieaugušiem pacientiem ar nesen diagnosticētu multiformo glioblastomu vienlaikus ar staru terapiju (rt) un vēlāk kā monoterapijas terapiju. par attieksmi pret bērniem vecumā no trīs gadiem, pusaudžiem un pieaugušiem pacientiem ar ļaundabīgiem glioma, piemēram, glioblastoma multiforme vai anaplastic astrocytoma, parādot atkārtošanās vai progresēšanu pēc tam, kad standarta terapija.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

sanofi winthrop industrie - isatuximab - multiple mieloma - antineoplastiski līdzekļi - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.