Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - imūnsupresanti - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Latvia - Latvia - Adama

adama - šķīstošs koncentrāts - fludioksonils + tebukonazols - citi produkti

Kesatuan Eropah - Latvia - 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.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

ceva santé animale - benazepril hydrochloride, spironolactone - cardiovascular system - suņi - lai ārstētu sirds mazspēju, ko izraisa hroniskas deģeneratīvas vārstuļu slimības suņiem (ja nepieciešams, ar diurētisku līdzekli).

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - lumacaftor, ivacaftor - cistiskā fibroze - other respiratory system products - orkambi tabletes ir indicēts, lai ārstētu cistiskā fibroze (cf) pacientiem vecumā no 6 gadiem un vecākiem, kas ir homozygous par f508del cftr mutācija gēnu. orkambi granules are indicated for the treatment of cystic fibrosis (cf) in children aged 1 year and older who are homozygous for the f508del mutation in the cftr gene.

Latvia - Latvia - Pārtikas un veterinārais dienests, Zemkopības ministrija

queisser pharma gmbh&co.kg - cits, Šķīdums

Latvia - Latvia - Pārtikas un veterinārais dienests, Zemkopības ministrija

natures s.r.o. vai sia „medpro nutraceuticals” - kapsula

Latvia - Latvia - Zāļu valsts aģentūra

lv system service sia, latvia - sorafenibs - apvalkotā tablete - 200 mg

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

bioprojet pharma - pitolisant - narkolepsija - other nervous system drugs - wakix is indicated in adults, adolescents and children from the age of 6 years for the treatment of narcolepsy with or without cataplexy (see also section 5.

Kesatuan Eropah - Latvia - EMA (European Medicines Agency)

theravia - cholic acid - digestive system diseases; metabolism, inborn errors - Žultsskābes un to atvasinājumi - orphacol tiek norādīts iedzimts kļūdas primāro žults skābes sintēze 3β-hidroksi-Δ5-c27-steroid oxidoreductase trūkumu vai zīdaiņiem, Δ4-3-oxosteroid-5β-reduktāzes trūkumu dēļ ārstēšanai bērniem un pusaudžiem vecumā no viena mēneša līdz 18 gadiem un pieaugušajiem.