Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - a vakcinák - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

nordic group b.v. - tegafur, gimeracil, oteracil - gyomor-daganatok - daganatellenes szerek - teysuno is indicated in adults:- for the treatment of advanced gastric cancer when given in combination with cisplatin (see section 5. - as monotherapy or in combination with oxaliplatin or irinotecan, with or without bevacizumab, for the treatment of patients with metastatic colorectal cancer for whom it is not possible to continue treatment with another fluoropyrimidine due to hand-foot syndrome or cardiovascular toxicity that developed in the adjuvant or metastatic setting.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

sanofi winthrop industrie - isatuximab - myeloma multiplex - daganatellenes szerek - 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.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - lamivudin - hepatitis b, krónikus - vírusellenes szerek szisztémás alkalmazásra - zeffix is indicated for the treatment of chronic hepatitis b in adults with: , compensated liver disease with evidence of active viral replication, persistently elevated serum alanine aminotransferase (alt) levels and histological evidence of active liver inflammation and / or fibrosis. beavatás a lamivudin kezelés csak akkor kell figyelembe venni, amikor a használt alternatív vírusellenes szer nagyobb genetikai akadály nem áll rendelkezésre, vagy megfelelő;, dekompenzált májbetegségben kombinálva egy második ügynök nélkül keresztrezisztencia lamivudin.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

merck sharp & dohme b.v. - elbasvir, grazoprevir - hepatitis c, krónikus - direct acting antivirals, antivirals for systemic use, antivirals for treatment of hcv infections - zepatier is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients 12 years of age and older who weigh at least 30 kg (see sections 4. 2, 4. 4 és 5. a hepatitis c vírus (hcv) genotípus specifikus tevékenység, lásd 4. 4 és 5.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

merck sharp and dohme b.v - a ribavirin - hepatitis c, krónikus - antivirals for systemic use, antivirals for treatment of hcv infections - a rebetol felnőttek krónikus hepatitis c (chc) kezelésére szolgáló egyéb gyógyszerkészítményekkel kombinációban szerepel. a rebetol feltüntetett kombinációban más gyógyszerekkel, a kezelés a krónikus hepatitis c (chc) a gyermekkorú (gyermek 3 éves, vagy annál idősebb, serdülők) korábban nem kezelt nélkül máj dekompenzáció.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

accord healthcare s.l.u. - kabazitaxel - prosztata daganatok, kasztráció-rezisztens - daganatellenes szerek - treatment of patients with hormone refractory metastatic prostate cancer previously treated with a docetaxel-containing regimen.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

sandoz gmbh - alfa-epoetin - anemia; kidney failure, chronic - antianémiás készítmények - treatment of symptomatic anaemia associated with chronic renal failure (crf) in adult and paediatric patients: , treatment of anaemia associated with chronic renal failure in paediatric and adult patients on haemodialysis and adult patients on peritoneal dialysis;, treatment of severe anaemia of renal origin accompanied by clinical symptoms in adult patients with renal insufficiency not yet undergoing dialysis;, treatment of anaemia and reduction of transfusion requirements in adult patients receiving chemotherapy for solid tumours, malignant lymphoma or multiple myeloma, and at risk of transfusion as assessed by the patient's general status (e. kardiovaszkuláris állapot, a már meglévő vérszegénység elején kemoterápia).

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

mylan pharmaceuticals limited - emtricitabin, tenofovir-dizoproxil-maleát - hiv fertőzések - vírusellenes szerek szisztémás alkalmazásra - treatment of hiv-1 infection:emtricitabine/tenofovir disoproxil mylan is indicated in antiretroviral combination therapy for the treatment of hiv-1 infected adults (see section 5. emtricitabine/tenofovir disoproxil mylan is also indicated for the treatment of hiv-1 infected adolescents, with nrti resistance or toxicities precluding the use of first line agents, (see sections 4. 2, 4. 4 és 5. pre-exposure prophylaxis (prep):emtricitabine/tenofovir disoproxil mylan is indicated in combination with safer sex practices for pre-exposure prophylaxis to reduce the risk of sexually acquired hiv-1 infection in adults and adolescents at high risk (see sections 4. 2, 4. 4 és 5.

Եվրոպական Միություն - հունգարերեն - EMA (European Medicines Agency)

hexal ag - alfa-epoetin - anemia; kidney failure, chronic; cancer - antianémiás készítmények - treatment of symptomatic anaemia associated with chronic renal failure (crf) in adult and paediatric patients: , treatment of anaemia associated with chronic renal failure in paediatric and adult patients on haemodialysis and adult patients on peritoneal dialysis;, treatment of severe anaemia of renal origin accompanied by clinical symptoms in adult patients with renal insufficiency not yet undergoing dialysis. a kezelés a vérszegénység csökkentése, valamint a transzfúzió felnőtt betegek kemoterápiás kezelés alatt a szolid tumor, malignus lymphoma, vagy myeloma multiplex, valamint a kockázata, transzfúzió, értékelte a beteg általános állapota (e. kardiovaszkuláris állapot, a már meglévő vérszegénység elején kemoterápia).