Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international nv - esketamine-hidroklorid - depresszió - más antidepresszánsok - spravato, kombinálva egy ssri vagy snri, jelzi, hogy a felnőttek a kezelés-rezisztens súlyos depresszió, aki nem válaszolt, hogy legalább két különböző kezelések antidepresszánsok a jelenlegi mérsékelt vagy súlyos depressziós epizód.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international n.v.    - recombinant adenovirus type 26 (ad26) encoding the glycoprotein (gp) of the ebola virus zaire (zebov) mayinga strain - vérzéses láz, ebola - a vakcinák - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international n.v.    - recombinant modified vaccinia ankara bavarian nordic virus encoding the: ebola virus zaire (zebov) mayinga strain glycoprotein (gp); ebola virus sudan gulu strain gp; ebola virus taï forest strain nucleoprotein and the marburg virus musoke strain gp - vérzéses láz, ebola - a vakcinák - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international nv - rilpivirine - hiv fertőzések - vírusellenes szerek szisztémás alkalmazásra - rekambys is indicated, in combination with cabotegravir injection, for the treatment of human immunodeficiency virus type 1 (hiv 1) infection in adults who are virologically suppressed (hiv-1 rna < 50 copies/ml) on a stable antiretroviral regimen without present or past evidence of viral resistance to, and no prior virological failure with, agents of the nnrti and ini class.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - karcinóma, nem kissejtes tüdő - daganatellenes szerek - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - myeloma multiplex - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - myeloma multiplex - daganatellenes szerek - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - prosztata daganatok, kasztráció-rezisztens - daganatellenes szerek - treatment of adult patients with prostate cancer.

Europese Unie - Hongaars - EMA (European Medicines Agency)

janssen-cilag international n.v. - talquetamab - myeloma multiplex - daganatellenes szerek - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Hongarije - Hongaars - OGYÉI (Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézetről)

upjohn eesv - nicergoline -