Spravato Evropska unija - slovenščina - EMA (European Medicines Agency)

spravato

janssen-cilag international nv - esketamine hidroklorid - depresivno motnjo - drugi antidepresivi - spravato, v kombinaciji s ssri ali snri, je indiciran za zdravljenje odraslih z odporno huda depresivna motnja, ki se niso odzvali na vsaj dveh različnih načinov zdravljenja z antidepresivi v tekočem zmerna do huda depresivna epizoda.

Zeftera (previously Zevtera) Evropska unija - slovenščina - EMA (European Medicines Agency)

zeftera (previously zevtera)

janssen-cilag international nv - ceftobiprole medocaril - skin diseases, infectious; soft tissue infections

Zabdeno Evropska unija - slovenščina - EMA (European Medicines Agency)

zabdeno

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

Mvabea Evropska unija - slovenščina - EMA (European Medicines Agency)

mvabea

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 - hemoragične mrzlice, ebola - cepiva - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Rekambys Evropska unija - slovenščina - EMA (European Medicines Agency)

rekambys

janssen-cilag international nv - rilpivirine - okužbe z virusom hiv - antivirusi za sistemsko uporabo - 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.

Jcovden (previously COVID-19 Vaccine Janssen) Evropska unija - slovenščina - EMA (European Medicines Agency)

jcovden (previously covid-19 vaccine janssen)

janssen-cilag international nv - adenovirus type 26 encoding the sars-cov-2 spike glycoprotein (ad26.cov2-s) - covid-19 virus infection - cepiva - jcovden is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 years of age and older. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Ponvory Evropska unija - slovenščina - EMA (European Medicines Agency)

ponvory

janssen-cilag international n.v.    - ponesimod - multiplo sklerozo, recidivno-nakazila - imunosupresivi - ponvory is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Rybrevant Evropska unija - slovenščina - EMA (European Medicines Agency)

rybrevant

janssen-cilag international n.v.    - amivantamab - karcinom, pljučni pljuč - antineoplastična sredstva - 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.

Carvykti Evropska unija - slovenščina - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - multiple myeloma - 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.

Tecvayli Evropska unija - slovenščina - EMA (European Medicines Agency)

tecvayli

janssen-cilag international n.v. - teclistamab - multiple myeloma - antineoplastična sredstva - 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.