Evrópusambandið - þýska - 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 - hämorrhagische fieber, ebola - - impfstoffe - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - karzinom, nicht kleinzellige lunge - antineoplastische mittel - 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.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - multiples myelom - 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.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - multiples myelom - antineoplastische mittel - 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.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - prostatahyperplasie neubildungen, kastration-resistentem - antineoplastische mittel - treatment of adult patients with prostate cancer.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international n.v.    - rilpivirinhydrochlorid - hiv-infektionen - antivirale mittel zur systemischen anwendung - edurant, wird in kombination mit anderen antiretroviralen arzneimitteln für die behandlung des humanen immundefizienz-virus typ 1 (hiv‑1) infektion bei antiretroviralen treatment‑naïve patienten 12 jahre und älter mit einer viruslast ≤ 100.000 hiv‑1 rna kopien/ml. wie bei anderen antiretroviralen arzneimitteln, genotypischen resistenzprüfung sollte die richtschnur für den einsatz von edurant.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international n.v. - darunavir, cobicistat - hiv-infektionen - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - rezolsta ist in kombination mit anderen antiretroviralen arzneimitteln zur behandlung der infektion mit dem humanen immundefizienzvirus 1 (hiv 1) bei erwachsenen ab 18 jahren indiziert. genotypische tests sollten als richtschnur für die verwendung von rezolsta.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international nv - canagliflozin - diabetes mellitus, typ 2 - drogen bei diabetes verwendet - invokana is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise:as monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 und 5.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international n.v.   - decitabin - leukämie, myeloid - antineoplastische mittel - behandlung von erwachsenen patienten mit neu diagnostizierter de novo oder sekundärer akuter myeloischer leukämie (aml) nach der klassifikation der weltgesundheitsorganisation (who), die keine kandidaten für eine standard-induktionschemotherapie sind.

Evrópusambandið - þýska - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir, cobicistat, emtricitabin, tenofovir alafenamide - hiv-infektionen - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - symtuza ist indiziert zur behandlung der infektion mit dem humanen immundefizienzvirus typ 1 (hiv-1) bei erwachsenen und jugendlichen (ab 12 jahren mit einem körpergewicht von mindestens 40 kg).. genotypic testing should guide the use of symtuza.