Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

janssen-cilag a/s - fentanyl - depotplastre - 12 mikrogram/time

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

janssen-cilag a/s - risperidon - filmovertrukne tabletter - 0,5 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

janssen-cilag a/s - risperidon - oral opløsning - 1 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

janssen-cilag a/s - risperidon - depotinjektionsvæske, pulver og solvens til suspension - 25 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

janssen-cilag international n.v. - darunavir, cobicistat - hiv infektioner - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - rezolsta, er indiceret i kombination med andre antiretrovirale lægemidler til behandling af human immunodeficiency virus 1 (hiv 1) infektion hos voksne i alderen 18 år eller derover. genotypiske test bør vejlede i brugen af rezolsta.

Den Europæiske Union - dansk - 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 - hæmoragisk feber, ebola - vacciner - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Den Europæiske Union - dansk - 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 - hæmoragisk feber, ebola - vacciner - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

janssen-cilag international n.v. - daratumumab - multipelt myelom - 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. i kombination med bortezomib, thalidomid og dexamethason til behandling af voksne patienter med nyligt diagnosticeret med myelomatose, der er berettiget til autolog stamcelletransplantation. i kombination med lenalidomid og dexamethason, eller bortezomib og dexamethason til behandling af voksne patienter med myelomatose, som har modtaget mindst én tidligere behandling. 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. som monoterapi til behandling af voksne patienter med recidiverende og refraktær myelomatose, hvis tidligere behandling indgår en proteasome-hæmmer og et immunmodulerende agent, og som har vist, sygdommens progression på den sidste terapi. 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.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

janssen-cilag international nv - ibrutinib - lymphoma, mantle-cell; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, protein kinase inhibitors - imbruvica as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl). imbruvica as a single agent or in combination with rituximab or obinutuzumab or venetoclax is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. imbruvica as a single agent or in combination with bendamustine and rituximab (br) is indicated for the treatment of adult patients with cll who have received at least one prior therapy. imbruvica as a single agent is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo immunotherapy. imbruvica in combination with rituximab is indicated for the treatment of adult patients with wm.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

janssen-cilag international nv - bedaquilinfumarat - tuberkulose, multidrugt-resistent - antimyco-bakterielle midler - sirturo er indiceret til brug som en del af en passende kombination regime for pulmonal multidrug resistente tuberkulose (mdr-tb) hos voksne og unge patienter (12 år til mindre end 18 år, og som vejer mindst 30 kg), når en effektiv behandling regime ellers ikke kan være sammensat på grund af resistens eller tolerance. det bør overvejes at officielle vejledning om hensigtsmæssig brug af antibakterielle midler..