Europeiska unionen - svenska - 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.

Europeiska unionen - svenska - EMA (European Medicines Agency)

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - ritonavir - filmdragerad tablett - 100 mg - ritonavir 100 mg aktiv substans

Europeiska unionen - svenska - EMA (European Medicines Agency)

hra pharma rare diseases - ketokonazol - cushing syndrom - antimykotika för systemisk användning - ketokonazol hra är indicerat för behandling av endogent cushings syndrom hos vuxna och ungdomar över 12 år.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

accord healthcare b.v. - lopinavir; ritonavir - filmdragerad tablett - 200 mg/50 mg - lopinavir 200 mg aktiv substans; ritonavir 50 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - lopinavir; ritonavir - filmdragerad tablett - 200 mg/50 mg - ritonavir 50 mg aktiv substans; lopinavir 200 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pfizer ab - flukonazol - pulver till oral suspension - 10 mg/ml - natriumbensoat hjälpämne; flukonazol 10 mg aktiv substans; sackaros hjälpämne - flukonazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

omnia läkemedel ab - flukonazol - pulver till oral suspension - 10 mg/ml - sackaros hjälpämne; natriumbensoat hjälpämne; flukonazol 10 mg aktiv substans - flukonazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

omnia läkemedel ab - flukonazol - pulver till oral suspension - 10 mg/ml - sackaros hjälpämne; natriumbensoat hjälpämne; flukonazol 10 mg aktiv substans - flukonazol

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

omnia läkemedel ab - flukonazol - pulver till oral suspension - 10 mg/ml - flukonazol 10 mg aktiv substans; sackaros hjälpämne; natriumbensoat hjälpämne - flukonazol