Sverige - svenska - Läkemedelsverket (Medical Products Agency)

abbvie ab - ribavirin - filmdragerad tablett - 600 mg - ribavirin 600 mg aktiv substans; laktosmonohydrat hjälpämne - ribavirin

Europeiska unionen - svenska - EMA (European Medicines Agency)

gilead sciences ireland uc - bulevirtide acetate - hepatitis d, chronic - antivirala medel för systemisk användning - hepcludex is indicated for the treatment of chronic hepatitis delta virus (hdv) infection in plasma (or serum) hdv-rna positive adult patients with compensated liver disease.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - ribavirin - filmdragerad tablett - 200 mg - natriumlaurilsulfat hjälpämne; cetylalkohol hjälpämne; ribavirin 200 mg aktiv substans - ribavirin

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medartuum ab - ribavirin - filmdragerad tablett - 200 mg - cetylalkohol hjälpämne; natriumlaurilsulfat hjälpämne; ribavirin 200 mg aktiv substans - ribavirin

Europeiska unionen - svenska - EMA (European Medicines Agency)

novartis europharm limited - eltrombopag - purpura, trombocytopenisk, idiopatisk - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 och 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 och 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medac gesellschaft für klinische spezialpräparate mbh - azatioprin - filmdragerad tablett - 25 mg - laktosmonohydrat hjälpämne; azatioprin 25 mg aktiv substans - azatioprin

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medac gesellschaft für klinische spezialpräparate mbh - azatioprin - filmdragerad tablett - 50 mg - azatioprin 50 mg aktiv substans; laktosmonohydrat hjälpämne - azatioprin