Sverige - svenska - Läkemedelsverket (Medical Products Agency)

octapharma ab - anti-d immunglobulin, humant - injektionsvätska, lösning i förfylld spruta - 625 ie/ml - anti-d immunglobulin, humant 625 ie aktiv substans - immunglobulin mot rh-immunisering

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

octapharma ab - anti-hepatit b-immunglobulin, humant - injektionsvätska, lösning - 200 ie/ml - anti-hepatit b-immunglobulin, humant 200 ie aktiv substans - immunglobulin mot hepatit b

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

omrix biopharmaceuticals sa - anti-hepatit b-immunglobulin, humant - infusionsvätska, lösning - 50 ie/ml - anti-hepatit b-immunglobulin, humant 50 ie aktiv substans - immunglobulin mot hepatit b

Europeiska unionen - svenska - EMA (European Medicines Agency)

takeda manufacturing austria ag - humant normalt immunoglobulin (ivig) - purpura, thrombocytopenic, idiopathic; bone marrow transplantation; immunologic deficiency syndromes; guillain-barre syndrome; mucocutaneous lymph node syndrome - immunförsvaret sera och immunglobuliner, - substitutionsterapi hos vuxna, samt barn och ungdomar (0-18 år) i:primär immunbrist syndrom med nedsatt antikroppar;hypogammaglobulinaemia och återkommande bakteriella infektioner hos patienter med kronisk lymfatisk leukemi, i vilken antibiotikaprofylax har misslyckats. hypogammaglobulinaemia och återkommande bakteriella infektioner i platå-fas-multipel myelom patienter som har misslyckats att svara på pneumokock-immunisering, hypogammaglobulinaemia hos patienter efter allogen hematopoetisk-stamcellstransplantation (hsct), medfödd aids och återkommande bakteriella infektioner. immunmodulering hos vuxna, samt barn och ungdomar (0-18 år) i:primära immun trombocytopeni (itp) hos patienter med hög risk för blödningar eller före en operation för att korrigera det antal blodplättar;guillain barré syndrom;kawasakis sjukdom;multifokal motorisk neuropati (mmn).

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

octapharma ab - anti-d immunglobulin, humant - injektionsvätska, lösning - 750 ie/ml - anti-d immunglobulin, humant 750 ie aktiv substans

Europeiska unionen - svenska - EMA (European Medicines Agency)

amgen europe b.v. - romiplostim - purpura, trombocytopenisk, idiopatisk - hemostatika - adults:nplate is indicated for the treatment of primary immune thrombocytopenia  (itp) in adult patients who are refractory to other treatments (e. kortikosteroider, immunoglobuliner). paediatrics:nplate is indicated for the treatment of chronic primary immune thrombocytopenia (itp) in paediatric patients one year of age and older who are refractory to other treatments (e. kortikosteroider, immunoglobuliner).

Europeiska unionen - svenska - EMA (European Medicines Agency)

stada arzneimittel ag - budesonide, micronised - glomerulonephritis, iga - antidiarrheals, tarm -, antiinflammatoriska / antiinfective agenter - kinpeygo is indicated for the treatment of primary immunoglobulin a (iga) nephropathy (igan) in adults at risk of rapid disease progression with a urine protein-to-creatinine ratio (upcr) ≥1. 5 g/gram.

Europeiska unionen - svenska - EMA (European Medicines Agency)

sanofi pasteur - chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated) - denguefeber - vacciner - dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 och 4. användning av dengvaxia bör ske i enlighet med officiella rekommendationer.

Europeiska unionen - svenska - EMA (European Medicines Agency)

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - denguefeber - vacciner - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

Europeiska unionen - svenska - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - immunsuppressiva - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.