European Union - Swedish - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - multipelt myelom - antineoplastiska medel - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

European Union - Swedish - EMA (European Medicines Agency)

mylan ireland limited - fingolimod hydroklorid - multipel skleros, skovvis förlöpande - immunsuppressiva - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 och 5. 1)orpatients med snabbt föränderliga svår skovvis förlöpande multipel skleros definieras av 2 eller flera funktionsnedsättande skov under ett år och med 1 eller flera gadolinium öka skador på hjärnan mri eller en avsevärd ökning av t2-lesioner belastning jämfört med en tidigare senaste mrt.

European Union - Swedish - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - antineoplastiska medel - abecma 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.

European Union - Swedish - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - multipelt 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.

European Union - Swedish - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - multipelt myelom - antineoplastiska medel - 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.

European Union - Swedish - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - irbesartan - hypertension - agenter som verkar på renin-angiotensinsystemet - behandling av essentiell hypertoni. behandling av njursjukdom hos patienter med hypertoni och typ 2-diabetes mellitus som en del av ett blodtryckssänkande läkemedel regim (se avsnitt 5.

European Union - Swedish - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - irbesartan, hydroklortiazid - hypertension - agenter som verkar på renin-angiotensinsystemet - behandling av essentiell hypertoni. detta fast dos kombination är indicerat hos vuxna patienter vars blodtryck inte är adekvat kontrollerat om irbesartan eller hydroklortiazid ensam (se avsnitt 5.

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

boehringer ingelheim vetmedica gmbh - infektiöst fågelbronkitvirus, stam massachusetts h120, levande försvagat - brustablett till okulonasal suspension - infektiöst fågelbronkitvirus, stam massachusetts h120, levande försvagat 3,7 - 4,7 log10 eid50 aktiv substans; mannitol hjälpämne; para-orange hjälpämne - fjäderfä

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

orifarm ab - hepatit a-virus, inaktiverat antigen - injektionsvätska, suspension - 1440 elisa u/ml - fenylalanin hjälpämne; aluminiumoxid, hydratiserad 0,95 mg adjuvans; hepatit a-virus, inaktiverat antigen 1440 elisa e aktiv substans - inaktiverat helvirusvaccin

Sweden - Swedish - Läkemedelsverket (Medical Products Agency)

orifarm ab - hepatit b-virus, ytantigen (hbsag) - injektionsvätska, suspension, förfylld spruta - 10 mikrogram/0,5 ml - aluminiumoxid, hydratiserad 0,95 mg adjuvans; hepatit b-virus, ytantigen (hbsag) 20 mikrog aktiv substans - renat antigen