Evropska unija - slovenščina - EMA (European Medicines Agency)

sandoz gmbh - rituksimab - lymphoma, non-hodgkin; arthritis, rheumatoid; microscopic polyangiitis; wegener granulomatosis - antineoplastična sredstva - riximyo is indicated in adults for the following indications:non-hodgkin’s lymphoma (nhl)riximyo is indicated for the treatment of previously untreated adult patients with stage iii-iv follicular lymphoma in combination with chemotherapy. riximyo maintenance therapy is indicated for the treatment of adult follicular lymphoma patients responding to induction therapy. riximyo monotherapy is indicated for treatment of adult patients with stage iii-iv follicular lymphoma who are chemoresistant or are in their second or subsequent relapse after chemotherapy. riximyo is indicated for the treatment of adult patients with cd20 positive diffuse large b cell non-hodgkin’s lymphoma in combination with chop (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy. riximyo in combination with chemotherapy is indicated for the treatment of paediatric patients (aged ≥ 6 months to < 18 years old) with previously untreated advanced stage cd20 positive diffuse large b-cell lymphoma (dlbcl), burkitt lymphoma (bl)/burkitt leukaemia (mature b-cell acute leukaemia) (bal) or burkitt-like lymphoma (bll). chronic lymphocytic leukaemia (cll)riximyo in combination with chemotherapy is indicated for the treatment of patients with previously untreated and relapsed/refractory chronic lymphocytic leukaemia. samo omejeni so na voljo podatki o učinkovitosti in varnosti za bolnike predhodno zdravljenih z monoklonalna protitelesa, vključno z rituksimabom ali bolniki, ognjevzdržni, da prejšnji rituksimabom plus kemoterapijo. glej oddelek 5. 1 za nadaljnje informacije. rheumatoid arthritisriximyo in combination with methotrexate is indicated for the treatment of adult patients with severe active rheumatoid arthritis who have had an inadequate response or intolerance to other disease-modifying anti-rheumatic drugs (dmard) including one or more tumour necrosis factor (tnf) inhibitor therapies. rituksimabom je dokazano, da zmanjša stopnjo napredovanja skupno škodo, merjeno z x-ray in izboljšati telesno funkcijo, če bi imeli v kombinaciji z metotreksatom. granulomatosis with polyangiitis and microscopic polyangiitisriximyo, in combination with glucocorticoids, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (wegener’s) (gpa) and microscopic polyangiitis (mpa). riximyo, in combination with glucocorticoids, is indicated for the induction of remission in paediatric patients (aged ≥ 2 to < 18 years old) with severe, active gpa (wegener’s) and mpa. pemphigus vulgarisriximyo is indicated for the treatment of patients with moderate to severe pemphigus vulgaris (pv).

Evropska unija - slovenščina - EMA (European Medicines Agency)

gsk vaccines s.r.l. - zunanjo membrano semenskih mešičkov iz neisseria meningitidis skupina b (sev nz 98/254), rekombinantne neisseria meningitidis skupina b fhbp fuzijski protein, rekombinantne neisseria meningitidis skupina b nada beljakovin, rekombinantne neisseria meningitidis skupina b nhba fuzijski protein - meningitis, meningokokni - meningococcal cepiva - aktivna imunizacija proti invazivni bolezni, ki jo povzročajo sevi neisseria meningitidis serogroup-b.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

gsk vaccines srl - beljakovina nhba iz neisseria meningitidis skupine b, rekombinantna, fuzijska, beljakovina nada iz neisseria meningitidis skupine b, rekombinantna, beljakovina fhbp iz neisseria meningitidis skupine b, rekombinantna, fuzijska, vezikli zunanje membrane iz neisseria meningitidis skupine b sev nz98/254 - suspenzija za injiciranje - beljakovina nhba iz neisseria meningitidis skupine b, rekombinantna, fuzijska 50 µg / 0,5 ml; beljakovina nada iz neisseria meningitidis skupine b, rekombinantna 50 µg / 0,5 ml; beljakovina fhbp iz neisseria meningitidis skupine b, rekombinantna, fuzijska 50 µg / 0,5 ml; vezikli zunanje membrane iz neisseria meningitidis skupine b sev nz98/254 25 µg / 0,5 ml - večkomponentno cepivo proti meningokokom b

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

sandoz gmbh - rituksimab - koncentrat za raztopino za infundiranje - rituksimab 100 mg / 1 viala - rituksimab

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

sandoz gmbh - rituksimab - koncentrat za raztopino za infundiranje - rituksimab 500 mg / 1 viala - rituksimab

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

sandoz gmbh - rituksimab - koncentrat za raztopino za infundiranje - rituksimab 100 mg / 1 viala - rituksimab

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

sandoz gmbh - rituksimab - koncentrat za raztopino za infundiranje - rituksimab 500 mg / 1 viala - rituksimab

Evropska unija - slovenščina - EMA (European Medicines Agency)

gsk vaccines s.r.l. - konjugirano cepivo proti meningokokom skupine a, c, w-135 in y - immunization; meningitis, meningococcal - bakterijska cepiva - vialsmenveo je označen za aktivno imunizacijo otrok (od dveh let starosti), mladostnikom in odraslim na tveganje izpostavljenosti neisseria meningitidis skupine a, c, w135 in y, za preprečevanje invazivnih bolezni. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meningitis, meningokokni - cepiva - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

gsk d.o.o., ljubljana - virus mumpsa (sev jeryl lynn), živ, oslabljen; virus rdečk (sev wistar ra 27/3), živ, oslabljen; virus ošpic (sev schwarz), živ, oslabljen - prašek in vehikel za raztopino za injiciranje - virus mumpsa (sev jeryl lynn), živ, oslabljen 5011,87 ccid50 / 0,5 ml  virus rdečk (sev wistar ra 27/3), živ, oslabljen1000 ccid50 / 0,5 ml  virus ošpic (sev schwarz), živ, oslabljen1000 ccid50 / 0,5 ml; virus rdečk (sev wistar ra 27/3), živ, oslabljen 1000 ccid50 / 0,5 ml  virus ošpic (sev schwarz), živ, oslabljen1000 ccid50 / 0,5 ml; virus ošpic (sev schwarz), živ, oslabljen 1000 ccid50 / 0,5 ml - mešano cepivo proti ošpicam, mumpsu in rdečkam z oslabljenimi virusi