Thalidomide Lipomed Europska Unija - litavski - EMA (European Medicines Agency)

thalidomide lipomed

lipomed gmbh - talidomidas - daugybinė mieloma - imunosupresantai - thalidomide lipomed in combination with melphalan and prednisone is indicated as first line treatment of patients with untreated multiple myeloma, aged ≥ 65 years or ineligible for high dose chemotherapy. thalidomide lipomed is prescribed and dispensed in accordance with the thalidomide lipomed pregnancy prevention programme (see section 4.

Kyleena Litva - litavski - SMCA (Valstybinė vaistų kontrolės tarnyba)

kyleena

bayer ag - levonorgestrelis - vartojimo į gimdos ertmę sistema - 19,5 mg - plastic iud with progestogen

Fleree Litva - litavski - SMCA (Valstybinė vaistų kontrolės tarnyba)

fleree

bayer ag - levonorgestrelis - vartojimo į gimdos ertmę sistema - 13,5 mg - plastic iud with progestogen

Cardace Litva - litavski - SMCA (Valstybinė vaistų kontrolės tarnyba)

cardace

sanofi winthrop industrie - ramiprilis - tabletės - 2,5 mg; 10 mg - ramipril

Etrixenal Litva - litavski - SMCA (Valstybinė vaistų kontrolės tarnyba)

etrixenal

proenzi s.r.o. - naproksenas - tabletės - 250 mg - naproxen

Tobramycin Via pharma Litva - litavski - SMCA (Valstybinė vaistų kontrolės tarnyba)

tobramycin via pharma

via pharma, uab - tobramicinas - purškiamasis įkvepiamasis tirpalas - 300 mg/5 ml - tobramycin

CARPET B Litva - litavski - Ecolab

carpet b

ecolab deutschland gmbh -

Riximyo Europska Unija - litavski - EMA (European Medicines Agency)

riximyo

sandoz gmbh - rituksimabas - lymphoma, non-hodgkin; arthritis, rheumatoid; microscopic polyangiitis; wegener granulomatosis - antinavikiniai vaistai - 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. tik ribotą duomenų apie veiksmingumą ir saugumą pacientams, anksčiau gydomi monokloniniai antikūnai, įskaitant rituximab ar pacientams, ugniai atsparios į ankstesnį rituximab plius chemoterapija. Žr. skyrių 5. 1, jei norite gauti daugiau informacijos. 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. rituximab buvo įrodyta, kad sumažinti greitį progresavimą, bendrą žalą, vertinant pagal x-ray ir gerinti fizinę funkciją, skiriant kartu su metotreksatu. 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).