Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

sanofi-aventis lietuva, uab - levofloksacinas - plėvele dengtos tabletės - 250 mg - levofloxacin

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

sanofi winthrop industrie - levofloksacinas - plėvele dengtos tabletės - 500 mg - levofloxacin

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

sanofi-aventis lietuva, uab, lietuva - levofloksacinas - plėvele dengtos tabletės - 250 mg - levofloxacin

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

sanofi-aventis lietuva, uab - levofloksacinas - infuzinis tirpalas - 5 mg/ml - levofloxacin

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

sanofi-aventis lietuva, uab - levofloksacinas - infuzinis tirpalas - 5 mg/ml - levofloxacin

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antinavikiniai vaistai - tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) after two or more lines of systemic therapy.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

janssen-cilag international n.v. - talquetamab - daugybinė mieloma - antinavikiniai vaistai - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - daugybinė mieloma - 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.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

amgen europe b.v. - blinatumomabas - prekursorių ląstelių limfoblastinė leukemija-limfoma - antinavikiniai vaistai - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

amivas ireland ltd - artesunate - maliarija - antiprotoziniai preparatai - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. reikėtų atsižvelgti į oficialius nurodymus, kaip tinkamai naudoti vaistus nuo maliarijos sukėlėjų.