Bulgària - búlgar - БАБХ (Българска агенция по безопасност на храните)

krka - Марбофлоксацин - инжекционен разтвор - 20 mg/ml - котки, кучета, свине, телета

Bulgària - búlgar - БАБХ (Българска агенция по безопасност на храните)

Асклеп- фарма ООД - Триметоприм; sulphadiazine - инжекционен разтвор - 40 mg /ml; 200 mg/ml - говеда, коне, котки, кучета, свине

Bulgària - búlgar - БАБХ (Българска агенция по безопасност на храните)

Асклеп- фарма ООД - Витамин А пальмитат, холекальциферол (витамин d3), витамин е ацетат, тиамин хидрохлорид (витамин В1), рибофлавин фосфат натрий (витамин В2), пиридоксин хидрохлорид (витамин В6), никотинамид, Декспантенол, цианокобаламин (витамин В12) - инжекционен разтвор - 15 000 iu/ml; 25 µg/ml; 20 mg/ml; 10 mg/ml; 5 mg/ml; 3 mg/ml; 35 mg/ml; 25 mg/ml; 25 µg/ml - говеда, коне, овце, свине

Bulgària - búlgar - БАБХ (Българска агенция по безопасност на храните)

bioveta, a.s. - cloprostenolum - инжекционен разтвор - 0, 250 mg/ml - кобили, крави, свине, юници

Bulgària - búlgar - БАБХ (Българска агенция по безопасност на храните)

vetviva richter ag - Бупренорфин - инжекционен разтвор - 0.3 mg/ml - котки, кучета

Unió Europea - búlgar - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - Антинеопластични средства - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Unió Europea - búlgar - EMA (European Medicines Agency)

bluebird bio (netherlands) b.v. - elivaldogene autotemcel - adrenoleukodystrophy - Други лекарства в нервната система - treatment of early cerebral adrenoleukodystrophy in patients less than 18 years of age, with an abcd1 genetic mutation, and for whom a human leukocyte antigen (hla) matched sibling haematopoietic stem cell donor is not available.

Unió Europea - búlgar - 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 - Антинеопластични средства - 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.

Unió Europea - búlgar - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - Антинеопластични средства - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.

Unió Europea - búlgar - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - Множествена миелома - 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.