ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - псориазис - Имуносупресори - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

accord healthcare s.l.u. - icatibant acetate - Ангиоедем, наследствено - other hematological agents - icatibant accord is indicated for symptomatic treatment of acute attacks of hereditary angioedema (hae) in adults, adolescents and children aged 2 years and older, with c1 esterase inhibitor deficiency.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

pfizer europe ma eeig  - tanezumab - osteoarthritis; pain - Аналгетици - treatment of moderate to severe chronic pain associated with osteoarthritis (oa) of the hip or knee in adult patients for whom treatment with non-steroidal anti-inflammatory drugs (nsaids) and/or any opioid is ineffective, not tolerated or inappropriate.

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

nordic group b.v. - Метотрексат - arthritis, psoriatic; psoriasis; arthritis, juvenile rheumatoid; arthritis, rheumatoid - Антинеопластични средства - nordimet is indicated for the treatment of:active rheumatoid arthritis in adult patients,polyarthritic forms of severe, active juvenile idiopathic arthritis (jia), when the response to nonsteroidal anti-inflammatory drugs (nsaids) has been inadequate,moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, and severe psoriatic arthritis in adult patients, induction of remission in moderate steroid-dependent crohn's disease in adult patients, in combination with corticosteroids and for maintenance of remission, as monotherapy, in patients who have responded to methotrexate.

বুলগেরিয়া - বুলগেরিয় - БАБХ (Българска агенция по безопасност на храните)

provet s. a. - Прокаин пеницилин g - инжекционна суспензия - 300 000 iu/ml - котки, кучета, овце, свине

বুলগেরিয়া - বুলগেরিয় - БАБХ (Българска агенция по безопасност на храните)

vetoquinol italia s.r.l. - Амоксицилин (като Амоксициллина тригидрат) - перорален прах - 800 mg/g - бройлери, прасета, пуйки

বুলগেরিয়া - বুলগেরিয় - БАБХ (Българска агенция по безопасност на храните)

industrial veterinaria, s.a. - Клоксациллин (бензатин) - интрамамарна суспензия - 500 mg/10 g - кози, крави, овце

বুলগেরিয়া - বুলগেরিয় - БАБХ (Българска агенция по безопасност на храните)

ДСМ ДЕНИТРАНС ООД - Бензилпенициллин прокаин; Дигидрострептомицин сулфат - инжекционна суспензия - 200 000 iu/ml; 250 mg/l - говеда, коне, кучета, овце, свине

বুলগেরিয়া - বুলগেরিয় - БАБХ (Българска агенция по безопасност на храните)

ВЕТПРОМ АД - sulfathiazole - перорален прах - 50 g/50 g - говеда, кози, коне, овце, свине

ইউরোপীয় ইউনিয়ন - বুলগেরিয় - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - lanadelumab - Ангиоедем, наследствено - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.