Европейски съюз - български - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - Артрит, ревматоиден - Имуносупресори - rheumatoid arthritisbaricitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). olumiant може да се използва като монотерапия или в комбинация с метотрексат. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.

Европейски съюз - български - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - Артрит, ревматоиден - Имуносупресори - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Европейски съюз - български - EMA (European Medicines Agency)

shionogi b.v. - оспемифен - postmenopause - Полови хормони и слиза на половата система, - senshio is indicated for the treatment of moderate to severe symptomatic vulvar and vaginal atrophy (vva) in post-menopausal women.

Европейски съюз - български - EMA (European Medicines Agency)

roche registration gmbh  - risdiplam - Мускулна атрофия, спинална - Други лекарства за нарушения на мускулно-скелетната система - evrysdi is indicated for the treatment of 5q spinal muscular atrophy (sma) in patients with a clinical diagnosis of sma type 1, type 2 or type 3 or with one to four smn2 copies.

Европейски съюз - български - EMA (European Medicines Agency)

zoetis belgium sa - оклацитиниб малеат - Средства за дерматит, с изключение на кортикостероиди - Кучета - - treatment of pruritus associated with allergic dermatitis in dogs. - treatment of clinical manifestations of atopic dermatitis in dogs.

Европейски съюз - български - EMA (European Medicines Agency)

virbac s.a. - хидрокортизон ацепонат - Кортикостероиди, дерматологични препарати - Кучета - За симптоматично лечение на възпалителни и сърбежни дерматози при кучета. for alleviation of clinical signs associated with atopic dermatitis in dogs.

Европейски съюз - български - EMA (European Medicines Agency)

ecuphar - хидрокортизон ацепонат - Кортикостероиди, дерматологични препарати - Кучета - За симптоматично лечение на възпалителни и сърбежни дерматози при кучета. for alleviation of clinical signs associated with atopic dermatitis in dogs.

Европейски съюз - български - EMA (European Medicines Agency)

leo pharma a/s - tralokinumab - Дерматит, Атопич - Други дерматологични препарати - adtralza is indicated for the treatment of moderate to severe atopic dermatitis in adult and adolescent patients 12 years and older who are candidates for systemic therapy.

Европейски съюз - български - EMA (European Medicines Agency)

pfizer europe ma eeig  - abrocitinib - Дерматит, Атопич - Други дерматологични препарати - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

Европейски съюз - български - EMA (European Medicines Agency)

almirall, s.a. - lebrikizumab - Дерматит, Атопич - Други дерматологични препарати - ebglyss is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older with a body weight of at least 40 kg who are candidates for systemic therapy.