Euroopa Liit - eesti - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - artriit, reumatoidartriit - immunosupressandid - 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 võib kasutada monoteraapiana või kombinatsioonis metotreksaadiga. 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.

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accord healthcare b.v. - metotreksaat - infusioonilahuse kontsentraat - 100mg 1ml 5ml 5tk

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sandoz pharmaceuticals d.d. - metotreksaat - süstelahus süstlis - 10mg 1ml 2ml 4tk

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mepha-investigacao, desenvolvimento e fabricacao farmaceutica, lda - ibuprofeen - õhukese polümeerikattega tablett - 400mg 10tk; 400mg 100tk; 400mg 60tk; 400mg 20tk

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first pharma oÜ - metotreksaat - tablett - 2,5mg 100tk

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g.l. pharma gmbh - fingolimood - kõvakapsel - 0,5mg 98tk; 0,5mg 7tk

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norameda uab - fingolimood - kõvakapsel - 0,5mg 100tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

accord healthcare s.l.u. - fingolimod vesinikkloriid - sclerosis multiplex, relapsing-remitting - immunosuppressants, valikuline immunosuppressants - märgitud ühe haigust moduleeriva ravi väga aktiivne relapsing remitting sclerosis multiplex järgmiste rühmade täiskasvanud patsientidel ja lastel patsientidel vanuses 10 aastat ja vanemad:patsiendid, kellel on väga aktiivne haiguse vaatamata täielikku ja piisavat ravi vältel vähemalt ühe haigust moduleeriva therapyorpatients kiiresti arenev raske relapsing remitting sclerosis multiplex määratud 2 või enam puuet ägenemiste ühe aasta, ja on 1 või enam gadoliinium suurendada kahjustused aju mri või olulist kasvu, t2 kahjustus koormus võrreldes varasema hiljutise mrt.

Euroopa Liit - eesti - EMA (European Medicines Agency)

gilead sciences ireland uc, galapagos nv - filgotinib maleate - artriit, reumatoidartriit - immunosupressandid - rheumatoid arthritisjyseleca 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). jyseleca may be used as monotherapy or in combination with methotrexate (mtx). ulcerative colitisjyseleca is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic agent.

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grindeks as - fingolimood - kõvakapsel - 0,5mg 28tk