Europäische Union - Deutsch - EMA (European Medicines Agency)

eli lilly nederland b.v. - baricitinib - arthritis, rheumatoide - immunsuppressiva - 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 kann als monotherapie oder in kombination mit methotrexat verwendet werden. 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.

Europäische Union - Deutsch - EMA (European Medicines Agency)

gilead sciences ireland uc, galapagos nv - filgotinib maleate - arthritis, rheumatoide - immunsuppressiva - 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.

Europäische Union - Deutsch - EMA (European Medicines Agency)

pfizer europe ma eeig - konjugierte östrogene, bazedoxifene - nach den wechseljahren - conjugated estrogens und bazedoxifene - duavive ist indiziert zur:behandlung der östrogenmangel-symptome bei postmenopausalen frauen mit einer gebärmutter (mit mindestens 12 monate seit der letzten menstruation), bei denen eine behandlung mit gestagen-haltige therapie nicht geeignet ist. die erfahrung in der behandlung von frauen, die älter als 65 jahre ist begrenzt.

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

tetesept pharma gmbh - ascorbinsäure, pfefferminzöl, anisöl, bitterfenchelöl - lutschpastille - ascorbinsäure 10.mg; pfefferminzöl 6.mg; anisöl 2.mg; bitterfenchelöl 0.25mg

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

hra pharma rare diseases sas (8191301) - metyrapon - weichkapsel - teil 1 - weichkapsel; metyrapon (07640) 250 milligramm

Österreich - Deutsch - AGES (Agentur für Gesundheit und Ernährungssicherheit)

+pharma arzneimittel gmbh - levocetirizin dihydrochlorid -

Europäische Union - Deutsch - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - selektive immunsuppressiva - colitis colitisentyvio ist indiziert für die behandlung von erwachsenen patienten mit mittelschwerer bis schwerer aktiver colitis ulcerosa, die unzureichend mit, verloren, antwort, oder waren intolerant entweder konventionelle therapie oder tumor-nekrose-faktor alpha (tnfa) - antagonisten. morbus crohn diseaseentyvio ist indiziert für die behandlung von erwachsenen patienten mit mäßig bis schwer aktivem morbus crohn, die haben eine unzureichende antwort mit, verloren, antwort, oder waren intolerant entweder konventionelle therapie oder tumor-nekrose-faktor alpha (tnfa) - antagonisten. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Europäische Union - Deutsch - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - immunsuppressiva - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), 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). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Österreich - Deutsch - AGES (Agentur für Gesundheit und Ernährungssicherheit)

ucb pharma gmbh - levocetirizin dihydrochlorid - levocetirizin