Olumiant Uniunea Europeană - română - EMA (European Medicines Agency)

olumiant

eli lilly nederland b.v. - baricitinib - artrita, reumatoida - imunosupresoare - 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 poate fi utilizat ca monoterapie sau în asociere cu metotrexat. 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.

OLUMIANT 2 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

olumiant 2 mg

lilly s.a. - spania - baricitinibum - compr. film. - 2mg - imunosupresoare imunosupresoare selective

OLUMIANT 4 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

olumiant 4 mg

lilly s.a. - spania - baricitinibum - compr. film. - 4mg - imunosupresoare imunosupresoare selective

Ontozry Uniunea Europeană - română - EMA (European Medicines Agency)

ontozry

angelini pharma s.p.a - cenobamate - epilepsie - antiepileptice, - adjunctive treatment of focal-onset seizures with or without secondary generalisation in adult patients with epilepsy who have not been adequately controlled despite a history of treatment with at least 2 anti-epileptic medicinal products.

Cibinqo Uniunea Europeană - română - EMA (European Medicines Agency)

cibinqo

pfizer europe ma eeig  - abrocitinib - dermatita, atopică - alte preparate dermatologice - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

CIBINQO 100 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cibinqo 100 mg

pfizer manufacturing deutschland gmbh - germania - abrocitinibum - compr. film. - 100mg - preparate de uz dermatologic alte preparate de uz dermatologic

CIBINQO 200 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cibinqo 200 mg

pfizer manufacturing deutschland gmbh - germania - abrocitinibum - compr. film. - 200mg - preparate de uz dermatologic alte preparate de uz dermatologic

CIBINQO 50 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cibinqo 50 mg

pfizer manufacturing deutschland gmbh - germania - abrocitinibum - compr. film. - 50mg - preparate de uz dermatologic alte preparate de uz dermatologic

DIFLUCAN 10 mg/ml România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

diflucan 10 mg/ml

fareva amboise - franta - fluconazolum - pulb. pt. susp. orala - 10mg/ml - antimicotice de uz sistemic derivati de triazol

DIFLUCAN 150 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

diflucan 150 mg

fareva amboise - franta - fluconazolum - caps. - 150mg - antimicotice de uz sistemic derivati de triazol