Olumiant Europska Unija - hrvatski - EMA (European Medicines Agency)

olumiant

eli lilly nederland b.v. - baricitinib - artritis, reumatoidni - imunosupresivi - 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 se može koristiti kao monoterapija ili u kombinaciji s metotreksatom. 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.

Pregabalin Zentiva k.s. Europska Unija - hrvatski - EMA (European Medicines Agency)

pregabalin zentiva k.s.

zentiva k.s. - pregabalin - anxiety disorders; neuralgia; epilepsy - antiepileptici sredstva, - Нейропатическая painpregabalin Зентива k.. je indiciran za liječenje periferne i središnje neuropatske boli kod odraslih osoba. epilepsypregabalin Зентива k.. prikazuje se kao dodatna terapija kod osoba s парциальными судорогами sa ili bez sekundarne generalizacije. postati generalizirani anksioznosti disorderpregabalin Зентива k.. indiciran za liječenje generalizirani anksiozni poremećaj (gap) kod odraslih.

Pregabalin Zentiva Europska Unija - hrvatski - EMA (European Medicines Agency)

pregabalin zentiva

zentiva, k.s. - pregabalin - anxiety disorders; epilepsy - antiepileptici sredstva, - neuropathic pain , pregabalin zentiva is indicated for the treatment of peripheral and central neuropathic pain in adults. , epilepsy , pregabalin zentiva is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. , generalised anxiety disorder , pregabalin zentiva is indicated for the treatment of generalised anxiety disorder (gad) in adults.

Procoralan Europska Unija - hrvatski - EMA (European Medicines Agency)

procoralan

les laboratoires servier - ivabradin hidroklorid - angina pectoris; heart failure - srčana terapija - simptomatsko liječenje kronične stabilne angine pektoris ivabradin je indiciran za simptomatsko liječenje kronične stabilne angine pektoris u koronarne bolesti odraslih normalan sinusni ritam i puls ≥ 70 otkucaja u minuti. ivabradine is indicated :in adults unable to tolerate or with a contraindication to the use of beta-blockersor in combination with beta-blockers in patients inadequately controlled with an optimal beta-blocker dose. liječenje kroničnog zatajenja srca ivabradin je indiciran u kroničnom zatajenju srca nyha ii do iv sa sistoličkom u bolesnika u sinusni ritam i čiji je ≥ 75 otkucaja u minuti, u kombinaciji sa standardnom terapijom uključujući terapiju beta-blokator ili kada se beta-blokator terapija kontraindicirana ili ne podnosi.

Rasagiline ratiopharm Europska Unija - hrvatski - EMA (European Medicines Agency)

rasagiline ratiopharm

teva b.v. - rasagilin - parkinsonova bolest - antiparkinsonski lijekovi - rasagiline ratiopharm je indiciran za liječenje idiopatska parkinsonova bolest (pd) kao monoterapija (bez levodope) ili kao dodatak terapija (s levodopom) u bolesnika s kraja doze fluktuacije.

Silodyx Europska Unija - hrvatski - EMA (European Medicines Agency)

silodyx

recordati ireland ltd - silodosin - prostata hyperplasia - urologicals - liječenje znakova i simptoma benigne hiperplazije prostate (bph).

Tadalafil Lilly Europska Unija - hrvatski - EMA (European Medicines Agency)

tadalafil lilly

eli lilly nederland b.v. - tadalafil - poremećaj erekcije - urologicals - liječenje erektilne disfunkcije kod odraslih muškaraca. da bi tadalafil bio učinkovit, potrebna je seksualna stimulacija. tadalafil lilly ne navodi za žene. liječenje znakova i simptoma benigne hiperplazije prostate kod odraslih muškaraca.

Tadalafil Mylan Europska Unija - hrvatski - EMA (European Medicines Agency)

tadalafil mylan

mylan pharmaceuticals limited - tadalafil - poremećaj erekcije - urologicals - liječenje erektilne disfunkcije kod odraslih muškaraca. da bi tadalafil bio učinkovit, potrebna je seksualna stimulacija. tadalafil mylan u se ne navodi za žene.

Tysabri Europska Unija - hrvatski - EMA (European Medicines Agency)

tysabri

biogen netherlands b.v. - natalizumab - multipla skleroza - selektivni imunosupresivi - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 i 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Zoledronic acid Actavis Europska Unija - hrvatski - EMA (European Medicines Agency)

zoledronic acid actavis

actavis group ptc ehf   - monohidrat zoledronske kiseline - prijelom, kosti - lijekovi za liječenje bolesti kostiju - prevencija koštanog događaja (patološki prijelomi, spinalne kompresije, zračenja ili operacije na kostima, ili hiperkalcijemije) u odraslih bolesnika s uznapredovalim zloćudnim bolestima koje uključuju kosti. liječenje odraslih bolesnika s tumorom-induced гиперкальциемии.