Cimzia यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

cimzia

ucb pharma sa  - Цертолизумаб pegol - artritis, reumatoidni - imunosupresivi - reumatoidni arthritiscimzia, u kombinaciji sa metotreksatom (mtx), prikazan je za:liječenje umjereni do teški, aktivni reumatoidni artritis (ra) kod odraslih pacijenata, kada je u odgovoru na заболевани-razrađen antirheumatic napitke (dmards), uključujući i metotreksat, bio je neadekvatno. cimzia može biti dano kao monoterapija u slučaju netolerancije na mtx ili pri nastavak liječenja s mtx je inappropriatethe liječenje teških, aktivnog i uznapredovalog ra kod odraslih, koji nisu prethodno tretirani s mtx ili drugim lijekovima базисными. cimzia je pokazala da smanjuju brzinu progresije poraza zglobova, mjerene x-zračenja i poboljšati fizičku funkciju, kada se daje u kombinaciji s mtx. Аксиальный спондилоартрит cimzia indiciran za liječenje odraslih bolesnika s teškim aktivnim аксиальным спондилоартритом, uključujući:ankilozantni spondilitis (as)odrasle osobe s teškim aktivnim анкилозирующим спондилитом koji su imali neadekvatan odgovor ili netoleranciju nesteroidni protuupalni lijekovi (nsar). Аксиальный спон

Cimzia यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

cimzia

ucb pharma sa - Цертолизумаб pegol - crohn disease - imunosupresivi - cimzia, in combination with methotrexate (mtx), is indicated for the treatment of moderate to severe, active rheumatoid arthritis (ra) in adult patients when the response to disease-modifying antirheumatic drugs (dmard) including methotrexate, has been inadequate. cimzia može biti dano kao monoterapija u slučaju netolerancije метотрексата ili pri stalnom liječenju s metotreksat je nepraktično. cimzia has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function, when given in combination with methotrexate.

Entyvio यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

entyvio

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - selektivni imunosupresivi - colitisentyvio ulcerozni indiciran za liječenje odraslih bolesnika s вмеру na strogo aktivno язвенному колиту, koji su imali neadekvatan odgovor, izgubila odgovor, ili iz netrpeljivosti ili tradicionalne terapije ili faktor nekroze tumora alfa (Фноа) antagonist. diseaseentyvio kruna je indiciran za liječenje odraslih bolesnika s bolešću reumatoidnim kruna, koji su imali neadekvatan odgovor, izgubila odgovor, ili iz netrpeljivosti ili tradicionalne terapije ili faktor nekroze tumora alfa (Фноа) antagonist. 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.

ENTYVIO 300 mg/1 bočica prašak za koncentrat za otopinu za infuziju बोस्निया और हर्ज़ेगोविना - क्रोएशियाई - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

entyvio 300 mg/1 bočica prašak za koncentrat za otopinu za infuziju

takeda pharmaceuticals bh d.o.o. sarajevo - vedolizumab - prašak za koncentrat za otopinu za infuziju - 300 mg/1 bočica - 1 bočica praška za koncentrat za otopinu za infuziju sadrži: 300 mg vedolizumab

ENTYVIO 108 mg/1 šprica rastvor za injekciju u napunjenoj šprici बोस्निया और हर्ज़ेगोविना - क्रोएशियाई - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

entyvio 108 mg/1 šprica rastvor za injekciju u napunjenoj šprici

takeda pharmaceuticals bh d.o.o. sarajevo - vedolizumab - rastvor za injekciju u napunjenoj šprici - 108 mg/1 šprica - 1 napunjena šprica sa 0,68 ml rastvora za injekciju sadrži: 108 mg vedolizumaba

Nucala यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

nucala

glaxosmithkline trading services - mepolizumab - astma - lijekovi za opstruktivne plućne bolesti dišnih putova, - severe eosinophilic asthmanucala is indicated as an add-on treatment for severe refractory eosinophilic asthma in adults, adolescents and children aged 6 years and older. chronic rhinosinusitis with nasal polyps (crswnp)nucala is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adult patients with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate control. eosinophilic granulomatosis with polyangiitis (egpa)nucala is indicated as an add-on treatment for patients aged 6 years and older with relapsing-remitting or refractory eosinophilic granulomatosis with polyangiitis (egpa). hypereosinophilic syndrome (hes)nucala is indicated as an add-on treatment for adult patients with inadequately controlled hypereosinophilic syndrome without an identifiable non-haematologic secondary cause.

Tysabri यूरोपीय संघ - क्रोएशियाई - 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.

TYSABRI 300 mg/15 mL koncentrat za rastvor za infuziju बोस्निया और हर्ज़ेगोविना - क्रोएशियाई - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

tysabri 300 mg/15 ml koncentrat za rastvor za infuziju

medis international d.o.o. sarajevo - natalizumab - koncentrat za rastvor za infuziju - 300 mg/15 ml - 1 bočica sa 15 ml koncetrata za rastvor za infuziju sadrži: 300 mg natalizumaba

Tyruko यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

tyruko

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunosupresivi - tyruko is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis (rrms) for the following patient groups: patients with highly active disease 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 rrms defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain magnetic resonance imaging (mri) or a significant increase in t2 lesion load as compared to a previous recent mri.

ENTYVIO 108 mg/1 Pen rastvor za injekciju u napunjenom penu बोस्निया और हर्ज़ेगोविना - क्रोएशियाई - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

entyvio 108 mg/1 pen rastvor za injekciju u napunjenom penu

takeda pharmaceuticals bh d.o.o. sarajevo - vedolizumab - rastvor za injekciju u napunjenom penu - 108 mg/1 pen - 1 napunjen pen sa 0,68 ml rastvora za injekciju sadrži: 108 mg vedolizumaba