Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

bayer ag - aflibercept - wet macular degeneration; macular edema; diabetes complications - oftalmoloġiċi - eylea huwa indikat għall-adulti għat-trattament ta': neovaskulari (imxarrba) relatata mal-età deġenerazzjoni makulari (amd);indeboliment tal-vista minħabba l-edima makulari sekondarja għal okklużjoni tal-vina tar-retina (il-fergħa rvo jew ċentrali rvo);indeboliment tal-vista minħabba ta 'edima makulari dijabetika (dme);indeboliment tal-vista minħabba myopic ġrieħi ta' neovaskularizzazzjoni korojdali (myopic cnv).

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - lanadelumab - angioedemas, ereditarji - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

bayer ag - vericiguat - insuffiċjenza tal-qalb - terapija kardijaka - treatment of symptomatic chronic heart failure.

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

bayer ag - riociguat - pressjoni għolja, pulmonari - antihypertensives għall-ipertensjoni arterjali pulmonari - chronic thromboembolic pulmonary hypertension (cteph)adempas is indicated for the treatment of adult patients with who functional class (fc) ii to iii withinoperable cteph,persistent or recurrent cteph after surgical treatment,to improve exercise capacity. pulmonary arterial hypertension (pah)adultsadempas, as monotherapy or in combination with endothelin receptor antagonists, is indicated for the treatment of adult patients with pulmonary arterial hypertension (pah) with who functional class (fc) ii to iii to improve exercise capacity. l-effikaċja ġiet murija fil-pah popolazzjoni inklużi l-etjoloġiji ta idjopatika jew li tintiret-pah jew pah assoċċjata ma'mard tal-connective tissue. paediatricsadempas is indicated for the treatment of pah in paediatric patients aged less than 18 years of age and body weight ≥ 50 kg with who functional class (fc) ii to iii in combination with endothelin receptor antagonists.

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

bpl bioproducts laboratory gmbh - - fattur tal-koagulazzjoni x - fattur x defiċjenza - vitamin k and other hemostatics, antihemorrhagics, coagulation factor x - coagadex huwa indikat għat-trattament u profilassi ta 'episodji ta' fsada u għal ġestjoni perioperattiva f'pazjenti b'defiċjenza ereditarja ta 'fattur x. coagadex huwa indikat fil-gruppi kollha tal-età.

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

pfizer europe ma eeig - nonacog alfa - hemofilja b - sustanzi kontra l-emorraġija - trattament u profilassi ta 'fsada f'pazjenti b'emofilja b (nuqqas konġenitali ta' fattur ix).

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

sanquin plasma products b.v. - fattur tal-koagulazzjoni uman ix - hemofilja b - sustanzi kontra l-emorraġija - trattament u profilassi ta 'fsada f'pazjenti b'emofilja b (defiċjenza konġenitali tal-fattur ix).

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

novo nordisk a/s - turoctocog alfa - hemofilja a - fattur viii tal-koagulazzjoni - trattament u profilassi ta 'fsada f'pazjenti b'emofilja a (nuqqas konġenitali ta' fattur viii). novoeight jista 'jintuża għall-etajiet kollha.

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

pfizer europe ma eeig - moroctocog alfa - hemofilja a - sustanzi kontra l-emorraġija - trattament u profilassi ta 'fsada f'pazjenti b'emofilja a (nuqqas konġenitali ta' fattur viii). refacto af hu adattat għall-użu fl-adulti u t-tfal ta ' kull età, inkluż trabi tat-twelid. refacto af ma fih l-von willebrand il-fattur, u għaldaqstant mhuwiex indikat fil-von willebrand-marda tal -.

Den Europæiske Union - maltesisk - EMA (European Medicines Agency)

baxalta innovations gmbh - nonacog gamma - hemofilja b - sustanzi kontra l-emorraġija - trattament u profilassi ta 'fsada f'pazjenti b'emofilja b (defiċjenza konġenitali tal-fattur ix).