Unjoni Ewropea - Malti - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - afoxolaner - ectoparasiticides għal użu sistemiku - klieb - it-trattament tal-briegħed (ctenocephalides felis u c. canis) infestazzjonijiet. il-prodott jista 'jintuża bħala parti minn strateġija ta' trattament għall-kontroll tad-dermatite tal-allerġija tal-briegħed (fad). it-trattament ta ' qurdien (dermacentor reticulatus, ixodes ricinus, rhipicephalus sanguineus) infestazzjonijiet. trattament ta ' domodikosis (ikkawżata minn demodex canis). kura għal sarcoptic mange (ikkawżata minn sarcoptes scabiei var. canis).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ucb pharma s.a. - lacosamide - epilettiji, parzjali - anti-epilettiċi, - lacosamide ucb huwa indikat bħala monoterapija u terapija aġġuntiva fil-kura ta 'aċċessjonijiet ta' bidu parzjali bi jew mingħajr ġeneralizzazzjoni sekondarja f'adulti, adolexxenti u tfal minn 4 snin b'epilessija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - eprinomectin, esafoxolaner, praziquantel - eprinomectin, combinations, , avermectins, antiparasitic products, insecticides and repellents - qtates - for cats with, or at risk from mixed infections by cestodes, nematodes and ectoparasites. il-prodott mediċinali veterinarju huwa esklussivament indikat meta l-tliet gruppi huma maħsuba fl-istess ħin.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - psorajiżi - immunosoppressanti - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, 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). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

baxter holding b.v. - insulin human (rdna) - diabetes mellitus - drogi użati fid-dijabete - inpremzia is indicated for the treatment of diabetes mellitus.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

oncopeptides ab - melphalan flufenamide hydrochloride - majloma multipla - aġenti antineoplastiċi - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

substipharm - prasugrel - acute coronary syndrome; angina, unstable; myocardial infarction - aġenti antitrombotiċi - efient, ko amministrati bl-aċidu aċetilsaliċiliku (asa), huwa indikat għall-prevenzjoni ta ' avvenimenti ta ' atherothrombotic fil-pazjenti bl-sindromu coronary akuta (i. anġina instabbli, mhux-st-segment-elevazzjoni myocardial infarzjoni [ua / nstemi] jew st-segment-elevazzjoni myocardial infarzjoni [stemi]) li jkunu għaddejjin minn intervent coronary perkutanja (pci) ta ' primarja jew mdewma.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

merck sharp & dohme b.v. - sitagliptin - diabetes mellitus, tip 2 - drogi użati fid-dijabete - għall-pazjenti adulti b'dijabete tat-tip 2 mellitus, xelevia huwa indikat biex itejbu l-kontroll gliċemiku:bħala monoterapija:f'pazjenti li mhumiex ikkontrollati biżżejjed bid-dieta u l-eżerċizzju waħidhom u li għalihom metformin mhux adattat minħabba kontra-indikazzjonijiet jew intolleranza;bħala terapija dupliċi orali flimkien mal:metformin meta d-dieta u l-eżerċizzju flimkien ma 'metformin waħdu ma jipprovdux kontroll gliċemiku adegwat;sulphonylurea meta d-dieta u l-eżerċizzju flimkien ma' doża massima tollerata ta ' sulphonylurea waħedhom ma jipprovdux kontroll gliċemiku adegwat u meta metformin ma jkunx adegwat minħabba kontraindikazzjonijiet jew intolleranza;a peroxisome proliferator-activated receptor gamma (ppary) agonist (i. thiazolidinedione) meta l-użu ta'l-agonist ppary huwa xieraq u meta d-dieta u l-eżerċizzju flimkien ma 'l-agonist ppary waħdu ma jipprovdux kontroll gliċemiku adegwat;bħala terapija trippla orali f'kombinazzjoni ma': sulphonylurea u metformin meta d-dieta u l-eżerċizzju flimkien ma doppju it-terapija b'dawn il-prodotti mediċinali ma jipprovdux kontroll gliċemiku adegwat;ppary agonista u metformin meta l-użu ta'l-agonist ppary huwa xieraq u meta d-dieta u l-eżerċizzju flimkien ma doppju it-terapija b'dawn il-prodotti mediċinali ma jipprovdux kontroll gliċemiku adegwat. xelevia huwa wkoll indikat bħala żieda mal-insulina (bil-metformina jew mingħajrha) meta d-dieta u l-eżerċizzju flimkien ma doża stabbli ta ' l-insulina ma jipprovdux kontroll gliċemiku adegwat.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

merck sharp & dohme b.v. - sitagliptin, metformin hydrochloride - diabetes mellitus, tip 2 - drogi użati fid-dijabete - għall-pazjenti b'dijabete tat-tip 2 mellitus:velmetia huwa indikat bħala żieda mad-dieta u l-eżerċizzju biex itejjeb il-kontroll gliċemiku għal pazjenti mhux ikkontrollati adegwatament fuq id-doża massima ttollerata ta 'metformin waħdu jew għal dawk li diġà qegħdin jiġu kkurati b'kumbinazzjoni ta' sitagliptin u metformin. velmetia huwa indikat f'kombinazzjoni ma ' sulphonylurea (i. terapija ta 'kumbinazzjoni tripla) bħala żieda mad-dieta u l-eżerċizzju f'pazjenti mhux ikkontrollati adegwatament fuq id-doża massima ttollerata ta' metformin u sulphonylurea. velmetia huwa indikat bħala terapija ta 'kumbinazzjoni tripla ma' ppar-agonist (i. thiazolidinedione) bħala żieda mad-dieta u l-eżerċizzju f'pazjenti mhux ikkontrollati adegwatament fuq id-doża massima ttollerata ta ' metformin u agonista ppar. velmetia huwa indikat ukoll bħala add-on għall-insulina (i. terapija ta 'kumbinazzjoni tripla) bħala żieda mad-dieta u l-eżerċizzju biex itejjeb il-kontroll gliċemiku f'pazjenti meta stabbli fid-dożaġġ ta' l-insulina u metformin waħdu ma jipprovdux kontroll gliċemiku adegwat.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - majloma multipla - aġenti antineoplastiċi - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.