Unjoni Ewropea - Malti - EMA (European Medicines Agency)

neuraxpharm pharmaceuticals s.l. - ublituximab - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosoppressanti - briumvi is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pfizer europe ma eeig - ritlecitinib tosilate - alopecia areata - immunosoppressanti - litfulo is indicated for the treatment of severe alopecia areata in adults and adolescents 12 years of age and older.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - aġenti antineoplastiċi oħra - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi b.v. - imiglucerase - mard gaucher - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - cerezyme (imiglucerase) huwa indikat għall-użu bħala longterm enżima terapija ta ' sostituzzjoni fil-pazjenti bl-djanjosi konfermat ta ' non-neuronopathic (tip 1) jew neuronopathic kronika (tip 3) mard gaucher li jesebixxu klinikament sinifikanti nonneurological manifestazzjonijiet tal-marda. il-manifestazzjonijiet mhux newroloġiċi tal-marda gaucher jinkludu wieħed jew aktar mill-kondizzjonijiet li ġejjin:anemija wara l-esklużjoni ta 'kawżi oħra, bħal iron deficiencythrombocytopeniabone-marda wara l-esklużjoni ta' kawżi oħra bħal vitamina d deficiencyhepatomegaly jew splenomegalija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

alexion europe sas - asfotase alfa - hypofosfatija - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - strensiq huwa indikat għat-terapija tibdil fit-tul tal-enżima fil-pazjenti bl-iskoppjar paediatric hypophosphatasia biex jittrattaw il-manifestazzjonijiet tal-għadam tal-marda.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infezzjonijiet pnewmokokkali - vaċċini - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. ara t-taqsimiet 4. 4 u 5. 1 għal informazzjoni dwar il-protezzjoni kontra serotipi pnewmokokkiċi speċifiċi. apexxnar should be used in accordance with official recommendations. .

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - immunosoppressanti - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

amicus therapeutics europe limited - cipaglucosidase alfa - mard tal-Ħażna tal-glukoġen tat-tip ii - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - pombiliti (cipaglucosidase alfa) is a long-term enzyme replacement therapy used in combination with the enzyme stabiliser miglustat for the treatment of adults with late-onset pompe disease (acid α-glucosidase [gaa] deficiency).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - omalizumab - asthma; urticaria - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - allerġiċi asthmaxolair huwa indikat fl-adulti, l-adoloxxenti u t-tfal (6 sa.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

united therapeutics europe ltd - dinutuximab - neuroblastoma - aġenti antineoplastiċi - unituxin huwa indikat għat-trattament ta ' riskju għoli neuroblastoma fil-pazjenti l-età ta ' 12-il xahar li 17years, li kienu riċevuti induzzjoni chemotherapy qabel u miksub mill-inqas tweġiba parzjali, segwita minn terapija myeloablative u ċelluli staminali awtologi trapjant (asct). jingħata flimkien ma 'fattur li jistimula l-kolonja tal-granuloċit-makrofagi (gm-csf), interleukin-2 (il-2), u isotretinoin.