Onpattro האיחוד האירופי - מלטית - EMA (European Medicines Agency)

onpattro

alnylam netherlands b.v. - patisiran sodium - amilojdożi, familjali - drogi oħra tas-sistema nervuża - onpattro huwa indikat għall-kura ta ' transthyretin medjat amilojdożi (hattr amilojdożi) f'pazjenti adulti bil-istadju ta'l-1 jew l-istadju 2 polinewropatija.

Pepaxti האיחוד האירופי - מלטית - EMA (European Medicines Agency)

pepaxti

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.

Yselty האיחוד האירופי - מלטית - EMA (European Medicines Agency)

yselty

theramex ireland limited - linzagolix choline - leiomyoma - ormoni u analogi pitwitarji u ipotalamiċi - yselty is indicated for the treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.

Plerixafor Accord האיחוד האירופי - מלטית - EMA (European Medicines Agency)

plerixafor accord

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - immunostimulanti, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Mycapssa האיחוד האירופי - מלטית - EMA (European Medicines Agency)

mycapssa

amryt pharmaceuticals dac - octreotide acetate - acromegaly - ormoni u analogi pitwitarji u ipotalamiċi - mycapssa is indicated for maintenance treatment in adult patients with acromegaly who have responded to and tolerated treatment with somatostatin analogues.

Bondenza (previously Ibandronic Acid Roche) האיחוד האירופי - מלטית - EMA (European Medicines Agency)

bondenza (previously ibandronic acid roche)

roche registration ltd. - ibandronic acid - l-osteoporożi, il-menopawża - drogi għat-trattament ta 'mard tal-għadam - trattament ta 'l-osteoporożi f'nisa wara l-menopawża b'riskju akbar ta' ksur. tnaqqis fir-riskju ta ' ksur vertebrali ġie muri. l-effikaċja fuq tal-femora-għonq ksur għadha ma ġietx stabbilita.

Capecitabine Accord האיחוד האירופי - מלטית - EMA (European Medicines Agency)

capecitabine accord

accord healthcare s.l.u. - capecitabine - colonic neoplasms; breast neoplasms; colorectal neoplasms; stomach neoplasms - aġenti antineoplastiċi - capecitabine accord huwa indikat għat-trattament awżiljarju ta 'pazjenti wara l-kirurġija ta' stadju iii (dukes 'stage-c) kanċer tal-kolon. capecitabine qbil huwa indikat għat-trattament tal-kanċer metastatiku tal-kolorektum. capecitabine qbil huwa indikat għall-kura preferita tal-kanċer gastriku avvanzat flimkien ma ' reġim ibbażat fuq il -. capecitabine qbil flimkien ma 'docetaxel huwa indikat għall-kura ta' pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment tal-kimoterapija ċitotossika. it-terapija ta 'qabel kellha tinkludi anthracycline. capecitabine qbil huwa wkoll indikat bħala monoterapija għall-kura ta 'pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment ta' taxanes u ta 'kors ta' kimoterapija li fihom jew li għalihom l-aktar anthracycline ma tkunx indikata t-terapija.

Capecitabine Medac האיחוד האירופי - מלטית - EMA (European Medicines Agency)

capecitabine medac

medac gesellschaft für klinische spezialpräparate mbh - capecitabine - neoplażmi kolorettali - aġenti antineoplastiċi - capecitabine medac huwa indikat għall-adjuvant trattament tal-pazjenti wara l-kirurġija fl-istadju tal-iii (dukes ta' stadju-c) tal-colon cancer. capecitabine medac huwa indikat għat-trattament tal-kanċer metastatiku tal-kolorektum. capecitabine medac huwa indikat għall-kura preferita tal-kanċer gastriku avvanzat flimkien ma ' reġim ibbażat fuq il -. capecitabine medac flimkien ma 'docetaxel huwa indikat għall-kura ta' pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment tal-kimoterapija ċitotossika. it-terapija ta 'qabel kellha tinkludi anthracycline. capecitabine medac huwa wkoll indikat bħala monoterapija għall-kura ta 'pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment ta' taxanes u ta 'kors ta' kimoterapija li fihom jew li għalihom l-aktar anthracycline ma tkunx indikata t-terapija.

Capecitabine Teva האיחוד האירופי - מלטית - EMA (European Medicines Agency)

capecitabine teva

teva pharma b.v. - capecitabine - colonic neoplasms; breast neoplasms; colorectal neoplasms; stomach neoplasms - aġenti antineoplastiċi - capecitabine teva huwa indikat għat-trattament awżiljarju ta 'pazjenti wara l-operazzjoni tal-istadju iii (dukes' stage c) kanċer tal-kolon. capecitabine teva huwa indikat għall-kura ta ' kanċer metastatiku tal-kolorektum. capecitabine teva huwa indikat għall‑kura preferita tal-kanċer gastriku avvanzat flimkien ma ' reġim ibbażat fuq il -. capecitabine teva flimkien ma 'docetaxel huwa indikat għall-kura ta' pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment tal-kimoterapija ċitotossika. it-terapija ta 'qabel kellha tinkludi anthracycline. capecitabine teva huwa wkoll indikat bħala monoterapija għall-kura ta 'pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment ta' taxanes u ta 'kors ta' kimoterapija li fihom jew li għalihom l-aktar anthracycline ma tkunx indikata t-terapija.

Ecansya (previously Capecitabine Krka) האיחוד האירופי - מלטית - EMA (European Medicines Agency)

ecansya (previously capecitabine krka)

krka, d.d., novo mesto - capecitabine - colonic neoplasms; breast neoplasms; colorectal neoplasms; stomach neoplasms - aġenti antineoplastiċi - ecansya huwa indikat għat-trattament awżiljarju ta 'pazjenti wara kirurġija ta' stadju iii (dukes 'stage-c) kanċer tal-kolon. ecansya huwa indikat għat-trattament tal-kanċer metastatiku tal-kolorektum. ecansya huwa indikat għall-kura preferita tal-kanċer gastriku avvanzat flimkien ma ' reġim ibbażat fuq il -. ecansya flimkien ma 'docetaxel huwa indikat għall-kura ta' pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment tal-kimoterapija ċitotossika. it-terapija ta 'qabel kellha tinkludi anthracycline. ecansya huwa wkoll indikat bħala monoterapija għall-kura ta 'pazjenti b'lokalment avvanzat jew tal-kanċer tas-sider metastatiku wara l-falliment ta' taxanes u ta 'kors ta' kimoterapija li fihom jew li għalihom l-aktar anthracycline ma tkunx indikata t-terapija.