Den europeiske union - maltesisk - EMA (European Medicines Agency)

avimedical b.v. - itraconazole - antimikotiċi għall-użu sistemiku-derivati triazole, itraconazole - avjan - għat-trattament ta ' asperġillożi u kandidjasi fil-ħbieb l-għasafar,.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

pierre fabre medicament - vinflunine - carcinoma, transitional cell; urologic neoplasms - aġenti antineoplastiċi - javlor huwa indikat fil-monotherapy għat-trattament tal-pazjenti adulti b ' karċinoma transitorju b ' ċellola avvanzat jew metastatic tal-urothelial wara l-falliment tad-dożaġġ minn qabel li fihom il-platinu. l-effikaċja u s-sigurtà tal-vinflunine ma ġewx studjati f'pazjenti bi stejtus ta ' prestazzjoni ≥ 2.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

passauer pharma gmbh - mycophenolate mofetil - rifjut ta 'graft - immunosoppressanti - myclausen hija indikata fil kombinazzjoni ma ' ciclosporin u corticosteroids għall-profilassi ta ' rifjut transplant akuta fil-pazjenti li jirċievu trapjanti renali, kardijaċi jew epatiċi alloġenejċi.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

swedish orphan biovitrum ab - collagenase clostridium histolyticum - kuntratt dupuytren - mediċini oħra għal disturbi fis-sistema muskoloskeletali - , the treatment of dupuytren’s contracture in adult patients with a palpable cord. , it-trattament ta'rġiel adulti bil-marda ta'peyronie bil-kundizzjoni tal-plakka u l-liwi deformità tal mill-inqas 30 grad fil-bidu tat-terapija.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

ratiopharm gmbh - filgrastim - neutropenia; hematopoietic stem cell transplantation; cancer - immunostimulanti, - ratiograstim huwa indikat għall-tnaqqis fit-tul tal-neutropenia u l-inċidenza tal-marda bid-deni neutropenia fil-pazjenti trattati ma chemotherapy ċitotossiċi stabbiliti għall-malignancy (bl-eċċezzjoni tal-lewċemja myeloid kronika u myelodysplastic sindromi) u għat-tnaqqis fit-tul tal-neutropenia fil-pazjenti sottoposti għal terapija myeloablative segwit mill-mudullun trapjant meqjusa li huma f'riskju akbar ta ' neutropenia ħorox imtawla. is-sigurtà u l-effikaċja ta 'filgrastim huma simili fl-adulti u fit-tfal li qed jirċievu kimoterapija ċitotossika. ratiograstim huwa indikat għall-mobilizzazzjoni tal-taċ-ċelluli proġenitriċi tad-demm periferali (pbpc). f'pazjenti, tfal jew adulti, b'severa konġenitali, ċiklika, jew newtropenja idjopatika bl-għadd assolut ta 'newtrofili (anc) ta' ≤ 0. 5 x 109/l, u storja ta severi jew infezzjonijiet rikorrenti fit-tul fit-amministrazzjoni ta 'ratiograstim huwa indikat biex jiżdied l-għadd ta'newtrofili u biex inaqqas l-inċidenza u t-tul ta' l-infezzjoni avvenimenti relatati mal-. ratiograstim huwa indikat għall-kura ta ' newtropenja persistenti (anc ≤ 1. 0 x 109 / l) f'pazjenti b'infezzjoni avvanzata ta 'l-hiv, sabiex jitnaqqas ir-riskju ta' infezzjonijiet batteriċi meta għażliet oħra biex tiġi amministrata n-newtropenija mhumiex xierqa.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

alexion europe sas - eculizumab - emoglobinurja, paroxysmal - immunosoppressanti - soliris huwa indikat fl-adulti u t-tfal għall-kura ta': emoglobinurja notturnali parossimali (pnh). l-evidenza ta 'benefiċċju kliniku hija murija f'pazjenti b'emodijalisi ma' sintomi kliniċi(i) indikattiv ta'l-attività għolja tal-marda, irrispettivament mill-trasfużjoni-istorja (ara sezzjoni 5. atipiċi sindromu uremiku emolitiku (ahus). soliris huwa indikat fl-adulti għall-kura ta': ġeneralizzati refrattarji myasthenia gravis (gmg) f'pazjenti li huma kontra l-acetylcholine-riċettur (achr) antikorpi pożittivi (ara sezzjoni 5. neuromyelitis maws ottiku għall-logħob tal-ispettru disturb (nmosd) f'pazjenti li huma kontra l-aquaporin-4 (aqp4) antikorpi pożittivi bl-isklerożi multipla reċidiva-kors tal-marda.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

teva gmbh - filgrastim - neutropenia; hematopoietic stem cell transplantation; cancer - immunostimulanti, - tevagrastim huwa indikat għall-tnaqqis fit-tul tal-neutropenia u l-inċidenza tal-marda bid-deni neutropenia fil-pazjenti trattati ma chemotherapy ċitotossiċi stabbiliti għall-malignancy (bl-eċċezzjoni tal-lewċemja myeloid kronika u myelodysplastic sindromi) u għat-tnaqqis fit-tul tal-neutropenia fil-pazjenti sottoposti għal terapija myeloablative segwit mill-mudullun trapjant meqjusa li huma f'riskju akbar ta ' neutropenia ħorox imtawla. is-sigurtà u l-effikaċja ta 'filgrastim huma simili fl-adulti u fit-tfal li qed jirċievu kimoterapija ċitotossika. tevagrastim huwa indikat għall-mobilizzazzjoni tal-taċ-ċelluli proġenitriċi tad-demm periferali (pbpc). f'pazjenti, tfal jew adulti, b'severa konġenitali, ċiklika, jew newtropenja idjopatika bl-għadd assolut ta 'newtrofili (anc) ta' 0. 5 x 109/l, u storja ta severi jew infezzjonijiet rikorrenti fit-tul fit-amministrazzjoni ta 'tevagrastim huwa indikat biex jiżdied l-għadd ta'newtrofili u biex inaqqas l-inċidenza u t-tul ta' l-infezzjoni avvenimenti relatati mal-. tevagrastim huwa indikat għall-kura ta 'newtropenja persistenti (anc ta' inqas minn jew ugwali għal 1. 0 x 109 / l) f'pazjenti b'infezzjoni avvanzata ta 'l-hiv, sabiex jitnaqqas ir-riskju ta' infezzjonijiet batteriċi meta għażliet oħra biex tiġi amministrata n-newtropenija mhumiex xierqa.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

pfizer ireland pharmaceuticals - ceftaroline fosamil - community-acquired infections; skin diseases, infectious; pneumonia - antibatteriċi għal użu sistemiku, - zinforo is indicated for the treatment of the following infections in neonates, infants, children, adolescents and adults: , complicated skin and soft tissue infections (cssti), community-acquired pneumonia (cap) , consideration should be given to official guidance on the appropriate use of antibacterial agents.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

samsung bioepis nl b.v. - eculizumab - emoglobinurja, paroxysmal - immunosoppressanti - epysqli is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). evidence of clinical benefit is demonstrated in patients with haemolysis with clinical symptom(s) indicative of high disease activity, regardless of transfusion history.