Európai Unió - máltai - EMA (European Medicines Agency)

krka, d.d., novo mesto - repaglinide - diabetes mellitus, tip 2 - drogi użati fid-dijabete - repaglinide huwa indikat fil-pazjenti bl-dijabete tat-tip-2 (mhux-insulina - dipendenti diabetes mellitus (niddm)) tagħhom hyperglycaemia jistgħu aktar jiġu kkontrollati b'mod sodisfaċenti minn dieta, piż tnaqqis u l-eżerċizzju. il-kura għandha tinbeda bħala żieda mad-dieta u l-eżerċizzju biex ibaxxi l-glucose fid-demm fir-rigward ta'l-ikel.

Európai Unió - máltai - EMA (European Medicines Agency)

bioprojet pharma - pitolisant - sleep apnea, obstructive - drogi oħra tas-sistema nervuża - ozawade is indicated to improve wakefulness and reduce excessive daytime sleepiness (eds) in adult patients with obstructive sleep apnoea (osa).

Európai Unió - máltai - EMA (European Medicines Agency)

dipharma arzneimittel gmbh - sapropterin dihydrochloride - phenylketonurias - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

Európai Unió - máltai - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - qasma-virus tal-influwenza, inattivat, li fih antiġen*:/california/7/2009 (h1n1)v like strain (x-179a)*propagati fil-bajd. - influenza, human; immunization; disease outbreaks - vaċċini ta 'l-influwenza - profilassi tal-influwenza f'sitwazzjoni pandemika ddikjarata uffiċjalment. il-vaċċin kontra l-influwenza pandemika għandu jintuża skond il-gwida uffiċjali.

Európai Unió - máltai - EMA (European Medicines Agency)

takeda manufacturing austria ag - proteina umana c - purpura fulminans; protein c deficiency - aġenti antitrombotiċi - ceprotin is indicated for prophylaxis and treatment of  purpura fulminans  coumarin-induced skin necrosis and venous thrombotic events in patients with severe congenital protein c deficiency.

Európai Unió - máltai - 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.

Európai Unió - máltai - EMA (European Medicines Agency)

accord healthcare s.l.u. - voriconazole - aspergillosis; candidiasis; mycoses - antimikotiċi għall-użu sistemiku-derivattivi tat-triazole - voriconazole huwa aġent broad-spectrum, aġent antifungali triazole u hija indikata fl-adulti u t-tfal li għandhom sentejn u aktar kif ġej:trattament ta 'asperġillożi invażiva;it-trattament ta'candidaemia f'pazjenti mhux newtropeniċi;il-kura ta' fluconazole-'infezzjonijiet invażivi serji candida reżistenti (inkluż c. krusei);il-kura ta'infezzjonijiet fungali serji kkawżati minn scedosporium spp. u fusarium spp. voriconazole għandu jingħata primarjament lil pazjenti b'progressiva, possibbilment ta'theddida għall-ħajja infezzjonijiet.

Európai Unió - máltai - EMA (European Medicines Agency)

torbet laboratories ireland limited - urea (13c) - breath tests; helicobacter infections - aġenti dijanjostiċi - dan il-prodott mediċinali huwa għal użu dijanjostiku biss. għal dijanjosi in vivo ta ' helicobacter pylori gastroduwodenali (h. pylori) .

Európai Unió - máltai - EMA (European Medicines Agency)

novartis europharm ltd - midostaurin - leukemia, myeloid, acute; mastocytosis - aġenti antineoplastiċi - rydapt huwa indikat:f'kombinazzjoni mal-istandard daunorubicin u cytarabine induzzjoni u doża għolja ta ' cytarabine konsolidazzjoni kimoterapija, u għall-pazjenti fil-rispons sħiħ segwit minn rydapt waħidha-manutenzjoni tal-kura, għall-pazjenti adulti li jkunu għadhom kif ġew dijanjostikati lewkimja majelojde akuta (aml) li huma flt3 mutazzjoni pożittivi (ara sezzjoni 4. 2);bħala monoterapija għall-kura ta ' pazjenti adulti b'aggressiva sistemika mastocytosis (asm), sistemika mastocytosis assoċjati mal-ematoloġiċi neoplażmi (sm ahn), jew tal-mast cell li lewkimja (mcl).

Európai Unió - máltai - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - doxorubicin hydrochloride - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - aġenti antineoplastiċi - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).