Unjoni Ewropea - Malti - EMA (European Medicines Agency)

theravia - aċidu kolesteriku - digestive system diseases; metabolism, inborn errors - - aċidi tal-bili u d-derivattivi - orphacol huwa indikat għall-kura ta ' l-iżbalji inborn fil-primarja tal-bili-aċidu sintesi minħabba n-nuqqas ta ' oxidoreductase 3β-hydroxy-Δ5-c27-steroid jew in-nuqqas ta ' Δ4-3-oxosteroid-5β-reductase fl-trabi, tfal u adolexxenti ta ' età xahar għal 18-il sena u adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

roche registration gmbh - methoxy polyethylene glycol-epoetin beta - anemia; kidney failure, chronic - preparazzjonijiet antianemiċi - treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adult patients (see section 5. treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (esa) after their haemoglobin level was stabilised with the previous esa (see section 5.

Unjoni Ewropea - Malti - 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.

Unjoni Ewropea - Malti - 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).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

crealta pharmaceuticals ireland limited - pegloticase - gotta - preparazzjonijiet antigout - krystexxa huwa indikat għall-kura ta ' severi gout debilitanti tophaceous kronika fil-pazjenti adulti li jistgħu wkoll ikollhom l-involviment konġunt erosive u li jkunu naqsu milli joqogħdu normalizzati serum uric acid b ' xanthine oxidase inibituri fil-massimu xieraq tad-doża jew li għalihom huma contraindicated dawn il-mediċini.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

recordati rare diseases - tocofersolan - cholestasis; vitamin e deficiency - vitamini - vedrop huwa indikat fl-defiċjenza ta ' vitamina-e minħabba l-malassorbazzjoni tad-diġestjoni fil-pazjenti pedjatriċi li jsofru minn cholestasis kronika konġenitali jew cholestasis kronika ereditarji, mit-twelid (fil-kelma newborns) sa 16 jew 18-il sena, skond ir-reġjun.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

merck sharp & dohme b.v. - peginterferon alfa-2b - epatite Ċ, kronika - immunostimulanti, - adults (tritherapy)pegintron in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. jekk jogħġbok irreferi għall-ribavirin u boceprevir-sommarji tal-karatteristiċi tal-prodott (smpcs) meta pegintron ikun ser jintuża flimkien ma ' dawn il-mediċini. adults (bitherapy and monotherapy)pegintron is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv. pegintron f'kombinazzjoni ma 'ribavirin (bitherapy) huwa indikat għall-kura ta chc infezzjoni fil-pazjenti adulti li ma kienux trattati qabel inkluż pazjenti b'hiv klinikament stabbli ko-infezzjoni u f'pazjenti adulti li jkunu fallew it-trattament preċedenti bl-interferon-alpha (pegilata jew mhux pegilata) u terapija kombinata b'ribavirin jew ma' interferon-alpha monoterapija. il-monoterapija b'interferon, li tinkludi pegintron, tintuża l-aktar f'każ ta 'intolleranza jew ta' kontra-indikazzjoni għal ribavirin. jekk jogħġbok irreferi għall-ribavirin smpc meta pegintron ikun ser jintuża flimkien ma ' ribavirin. paediatric population (bitherapy)pegintron is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents who have chc, previously untreated, without liver decompensation, and who are positive for hcv-rna. meta tiddeċiedi li ma li tipposponi it-trattament sakemm il-ħajja adulta, huwa importanti li wieħed jikkunsidra li l-terapija kombinata indotta-inibizzjoni tat-tkabbir li jista'jkun irriversibbli f'xi pazjenti. id-deċiżjoni li l-kura għandha tittieħed każ b'każ. jekk jogħġbok irreferi għall-ribavirin smpc għal kapsuli jew soluzzjoni orali meta pegintron ikun ser jintuża flimkien ma ' ribavirin.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zoetis belgium sa - virus tal-marda aujeszky ħaj attenwat - immunoloġiċi - majjali - immunizzazzjoni attiva ta 'majjali mill-età ta' 10 ġimgħat biex tevita l-mortalità u s-sinjali kliniċi tal-marda ta 'aujeszky u tnaqqas it-tneħħija tal-virus tal-qasam ta' aujeszky's disease. immunizzazzjoni passiva tal-frieħ tal-majjaliet vaċċinati sabiex titnaqqas il-mortalità u sinjali kliniċi tal-marda aujeszky u sabiex jitnaqqas l-eskrezzjoni tal-marda aujeszky-virus fil-qasam.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

bracco international b.v. - hexafluworidu tal-kubrit - ultrasonography; echocardiography - midja ta 'kuntrast - dan il-prodott mediċinali huwa għal użu dijanjostiku biss. sonovue hu għall-użu mal-viżjoni bl-ultrasawnd biex itejbu l-echogenicity tad-demm, jew ta ' fluwidi fil-apparat tal-awrina li jirriżulta f'titjib signal to noise ratio. sonovue għandu jintuża biss f'pazjenti fejn l-istudju mingħajr titjib tal-kuntrast ikun inkonklussiv. echocardiographysonovue huwa tal-kuntrast ekokardjografiku transpulmonari għall-użu f'pazjenti adulti b'suspett jew stabbilita mard kardjovaskulari biex jipprovdu opacification tal-kmamar tal-qalb u jsaħħaħ-ventrikolu tax-xellug endocardial-delineazzjoni tal-fruntiera. doppler tal-macrovasculaturesonovue iżid il-preċiżjoni fil-kxif jew l-esklużjoni ta ' anormalitajiet fl-arterji ċerebrali u extracranial karotide jew fl-arterji periferali f'pazjenti adulti billi jtejbu l-doppler signal to noise ratio. sonovue jżid il-kwalità tal-doppler tal-fluss tal-immaġni u l-tul tal-klinikament utli titjib tas-sinjal fl-evalwazzjoni tal-vina portali f'pazjenti adulti. doppler tal-microvasculaturesonovue itejjeb il-wiri tal-vaskularità tal-fwied u fis-sider feriti waqt il-doppler sonography f'pazjenti adulti li jwassal għal karatterizzazzjoni aktar speċifika tal-leżjonijiet. ultrasonografija tal-ħmieġ ta'l-imsaren fl-awrina tractsonovue huwa indikat għall-użu fil-ultrasonografija tal-ħmieġ ta'l-imsaren fl-apparat f'pazjenti pedjatriċi mill-tarbija tat-twelid sa 18-il sena li jiġi lokalizzat vesicoureteral rifluss. għal-limitazzjoni fl-interpretazzjoni ta negattiv urosonography.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - stavudine - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - iebes capsuleszerit huwa indikat flimkien ma ' prodotti mediċinali antiretrovirali oħra għat-trattament ta infettati bl-hiv pazjenti adulti u pazjenti pedjatriċi ('l fuq minn l-età ta'tliet xhur) biss meta l-mediċini antiretrovirali oħra ma jistgħux jintużaw. it-tul tat-terapija b'zerit għandha tiġi limitata għall-iqsar żmien possibbli. trab għall-ħalq solutionzerit huwa indikat flimkien ma ' prodotti mediċinali antiretrovirali oħra għat-trattament ta infettati bl-hiv pazjenti adulti u pazjenti pedjatriċi (mit-twelid) biss meta l-mediċini antiretrovirali oħra ma jistgħux jintużaw. it-tul tat-terapija b'zerit għandha tiġi limitata għall-iqsar żmien possibbli.