Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ipsen pharma - cabozantinib - neoplażmi tat-tirojde - aġenti antineoplastiċi - trattament ta 'pazjenti adulti b'karċinoma medjulari tat-tirojde progressiva, li ma tistax tiġi mneħħija lokalment jew metastatika.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

takeda gmbh - pantoprazole - reflux gastroesofagi - inibituri tal-proton pump - trattament fuq medda qasira ta 'żmien ta' sintomi ta 'rifluss (e. ħruq ta 'stonku, riġenerazzjoni tal-aċidu) fl-adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - valsartan, amlodipine (as amlodipine besilate) - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'ipertensjoni essenzjali. copalia huwa indikat f'pazjenti li l-pressjoni tad-demm mhijiex ikkontrollata adegwatament bl-amlodipina jew valsartan monoterapija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

les laboratoires servier - ivabradine hydrochloride - angina pectoris; heart failure - it-terapija tal-qalb - kura sintomatika ta kronika stabbli, anġina pectorisivabradine huwa indikat għat-trattament tas-sintomi ta ' angina pectoris kronika stabbli fil-mard tal-arterji koronarji adulti b'ritmu sinusali normali u rata tal-qalb ≥ 70 bpm. ivabradine huwa indikat:fl-adulti li ma jistgħux jittolleraw jew bil-kontra-indikazzjoni għall-użu tal-beta-blockersor flimkien ma ' beta blockers f'pazjenti mhux ikkontrollati adegwatament bil-aħjar beta-blocker-doża. it-trattament tal-qalb kroniku failureivabradine huwa indikat f'insuffiċjenza kronika tal-qalb nyha ii-iv tal-klassi b'disfunzjoni sistolika, fil-pazjenti fl-sinus ritmiku u li d-rata tal-qalb huwa ≥ 75 bpm, f'kombinazzjoni ma ' terapija standard, inklużi l-beta-blockers jew meta beta-blockers huwa kontra-indikati jew mhux ittollerati.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - secukinumab - arthritis, psoriatic; psoriasis; spondylitis, ankylosing - immunosoppressanti - plaque psoriasiscosentyx is indicated for the treatment of moderate to severe plaque psoriasis in adults and children from the age of 6 years old who are candidates for systemic therapy. hidradenitis suppurativa (hs)cosentyx is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adults with an inadequate response to conventional systemic hs therapy. psorjatika arthritiscosentyx, waħdu jew f'taħlita ma 'methotrexate (mtx), huwa indikat għall-kura ta' artrite psorjatika attiva f'pazjenti adulti meta r-rispons għall-preċedenti li timmodifika l-marda anti rewmatiċi tad-droga (dmard) it-terapija kienet inadegwata. assjali aksjali (axspa)ankylosing spondylitis (as, radjografiku assjali aksjali)cosentyx huwa indikat għat-trattament ta ' ankylosing spondylitis attiva fl-adulti li ma kellhomx rispons xieraq għat-terapija konvenzjonali. non-radiographic axial spondyloarthritis (nr-axspa)cosentyx is indicated for the treatment of active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) evidence in adults who have responded inadequately to non steroidal anti inflammatory drugs (nsaids). juvenile idiopathic arthritis (jia)enthesitis-related arthritis (era)cosentyx, alone or in combination with methotrexate (mtx), is indicated for the treatment of active enthesitis-related arthritis in patients 6 years and older whose disease has responded inadequately to, or who cannot tolerate, conventional therapy. juvenile psoriatic arthritis (jpsa)cosentyx, alone or in combination with methotrexate (mtx), is indicated for the treatment of active juvenile psoriatic arthritis in patients 6 years and older whose disease has responded inadequately to, or who cannot tolerate, conventional therapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

recordati rare diseases - betaine anidru - homocystinurja - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - adjunctive treatment of homocystinuria, involving deficiencies or defects in:cystathionine beta-synthase (cbs);5,10-methylene-tetrahydrofolate reductase (mthfr);cobalamin cofactor metabolism (cbl). cystadane should be used as supplement to other therapies such as vitamin b6 (pyridoxine), vitamin b12 (cobalamin), folate and a specific diet.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

recordati rare diseases - mercaptamine hydrochloride - Ċistinosi - oftalmoloġiċi - cystadrops huwa indikat għat-trattament tad-depożiti tal-kristalli taċ-ċistini tal-kornea f'adulti u tfal minn sentejn b'ċistinosi.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

recordati rare diseases - mercaptamine bitartrate - Ċistinosi - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - cystagon huwa indikat għat-trattament ta 'ċistinosi nefropatika ppruvata. cysteamine jnaqqas l-akkumulazzjoni taċ-ċistina f'xi ċelluli (e. lewkoċiti, iċ-ċelloli tal-muskoli u l-fwied) tal-pazjenti nephropathic cystinosis u, meta t-trattament jibda kmieni, huwa dewmien l-iżvilupp tal-falliment renali.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

janssen-cilag international n.v.   - decitabine - lewkimja, myeloid - aġenti antineoplastiċi - trattament tal-pazjenti adulti ma intomx ġodda de novo jew sekondarja akuta myeloid lewċemja (aml), skond il-klassifika ta ' l-organizzazzjoni dinjija tas-saħħa (who), li ma jkunux dawk il-kandidati għall-induzzjoni standard chemotherapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - l-amlodipina, valsartan - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'ipertensjoni essenzjali. dafiro huwa indikat f'pazjenti li l-pressjoni tad-demm mhijiex ikkontrollata adegwatament bl-amlodipina jew valsartan monoterapija.