DuoResp Spiromax Unjoni Ewropea - Malti - EMA (European Medicines Agency)

duoresp spiromax

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - asthma duoresp spiromax is indicated in adults and adolescents (12 years and older) for the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β₂ adrenoceptor agonist) is appropriate:in patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β₂ adrenoceptor agonists. orin patients already adequately controlled on both inhaled corticosteroids and long-acting β₂ adrenoceptor agonists. copdduoresp spiromax is indicated in adults, aged 18 years and older for the symptomatic treatment of patients with copd with forced expiratory volume in 1 second (fev₁).

Panretin Unjoni Ewropea - Malti - EMA (European Medicines Agency)

panretin

eisai gmbh - alitretinoin - sarcoma, kaposi - aġenti antineoplastiċi - panretin gel hija indikata għat-trattament topiku ta ' leżjonijiet fil-ġilda f'pazjenti b'akkwistat-immuni-defiċjenza tal-syndrome (aids) relatati mal-sarkoma ta'kaposi (ks) meta: - leżjonijiet ma jkunux ulcerated jew lymphoedematous, u;it-trattament tal-vixxri ks ma hija meħtieġa, u; - leżjonijiet huma li ma jkunux qed jirrispondu għal sistemika-terapija kombinata antiretrovirali, u;ir-radjuterapija jew kimoterapija mhumiex xierqa.

Kirsty (previously Kixelle) Unjoni Ewropea - Malti - EMA (European Medicines Agency)

kirsty (previously kixelle)

biosimilar collaborations ireland limited - insulin aspart - diabetes mellitus - drogi użati fid-dijabete - kirsty is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Truvelog Mix 30 Unjoni Ewropea - Malti - EMA (European Medicines Agency)

truvelog mix 30

sanofi winthrop industrie - insulin aspart - diabetes mellitus - drogi użati fid-dijabete - truvelog mix 30 is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 10 years and above.

Cystadane Unjoni Ewropea - Malti - EMA (European Medicines Agency)

cystadane

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.

Spikevax (previously COVID-19 Vaccine Moderna) Unjoni Ewropea - Malti - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vaċċini - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Conbriza Unjoni Ewropea - Malti - EMA (European Medicines Agency)

conbriza

pfizer europe ma eeig - bazedoxifene - l-osteoporożi, il-menopawża - - ormoni tas-sess u modulaturi ta ' l-ġenitali-sistema, - conbriza huwa indikat għall-kura tal-postmenopausal b'impenn li jissegwew għanijiet fin-nisa f'riskju akbar ta ' ksur. Ġie muri tnaqqis sinifikanti fl-inċidenza ta 'ksur vertebrali; l-effikaċja fuq il-ksur tal-ġenbejn ma ġietx stabbilita. meta jiddeterminaw l-għażla ta'conbriza jew terapiji oħra, inklużi l-estroġeni, għall-individwu mara wara l-menopawża, għandha tingħata konsiderazzjoni lill-sintomi tal-menopawsa, l-effetti fuq l-utru u tas-sider-tessuti, u kardjovaskulari ir-riskji u l-benefiċċji.

Dutrebis Unjoni Ewropea - Malti - EMA (European Medicines Agency)

dutrebis

merck sharp dohme limited - lamivudine, raltegravir potassju - infezzjonijiet ta 'hiv - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - dutrebis huwa indikat f ' għaqda ma ' oħrajn anti‑retroviral prodotti mediċinali għat-trattament ta ' l-infezzjoni tal-virus ta ' immunodefiċjenza umani (hiv‑1) fl-adulti, adolixxenti u tfal mill-età ta ' 6 snin u mill-anqas 30 kg mingħajr preżent użin jew imgħoddi evidenza ta ' reżistenza virali għal aġenti antivirali tal-insti (integrase il-faxxa trasferiment inhibitor) u nrti (inibitur ta ' rivers transcriptase nukleosidi) klassijiet (ara sezzjonijiet 4. 2, 4. 4 u 5.

Inovelon Unjoni Ewropea - Malti - EMA (European Medicines Agency)

inovelon

eisai gmbh - rufinamide - epilessija - anti-epilettiċi, - inovelon huwa indikat bhala terapija aġġuntiva fit-trattament ta 'aċċessjonijiet assoċjati mas-sindrome lennox gastaut f'pazjenti li għandhom 4 snin ta' età u anzjani.

Mircera Unjoni Ewropea - Malti - EMA (European Medicines Agency)

mircera

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.