União Europeia - maltês - EMA (European Medicines Agency)

biogen netherlands b.v. - diroximel fumarate (biib098) - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

União Europeia - maltês - EMA (European Medicines Agency)

mylan ireland limited - dimetil fumarate - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

União Europeia - maltês - EMA (European Medicines Agency)

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetil fumarate - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

União Europeia - maltês - EMA (European Medicines Agency)

teva gmbh - dimetil fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosoppressanti - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

União Europeia - maltês - EMA (European Medicines Agency)

accord healthcare s.l.u. - dimetil fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosoppressanti - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

União Europeia - maltês - EMA (European Medicines Agency)

atnahs pharma netherlands b.v. - ibandronic acid - l-osteoporożi, il-menopawża - drogi għat-trattament ta 'mard tal-għadam - it-trattament ta'l-osteoporożi f'nisa wara l-menopawża f'riskju miżjud ta'ksur (ara sezzjoni 5. tnaqqis fir-riskju ta ' ksur vertebrali ġie muri, l-effikaċja fuq il-ksur fl-għonq tal-femora ma ġietx stabbilita.

União Europeia - maltês - EMA (European Medicines Agency)

emdoka bvba - halofuginone lactate - halofuginone, oħra proto \ - aġenti tal - - għoġġiela, twelid - fl-għoġġiela tat-twelid:il-prevenzjoni ta 'dijarea \ ata minn cryptosoridium pavarum infezzjoni, f'irziezet bi storja ta' il-kriptosporidjosi. l-amministrazzjoni għandha tibda fl-ewwel 24 sa 48 siegħa. it-tnaqqis tad-dijarea \ ata minn cryptosoridium pavarum infezzjoni. l-amministrazzjoni għandha tibda fi żmien 24 siegħa wara l-bidu tad-dijarea. fiż-żewġ każijiet, it-tnaqqis ta 'l-eliminazzjoni ta' l-ooċisti intwera.

União Europeia - maltês - EMA (European Medicines Agency)

intervet international bv - halofuginone - antiprotozoali - għoġġiela, twelid - fil-tarbija tat-twelid calvesprevention ta 'dijarea minħabba dijanjostikati cryptosporidium parvum fl-irziezet bi storja ta' il-kriptosporidjosi. l-amministrazzjoni għandha tibda fl-ewwel 24 sa 48 siegħa. tnaqqis ta 'dijarrea minħabba dijanjożi cryptosporidium parvum. l-amministrazzjoni għandha tibda fi żmien 24 siegħa wara l-bidu tad-dijarea. fiż-żewġ każijiet, it-tnaqqis ta 'l-eskrezzjoni ta' l-ooċista ntwera.

União Europeia - maltês - EMA (European Medicines Agency)

virbac s.a. - halofuginone - antiprotozoali - għoġġiela, twelid - in new born calves:- prevention of diarrhoea due to diagnosed cryptosporidium parvum, in farms with history of cryptosporidiosis,administration should start in the first 24 to 48 hours of age- reduction of diarrhoea due to diagnosed cryptosporidium parvum. l-amministrazzjoni għandha tibda fi żmien 24 siegħa wara l-bidu tad-dijarea. fiż-żewġ każijiet, it-tnaqqis ta 'l-eliminazzjoni ta' l-ooċisti intwera.

União Europeia - maltês - EMA (European Medicines Agency)

univar solutions bv - trientene dihydrochloride - deġenerazzjoni epatoġenika - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - cufence huwa indikat għall-kura ta ' wilson tal-marda fil-pazjenti li ma jittollerawx d-penicillamine-terapija, fl-adulti u tfal 5 snin jew iktar.