Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pacira ireland limited - bupivacaine - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

advanced accelerator applications - l-arginine hydrochloride, l-lysine hydrochloride - ir-radjazzjoni korrimenti - detoxifying agents for antineoplastic treatment - lysakare huwa indikat għat-tnaqqis tal-kliewi espożizzjoni għar-radjazzjoni matul il-peptide-riċettur radjunuklidi-terapija (prrt) ma lutetium (177lu) oxodotreotide fl-adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi b.v. - laronidase - mucopolysaccharidosis i - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - aldurazyme hu indikat għal enżimi fuq żmien twil terapija tas-sostituzzjoni f'pazjenti b'dijanjosi kkonfermata ta ' mucopolysaccharidosis i (mps i; alfa-l-iduronidase defiċjenza) biex jikkura l-nonneurological manifestazzjonijiet tal-marda.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

recordati ireland ltd. - lidocaine, prilocaine - disfunzjoni sesswali, fiżjoloġika - anestetiċi - trattament tal-eġakulazzjoni primarja prematura fl-irġiel adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

mallinckrodt pharmaceuticals ireland limited - fibrinoġen uman, trombina umana - hemostasi, kirurġiċi - sustanzi kontra l-emorraġija - trattament ta 'sostenn fejn it-tekniki kirurġiċi standard mhumiex biżżejjed għat-titjib tal-emostasi. raplixa għandu jintuża f'kombinazzjoni ma approvat ġelatina sponża. raplixa huwa indikat fl-adulti minn 18-il sena.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

viatris healthcare limited - tolcapone - marda ta 'parkinson - kontra l-marda ta ' parkinson id-drogi, aġenti dopaminerġiċi oħra - tasmar hija indikata fil kombinazzjoni ma ' ticlopidine hydrochloride / benserazide jew ticlopidine hydrochloride / carbidopa għall-użu fil-pazjenti ma ticlopidine hydrochloride-responsivi idiopathic parkinson's marda u oxxillazzjonijiet vetturi bil-mutur, li naqas milli jirrispondi għal jew huma intolerant ta ' xulxin inibituri ta ' catechol-o-methyltransferase (comt). minħabba r-riskju ta potenzjalment fatali, ħsara fil-fwied akut, tasmar ma għandhomx jiġu kkunsidrati bħala l-ewwel linja ta 'trattament miżjud ma' levodopa / benserazide jew levodopa / carbidopa. peress li tasmar għandu jiġi użat biss flimkien ma 'levodopa / benserazide u b'levodopa / carbidopa, l-tagħrif preskritt individwalment għal dawn l-sustanzi ta' levodopa hija applikabbli għall-użu tagħhom flimkien ma ' tasmar.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

fatro s.p.a - rabbit hemorrhagic disease virus 2 vp1ab, rabbit hemorrhagic disease virus vp1a - immunoloġiċi għall-leporidae - fniek - for active immunisation of rabbits from the age of 28 days to reduce mortality, infection, clinical signs and organ lesions of rabbit haemorrhagic disease caused by rhdv1 and rhdv2.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

corza medical gmbh - fibrinoġen uman, trombina umana - hemostasi, kirurġiċi - sustanzi kontra l-emorraġija - tachosil is indicated in adults and children from 1 month of age for supportive treatment in surgery for improvement of haemostasis, to promote tissue sealing and for suture support in vascular surgery where standard techniques are insufficient. tachosil is indicated in adults for supportive sealing of the dura mater to prevent postoperative cerebrospinal leakage following neurological surgery (see section 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - regdanvimab - covid-19 virus infection - sera immuni u immunoglobulini, - regdanvimab is indicated for the treatment of adults with coronavirus disease 2019 (covid-19) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

immedica pharma ab - glycerol phenylbutyrate - disturbi taċ-Ċiklu ta 'l-urea, inborn - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - ravicti huwa indikat għall-użu bħala terapija aġġuntiva għall-kroniku tal-ġestjoni ta 'pazjenti bil-urea disturbi fiċ-ċiklu (ucds) inklużi n-nuqqasijiet tal-carbamoyl phosphate-synthase-i (cps), ornithine carbamoyltransferase (otc), argininosuccinate synthetase (ass), argininosuccinate lyase (asl), arginase i (arg) u ornithine translocase defiċjenza hyperornithinaemia-iperammonemija homocitrullinuria sindromu (hhh) li ma jistgħux ikunu ġestiti mill-restrizzjoni ta' proteini tad-dieta u/jew l-aċidu amminiku supplimentazzjoni waħdu. ravicti għandhom jiġu użati mal-restrizzjoni ta ' proteini tad-dieta u, f'xi każijiet, supplimenti tad-dieta (e. , amino acids essenzjali, arginine, citrulline, supplimenti ta 'kaloriji mingħajr proteini).