الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

virbac s.a. - omega interferon rikombinanti ta 'oriġini qtates - immunostimulanti, - dogs; cats - dogsreduction of mortality and clinical signs of parvovirosis (enteric form) in dogs from one month of age. catstreatment of cats infected with feline leukaemia virus (felv) and / or feline immunodeficiency virus (fiv), in non-terminal clinical stages, from the age of nine weeks. in a field study conducted, it was observed that there was:a reduction of clinical signs during the symptomatic phase (four months);a reduction of mortality:in anaemic cats, mortality rate of about 60% at four, six, nine and 12 months was reduced by approximately 30% following treatment with interferon;in non-anaemic cats, mortality rate of 50% in cats infected by felv was reduced by 20% following treatment with interferon. fil-qtates infettati mill-fiv, il-mortalità kienet baxxa (5%) u ma kinitx influwenzata mit-trattament.

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

merck europe b.v.  - lutropin alfa - ovulation induction; infertility, female - - ormoni tas-sess u modulaturi ta ' l-ġenitali-sistema, - luveris fl-assoċjazzjoni mal-preparazzjoni (fsh) follicle-istimulazzjoni-ormoni huwa rakkomandat għall-istimulazzjoni ta ' l-iżvilupp follicular fin-nisa ma severi luteinising-ormoni (lh) u fsh defiċjenza. fi provi kliniċi, dawn il-pazjenti ġew definiti bil-livelli endoġeni tas-serum lh.

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

united therapeutics europe ltd - dinutuximab - neuroblastoma - aġenti antineoplastiċi - unituxin huwa indikat għat-trattament ta ' riskju għoli neuroblastoma fil-pazjenti l-età ta ' 12-il xahar li 17years, li kienu riċevuti induzzjoni chemotherapy qabel u miksub mill-inqas tweġiba parzjali, segwita minn terapija myeloablative u ċelluli staminali awtologi trapjant (asct). jingħata flimkien ma 'fattur li jistimula l-kolonja tal-granuloċit-makrofagi (gm-csf), interleukin-2 (il-2), u isotretinoin.

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

kyowa kirin holdings b.v. - naloxegol oxalate - constipation; opioid-related disorders - periferali tal-opioid antagonisti tar-riċettur-mediċini għall-istitikezza - trattament ta 'stitikezza kkawżata mill-opjojdi (oic) f'pazjenti adulti li kellhom rispons inadegwat għal-lassattiv (i).

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

esteve pharmaceuticals gmbh - ziconotide - injections, spinal; pain - analġeżiċi - ziconotide huwa indikat għall-kura ta 'uġigħ sever u kroniku f'pazjenti li jeħtieġu analġeżija intrateġika (it).

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabetes mellitus - drogi użati fid-dijabete - dijabete mellitus fejn huwa meħtieġ it-trattament bl-insulina. insulina bniedem winthrop mgħaġġla huwa wkoll adattat għat-trattament ta ' koma hyperglycaemic u ketoacidosis, kif ukoll għall-kisba minn qabel, intra - u postoperative stabbilizzazzjoni fil-pazjenti bl-diabetes mellitus.

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

laboratoire aguettant - sufentanil citrate - uġigħ - anestetiċi - dzuveo is indicated for the management of acute moderate to severe pain in adult patients.

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

helsinn birex pharmaceuticals ltd - netupitant, palonosetron hydrochloride - vomiting; neoplasms; nausea; cancer - anti-emetiċi u anti-nawżjanti, - akynzeo huwa indikat fl-adulti għall -: il-prevenzjoni tal-akuta u ttardjata dardir u r-rimettar assoċjati mal ferm emetoġenika bbażata fuq cisplatin kimoterapija tal-kanċer. il-prevenzjoni ta akuta u ttardjata'nawseja u rimettar assoċjati ma'kimoterapija tal-kanċer moderatament emetoġenika.

الاتحاد الأوروبي - المالطية - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabetes mellitus - drogi użati fid-dijabete - dijabete mellitus fejn huwa meħtieġ it-trattament bl-insulina. insuman rapid huwa wkoll adattat għall-kura ta 'koma ipergliċemika u ketoaċidożi, kif ukoll għall-kisba ta' stabilizzazzjoni minn qabel, intra u wara l-operazzjoni f'pazjenti bid-dijabete mellitus.

الاتحاد الأوروبي - المالطية - 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.