Unjoni Ewropea - Malti - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97) - immunoloġiċi għall-felini, - qtates - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs ;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - rikombinanti turkija herpesvirus, tar-razza vhvt013-69, ħaj - immunoloġiċi għall-aves, tjur domestiċi, immunoloġiċi - embryonated eggs; chicken - għall-immunizzazzjoni attiva tal-flieles:biex tipprevjeni mwiet u biex tnaqqas sinjali kliniċi u leżjonijiet tal-marda infettiva bursal. biex tnaqqas l-imwiet, sinjali kliniċi u leżjonijiet tal-marda ta'marek.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

merial - eprinomectin - endectoċidi - bhejjem - it-trattament ta ' l-parassiti li ġejjin:roundworms gastrointestinali (adulti u l4):- ostertagia ostertagi/lyrata, cooperia oncophora/surnabada, c. punctata, haemonchus contortus, trichostrongylus axei, t. colubriformis, bunostomum phlebotomum, nematodirus helvetianus, oesophagostomum radiatumlungworm (adulti u l4):- dictyocaulus viviparuswarbles (parassiti-istadji):- hypoderma bovis, h. lineatummange dud:- sarcoptes scabiei var. bovis qamel: linognathus vituli, haematopinus eurysternus, solenoptes capillatushorn dubbien: haematobia irritansprevention tal-reinfections bil-parassiti li ġejjin:- dictyocaulus viviparus, ostertagia ostertagi/lyrata, trichostrongylus colubriformis, haemonchus contortus, u bunostomum phlebotomum;- oesophagostomum radiatum, cooperia oncophora/surnabada, c. punctata u trichostrongylus axei.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

viatris healthcare limited - fenofibrate, simvastatin - dyslipidemias - aġenti li jimmodifikaw il-lipidi - cholib huwa indikat bħala terapija adjunctive tad-dieta u jeżerċita fir-riskju għoli kardjovaskulari pazjenti adulti ma dyslipidaemia imħallat li tnaqqas it-trigliċeridi u jżidu l-livelli hdl c meta livelli ldl c huma kkontrollati b'mod adegwat bl-doża korrispondenti ta ' l- simvastatin monotherapy.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

allergan pharmaceuticals international ltd - trab tal-frixa - insuffiċjenza pankreatika exocrine - diġestivi, inkl. enżimi - trattament ta 'sostituzzjoni ta' enzimi pankreatiċi f'insuffiċjenza pankreatika exocrine minħabba fibrożi ċistika jew kundizzjonijiet oħra (e. pankreatite kronika, pankreatectomija ta 'wara jew kanċer tal-frixa). enzepi huwa indikat fit-trabi, tfal, l-adoloxxenti u l-adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

torbet laboratories ireland limited - urea (13c) - breath tests; helicobacter infections - aġenti dijanjostiċi - dan il-prodott mediċinali huwa għal użu dijanjostiku biss. għal dijanjosi in vivo ta ' helicobacter pylori gastroduwodenali (h. pylori) .

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - tolvaptan - kliewi poliċistiku, autosomal dominanti - id-dijuretiċi, - jinarc huwa indikat biex tnaqqas il-progressjoni tal-iżvilupp tal-Ġlata u insuffiċjenza renali tal-marda tal-kliewi polycystic dominanti autosomal (adpkd) fl-adulti b ' ckd stadju 1 sa 3 fil-bidu tat-trattament bi prova tal-marda malajr jipprogressa b ' mod.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

alexion europe sas - sebelipase alfa - metaboliżmu tal-lipidi, Żbalji inborn - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - kanuma huwa indikat għal terapija ta 'sostituzzjoni ta' enżimi fit-tul (ert) f'pazjenti ta 'etajiet kollha b'defiċjenza ta' lipase ta 'lysosomal acid (lal).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

alexion europe sas - eculizumab - emoglobinurja, paroxysmal - immunosoppressanti - soliris huwa indikat fl-adulti u t-tfal għall-kura ta': emoglobinurja notturnali parossimali (pnh). l-evidenza ta 'benefiċċju kliniku hija murija f'pazjenti b'emodijalisi ma' sintomi kliniċi(i) indikattiv ta'l-attività għolja tal-marda, irrispettivament mill-trasfużjoni-istorja (ara sezzjoni 5. atipiċi sindromu uremiku emolitiku (ahus). soliris huwa indikat fl-adulti għall-kura ta': ġeneralizzati refrattarji myasthenia gravis (gmg) f'pazjenti li huma kontra l-acetylcholine-riċettur (achr) antikorpi pożittivi (ara sezzjoni 5. neuromyelitis maws ottiku għall-logħob tal-ispettru disturb (nmosd) f'pazjenti li huma kontra l-aquaporin-4 (aqp4) antikorpi pożittivi bl-isklerożi multipla reċidiva-kors tal-marda.