Европейский союз - мальтийский - EMA (European Medicines Agency)

grunenthal gmbh - allopurinol, lesinurad - gotta - preparazzjonijiet antigout - duzallo huwa indikat fl-adulti għat-trattament ta'l-iperuriċemija fil-gotta pazjenti li ma kisbux-mira tal-uric acid fis-serum livelli b'doża adegwata ta ' allopurinol waħdu.

Европейский союз - мальтийский - EMA (European Medicines Agency)

bayer animal health gmbh - iron(iii) ion, toltrazuril - toltrazuril, kombinazzjonijiet - majjali (ħnienes) - għall-konkorrenti-prevenzjoni ta 'sinjali kliniċi tal-koċċidjożi (bħal dijarea) fit-trabi tat-twelid qżieqeż fuq l-irziezet kkonfermati b'-istorja tal-koċċidjożi kkawżati minn cystoisospora suis, u l-prevenzjoni ta 'defiċjenza ta' ħadid anemija.

Европейский союз - мальтийский - EMA (European Medicines Agency)

cis bio international - ioflupane (123l) - radionuclide imaging; dementia; movement disorders - radjofarmaċewtiċi dijanjostiċi - dan il-prodott mediċinali huwa għal użu dijanjostiku biss. striascan huwa indikat għall-osservazzjoni telf tal-funzjonali tan-newroni dopaminerġiċi terminali fl-istriatum:f'pazjenti adulti b'klinikament inċerti u sindromi ta'parkinson, per eżempju dawk b'sintomi bikrija, biex jgħin jagħraf bejn tregħid essenzjali u sindromi ta'parkinson relatati mal-marda idjopatika ta ' parkinson, atrofija multipla tas-sistema u progressive supranuclear palsy. striascan hija f'pożizzjoni li jiddistingwi bejn il-marda ta'parkinson, atrofija multipla tas-sistema u progressive supranuclear palsy. f'pazjenti adulti, li jgħin biex jiddistingwi-probabbiltà ta ' dimenzja b'lewy bodies mill-marda ta'alzheimer. striascan hija f'pożizzjoni li jiddiskriminaw bejn dimenzja mal-korpi lewy u l-marda ta ' parkinson id-dimenzja.

Европейский союз - мальтийский - EMA (European Medicines Agency)

intervet international b.v. - cell-associated live recombinant turkey herpesvirus (strain hvt/ndv/ilt) expressing the fusion protein of newcastle disease virus and the glycoproteins gd and gi of infectious laryngotracheitis virus - immunoloġiċi għall-għasafar - embryonated chicken eggs; chicken - for active immunisation of one-day-old chicks or embryonated chicken eggs:to reduce mortality and clinical signs caused by newcastle disease (nd) virus,to reduce mortality, clinical signs and lesions caused by avian infectious laryngotracheitis (ilt) virus and marek’s disease (md) virus.

Европейский союз - мальтийский - EMA (European Medicines Agency)

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Европейский союз - мальтийский - EMA (European Medicines Agency)

ascendis pharma endocrinology division a/s - lonapegsomatropin - growth and development - ormoni u analogi pitwitarji u ipotalamiċi - growth failure in children and adolescents aged from 3 years up to 18 years due to insufficient endogenous growth hormone secretion (growth hormone deficiency [ghd]),.

Европейский союз - мальтийский - EMA (European Medicines Agency)

horizon therapeutics ireland dac - inebilizumab - neuromyelitis optica - immunosoppressanti - uplizna is indicated as monotherapy for the treatment of adult patients with neuromyelitis optica spectrum disorders (nmosd) who are anti-aquaporin 4 immunoglobulin g (aqp4-igg) seropositive (see section 5.

Европейский союз - мальтийский - EMA (European Medicines Agency)

pfizer europe ma eeig  - rimegepant - disturbi fl-emigranja - antimigraine preparations, calcitonin gene-related peptide (cgrp) antagonists - vydura is indicated for theacute treatment of migraine with or without aura in adults;preventative treatment of episodic migraine in adults who have at least 4 migraine attacks per month.

Европейский союз - мальтийский - EMA (European Medicines Agency)

billev pharma aps - lutetium (177lu) chloride - radjonuklidi imaging - radjofarmaċewtiċi terapewtiċi - lutetium (177lu) chloride billev is a radiopharmaceutical precursor, and it is not intended for direct use in patients. it is to be used only for the radiolabelling of carrier molecules that have been specifically developed and authorised for radiolabelling with lutetium (177lu) chloride.

Европейский союз - мальтийский - EMA (European Medicines Agency)

novartis europharm limited - asciminib hydrochloride - lewkimja, mjeloġenika, kronika, bcr-abl pożittiva - aġenti antineoplastiċi - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.