União Europeia - maltês - EMA (European Medicines Agency)

bayer animal health gmbh - florfenicol, terbinafine hydrochloride, mometasone furoate - otologicals, kortikosterojdi u antiinfectives flimkien - klieb - għat-trattament ta 'klieb otite esterna jew l-aggravament akut ta' otite rikurrenti kkawżati minn infezzjonijiet imħalta tal suxxettibbli razez ta ' batterji sensittivi għall-florfenicol (staphylococcus pseudintermedius) u fungi sensittivi għall-terbinafine (malassezia pakidermatite).

União Europeia - maltês - EMA (European Medicines Agency)

vetcare oy - medetomidine hydrochloride, vatinoxan hydrochloride - psikoterapewtiċi, ipnotiċi u sedattivi - klieb - to provide restraint, sedation and analgesia during conduct of non-invasive, non-painful or mildly painful procedures and examinations intended to last no more than 30 minutes.

União Europeia - maltês - EMA (European Medicines Agency)

proveca pharma limited - glycopyrronium bromide - sialorrea - drogi għal disturbi gastro-intestinali funzjonali - trattament sintomatiċi tal sialorrhoea severa (drooling kronika patoloġiċi) fit-tfal u adolexxenti li għandhom 3 snin u aktar antiki b ' diżordni newroloġika kronika.

União Europeia - maltês - EMA (European Medicines Agency)

uniqure biopharma b.v.  - alipogene tiparvovec - iperlipoproteinemija tip i - aġenti li jimmodifikaw il-lipidi - glybera huwa indikat għal pazjenti adulti dijanjostikati b'defiċjenza ta 'lipoproteina lipase familjali (lpld) u li jbatu minn attakki severi jew multipli ta' pankreatite minkejja r-restrizzjonijiet tad-dieta tax-xaħam. id-dijanjożi ta 'lpld trid tiġi kkonfermata b'testjar ġenetiku. l-indikazzjoni hija ristretta għal pazjenti b'livelli li jistgħu jiġu osservati ta 'proteina lpl.

União Europeia - maltês - EMA (European Medicines Agency)

krka, d.d., novo mesto - irbesartan hydrochloride - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'ipertensjoni essenzjali. it-trattament tal-mard renali fil-pazjenti b'ipertensjoni u b'dijabete mellitus tip 2 bħala parti mill kontra l-pressjoni il-prodott mediċinali reġimen.

União Europeia - maltês - EMA (European Medicines Agency)

seqirus netherlands b.v. - a/darwin/6/2021(h3n2)-like strain (a/darwin/11/2021, wild type) / a/wisconsin/67/2022 (h1n1)pdm09-like strain (a/georgia/12/2022 cvr-167) / b/austria/1359417/2021-like strain (b/singapore/wuh4618/2021) / b/phuket/3073/2013-like virus (b/singapore/inftt-16-0610/2016, wild type) - influwenza, bniedem - l-influwenza, mhux attivat, maqsuma virus jew antiġen tal-wiċċ - prophylaxis of influenza in adults and children from 2 years of age. flucelvax tetra għandu jintuża skond ir-rakkomandazzjonijiet uffiċjali.

União Europeia - maltês - EMA (European Medicines Agency)

vericel denmark aps - kondroċiti kkultivati ​​awtologi - fratturi, qarquċa - mediċini oħra għal disturbi fis-sistema muskoloskeletali - tiswija ta 'difetti sintomiċi tal-qarquċa tal-irkoppa.

União Europeia - maltês - EMA (European Medicines Agency)

seqirus s.r.l.  - zoonotic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted), influenza virus surface antigens (haemagglutinin and neuraminidase) of strain: a/turkey/turkey/1/05 (h5n1)-like strain (nibrg-23) - influenza a virus, h5n1 subtype - vaċċini - active immunisation against h5 subtype of influenza a virus.

União Europeia - maltês - EMA (European Medicines Agency)

vbi vaccines b.v. - antigen tal-wiċċ ta 'l-epatite b - epatite b - vaċċini - prehevbri is indicated for active immunisation against infection caused by all known subtypes of the hepatitis b virus in adults. it can be expected that hepatitis d will also be prevented by immunisation with prehevbri as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection. the use of prehevbri should be in accordance with official recommendations.

União Europeia - maltês - EMA (European Medicines Agency)

sanofi pasteur - sars-cov-2 prefusion spike delta tm protein, recombinant (b.1.351 strain) - covid-19 virus infection - vaċċini - vidprevtyn beta is indicated as a booster for active immunisation to prevent covid-19 in adults who have previously received an mrna or adenoviral vector covid-19 vaccine (see sections 4. 2 u 5. 1 in product information document). l-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.