Unión Europea - maltés - EMA (European Medicines Agency)

valneva austria gmbh - covid-19 vaccine (inactivated, adjuvanted, adsorbed) - covid-19 virus infection - vaċċini - covid-19 vaccine (inactivated, adjuvanted) valneva is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 to 50 years of age.  the use of this vaccine should be in accordance with official recommendations.

Unión Europea - maltés - EMA (European Medicines Agency)

biogen netherlands b.v. - diroximel fumarate (biib098) - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

Unión Europea - maltés - EMA (European Medicines Agency)

pierre fabre medicament - busulfan - trapjant ta 'ċelloli staminali ematopojetiċi - aġenti antineoplastiċi - busilvex segwit minn cyclophosphamide (bucy2) huwa indikat bħala kondizzjonament trattament qabel haematopoietic konvenzjonali trapjant ta ' proġenitur taċ-ċelloli (hpct) fil-pazjenti adulti meta l-għaqda hija kkunsidrata l-aħjar għażla disponibbli. il-busilvex li ġejjin fludarabine (fb) hu indikat bħala trattament kondizzjonarju t-trapjant taċ-ċelluli ematopojetiċi proġenitriċi (hpct) f'pazjenti adulti li huma kandidati għall-imnaqqas-intensità tal-kondizzjonament (ric) reġimen. busilvex il-ċiklofosfamid (regimen bucy4) jew melfalan (bumel) hu indikat bħala trattament kondizzjonarju konvenzjonali taċ-ċelluli ematopojetiċi tat-trapjant fil-pazjenti pedjatriċi.

Unión Europea - maltés - EMA (European Medicines Agency)

fresenius kabi deutschland gmbh - busulfan - trapjant ta 'ċelloli staminali ematopojetiċi - alkyl sulfonates - busulfan fresenius kabi warajh cyclophosphamide (bucy2) huwa indikat bħala kondizzjonament trattament qabel haematopoietic konvenzjonali trapjant ta ' proġenitur taċ-ċelloli (hpct) fil-pazjenti adulti meta l-għaqda hija kkunsidrata l-aħjar għażla disponibbli. busulfan fresenius kabi-ċiklofosfamid (regimen bucy4) jew melfalan (bumel) hu indikat bħala trattament kondizzjonarju konvenzjonali taċ-ċelluli ematopojetiċi tat-trapjant fil-pazjenti pedjatriċi.

Unión Europea - maltés - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - qasma-virus tal-influwenza, inattivat, li fih antiġen*:/california/7/2009 (h1n1)v like strain (x-179a)*propagati fil-bajd. - influenza, human; immunization; disease outbreaks - vaċċini ta 'l-influwenza - profilassi tal-influwenza f'sitwazzjoni pandemika ddikjarata uffiċjalment. il-vaċċin kontra l-influwenza pandemika għandu jintuża skond il-gwida uffiċjali.

Unión Europea - maltés - EMA (European Medicines Agency)

pfizer europe ma eeig - inotuzumab ozogamicin - leukimija limfoblastika taċ-Ċelluli prekursuri-linfoma - aġenti antineoplastiċi - besponsa huwa indikat bħala monoterapija għall-kura ta ' adulti b'all rikadut jew refrattarju cd22-pożittivi taċ-ċellula b prekursur li għandhom lewkimja limfoblastika akuta (all). pazjenti adulti bi prekursur taċ-ċelluli b tal-kromożomi posittivi (ph +) li rkadew jew refrattarji ta 'philadelphia kollha kellhom ikunu fallew il-kura b'inqas minn 1 tyrosine kinase inhibitor (tki).

Unión Europea - maltés - EMA (European Medicines Agency)

merck sharp & dohme b.v. - doravirine, lamivudine, tenofovir disoproxil fumarate - infezzjonijiet ta 'hiv - antivirali għat-trattament ta 'infezzjonijiet bl-hiv, kombinazzjonijiet - delstrigo huwa indikat għat-trattament ta 'adulti infettati bl-hiv-1 mingħajr passat jew fil-preżent evidenza ta' reżistenza għall-klassi nnrti, lamivudine, jew tenofovir. delstrigo is also indicated for the treatment of adolescents aged 12 years and older weighing at least 35 kg who are infected with hiv-1 without past or present evidence of resistance to the nnrti class, lamivudine, or tenofovir and who have experienced toxicities which preclude the use of other regimens that do not contain tenofovir disoproxil.

Unión Europea - maltés - EMA (European Medicines Agency)

merck sharp & dohme b.v. - doravirine - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - pifeltro is indicated, in combination with other antiretroviral medicinal products, for the treatment of adults, and adolescents aged 12 years and older weighing at least 35 kg infected with hiv 1 without past or present evidence of resistance to the nnrti class.

Unión Europea - maltés - EMA (European Medicines Agency)

orchard therapeutics (netherlands) bv - atidarsagene autotemcel - leukodystrophy, metachromatic - drogi oħra tas-sistema nervuża - libmeldy is indicated for the treatment of metachromatic leukodystrophy (mld) characterized by biallelic mutations in the arysulfatase a (arsa) gene leading to a reduction of the arsa enzymatic activity:in children with late infantile or early juvenile forms, without clinical manifestations of the disease,in children with the early juvenile form, with early clinical manifestations of the disease, who still  have the ability to walk independently and before the onset of cognitive decline.

Unión Europea - maltés - EMA (European Medicines Agency)

vifor fresenius medical care renal pharma france - avacopan - microscopic polyangiitis; wegener granulomatosis - immunosoppressanti - tavneos, in combination with a rituximab or cyclophosphamide regimen, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (gpa) or microscopic polyangiitis (mpa).