Uniunea Europeană - română - EMA (European Medicines Agency)

gsk vaccines s.r.l. - meningococic a, c, w-135 și y conjugat vaccin - immunization; meningitis, meningococcal - vaccinuri bacteriene - vialsmenveo este indicat pentru imunizarea activă a copiilor (de la vârsta de doi ani), adolescenți și adulți cu risc de expunere la neisseria meningitidis grupele a, c, w135 și y, pentru prevenirea bolii invazive. utilizarea acestui vaccin ar trebui să fie în conformitate cu recomandările oficiale.

Uniunea Europeană - română - EMA (European Medicines Agency)

pfizer europe ma eeig - neisseria meningitidis serogrupul b fhbp (fhbp recombinant lipidizat (proteina de legare a factorului h)) subfamilia a; neisseria meningitidis serogrupul b fhbp (fhbp recombinant lipidizat (proteina de legare a factorului h)) subfamilia b - meningită, meningococică - bacterial vaccines, meningococcal vaccines - trumenba este indicat pentru imunizarea activă a persoanelor cu vârsta de 10 ani și peste pentru a preveni boala meningococică invazivă cauzată de serogroupul neisseria meningitidis. utilizarea acestui vaccin ar trebui să fie în conformitate cu recomandările oficiale.

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

pfizer manufacturing austria gmbh - austria - vaccin meningococic polizaharidic de grup c - susp. inj. in seringa preumpluta - 0,5ml - vaccinuri bacteriene vaccinuri meningococice

Uniunea Europeană - română - EMA (European Medicines Agency)

gsk vaccines s.r.l. - exterior membrana veziculelor de neisseria meningitidis grup b (tulpina nz 98/254), recombinant neisseria meningitidis grup b fhbp proteină de fuziune, recombinant neisseria meningitidis grup b nada proteine, recombinant neisseria meningitidis grup b nhba proteină de fuziune - meningită, meningococică - vaccinuri meningococice - imunizarea activă împotriva bolilor invazive cauzate de tulpinile serogrup-b ale neisseria meningitidis.

Uniunea Europeană - română - EMA (European Medicines Agency)

pfizer europe ma eeig - neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid - meningită, meningococică - vaccinuri - nimenrix este indicat pentru imunizarea activă a persoanelor de la vârsta de 6 săptămâni împotriva bolilor meningococice invazive cauzate de grupul neisseria meningitidis a, c, w-135 și y.

Uniunea Europeană - română - EMA (European Medicines Agency)

sanofi pasteur - neisseria meningitidis group c polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group a polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group y polysaccharide conjugated to tetanus toxoid, neisseria meningitidis group w-135 polysaccharide conjugated to tetanus toxoid - meningită, meningococică - vaccinuri - menquadfi is indicated for active immunisation of individuals from the age of 12 months and older against invasive meningococcal disease caused by neisseria meningitidis serogroups a, c, w, and y. the use of this vaccine should be in accordance with available official recommendations.

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

pfizer europe ma eeig - vaccin meningococic polizaharidic de grup c - susp. inj. in seringa preumpluta - 0,5ml - vaccinuri bacteriene vaccinuri meningococice

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

glaxosmithkline biologicals s.a. - vaccin meningococic polizaharidic tetravalent - liofilizat şi solvent pentru soluţie injectabilă - 1 doză

Uniunea Europeană - română - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinurie, paroxismal - imunosupresoare selective - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

helba phamaceuticals inc. co. - spiramycinum - comprimate filmate - 1500000 ui