ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

astrazeneca ab - anifrolumab - lupus erythematosus, sistemic - imunosupresoare - saphnelo is indicated as an add-on therapy for the treatment of adult patients with moderate to severe, active autoantibody-positive systemic lupus erythematosus (sle), despite standard therapy.

রুমানিয়া - রোমানীয় - Ecolab

ecolab deutschland gmbh -

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

vbi vaccines b.v. - hepatita b antigen de suprafață - hepatita b - vaccinuri - 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.

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunosupresoare - tyruko is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis (rrms) for the following patient groups: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 și 5. 1), or, patients with rapidly evolving severe rrms defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain magnetic resonance imaging (mri) or a significant increase in t2 lesion load as compared to a previous recent mri.

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - infecții ale virusului sincițial respirator - vaccinuri - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. vezi secțiunile 4. 2 și 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. utilizarea acestui vaccin ar trebui să fie în conformitate cu recomandările oficiale.

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

bavarian nordic a/s - vaccinia modificată ankara - virusul nordic bavarez (mva-bn) - smallpox vaccine; monkeypox virus - alte vaccinuri virale, - active immunisation against smallpox, monkeypox and disease caused by vaccinia virus in adults (see sections 4. 4 și 5. utilizarea acestui vaccin ar trebui să fie în conformitate cu recomandările oficiale.

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline panleucopenia virus (pli iv) - produsele imunologice pentru felidae, - pisici - active immunisation of cats aged eight 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. onset of immunity is one week after primary vaccination course the duration of immunity is one year after the primary vaccination course and three years after the last re-vaccination.

ইউরোপীয় ইউনিয়ন - রোমানীয় - 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 chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - produsele imunologice pentru felidae, - pisici - active immunisation of cats aged eight weeks and older:• against feline viral rhinotracheitis to reduce clinical signs;• against calicivirus infection to reduce clinical signs;• against chlamydophila felis infection to reduce clinical signs;• against feline panleucopenia to prevent mortality and clinical signs. incidența imunității a fost demonstrată la o săptămână după vaccinarea primară pentru rinotraheită, calicivirus, chlamydophila felis și componentele panleucopeniei. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

zoetis belgium - virus inactivat al bolii limbii albastre, serotip 8, tulpina btv-8/bel2006/02 - immunologicals - bovine - active immunisation of cattle from three months of age for the prevention of viraemia caused by bluetongue virus, serotype 8.

ইউরোপীয় ইউনিয়ন - রোমানীয় - EMA (European Medicines Agency)

janssen-cilag international n.v.    - recombinant adenovirus type 26 (ad26) encoding the glycoprotein (gp) of the ebola virus zaire (zebov) mayinga strain - febra hemoragica ebola - vaccinuri - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.