Pandemic Influenza Vaccine H5N1 Baxter AG Uniunea Europeană - letonă - EMA (European Medicines Agency)

pandemic influenza vaccine h5n1 baxter ag

resilience biomanufacturing ireland limited - gripas vakcīna (viss virions, inaktivēts), kas satur antigēnu no: a / vietnam / 1203/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vakcīnas - gripas profilakse oficiāli paziņotajā pandēmijas situācijā. pandēmiskās gripas vakcīna jāizmanto saskaņā ar oficiālajām vadlīnijām.

Prepandemic Influenza Vaccine (H5N1) (Split Virion, Inactivated, Adjuvanted) GlaxoSmithKline Biologicals Uniunea Europeană - letonă - EMA (European Medicines Agency)

prepandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted) glaxosmithkline biologicals

glaxosmithkline biologicals s.a. - split gripas vīruss, inaktivēts, satur antigēnu: lietots a / vietnam / 1194/2004 (h5n1) līdzīgais celms (nibrg-14) - influenza, human; immunization; disease outbreaks - vakcīnas - aktīvā imunizācija pret a gripas vīrusa h5n1 apakštipa. Šī norāde ir balstīta uz immunogenicity datus no veseliem vecumā no 18 gadiem pēc administrācijas divas devas vakcīnas, kas gatavoti no a/vjetnama/1194/2004 nibrg-14 (h5n1) (skatīt 5. iedaļu. prepandemic gripas vakcīna (h5n1) (split virion, inaktivēta, adjuvanted) glaxosmithkline bioloģiskās izcelsmes zālēm 3. 75 µg būtu jāizmanto saskaņā ar oficiālās vadlīnijas.

Meningococcal polysaccharide A + C vaccine pulveris un šķīdinātājs injekciju suspensijas pagatavošanai pilnšļircē Letonia - letonă - Zāļu valsts aģentūra

meningococcal polysaccharide a + c vaccine pulveris un šķīdinātājs injekciju suspensijas pagatavošanai pilnšļircē

sanofi pasteur, france - meningokoku polisaharīdu vakcīna - pulveris un suspensija injekciju suspensijas pagatavošanai pilnšļircē

Spikevax (previously COVID-19 Vaccine Moderna) Uniunea Europeană - letonă - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vakcīnas - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Vaxzevria (previously COVID-19 Vaccine AstraZeneca) Uniunea Europeană - letonă - EMA (European Medicines Agency)

vaxzevria (previously covid-19 vaccine astrazeneca)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - vakcīnas - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. izmantojot šo vakcīnu, kas būtu saskaņā ar oficiālās rekomendācijas.

Adjupanrix (previously Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals) Uniunea Europeană - letonă - EMA (European Medicines Agency)

adjupanrix (previously pandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted) glaxosmithkline biologicals)

glaxosmithkline biologicals s.a. - split gripas vīruss, inaktivēts, satur antigēnu: lietots a / vietnam / 1194/2004 (h5n1) līdzīgais celms (nibrg-14) - influenza, human; immunization; disease outbreaks - vakcīnas - gripas profilakse oficiāli paziņotajā pandēmijas situācijā. pandēmiskās gripas vakcīna jāizmanto saskaņā ar oficiālajām vadlīnijām.

Celvapan Uniunea Europeană - letonă - EMA (European Medicines Agency)

celvapan

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - vakcīnas - profilaksei gripas vīrusu (h1n1) v 2009. celvapan būtu jāizmanto saskaņā ar oficiālās vadlīnijas.

Vaxelis Uniunea Europeană - letonă - EMA (European Medicines Agency)

vaxelis

mcm vaccine b.v. - difterija toxoid, tetanus toxoid, bordetella pertussis antigēnus: klepus toxoid, hemaglutinīna pertaktīna, fimbriae veidi 2 un 3, b hepatīta virsmas antigēnu, kas ražoti rauga šūnām, poliomielīta (inaktivēta): tips 1 (mahoney), tips 2 (mef-1), tips 3 (saukett), kas ražoti vero šūnas/ haemophilus influenzae b tipa polisaharīds (polyribosylribitol fosfāts), kas konjugēts pret meningokoku olbaltumvielu. - meningitis, haemophilus; poliomyelitis; tetanus; diphtheria; whooping cough; hepatitis b - vakcīnas - vaxelis (dtap-hb-ipv-hib) ir indicēts pamatskolu un pastiprinātājs vakcinācija zīdaiņiem un maziem bērniem vecumā no 6 nedēļām pret difterija, stingumkrampji, garais klepus, b hepatīts, poliomielīta un invazīvajām slimībām, ko izraisa haemophilus influenzae tips b (hib). vaxel lietošanai jāatbilst oficiālajiem ieteikumiem.

RotaTeq Uniunea Europeană - letonă - EMA (European Medicines Agency)

rotateq

merck sharp & dohme b.v. - rotavīrusa serotips g1, serotips g2, serotips g3, serotips g4, serotips p1 - immunization; rotavirus infections - vaccines, viral vaccines - rotateq ir indicēts zīdaiņu aktīvai imunizācijai no sešu nedēļu vecās līdz 32 nedēļas, lai novērstu rotavīrusa infekcijas izraisītu gastroenterītu. rotateq ir jāizmanto, pamatojoties uz oficiālās rekomendācijas.

PreHevbri Uniunea Europeană - letonă - EMA (European Medicines Agency)

prehevbri

vbi vaccines b.v. - hepatīta b virsmas antigēns - b hepatīts - vakcīnas - 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.