유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

valneva austria gmbh - japānas encefalīta vīruss, inaktivēts (attenuēts sa14-14-2 celms, kas audzēts vero šūnās) - encephalitis, japanese; immunization - vakcīnas - ixiaro ir indicēts aktīvai imunizācijai pret japāņu encefalītu pieaugušajiem, pusaudžiem, bērniem un zīdaiņiem vecumā no diviem mēnešiem un vecākiem. ixiaro būtu jāuzskata par lietošanai personu riska iedarbības ar ceļojumu vai tās laikā savas profesionālās darbības.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - palifermin - mucosīts - visi pārējie terapeitiskie produkti - kepivance norādīja, lai samazinātu biežumu, ilgumu un smagumu mutvārdu mucositis pieaugušiem pacientiem ar hematoloģisko malignancies saņem myeloablative radiochemotherapy, kas saistītas ar augsta saslimstība ar nopietnu mucositis un prasa autologās-asinsrades-cilmes šūnu atbalsts.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

theramex ireland limited - follitropin alfa - anovulācija - dzimumhormoni un dzimumsistēmas modulatori dzimumorgānu sistēma, - pieaugušo womenanovulation (ieskaitot policistisko olnīcu sindroms) sievietes, kas ir bijis nereaģē uz ārstēšanu ar clomifene citrāts;stimulēšana multifollicular attīstības sievietēm notiek superovulation apaugļošanas tehnoloģijas (mĀksla), piemēram, in vitro apaugļošana (ivf), gamete iekšējo fallopian nodošanas un zygote iekšējo fallopian nodošanu;ovaleap sadarbībā ar luteinizējošs hormons (lh) preparāts ir ieteicams stimulēt folikulu attīstību sievietēm ar smagu lh un fsh deficīts. klīniskajos pētījumos pacientiem, tika noteikti ar endogēns seruma lh līmenis < 1. 2 iu/l. pieaugušo menovaleap ir norādīts stimulē spermatoģenēzi vīriešiem, kuriem ir iedzimtas vai iegūtas hypogonadotropic hipogonādisms ar vienlaicīgu cilvēka horiona gonadotropin (hcg) terapija.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - difterija toxoid, tetanus toxoid, inaktivēta bordetella pertussis, b hepatīta virsmas antigēna (rdna), haemophilus influenzae b tipa polisaharīds - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; diphtheria - vakcīnas - quintanrix ir norādīta primārā imunizācijas zīdaiņiem (laikā pirmajā dzīves gadā) pret difterija, stingumkrampji, garais klepus, b hepatīta un invazīvo slimību izraisa, haemophilus influenzae b tipa un pastiprinātājs imunizācijas bērniem laikā otrajā dzīves gadā. izmantot quintanrix būtu jānosaka, pamatojoties uz oficiālās rekomendācijas.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

bausch + lomb ireland limited - bromfenaka nātrija seskvihidrāts - pain, postoperative; ophthalmologic surgical procedures - oftalmoloģiskie līdzekļi - pēcoperācijas acu iekaisuma ārstēšana pēc kataraktas ekstrakcijas pieaugušajiem.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - rekombinanto vezikulārā stomatīta vīruss (celms, indiana), ar dzēšanas aploksnes glikoproteīnu, aizstāj ar zaira ebolavirus (celms kikwit 1995) virsmas glikoproteīnu - hemorāģisko drudzi, ebola - vakcīnas - ervebo is indicated for active immunization of individuals 1 year of age or older to protect against ebola virus disease (evd) caused by zaire ebola virus. izmantot ervebo būtu saskaņā ar oficiālās rekomendācijas.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

santen oy - netarsudil - glaucoma, open-angle; ocular hypertension - oftalmoloģiskie līdzekļi - samazināt paaugstinātu intraokulāro spiedienu (ias) pieaugušiem pacientiem ar primāra atvērta kakta glaukoma vai acs hipertensijas.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna 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 - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. izmantojot šo vakcīnu, kas būtu saskaņā ar oficiālās rekomendācijas.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneimokoku infekcijas - pneimokoku vakcīna, polisaharīdu antigēns, attīrīts, konjugēts - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. skatīt nodaļas 4. 4 un 5. 1, lai iegūtu informāciju par aizsardzību pret specifiskiem pneimokoku serotipiem. the use of vaxneuvance should be in accordance with official recommendations.

유럽 연합 - 라트비아어 - EMA (European Medicines Agency)

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - denges - vakcīnas - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.