Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13164
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dc.contributor.authorChotpitayasunondh T.
dc.contributor.authorPruekprasert P.
dc.contributor.authorPuthanakit T.
dc.contributor.authorPancharoen C.
dc.contributor.authorTangsathapornpong A.
dc.contributor.authorOberdorfer P.
dc.contributor.authorKosalaraksa P.
dc.contributor.authorPrommalikit O.
dc.contributor.authorTangkittithaworn S.
dc.contributor.authorKerdpanich P.
dc.contributor.authorTechasaensiri C.
dc.contributor.authorKorejwo J.
dc.contributor.authorChuenkitmongkol S.
dc.contributor.authorHouillon G.
dc.date.accessioned2021-04-05T03:22:32Z-
dc.date.available2021-04-05T03:22:32Z-
dc.date.issued2017
dc.identifier.issn0264410X
dc.identifier.other2-s2.0-85006966243
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13164-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85006966243&doi=10.1016%2fj.vaccine.2016.11.062&partnerID=40&md5=5f84f81d084334af01bfa9bd6bb01e7b
dc.description.abstractBackground Japanese encephalitis is a mosquito-borne viral disease endemic in most countries in Asia. A recombinant live, attenuated Japanese encephalitis virus vaccine, JE-CV, is licensed in 14 countries, including Thailand, for the prevention of Japanese encephalitis in adults and children. Methods This was a prospective, phase IV, open-label, multicentre, safety study of JE-CV conducted from November 2013 to April 2015, to evaluate rare serious adverse events (AEs). JE-CV was administered to 10,000 healthy children aged 9 months to <5 years in Thailand as a primary (Group 1) or booster (Group 2) vaccination. Serious AEs (SAEs), including AEs of special interest, up to 60 days after administration were evaluated. Immediate Grade 3 systemic AEs up to 30 min after JE-CV administration were also described. Results The median age of participants was 1.1 years in Group 1 and 3.8 years in Group 2. SAEs were reported in 204 (3.0%) participants in Group 1 and 59 (1.9%) participants in Group 2. Among a total of 294 SAEs in 263 participants, only three events occurring in two participants were considered related to vaccination. All three cases were moderate urticaria, none of which met the definition of AEs of special interest for hypersensitivity. AEs of special interest were reported in 28 (0.4%) participants in Group 1 and 4 (0.1%) participants in Group 2; none were considered related to vaccination. Febrile convulsion was the most frequently reported AE of special interest: 25 (0.4%) participants in Group 1; and 2 (<0.1%) in Group 2. There were no cases of Japanese encephalitis reported. No Grade 3 immediate systemic AEs were reported after any JE-CV vaccination. Conclusions Our study did not identify any new safety concerns with JE-CV and confirms its good safety profile. This study was registered on www.clinicaltrials.gov (NCT01981967; Universal Trial Number: U1111-1127-7052). © 2016 The Authors
dc.subjectJapanese encephalitis vaccine
dc.subjectlive vaccine
dc.subjectrecombinant vaccine
dc.subjectJapanese encephalitis vaccine
dc.subjectlive vaccine
dc.subjectrecombinant vaccine
dc.subjectacute disseminated encephalomyelitis
dc.subjectallergic reaction
dc.subjectanaphylaxis
dc.subjectArticle
dc.subjectBell palsy
dc.subjectbrain disease
dc.subjectbronchitis
dc.subjectchild
dc.subjectchild hospitalization
dc.subjectcongenital malformation
dc.subjectconvulsion
dc.subjectdeath
dc.subjectdengue
dc.subjectdiarrhea
dc.subjectdisability
dc.subjectdrug marketing
dc.subjectdrug safety
dc.subjectdyspepsia
dc.subjectencephalitis
dc.subjectenteritis
dc.subjectepilepsy
dc.subjectfebrile convulsion
dc.subjectfemale
dc.subjectfever
dc.subjectfood poisoning
dc.subjectgastritis
dc.subjectgastroenteritis
dc.subjecthuman
dc.subjectinfant
dc.subjectinfluenza
dc.subjectJapanese encephalitis
dc.subjectlicensing
dc.subjectmale
dc.subjectmouth ulcer
dc.subjectmulticenter study
dc.subjectmyelitis
dc.subjectneurologic disease
dc.subjectnormal human
dc.subjectopen study
dc.subjectperipheral neuropathy
dc.subjectpharyngitis
dc.subjectphase 4 clinical trial
dc.subjectpneumonia
dc.subjectpreschool child
dc.subjectpriority journal
dc.subjectprospective study
dc.subjectpyrexia idiopathica
dc.subjectrhinopharyngitis
dc.subjectside effect
dc.subjectsingle drug dose
dc.subjectThailand
dc.subjecturticaria
dc.subjectvaccination
dc.subjectvaccination reaction
dc.subjectvaccine failure
dc.subjectviremia
dc.subjectvirus infection
dc.subjectvirus pneumonia
dc.subjectadverse drug reaction
dc.subjectclinical trial
dc.subjectJapanese encephalitis
dc.subjectpathology
dc.subjectChild, Preschool
dc.subjectDrug-Related Side Effects and Adverse Reactions
dc.subjectEncephalitis, Japanese
dc.subjectFemale
dc.subjectHealthy Volunteers
dc.subjectHumans
dc.subjectInfant
dc.subjectJapanese Encephalitis Vaccines
dc.subjectMale
dc.subjectProspective Studies
dc.subjectThailand
dc.subjectVaccines, Attenuated
dc.subjectVaccines, Synthetic
dc.titlePost-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailand
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationVaccine. Vol 35, No.2 (2017), p.299-304
dc.identifier.doi10.1016/j.vaccine.2016.11.062
Appears in Collections:Scopus 1983-2021

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