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DC Field | Value | Language |
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dc.contributor.author | Chotpitayasunondh T. | |
dc.contributor.author | Pruekprasert P. | |
dc.contributor.author | Puthanakit T. | |
dc.contributor.author | Pancharoen C. | |
dc.contributor.author | Tangsathapornpong A. | |
dc.contributor.author | Oberdorfer P. | |
dc.contributor.author | Kosalaraksa P. | |
dc.contributor.author | Prommalikit O. | |
dc.contributor.author | Tangkittithaworn S. | |
dc.contributor.author | Kerdpanich P. | |
dc.contributor.author | Techasaensiri C. | |
dc.contributor.author | Korejwo J. | |
dc.contributor.author | Chuenkitmongkol S. | |
dc.contributor.author | Houillon G. | |
dc.date.accessioned | 2021-04-05T03:22:32Z | - |
dc.date.available | 2021-04-05T03:22:32Z | - |
dc.date.issued | 2017 | |
dc.identifier.issn | 0264410X | |
dc.identifier.other | 2-s2.0-85006966243 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13164 | - |
dc.identifier.uri | https://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.abstract | Background 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.subject | Japanese encephalitis vaccine | |
dc.subject | live vaccine | |
dc.subject | recombinant vaccine | |
dc.subject | Japanese encephalitis vaccine | |
dc.subject | live vaccine | |
dc.subject | recombinant vaccine | |
dc.subject | acute disseminated encephalomyelitis | |
dc.subject | allergic reaction | |
dc.subject | anaphylaxis | |
dc.subject | Article | |
dc.subject | Bell palsy | |
dc.subject | brain disease | |
dc.subject | bronchitis | |
dc.subject | child | |
dc.subject | child hospitalization | |
dc.subject | congenital malformation | |
dc.subject | convulsion | |
dc.subject | death | |
dc.subject | dengue | |
dc.subject | diarrhea | |
dc.subject | disability | |
dc.subject | drug marketing | |
dc.subject | drug safety | |
dc.subject | dyspepsia | |
dc.subject | encephalitis | |
dc.subject | enteritis | |
dc.subject | epilepsy | |
dc.subject | febrile convulsion | |
dc.subject | female | |
dc.subject | fever | |
dc.subject | food poisoning | |
dc.subject | gastritis | |
dc.subject | gastroenteritis | |
dc.subject | human | |
dc.subject | infant | |
dc.subject | influenza | |
dc.subject | Japanese encephalitis | |
dc.subject | licensing | |
dc.subject | male | |
dc.subject | mouth ulcer | |
dc.subject | multicenter study | |
dc.subject | myelitis | |
dc.subject | neurologic disease | |
dc.subject | normal human | |
dc.subject | open study | |
dc.subject | peripheral neuropathy | |
dc.subject | pharyngitis | |
dc.subject | phase 4 clinical trial | |
dc.subject | pneumonia | |
dc.subject | preschool child | |
dc.subject | priority journal | |
dc.subject | prospective study | |
dc.subject | pyrexia idiopathica | |
dc.subject | rhinopharyngitis | |
dc.subject | side effect | |
dc.subject | single drug dose | |
dc.subject | Thailand | |
dc.subject | urticaria | |
dc.subject | vaccination | |
dc.subject | vaccination reaction | |
dc.subject | vaccine failure | |
dc.subject | viremia | |
dc.subject | virus infection | |
dc.subject | virus pneumonia | |
dc.subject | adverse drug reaction | |
dc.subject | clinical trial | |
dc.subject | Japanese encephalitis | |
dc.subject | pathology | |
dc.subject | Child, Preschool | |
dc.subject | Drug-Related Side Effects and Adverse Reactions | |
dc.subject | Encephalitis, Japanese | |
dc.subject | Female | |
dc.subject | Healthy Volunteers | |
dc.subject | Humans | |
dc.subject | Infant | |
dc.subject | Japanese Encephalitis Vaccines | |
dc.subject | Male | |
dc.subject | Prospective Studies | |
dc.subject | Thailand | |
dc.subject | Vaccines, Attenuated | |
dc.subject | Vaccines, Synthetic | |
dc.title | Post-licensure, phase IV, safety study of a live attenuated Japanese encephalitis recombinant vaccine in children in Thailand | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Vaccine. Vol 35, No.2 (2017), p.299-304 | |
dc.identifier.doi | 10.1016/j.vaccine.2016.11.062 | |
Appears in Collections: | Scopus 1983-2021 |
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