A nationwide prospective cohort study on safety of the 17D-204 yellow fever vaccine during a vaccine shortage in Japan.
Autor: |
Miyazato, Yusuke, Terada, Mari, Ujiie, Mugen, Saito, Sho, Moriya, Akinari, Ando, Masao, Ohmagari, Norio |
Předmět: |
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Zdroj: |
Journal of Travel Medicine; Mar2023, Vol. 30 Issue 2, p1-4, 4p |
Abstrakt: |
He was diagnosed with adhesive bowel obstruction, which was treated conservatively and the patient recovered |
M/22 | Tonsillitis | 29 | Serious | Related/cannot be ruled out | The subject with no previous medical history presented with mild sore throat and fever appearing on Day 6 post-vaccination, which was judged to have been caused by the vaccination by the site physician. No adverse event occurred to the baby |
ht Onset time is counted from vaccination day (vaccination = Day 0). He was diagnosed with adhesive bowel obstruction, which was treated conservatively and the patient recovered
M/22 | Tonsillitis | 29 | Serious | Related/cannot be ruled out | The subject with no previous medical history presented with mild sore throat and fever appearing on Day 6 post-vaccination, which was judged to have been caused by the vaccination by the site physician. On 24 July 2017, Sanofi Pasteur, yellow fever vaccine (YF-VAX) manufacturer, announced a vaccine shortage caused by manufacturing delays.[1] Consequently, some countries were forced to take compensatory measures. [Extracted from the article] |
Databáze: |
Complementary Index |
Externí odkaz: |
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