Professional Documents
Culture Documents
The live recombinant tetravalent vaccine, Dengvaxia, had a high-profile debut in the
Philippines in the spring of 2016. The nation had participated in every stage of clinical
development and was the first in the world to get access to it. With a goal of immunizing a
million kids by the end of the year, the Department of Health launched a mass vaccination
program and spent $67 million on Dengvaxia.
With Dengvaxia, whose development had taken 20 years and cost roughly $1.8 billion,
Sanofi likewise had great expectations. Infection rates were expected to drop by 24% within the
next five years thanks to the vaccine, which helps protect against all four dengue serotypes.
Sanofi appeared to be well-positioned to profit from the introduction of the first-ever dengue
vaccine to international markets. By October 2016, 10 other nations, including Mexico, Brazil,
and Indonesia, had given their regulatory clearance for Dengvaxia.
Dengvaxia is given as three injections spaced six months apart, but after more than six
months had passed and more than 830,000 kids had received at least one dose, Sanofi declared
that it was changing its label to limit its use to only those who had already been exposed to
dengue virus. Sanofi said the findings revealed that recipients of the vaccine who were dengue-
naive might be more susceptible to more serious infections after reexamining the trial's
outcomes. The Dengvaxia controversy was sparked by this news.
Therefore, to prevent the occurrence of the same issue, the following solutions have been
proposed:
HHS.gov. https://www.hhs.gov/immunization/basics/safety/index.html
Petersen, M. B., Bor, A., Jørgensen, F., & Lindholt, M. F. (2021). Transparent communication
about negative features of COVID-19 vaccines decreases acceptance but increases trust.
https://doi.org/10.1073/pnas.2024597118
World Health Organization. (2016). Vaccine Safety communication Guide for immunization
https://apps.who.int/iris/rest/bitstreams/1247065/retrieve