Clinical Trial Info

Drug Use Investigation of COMIRNATY Intramuscular Injection

Authored by
Staff
Last Reviewed
August 9, 2021

The 20,000 healthcare professionals who are vaccinated with this product early after the marketing approval of COMIRNATY(participants in the Investigation of Health Status of Recipients Vaccinated First conducted by the Science Research Group of the Ministry of Health, Labour and Welfare) will be followed for 11 months from the day following 28 days after the final vaccination of this product (end date of observation period in Investigation of Health Status of Recipients Vaccinated First) to 12 months after the final vaccination of this product, information on serious adverse events and COVID-19 observed during the follow-up period will be collected, and the long-term safety of this product will be assessed (to be conducted as 11-month follow-up investigation after completion of Investigation of Health Status of Recipients Vaccinated First).