COVID-19 vaccine Adverse Response & Evaluation (CARE) Programme:

Intensive Monitoring

Part IV of the study aims to actively recruit participants and intensively monitor their potential adverse reactions

Study Purpose

The study aims to understand the potential adverse reactions seen in people of different age groups and health statues following COVID-19 vaccination.

This study will be conducted in the form of follow-up surveys

Study Content

Each vaccine recipient or their caregiver completed an online or paper survey 1, 2, 3, 7, 14 & 28 days after each COVID-19 vaccine injection (two doses in total), a maximum of 12 surveys.

The survey recorded the health status and any adverse reactions seen in the vaccine recipient.

Recruited Subject

4000

As of 13/08/2021

(Target reached)

Materials and Samples