Explore Active Surveillance Mode of the Community's Adverse Event Following Immunization(AEFI)

Beijing Center for Disease Control and Prevention1,000 enrolled

Overview

The investigators would remind the guardians of observation after immunization via sending short message and collect the information of AEFI by two ways, short message/telephone and website questionnaire.

The investigators will compare the rate between active and inactive surveillance of AEFI

Study Type

INTERVENTIONAL

Allocation

Purpose

PREVENTION

Masking

NONE

Enrollment

1,000

Conditions

Adverse Reaction to Drug

Interventions

sending messageOTHER

Sending the suggestive short message

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * According with the regular vaccination * Immunization the acellular pertussis diphtheria tetanus vaccine and Measles and rubella combined vaccine Exclusion Criteria: * Disapproval the AEFI information

Outcomes

Primary Outcomes

Incidence about AEFI

Incidence about AEFI comes from the rate between number of adverse event and the all quantity for immunization about MR and APDT

Time frame: 1.5years

Data from ClinicalTrials.gov

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