tracking Adverse Effects of vaccines on all patients...especially Children. Be more like Dr. Bhatacharya on this subject...i.e. trust the established Science built over many decades of hard work by medical scientists and physicians...leave your Non-Stop Politicking out of it.
For others...here's a quick AI summary of VAERS...
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AI Overview
Yes, the Vaccine Adverse Event Reporting System (VAERS) actively tracks vaccine effects on children.In fact, the system was originally established under the National Childhood Vaccine Injury Act of 1986specifically to monitor the safety of vaccines, with a heavy emphasis on pediatric populations. [1, 2]
How VAERS Monitors Pediatric Vaccine Safety
• Passive Surveillance: VAERS relies on healthcare providers, vaccine manufacturers, and parents to voluntarily submit reports of health problems—known as adverse events—that occur after a child receives a vaccine. [1, 2]
• Mandatory Reporting: By law, healthcare providers are required to report certain adverse events that occur within specific timeframes after childhood immunizations. [1, 2]
• Early Warning Signal: Agencies like the Centers for Disease Control and Prevention (CDC) and the FDA use the data as a flagging system to detect unusual or unexpected patterns in children, which then prompt deeper scientific investigations
Important Data Limitations
When reviewing pediatric data in VAERS, public health officials keep several unique factors in mind:
• Causation vs. Coincidence: A report submitted to VAERS does not mean the vaccine caused the health problem. Millions of infants receive vaccines during the first year of life—a period when natural health milestones, sudden illnesses, or developmental conditions frequently emerge purely by coincidence. [1, 2, 3]
• Encouraged Reporting: Parents and doctors are instructed by the CDC Guide to Interpreting VAERS Data to report any significant health event following a vaccination, regardless of whether they think the shot was responsible. [1]
• Safety Context: Decades of data gathered from VAERS, alongside more rigorous active surveillance networks, show that the vast majority of pediatric reports involve mild and temporary reactions like low-grade fevers or soreness at the injection site
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