Bill

Bill > S767


NJ S767

NJ S767
Establishes Children's Vaccine Adverse Event Reporting System.


summary

Introduced
01/13/2026
In Committee
01/13/2026
Crossed Over
Passed
Dead

Introduced Session

2026-2027 Regular Session

Bill Summary

This bill requires the establishment of a Children's Vaccine Adverse Event Reporting System in the Department of Health to receive and maintain reports of adverse events experienced by a child under 19 years of age, in the eight weeks following the administration of a vaccine. The bill requires that health care providers report any adverse event experienced by a child in the provider's care or to whom the health care provider administered a vaccine(s), regardless of whether the vaccine(s) is deemed, in the professional opinion of the health care provider, to be the cause of the adverse event. The reporting requirements would apply to a physician, physician assistant, advanced practice nurse, registered nurse, pharmacist, or other professional licensed pursuant to Title 45 of the Revised Statutes and authorized to administer vaccines, including those who provide care to a child in the emergency department of a hospital or an urgent care center in the State. The bill provides that the Commissioner of Health is to determine the form and manner of reports made to the system and that such reports include the name and address of the health care provider submitting the report, the name, age, and address of the child, the adverse event or events experienced by the child, the date of administration of the child's most recent vaccine, the vaccine or vaccines that were administered, any product inserts that were packaged with the vaccine, and any other pertinent information as may be required by the commissioner. The bill authorizes the commissioner to share the adverse event reports only with: (1) recognized public health entities that analyze data on vaccines and adverse events, except that the identity of any child or health care provider shall not be disclosed or made public; and, (2) with the Vaccine Adverse Event Reporting System (VAERS) operated by the federal Centers for Disease Control and Prevention and the United States Food and Drug Administration, in the event that the healthcare provider was not required to report the particular adverse event to VAERS under the provisions of federal law. The bill would take effect on the first day of the sixth month next following enactment.

AI Summary

This bill establishes a Children's Vaccine Adverse Event Reporting System within the Department of Health to collect and maintain reports of negative health occurrences, called "adverse events," experienced by children under 19 years old within eight weeks of receiving a vaccine. Healthcare providers, including doctors, nurses, and pharmacists authorized to administer vaccines, are required to report any adverse event a child in their care experiences after vaccination, regardless of whether they believe the vaccine caused it. The Commissioner of Health will decide the format of these reports, which must include details about the provider, the child, the adverse event, the date and type of vaccine administered, and any accompanying product information. This system aims to gather more data on vaccine safety in children, and the Commissioner can share these reports with public health organizations that study vaccines and adverse events, ensuring the identities of children and providers remain confidential, and also with the federal Vaccine Adverse Event Reporting System (VAERS) if a report wasn't already required by federal law. This new system will become active six months after the bill is signed into law.

Committee Categories

Health and Social Services

Sponsors (1)

Last Action

Introduced in the Senate, Referred to Senate Health, Human Services and Senior Citizens Committee (on 01/13/2026)

bill text


bill summary

Loading...

bill summary

Loading...

bill summary

Loading...