Jan 8, 2024 · Events described in manufacturer’s package insert as contraindications to additional doses of vaccine (interval - see package insert) Effective date: January 8, 2024. The …

**Represents the onset interval between vaccination and the adverse event. For a detailed explanation of terms, see the Vaccine Injury Table at

Checklist of information to complete the VAERS form (VAERS will still accept a report even if you cannot provide all this information)

1. Important Information About VAERS The Vaccine Adverse Event Reporting System (VAERS) was created by the Food and Drug Administration (FDA) and Centers for Disease Control and …

Any other vaccines received within one month prior to the date listed in item 4: Use Continuation Page if needed

In addition, it is often the case that more than one vaccine was administered, making it difficult to know to which of the vaccines the event might be attributed. In analyzing individual reports, …

Usted debe reportar cualquier reacción adversa que se presente después de recibir una vacuna, aun cuando no esté seguro de que la vacuna haya causado dicha reacción. Es de particular …