Under NCVIA, which types of events must be reported to VAERS?

• A. Any event listed by the vaccine manufacturer as a contraindication to subsequent doses.
• B. Any event listed in the Reportable Events Table that occurs within the specified time period after vaccination.
• C. Any event listed by the vaccine manufacturer as a contraindication OR any event listed in the Reportable Events Table that occurs within the specified time period after vaccination.
• D. All adverse events regardless of timing.

Answer: (C)