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Table of Reportable Events
Following Vaccination (RET)

Vaccine/Toxoid
(click on link
for
CDC VIS)
Event
(click on link for definitions)
Interval from Vaccination
(click on link for inserts)
Tetanus in any combination;
DTaP, DTP, DTP-HiB, DT, Td, or TT)
A. Anaphylaxis or anaphylactic shock 7 days
B. Brachial neuritis 28 days
C. Any sequelae (including death) of above events Not applicable
D. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Pertussis in any combination; DTaP, DTP, DTP-HiB, P A. Anaphylaxis or anaphylactic shock 7 days
B. Encephalopathy (or encephalitis) 7 days
C. Any sequelae (including death) of above events Not applicable
D. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Measles, mumps and rubella in any combination; MMR, MR, M, or R A. Anaphylaxis or anaphylactic shock 7 days
B. Encephalopathy (or encephalitis) 15 days
C. Any sequelae (including death) of above events Not applicable
D. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Rubella in any combination; MMR, MR, R A. Chronic arthritis 42 days
B. Any sequelae (including death) of above event Not applicable
C. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Measles in any combination; MMR, MR, M A. Thrombocytopenic purpura 7-30 days
B. Vaccine-strain measles viral infection in an immunodeficient recipient 6 months
C. Any sequelae (including death) of above event Not applicable
D. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Oral Polio (OPV) A. Paralytic polio 30 days/ 6 months
B. Vaccine-strain polio viral infection 30 days/ 6 months
C. Any sequelae (including death) of above events Not applicable
D. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Inactivated Polio (IPV) A. Anaphylaxis or anaphylactic shock 7 days
B. Any sequelae (including death) of the above event Not applicable
C. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Hepatitis B A. Anaphylaxis or anaphylactic shock 7 days
B. Any sequelae (including death) of the above event Not applicable
C. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Hemophilus influenzae, Type b, (conjugate) A. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Varicella A. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Rotavirus A. Intussusception 30 days
B. Any sequela (including death) of the above event Not applicable
C. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert
Pneumococcal conjugate A. Events described in manufacturer's package insert as contraindications to additional doses of vaccine See package insert

*Effective date: August 26,2002.
The Reportable Events Table (RET) reflects what is reportable by law (42 USC 300aa-25) to the Vaccine Adverse Event Reporting System (VAERS) including conditions found in the manufacturers package insert. In addition, individuals are encouraged to report any clinically significant or unexpected events (even if you are not certain the vaccine caused the event) for any vaccine, whether or not it is listed on the RET. Manufacturers are also required by regulation (21CFR 600.80) to report to the VAERS program all adverse events made known to them for any vaccine.


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