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Data source: VAERS (Vaccine Adverse Event Reporting System)

Data through 2026 · Updated quarterly

Built by TheDataProject.ai · © 2026 VaccineWatch

Important: VAERS accepts reports of adverse events following vaccination. For any given report, there is no certainty that the reported event was caused by the vaccine. Reports may contain information that is incomplete, inaccurate, coincidental, or unverifiable. Most reports to VAERS are voluntary, which means they are subject to biases. This data cannot be used to determine if vaccines cause or contribute to adverse events.

⚠️

Important: VAERS reports alone cannot determine if a vaccine caused an adverse event. Reports may contain incomplete, inaccurate, or unverified information. Correlation does not equal causation.

  1. Home
  2. Vaccine Side Effects
  3. DTaP Vaccine
6 min read
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DTaP Vaccine Side Effects

DTaP protects children against diphtheria, tetanus, and pertussis (whooping cough). Given as a 5-dose series between ages 2 months and 6 years, it's one of the most frequently administered childhood vaccines — and one of the most reported in VAERS.

93,278
Total Reports
2,414
Deaths Reported
9,116
Hospitalizations
37,224
ER Visits
ℹ️ Historical context: The older DTP (whole-cell pertussis) vaccine had higher reactogenicity and was replaced by DTaP (acellular pertussis) in the late 1990s. VAERS data includes both, and many early reports reflect the older, more reactive formulation.

Most Commonly Reported Side Effects

The following symptoms are most frequently reported after DTaP vaccination:

#1Pyrexia
16,011
#2Injection site erythema
15,414
#3Injection site swelling
8,523
#4Erythema
7,318
#5Injection site oedema
6,374
#6Injection site warmth
5,853
#7Vomiting
5,394
#8Rash
5,273
#9Urticaria
4,953
#10Injection site pain
4,760
#11Convulsion
4,183
#12Injection site induration
3,964

DTaP vs DTP: A Critical Distinction

The original DTP vaccine used whole pertussis bacteria and was associated with higher rates of fever, fussiness, and rare neurological events. The modern DTaP uses purified (acellular) pertussis components and has a significantly improved safety profile.

When looking at VAERS data, it's important to separate pre-1997 DTP reports from modern DTaP reports. The 2,414 death reports across both formulations largely reflect the older vaccine and the era before improved infant health monitoring.

Expected Side Effects

Common (up to 50% of doses):

  • Fussiness and irritability (very common in infants)
  • Pain, redness, or swelling at injection site
  • Fever (mild to moderate)
  • Decreased appetite
  • Drowsiness

Less common:

  • Vomiting
  • Extensive limb swelling (usually with 4th or 5th dose)
  • Persistent crying lasting 3+ hours

Rare:

  • Febrile seizures
  • High fever (>105°F)
  • Hypotonic-hyporesponsive episodes (sudden limpness)
  • Severe allergic reaction

Co-Administration Context

DTaP is almost always given alongside other vaccines (Hib, IPV, PCV13, hepatitis B, rotavirus) at the 2, 4, and 6-month visits. This means many VAERS reports listing DTaP also list other vaccines — making it impossible to attribute symptoms to DTaP alone from VAERS data.

DTaP is given as a 5-dose series in early childhood. See exactly when each dose is due on the CDC vaccine schedule and our 2026 vaccine schedule analysis.

⚠️ Remember: VAERS reports show correlation, not causation. Many death reports in infants reflect SIDS and other causes that occurred after vaccination by coincidence, not because of the vaccine. Always consult your healthcare provider for medical advice.

Explore This Data

DTaP Vaccine Detail →
Full VAERS profile
Pediatric Analysis →
Children's vaccine data
Tdap Side Effects →
Adult booster version

2026 Safety Monitoring Update

As of mid-2026, the DTaP vaccine continues to be monitored through VAERS and complementary surveillance systems including the Vaccine Safety Datalink (VSD) and the Clinical Immunization Safety Assessment (CISA) project. No new safety signals have been identified in recent data that would change the established safety profile of this vaccine.

The HHS administration's announced development of AI-powered VAERS analysis tools may provide additional insights into DTaP vaccine adverse event patterns. These tools aim to detect subtle signals that traditional statistical methods might miss, though their implementation timeline and methodology remain under development.

It's worth noting that VAERS reporting for routine vaccines like DTaP has remained stable through the post-pandemic period. While COVID-19 vaccine reports surged and then declined, reporting patterns for established childhood and adult vaccines have been remarkably consistent, suggesting that the VAERS system continues to function as designed for ongoing safety surveillance.

Understanding VAERS Data for DTaP

When interpreting VAERS data for DTaP vaccines, several key principles apply:

  • Reports ≠ Causation: A VAERS report means an event occurred after vaccination. It does not establish that the vaccine caused the event. Many reported symptoms are common health occurrences that would happen regardless of vaccination.
  • No denominator: VAERS does not track the number of doses administered. Without knowing how many people received the vaccine, raw report counts cannot be used to calculate risk rates or compare safety across vaccines.
  • Co-administration: Many vaccines are given at the same visit. When a VAERS report lists multiple vaccines, it's impossible to determine which vaccine (if any) was responsible for the reported adverse event.
  • Reporting variability: Healthcare provider awareness, media attention, and public concern all influence how many reports are filed. Changes in report volume may reflect changes in reporting behavior rather than changes in actual safety.

How to Use This Data Responsibly

VAERS data is most useful as a starting point for conversation with your healthcare provider, not as a basis for medical decisions. If you're concerned about DTaP vaccine side effects:

  • Discuss your specific risk factors with your doctor or pharmacist
  • Ask about the relative risks of the disease the vaccine prevents vs. the vaccine itself
  • Consider your age, health status, and any previous vaccine reactions
  • Remember that clinical trials and post-market studies provide much stronger safety evidence than VAERS alone

For the most up-to-date safety information, consult the CDC's vaccine information pages or speak with a qualified healthcare professional.

More Resources

When Do Side Effects Start?
73% occur within 3 days of vaccination
Serious vs Non-Serious Outcomes
The full severity spectrum in VAERS
Report an Adverse Event
How to file a VAERS report
Our Methodology
How we process VAERS data

2026 Safety Monitoring Update

As of mid-2026, the DTaP vaccine continues to be monitored through VAERS and complementary surveillance systems including the Vaccine Safety Datalink (VSD) and the Clinical Immunization Safety Assessment (CISA) project. No new safety signals have been identified in recent data that would change the established safety profile of this vaccine.

The HHS administration's announced development of AI-powered VAERS analysis tools may provide additional insights into DTaP vaccine adverse event patterns. These tools aim to detect subtle signals that traditional statistical methods might miss, though their implementation timeline and methodology remain under development.

It's worth noting that VAERS reporting for routine vaccines like DTaP has remained stable through the post-pandemic period. While COVID-19 vaccine reports surged and then declined, reporting patterns for established childhood and adult vaccines have been remarkably consistent, suggesting that the VAERS system continues to function as designed for ongoing safety surveillance.

Understanding VAERS Data for DTaP

When interpreting VAERS data for DTaP vaccines, several key principles apply:

  • Reports ≠ Causation: A VAERS report means an event occurred after vaccination. It does not establish that the vaccine caused the event. Many reported symptoms are common health occurrences that would happen regardless of vaccination.
  • No denominator: VAERS does not track the number of doses administered. Without knowing how many people received the vaccine, raw report counts cannot be used to calculate risk rates or compare safety across vaccines.
  • Co-administration: Many vaccines are given at the same visit. When a VAERS report lists multiple vaccines, it's impossible to determine which vaccine (if any) was responsible for the reported adverse event.
  • Reporting variability: Healthcare provider awareness, media attention, and public concern all influence how many reports are filed. Changes in report volume may reflect changes in reporting behavior rather than changes in actual safety.

How to Use This Data Responsibly

VAERS data is most useful as a starting point for conversation with your healthcare provider, not as a basis for medical decisions. If you're concerned about DTaP vaccine side effects:

  • Discuss your specific risk factors with your doctor or pharmacist
  • Ask about the relative risks of the disease the vaccine prevents vs. the vaccine itself
  • Consider your age, health status, and any previous vaccine reactions
  • Remember that clinical trials and post-market studies provide much stronger safety evidence than VAERS alone

For the most up-to-date safety information, consult the CDC's vaccine information pages or speak with a qualified healthcare professional.

More Resources

When Do Side Effects Start?
73% occur within 3 days of vaccination
Serious vs Non-Serious Outcomes
The full severity spectrum in VAERS
Report an Adverse Event
How to file a VAERS report
Our Methodology
How we process VAERS data

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