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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.
DTaP + IPV (Kinrix)
DTAPIPV13,957 total reports
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Manufacturers:
13,957
Total Reports
13
Deaths
314
Hospitalizations
2,851
ER Visits
76
Disabilities
About DTaP + IPV (Kinrix)
DTaP + IPV (Kinrix) has 13,957 reports in VAERS spanning from 1990 to 2026.
Of these reports, 13 mentioned death, 314 involved hospitalization, and 2,851 required emergency department visits.
This vaccine is manufactured by: GlaxoSmithKline, Sanofi Pasteur, Unknown Manufacturer.
This vaccine accounts for 0.7% of all 1,983,260 reports in the VAERS database.
Reporting Rate
This vaccine averages 735 reports per year over 19 years of reporting (2008–2026).
Understanding These Numbers
•Reports don't prove causation. They represent temporal associations where someone experienced an event after vaccination.
•Background rates matter. Many conditions occur naturally and may coincidentally happen after vaccination.
•Reporting varies by vaccine. Newer vaccines or those in the news may have higher reporting rates due to increased awareness.
Most Reported Symptoms
1,267
1,248
Top Reporting States
Explore Further
Related Analysis
Data Source
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.