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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 + Hib (Trihibit)
DTAPH751 total reports
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Manufacturers:
751
Total Reports
4
Deaths
65
Hospitalizations
315
ER Visits
20
Disabilities
About DTaP + Hib (Trihibit)
DTaP + Hib (Trihibit) has 751 reports in VAERS spanning from 1990 to 2026.
Of these reports, 4 mentioned death, 65 involved hospitalization, and 315 required emergency department visits.
This vaccine is manufactured by: Sanofi Pasteur, Unknown Manufacturer.
This vaccine accounts for 0.0% of all 1,983,260 reports in the VAERS database.
Reporting Rate
This vaccine averages 36 reports per year over 21 years of reporting (1999–2022).
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
Top Reporting States
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Related Analysis
Data Source
This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.