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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.

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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.

  1. Home
  2. Vaccines
  3. DTaP
  4. Wrong patient received product
DTaP×Wrong patient received product

Wrong patient received product Reports for DTaP

#947 most reported symptom for this vaccine

11
Reports
0
Deaths
0
Hospitalizations
0
Mortality Rate
%
0
Hosp. Rate
%

Wrong patient received product and DTaP

Wrong patient received product has been reported 11 times in association with DTaP vaccination in VAERS. This represents 0.0% of all 66,714 reports for this vaccine.

Among these reports, 0 mentioned death (0.00%) and 0 involved hospitalization (0.0%).

Wrong patient received product is the #947 most frequently reported symptom for DTaP out of 1943 total symptoms.

Disclaimer: VAERS reports describe events that occurred after vaccination but do not establish that the vaccine caused the event. Many reported symptoms may be coincidental or related to underlying conditions.

What This Means

Seeing 11 reports of Wrong patient received product after DTaP vaccination may seem alarming, but context is critical.

The mortality rate among these reports is very low at 0.00%, suggesting most cases are non-fatal.

Important Context

•Association, not causation: These reports show Wrong patient received product occurred after vaccination, not that the vaccine caused it.
•Background rates: Wrong patient received product may occur naturally at baseline rates in the population, unrelated to vaccination.
•Anyone can report: VAERS accepts reports from anyone — patients, parents, healthcare providers — without requiring medical verification.
•Denominator missing: VAERS counts reports, not rates per dose. Without knowing how many doses were given, raw counts can be misleading. Learn more →

Similarly Ranked Symptoms

Swelling of eyelid11 reportsCOVID-1911 reportsCerebral infarction10 reportsFuruncle10 reports

Quick Facts

Reports:11
Deaths:0
Hospitalizations:0
% of Vaccine:0.0%
Rank:#947 of 1943

Related Pages

DTaP OverviewWrong patient received product (All Vaccines)Why Raw Numbers MisleadTop Symptoms Analysis

Data Source

This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.