VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U7931AB: VAERS reports

30 VAERS reports list lot U7931AB as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2023-11-10 and 2024-12-04. Data: VAERS public files through 31 December 2024 (site extract 2026-07-04).

Read this first. VAERS accepts reports from anyone, and a report does not establish that the vaccine caused the event. A lot's report count mostly reflects how many doses it contained, when it was used and who received it; no administered-dose counts are published for this lot, so counts are not rates and cannot rank lots against each other. Lot numbers in VAERS reports are typed by reporters and are sometimes wrong.
30
Reports
0%
Marked serious
0
With a death outcome
12
Months with reports

Symptom categories in these reports

A report can mention several categories, so the counts add up to more than the number of reports.

CategoryCount%
Injection-site / Local reaction2459%
Dermatological (non-injection-site)922%
Allergic / Anaphylactic410%
Neurological25%
General / Systemic (non-local)25%

Where reports came from

U.S. state of the reporter, where given (top 12).

Michigan6
Texas4
Massachusetts3
New Jersey2
New York2
Washington2
Illinois1
Tennessee1
Missouri1
Pennsylvania1
Ohio1
Maryland1

Reports by month received

2023-111
2023-122
2024-021
2024-033
2024-042
2024-055
2024-063
2024-074
2024-084
2024-092
2024-102
2024-121

Products recorded with this lot

Manufacturer and product as reported in VAERS. Reports listing the lot under more than one product are counted once.

Related

Source: VAERS public data (CDC/FDA), grouped by manufacturer and lot by the Open Source Medicine Foundation; extract 2026-07-04 16:35 UTC. Not medical advice. Report errors via contact.