VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U6831AA: VAERS reports

28 VAERS reports list lot U6831AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2021-07-31 and 2023-05-11. 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.
28
Reports
0%
Marked serious
0
With a death outcome
11
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 reaction1032%
Musculoskeletal826%
General / Systemic (non-local)619%
Neurological310%
Cardiac / Cardiovascular26%
Allergic / Anaphylactic13%
Gastrointestinal13%

Where reports came from

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

Florida5
Illinois2
Oklahoma2
Virginia2
Pennsylvania2
Arizona1
New York1
California1
Texas1
Mississippi1
Colorado1
Maine1

Reports by month received

2021-071
2021-083
2021-103
2021-122
2022-011
2022-022
2022-051
2022-106
2022-116
2022-122
2023-051

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.