VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U3051AA: VAERS reports

23 VAERS reports list lot U3051AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2010-03-30 and 2011-10-10. 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.
23
Reports
43%
Marked serious
1
With a death outcome
9
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 reaction2225%
General / Systemic (non-local)2124%
Neurological1213%
Gastrointestinal1213%
Cardiac / Cardiovascular1011%
Musculoskeletal44%
Dermatological (non-injection-site)44%
Allergic / Anaphylactic33%
Respiratory11%

Where reports came from

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

Georgia11
Minnesota1
Oklahoma1
Maryland1
Missouri1
Iowa1
California1
North Carolina1
Pennsylvania1
Colorado1
Wisconsin1
New Jersey1

Reports by month received

2010-031
2010-051
2010-083
2010-096
2010-107
2010-112
2011-031
2011-081
2011-101

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.