VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4393BA: VAERS reports

20 VAERS reports list lot U4393BA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2012-08-15 and 2015-08-18. 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.
20
Reports
50%
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%
Cardiac / Cardiovascular3130%
Injection-site / Local reaction2524%
General / Systemic (non-local)1616%
Neurological77%
Dermatological (non-injection-site)77%
Allergic / Anaphylactic55%
Musculoskeletal44%
Thrombotic / Hematological33%
Gastrointestinal33%
Autoimmune / Immune-mediated11%
Psychiatric / Neuropsychiatric11%

Where reports came from

U.S. state of the reporter, where given (top 9).

California5
Washington4
South Carolina3
Colorado2
North Carolina2
Florida1
Kansas1
Georgia1
Missouri1

Reports by month received

2012-083
2012-094
2012-103
2012-111
2013-041
2013-051
2013-061
2013-071
2013-081
2013-091
2015-041
2015-082

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.