VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4939AA: VAERS reports

22 VAERS reports list lot U4939AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2014-08-21 and 2016-06-17. 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.
22
Reports
50%
Marked serious
0
With a death outcome
10
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 reaction2228%
General / Systemic (non-local)1418%
Dermatological (non-injection-site)1215%
Allergic / Anaphylactic1114%
Neurological68%
Musculoskeletal68%
Cardiac / Cardiovascular23%
Respiratory23%
Thrombotic / Hematological11%
Gastrointestinal11%
Psychiatric / Neuropsychiatric11%

Where reports came from

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

Alabama3
District of Columbia2
Texas2
Florida2
Georgia2
Oklahoma2
New York1
California1
Michigan1
Missouri1
Wyoming1
Virginia1

Reports by month received

2014-085
2014-094
2014-103
2014-121
2015-022
2015-031
2015-052
2015-111
2016-042
2016-061

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.