VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5213BA: VAERS reports

31 VAERS reports list lot U5213BA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2015-05-01 and 2016-05-16. 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.
31
Reports
26%
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 reaction4350%
Allergic / Anaphylactic1214%
General / Systemic (non-local)89%
Neurological56%
Musculoskeletal56%
Dermatological (non-injection-site)56%
Cardiac / Cardiovascular45%
Respiratory22%
Gastrointestinal22%

Where reports came from

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

California5
Ohio4
Alabama3
Missouri2
Pennsylvania2
Kansas2
Maryland1
North Carolina1
New Jersey1
Maine1
Oregon1
Kentucky1

Reports by month received

2015-053
2015-063
2015-073
2015-084
2015-095
2015-102
2015-111
2015-121
2016-011
2016-031
2016-045
2016-052

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.