VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5081AA: VAERS reports

23 VAERS reports list lot U5081AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2015-03-11 and 2019-09-03. 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
61%
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%
Neurological1617%
General / Systemic (non-local)1617%
Injection-site / Local reaction1415%
Cardiac / Cardiovascular1112%
Musculoskeletal1011%
Allergic / Anaphylactic77%
Respiratory77%
Gastrointestinal77%
Dermatological (non-injection-site)55%
Psychiatric / Neuropsychiatric22%

Where reports came from

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

Illinois6
California3
Maryland2
Florida2
Texas2
New Jersey1
Alaska1
Washington1
North Dakota1
Montana1
Nebraska1
Pennsylvania1

Reports by month received

2015-0311
2015-044
2015-051
2015-061
2015-071
2015-081
2015-111
2016-041
2016-051
2019-091

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.