VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5726AA: VAERS reports

21 VAERS reports list lot U5726AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2017-07-22 and 2019-09-16. 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.
21
Reports
5%
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 reaction2835%
General / Systemic (non-local)1721%
Musculoskeletal911%
Neurological810%
Gastrointestinal79%
Respiratory45%
Cardiac / Cardiovascular34%
Dermatological (non-injection-site)34%
Allergic / Anaphylactic11%

Where reports came from

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

Wisconsin4
Oregon3
California2
South Carolina2
District of Columbia1
Ohio1
Massachusetts1
Colorado1
Washington1
Minnesota1
Pennsylvania1
Wyoming1

Reports by month received

2017-071
2017-082
2017-092
2017-105
2017-112
2018-011
2018-021
2018-033
2018-041
2018-091
2019-071
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.