VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5850AA: VAERS reports

24 VAERS reports list lot U5850AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2018-05-05 and 2019-10-01. 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.
24
Reports
4%
Marked serious
0
With a death outcome
11
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 reaction2830%
Dermatological (non-injection-site)1516%
Neurological1213%
General / Systemic (non-local)1112%
Musculoskeletal1011%
Allergic / Anaphylactic67%
Cardiac / Cardiovascular44%
Gastrointestinal33%
Psychiatric / Neuropsychiatric33%

Where reports came from

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

California7
Minnesota3
Washington2
Oregon2
Colorado1
Arizona1
Utah1
Iowa1
Montana1
Virginia1
Tennessee1
Kansas1

Reports by month received

2018-054
2018-063
2018-074
2018-084
2018-101
2018-113
2018-121
2019-011
2019-041
2019-051
2019-101

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.