VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5318AA: VAERS reports

42 VAERS reports list lot U5318AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2016-01-28 and 2018-05-11. 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.
42
Reports
19%
Marked serious
0
With a death outcome
16
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 reaction4940%
General / Systemic (non-local)2117%
Musculoskeletal1311%
Neurological1210%
Dermatological (non-injection-site)108%
Allergic / Anaphylactic87%
Gastrointestinal43%
Respiratory22%
Cardiac / Cardiovascular11%
Thrombotic / Hematological11%

Where reports came from

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

California7
Illinois3
North Carolina2
Utah2
Alabama2
West Virginia2
Maryland2
South Carolina2
Pennsylvania2
Tennessee1
Indiana1
Ohio1

Reports by month received

2016-011
2016-032
2016-043
2016-052
2016-069
2016-077
2016-085
2016-093
2016-103
2016-111
2017-021
2017-061
2017-071
2017-081
2017-101
2018-051

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.