VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4875AA: VAERS reports

38 VAERS reports list lot U4875AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2014-05-27 and 2016-04-19. 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.
38
Reports
47%
Marked serious
0
With a death outcome
15
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 reaction2623%
General / Systemic (non-local)2018%
Allergic / Anaphylactic1513%
Neurological1312%
Cardiac / Cardiovascular1211%
Musculoskeletal87%
Dermatological (non-injection-site)76%
Respiratory54%
Gastrointestinal44%
Psychiatric / Neuropsychiatric11%
Reproductive / Menstrual11%

Where reports came from

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

Pennsylvania6
California4
Texas3
New Jersey3
New York3
Massachusetts3
Alabama2
Michigan2
Ohio2
Oregon1
New Hampshire1
Colorado1

Reports by month received

2014-051
2014-068
2014-074
2014-084
2014-093
2014-112
2014-123
2015-011
2015-023
2015-031
2015-043
2015-061
2015-102
2016-031
2016-041

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.