VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4870BA: VAERS reports

33 VAERS reports list lot U4870BA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2014-05-19 and 2015-11-19. 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.
33
Reports
42%
Marked serious
0
With a death outcome
9
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%
General / Systemic (non-local)2824%
Injection-site / Local reaction2824%
Musculoskeletal1412%
Dermatological (non-injection-site)1412%
Neurological1311%
Cardiac / Cardiovascular54%
Allergic / Anaphylactic43%
Respiratory43%
Gastrointestinal43%
Autoimmune / Immune-mediated22%
Psychiatric / Neuropsychiatric11%

Where reports came from

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

New York5
Missouri4
Ohio4
Michigan3
Washington2
Oregon2
Colorado1
Minnesota1
Arizona1
Oklahoma1
Florida1
Utah1

Reports by month received

2014-052
2014-102
2014-114
2014-127
2015-0110
2015-035
2015-051
2015-061
2015-111

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.