VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4612AA: VAERS reports

63 VAERS reports list lot U4612AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2013-04-30 and 2019-12-24. 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.
63
Reports
14%
Marked serious
0
With a death outcome
14
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 reaction3338%
General / Systemic (non-local)1517%
Neurological1112%
Allergic / Anaphylactic78%
Gastrointestinal67%
Dermatological (non-injection-site)67%
Cardiac / Cardiovascular33%
Musculoskeletal33%
Respiratory22%
Autoimmune / Immune-mediated11%
Psychiatric / Neuropsychiatric11%

Where reports came from

U.S. state of the reporter, where given (top 11).

South Carolina39
Missouri9
California2
Virginia2
North Carolina2
Rhode Island2
Florida2
Michigan1
Georgia1
Minnesota1
Texas1

Reports by month received

2013-041
2013-051
2013-061
2013-074
2013-085
2013-091
2013-102
2013-111
2014-013
2014-021
2014-081
2015-0140
2016-051
2019-121

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.