VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot C3837BA: VAERS reports

21 VAERS reports list lot C3837BA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2011-04-05 and 2012-08-02. 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.
21
Reports
43%
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%
Injection-site / Local reaction2533%
Neurological1418%
General / Systemic (non-local)1317%
Allergic / Anaphylactic68%
Musculoskeletal57%
Dermatological (non-injection-site)57%
Gastrointestinal45%
Psychiatric / Neuropsychiatric23%
Thrombotic / Hematological11%
Respiratory11%

Where reports came from

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

California8
Florida3
Massachusetts2
Virginia1
Maryland1
New York1
Arizona1
Connecticut1
Georgia1
Wisconsin1
Kansas1

Reports by month received

2011-043
2011-054
2011-064
2011-073
2011-083
2011-101
2012-051
2012-071
2012-081

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.