VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot C3030AA: VAERS reports

29 VAERS reports list lot C3030AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2008-10-20 and 2010-01-08. 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.
29
Reports
34%
Marked serious
0
With a death outcome
11
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 reaction3630%
General / Systemic (non-local)2722%
Neurological1613%
Dermatological (non-injection-site)1311%
Gastrointestinal97%
Musculoskeletal87%
Cardiac / Cardiovascular54%
Allergic / Anaphylactic54%
Respiratory32%

Where reports came from

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

Pennsylvania6
New York4
Michigan3
Ohio2
Maryland2
Maine2
Florida2
California1
Missouri1
Georgia1
West Virginia1
Idaho1

Reports by month received

2008-105
2008-114
2008-123
2009-017
2009-023
2009-041
2009-061
2009-071
2009-082
2009-091
2010-011

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.