VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4618AA: VAERS reports

30 VAERS reports list lot U4618AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2013-07-28 and 2015-11-04. 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.
30
Reports
10%
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 reaction3739%
General / Systemic (non-local)1920%
Allergic / Anaphylactic910%
Gastrointestinal89%
Musculoskeletal66%
Dermatological (non-injection-site)66%
Cardiac / Cardiovascular55%
Neurological22%
Thrombotic / Hematological11%
Respiratory11%

Where reports came from

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

Rhode Island5
Illinois3
New Jersey3
New York3
Pennsylvania3
Michigan2
Georgia1
Texas1
Maryland1
California1
Kentucky1
Missouri1

Reports by month received

2013-071
2013-0811
2013-092
2013-106
2013-111
2013-122
2014-111
2015-015
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.