VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U4384AA: VAERS reports

31 VAERS reports list lot U4384AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2012-08-11 and 2017-09-07. 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.
31
Reports
61%
Marked serious
0
With a death outcome
10
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 reaction3435%
Neurological1718%
General / Systemic (non-local)1314%
Allergic / Anaphylactic1010%
Thrombotic / Hematological55%
Respiratory44%
Gastrointestinal44%
Dermatological (non-injection-site)44%
Musculoskeletal33%
Cardiac / Cardiovascular11%
Psychiatric / Neuropsychiatric11%

Where reports came from

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

South Carolina7
Illinois3
Texas3
North Carolina3
Minnesota2
California2
Rhode Island2
Massachusetts1
Maryland1
Virginia1
Missouri1
New Hampshire1

Reports by month received

2012-084
2012-095
2012-105
2012-115
2013-011
2013-051
2013-071
2013-096
2015-012
2017-091

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.