VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5030AA: VAERS reports

22 VAERS reports list lot U5030AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2015-01-27 and 2015-10-12. 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.
22
Reports
32%
Marked serious
0
With a death outcome
8
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 reaction3647%
General / Systemic (non-local)912%
Musculoskeletal810%
Allergic / Anaphylactic79%
Neurological56%
Cardiac / Cardiovascular34%
Gastrointestinal34%
Dermatological (non-injection-site)34%
Autoimmune / Immune-mediated11%
Respiratory11%
Psychiatric / Neuropsychiatric11%

Where reports came from

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

Pennsylvania3
Kansas2
Washington2
Massachusetts2
South Carolina2
Tennessee1
Louisiana1
New Mexico1
Florida1
West Virginia1
Oregon1
California1

Reports by month received

2015-011
2015-024
2015-033
2015-044
2015-051
2015-065
2015-073
2015-101

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.