VAERS reports by lot

Sanofi Pasteur DTaP/Tdap lot U5770AA: VAERS reports

22 VAERS reports list lot U5770AA as a Sanofi Pasteur DTaP/Tdap vaccine, received between 2017-08-30 and 2019-06-19. 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
0%
Marked serious
0
With a death outcome
13
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 reaction2432%
General / Systemic (non-local)1925%
Dermatological (non-injection-site)811%
Musculoskeletal79%
Neurological68%
Cardiac / Cardiovascular34%
Allergic / Anaphylactic34%
Respiratory23%
Gastrointestinal23%
Psychiatric / Neuropsychiatric11%

Where reports came from

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

Michigan4
California3
Texas3
Virginia2
Ohio2
Maine1
Illinois1
Florida1
Rhode Island1
Missouri1
Nebraska1
New Jersey1

Reports by month received

2017-081
2017-091
2017-104
2017-113
2018-011
2018-021
2018-033
2018-042
2018-051
2018-061
2018-071
2018-092
2019-061

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.