VAERS reports by lot
GSK DTaP/Tdap lot AC52B031AB: VAERS reports
21 VAERS reports list lot AC52B031AB as a GSK DTaP/Tdap vaccine, received between 2009-03-11 and 2009-12-08. 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.
21
Reports
57%
Marked serious
0
With a death outcome
7
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.
| Category | Count | % |
|---|---|---|
| Injection-site / Local reaction | 29 | 36% |
| General / Systemic (non-local) | 15 | 19% |
| Neurological | 12 | 15% |
| Musculoskeletal | 12 | 15% |
| Cardiac / Cardiovascular | 8 | 10% |
| Dermatological (non-injection-site) | 3 | 4% |
| Allergic / Anaphylactic | 1 | 1% |
| Gastrointestinal | 1 | 1% |
Where reports came from
U.S. state of the reporter, where given (top 11).
| North Carolina | 7 |
| Minnesota | 2 |
| Pennsylvania | 2 |
| Illinois | 2 |
| Texas | 2 |
| Georgia | 1 |
| Virginia | 1 |
| Indiana | 1 |
| Florida | 1 |
| Wisconsin | 1 |
| New York | 1 |
Reports by month received
| 2009-03 | 1 | |
| 2009-04 | 2 | |
| 2009-05 | 3 | |
| 2009-06 | 3 | |
| 2009-08 | 2 | |
| 2009-11 | 1 | |
| 2009-12 | 9 |
Products recorded with this lot
- Tdap — Glaxosmithkline Biologicals (21 reports)
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.