Received Mar 30, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| MNQ | MENINGOCOCCAL CONJUGATE (MENQUADFI) | SANOFI PASTEUR | 1 | — | AR |
On March 30, 2026, at approximately 11:05 am, I received a MenQuadfi (meningococcal ACWY) vaccine at your facility. Approximately 15 minutes after the injection, I experienced a sudden loss of consciousness with complete temporary inability to move my arms or legs. I fell into a door and remained weak for over an hour afterward. I had no pain or anxiety prior to the event. I have already provided full details of this adverse reaction to your staff. This incident qualifies as a serious vaccine-related event, and I am in the process of documenting it thoroughly, including filing a report with VAERS and notifying the manufacturer (Sanofi).
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