Report #2861268

Received Sep 25, 2025

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex: Unknown
Age: 56 yrs
State: CO
Recovered: Unknown
Vaccinated: Sep 20, 2025
Onset: Sep 21, 2025
Days to onset: 1
Hospital days: —

Vaccines (2)

Type	Name	Manufacturer	Dose	Lot	Route / Site
COVID19	COVID19 (COVID19 (MODERNA))	MODERNA	UNK	3052671	IM / RA
FLU3	INFLUENZA (SEASONAL) (FLUBLOK)	SANOFI PASTEUR	UNK	U8832DA	IM / RA

Symptoms (3)

MalaisePainPyrexia

Symptom narrative

I'm a patient who is also a nurse. On 20Sep2025 at 1600 MDT, I received Sanofi's Flublok 0.5mL 2025-26 (NDC 49281-0725-10, LOT U8832DA or U8B32DA), Serial 13214KD21EAKMH, Exp 06/31/26) and Moderna's Spikevax 05mcg/0.5mL (NDC 80777-0112-96, LOT 3052671, Serial 2XFFSBFVT3T9 or 2XFFSBFV73T9, Exp 06/16/26). Both were given IM in my right deltoid. on 21Sep2025 at approximately 0400 MDT, I began to experience a low-grade fever, aches, and generally feeling as if I'm getting sick. While I consider these signs that my body is doing exactly what it's supposed to do in response to these vaccines, as a HCP, I still wanted to report them.