Report #2852736

Received Aug 5, 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: Female
Age: Age unknown
State: DC
Recovered: Unknown
Vaccinated: —
Onset: Feb 8, 2025
Days to onset: —
Hospital days: —

Vaccines (1)

Type	Name	Manufacturer	Dose	Lot	Route / Site
FLUX	INFLUENZA (SEASONAL) (NO BRAND NAME)	UNKNOWN MANUFACTURER	UNK	—	—

Symptoms (1)

Contraindication to vaccination

Symptom narrative

Reported Symptoms: 10002218:ANAPHYLAXIS; Narrative: A 69yo female with PMH of Osteopenia, Environmental Allergies, Osteoarthritis, Breast Cancer, long term use of anticoagulant, Atrial Flutter, Cardiomyopathy, Colonic Polyp and Cerebrovascular Accident s/p Arrhythmia. On February 8, 2025, PCC/WHC attending physician reported the patient had a historical ADR of Influenza vaccine induced Anaphylaxis classified as severe and updated the patient's ADR/Allergy profile. PCC attending physician also added an addendum note regarding influenza vaccine contraindication as "severe reaction in previous dose/contraindicated" No other detailed information was provided regarding reaction treatment, the product, when and where it occurred, who administered the vaccine, vaccine manufacturer, Expiration date, lot number etc. Unable to find on patient immunization profile. Other Relevant HX: Other: ANAPHYLAXIS