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Report #2873915

Received Nov 20, 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
NJ
Recovered
Not recovered
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
PNC20PNEUMO (PREVNAR20)PFIZER\WYETH1MA2506OT

Symptoms (2)

Vaccination site erythemaVaccination site pain

Symptom narrative

red and sore after the shot; red and sore after the shot; The initial case was missing the following minimum criteria: unspecified adverse event. Upon receipt of follow-up information on 12Nov2025, this case now contains all required information to be considered valid. This is a spontaneous report received from a Consumer or other non HCP. A 57-year-old female patient received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), as dose 1, 0.5 ml single (Lot number: MA2506, Expiration Date: 31Oct2026) intramuscular for immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PAIN (non-serious), outcome "recovering" and all described as "red and sore after the shot". Therapeutic measures were not taken as a result of vaccination site erythema, vaccination site pain. Additional information: After the shot and still a week after.

Medical history

Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None