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Report #2849437

Received Jul 11, 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
59 yrs
State
SC
Recovered
Not recovered
Vaccinated
Jun 1, 2025
Onset
Jul 1, 2025
Days to onset
30
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
PNC20PNEUMO (PREVNAR20)PFIZER\WYETHUNK——

Symptoms (2)

Injection site painMobility decreased

Symptom narrative

Pain at the injection where she has lost full movement of moving her arm all the way up and down; Pain at the injection where she has lost full movement of moving her arm all the way up and down; This is a spontaneous report received from an Other HCP from a sales representative. A 59-year-old female patient (not pregnant) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), in Jun2025 as dose number unknown, single (Batch/Lot number: unknown) at the age of 59 years for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION SITE PAIN (non-serious), INJECTED LIMB MOBILITY DECREASED (non-serious) all with onset Jul2025, latency 2 weeks after the suspect product(s) administration, outcome "not recovered" and all described as "Pain at the injection where she has lost full movement of moving her arm all the way up and down". Therapeutic measures were not taken as a result of vaccination site pain, injected limb mobility decreased. Additional information: The patient didn't receive any other vaccines on the same date as the vaccine reported. It was unknown if the patient received any other vaccines within 4 weeks prior to the vaccine reported. It was unknown if the patient was taking any other medications within 2 weeks of the event starting. Pain at the injection where the patient has lost full movement of moving her arm all the way up and down. This was 2 weeks later from vaccine administered. The reporter classified the event as non-serious. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.