VAERS Explorer
Back to explore

Report #2835485

Received Apr 10, 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
78 yrs
State
NY
Recovered
Not recovered
Vaccinated
Dec 2, 2024
Onset
Dec 9, 2024
Days to onset
7
Hospital days
—

Vaccines (1)

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

Symptoms (15)

Abdominal painAbdominal pain upperAlopeciaAmnesiaArthralgiaDizzinessErythemaEye disorderHepatic painInflammationInjection site painMuscle atrophyPruritusRashVomiting

Symptom narrative

memory loss; rash; itchy skin; stomach pain; liver pain; abdominal pain; dizziness; eye problem; inflammation of the ankle; vomiting; red face; hair loss; shoulder and arm pain of the injection; shoulder and arm pain of the injection; reduction of muscular tissue; This is a spontaneous report received from a Consumer or other non HCP. A 78-year-old female patient (not pregnant) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), on 02Dec2024 as dose number unknown, single (Batch/Lot number: unknown) at the age of 78 years for immunisation. The patient's relevant medical history included: "Cardiac ablation", start date: 2024 (unspecified if ongoing); "Lung cancer", start date: 2019 (unspecified if ongoing). The patient had no known allergies. The patient's concomitant medications were not reported. The following information was reported: ABDOMINAL PAIN (non-serious) with onset 09Dec2024, outcome "not recovered"; DIZZINESS (non-serious) with onset 09Dec2024, outcome "not recovered"; EYE DISORDER (non-serious) with onset 09Dec2024, outcome "not recovered", described as "eye problem"; ALOPECIA (non-serious) with onset 09Dec2024, outcome "not recovered", described as "hair loss"; ARTHRITIS (non-serious) with onset 09Dec2024, outcome "not recovered", described as "inflammation of the ankle"; PRURITUS (non-serious) with onset 09Dec2024, outcome "not recovered", described as "itchy skin"; HEPATIC PAIN (non-serious) with onset 09Dec2024, outcome "not recovered", described as "liver pain"; AMNESIA (non-serious) with onset 09Dec2024, outcome "not recovered", described as "memory loss"; RASH (non-serious) with onset 09Dec2024, outcome "not recovered"; ERYTHEMA (non-serious) with onset 09Dec2024, outcome "not recovered", described as "red face"; MUSCLE ATROPHY (non-serious) with onset 09Dec2024, outcome "not recovered", described as "reduction of muscular tissue"; VACCINATION SITE PAIN (non-serious), ARTHRALGIA (non-serious) all with onset 09Dec2024, outcome "not recovered" and all described as "shoulder and arm pain of the injection"; ABDOMINAL PAIN UPPER (non-serious) with onset 09Dec2024, outcome "not recovered", described as "stomach pain"; VOMITING (non-serious) with onset 09Dec2024, outcome "not recovered". Therapeutic measures were not taken as a result of amnesia, rash, pruritus, abdominal pain upper, hepatic pain, abdominal pain, dizziness, eye disorder, arthritis, vomiting, erythema, alopecia, vaccination site pain, arthralgia, muscle atrophy. The information on the batch/lot number for pneumococcal 20-val conj vac (dipht CRM197 protein) will be requested and submitted if and when received.

Medical history

Medical History/Concurrent Conditions: Cardiac ablation; Lung cancer