Skip to main content
VaccineWatch
VaccinesSymptomsStatesAnalysisToolsDashboardCompare

VaccineWatch

Transparent access to VAERS data for informed decision-making. We present the data as-is, with appropriate context and disclaimers.

Explore Data

  • Vaccines
  • Symptoms
  • Manufacturers
  • States
  • Dashboard
  • Compare Tool
  • Search

Deep Dives

  • The Denominator Problem
  • Onset Timing
  • Lot Number Analysis
  • COVID Impact
  • Myocarditis
  • Death Reports
  • Interactive Tools
  • Reporting Rate Calculator
  • Signal Detection
  • All 23 Articles →

Resources

  • About
  • Methodology
  • FAQ
  • Glossary
  • Side Effects Guide
  • Vaccine Schedule
  • Vaccine Safety
  • Safety Timeline
  • Adverse Events
  • Is VAERS Reliable?
  • Myocarditis
  • Guillain-Barré
  • Allergic Reactions
  • Report an Event
  • Disclaimer
  • VAERS Official Site ↗

Sister Sites

  • OpenMedicaid
  • OpenFeds
  • OpenImmigration
  • OpenCrime
  • OpenSpending
  • OpenMedicare
  • OpenLobby
  • WarCosts
  • OpenPrescriber
  • GiveScope
  • SPACGraveyard
  • AI Exposure
  • AutoPilotWatch
  • TariffTax
  • ShelterScope
  • TheDataProject.ai

Data source: VAERS (Vaccine Adverse Event Reporting System)

Data through 2026 · Updated quarterly

Built by TheDataProject.ai · © 2026 VaccineWatch

Important: VAERS accepts reports of adverse events following vaccination. For any given report, there is no certainty that the reported event was caused by the vaccine. Reports may contain information that is incomplete, inaccurate, coincidental, or unverifiable. Most reports to VAERS are voluntary, which means they are subject to biases. This data cannot be used to determine if vaccines cause or contribute to adverse events.

⚠️

Important: VAERS reports alone cannot determine if a vaccine caused an adverse event. Reports may contain incomplete, inaccurate, or unverified information. Correlation does not equal causation.

  1. Home
  2. Vaccines
  3. Pneumococcal (Pneumovax)
  4. Poor quality device used
Pneumococcal (Pneumovax)×Poor quality device used

Poor quality device used Reports for Pneumococcal (Pneumovax)

#2045 most reported symptom for this vaccine

3
Reports
0
Deaths
0
Hospitalizations
0
Mortality Rate
%
0
Hosp. Rate
%

Poor quality device used and Pneumococcal (Pneumovax)

Poor quality device used has been reported 3 times in association with Pneumococcal (Pneumovax) vaccination in VAERS. This represents 0.0% of all 71,157 reports for this vaccine.

Among these reports, 0 mentioned death (0.00%) and 0 involved hospitalization (0.0%).

Poor quality device used is the #2045 most frequently reported symptom for Pneumococcal (Pneumovax) out of 2065 total symptoms.

Disclaimer: VAERS reports describe events that occurred after vaccination but do not establish that the vaccine caused the event. Many reported symptoms may be coincidental or related to underlying conditions.

What This Means

Seeing 3 reports of Poor quality device used after Pneumococcal (Pneumovax) vaccination may seem alarming, but context is critical.

The mortality rate among these reports is very low at 0.00%, suggesting most cases are non-fatal.

Important Context

•Association, not causation: These reports show Poor quality device used occurred after vaccination, not that the vaccine caused it.
•Background rates: Poor quality device used may occur naturally at baseline rates in the population, unrelated to vaccination.
•Anyone can report: VAERS accepts reports from anyone — patients, parents, healthcare providers — without requiring medical verification.
•Denominator missing: VAERS counts reports, not rates per dose. Without knowing how many doses were given, raw counts can be misleading. Learn more →

Similarly Ranked Symptoms

Stem cell transplant3 reportsNasal discomfort3 reportsPeriorbital swelling3 reportsEuphoric mood3 reports

Quick Facts

Reports:3
Deaths:0
Hospitalizations:0
% of Vaccine:0.0%
Rank:#2045 of 2065

Related Pages

Pneumococcal (Pneumovax) OverviewPoor quality device used (All Vaccines)Why Raw Numbers MisleadTop Symptoms Analysis

Data Source

This data comes from the Vaccine Adverse Event Reporting System (VAERS), jointly managed by CDC and FDA.