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
  • All 23 Articles →

Resources

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

Sister Sites

  • OpenMedicaid
  • OpenFeds
  • OpenSpending
  • OpenMedicare
  • OpenLobby
  • 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. Influenza, Seasonal (Flucelvax Quadrivalent)
  4. Incorrect route of product administration
Influenza, Seasonal (Flucelvax Quadrivalent)×Incorrect route of product administration

Incorrect route of product administration Reports for Influenza, Seasonal (Flucelvax Quadrivalent)

#151 most reported symptom for this vaccine

38
Reports
0
Deaths
0
Hospitalizations
0
Mortality Rate
%
0
Hosp. Rate
%

Incorrect route of product administration and Influenza, Seasonal (Flucelvax Quadrivalent)

Incorrect route of product administration has been reported 38 times in association with Influenza, Seasonal (Flucelvax Quadrivalent) vaccination in VAERS. This represents 0.4% of all 8,852 reports for this vaccine.

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

Incorrect route of product administration is the #151 most frequently reported symptom for Influenza, Seasonal (Flucelvax Quadrivalent) out of 844 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 38 reports of Incorrect route of product administration after Influenza, Seasonal (Flucelvax Quadrivalent) 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 Incorrect route of product administration occurred after vaccination, not that the vaccine caused it.
•Background rates: Incorrect route of product administration 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

Nasal congestion38 reportsFull blood count38 reportsDysphagia37 reportsRash papular37 reports

Quick Facts

Reports:38
Deaths:0
Hospitalizations:0
% of Vaccine:0.4%
Rank:#151 of 844

Related Pages

Influenza, Seasonal (Flucelvax Quadrivalent) OverviewIncorrect route of product administration (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.