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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.

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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. Polio (Inactivated) (Ipol)
  4. Inappropriate schedule of product administration
Polio (Inactivated) (Ipol)×Inappropriate schedule of product administration

Inappropriate schedule of product administration Reports for Polio (Inactivated) (Ipol)

#161 most reported symptom for this vaccine

124
Reports
1
Deaths
1
Hospitalizations
0.81
Mortality Rate
%
0.8
Hosp. Rate
%

Inappropriate schedule of product administration and Polio (Inactivated) (Ipol)

Inappropriate schedule of product administration has been reported 124 times in association with Polio (Inactivated) (Ipol) vaccination in VAERS. This represents 0.3% of all 44,360 reports for this vaccine.

Among these reports, 1 mentioned death (0.81%) and 1 involved hospitalization (0.8%).

Inappropriate schedule of product administration is the #161 most frequently reported symptom for Polio (Inactivated) (Ipol) out of 1646 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 124 reports of Inappropriate schedule of product administration after Polio (Inactivated) (Ipol) vaccination may seem alarming, but context is critical.

The mortality rate among these reports is very low at 0.81%, suggesting most cases are non-fatal.

Important Context

•Association, not causation: These reports show Inappropriate schedule of product administration occurred after vaccination, not that the vaccine caused it.
•Background rates: Inappropriate schedule 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

Ocular hyperaemia126 reportsEyelid oedema126 reportsBlood test123 reportsMuscular weakness123 reports

Quick Facts

Reports:124
Deaths:1
Hospitalizations:1
% of Vaccine:0.3%
Rank:#161 of 1646

Related Pages

Polio (Inactivated) (Ipol) OverviewInappropriate schedule 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.