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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.

Influenza, Seasonal (Fluvirin)×Headache

Headache Reports for Influenza, Seasonal (Fluvirin)

#8 most reported symptom for this vaccine

8,484
Reports
32
Deaths
716
Hospitalizations
0.38
Mortality Rate
%
8.4
Hosp. Rate
%

Headache and Influenza, Seasonal (Fluvirin)

Headache has been reported 8,484 times in association with Influenza, Seasonal (Fluvirin) vaccination in VAERS. This represents 7.1% of all 119,695 reports for this vaccine.

Among these reports, 32 mentioned death (0.38%) and 716 involved hospitalization (8.4%).

Headache is the #8 most frequently reported symptom for Influenza, Seasonal (Fluvirin) out of 3021 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 8,484 reports of Headache after Influenza, Seasonal (Fluvirin) vaccination may seem alarming, but context is critical. With 119,695 total reports for this vaccine (representing many millions of doses), Headache appears in only 7.1% of reports.

The mortality rate among these reports is very low at 0.38%, suggesting most cases are non-fatal.

Important Context

Association, not causation: These reports show Headache occurred after vaccination, not that the vaccine caused it.
Background rates: Headache 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 →

Quick Facts

Reports:8,484
Deaths:32
Hospitalizations:716
% of Vaccine:7.1%
Rank:#8 of 3021

Data Source

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