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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. Influenza, Seasonal (Fluvirin)
  4. Fluid retention
Influenza, Seasonal (Fluvirin)×Fluid retention

Fluid retention Reports for Influenza, Seasonal (Fluvirin)

#631 most reported symptom for this vaccine

55
Reports
0
Deaths
12
Hospitalizations
0
Mortality Rate
%
21.8
Hosp. Rate
%

Fluid retention and Influenza, Seasonal (Fluvirin)

Fluid retention has been reported 55 times in association with Influenza, Seasonal (Fluvirin) vaccination in VAERS. This represents 0.0% of all 119,695 reports for this vaccine.

Among these reports, 0 mentioned death (0.00%) and 12 involved hospitalization (21.8%).

Fluid retention is the #631 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 55 reports of Fluid retention 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), Fluid retention appears in only 0.0% of reports.

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 Fluid retention occurred after vaccination, not that the vaccine caused it.
•Background rates: Fluid retention 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

Eczema55 reportsDermatitis55 reportsLymphadenitis55 reportsIdiopathic thrombocytopenic purpura55 reports

Quick Facts

Reports:55
Deaths:0
Hospitalizations:12
% of Vaccine:0.0%
Rank:#631 of 3021

Related Pages

Influenza, Seasonal (Fluvirin) OverviewFluid retention (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.