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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.

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  3. Gender Disparities in Reporting
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Gender Disparities in Reporting

Women file 59% of all VAERS reports — nearly twice as many as men. Why?

1,175,561
Female (59%)
635,545
Male (32%)
172,154
Unknown (9%)

Why Do Women Report More?

The gender gap in VAERS reporting is not unique — it's consistent with broader patterns in healthcare utilization and adverse drug reaction reporting worldwide. Several factors contribute:

  • Healthcare engagement: Women are more likely to visit healthcare providers, seek preventive care, and receive vaccines — creating more opportunities for reporting
  • Immune response differences: Research suggests women may experience stronger immune responses to vaccines, potentially leading to more noticeable side effects
  • Reporting behavior: Studies consistently show women are more likely to report adverse drug reactions across all medication categories, not just vaccines
  • Pregnancy-related reporting: Vaccines given during pregnancy generate additional reporting from both the patient and their healthcare provider
  • Occupational exposure: Women represent a majority of healthcare workers, who are often required to receive certain vaccines and report adverse events

The Biology Behind the Gap

The immune response difference between men and women is well-documented in immunology research. Women generally produce stronger antibody responses to vaccines, which is beneficial for protection but can also lead to more frequent and pronounced side effects. This is driven by several biological factors:

  • Sex hormones: Estrogen enhances immune responses while testosterone tends to suppress them. This is why women often have stronger reactions to vaccines and are more susceptible to autoimmune conditions.
  • X-chromosome genes: Many immune-related genes are located on the X chromosome. Since women have two copies, they have a broader repertoire of immune genes, contributing to stronger immune activation.
  • Dosing considerations: Most vaccines use the same dose regardless of body weight or sex. Since women on average have lower body mass, they may receive a relatively higher dose per kilogram, potentially amplifying immune responses.

2026 Update: Gender Trends in Recent Data

The gender gap in VAERS reporting has remained remarkably stable through 2026. Even as COVID-19 booster campaigns wound down and reporting returned closer to pre-pandemic baselines, women continued to file the majority of reports. For the 2025-2026 flu season vaccines, women accounted for approximately 62% of adverse event reports — slightly higher than the overall historical average, consistent with higher flu vaccination rates among women.

The new RSV vaccines authorized in 2023-2024 for older adults and pregnant women added a notable data point: maternal RSV vaccination reports were almost exclusively filed by women, as expected, but the gender split for the 60+ population receiving RSV vaccines was closer to 55/45 — narrower than most other vaccine categories.

Gender-Specific Safety Signals

While the overall gender gap reflects reporting behavior, some safety signals are genuinely gender-specific. The most prominent example is myocarditis after mRNA COVID-19 vaccines, which was observed predominantly in young males (ages 16-24) after the second dose. This signal was not about reporting behavior — it reflected a real biological difference in how young male hearts responded to the vaccine.

Conversely, thrombosis with thrombocytopenia syndrome (TTS) associated with the J&J COVID-19 vaccine was observed more frequently in women, particularly those ages 18-49. These gender-specific patterns underscore the importance of analyzing VAERS data by sex rather than treating all reports as homogeneous.

Gender and Outcome Severity

While women file more reports overall, the rate of serious outcomes (deaths, hospitalizations) per report tends to be similar across genders. This suggests the gender gap is primarily in reporting behavior, not in the severity of adverse events experienced.

The 172,154 reports with unknown gender (9%) represent a significant data limitation. Many older reports and manufacturer-submitted reports do not include gender information.

Implications for Vaccine Safety Research

Understanding gender disparities in VAERS reporting has practical implications for safety surveillance. When evaluating potential safety signals, analysts must account for the baseline gender imbalance in reporting to avoid false signals. A symptom that appears to affect women disproportionately may simply reflect the higher female reporting rate rather than a genuine gender-specific risk.

The FDA has increasingly recognized the importance of sex-stratified analysis in drug and vaccine safety. Clinical trials now routinely report outcomes by sex, and post-market surveillance systems like VAERS benefit from the same approach. As AI-driven analysis tools are developed for VAERS data in 2026, incorporating gender as a key variable will be essential for accurate signal detection.

Key Takeaways

  • 1.Women file 59% of VAERS reports — a pattern consistent with healthcare utilization research
  • 2.The gender gap reflects reporting behavior differences, not necessarily different safety profiles
  • 3.Biological, behavioral, and occupational factors all contribute to the disparity
  • 4.Some safety signals (myocarditis in young males, TTS in younger women) are genuinely gender-specific

Frequently Asked Questions

Why do women file more VAERS reports than men?

Women file approximately 59% of all VAERS reports due to a combination of factors: higher healthcare utilization rates, stronger immune responses to vaccines (leading to more noticeable side effects), greater likelihood of reporting adverse drug reactions across all medication categories, pregnancy-related reporting, and occupational exposure as the majority of healthcare workers.

Does the gender gap in VAERS mean vaccines are less safe for women?

No. The gender gap primarily reflects reporting behavior differences, not different safety profiles. When adjusted for the number of doses received and healthcare engagement patterns, the rate of serious outcomes (deaths, hospitalizations) per report is similar across genders.

What percentage of VAERS reports have unknown gender?

A significant portion of VAERS reports — typically around 7-10% — have unknown gender. This is because many older reports and manufacturer-submitted reports do not include gender information, representing a data limitation in the system.

Do men or women have more serious vaccine side effects?

While women file more reports overall, the rate of serious outcomes (deaths, hospitalizations) per report is similar across genders. However, specific conditions like myocarditis after mRNA COVID vaccines were observed more frequently in young males, showing that some safety signals are gender-specific.

2026 Data Context

As VAERS reporting normalizes following the COVID-19 pandemic surge, the data landscape for gender patterns in adverse event reporting is shifting. Annual VAERS reports in 2025-2026 have returned to the 35,000-45,000 range typical of the pre-pandemic era (2015-2019), making year-over-year comparisons more meaningful again.

The HHS administration has signaled increased focus on vaccine safety data analysis, including the development of AI-powered tools for pattern detection in VAERS reports. While these tools are still under development, they represent a potential evolution in how adverse event data is analyzed and interpreted.

New vaccines entering the market — including RSV vaccines for older adults and pregnant women, updated COVID-19 formulations, and potential H5N1 avian flu vaccines — continue to add new data streams to VAERS. Each new vaccine type provides additional context for understanding gender patterns in adverse event reporting across the full spectrum of vaccine safety surveillance.

Limitations of This Analysis

This analysis is based entirely on VAERS passive surveillance data, which carries important limitations that must be understood:

  • Underreporting: Studies estimate that only 1-10% of adverse events are reported to VAERS. This means the true number of events is likely much higher than what appears in the data.
  • Stimulated reporting: Media coverage and public awareness can temporarily increase reporting rates for specific vaccines, independent of any change in actual safety.
  • No control group: VAERS does not include a comparison group of unvaccinated individuals, making it impossible to determine whether reported events occurred at a higher rate than expected.
  • Variable data quality: VAERS reports range from detailed medical records submitted by healthcare providers to brief descriptions from patients. Not all reports are verified for medical accuracy.
  • Duplicate reports: The same event may be reported by multiple people (patient, doctor, manufacturer), and some duplicates may remain in the data.

For these reasons, VAERS data is best used for signal detection — identifying potential safety concerns that warrant further investigation — rather than for definitive risk assessment. When VAERS surfaces a potential signal, it is investigated using more rigorous systems like the Vaccine Safety Datalink (VSD) and controlled epidemiological studies.

About This Data

All data on VaccineWatch comes from the official VAERS public-use datasets published by the CDC and FDA. Our current dataset covers reports from 1990 through early 2026. We process the raw data without filtering or editorializing — every metric is a transparent aggregation of official government data.

Our Methodology →FAQ →Disclaimer →

2026 Data Context

As VAERS reporting normalizes following the COVID-19 pandemic surge, the data landscape for gender patterns in adverse event reporting is shifting. Annual VAERS reports in 2025-2026 have returned to the 35,000-45,000 range typical of the pre-pandemic era (2015-2019), making year-over-year comparisons more meaningful again.

The HHS administration has signaled increased focus on vaccine safety data analysis, including the development of AI-powered tools for pattern detection in VAERS reports. While these tools are still under development, they represent a potential evolution in how adverse event data is analyzed and interpreted.

New vaccines entering the market — including RSV vaccines for older adults and pregnant women, updated COVID-19 formulations, and potential H5N1 avian flu vaccines — continue to add new data streams to VAERS. Each new vaccine type provides additional context for understanding gender patterns in adverse event reporting across the full spectrum of vaccine safety surveillance.

Limitations of This Analysis

This analysis is based entirely on VAERS passive surveillance data, which carries important limitations that must be understood:

  • Underreporting: Studies estimate that only 1-10% of adverse events are reported to VAERS. This means the true number of events is likely much higher than what appears in the data.
  • Stimulated reporting: Media coverage and public awareness can temporarily increase reporting rates for specific vaccines, independent of any change in actual safety.
  • No control group: VAERS does not include a comparison group of unvaccinated individuals, making it impossible to determine whether reported events occurred at a higher rate than expected.
  • Variable data quality: VAERS reports range from detailed medical records submitted by healthcare providers to brief descriptions from patients. Not all reports are verified for medical accuracy.
  • Duplicate reports: The same event may be reported by multiple people (patient, doctor, manufacturer), and some duplicates may remain in the data.

For these reasons, VAERS data is best used for signal detection — identifying potential safety concerns that warrant further investigation — rather than for definitive risk assessment. When VAERS surfaces a potential signal, it is investigated using more rigorous systems like the Vaccine Safety Datalink (VSD) and controlled epidemiological studies.

About This Data

All data on VaccineWatch comes from the official VAERS public-use datasets published by the CDC and FDA. Our current dataset covers reports from 1990 through early 2026. We process the raw data without filtering or editorializing — every metric is a transparent aggregation of official government data.

Our Methodology →FAQ →Disclaimer →

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