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Transparent access to VAERS data for informed decision-making. We present the data as-is, with appropriate context and disclaimers.

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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. Msp Vaccine Company

Msp Vaccine Company

2,414 total reports0.1% market share
2,414
Total Reports
30
Deaths
99
Hospitalizations
1
Vaccines

About Msp Vaccine Company

Msp Vaccine Company has 2,414 adverse event reports in VAERS, representing 0.1% of all manufacturer-attributed reports.

Of these reports, 30 mentioned death and 99 involved hospitalization.

Msp Vaccine Company produces 1 vaccine tracked in VAERS. Their relatively low report count reflects a smaller market presence or specialized vaccine portfolio.

Vaccines by Msp Vaccine Company

VaccineReportsDeathsHospitalizations
DTPPVHBHPB2,0232487

Understanding Manufacturer Data

•Market presence matters: More reports often reflect more doses distributed, not necessarily more safety issues.
•Reporting varies: Newer vaccines and those under heightened scrutiny tend to have higher reporting rates.
•All manufacturers meet FDA standards: Safety and efficacy requirements apply equally to all approved vaccines.

Top Vaccines

1. DTPPVHBHPB2,414

Explore Further

Top Vaccine: DTPPVHBHPBAll ManufacturersManufacturer LandscapeCompare Vaccines

Data Source

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