🏥 VAERS Vaccine Data Browser

🔒 Privacy & Data Disclaimer

About This Site

This is a public data browser for the Vaccine Adverse Event Reporting System (VAERS). By using this site, you acknowledge and agree to the following:

Data Source & Accuracy

  • Public Data: All data displayed comes from the publicly available VAERS database maintained by the CDC and FDA.
  • No Verification: VAERS accepts all reports without verifying medical accuracy. Reports do not prove causation between vaccines and adverse events.
  • Anyone Can Report: Healthcare providers, patients, family members, and anyone else can submit reports to VAERS.
  • Research Purpose: This data is for transparency, research, and monitoring vaccine safety signals only.

Your Privacy

  • No Personal Data Collection: This site does not collect, store, or track any personal information about visitors.
  • No Cookies: We do not use cookies except for remembering that you've seen this disclaimer (stored locally in your browser).
  • No Analytics: We do not use Google Analytics or any other tracking services.
  • Search Privacy: Your searches and filters are not logged or stored on our servers.
  • Public Data Only: The VAERS data shown here is already public and contains no personally identifiable information.

Medical Disclaimer

  • Not Medical Advice: This tool is for informational purposes only and does not provide medical advice.
  • Consult Healthcare Providers: Always consult qualified healthcare professionals for medical decisions.
  • No Liability: We are not responsible for decisions made based on this data.

Data Interpretation

  • The presence of a report does not mean the vaccine caused the adverse event.
  • Coincidental events are often reported (e.g., a heart attack that happened to occur after vaccination).
  • Serious adverse events must be reported by law, even if unrelated to the vaccine.
  • The database is useful for detecting safety signals that require further investigation.

📖 Help & Search Guide

Column Icons Legend

💀 Death
🏥 Hospitalized
🚑 Emergency Room
♿ Disability
⚠️ Life Threatening

How to Search

💡 Search Tips:
  • Select Year: Choose a specific year OR "All Years" to search across all data
  • All Years requires filters: When searching all years, you must select at least one filter (lot number, vaccine type, outcome, etc.) for performance
  • Lot number tracking: Use "All Years" + Lot Number to track lots across multiple years
  • Combine filters: Use multiple filters together to narrow results (e.g., Age + Vaccine Type + Death)
  • VAERS ID: Search for specific report by ID number
  • Age: Enter exact age (e.g., 25) or decimal (e.g., 0.5 for 6 months)
  • State: Enter 2-letter state code (e.g., CA, NY, TX)
  • Vaccine Type: Search partial names (e.g., "COVID19", "FLU", "HPV")
  • Manufacturer: Search by company (e.g., "PFIZER", "MODERNA")
  • Lot Number: Search specific vaccine lot (works great with "All Years")
  • Symptoms: Search for any symptom keyword (e.g., "fever", "rash")
  • Death/Hospitalized: Filter to only show cases with these outcomes

Understanding the Data

  • Reports are unverified: VAERS accepts all reports without medical verification
  • Not proof of causation: A report does not mean the vaccine caused the event
  • Anyone can report: Healthcare providers, patients, and family members can submit reports
  • Multiple vaccines: One report may list multiple vaccines given at the same time
  • Blank fields: Not all fields are required, so some data may be missing

Using the Table

  • Sort columns: Click column headers (ID, Age, Sex, Date, Died) to sort
  • Expand text: Click "More" to see full narrative or symptom text
  • Navigate pages: Use pagination controls at top and bottom of table
  • Export results: Click "📥 Export CSV" to download filtered data (max 10,000 records)

💡 Frequently Asked Questions (FAQ)

What is this site?

🏥 VAERS Vaccine Data Browser is an independent, third-party data browser for publicly available VAERS (Vaccine Adverse Event Reporting System) data.

Important: This site is NOT affiliated with, endorsed by, or operated by the CDC, FDA, or any government agency. We are an independent service that makes public VAERS data easier to search and analyze.

What is VAERS?

VAERS (Vaccine Adverse Event Reporting System) is a national early warning system established in 1990 to detect possible safety problems with vaccines. It's co-managed by the CDC (Centers for Disease Control and Prevention) and FDA (Food and Drug Administration).

VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination.

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

  • Publicly available - Published by the CDC/FDA on their official website
  • De-identified - Contains no personally identifiable information (names, addresses, contact info removed)
  • Legally accessible - Available to researchers, media, and the general public under FOIA (Freedom of Information Act)
  • Not protected health information - Once de-identified and published by the government, it's no longer covered by HIPAA restrictions

This site displays the same public data available at vaers.hhs.gov/data.

Why does this site exist?

We believe in transparency and public access to health data. While the CDC/FDA provide VAERS data, their official site:

  • Is difficult to search and filter
  • Requires downloading large CSV files and technical knowledge
  • Is not user-friendly for the average person

This independent site makes the same publicly available data easier to search, filter, and understand for researchers, journalists, healthcare workers, and concerned citizens.

Where does the data come from?

All data is downloaded directly from the official CDC/FDA VAERS website at vaers.hhs.gov/data.

The data is:

  • Publicly released by the CDC/FDA every week
  • Available as downloadable CSV files
  • Imported into this site's database for easier searching
  • Displayed exactly as provided (no modifications or filtering)

This site does not collect, modify, or add to the official VAERS data.

My vaccine lot number matches one with deaths/serious events - should I be worried?

Important context:

  • VAERS reports do NOT prove causation - A report means an event occurred after vaccination, but doesn't mean the vaccine caused it
  • Anyone can report - Reports are not verified for medical accuracy before being published
  • Coincidences happen - When millions of people get vaccinated, some will experience unrelated medical events afterward
  • Large lot numbers - Popular vaccines may have hundreds of thousands of doses from one lot number
  • More vaccinations = more reports - Lots used widely will naturally have more reports

What to do:

  • Don't panic - VAERS data requires expert analysis to interpret
  • Talk to your doctor if you have concerns
  • Check official CDC/FDA safety communications for genuine safety signals
  • Remember: billions of vaccine doses have been safely administered

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

  • ✅ Early warning system for potential safety signals
  • ✅ Open and transparent - publicly accessible
  • ✅ Accepts all reports regardless of likelihood of causation
  • ✅ Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • ⚠️ Reports are unverified - not investigated before publication
  • ⚠️ Cannot determine if vaccine caused the event
  • ⚠️ Underreporting - not all adverse events are reported
  • ⚠️ Overreporting - coincidental events may be reported
  • ⚠️ Incomplete data - not all fields are required

Bottom line: VAERS is an important tool for safety monitoring, but individual reports should not be used as proof that a vaccine caused harm.

What are "adverse events"?

An adverse event is any undesirable health occurrence that happens after vaccination, including:

  • Common reactions: Sore arm, mild fever, fatigue (usually expected)
  • Serious events: Hospitalization, disability, life-threatening illness, death
  • Coincidental events: Medical conditions that would have occurred anyway

Important: An adverse event doesn't mean the vaccine caused it - only that it occurred after vaccination. Many reported events are coincidental or unrelated.

Why are some lot numbers listed multiple times?

This is normal and expected! A person may receive multiple doses of the same vaccine from the same lot number:

  • COVID vaccines require 2-3 doses
  • HPV, Hepatitis B, and other vaccines have multi-dose schedules
  • Each dose is recorded as a separate entry

Example: Person receives Pfizer COVID dose 1 (lot ABC123) and dose 2 (lot ABC123) - lot ABC123 appears twice in their report.

How often is this data updated?

The CDC/FDA releases new VAERS data every Friday. This site is typically updated:

  • Weekly or bi-weekly for recent data
  • Check the available years to see what data is currently loaded
  • During updates, the site may be in maintenance mode temporarily

Where can I learn more?

⚠️ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
🔄 Reset 📥 Export CSV
ID Age Sex State Date ▼ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative 💀 🏥 🚑 ♿ ⚠️
2828376 29 F ME 02/26/2025 FLU3
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 K9XL5
U7999AA
No adverse event, Product storage error; No adverse event, Product storage error No adverse event, Product storage error; No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828377 34 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999AA
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828378 18 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999AA
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828379 65 M PA 02/26/2025 COVID19
 MODERNA
 013A21A
Arthralgia, Contusion, Magnetic resonance imaging joint, Osteonecrosis Arthralgia, Contusion, Magnetic resonance imaging joint, Osteonecrosis
One week after injections, I noted in my diary left shoulder pain and a bruise. I attributed the pai... One week after injections, I noted in my diary left shoulder pain and a bruise. I attributed the pain and bruise to moving some furniture but now think that the injection may have been responsible. Subsequently, in 2025, I was diagnosed by an orthopedic surgeon with Avascular Necrosis in that shoulder that involved my Humeral Head. There was no other explanation for that development. More
2828380 37 F ME 02/26/2025 FLU3
RSV
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
SANOFI PASTEUR
 K9XL5
HY1812
U79999a
No adverse event, Product storage error; No adverse event, Product storage error... No adverse event, Product storage error; No adverse event, Product storage error; No adverse event, Product storage error More
Out of range temperature for refrigerator. No adverse reactions. Out of range temperature for refrigerator. No adverse reactions.
2828381 32 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999A
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828382 35 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999A
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828383 34 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999A
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828384 33 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828385 23 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999A
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828386 26 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999A
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828387 11 M IA 02/26/2025 HPV9
 MERCK & CO. INC.
 1965046
Cognitive disorder, Mobility decreased, Pain in extremity Cognitive disorder, Mobility decreased, Pain in extremity
His arm was in intense pain for a couple of days and he wasn't physically able to grip anything... His arm was in intense pain for a couple of days and he wasn't physically able to grip anything or squeeze with that hand. Even cognitively he was really off for a couple of days. No treatment given aside from symptomatic cares at home and monitoring. More
2828388 17 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999A
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828389 31 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828390 6 F GA 02/26/2025 DTAP
FLU3
HEP
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 9R2D7
U8442BA
F5L5E
Extra dose administered; Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered; Extra dose administered
Patient was given Hepatitis B vaccine that was not needed. Patient was given Hepatitis B vaccine that was not needed.
2828391 02/26/2025 COVID19
 JANSSEN
 Unknown
Mass, Unevaluable event Mass, Unevaluable event
unspecified mass; body does not work the same; This spontaneous report received from a health care p... unspecified mass; body does not work the same; This spontaneous report received from a health care professional concerned a patient of unspecified age and sex. The patient's height and weight were not reported. Age at time of vaccination was unknown. No past medical history, concurrent conditions or pre-existing medical conditions were reported. The patient received janssen covid-19 vaccine (suspension for injection, route of admin not reported, batch number: Unknown) dose, frequency and therapy dates not reported, additional dosage information included: dose series 1, for covid-19 prophylaxis. The batch number was not reported. The company is unable to perform follow up. No concomitant medications were reported. On an unspecified date, the patient experienced unspecified mass and body does not work the same. (dose series 1). The doctors found a mass in my body, and know have to get it removed. Patient do not have the money to get it removed because patient was not working . Ever sense patient got the Covid-19 vaccine, body does not work the same. They are not looking for money, just for someone to help with this. The action taken with janssen covid-19 vaccine was not applicable. The outcome of unspecified mass and body does not work the same was not reported. This report was associated with a product quality complaint: Product Complaint 90000351091. This report was serious (other medically important condition).; Sender's Comments: V0: Mass. Insufficient information is available to make a causality assessment. Therefore, this event is considered unclassifiable. More
2828392 31 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828393 23 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828394 33 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828395 35 F ME 02/26/2025 RSV
 PFIZER\WYETH
 LN5490
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828396 18 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828397 34 F ME 02/26/2025 FLU3
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 K9XL05
U7999AA
No adverse event, Product storage error; No adverse event, Product storage error No adverse event, Product storage error; No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828398 11 M TN 02/26/2025 FLU3
MNQ
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
 AE2J7
U8370AA
3CA30C1
Dizziness, Feeling abnormal, Pallor; Dizziness, Feeling abnormal, Pallor; Dizzin... Dizziness, Feeling abnormal, Pallor; Dizziness, Feeling abnormal, Pallor; Dizziness, Feeling abnormal, Pallor More
Pt received 3 vaccinations. Less than 5 minutes after receiving vaccinations patient begins complain... Pt received 3 vaccinations. Less than 5 minutes after receiving vaccinations patient begins complaining of dizziness. Pt became pale. Juice and crackers given to patient. Pt stated he was feeling worse. BP taken at 1041 was 78/52. Pt laid down and feet were elevated. Pt remained conscious entire time and was talking to this RN. MD was present at bedside d/t pt history of seizures. BP repeated at 1044 was 126/76. Pt color returned and he stated he was no longer dizzy. Pt moved to sitting position and BP repeated at 1046 107/58. Pt stated he felt fine and was no longer dizzy. Pt color returned to baseline and all vitals WNL. Pt monitored in clinic for additional 30 minutes d/t history. Interpreter present for incident. More
2828399 25 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999AA
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828400 28 F ME 02/26/2025 FLU3
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 K9XL5
U7999AA
No adverse event, Product storage error; No adverse event, Product storage error No adverse event, Product storage error; No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828401 47 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828402 17 F ME 02/26/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828403 34 F TN 02/26/2025 HPV9
 MERCK & CO. INC.
Arthralgia, Joint stiffness, Musculoskeletal stiffness, Myalgia Arthralgia, Joint stiffness, Musculoskeletal stiffness, Myalgia
Muscle and Joint stiffness and pain, ibuprofen and topical muscle cream Muscle and Joint stiffness and pain, ibuprofen and topical muscle cream
2828404 37 F ME 02/26/2025 TDAP
 SANOFI PASTEUR
 U7999AA
No adverse event, Product storage error No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828405 56 F FL 02/26/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Chest injury, Dizziness, Face injury, Headache, Mobility decreased; Nausea, Sync... Chest injury, Dizziness, Face injury, Headache, Mobility decreased; Nausea, Syncope, Vomiting More
Severe headache, Dizziness that resulted in fainting three times (which caused injuries to my face a... Severe headache, Dizziness that resulted in fainting three times (which caused injuries to my face and ribcage), Nausea resulting in vomiting. All symptoms persisted for more than 24 hours. More
2828406 90 F TX 02/26/2025 TDAP
 SANOFI PASTEUR
 U8352AA
Cellulitis, Erythema Cellulitis, Erythema
Developed redness that spread to elbow area. Was diagnosed with cellulitis and given antibiotic pre... Developed redness that spread to elbow area. Was diagnosed with cellulitis and given antibiotic prescription x 7 days. 1-week later redness started to subside. More
2828407 44 F WI 02/26/2025 FLU3
HEPAB
IPV
VARCEL
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 U8523BA
4DS4N
X1B141M
Y011019
Loss of personal independence in daily activities, Pain, Pain in extremity, Tend... Loss of personal independence in daily activities, Pain, Pain in extremity, Tenderness; Loss of personal independence in daily activities, Pain, Pain in extremity, Tenderness; Loss of personal independence in daily activities, Pain, Pain in extremity, Tenderness; Loss of personal independence in daily activities, Pain, Pain in extremity, Tenderness More
Patient reported experiencing bilateral arm pain after receiving vaccines in both arms. However, pai... Patient reported experiencing bilateral arm pain after receiving vaccines in both arms. However, pain in left upper arm continued. Patient returned 1 month later for second doses and reported pain to RN. Adacel received in left deltoid on 1/21/25. Client reported bilateral arm pain due to vaccination, pain in left upper arm continued. Patient returned to clinic on 2/25/25 to report pain. Describes pain as sharp like a needlestick upon palpation, soreness with movement- hurts/makes getting dressed difficult. Upon evaluation, no obvious bruises, masses, redness, swelling present. Patient denies injury or trauma to site before or after vaccination and reports she does not sleep on that side nor does any work that strains the muscle. Describes pain as 8/10- still feels like she was recently vaccinated. More
2828408 50 M CA 02/26/2025 PNC13
PNC13
 PFIZER\WYETH
PFIZER\WYETH

Asthenia, Headache, Immediate post-injection reaction, Influenza, Nausea; Night ... Asthenia, Headache, Immediate post-injection reaction, Influenza, Nausea; Night sweats, Pyrexia, Rash, Rash pruritic More
Immediate flu symptoms. 101.5 fever. Rash on inner arm for one week thus far. Night sweats for a w... Immediate flu symptoms. 101.5 fever. Rash on inner arm for one week thus far. Night sweats for a week and thus far. Severe headache. Felt like I was getting better but on day 7 feeling very weak, nausea and headache is back. Still itchy rash. More
2828409 7 M 02/26/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 LM2221
U8518DA
No adverse event, Product administered to patient of inappropriate age; No adver... No adverse event, Product administered to patient of inappropriate age; No adverse event, Product administered to patient of inappropriate age More
No adverse reaction. Pfizer-BioNTech for age 12 years and up was administered to a 7 year old patien... No adverse reaction. Pfizer-BioNTech for age 12 years and up was administered to a 7 year old patient. More
2828410 PA 02/26/2025 COVID19
 MODERNA
Cardiac arrest, Post-anoxic myoclonus Cardiac arrest, Post-anoxic myoclonus
have a cardiac arrest and I was dead for 16 minutes; Lance Adam's syndrome; This spontaneous ca... have a cardiac arrest and I was dead for 16 minutes; Lance Adam's syndrome; This spontaneous case was reported by a patient and describes the occurrence of CARDIAC ARREST (have a cardiac arrest and I was dead for 16 minutes) and POST-ANOXIC MYOCLONUS (Lance Adam's syndrome) in a patient of an unknown age and gender who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 vaccination. The patient's past medical history included Physical therapy (for 4 years.). On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (unknown route) 1 dosage form. On an unknown date, the patient experienced CARDIAC ARREST (have a cardiac arrest and I was dead for 16 minutes) (seriousness criterion medically significant) and POST-ANOXIC MYOCLONUS (Lance Adam's syndrome) (seriousness criterion disability). The patient was treated with Physical therapy for Post-anoxic myoclonus. At the time of the report, CARDIAC ARREST (have a cardiac arrest and I was dead for 16 minutes) and POST-ANOXIC MYOCLONUS (Lance Adam's syndrome) outcome was unknown. The action taken with SPIKEVAX NOS (SPIKEVAX NOS) (Unknown) was unknown. No concomitant medications were reported. The patient had own construction company for 30 years and now in physical therapy for 4 years and can barely walk. The patient can't use left hand either. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 20-Feb-2025: Live follow up received that contains no new significant information. On 20-Feb-2025: Live follow up received that contains no new significant information.; Reporter's Comments: The benefit-risk relationship of the product is not affected by this report. More
✓
2828411 13 M CO 02/26/2025 HEP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 42D7A
CX4HL
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
Patient and guardian did not consent to vaccination but doses were administered. No physical symptom... Patient and guardian did not consent to vaccination but doses were administered. No physical symptoms or adverse reaction occurred. 02/27/2025 Phone follow-up: Patient believes they did not consent states they did not consent to vaccine. More
2828412 7 F MT 02/26/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 YC239
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Dtap given to 7 year old Dtap given to 7 year old
2828413 1 M GA 02/26/2025 HEPA
HIBV
MMR
PNC20
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
MERCK & CO. INC.
 t5727
y006391
X027446
lc5483
y011015
Decreased appetite, Rash, Rash morbilliform, Rash pruritic; Decreased appetite, ... Decreased appetite, Rash, Rash morbilliform, Rash pruritic; Decreased appetite, Rash, Rash morbilliform, Rash pruritic; Decreased appetite, Rash, Rash morbilliform, Rash pruritic; Decreased appetite, Rash, Rash morbilliform, Rash pruritic; Decreased appetite, Rash, Rash morbilliform, Rash pruritic More
Rash on the back and abdomen began two days ago. Mom applied hydrocortisone twice yesterday and agai... Rash on the back and abdomen began two days ago. Mom applied hydrocortisone twice yesterday and again this morning, but the rash remains unchanged and continues to itch. No fever, patient is drinking well, but appetite temporarily decreased after vaccination and is now improving. No known sick contacts. Rash appears measles-like, likely a reaction to the MMR vaccine, with no signs of active measles. Parents were educated that the rash is self-limiting and will resolve on its own. No medication needed at this time. More
2828414 0.17 F 02/26/2025 RV1
 GLAXOSMITHKLINE BIOLOGICALS
 5N2AN
Haematemesis Haematemesis
1 episode of frank hematemesis that the day after vaccine administration 1 episode of frank hematemesis that the day after vaccine administration
✓
2828415 19 M PA 02/26/2025 COVID19
 MODERNA
 8080803
Expired product administered, No adverse event Expired product administered, No adverse event
Box expiration date is 06/11/2025. After vaccine administered and patient left, RN realized that the... Box expiration date is 06/11/2025. After vaccine administered and patient left, RN realized that the BUD date was 02/08/2025 (as it was in the fridge). No adverse reactions in office. More
2828416 0.33 M VA 02/26/2025 DTAPHEPBIP
HIBV
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH


Erythema, Induration, Peripheral swelling; Erythema, Induration, Peripheral swel... Erythema, Induration, Peripheral swelling; Erythema, Induration, Peripheral swelling; Erythema, Induration, Peripheral swelling More
Erythema and swelling of thigh, with residual induration palpable Erythema and swelling of thigh, with residual induration palpable
2828417 28 F MI 02/26/2025 MMRV
 MERCK & CO. INC.
 y011210
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no noted adverse events no noted adverse events
2828418 16 M AZ 02/26/2025 MENB
MENB
MNQ
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
 A274J
A274J
9M2R7
9M2R7
Disorientation, Dizziness, Headache, Heart rate increased, Immediate post-inject... Disorientation, Dizziness, Headache, Heart rate increased, Immediate post-injection reaction; Seizure like phenomena; Disorientation, Dizziness, Headache, Heart rate increased, Immediate post-injection reaction; Seizure like phenomena More
Spoke to mother, she explains right after he received the vaccines, he begun feeling disorientated,... Spoke to mother, she explains right after he received the vaccines, he begun feeling disorientated, dizzy, HR was elevated, and stated he felt like he was going to have a seizure. I asked mother if he had a history of seizures and she stated no history of seizures. After about 2 hours, the symptoms subsided, but had a HA that lasted a couple days after. Mother feels it may have been the Menveo or Bexsero he had received that day. I explained to mother I would report his reaction to vaers. And if any other information is needed from mother, she would ne contacted. More
2828419 71 M OH 02/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Blood pressure fluctuation, Heart rate decreased Blood pressure fluctuation, Heart rate decreased
Blood pressure spikes and dives. Resting heart rate lower. Blood pressure spikes and dives. Resting heart rate lower.
2828420 70 M VA 02/26/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FD 7218
FD 7218
Cardiac failure congestive, Catheterisation cardiac, Computerised tomogram thora... Cardiac failure congestive, Catheterisation cardiac, Computerised tomogram thorax, Echocardiogram, Electrocardiogram; Heart valve incompetence, Scan with contrast More
Developed Acute congestive cardiac failure 4 months after 3rd vaccine. Follow on testing indicated ... Developed Acute congestive cardiac failure 4 months after 3rd vaccine. Follow on testing indicated leaking aortic heart valve. No family history of heart issues. More
2828421 5 M VA 02/26/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 U7838AA
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Mom called yesterday afternoon 2/25 about patient's right thigh becoming swollen, painful and r... Mom called yesterday afternoon 2/25 about patient's right thigh becoming swollen, painful and red the day after patient was vaccinated on 2/24. DTAP/IPV given to patient in that thigh. Mom instructed to apply cold compresses and give Ibuprofen, and to monitor site. Mother brought patient in to the clinic today. Patient evaluated by doctor and sent home with instructions on what to monitor for and further instructions. More
2828422 0.33 F CA 02/26/2025 DTAP
RV5
 SANOFI PASTEUR
MERCK & CO. INC.

Crying, Injection site reaction, Pyrexia, Rash erythematous; Crying, Injection s... Crying, Injection site reaction, Pyrexia, Rash erythematous; Crying, Injection site reaction, Pyrexia, Rash erythematous More
inconsolable crying for 3 days, fever, reddened site with bumps. inconsolable crying for 3 days, fever, reddened site with bumps.
2828423 56 F SC 02/26/2025 PNC21
 MERCK & CO. INC.
 yo11819
Erythema Erythema
pt had allergic rx after 3 days its only reddness no fever or any signs of infection pt had allergic rx after 3 days its only reddness no fever or any signs of infection
2828424 1 M MI 02/26/2025 HEPA
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 DN273
Y013073
Vomiting; Vomiting Vomiting; Vomiting
Had 3 episodes of vomiting on 2/21/2025. Starting at 6:30 AM. Had 3 episodes of vomiting on 2/21/2025. Starting at 6:30 AM.
2828425 1 FL 02/26/2025 VARCEL
 MERCK & CO. INC.
 Y011018
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Patient was given a live virus too soon to the previously given live vaccine. The dosing betweeen MM... Patient was given a live virus too soon to the previously given live vaccine. The dosing betweeen MMR and Varicella was only 2 weeks instead of the 4 week guideline. Per vaccine guidelines, the child will not have immunity given from the varicella vaccine and will require 2 doses appropriately spaced. No other symptoms reported by parents. More
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