🏥 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 💀 🏥 🚑 ♿ ⚠️
2827985 20 F KY 02/25/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 42B22
Underdose Underdose
dose 1 given was a pediatric dose; dose 1 given was a pediatric dose; This non-serious case was repo... dose 1 given was a pediatric dose; dose 1 given was a pediatric dose; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of underdose in a 20-year-old female patient who received HBV (Engerix B pediatric) (batch number 42B22, expiry date 07-MAR-2026) for prophylaxis. On 25-JUL-2024, the patient received the 1st dose of Engerix B pediatric. On 25-JUL-2024, an unknown time after receiving Engerix B pediatric, the patient experienced underdose (Verbatim: dose 1 given was a pediatric dose) and adult use of a child product (Verbatim: dose 1 given was a pediatric dose). The outcome of the underdose and adult use of a child product were not applicable. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 30-JAN-2025 The pharmacist reported that 21 year old female patient was in pharmacy requesting third dose of Engerix-B series. The first two doses were administered at another facility. Upon looking at the records, dose 1 was given was a pediatric dose which led to underdose and adult use of a child product. On 27th August 2024, dose 2 was given was an adult dose. The patient was 20 years old at the time of both doses. At the time of call, the pharmacist had not yet administered a third dose. More
2827986 78 F AL 02/25/2025 COVID19
COVID19
 MODERNA
MODERNA

Atrial fibrillation, Blood disorder, Cerebral thrombosis, Cerebrovascular accide... Atrial fibrillation, Blood disorder, Cerebral thrombosis, Cerebrovascular accident, Death; Fluid retention More
developed atrial fibrillation/atrial fibrillation worsened; stroke; blood clot was found in her brai... developed atrial fibrillation/atrial fibrillation worsened; stroke; blood clot was found in her brain; having blood issues after her first vaccine; we lost her; she started retaining water 2 weeks before we lost her; This spontaneous case was reported by a patient family member or friend and describes the occurrence of DEATH (we lost her), ATRIAL FIBRILLATION (developed atrial fibrillation/atrial fibrillation worsened), CEREBROVASCULAR ACCIDENT (stroke) and CEREBRAL THROMBOSIS (blood clot was found in her brain) in a 78-year-old female patient who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On an unknown date, the patient received first dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. On an unknown date, received second dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) dosage was changed to 1 dosage form and third dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) dosage was changed to 1 dosage form. In August 2022, the patient experienced FLUID RETENTION (she started retaining water 2 weeks before we lost her). On an unknown date, the patient experienced ATRIAL FIBRILLATION (developed atrial fibrillation/atrial fibrillation worsened) (seriousness criterion medically significant), CEREBROVASCULAR ACCIDENT (stroke) (seriousness criterion medically significant), CEREBRAL THROMBOSIS (blood clot was found in her brain) (seriousness criterion medically significant) and BLOOD DISORDER (having blood issues after her first vaccine). The patient died on 14-Sep-2022. The cause of death was not reported. It is unknown if an autopsy was performed. At the time of death, ATRIAL FIBRILLATION (developed atrial fibrillation/atrial fibrillation worsened), CEREBROVASCULAR ACCIDENT (stroke), CEREBRAL THROMBOSIS (blood clot was found in her brain), FLUID RETENTION (she started retaining water 2 weeks before we lost her) and BLOOD DISORDER (having blood issues after her first vaccine) outcome was unknown. Concomitant medication was not reported. Patient started having blood issues after her first vaccine. After her second vaccine she developed atrial fibrillation issues and was rushed to the emergency room for a stroke, and a blood clot was found in her brain. After the third vaccine the atrial fibrillation worsened, and she started retaining water 2 weeks before her death. It was unknown if the patient experienced any additional symptoms/events. Treatment medication was not reported.; Reporter's Comments: Company comment: The benefit-risk relationship of product is not affected by this report.; Reported Cause(s) of Death: we lost her More
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2827987 NY 02/25/2025 DTPPVHBHPB
 MSP VACCINE COMPANY
 U7907AA
Extra dose administered Extra dose administered
administered a 4th dose of the vaccine on 10/21/2024 while they were 9 months old. Nurse confirmed t... administered a 4th dose of the vaccine on 10/21/2024 while they were 9 months old. Nurse confirmed the patient adhered to the 3 dose series of VAXELIS, but were inadvertently administered a 4th dose.; administered a 4th dose of the vaccine on 10/21/2024 while they were 9 months old. Nurse confirmed the patient adhered to the 3 dose series of VAXELIS, but were inadvertently administered a 4th dose.; administered a 4th dose of the vaccine on 10/21/2024 while they were 9 months old. Nurse confirmed the patient adhered to the 3 dose series of VAXELIS, but were inadvertently administered a 4th dose.; This non-serious spontaneous safety report, with reference number 02739314 (interaction number: 02739305), was received by partner on 21-JAN-2025 and forwarded to agency on 21-JAN-2025 from other health professional. Off-label classification was added due to Vaxelis being administered to a 9-month-old patient. Due to the nature of the event, the causality between the events 'administered a 4th dose of the vaccine on 10/21/2024 while they were 9 months old. Nurse confirmed the patient adhered to the 3 dose series of VAXELIS but were inadvertently administered a 4th dose' and Vaxelis was not applicable. Further information is expected. More
2827989 66 M MT 02/25/2025 COVID19
 PFIZER\BIONTECH
Cardiac amyloidosis, Carpal tunnel syndrome, Magnetic resonance imaging heart, M... Cardiac amyloidosis, Carpal tunnel syndrome, Magnetic resonance imaging heart, Muscle injury, Tendon rupture More
Patient received Pfizer covid 19 vaccine doses on 2/5/21 and 2/26/21. Following those Pfizer Covid 1... Patient received Pfizer covid 19 vaccine doses on 2/5/21 and 2/26/21. Following those Pfizer Covid 19 doses patient experienced bilateral bicep tears, bilateral ham [INVALID]te, and bilateral carpal tunnel syndromes. Patient was concerned about possible amyloidosis following these symptoms as muscle and carpal tunnel manifestations are known complications of amyloidosis. In August of 2023 (~18 months follow covid vaccine doses) he was diagnosed with cardiac amyloidosis. Case reports of covid 19 vaccine induced amyloidosis are available in published literature. More
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2827990 35 M NY 02/25/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 x449y
Hypoaesthesia, Paraesthesia Hypoaesthesia, Paraesthesia
Patient states they have arm tingling and numbness radiating through their shoulder into their finge... Patient states they have arm tingling and numbness radiating through their shoulder into their fingers on the arm the vaccine was administered. it has been over 4 months since then and it still comes and goes, has not gotten better. More
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2827991 F IN 02/25/2025 COVID19
 MODERNA
Computerised tomogram abnormal, Lymphadenopathy, Neoplasm Computerised tomogram abnormal, Lymphadenopathy, Neoplasm
I am a 56 y/o woman with a history of Type 1 Diabetes (LADA) Lupus, Stage 3A Kidney Disease, Non-Alc... I am a 56 y/o woman with a history of Type 1 Diabetes (LADA) Lupus, Stage 3A Kidney Disease, Non-Alcoholic Cirrhosis of the Liver and Breast Cancer. After receiving my second Moderna vaccination for Covid 19, (that made me so ill I spent close to a week in bed) I noticed that the lymph nodes on the underneath side of my arms from my armpits down and my groin, became swollen and dense feeling. I put it down to being chronically sick. However, when I mentioned it to my endocrinologist literally a few years later, she ordered a CT scan. It showed lymph nodes of various sizes with flow, having fatty hilums. ranging from 0.5 to 2.5 cm The lymph nodes have times when they slightly reduced in size only to come back and get larger. They currently feel the largest they have even been. Especially in the armpit next to the breast where I had my lumpectomy and radiation treatment for breast cancer. I have an MRI scheduled for 2/25/25. It is for a couple of different things, but my endocrinologist will be looking at the state of my lymph nodes. Having had cancer and still having several tumors is what is concerning to my doctor. There lines of swollen lymph nodes never existed prior to the Moderna Covid vaccination, which I received approximately 4/21 from the pharmacy at our local store. Although I have many co-morbid conditions, permanently swollen lymph nodes were never one of them. I would like to know if the Moderna vaccination indeed caused this, and will this do me further harm given my medical history of cancer and currently having multiple tumors? Knowledge is power and staying on top of my medical conditions is imperative. I'm sure that is understandable. Thank you for your time and consideration We will find out after the 25th if there are additional changes to the lymph nodes and the existing tumors. More
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2827992 F MI 02/25/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Stevens-Johnson syndrome Stevens-Johnson syndrome
I received a GSK RSV vaccine and had a late onset reaction that turned out to be SJS I went to Urgen... I received a GSK RSV vaccine and had a late onset reaction that turned out to be SJS I went to Urgent Care Clinic and no test was performed. More
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2827993 55 M MI 02/25/2025 COVID19
 PFIZER\BIONTECH
Alpha-1 antitrypsin deficiency, Chronic lymphocytic leukaemia Alpha-1 antitrypsin deficiency, Chronic lymphocytic leukaemia
Since taking the first two Covid vaccines, I have been diagnosed with alpha 1 antitrypsen deficiency... Since taking the first two Covid vaccines, I have been diagnosed with alpha 1 antitrypsen deficiency (no family history) and chronic lymphocytic leukemia. Perfectly health prior to Covid. More
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2827994 12 M FL 02/25/2025 HPV9
 MERCK & CO. INC.
Dysphagia, Facial paralysis, Hypoaesthesia, Mastication disorder, Paraesthesia Dysphagia, Facial paralysis, Hypoaesthesia, Mastication disorder, Paraesthesia
The evening after the vaccine, pt. began to feel tingling sensation in left cheek and jaw, the follo... The evening after the vaccine, pt. began to feel tingling sensation in left cheek and jaw, the following day at school his friends noted his "uneven facies, left side drooping", mom then noted significant facial differences when she saw him after school that day and took him straight to ER. There they performed a physical exam and labs. His vital signs and labs were normal, face was still numb on left side, weak with inability to smile and fully close left eye, mild difficulty chewing and swallowing. Per mother's report the providers at the ER did not feel that imaging was necessary. He was sent home on a oral steroid wean. When seen in PCP office on 2/22/25, weakness and numbness per More
2827995 1 M MA 02/25/2025 MMRV
PNC20
VARCEL
 MERCK & CO. INC.
PFIZER\WYETH
MERCK & CO. INC.
 Y017205
HR3650
Y011020
Unevaluable event; Unevaluable event; Unevaluable event Unevaluable event; Unevaluable event; Unevaluable event
None reported at this time None reported at this time
2828031 40 M CA 02/25/2025 COVID19
 PFIZER\BIONTECH
Ageusia, Anosmia, Magnetic resonance imaging Ageusia, Anosmia, Magnetic resonance imaging
Complete loss of taste and smell for more than two years. Smell and taste never went back to normal... Complete loss of taste and smell for more than two years. Smell and taste never went back to normal. More
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2828032 54 F SD 02/25/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EH9899
EL3246
FH8028
Ear congestion, Persistent postural-perceptual dizziness, Tinnitus, Vertigo posi... Ear congestion, Persistent postural-perceptual dizziness, Tinnitus, Vertigo positional; Ear congestion, Persistent postural-perceptual dizziness, Tinnitus, Vertigo positional; Ear congestion, Persistent postural-perceptual dizziness, Tinnitus, Vertigo positional More
Fullness in ears happened within an hour after first shot. Tinnitus started a few days later and ca... Fullness in ears happened within an hour after first shot. Tinnitus started a few days later and came and went at first becoming more frequent and the volume increasing after the second shot one month later. It didn't come and go after that, it just remained. I don't remember a change after the 3rd shot but the tinnitus is now permanent and loud. I am now dealing with BPPV and PPPD and constant tinnitus. More
2828033 61 M MI 02/25/2025 COVID19
COVID19
 MODERNA
MODERNA
 018b21a
043b21a
Excessive cerumen production, Tinnitus; Excessive cerumen production, Tinnitus Excessive cerumen production, Tinnitus; Excessive cerumen production, Tinnitus
Noticeable ringing in ears. Thought I had a wax plug so went to doctor to have ears checked out. D... Noticeable ringing in ears. Thought I had a wax plug so went to doctor to have ears checked out. During visit had a hearing exam. Noted to technician that I had ringing in my ears. Having worked in an industry that demanded hearing tests yearly, I knew that driving, which I had to drive 60 miles to appointment, may cause some hearing distortion. The doctor was also told of the ringing in the ears but no mention was made except for ear leaning. After visit and continuing on till today, the tinnitus remains. There is no relief able to be provided. As mentioned, I wore hearing protection every day and my hearing tests performed provided no abnormal impacts to hearing. The tinnitus did not occur during my working career. More
2828034 10 F GA 02/25/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 SKBT5727
Pruritus, Urticaria Pruritus, Urticaria
400pm developed localized left arm only urticaria and itching 400pm developed localized left arm only urticaria and itching
2828035 70 M SC 02/25/2025 PNC20
 PFIZER\WYETH
 lj5283
Extra dose administered Extra dose administered
patient received a second dose of vaccine after having received a dose less than 2 years ago. vaccin... patient received a second dose of vaccine after having received a dose less than 2 years ago. vaccines given too close together More
2828036 46 F GA 02/25/2025 HEP
MMR
 DYNAVAX TECHNOLOGIES CORPORATION
MERCK & CO. INC.
 944917
X026222
Fatigue, Flushing, Product preparation error, Rash, Vision blurred; Fatigue, Flu... Fatigue, Flushing, Product preparation error, Rash, Vision blurred; Fatigue, Flushing, Product preparation error, Rash, Vision blurred More
After administration of MMR vaccine subcutaneous to the left upper arm, noticed the MMR vaccine had ... After administration of MMR vaccine subcutaneous to the left upper arm, noticed the MMR vaccine had been reconstituted with the HEPLISAV-B vaccine instead of the sterile diluent. Subcutaneous injection was given at 11:30 AM. At 11:45 AM began c/o feeling flushed, slight blurry vision, rash noticed on bilateral sides of neck and on upper right scapula. Denied any symptoms of Anaphylaxis. 11:56 AM VS: BP 151/95 Pulse 75 Resp 16 O2 sat 98%. 12:05 PM Diphenhydramine 50 mg IM. 1225 rash and flushing has disappeared. Pt is feeling drowsy from the Benadryl injection. VSS. Monitored pt until daughter came to clinic to take her home. Pt denies any symptoms upon leaving with the exception of tiredness. Pt ambulated with assistance of RN to daughter's vehicle. Advised pt and daughter if patient were to experience any anaphylactic symptoms such as difficulty breathing, lip or tongue swelling or any other emergent conditions to report to the nearest emergency room for evaluation. Pt vitals upon clinic discharge at 1405 were: BP 134/83 heart rate 78, respirations 16, 02 sat 98%. More
2828037 64 M GA 02/25/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K72S4
Extra dose administered, No adverse event Extra dose administered, No adverse event
This dose of the influenza vaccine was administered on 1/30/2025. Unfortunately, the nurse administe... This dose of the influenza vaccine was administered on 1/30/2025. Unfortunately, the nurse administering the vaccine was unaware that the patient received a previous dose of the influenza vaccine on 1/02/2025. The patient had no symptoms, treatment was not required, and there were no adverse outcomes. More
2828038 9 F TX 02/25/2025 MMR
 MERCK & CO. INC.
 X004346
Expired product administered, No adverse event Expired product administered, No adverse event
Gave an expired MMR vaccine to child. MMR vaccine expired on 02/08/2025 and it was given on 02/20/20... Gave an expired MMR vaccine to child. MMR vaccine expired on 02/08/2025 and it was given on 02/20/2025. No adverse reactions noted. More
2828039 77 F 02/25/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3ext9
Erythema, Peripheral swelling, Rash, Swelling face Erythema, Peripheral swelling, Rash, Swelling face
Pt had severe reaction post vaccination for about 3 weeks. Their arm was red and swollen, then about... Pt had severe reaction post vaccination for about 3 weeks. Their arm was red and swollen, then about 2-3 weeks after vaccination she developed a red rash on her face with some swelling. More
2828040 15 F TX 02/25/2025 FLU3
HEP
HEPA
IPV
MMR
MNQ
TDAP
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 J245K
X024135
X025908
W1C831M
X004346
U7827AA
H95RD
X024649
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event More
Gave an expired MMR vaccine to child. MMR vaccine expired on 02/08/2025 and it was given on 02/20/20... Gave an expired MMR vaccine to child. MMR vaccine expired on 02/08/2025 and it was given on 02/20/2025. No adverse reactions noted. More
2828041 27 M VA 02/25/2025 IPV
MMR
 SANOFI PASTEUR
MERCK & CO. INC.
 Y1A201M
Y010372
Fall, Head injury, Syncope; Fall, Head injury, Syncope Fall, Head injury, Syncope; Fall, Head injury, Syncope
PT FAINTED 2-3 MINS AFTER ADMINISTRATION, HE WAS WALKING AWAY THEN FELL AND HIT HIS HEAD ON THE GROU... PT FAINTED 2-3 MINS AFTER ADMINISTRATION, HE WAS WALKING AWAY THEN FELL AND HIT HIS HEAD ON THE GROUND. More
2828042 42 F OH 02/25/2025 RAB
 SANOFI PASTEUR
 X1D401M
Fatigue, Lymphadenopathy, Pyrexia Fatigue, Lymphadenopathy, Pyrexia
Fatigue began 2/20/2025 and lasted through 2/21/2025. Reported fever in the middle of the night 2/20... Fatigue began 2/20/2025 and lasted through 2/21/2025. Reported fever in the middle of the night 2/20/25-2/21/25 that broke by morning, never took temperature. Reported waking up with a lima bean sized swollen lymph node on the morning of 2/21/25. Lymph node remains swollen but decreasing on 2/25/2025. More
2828043 21 F ME 02/25/2025 RSV
 PFIZER\WYETH
 LN5502
Exposure during pregnancy, No adverse event, Product storage error Exposure during pregnancy, No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions. Out of range temperature for refrigerator. No adverse reactions.
2828044 25 F ME 02/25/2025 RSV
 PFIZER\WYETH
 LN5502
Exposure during pregnancy, No adverse event, Product storage error Exposure during pregnancy, No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828045 64 M 02/25/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 YZ9CY
Chills, Extra dose administered, Myalgia, Pyrexia, Urticaria Chills, Extra dose administered, Myalgia, Pyrexia, Urticaria
Patient reported experiencing fever, chills, hives, and myalgia approximately 48-72 hr after receivi... Patient reported experiencing fever, chills, hives, and myalgia approximately 48-72 hr after receiving a third Shingrix dose. Previous doses 1&2 of Shingrix were administered in 2022. More
2828046 43 F ME 02/25/2025 TDAP
 SANOFI PASTEUR
 U7904AA
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
2828047 85 F ME 02/25/2025 FLU3
 SANOFI PASTEUR
 UT9409EA
Product storage error Product storage error
It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperatu... It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperature range More
2828049 37 F ME 02/25/2025 TDAP
 SANOFI PASTEUR
 3CA07C1
Exposure during pregnancy, No adverse event, Product storage error Exposure during pregnancy, No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828050 21 F ME 02/25/2025 TDAP
 SANOFI PASTEUR
 U7904AA
Exposure during pregnancy, No adverse event, Product storage error Exposure during pregnancy, No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828051 16 F TX 02/25/2025 HEP
HEPA
IPV
MENB
MMR
MNQ
TDAP
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
SANOFI PASTEUR
NOVARTIS VACCINES AND DIAGNOSTICS
MERCK & CO. INC.
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 X024135
X025908
W1C831M
XX33P
X004346
U7827AA
H95RD
X024649
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event More
Gave an expired MMR vaccine to a child. the MMR vaccine expired 02/08/2025 and it was given on 02/20... Gave an expired MMR vaccine to a child. the MMR vaccine expired 02/08/2025 and it was given on 02/20/2025. No adverse reactions noted. More
2828052 22 F ME 02/25/2025 TDAP
 SANOFI PASTEUR
 3CA07C1
Exposure during pregnancy, No adverse event, Product storage error Exposure during pregnancy, No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reaction Out of range temperature for refrigerator. No adverse reaction
2828053 27 F ME 02/25/2025 TDAP
 SANOFI PASTEUR
 U79529AA
Exposure during pregnancy, No adverse event, Product storage error Exposure during pregnancy, No adverse event, Product storage error
Out of range temperature for refrigerator. No adverse reactions Out of range temperature for refrigerator. No adverse reactions
2828054 35 F ME 02/25/2025 TDAP
 SANOFI PASTEUR
 U7929AA
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
2828055 33 F ME 02/25/2025 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
2828056 55 M WA 02/25/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 943191
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Employee given Heplisav-B on 12/4/24 and then again on 12/10/24. No adverse event. Employee given Heplisav-B on 12/4/24 and then again on 12/10/24. No adverse event.
2828057 87 F ME 02/25/2025 COVID19
 MODERNA
 031H21A
Death, Myocardial infarction, Thrombosis Death, Myocardial infarction, Thrombosis
clot developed causing fatal heart attack clot developed causing fatal heart attack
✓ ✓
2828058 20 F ME 02/25/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
Unevaluable event Unevaluable event
None None
2828059 56 F 02/25/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Chills, Dyspnoea, Pain, Pyrexia, Swelling face; Urticaria Chills, Dyspnoea, Pain, Pyrexia, Swelling face; Urticaria
Hives all over body, difficulty breathing, swelling of face, fever, body aches and chills Hives all over body, difficulty breathing, swelling of face, fever, body aches and chills
2828060 74 F 02/25/2025 COVID19
 MODERNA
 3043835
Computerised tomogram head, Gait inability, Muscular weakness, Musculoskeletal s... Computerised tomogram head, Gait inability, Muscular weakness, Musculoskeletal stiffness, Pain More
Muscles stiffness, pain, weakness in RUE and RLE. Sevre enough unable to ambulate. Muscles stiffness, pain, weakness in RUE and RLE. Sevre enough unable to ambulate.
2828061 40 F ME 02/25/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
Product storage error Product storage error
It was discovered after the vaccine was given that the refrigerator that it was kept in was out of t... It was discovered after the vaccine was given that the refrigerator that it was kept in was out of temperature range. More
2828062 79 F ME 02/25/2025 FLU3
 SANOFI PASTEUR
 UT8409EA
Product storage error Product storage error
Patient received a vaccine from a fridge that was out of temperature range at that time. Patient received a vaccine from a fridge that was out of temperature range at that time.
2828064 41 F ME 02/25/2025 RSV
 PFIZER\WYETH
 LN5502
Exposure during pregnancy, Product storage error Exposure during pregnancy, Product storage error
It was discovered after the vaccine was given that the refrigerator that it was kept in was out of t... It was discovered after the vaccine was given that the refrigerator that it was kept in was out of temperature range. More
2828065 37 F ME 02/25/2025 RSV
TDAP
 PFIZER\WYETH
SANOFI PASTEUR
 LN5502
U8231AA
Exposure during pregnancy, Product storage error; Exposure during pregnancy, Pro... Exposure during pregnancy, Product storage error; Exposure during pregnancy, Product storage error More
It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperatu... It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperature range at the time the vaccine was administered. More
2828066 43 F ME 02/25/2025 COVID19
FLU3
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
 3043157
DA7P5
Unevaluable event; Unevaluable event Unevaluable event; Unevaluable event
None stated. None stated.
2828067 1.67 M NE 02/25/2025 DTAPHEPBIP
 GLAXOSMITHKLINE BIOLOGICALS
Cardiac monitoring, Dysstasia, Hyporesponsive to stimuli, Seizure, Unresponsive ... Cardiac monitoring, Dysstasia, Hyporesponsive to stimuli, Seizure, Unresponsive to stimuli More
My son had a seizure and was unresponsive the saturday 2/22/25 after having his Dtap vaccine. We to... My son had a seizure and was unresponsive the saturday 2/22/25 after having his Dtap vaccine. We took him to the ER and he was responsive by the time we got there but still sluggish and had trouble standing. More
2828068 27 F ME 02/25/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 U8231AA
Product storage error Product storage error
It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperatu... It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperature range at the time the vaccine was administered. More
2828069 17 F ME 02/25/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL%
Exposure during pregnancy, Product storage error Exposure during pregnancy, Product storage error
It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperatu... It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperature range at the time the vaccine was administered. More
2828070 19 M ME 02/25/2025 FLU3
 SEQIRUS, INC.
 K9XL5
Product storage error Product storage error
It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperatu... It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperature range at the time the vaccine was administered. More
2828071 36 F ME 02/25/2025 HPV9
 MERCK & CO. INC.
 X019862
Product storage error Product storage error
It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperatu... It was discovered after vaccine was given, that the refrigerator it was kept in was out of temperature range at the time the vaccine was administered. More
2828072 11 F VA 02/25/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 22GP3
Inappropriate schedule of product administration Inappropriate schedule of product administration
Patient was given Hepatitis A vaccine too early. 2nd dose in series due 6/5/2024, was accidentally ... Patient was given Hepatitis A vaccine too early. 2nd dose in series due 6/5/2024, was accidentally given today 2/25/2025. Father made aware. He gave verbal understanding. More
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