🏥 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 💀 🏥 🚑 ♿ ⚠️
2854491 58 F IL 08/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 5y49c
Product preparation issue Product preparation issue
Only AS01B adjuvant administered; Inappropriate dose of vaccine administered; This non-serious case ... Only AS01B adjuvant administered; Inappropriate dose of vaccine administered; This non-serious case was reported by a nurse via call center representative and described the occurrence of inappropriate preparation of medication in a 58-year-old female patient who received Herpes zoster (Shingrix) (batch number 5y49c, expiry date 04-APR-2027) for prophylaxis. On 11-AUG-2025, the patient received Shingrix. On 11-AUG-2025, an unknown time after receiving Shingrix, the patient experienced inappropriate preparation of medication (Verbatim: Only AS01B adjuvant administered) and inappropriate dose of vaccine administered (Verbatim: Inappropriate dose of vaccine administered). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date: 11-AUG-2025 A nurse practitioner started a chat and informed that a patient was given a dose of AS01b sterile diluent without the antigen component, which led to an inappropriate preparation of medication and inappropriate dose of vaccine administered. The reporter wanted to know how should they proceed after this. Reporter informed that such was administered earlier that day. The vaccine administration facility was the same as primary reporter. More
2854492 M FL 08/18/2025 COVID19
 MODERNA
Near death experience Near death experience
almost killed him; This spontaneous case was reported by a physician and describes the occurrence of... almost killed him; This spontaneous case was reported by a physician and describes the occurrence of NEAR DEATH EXPERIENCE (almost killed him) in a male patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported. 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 NEAR DEATH EXPERIENCE (almost killed him) (seriousness criterion medically significant). At the time of the report, NEAR DEATH EXPERIENCE (almost killed him) outcome was unknown. The action taken with SPIKEVAX NOS (SPIKEVAX NOS) (Unknown) was unknown. For SPIKEVAX NOS (SPIKEVAX NOS) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. It was stated reporter was trying to find someone that offered the Novavax Covid vaccine and he could not find anyone. In other places, he was unable to find it. He was worried about Covid because it was rising to epidemic levels again and it has a real bad impact on him. Patient might like to be vaccinated on this weekend. It was reported that there were 2 seasons for Covid; one was when it was too hot and everyone was inside under the air conditioning, and the other was when it was too cold and people were hiding, and during that time, it was summer season in the reporter's place. It was reported that he did not like the mRNA vaccines and it was reported that Moderna almost killed him, and several of his friends stroke out in different things as well as it seemed to be not very effective. Patient would prefer to be vaccinated with Novavax Covid vaccine or he might would have Pfizer vaccine. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2025-788613 (E2B Linked Report).; Reporter's Comments: The benefit -risk relationship of product is not affected by this report.; Sender's Comments: US-MODERNATX, INC.-MOD-2025-788613:invalid case for multiple patients More
2854493 M WI 08/18/2025 COVID19
 MODERNA
COVID-19 COVID-19
we both got Covid; This spontaneous case was reported by a nurse and describes the occurrence of COV... we both got Covid; This spontaneous case was reported by a nurse and describes the occurrence of COVID-19 (we both got Covid) in a male patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported. 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 COVID-19 (we both got Covid). At the time of the report, COVID-19 (we both got Covid) outcome was unknown. The action taken with SPIKEVAX NOS (SPIKEVAX NOS) (Unknown) was unknown. For SPIKEVAX NOS (SPIKEVAX NOS) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient and his wife were well vaccinated and so, they took a trip out of the country, and both got covid very mild and came back. Then nothing happened. They did not travel again for a while and then traveled again out of the country with friends. And again, they got covid again, very mild. They had kept up with their vaccines all the way along. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2025-788543 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2025-788543:wife case More
2854494 80 F 08/18/2025 COVID19
 MODERNA
COVID-19 COVID-19
got COVID, but the symptoms were very mild; This spontaneous case was reported by a nurse and descri... got COVID, but the symptoms were very mild; This spontaneous case was reported by a nurse and describes the occurrence of COVID-19 (got COVID, but the symptoms were very mild) in an 80-year-old female patient who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: tetanus. Past adverse reactions to the above products included No adverse effect with tetanus. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced COVID-19 (got COVID, but the symptoms were very mild). At the time of the report, COVID-19 (got COVID, but the symptoms were very mild) had resolved. For SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use), the reporter did not provide any causality assessments. Concomitant medication was not reported. Patient had her pneumonia, shingles vaccine already, she was good for a while until any of those come up. It was reported that, patient saw in newspaper that unfortunately, the administration and government was going to withdraw funding for development of Covid and Covid like vaccines and MRNA vaccines in general and wanted to know the status of the current Moderna vaccine. It was reported that, patient received first Moderna dose on 22-Feb-2021, second dose on 22-Mar-2021, third dose on 29-Oct-2021, fourth 26-May-2022, Fifth dose on 04-Oct-2022 sixth dose on 21-Apr-2023, seventh dose on 13-Oct-2023, eight dose on 4-Sep-2024, 9th dose on 07-Apr- 2025 with Batch Number unknown. Her most recent booster Covid vaccine was from Moderna and all covid vaccines had been Moderna. Most recent one was in April, and the consensus patient heard from healthcare provider and others was that seniors like herself and her husband were generally recommended to get a kind of a spring shot to cover the summer surge and a fall shot to cover the winter surge. She had taken covid vaccine as regularly as it was recommended ever since they first came out in January of 2021. She did not travel outside of the country for a couple of years after covid developed, until finally thought it was a bit safer and were well vaccinated and so, they took a trip and they both got covid very mild and came back. Then nothing happened. They didn't travel again for a while and then traveled again with friends. And got covid again very mild. They had kept up with our vaccines all the way along. Patient was planning to get shot of the newest formulation and she likely to call as they get closer to October. It was unknown if the patient experienced any additional symptoms/events. Treatment medication was not reported. This case was linked to US-MODERNATX, INC.-MOD-2025-788682 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 06-Aug-2025: Follow-up received with non-significant: Historical vaccines were added.; Sender's Comments: US-MODERNATX, INC.-MOD-2025-788682:husband case More
2854495 08/18/2025 COVID19
 PFIZER\BIONTECH
Gastrointestinal disorder, Muscular dystrophy, Weight gain poor Gastrointestinal disorder, Muscular dystrophy, Weight gain poor
problems especially with my muscles, in both arms seem to/ but it shrunk; stomach problem; I am not ... problems especially with my muscles, in both arms seem to/ but it shrunk; stomach problem; I am not able to gain weight; This is a spontaneous report received from a Consumer or other non HCP. A patient (age and gender not provided) received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: MUSCULAR DYSTROPHY (non-serious), outcome "unknown", described as "problems especially with my muscles, in both arms seem to/ but it shrunk"; GASTROINTESTINAL DISORDER (non-serious), outcome "unknown", described as "stomach problem"; WEIGHT GAIN POOR (non-serious), outcome "unknown", described as "I am not able to gain weight". Additional information: Ever since the patient had the shot, the patient had problems especially with muscles, in both arms seem to, it has caused him/her nothing, but it shrunk and had stomach problem. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2854496 M 08/18/2025 COVID19
 PFIZER\BIONTECH
COVID-19, Drug ineffective, SARS-CoV-2 test COVID-19, Drug ineffective, SARS-CoV-2 test
tested positive with covid 19; tested positive with covid 19; This is a spontaneous report received ... tested positive with covid 19; tested positive with covid 19; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A male patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "tested positive with covid 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2854497 36 M MN 08/18/2025 COVID19
 PFIZER\BIONTECH
Laboratory test, Myocardial infarction Laboratory test, Myocardial infarction
2 heartattacks 2 heartattacks
✓ ✓ ✓
2854498 M NC 08/18/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 9K34M
Incorrect dose administered Incorrect dose administered
Adult dose of hep b Given to 4 week old-no noted reaction after 72 hours Adult dose of hep b Given to 4 week old-no noted reaction after 72 hours
2854499 74 M MN 08/18/2025 COVID19
 PFIZER\BIONTECH
 ME6072
Loss of consciousness Loss of consciousness
Patient received vaccine and waited 15 min before leaving facility. Approx 45 min later patient blac... Patient received vaccine and waited 15 min before leaving facility. Approx 45 min later patient blacked out while driving and have car accident totaling his vehicle. Patient was assessed in the ED. More
2854500 5 F AR 08/18/2025 DTAPIPV
MMR
 SANOFI PASTEUR
MERCK & CO. INC.
 U8198AA
Y004114
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered More
Received Quadracel for second dose of DTaP and IPV. The combo vaccine was only for the 5th dose of D... Received Quadracel for second dose of DTaP and IPV. The combo vaccine was only for the 5th dose of DTaP and the 4th/5th dose of Polio. No adverse reaction noted More
2854501 77 M IN 08/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 PJ353
Injection site pain, Pain Injection site pain, Pain
PT had injection sight tenderness until yesterday when it vastly resolved. Pain would radiate down ... PT had injection sight tenderness until yesterday when it vastly resolved. Pain would radiate down to fingers and sometimes could be felt in his lateral trunk. More
2854502 34 F DE 08/18/2025 MMR
 MERCK & CO. INC.
 Y015022
Discomfort, Erythema, Headache, Skin warm, Swelling Discomfort, Erythema, Headache, Skin warm, Swelling
redness, warmth, some swelling like a bug bite to area, mild discomfort. Also had a headache a coupl... redness, warmth, some swelling like a bug bite to area, mild discomfort. Also had a headache a couple days later. Took some ibuprofen. More
2854503 84 F ME 08/18/2025 PNC21
 MERCK & CO. INC.
 lx4482
Injection site reaction, Rash erythematous, Rash pruritic Injection site reaction, Rash erythematous, Rash pruritic
Itchy red rash near cite Itchy red rash near cite
2854504 17 F VA 08/18/2025 YF
YF
 SANOFI PASTEUR
SANOFI PASTEUR
 UK136AB
UK136AB
Asthenia, Cyanosis, Dizziness, Loss of consciousness, Pallor; Somnolence Asthenia, Cyanosis, Dizziness, Loss of consciousness, Pallor; Somnolence
After administering the Yellow Fever vaccine, the pt stated "I feel like I'm going to pass... After administering the Yellow Fever vaccine, the pt stated "I feel like I'm going to pass out." When the pt lost consciousness, the RN was able to lie the pt down on the exam table. The pt was unconscious for no longer than 5 seconds. When the pt fully regained consciousness she was noted to be drowsy, weak, pale, and her lips were cyanotic. The pt was A&O X4. The RN helped sit the pt up and asked if she would like saltine crackers. The pt accepted the crackers with some water. The pt admitted to the nurse that she did not eat breakfast that morning. Prior to administration of the vaccine, the RN and the pt had discussed the pt's fear of needles, but not if she had eaten. The RN was able to contact the pt's mother the following business day and the pt's mother was able to report that the pt had recovered well. More
2854505 12 F AZ 08/18/2025 HPV9
HPV9
 MERCK & CO. INC.
MERCK & CO. INC.
 BHCQC
BHCQC
Face and mouth X-ray normal, Jaw clicking, Osteoarthritis, Pain in jaw, Trismus;... Face and mouth X-ray normal, Jaw clicking, Osteoarthritis, Pain in jaw, Trismus; X-ray dental normal More
Patient started complaining about Jaw pain around November fallowing the shot, was dealing with clic... Patient started complaining about Jaw pain around November fallowing the shot, was dealing with clicking, as the months went on it went from, jaw feeling weird to clicking to locking to January is when her jaw popped and then locked completely, we took her to dentist first because we thought it would be her wisdom teeth, after x rays there they stated her wisdom teeth were fine and nothing abnormal, then we went to ER later that day. They x-ray her there and they stated that they couldn't find anything wrong and that we would need to go to a TMJ specialist. We had to wait till JUNE for her fist visit. After several visits with the TMJ specialist said that my 13 yr old daughter has arthritis on her right side of her Jaw. More
✓
2854506 58 F CA 08/18/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.

Dyspnoea, Erythema, Gastrointestinal pain, Lip erythema, Nausea; Oral mucosal er... Dyspnoea, Erythema, Gastrointestinal pain, Lip erythema, Nausea; Oral mucosal erythema, Paraesthesia, Pharyngeal swelling, Rash, Vomiting More
I was fine, I got my vaccine around Noon, Around 6:30 i started getting gastro pain, I started vomit... I was fine, I got my vaccine around Noon, Around 6:30 i started getting gastro pain, I started vomiting and my feet and hands began to tingle and then turned red. My lips turned red and around my mouth. My throat got swollen and it was had to breathe and broke out in a rash all over my body. I then i went to ER they took me right back and they gave me Benadryl something for nauseas, IV fluids and they kept me for observation. They did not keep my over night just until my throat opened up. More
2854507 1.33 M MI 08/18/2025 DTPPVHBHPB
HEP
HEPA
MMR
PNC20
VARCEL
 MSP VACCINE COMPANY
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
PFIZER\WYETH
MERCK & CO. INC.
 U8265AA
LG749
32559
Y018962
LN4931
Z005455
Extra dose administered, Injection site pain; Extra dose administered, Injection... Extra dose administered, Injection site pain; Extra dose administered, Injection site pain; Extra dose administered, Injection site pain; Extra dose administered, Injection site pain; Extra dose administered, Injection site pain; Extra dose administered, Injection site pain More
Client received combo Vaxelis with an additional HepB single antigen dose. This was an oversight on ... Client received combo Vaxelis with an additional HepB single antigen dose. This was an oversight on my part when checking vaccines required with vaccines pulled for administration. Spoke with the mother of the client, who informed me her son, "did not have any additional side effects or fever, only a sore leg." More
2854508 16 F AR 08/18/2025 MMRV
 MERCK & CO. INC.
 Z2007869
Wrong product administered Wrong product administered
Patient was in clinic for scheduled visit and was due for vaccines. Patient had a shot record with p... Patient was in clinic for scheduled visit and was due for vaccines. Patient had a shot record with previous MMR and Varicella vaccines given, but shown as invalid on shot record, so another MMR and varicella was due. LPN and CSM and 3rd nurse discussed and reviewed chart vs. Web shot record. Determined patient needed MMR and varicella. Patient received MMRV instead of MMR and varicella separately. On Thursday, 8/14, became apparent that a vaccine error was made. Spoke to the CS and VFC rep and discussed no adverse effects expected from error. On Friday, CS called vaccine manufacturer who confirmed the same. Parent contacted, incident reporting entered, re-education with staff addressed, label added to Proquad box for age alert. More
2854509 65 F DE 08/18/2025 TDAP
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 KR75K
7523K
Injection site erythema, Injection site swelling; Injection site erythema, Injec... Injection site erythema, Injection site swelling; Injection site erythema, Injection site swelling More
PATIENT REPORTS REDNESS AND SWELLING IN THE INJECTION SITE OF THE RIGHT ARM AND SURROUNDING AREA (LA... PATIENT REPORTS REDNESS AND SWELLING IN THE INJECTION SITE OF THE RIGHT ARM AND SURROUNDING AREA (LARGE AREA) More
2854510 11 M IL 08/18/2025 HPV9
HPV9
MNQ
MNQ
TDAP
TDAP
 MERCK & CO. INC.
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 Y015180
Y015180
U8599AA
U8599AA
9JT4S
9JT4S
Erythema, Induration, Injection site pruritus, Injection site reaction, Injectio... Erythema, Induration, Injection site pruritus, Injection site reaction, Injection site swelling; Injection site warmth, Rash macular; Erythema, Induration, Injection site pruritus, Injection site reaction, Injection site swelling; Injection site warmth, Rash macular; Erythema, Induration, Injection site pruritus, Injection site reaction, Injection site swelling; Injection site warmth, Rash macular More
Mother called on 08/01/2025 to report patients left shoulder on the evening of immunization was hard... Mother called on 08/01/2025 to report patients left shoulder on the evening of immunization was hard and red. On 07/31/2025, the same shoulder was also "itchy and blotchy from shoulder to elbow". Today, 08/01/2025, it is no longer itchy or blotchy but is swollen and hot to the touch. States he has used warm compresses on shoulder. 08/18/2025, called to check on patient to see if there were any ongoing problems, patients mother stated the redness and swelling dissipated and was gone within a couple of days from last contact (08/01/2025). More
2854511 4 M FL 08/18/2025 MMR
 MERCK & CO. INC.
Product storage error Product storage error
Patient was given a vaccine that was non-viable due to it being out of temperature range for too lon... Patient was given a vaccine that was non-viable due to it being out of temperature range for too long. More
2854512 19 M 08/18/2025 MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
Immune system disorder Immune system disorder
Patient reports that according to the doctor at the ER, the immunization "compromised my immune... Patient reports that according to the doctor at the ER, the immunization "compromised my immune system" and the the Tylenol he had taken triggered a reaction. He was given steroids and other medication. Was released after 2 hours and is now feeling well. More
2854513 17 F IL 08/18/2025 MNQ
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
 DL4YY
DL4YY
Injection site cellulitis, Injection site erythema, Injection site induration, I... Injection site cellulitis, Injection site erythema, Injection site induration, Injection site pain, Injection site warmth; Peripheral swelling More
Patient reported that her arm started swelling and the swelling increased over the days from the tim... Patient reported that her arm started swelling and the swelling increased over the days from the time that she received the vaccine to the time that she was seen in the clinic on 8/15/25. Also was experiencing pain, redness, warmth and hardness to vaccine site. MD diagnosis was cellulitis and patient was started on 7 day course of cephalexin 500 mg capsule q6 hours. More
2854514 29 F 08/18/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Nausea, Vomiting Nausea, Vomiting
NAUSEA/VOMITTED NAUSEA/VOMITTED
2854515 5 F OK 08/18/2025 DTAPIPV
 SANOFI PASTEUR
 U8383AB
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Localized swelling and redness at injection site Localized swelling and redness at injection site
2854516 17 F IL 08/18/2025 MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
 DL4YY
Injection site cellulitis, Injection site induration, Injection site pain, Injec... Injection site cellulitis, Injection site induration, Injection site pain, Injection site warmth, Peripheral swelling More
Patient was seen in our office on 8/11/25 and received the Menveo vaccine. Pt was then seen on 8/15... Patient was seen in our office on 8/11/25 and received the Menveo vaccine. Pt was then seen on 8/15/25 in our office with swelling to right arm which she stated started the day she received the vaccine and which increased over time until she was seen in our office. Also reported that arm was painful, felt warm to touch and the site felt hard. MD diagnosed cellulitis and prescribed a 7 day course of cephalexin 500 mg capsules q 6 hours. More
2854517 4 M CO 08/18/2025 DTAPIPV
 SANOFI PASTEUR
 U7838AA
Extra dose administered, No adverse event Extra dose administered, No adverse event
No none adverse reaction No none adverse reaction
2854518 4 M CO 08/18/2025 DTAPIPV
 SANOFI PASTEUR
 U7838AA
Expired product administered, No adverse event Expired product administered, No adverse event
The Vaccine was expired. No adverse effects The Vaccine was expired. No adverse effects
2854519 18 M 08/18/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 CD44A
Loss of consciousness, Pallor Loss of consciousness, Pallor
Patient here for a 2nd of 3 Series Meningitis B vaccine and a Lipid Panel. Per Dr.'s Notes, pat... Patient here for a 2nd of 3 Series Meningitis B vaccine and a Lipid Panel. Per Dr.'s Notes, patient to present back for Nurse visit for 2nd Dose Mid August. Patient received dose around 1019 am in the left deltoid and tolerated well. Patient states his first dose he just had a sore arm muscle with no other issues. Patient was then walked over to the lab area for his blood draw. Patient was doing well and draw was completed when patient passed out and became pale. Patient was laid flat and cold pack placed behind his neck. Within about 15 seconds patient came too. Patient was diaphoretic. Answered questions appropriately and color returned to his face. Patient had some apple juice and graham crackers. After about 20 minutes he felt ready to return home. Patient was up and about with no concerns. Obtained verbal consent to call mother and update her. This was done right after patient departed. Patient should return around January 3rd for 3rd dose of Men. B vaccine. More
2854520 1.25 M NJ 08/18/2025 PNC20
 PFIZER\WYETH
 LN4929
Rash pruritic Rash pruritic
Patient's parents describe intermittent body rash that is itchy. It has been persistent for the... Patient's parents describe intermittent body rash that is itchy. It has been persistent for the last 2 months and required both oral and topical steroids. More
2854521 84 F PA 08/18/2025 PNC20
 PFIZER\WYETH
Injected limb mobility decreased, Injection site bruising, Injection site pain, ... Injected limb mobility decreased, Injection site bruising, Injection site pain, Muscular weakness, Pain in extremity More
pt says that the day after being vaccinated she had pain in the arm about 2 or 3 inches below the in... pt says that the day after being vaccinated she had pain in the arm about 2 or 3 inches below the injection site. The following week after the vaccine she had a big black and blue mark that appeared. She called the doctors office about it and was told to apply heat. Now she is starting to loose mobility in the left arm and her right arm is becoming very weak. She has a lot of pain in in the left arm. She went to the doctor and was told to apply ice. This helped very little. She uses a heating pad to help with the pain so she can sleep, but the pain is still present when waking up. She continues to loose strength in both arms and continues to have pain in the left arm. More
2854522 56 F TX 08/18/2025 PNC20
 PFIZER\WYETH
 LJ5280
Erythema, Peripheral swelling Erythema, Peripheral swelling
Patient received Prevnar 20 vaccine on 8/12/25 on left deltoid. She came in today and showed us tha... Patient received Prevnar 20 vaccine on 8/12/25 on left deltoid. She came in today and showed us that her arm was red and swollen. She stated that it occurred right away when she got home. She called health insurance and they advised her to take Tylenol for the reaction. Despite taking the Tylenol, the redness seems to be getting bigger and not better. She will go to her doctor today to be evaluated. More
2854523 13 F NC 08/18/2025 HPV9
 MERCK & CO. INC.
 2007667
Lymphadenitis, Oedema, Skin warm, Tenderness Lymphadenitis, Oedema, Skin warm, Tenderness
Axillary lymphadenitis on ipsilateral side, warmth, edema, tenderness. Treated successfully with Au... Axillary lymphadenitis on ipsilateral side, warmth, edema, tenderness. Treated successfully with Augmentin with resolution of symptoms. More
2854524 18 M MI 08/18/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 55N34
Pain Pain
The patient has pain 3/10 when he lifts his arm over his head. He has been using ice, moves it, use... The patient has pain 3/10 when he lifts his arm over his head. He has been using ice, moves it, uses warm compress, is taking Motrin. It is getting a little better but improving slowly. I advised him to call his PCP today. I consulted with Dr., he agreed that the patient needs to call his PCP. The patient plays college basketball and it hurts when he raises his arm up over his head. The arm is not red and not swollen per the patient phone call. He will call his PCP. I called the patient to see if he called his PCP. It went to voicemail. I left a message. More
2854525 77 F IA 08/18/2025 RSV
 PFIZER\WYETH
 md5462
Extra dose administered Extra dose administered
Patient given 2nd dose of RSV. First dose received in 9/2024, but was not documented. Found upon ent... Patient given 2nd dose of RSV. First dose received in 9/2024, but was not documented. Found upon entering insurance. More
2854526 4 F CA 08/18/2025 DTAP
IPV
 SANOFI PASTEUR
SANOFI PASTEUR
 3CA03C3
Y1A201M
Irritability, Lethargy, Loss of personal independence in daily activities, Pruri... Irritability, Lethargy, Loss of personal independence in daily activities, Pruritus, Urticaria; Irritability, Lethargy, Loss of personal independence in daily activities, Pruritus, Urticaria More
Child woke up on 3/29/25 with hives down her Left Arm. Child's parents contacted the provider.... Child woke up on 3/29/25 with hives down her Left Arm. Child's parents contacted the provider. Child continued to experience hives even seven days after the vaccinations. Child missed out on her recreational soccer game that week due to itching, her being lethargic, and extremely irritable. Child's preschool called the parents multiple times that month to come pick the child up from school due to extreme itching. Child's parents contacted the provider again seven days after vaccination because the hives continued to be present. Discoloration of the arm was notable up until one month following the vaccines. More
2854527 55 F NC 08/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 55KB9
Nausea, Seizure Nausea, Seizure
Patient was given her second vaccine in our vaccination room. The patient complained of feeling nau... Patient was given her second vaccine in our vaccination room. The patient complained of feeling nauseous, so the administrator left the room to achieve an emesis bag. Upon arrival back into the vaccination room with the bag, the husband of the patient informed the administrator the patient had just had a seizure. Patient and her husband were allowed to remain in the immunization room until the patient felt she could walk out safely. More
2854528 0.17 F NY 08/18/2025 DTPPVHBHPB
 MSP VACCINE COMPANY
 U8313AA
Injection site mass Injection site mass
Provider at today's well child check was told about a "pen-tip" sized lump/bump to th... Provider at today's well child check was told about a "pen-tip" sized lump/bump to the left thigh that has been present since her 2 month vaccines. No other symptoms noted. More
2854529 81 F CO 08/18/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Cyanosis, Erythema, Immune thrombocytopenia, Pain, Pallor; Platelet count decrea... Cyanosis, Erythema, Immune thrombocytopenia, Pain, Pallor; Platelet count decreased, Raynaud's phenomenon, Skin ulcer More
pt says a couple of days later she was in pain from head to toe. Then her toes became really red. He... pt says a couple of days later she was in pain from head to toe. Then her toes became really red. Her toes would turn white, and then blue and then red. Then developed sores on them. She has raynaud's disease so had blood work and was sent to the ER. Her platelets were low and she has to have infusions. She is now on hepatitis meds that make her blood sugar go up. She has been diagnosed with ITP. She continues to have these infusions and believes the vaccine caused her symptoms . More
✓ ✓
2854530 86 F IA 08/18/2025 COVID19
 MODERNA
 3046731
Death Death
Expired Expired
✓
2854531 50 M 08/18/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FG3184
FF8841
Heart rate irregular, Hypertensive heart disease, Sudden death; Heart rate irreg... Heart rate irregular, Hypertensive heart disease, Sudden death; Heart rate irregular, Hypertensive heart disease, Sudden death More
My husband had no heart problem, but after getting the vaccine he had couple of irregular heartbeats... My husband had no heart problem, but after getting the vaccine he had couple of irregular heartbeats. Other then that his heart seemed okay but after 13 month of 2nd Covid Vaccination, he died suddenly due to Hypertension Cardio Vascular Disease. Medical Examiner said it is not related to Covid Vaccine, but as a spouse, I believe this is Vaccine related. More
✓
2854532 77 M IA 08/18/2025 COVID19
 MODERNA
 3046731
Death Death
resident expired resident expired
✓
2854533 50 F SC 08/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7523j
Product preparation issue Product preparation issue
patient was given just the diluent. It was not mixed. I reconstituted a full dose and gave the full ... patient was given just the diluent. It was not mixed. I reconstituted a full dose and gave the full dose right after the diluent was given More
2854534 62 M CA 08/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 F95YS
Extra dose administered, No adverse event Extra dose administered, No adverse event
On 05/31/2025, customer was administered an extra dose of Shingrix by a floater pharmacist. This wa... On 05/31/2025, customer was administered an extra dose of Shingrix by a floater pharmacist. This was discovered when customer came in to get his second dose on 08/15/2025. I checked records and found that he had already completed both doses in 2022. Customer reported not having any side effects after the administrating of the third doses of Shingrix. More
2854535 64 M VA 08/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 35A77
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling More
LOCALIZED INJECTION SITE BAD PAIN, REDNESS, SWELLING, ITCHINESS LOCALIZED INJECTION SITE BAD PAIN, REDNESS, SWELLING, ITCHINESS
2854536 1 F MI 08/18/2025 HEPA
MMRV
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 GP759
Z009076
Z008083
Pyrexia; Pyrexia; Pyrexia Pyrexia; Pyrexia; Pyrexia
Fever 102. Fever 102.
2854538 85 F IA 08/18/2025 PNC13
 PFIZER\WYETH
Death Death
Expired Expired
✓
2854539 16 M PA 08/18/2025 MENB
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS

Headache, Migraine; Headache, Migraine Headache, Migraine; Headache, Migraine
Patient has experienced more headache / migraine in the 7 weeks since receiving these 2 vaccines tha... Patient has experienced more headache / migraine in the 7 weeks since receiving these 2 vaccines than he normally would in an entire year. The first headache began the day after receiving these vaccines. More
2854540 17 F HI 08/18/2025 MNP
 PFIZER\WYETH
 LJ0075
Axillary pain, Erythema, Myalgia, Pain, Pyrexia Axillary pain, Erythema, Myalgia, Pain, Pyrexia
Moderate local pain, redness to deltoid area with mild pain into ipsilateral axilla and intermittent... Moderate local pain, redness to deltoid area with mild pain into ipsilateral axilla and intermittent fevers More
2854541 73 F FL 08/18/2025 FLU3
RSV
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 u876488
f4ac3
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
No adverse events were reported by patient. This is to report a second dose of RSV given. Database d... No adverse events were reported by patient. This is to report a second dose of RSV given. Database did not show a previous RSV vaccine given on 12/21/2023 therefore the patient was given what turned out to be a second dose. More
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