🏥 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 💀 🏥 🚑 ♿ ⚠️
2866230 77 F TN 10/15/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 163833-00
Dizziness, Muscle spasms, Neuralgia, Oesophageal pain, Teething Dizziness, Muscle spasms, Neuralgia, Oesophageal pain, Teething
For over 30 years, Infectious disease department under guidance of CDC did not want me to take the... For over 30 years, Infectious disease department under guidance of CDC did not want me to take the older version Shingles shot because my levels were so high from so many active cases (over 57) since the age of 19. (am now 77) My current physician and my endocrinologist both said this new shot works by a different mechanism and that I should get the 2 shots. I received the first one on July 2, 2025 with absoslutely no side effects including no soreness of the arm. I did not expect what happened with the second shot on October 10th. Reaction began about 8 hours following shot. Every site in my body where I have recurring neuralgias from past live occurences became very painful and my arms and legs had severe cramping that I could not relieve even after tonic water and several showers. I considered going to the emergency room but my husband died in the hospital after going to the emergency room for covid in January of 2022. I could not force myself to go. There were no respiratory issues.... just mostly dizziness and severe pain even in my esophagus and teeth etc. I am used to pain from all my neuralgia extended attacks over the years, but this was very bad and I live alone, now. severe symptoms lasted about 18 hours and entire event about 48 hours. No recurrence or negativity since then. I am not in any way complaining. I am only explaining this as guidance for you about possibe side effects for thos who have had multiplee Herpes Zoster attacks. More
2866231 70 F NM 10/15/2025 COVID19
 MODERNA
Brain fog, SARS-CoV-2 test negative Brain fog, SARS-CoV-2 test negative
I felt something like brain fog after eating. This happened for about three days starting three day... I felt something like brain fog after eating. This happened for about three days starting three days after I got the vaccine. This also happened to me when I got Covid in January 2024. So I went to get a Covid test and I was found it was negative. I think I got a similar reaction to another Covid vaccine in the past, but I?m not sure. More
2866232 70 F TX 10/15/2025 FLU3
 SANOFI PASTEUR
 u8859da
Injection site bruising, Injection site erythema, Injection site mass, Muscular ... Injection site bruising, Injection site erythema, Injection site mass, Muscular weakness, Pain in extremity More
pt report inject site reactions including redness, firm knot at injection site, and bruising. A few... pt report inject site reactions including redness, firm knot at injection site, and bruising. A few days later patient started experiencing weakness and soreness in opposite arm. More
2866233 72 F FL 10/15/2025 FLU3
VARZOS
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 UT8781DA
3T74X
Injection site cellulitis, Injection site discolouration, Injection site inflamm... Injection site cellulitis, Injection site discolouration, Injection site inflammation, Injection site pain, Injection site swelling; Injection site cellulitis, Injection site discolouration, Injection site inflammation, Injection site pain, Injection site swelling More
Patient experience swelling at the site of the injection, specifically for the Shingrix injection. P... Patient experience swelling at the site of the injection, specifically for the Shingrix injection. Patient said it swelled up like a "baseball" or the size of a "large orange" and was bright red. She went to the hospital to have it checked and was given cephalexin for cellulitis, and the swelling was marked and was advised to monitor if the swelling changes in size. The swelling and inflammation did increase in size from top of her shoulder and to the joint of her elbow. Patient had plans to travel and ended up stopping by the ER and was administered a dose of IM Rocephin and given doxycycline 100mg BID for 12 days. Patient is currently still recovering from the infection, and the swelling has gone down, but still tender to touch. More
2866234 67 F HI 10/15/2025 FLU3
 SEQIRUS, INC.
 AX4606A
Dizziness, Nausea Dizziness, Nausea
Spoke with patient at 345 pm. States has mild nausea and dizziness. No any other adverse side effect... Spoke with patient at 345 pm. States has mild nausea and dizziness. No any other adverse side effects reported. More
2866235 60 M NM 10/15/2025 COVID19
 PFIZER\BIONTECH
Angiogram, Chest pain Angiogram, Chest pain
Chest pain three days later, Chest pain three days later,
✓
2866238 3 F KY 10/15/2025 FLU3
 SANOFI PASTEUR
 UT8802MA
Extra dose administered Extra dose administered
At the time of adverse event, office internet was out of service. Child seen for illness and offered... At the time of adverse event, office internet was out of service. Child seen for illness and offered to provide flu vaccine. Mom agreed & signed consent. When EMR available (prior to family departing office) error was noted and family informed of error. Vaccine was noted and family informed of error. Vaccine had been provided 9/16/25 (Visit completed with interpreter). More
2865590 M NC 10/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Inappropriate schedule of product administration Inappropriate schedule of product administration
Inappropriate schedule of vaccine administered; This non-serious case was reported by a pharmacist v... Inappropriate schedule of vaccine administered; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of inappropriate schedule of vaccine administered in a male patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (1st dose received in 2022). On an unknown date, the patient received the 2nd dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced inappropriate schedule of vaccine administered (Verbatim: Inappropriate schedule of vaccine administered). The outcome of the inappropriate schedule of vaccine administered was not applicable. Additional Information: GSK receipt date: 03-OCT-2025 The pharmacist reported that the patient received his first Shingrix dose in 2022 and did not yet receive his second dose. The reported mentioned that he would be receive it today. More
2865591 F KY 10/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incomplete course of vaccination Incomplete course of vaccination
Shingrix Late second dose; This non-serious case was reported by a pharmacist via sales rep and desc... Shingrix Late second dose; This non-serious case was reported by a pharmacist via sales rep and described the occurrence of incomplete course of vaccination in a 75-year-old female patient who did not receive Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (in 2020 5 years ago). On an unknown date, the patient did not receive the 2nd dose of Shingrix. On an unknown date, the patient had incomplete course of vaccination (Verbatim: Shingrix Late second dose). The outcome of the incomplete course of vaccination was not applicable. Additional Information: GSK Receipt Date: 30-SEP-2025 The patient received 1st dose of Shingrix. The reporter asked regarding restart the series or just receive the 2nd dose of Shingrix and be done complete series. Batch number "ASKU": The batch number was not provided upon follow up with the reporter. More
2865592 PA 10/14/2025 COVID19
 PFIZER\BIONTECH
Product contamination with body fluid Product contamination with body fluid
styrofoam container with the last few doses was covered in the blood; This is a spontaneous report r... styrofoam container with the last few doses was covered in the blood; This is a spontaneous report received from a Consumer or other non HCP from product quality group. This report involves BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The following information was reported: PRODUCT CONTAMINATION WITH BODY FLUID (non-serious), outcome "unknown", described as "styrofoam container with the last few doses was covered in the blood". Additional information: The order they received of their Pfizer COVID-19 Vaccine they ordered 300 doses and the last package that they opened Styrofoam container with the last few doses was covered in the blood. Causality for "styrofoam container with the last few doses was covered in the blood" was determined associated to device constituent of BNT162b2 omicron (lp.8.1) (malfunction). Batch/lot number is not provided, and it cannot be obtained. More
2865612 63 M OH 10/14/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Arthralgia, Headache, Injection site swelling, Joint swelling, Pyrexia; Skin exf... Arthralgia, Headache, Injection site swelling, Joint swelling, Pyrexia; Skin exfoliation More
Swelling Of injection sitePeeling skin, swelling of joints, joint pain headache, fever 103.2 Swelling Of injection sitePeeling skin, swelling of joints, joint pain headache, fever 103.2
✓
2865670 F 10/14/2025 PPV
TDAP
 UNKNOWN MANUFACTURER
GLAXOSMITHKLINE BIOLOGICALS

Arthralgia, Complex regional pain syndrome, Inflammation, Injection site pain, W... Arthralgia, Complex regional pain syndrome, Inflammation, Injection site pain, Wrong technique in product usage process; Arthralgia, Complex regional pain syndrome, Inflammation, Injection site pain, Wrong technique in product usage process More
increased inflammation and pain in her shoulder/that the pneumococcal vaccine administration led to ... increased inflammation and pain in her shoulder/that the pneumococcal vaccine administration led to a nerve injury; Complex regional pain syndrome; Information has been received from a pharmacist regarding a case in litigation and refers to a female patient of unknown age. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On unspecified date in 2017, the patient was vaccinated with a dose of Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) (strength, dose, dose number, route, anatomical location, lot # and expiration date were not reported) for prophylaxis; on the same date (unclear which vaccination was administered first) the patient received a dose of Diphtheria vaccine toxoid;Pertussis vaccine acellular 3-component;Tetanus vaccine toxoid (BOOSTRIX) (strength, dose, dose number, route, anatomical location, lot # and expiration date were not reported) for prophylaxis too. The vaccinations were received sequentially and administered so close to the same spot that there was only 1 visible skin puncture. Upon administration of the first vaccination, the patient told the pharmacist that she felt pain and that "something was wrong." During the next 2 days (unspecified date in december 2017), the patient experienced increased inflammation and pain in her shoulder. The patient sought medical follow-up and was diagnosed with complex regional pain syndrome. Initially, it was alleged through expert testimony that the administration of the Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) vaccine was outside the standard of care, and another expert concluded that the Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) vaccine administration led to a nerve injury. The Act was passed to create a vaccine injury compensation (VIC) program for specific vaccine-related injury claims. The VIC program covers injuries related to the Diphtheria vaccine toxoid;Pertussis vaccine acellular 3-component;Tetanus vaccine toxoid (BOOSTRIX) but did not cover injuries related to the Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) vaccine. In December 2020, the patient filed a lawsuit against the pharmacy alleging that negligent administration of the pneumococcal vaccine led to "painful and permanent" nerve injuries. At the reporting time, the outcome of both adverse events was unknown. The reporter considered both events to be related to Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) The reporter considered both events to be disabling events.; Sender's Comments: Priority : 2 , Is case serious : Yes , Index user : (withheld) , Index date : 2025-10-07 , MNSC number : , CLIC number : 938859 , ESTAR number : , IRMS number : PI1166104 , Central date : 2025-10-07 , Classification : DMC, Attachment description : Post Marketing Basic , Safety case number : More
✓
2865671 64 F 10/14/2025 PNC21
 MERCK & CO. INC.
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
erythema, swelling and pain at the injection site; erythema, swelling and pain at the injection site... erythema, swelling and pain at the injection site; erythema, swelling and pain at the injection site; erythema, swelling and pain at the injection site; This spontaneous report was received regarding her mother, a 64-year-old female patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 06-Oct-2025, the patient started therapy with Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE), 0.5 mL (.5ML), (lot # and expiration date were not reported) for prophylaxis. On 06-Oct-2025, the patient experienced erythema, swelling and pain at the injection site after being administered Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE). At the reporting time, the outcome of erythema, swelling and pain at the injection site was unknown. The causal relationship between the events and Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE) was not reported. More
2865672 59 F MD 10/14/2025 FLU3
 SANOFI PASTEUR
 U8848BA
Urticaria Urticaria
Patient came in 6 days after vaccination, reporting she had been experiencing urticaria ever since r... Patient came in 6 days after vaccination, reporting she had been experiencing urticaria ever since receiving the flu vaccine. Patient states urticaria is worse at night. Patient has been taking Benadryl to relive symptoms. States no breathing issues. Patient was interviewed by (withheld name) and an on site physician who was volunteering at the flu drive. Patient was instructed to take non-drowsy medication during the work day, and to go to the emergency room if breathing grew difficult or speak with PCM if symptoms don't alleviate soon. More
2865673 57 M SC 10/14/2025 COVID19
COVID19
 MODERNA
MODERNA
 3052550
3052550
Asthenia, Chills, Decreased appetite, Headache, Heart rate irregular; Myalgia, N... Asthenia, Chills, Decreased appetite, Headache, Heart rate irregular; Myalgia, Nuchal rigidity, Pyrexia More
High grade fever x 48H (102.9), rigors, anorexia, weakness, headache (non-migrainous), mild nuchal r... High grade fever x 48H (102.9), rigors, anorexia, weakness, headache (non-migrainous), mild nuchal rigidity, generalized mm aches, irregular heart beat. More
2865674 60 M FL 10/14/2025 FLU3
 SANOFI PASTEUR
Arthralgia, Gait disturbance, Hypoaesthesia, Joint swelling, Pain in extremity Arthralgia, Gait disturbance, Hypoaesthesia, Joint swelling, Pain in extremity
Patient reports that on Wednesday, 10/01/25, he received the influenza vaccine in the left deltoid a... Patient reports that on Wednesday, 10/01/25, he received the influenza vaccine in the left deltoid at (withheld) Behavioral Hospital. The following morning, he awoke with pain, numbness, and swelling in the right ankle. He states that over the next two days, the pain and numbness progressed up the right lower extremity to the point where he was limping. Pt went to the ED / (withheld) and he is under care of Worker compensation provider for a follow up More
2865677 34 F NC 10/14/2025 FLU3
 SANOFI PASTEUR
 U8848AA
Ocular discomfort, Ocular hyperaemia Ocular discomfort, Ocular hyperaemia
Employee reports that she received the vaccine in the morning on 10/07 at the employee flu drive and... Employee reports that she received the vaccine in the morning on 10/07 at the employee flu drive and at 1430 that afternoon her right eye became red and had was feeling pressure in it. She states she was see by the optometrist on the following day, 10/08 and was prescribed NSAIDS and steroid eye drops. When I became aware of the event on 10/10, the employee reports that the pressure and redness in her right eye were gone. She declined to come to Occupational Health for follow-up but did state she was going to have a follow-up with optometry on 10/15. More
2865678 6 F MN 10/14/2025 COVID19
 PFIZER\BIONTECH
 my9550
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Patient is 6 years old and was given a vaccine indicated for individuals 12 and older. Patient is 6 years old and was given a vaccine indicated for individuals 12 and older.
2865679 51 F MI 10/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 72R4G
Fatigue, Headache, Influenza like illness, Pyrexia, Rash Fatigue, Headache, Influenza like illness, Pyrexia, Rash
Flu-like symptoms (headache, fatigue, fever starting evening of 10/12, Rash developed on torso 10/13... Flu-like symptoms (headache, fatigue, fever starting evening of 10/12, Rash developed on torso 10/13, starting to resolve morning of 10/14 More
2865680 11 F MN 10/14/2025 COVID19
 PFIZER\BIONTECH
 my9550
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Patient is 11 years old and was given a vaccine indicated for individuals 12 and older. Patient is 11 years old and was given a vaccine indicated for individuals 12 and older.
2865681 62 F GA 10/14/2025 COVID19
 PFIZER\BIONTECH
Oropharyngeal pain, Periorbital swelling, Pharyngeal paraesthesia, Pharyngeal sw... Oropharyngeal pain, Periorbital swelling, Pharyngeal paraesthesia, Pharyngeal swelling More
Tingling and soreness in throat, slightly swollen. Next day had puffy eyes. Resolved 10/13/2025. Use... Tingling and soreness in throat, slightly swollen. Next day had puffy eyes. Resolved 10/13/2025. Used cough drops and green tea to soothe throat. More
2865682 9 M MN 10/14/2025 COVID19
 PFIZER\BIONTECH
 my9550
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
patient is 9 years old and was given a vaccine indicated for individuals 12 and older. patient is 9 years old and was given a vaccine indicated for individuals 12 and older.
2865684 66 F NC 10/14/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 U8830AA
U8830AA
Burning sensation, Erythema, Injection site pruritus, Pain in extremity, Periphe... Burning sensation, Erythema, Injection site pruritus, Pain in extremity, Peripheral swelling; Product administered at inappropriate site, Skin warm More
Per employee written account: "After receiving the vaccine, I felt fine, my arm was sore and th... Per employee written account: "After receiving the vaccine, I felt fine, my arm was sore and the site was itching, but it felt like it was itching inside and not on the surface. As with most vaccines, my arm felt sore all day, but did not interrupt my work. When I got home that night, my right arm was extremely sore. I took some Ibuprofen an put an ice pack on my arm. The next morning when I work up, my arm was burring, itching, red, hot to the touch and swollen. When I looked at the injection sight, I notice it was on the side of my upper right arm and not in the deltoid. I received the Fluzone High dose 65+due to my age being 66, which I had last year and did not experience any issues. On the morning of 08 OCT 2025, I brought this to the attention of my supervisor, (name withheld). By the end of the day on Wednesday 08 OCT 2025, my arm was very swollen, red, burning, hot to the touch and the lump was the size of a softball. I again took some Ibuprofen and sat with an ice pack on it all night. The morning of 09 OCT 2025, the redness and itching were not as intense, and some of the swelling had gone down. I still have some soreness, but nothing like it was." This reporter became aware of the situation on 10/10 and spoke to the employee by phone. She reports the swelling was gone and declined to be seen at Occupational Health. I advised that in the future she should report to OH as soon as she experiences any adverse reaction, unless emergent and to then go to an ER. More
2865685 75 F FL 10/14/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 U8764BB
U8764BB
Conjunctival hyperaemia, Cough, Eye pruritus, Fatigue, Oropharyngeal pain; Pruri... Conjunctival hyperaemia, Cough, Eye pruritus, Fatigue, Oropharyngeal pain; Pruritus, Swelling face More
Woke next day (10/12/2025) with whites of both eyes completely red. Face and eye area were swollen/... Woke next day (10/12/2025) with whites of both eyes completely red. Face and eye area were swollen/ puffy and that continued for two days. Eyes, face and head itched. Had a fever of 100.2 which continued for three days. Had dry cough and slightly sore throat. Had fatigue which continued for four days. I am 75 years old and never get the 'senior / high dose' version of the flu vaccine, although I get the flu shot annually. I thought this year with the vaccine idiocy rampant in the (withheld), I would make sure to protect myself. After this experience I won't ever get the high dose version again; however, I will continue to get the regular flu shot. In the question below about recovery, I can say I have recovered now after four days , but am still tired. More
2865686 30 F NY 10/14/2025 RSV
 PFIZER\WYETH
Exposure during pregnancy, Injection site hypoaesthesia, Injection site pain, In... Exposure during pregnancy, Injection site hypoaesthesia, Injection site pain, Injection site pruritus, Injection site swelling More
4th pregnancy, first time receiving rsv vaccine, swelling at injection spot after 2 days, itching at... 4th pregnancy, first time receiving rsv vaccine, swelling at injection spot after 2 days, itching at the spot, numbness where swelling taken place, minor soreness More
2865687 50 F MI 10/14/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
 407009
407009
Abdominal discomfort, Chills, Dizziness, Headache, Injection site bruising; Leth... Abdominal discomfort, Chills, Dizziness, Headache, Injection site bruising; Lethargy, Pyrexia More
Severe bruising at injection site, continued severe headache, chills, fever, lethargy, dizziness, up... Severe bruising at injection site, continued severe headache, chills, fever, lethargy, dizziness, upset stomach. Still ongoing after 5 days. I felt 100 fine before the injection and have never had a reaction like this before. More
2865688 38 F PA 10/14/2025 FLU3
FLU3
FLU3
FLU3
FLU3
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 D5YS9
D5YS9
D5YS9
D5YS9
D5YS9
D5YS9
Anion gap, Blood chloride normal, Blood creatinine normal, Blood glucose increas... Anion gap, Blood chloride normal, Blood creatinine normal, Blood glucose increased, Blood potassium normal; Blood sodium normal, Blood urea normal, Carbon dioxide normal, Full blood count, Glomerular filtration rate normal; Haematocrit normal, Haemoglobin normal, Lymphocyte percentage increased, Mean cell haemoglobin concentration normal, Mean cell haemoglobin decreased; Mean cell volume decreased, Mean platelet volume normal, Metabolic function test, Neutrophil percentage decreased, Palpitations; Parosmia, Platelet count normal, Red blood cell count normal, Red blood cell nucleated morphology, Red cell distribution width normal; Throat tightness, White blood cell count normal More
Approx 7:45pm, employee had smelled a funny smell, heart started racing, throat felt like it was clo... Approx 7:45pm, employee had smelled a funny smell, heart started racing, throat felt like it was closing up. At 8:00pm employee was seen in the ER. More
2865690 88 F DE 10/14/2025 FLU3
 SANOFI PASTEUR
 U8855AA
Extra dose administered Extra dose administered
Received 2 flu vaccines. First one on 9/15/2025 and the second one 9/30/2025 Received 2 flu vaccines. First one on 9/15/2025 and the second one 9/30/2025
2865692 90 F 10/14/2025 FLU3
 SANOFI PASTEUR
 u8862ca
Needle issue, Underdose, Wrong technique in product usage process Needle issue, Underdose, Wrong technique in product usage process
While giving the vaccine half of the vaccine sprayed through the needle and didn't make it into... While giving the vaccine half of the vaccine sprayed through the needle and didn't make it into the patient, the remaining half of the vaccine was able to be administered. The needle was defective, I let the patient know about the issue and administered half of another fluzone HD flu shot to the patient. More
2865695 8 M WA 10/14/2025 FLU3
HEPA
IPV
MMRV
TDAP
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
 U8854AA
42DM9
Y1A212M
Z008224
U8353BA
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event More
The child needed the varicella vaccine only and had completed his MMR. MMRV was administered by acci... The child needed the varicella vaccine only and had completed his MMR. MMRV was administered by accident. There was not an adverse effect noted having given an extra dose of MMR. More
2865696 87 M FL 10/14/2025 FLU3
 SANOFI PASTEUR
 U8859DA
Diarrhoea, Vomiting Diarrhoea, Vomiting
Patient received his Fluzone High Dose vaccine on Sunday October 12th, 2025 at 1:47 PM. The patient ... Patient received his Fluzone High Dose vaccine on Sunday October 12th, 2025 at 1:47 PM. The patient reports that at approximately 9:00 PM on Monday October 13th, 2025 they became ill and experienced "violent diarrhea and vomiting." They called the pharmacy on Tuesday October 14, 2025 at 10:30 AM and spoke with Pharmacy Manager (withheld name) about the incident, stating that the symptoms lessened after about 2:00 AM and had resolved by the time they called the pharmacy. They reported considering taking the patient to the hospital given the severity of his symptoms and could not give him medication. They were rehydrating him with fluids as of the morning of October 14th. More
2865697 79 F GA 10/14/2025 FLU3
 SANOFI PASTEUR
 UT8781AA
Arthralgia, Mobility decreased Arthralgia, Mobility decreased
Patient reported shoulder pain and difficulty raising arm. Advised to go over with their primary car... Patient reported shoulder pain and difficulty raising arm. Advised to go over with their primary care physician as this could be a sign of a shoulder injury. Still reporting shoulder pain in October and patient has been to their physician's office. More
2865698 72 F KY 10/14/2025 COVID19
 MODERNA
 3052133
Diarrhoea, Pain, Vomiting Diarrhoea, Pain, Vomiting
Patient described extreme body aches, slight vomiting, and diarrhea Patient described extreme body aches, slight vomiting, and diarrhea
2865699 7 F WA 10/14/2025 DTAP
FLU3
HEP
IPV
MMRV
 SANOFI PASTEUR
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 3CA55C1
U8854AA
3N2ND
Y1A212M
Z008224
Extra dose administered; Extra dose administered; Extra dose administered; Extra... Extra dose administered; Extra dose administered; Extra dose administered; Extra dose administered; Extra dose administered More
The child was given MMRV when they only needed the single dose varicella vaccine. MMR series had alr... The child was given MMRV when they only needed the single dose varicella vaccine. MMR series had already been completed More
2865700 63 F TX 10/14/2025 FLU3
 SEQIRUS, INC.
Hemiplegia, Oropharyngeal pain, Pain Hemiplegia, Oropharyngeal pain, Pain
two days after receiving the vaccine, she developed severe pain in right side of throat, followed by... two days after receiving the vaccine, she developed severe pain in right side of throat, followed by pain to the entire right side of the body; followed by right sided paralysis. More
2865701 91 F ND 10/14/2025 FLU3
 SANOFI PASTEUR
Blood pressure decreased, Dysstasia, Gait inability, Malaise, Mobility decreased Blood pressure decreased, Dysstasia, Gait inability, Malaise, Mobility decreased
The evening after the shot was given, Pt started not to feel well. She states she couldn't mov... The evening after the shot was given, Pt started not to feel well. She states she couldn't move her legs or arms. She rolled off of the couch because she wasn't able to stand or get up. A young man that helps her around the house came over to find her, and he also called another person over who suggested she go to the ER. She still couldn't move her arms or legs, couldn't walk. Her Blood pressure was very low in the ER she stated. She was admitted overnight for observation. By morning the next day, she felt better. She was discharged that day after 1 night hospitalization. Her PCP stated she not have any more vaccines after that. More
✓
2865703 31 F CA 10/14/2025 HPV9
HPV9
 MERCK & CO. INC.
MERCK & CO. INC.

Adnexa uteri pain, Anti-Muellerian hormone level decreased, Confusional state, D... Adnexa uteri pain, Anti-Muellerian hormone level decreased, Confusional state, Dizziness, Magnetic resonance imaging abnormal; Ovarian cyst, Syncope More
On the third dose I had severe confusion and syncope for about 12 hours, then pain in my right ovary... On the third dose I had severe confusion and syncope for about 12 hours, then pain in my right ovary that night. Ovarian pain has persisted. Scan confirm cyst and labs a few years later show low AMF or fertility. Prior 2 doses had 15 minutes of syncope and dizziness. Other vaccines have been normal, mild syncope or arm soreness. More
✓
2865704 26 F NV 10/14/2025 FLU3
FLU3
FLUC4
FLUC4
 SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
 Unknown
Unknown
948410
948410
Myalgia; Injection site pain; Myalgia; Injection site pain Myalgia; Injection site pain; Myalgia; Injection site pain
L arm muscular pain continuing for 3 weeks. Has not yet resolved. Has worsened over the last week L arm muscular pain continuing for 3 weeks. Has not yet resolved. Has worsened over the last week
2865705 8 M TX 10/14/2025 COVID19
 MODERNA
 6M-11Y
Pruritus, Rash Pruritus, Rash
Rash to back and chest. Itching Rash to back and chest. Itching
2865706 41 F 10/14/2025 FLU3
HEP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
DYNAVAX TECHNOLOGIES CORPORATION
GLAXOSMITHKLINE BIOLOGICALS
 4gr2b
946062
h4279
Injection site erythema, Injection site swelling, Pruritus, Rash; Injection site... Injection site erythema, Injection site swelling, Pruritus, Rash; Injection site erythema, Injection site swelling, Pruritus, Rash; Injection site erythema, Injection site swelling, Pruritus, Rash More
Vaccines given on 10/8. Redness/swelling and 2 bumps formed at right arm injection site, where flu w... Vaccines given on 10/8. Redness/swelling and 2 bumps formed at right arm injection site, where flu was administered. Her ankles, back of knees, and right arm were extremely itchy. The itching finished on 10/9. The bumps went away on 10/10. No other symptoms noted. Has never had this reaction before. More
2865708 17 F SC 10/14/2025 HPV9
 MERCK & CO. INC.
 Y018416
Immediate post-injection reaction, Loss of consciousness, Pallor, Syncope Immediate post-injection reaction, Loss of consciousness, Pallor, Syncope
Patient sitting upright on patient bed with mother by her side. HPV vaccine administered into right ... Patient sitting upright on patient bed with mother by her side. HPV vaccine administered into right deltoid. Patient immediately became pale in her face and had brief syncopal episode lasting no more than 5 seconds. Mom able to guide her shoulders down to bed as needed. Patient immediately alert and oriented after coming to. Water given and monitored for 15 minutes. Patient able to safely ambulate herself from office. More
2865709 50 M CA 10/14/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR

Injected limb mobility decreased, Pain, Pain in extremity; Injected limb mobilit... Injected limb mobility decreased, Pain, Pain in extremity; Injected limb mobility decreased, Pain, Pain in extremity More
Patient received flu shot 10/9 at (withheld) Pharmacy. Believe right arm covid vaccine and left arm... Patient received flu shot 10/9 at (withheld) Pharmacy. Believe right arm covid vaccine and left arm flu shot. Some expected soreness for 2 days. Yesterday, left arm pain. Unable to lift arm. More
2865710 34 F TN 10/14/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 JS74H
Injection site pain, Limb discomfort, Product administered at inappropriate site... Injection site pain, Limb discomfort, Product administered at inappropriate site, Skin tightness More
The vaccine was administered extremely high up on my right arm, close to shoulder bone. i took a ph... The vaccine was administered extremely high up on my right arm, close to shoulder bone. i took a photo of bandaid placement for documentation. starting 1-2 days post vaccine, a dull ache/burning sensation around injection site, tightness/heaviness in right arm started. used ice pack, otc pain medication (tylenol/ibuprofen) and topical lidocaine without much relief. still experiencing pain today 10/14. messaged providers office to report symptoms and ask for guidance on how to proceed and waiting to hear back. More
2865711 45 M NC 10/14/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.

Feeling abnormal, Influenza virus test negative, Oropharyngeal pain, Pyrexia, SA... Feeling abnormal, Influenza virus test negative, Oropharyngeal pain, Pyrexia, SARS-CoV-2 test negative; Stomatitis, Streptococcus test negative More
Day after shot, got to feeling bad and run a low grade temp. Going on 6 days with no relief from tem... Day after shot, got to feeling bad and run a low grade temp. Going on 6 days with no relief from temp besides medication. Sore throat and mouth feels raw. . Was given Magic mouth wash and prednisone. More
2865712 40 M CA 10/14/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 MY9550
TFAA2501
Pain in extremity; Pain in extremity Pain in extremity; Pain in extremity
Pt received two immunizations on the same arm on 9/10/2025 and he has been experiencing arm pain sin... Pt received two immunizations on the same arm on 9/10/2025 and he has been experiencing arm pain since the vaccination. It has been more than a month and he will go to urgent care for treatment today per pt's mother. More
2865713 57 F FL 10/14/2025 FLU3
PNC20
 SANOFI PASTEUR
PFIZER\WYETH
 U8864BA
MA2488
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Patient Received Prevnar 20 on 10/12/2025, but she is not due because she got the same vaccine on 5/... Patient Received Prevnar 20 on 10/12/2025, but she is not due because she got the same vaccine on 5/8/2023 (not reported on state shots) per CDC guidelines one shot for life. More
2865714 97 F KS 10/14/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3052784
UT8804AA
Pallor, Rash, Rash erythematous, Rash pruritic; Pallor, Rash, Rash erythematous,... Pallor, Rash, Rash erythematous, Rash pruritic; Pallor, Rash, Rash erythematous, Rash pruritic More
Non-palpable, erythematous yet blanchable patches along Left bra line and between shoulderblades. Ra... Non-palpable, erythematous yet blanchable patches along Left bra line and between shoulderblades. Rash originally reported to be pruritic, though this has diminished significantly since onset and has never been bothersome to patient, only noticeable. More
2865715 24 F MD 10/14/2025 COVID19
COVID19
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Chills, Headache, Myalgia, Nausea, Pyrexia; Syncope, Tunnel vision Chills, Headache, Myalgia, Nausea, Pyrexia; Syncope, Tunnel vision
fever, chills, headache, muscle aches beginning approximately 5 hours after vaccination; nausea, tun... fever, chills, headache, muscle aches beginning approximately 5 hours after vaccination; nausea, tunnel vision, and syncope upon waking up approximately 12 hours after vaccination More
2865716 69 M TX 10/14/2025 FLU3
 SANOFI PASTEUR
 U8859DA
Dizziness, Vision blurred Dizziness, Vision blurred
PATIENT REPORTED HAVING DIZINESS AND BLURRED VISION FOR 24 HOURS AFTER ADMINISTRATION OF THE VACCINE... PATIENT REPORTED HAVING DIZINESS AND BLURRED VISION FOR 24 HOURS AFTER ADMINISTRATION OF THE VACCINE. More
2865717 50 F NM 10/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Erythema, Muscle tightness, Pain, Pyrexia, Swelling Erythema, Muscle tightness, Pain, Pyrexia, Swelling
Swelling, redness, severe body aches, tight, knotted muscles in legs, fever Swelling, redness, severe body aches, tight, knotted muscles in legs, fever
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