🏥 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 💀 🏥 🚑 ♿ ⚠️
2789503 60 M MD 09/09/2024 COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 LM2223
LM2223
LM2223
Pain in extremity, Vascular pain; Epistaxis; Epistaxis, Vascular pain; Epistaxis... Pain in extremity, Vascular pain; Epistaxis; Epistaxis, Vascular pain; Epistaxis; Epistaxis, Vascular pain More
Symptoms started on Saturday evening with pain in the blood vessel around the left arm, elbow, and ... Symptoms started on Saturday evening with pain in the blood vessel around the left arm, elbow, and the lower arm close to the hand and around the biceps area. The pain lasted over night and by Sunday morning the pain had subsided. More
2821714 65 F VA 01/19/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 9L5P2
9L5P2
Chills, Headache, Injection site erythema, Injection site pruritus, Injection si... Chills, Headache, Injection site erythema, Injection site pruritus, Injection site swelling; Nausea, Pruritus More
PATIENT REPORTED REDNESS & SWELLING AT THE INJECTION SITE, HEADACHE, SHIVERING, AND NAUSEA. ALS... PATIENT REPORTED REDNESS & SWELLING AT THE INJECTION SITE, HEADACHE, SHIVERING, AND NAUSEA. ALSO HAD ITCHING AT THE INJECTION SITE THAT SPREAD TO THE ABDOMINAL AREA. More
2821715 71 F FL 01/19/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 3959s
3959s
Erythema, Injected limb mobility decreased, Injection site pain, Injection site ... Erythema, Injected limb mobility decreased, Injection site pain, Injection site reaction, Neuralgia; Swelling More
PATIENT STATES THAT SHE IS EXSPERIENCING PAIN IN THE UPPER LEFT ARM. THERE IS NERVE PAIN AND BURNING... PATIENT STATES THAT SHE IS EXSPERIENCING PAIN IN THE UPPER LEFT ARM. THERE IS NERVE PAIN AND BURNING IN THAT AREA. DIFFICULTY LIFTING ARM; SHE DIDNT HAVE ANY SWELLING, REDNESS, OR PAIN UNTIL A FEW DAYS AFTER THE VACCINE. More
2821716 75 M GA 01/19/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255T2
Extra dose administered Extra dose administered
Not known. Unable to reach patient Not known. Unable to reach patient
2821717 81 M GA 01/19/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255T2
Extra dose administered Extra dose administered
PATIENT RECEIVED A SECOND DOSE OF AREXVY ONE YEAR AFTER THE FIRST DOSE. ONLY ONE DOSE INDICATED. PATIENT RECEIVED A SECOND DOSE OF AREXVY ONE YEAR AFTER THE FIRST DOSE. ONLY ONE DOSE INDICATED.
2821718 79 F GA 01/19/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255T2
Extra dose administered Extra dose administered
PATIENT RECEIVED A SECOND DOSE OF AREXVY ONE YEAR AFTER THE FIRST DOSE. ONLY ONE DOSE INDICATED. PATIENT RECEIVED A SECOND DOSE OF AREXVY ONE YEAR AFTER THE FIRST DOSE. ONLY ONE DOSE INDICATED.
2821719 85 M FL 01/19/2025 FLU3
PNC20
 SEQIRUS, INC.
PFIZER\WYETH
 388489
lj5281
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
Patient had already received Prevnar 20 on 06/26/2022 then received a second dose of Prevnar 20 on 0... Patient had already received Prevnar 20 on 06/26/2022 then received a second dose of Prevnar 20 on 01/14/2025. Patient is doing ok. More
2821720 69 F FL 01/19/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
duplicate dose of arexy was originally given 05/25/24 duplicate dose of arexy was originally given 05/25/24
2821721 54 F 01/19/2025 PNC21
 MERCK & CO. INC.
 Y011819
Erythema, Pain, Skin warm Erythema, Pain, Skin warm
Red, warm and painful - started a day after vaccine - Red, warm and painful - started a day after vaccine -
2821722 78 F FL 01/19/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 N77J2
Erythema, Swelling face Erythema, Swelling face
Patient claims 2 days later she had a red face and a little swelling of the face. Mouth and Tongue ... Patient claims 2 days later she had a red face and a little swelling of the face. Mouth and Tongue were not affected. She took an antihistamine and applied cool compresses and the next day she said she was doing better. More
2821723 46 F AR 01/19/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 8081564
TFAA2436
Erythema, Pain, Skin warm, Swelling, Tenderness; Erythema, Pain, Skin warm, Swel... Erythema, Pain, Skin warm, Swelling, Tenderness; Erythema, Pain, Skin warm, Swelling, Tenderness More
Patient called pharmacy informed pharmacist of a small raised 3 inch diameter red circle on her left... Patient called pharmacy informed pharmacist of a small raised 3 inch diameter red circle on her left arm. She said it was hot and tender to the touch. Recommended to take some ibuprofen or tylenol for the pain. Told her this is a known but rare side effect. She waited until 1/19/2025 to report because the swelling had not gone down. Will follow up with her for improvement of symptoms and told her to call back to inform us if it got worse. More
2821739 67 F FL 01/19/2025 COVID19
 MODERNA
 3043823
Chills, Fatigue, Headache, Pyrexia, Sluggishness Chills, Fatigue, Headache, Pyrexia, Sluggishness
The morning after receiving the vaccine (Jan 18, 2025) at 11AM patient woke up with headache, fever ... The morning after receiving the vaccine (Jan 18, 2025) at 11AM patient woke up with headache, fever (up to 102degrees F), chills, feeling tired and sluggish. As a result she took ER650mg of tylenol and 400mg of advil. She feels better today Jan 19, 2025. More
2821740 66 F GA 01/19/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255t2
Extra dose administered Extra dose administered
Patient received first dose of arexvy 12/1/2023 and this wasn't realized until after patient re... Patient received first dose of arexvy 12/1/2023 and this wasn't realized until after patient received a second dose 1/16/25. This is a one shot series. No second shot is needed. More
2821741 86 F TN 01/19/2025 PNC20
 PFIZER\WYETH
 LC1281
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient was given Prevnar20 on 1/17/25. On 1/18/25, it was discovered that patient got Prevnar 20 on... Patient was given Prevnar20 on 1/17/25. On 1/18/25, it was discovered that patient got Prevnar 20 on 6/19/24. I was able to reach the patient on 1/19/25 and told her that she got a duplicate vaccine. She was not experiencing any adverse effects. More
2821742 62 F VA 01/19/2025 PNC20
 PFIZER\WYETH
 LJ5280
Impaired work ability Impaired work ability
PT RETURNED TO THE PHARMACY REPORTING SYMPOMS LIST ON THE VIS INFORMATION SHEET PT RETURNED TO THE PHARMACY REPORTING SYMPOMS LIST ON THE VIS INFORMATION SHEET
2821743 36 M MI 01/19/2025 COVID19
FLU3
PNC20
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 30433332
9H5J5
LJ5283
Urticaria; Urticaria; Urticaria Urticaria; Urticaria; Urticaria
Urticaria of arms, legs, back w/ onset 48 hours after vaccine administration Urticaria of arms, legs, back w/ onset 48 hours after vaccine administration
2821654 34 F AZ 01/18/2025 HPV4
HPV4
HPV4
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.


Arthralgia, Blood test, Dizziness, Ear swelling, Erythema; Eye contusion, Gait d... Arthralgia, Blood test, Dizziness, Ear swelling, Erythema; Eye contusion, Gait disturbance, Headache, Inflammation, Loss of personal independence in daily activities; Polychondritis, Rash, Throat irritation More
Dizziness; throat irritation; painful mouth sores; hair loss; Relapsing polychondritis/Gardasil-indu... Dizziness; throat irritation; painful mouth sores; hair loss; Relapsing polychondritis/Gardasil-induced autoimmune disorder; had rashes all over her body; Headaches; Information has been received from a lawyer and refers to a 34-year-old female patient. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 24-AUG-2021 and 08-NOV-2021, the patient was vaccinated with the first and second dose of quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL) intramuscular injection, respectively, administered to prevent cancer (also reported as preventing cervical cancer) (strength, dose, frequency, lot #, expiry date, anatomical location, and route of administration were not provided). Within weeks of receiving the second quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL) dose, on an unspecified date in 2021, the patient experienced her nose and ears turning red from inflammation. She had rashes all over her body and crippling joint pain. The redness and inflammation were severe enough to cause her eyes to appear black, and her ears to swell shut. She began suffering from headaches. She scheduled an appointment with an eyes, nose, and throat (ENT) who conducted several blood tests (results not provided) before being diagnosed with relapsing polychondritis by one ENT and confirmed by another ENT before being treated for her diagnosis. She was informed that her condition was extremely rare, and she was the only patient in her physician's system with this condition. Patient was also informed that her illness might necessitate heart surgery or the use of a ventilator as she ages. Patient endured daily joint pain, dizziness, swelling, redness in her nose and ears, rashes, and throat irritation. On 20-APR-2022, the patient was vaccinated with the third dose of quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL) intramuscular injection. She was currently prescribed three medications, one of which was given by infusion and not covered by insurance. Some of the medication had caused hair loss and painful mouth sores, and another carries the risk of retinal detachment. Along with seeing her ENT, she needed continuous monitoring of labs and future cardiologist appointments to monitor her heart. Before the quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL) vaccine, patient eagerly anticipated starting a family and completing her PhD. She maintained a 4.0 GPA, graduated with her master's degree, and held a full-time job. She enjoyed exercise and visiting the zoo, but now cannot because of her joint pain and exhaustion. She had contemplated taking time from school and leaving the job she loved due to the difficulties of commuting caused by her joint pain. Because her future health was uncertain, she was now uncertain about starting a family. Patient contended that her quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine injections caused her to develop relapsing polychondritis, as well as a constellation of adverse symptoms, complications, injuries, and other adverse events, many of which are alleged herein and all of which were caused by quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL) or otherwise linked to her quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL)-induced autoimmune disorder. Patient had suffered and continued to suffer severe and permanent physical injuries and associated symptomology and had suffered severe and permanent emotional injuries, including pain and suffering. She also had a substantial fear of suffering additional and ongoing harms, including but not limited to now being at an increased risk of cancer, and future symptoms and harms associated with her autoimmune and neurological disease and other injuries caused by quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL) vaccine. As a direct and proximate result of her quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL)-induced injuries, patient had suffered and continued to suffer economic losses, including considerable financial expenses for medical care and treatment, and diminished income capacity, and she would continue to incur these losses and expenses in the future. At the time of reporting, the outcome of the events was not recovered. The reporter considered thee events to be related to quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (GARDASIL). Upon internal review, the event relapsing polychondritis was determined to be medically significant. The reporter considered relapsing polychondritis to be Disability event. More
✓
2821671 F VA 01/18/2025 UNK
 UNKNOWN MANUFACTURER
Blood bilirubin increased, Hyperbilirubinaemia, Jaundice Blood bilirubin increased, Hyperbilirubinaemia, Jaundice
Hyperbilirubinemia, jaundice, on the verge of getting readmitted to hospital for phototherapy treatm... Hyperbilirubinemia, jaundice, on the verge of getting readmitted to hospital for phototherapy treatment More
2821672 66 F CA 01/18/2025 RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 5J959
5J959
Arthralgia, Decreased appetite, Dizziness, Fatigue, Headache; Loss of personal i... Arthralgia, Decreased appetite, Dizziness, Fatigue, Headache; Loss of personal independence in daily activities, Myalgia More
Severe fatigue, headache, light headed, arthralgia,myalgia, total loss of appetite. Unable to go abo... Severe fatigue, headache, light headed, arthralgia,myalgia, total loss of appetite. Unable to go about any daily activities. Bed ridden for 24 hours More
2821673 1.42 M KY 01/18/2025 DTAPIPVHIB
DTAPIPVHIB
FLU3
FLU3
PNC20
PNC20
 SANOFI PASTEUR
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
PFIZER\WYETH
 UK042AB
UK042AB
J9M39
J9M39
LC5483
LC5483
Electroencephalogram normal, Febrile convulsion, Influenza virus test negative, ... Electroencephalogram normal, Febrile convulsion, Influenza virus test negative, Pyrexia, Respiratory syncytial virus test negative; SARS-CoV-2 test negative; Electroencephalogram normal, Febrile convulsion, Influenza virus test negative, Pyrexia, Respiratory syncytial virus test negative; SARS-CoV-2 test negative; Electroencephalogram normal, Febrile convulsion, Influenza virus test negative, Pyrexia, Respiratory syncytial virus test negative; SARS-CoV-2 test negative More
Complex febrile seizure. Patient had two short seizure episodes lasting less than 1 minute on 1/15/2... Complex febrile seizure. Patient had two short seizure episodes lasting less than 1 minute on 1/15/25 associated with fever. He had a third febrile seizure episode on 1/16. More
✓
2821674 75 U FL 01/18/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered, No adverse event Extra dose administered, No adverse event
no adverse effects noted, patient had received a prior dose in 2023 no adverse effects noted, patient had received a prior dose in 2023
2821675 11 M IL 01/18/2025 MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
Erythema, Peripheral swelling, Pruritus Erythema, Peripheral swelling, Pruritus
My son?s arm was very red and swollen from the shoulder to half-way down his upper arm. It was very ... My son?s arm was very red and swollen from the shoulder to half-way down his upper arm. It was very red in color and itchy. I have pictures More
2821676 21 F UT 01/18/2025 RAB
 SANOFI PASTEUR
 W1D182M
Vomiting Vomiting
Donor received the Rabies vaccination. A minute after the shot, the Donor stated that she was going ... Donor received the Rabies vaccination. A minute after the shot, the Donor stated that she was going to be sick. (the RN) gave her the garbage can. The Donor vomited 240 mL in the garbage can. The RN asked if this was from the vaccination, The Donor stated that she felt sick half way through her plasma donation & that it was her second time getting sick during plasma donation. RN informed the Donor that had she known that the donor was not feeling well, she would not have given the Donor the Rabies vaccine. Donor stated, "That makes sense." More
2821677 71 M OH 01/18/2025 RSV
 PFIZER\WYETH
 LN5463
Extra dose administered Extra dose administered
Patient said he never received previous dose of RSV, and was even counseled on his age and underlyin... Patient said he never received previous dose of RSV, and was even counseled on his age and underlying conditions and this is a single dose vaccine. Before receiving the vaccine, he was again counseled on this being a single dose. After giving the vaccine and dropping the Admin Record on his profile, I saw he received an initial dose in March 2024 More
2821678 58 M FL 01/18/2025 FLU3
 SEQIRUS, INC.
 946614
Flushing Flushing
Flush (redness) in patients face, arms and chest Flush (redness) in patients face, arms and chest
2821679 66 M MA 01/18/2025 COVID19
COVID19
 MODERNA
MODERNA

Borrelia test, Feeling abnormal, Laboratory test, Mental impairment, Muscular we... Borrelia test, Feeling abnormal, Laboratory test, Mental impairment, Muscular weakness; Nephrectomy, Tremor More
see prior pages see prior pages
2821680 49 F NY 01/18/2025 COVID19
 MODERNA
 8080803
Fatigue, Fluid intake reduced, Headache, Nausea, Pyrexia Fatigue, Fluid intake reduced, Headache, Nausea, Pyrexia
mild fever at 100f, tiredness, headache, worsening nausea that prevents fluid intake mild fever at 100f, tiredness, headache, worsening nausea that prevents fluid intake
2821681 51 F MD 01/18/2025 PNC20
 PFIZER\WYETH
Injection site erythema, Injection site induration, Injection site nodule, Injec... Injection site erythema, Injection site induration, Injection site nodule, Injection site pain, Injection site swelling More
Pain, hard knot, redness and swelling at injection site for at least five days. Pain with even light... Pain, hard knot, redness and swelling at injection site for at least five days. Pain with even light pressure for four days. More
2821682 72 F NH 01/18/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 YO11819
YO11819
Chills, Injection site bruising, Injection site reaction, Injection site swellin... Chills, Injection site bruising, Injection site reaction, Injection site swelling, Injection site warmth; Pain, Pyrexia, Rash erythematous More
Swelling, red rash, hot to touch, fever, aches, chills, bruising at injection site Swelling, red rash, hot to touch, fever, aches, chills, bruising at injection site
2821683 65 M TX 01/18/2025 COVID19
 MODERNA
Chills, Injection site pain, Pain of skin Chills, Injection site pain, Pain of skin
Chills, site soreness, felt like my skin hurt Chills, site soreness, felt like my skin hurt
2821684 58 F FL 01/18/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA



Chills, Decreased appetite, Diarrhoea, Dizziness, Fatigue; Feeling of body tempe... Chills, Decreased appetite, Diarrhoea, Dizziness, Fatigue; Feeling of body temperature change, Hyperhidrosis, Hypersomnia, Influenza like illness, Loss of consciousness; Malaise, Nausea, Pain, Seizure, Urinary incontinence; Vomiting More
1/15/2025, 9:10 am - Covid vaccine at pharmacy, vaccines for multiple patients loaded in syringes an... 1/15/2025, 9:10 am - Covid vaccine at pharmacy, vaccines for multiple patients loaded in syringes and stored in ziplock bags with name and prescription information on them (filled before our arrival, no idea of how long they were out). 1/16/2025, 1-4 am, woke up feeling like I had something similar to the flu - hot/cold, sweating/chills, exhausted, aches, queasy. 1/16/25 8 am-3 pm continued queasy feeling, exhaustion, hot/cold. 1/16/25 3 pm ate Salisbury steak and mashed potatoes. 1/16/25 started to feel faint, saw bright white light, passed out and started vomiting at the same time, lost control of bladder, convulsions.. Struggled to wake back up. Finally did (getting close to calling for an ambulance but didn?t). Ever since through today 1/18/25 at 2 pm, continued queasy, , diarrhea, exhaustion, sleeping a lot more than normal, feel lousy in general, not much interest in trying to eat (eating small amounts, followed by diarrhea). More
2821685 22 M 01/18/2025 COVID19
 MODERNA
Headache, Pyrexia Headache, Pyrexia
Fever and headache Fever and headache
2821686 67 M PA 01/18/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 E75e5
Lethargy, Peripheral swelling, Pruritus, Pyrexia Lethargy, Peripheral swelling, Pruritus, Pyrexia
Patient had vaccine several weeks ago but came in today to tell me she had what she considered to be... Patient had vaccine several weeks ago but came in today to tell me she had what she considered to be a bad reaction. Her arm was swollen for two weeks and still itches. It began at midnight the day she got. For 16 hours she was extremely lethargic. She had a fever of 102.8 for 1 day following vaccine. Did not seek medical attention for symptoms. More
2821687 70 F MI 01/18/2025 COVID19
 MODERNA
Nephrolithiasis, Pyrexia, Renal pain Nephrolithiasis, Pyrexia, Renal pain
Kidney stone pain and fever Kidney stone pain and fever
2821688 66 F NC 01/18/2025 FLU3
 SANOFI PASTEUR
 U8524BA
Myalgia Myalgia
PATIENT REPORTED THAT FOLLOWING VACCINATION WITH THE FLUZONE HIGH DOSE VACCINE ON 12/21/2024 HAVING ... PATIENT REPORTED THAT FOLLOWING VACCINATION WITH THE FLUZONE HIGH DOSE VACCINE ON 12/21/2024 HAVING "MUSCLE PAIN BUT I WOULD SAY FROM 0-10 IT WAS 7" . "I TYHINK I TOOK NAPROXEN SODIUM" AND THAT "DID HELP" . ACCORDING TO THE PATIENT, THE PAIN LASTED APPROXIMATELY "2 DAYS" . PATIENT STATED THAT THERE WAS "MUSCLE PAIN" AND "SORENESS" , AND THAT IT WOULD GO "REALLY DEEP". PATINET REPORTED THAT SHE HAD TO GO THROUGH CHEMO[THERAPY] AND THAT SHE HAD SIMILAR SYUMPTOMS TO THOSE FOLLOWING THE VACCINE. THE PATIENT ALSO REPORTED THAT SHE WAS "ACHY" . PATIENT ALSO REPORTED THAT SHE WAS ON ANTIBIOTICS IN THE PRECEDING WEEKS BEFORE THE INFLUENZA VACCINE (SHE COULD NOT RECALL THE EXACT ANTIBIOTIC REGIMEN AT THE TIME OF THIS WRITING). ALSO, THE PATIENT STATED THAT THE ADVERSE EVENTS RESOLVED AFTER SEVERAL DAYS. More
2821689 73 M AZ 01/18/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Fatigue, Headache, Pain Fatigue, Headache, Pain
Headache, body aches, extreme fatigue Headache, body aches, extreme fatigue
2821690 16 F 01/18/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH


Blood test normal, Brain stem syndrome, Central nervous system lesion, Chest X-r... Blood test normal, Brain stem syndrome, Central nervous system lesion, Chest X-ray normal, Clinically isolated syndrome; Computerised tomogram head, Hypoaesthesia, Lumbar puncture, Magnetic resonance imaging head abnormal, Magnetic resonance imaging neck normal; Migraine, Nausea, Scan with contrast abnormal More
I came into the hospital in the beginning of November with face numbness. Almost the entirety of the... I came into the hospital in the beginning of November with face numbness. Almost the entirety of the right side of my face was numb and when I would touch it I could not feel it. The doctors decided to give me a CT scan of my head, after that I had an MRI (no contrast,) that?s where they found a lesion on my brain stem. There was another lesion but it was very very small closer to the top of my head. They weren't sure if it was a tumor at first or something else so I had to go back and get an MRI with contrast this time and they saw that it was in fact a lesion. I was then admitted to the hospital over a period of 5 days in the middle of November. They had me hooked up to an IV over those 5 days with a heavy dose of steroids. (I believe it was 1,000 mg but I could be wrong.) Later they did another MRI on my neck to make sure there were no lesions there (I was clear.) I got a chest x-ray done just as a precaution (nothing was found there.) They took about 30 vials of blood in total during that month of me in and out of the hospital (it all looked normal.) They ended up diagnosing me with Isolated Case Syndrome, but they are talking about treating me for Multiple Sclerosis. They can?t say that it is Multiple Sclerosis due to the fact that there were not enough lesions to pinpoint it on that. My face numbness went away after the steroids and I was released from the hospital. It?s been a couple months since November and I have been nauseous most days and I have migraines most days. They gave me medicine to subside that and it helps and it has been a lot more manageable since then. I am not sure if this is related to the COVID-19 Pfizer shot but seeing that nothing in my life has changed before I had the shot or after it?s safe to assume that this could have definitely been the cause of what I may have. I also have permanent brain damage on my brain stem from this lesion. I forgot to mention I also had a spinal tap done. More
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2821691 79 F NY 01/18/2025 RSV
 PFIZER\WYETH
 LL8391
Extra dose administered Extra dose administered
Upon entering the vaccine administration information on the registry, we noticed the patient was pre... Upon entering the vaccine administration information on the registry, we noticed the patient was previously vaccinated with an RSV vaccine in 2023. Currently, the guidelines recommend only one dose of the RSV vaccine. The patient was contacted upon discovering this issue at 5:01 pm 1/18/2025 and we informed her that we will report this incident. Patient states that she is feeling fine but was instructed to contact the pharmacy or her doctor if she does not feel well or has any concerns. More
2821692 33 F GA 01/18/2025 COVID19
UNK
 JANSSEN
UNKNOWN MANUFACTURER

Arthralgia, Complex regional pain syndrome, Pain in extremity, Uterine haemorrha... Arthralgia, Complex regional pain syndrome, Pain in extremity, Uterine haemorrhage, Vaginal haemorrhage; Arthralgia, Complex regional pain syndrome, Pain in extremity, Uterine haemorrhage, Vaginal haemorrhage More
I received the COVID-19 injection. The shot was mandatory for some jobs; with that being said I was ... I received the COVID-19 injection. The shot was mandatory for some jobs; with that being said I was the Front Gate Runner at the time. While receiving the Janssen COVID 19 injection I felt normal as if this shot would be like a flu injections as describe by injection medical staff. April 2020 not even more than twenty-four hours later; I began to feel pain and soreness. I requested to see the doctor, and I was told the side effects of pain as well as soreness would be accepted, and I was prescribed some Ibuprofen 800mg at pill time. I still have extreme pain in left shoulder and arm I was diagnosed with CRPS(central regional pain syndrome). While dealing with the pain from the vaccination; I started bleeding from my vaginal area, not to mention that to this date and year of 2025 I am still experiencing vaginal bleeding, that recently has been diagnosed as Hemorrhaging of the uterus. More
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2821693 66 M TN 01/18/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52Z52
Extra dose administered, Myalgia Extra dose administered, Myalgia
Patient received a second dose of Arexvy on 1/16/25 after already receiving the vaccine on 12/16/23.... Patient received a second dose of Arexvy on 1/16/25 after already receiving the vaccine on 12/16/23. Muscle pain/soreness after vaccination that is better now a couple days after vaccination. He used ibuprofen to treat the symptoms and reported that the symptoms did not significantly affect his day-to-day activities. More
2821694 76 F AZ 01/18/2025 PNC20
PNC20
RSV
RSV
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 lc1281
lc1281
hy1811
hy1811
Middle insomnia, Pruritus, Rash, Rash erythematous, Rash pruritic; Skin irritati... Middle insomnia, Pruritus, Rash, Rash erythematous, Rash pruritic; Skin irritation; Middle insomnia, Pruritus, Rash, Rash erythematous, Rash pruritic; Skin irritation More
Patient was waking up in the middle of the night initially with itching however itching never got t... Patient was waking up in the middle of the night initially with itching however itching never got to the point where it was severe. The itching then spread over the next few weeks including a breakout around the patients entire waist with itchy red rash that was inflamed looking with no bleeding. Patient never got to the point where she took anything or went to seek medical attention and describes it more as an irritation. More
2821695 81 F FL 01/18/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255t2
Extra dose administered, No adverse event Extra dose administered, No adverse event
this vaccine was given twice (11/23 and 1/25). no adverse event reported by patient this vaccine was given twice (11/23 and 1/25). no adverse event reported by patient
2821696 68 M CO 01/18/2025 COVID19
 MODERNA
 027A21A
Cardiac monitoring, Cerebrovascular accident, Computerised tomogram, Lymphadenop... Cardiac monitoring, Cerebrovascular accident, Computerised tomogram, Lymphadenopathy, Rash More
Broke out in a rash with swollen lymph nodes on chest and under armpits. After second shot on 04-01-... Broke out in a rash with swollen lymph nodes on chest and under armpits. After second shot on 04-01-2021 at 10:30 a.m. Moderna 020B21A I had a stroke on June 5, 2021. More
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2821697 64 F FL 01/18/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255T2
Pain in extremity Pain in extremity
Sore arm. Sore arm.
2821698 76 F AZ 01/18/2025 DT
DT
DT
DT
DT
DT
RSV
RSV
VARZOS
VARZOS
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
MODERNA
MODERNA
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS









Chills, Cough, Headache, Myalgia, Nausea; Pain; Chills, Cough, Headache, Myalgia... Chills, Cough, Headache, Myalgia, Nausea; Pain; Chills, Cough, Headache, Myalgia, Nausea; Pain; Chills, Cough, Headache, Myalgia, Nausea; Pain; Chills, Cough, Headache, Myalgia, Nausea; Pain; Chills, Cough, Headache, Myalgia, Nausea; Pain More
Headache chills, cough nauseous body aches and muscles Headache chills, cough nauseous body aches and muscles
2821699 11 F OR 01/18/2025 HPV9
 MERCK & CO. INC.
 X024560
Cellulitis, Erythema, Swelling Cellulitis, Erythema, Swelling
redness/swelling the day of vaccination. Diagnosed with cellulitis on 1/17/2025 (4 days after vaccin... redness/swelling the day of vaccination. Diagnosed with cellulitis on 1/17/2025 (4 days after vaccination) More
2821700 50 F IN 01/18/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Erythema, Headache, Injection site induration, Injection site warmth, Pain; Swel... Erythema, Headache, Injection site induration, Injection site warmth, Pain; Swelling More
Swelling the size of a golf ball, blood red like a sunburn, excruciating pain, headache that hasn?t ... Swelling the size of a golf ball, blood red like a sunburn, excruciating pain, headache that hasn?t yet gone away. Arm where shot was given is hard as a rock and hot to the touch. More
2821701 67 M MI 01/18/2025 COVID19
 NOVAVAX
Atrial fibrillation, Computerised tomogram, Pericardial effusion, Ultrasound sca... Atrial fibrillation, Computerised tomogram, Pericardial effusion, Ultrasound scan More
Developed fluid around the heart resulting in hospitalization for AFIB. Pulse of 180. Meds reduced ... Developed fluid around the heart resulting in hospitalization for AFIB. Pulse of 180. Meds reduced fluid. More
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2821432 U 01/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
suspected vaccination failure; shingles; This serious case was reported by a consumer via interactiv... suspected vaccination failure; shingles; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced vaccination failure (Verbatim: suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: shingles). The outcome of the vaccination failure and shingles were not reported. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingrix. The company considered the vaccination failure to be unrelated to Shingrix. It was unknown if the company considered the shingles to be related to Shingrix. Additional Information: GSK Receipt Date: 08-JAN-2025. This case was reported by a patient via interactive digital media. Patient had the vaccine and then got shingles. Same with Covid, same with flu. Not sure if patient believed in vaccines anymore. This case was considered as suspected vaccination failure as detail regarding completion of primary vaccination, laboratory test confirming shingles and time to onset were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK vaccine Shingrix. More
2821433 61 F NY 01/17/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Immediate post-injection reaction, Injection site pain, Myalgia, Nasal congestio... Immediate post-injection reaction, Injection site pain, Myalgia, Nasal congestion, Nausea; Wrong technique in product usage process More
whole body myalgia; nasal congestion; The health professional administered the vaccine through a reg... whole body myalgia; nasal congestion; The health professional administered the vaccine through a regular band aid, rather than an intended barrier bandage; burning pain at the injection site; nausea; This non-serious case was reported by a consumer via call center representative and described the occurrence of injection site pain in a 61-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included COVID vaccine (she took vaccine 3 weeks ago). On 15-DEC-2024, the patient received the 1st dose of Shingrix (intramuscular, unknown deltoid). On 15-DEC-2024, immediately after receiving Shingrix, the patient experienced injection site pain (Verbatim: burning pain at the injection site), nausea (Verbatim: nausea) and wrong technique in product usage process (Verbatim: The health professional administered the vaccine through a regular band aid, rather than an intended barrier bandage). On 16-DEC-2024, the patient experienced myalgia (Verbatim: whole body myalgia) and nasal congestion (Verbatim: nasal congestion). The patient was treated with ibuprofen (Advil). On 15-DEC-2024, the outcome of the nausea was resolved. On 17-DEC-2024, the outcome of the myalgia was resolved (duration 1 day). The outcome of the injection site pain was not resolved and the outcome of the nasal congestion was resolved and the outcome of the wrong technique in product usage process was unknown. It was unknown if the reporter considered the injection site pain, nausea, myalgia and nasal congestion to be related to Shingrix. It was unknown if the company considered the injection site pain, nausea, myalgia and nasal congestion to be related to Shingrix. Additional Information: GSK Receipt Date: 18-DEC-2024 The health professional (pharmacist/vaccinator) administered the vaccine through a regular (opaque, gauze centered) band-Aid, rather than an intended barrier bandage, which led to wrong technique in product usage process. The patient immediately had burning pain at the injection site and immediately, briefly, had nausea. The patient believed the nausea may have been due to the intensity of the pain. The next day she had whole body myalgia and took Advil and the myalgia resolved after one day. She had nasal congestion the day after vaccination. The patient did not know the batch number or expiration date. Nothing else was reported. More
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