🏥 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 💀 🏥 🚑 ♿ ⚠️
2857067 55 F OH 09/05/2025 PNC20
 PFIZER\WYETH
Erythema, Pain in extremity, Skin warm Erythema, Pain in extremity, Skin warm
Patient received pneumococcal vaccine at local pharmacy on 8/22/2025 (not at our office). Within the... Patient received pneumococcal vaccine at local pharmacy on 8/22/2025 (not at our office). Within the next 1 to 2 days 8/23/2025 and 8/24/2025 patient developed right arm pain with associated redness and warmth. Patient was seen in office 8/27/2025 with redness and warmth to the right upper arm as documented in office visit. She was treated with Zyrtec 10 mg daily and Keflex for possible cellulitis. More
2857068 12 M MS 09/05/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 9jt4s
Loss of consciousness Loss of consciousness
pt passed out after getting the vaccine pt passed out after getting the vaccine
2857069 0.17 F ID 09/05/2025 DTPPVHBHPB
PNC20
 MSP VACCINE COMPANY
PFIZER\WYETH
 U7921AA
LC5483
Crying, Injection site haematoma, Injection site pain, Wrong technique in produc... Crying, Injection site haematoma, Injection site pain, Wrong technique in product usage process; Crying, Injection site haematoma, Injection site pain, Wrong technique in product usage process More
Mother reported "My 2 month old got her vaccinations yesterday and shortly after was inconsolab... Mother reported "My 2 month old got her vaccinations yesterday and shortly after was inconsolably crying for hours. We took her to her primary doctor where he diagnosed a large hematoma on her thigh due to improper administration. It is causing her a lot of pain and we re monitoring closely. I just wanted this reported so it may be prevented in the future." More
2857070 68 F CA 09/05/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Bell's palsy Bell's palsy
Bell's palsy Bell's palsy
2857071 65 F IL 09/05/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 342XP
Chills, Headache, Nausea, Palpitations Chills, Headache, Nausea, Palpitations
Racing heartbeat. Started occurring about 1am following more common reactions of chills, headache, ... Racing heartbeat. Started occurring about 1am following more common reactions of chills, headache, and nausea. Did not have these reactions after the first Shingrix shot. Since there weren't other allergic reactions (such as hives or swelling), I just monitored at home to make sure reaction didn't worsen. The racing heartbeat lasted until about 7am. More
2857072 4 M TN 09/05/2025 DTAPIPV
HEPA
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 4L454
42DM9
Y013130
Z005455
Injection site erythema, Injection site pain, Injection site swelling; Injection... Injection site erythema, Injection site pain, Injection site swelling; Injection site erythema, Injection site pain, Injection site swelling; Injection site erythema, Injection site pain, Injection site swelling; Injection site erythema, Injection site pain, Injection site swelling More
Grandmother brought grandchild to follow up because patient started with left arm swollen, redness ... Grandmother brought grandchild to follow up because patient started with left arm swollen, redness and pain. Left arm meausre 21 cm, and right arm 16 cm. Patient was prescribed ibuprofen 100 mg/5mL with indication of 7.5 mL by mouth three times a day as needed and was given an appointment follow up visit on Monday September 01, 2025. Patient did not show up but we called and patinet symptoms resolved by Monday 9/1/25 as stayed by grandmother. More
2857073 6 F TX 09/05/2025 UNK
 UNKNOWN MANUFACTURER
 Y97N7
Erythema, Swelling, Tenderness Erythema, Swelling, Tenderness
Localized swelling, erythema, and tenderness Localized swelling, erythema, and tenderness
2857074 0.75 M IL 09/05/2025 HEP
 MERCK & CO. INC.
 Y019252
Urticaria Urticaria
Hives were on both arms, thighs, legs, stomach. No recent sick symptoms. No new foods, lotions, soap... Hives were on both arms, thighs, legs, stomach. No recent sick symptoms. No new foods, lotions, soaps, detergents, medications. Not itchy. More
2857075 52 F MA 09/05/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 7NX57
Underdose Underdose
A pediatric dose was given to an adult. The patient was notified that of the incorrect dose and was ... A pediatric dose was given to an adult. The patient was notified that of the incorrect dose and was recommended to go to the pharmacy to receive the correct dose. Due to the patient's insurance, we do not have the adult vaccine in office to offer her. More
2857076 68 F TN 09/05/2025 PNC20
 PFIZER\WYETH
 lp4948
Contusion, Pain in extremity Contusion, Pain in extremity
Bruising , sore arm Bruising , sore arm
2857077 0.33 F OH 09/05/2025 DTAPIPV
HIBV
PNC20
RV1
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS



Dry skin, Injection site rash, Pyrexia; Dry skin, Injection site rash, Pyrexia; ... Dry skin, Injection site rash, Pyrexia; Dry skin, Injection site rash, Pyrexia; Dry skin, Injection site rash, Pyrexia; Dry skin, Injection site rash, Pyrexia More
Infant ran a fever 100-101F for 2+ days. Treatment with cool cloths, baths. On the third day, she b... Infant ran a fever 100-101F for 2+ days. Treatment with cool cloths, baths. On the third day, she broke out in a rash on both thighs from the injection sites to the knee. Treatment for the rash included the application of Aquaphor ointment. Evidence of the rash is still visible as dry skin. More
2857078 10 M MA 09/05/2025 HEP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 3N3ND
LX494
Rash, Rash erythematous; Rash, Rash erythematous Rash, Rash erythematous; Rash, Rash erythematous
Patient returned to the clinic on 9/4/25 for his PPD read. Parent stated that patient had developed ... Patient returned to the clinic on 9/4/25 for his PPD read. Parent stated that patient had developed a rash starting on 9/3/25. Nursing staff observed flat red areas on both upper extremities, as well as along Patient's flanks. Denies itching, SOB, and nausea. Lungs were clear to auscultation, denies any throat tightness or facial swelling. Parent advised to monitor symptoms and go to the nearest emergency room for evaluation. More
2857079 40 F MD 09/05/2025 HPV9
 MERCK & CO. INC.
Lichen planus Lichen planus
I was diagnosed with Lichen Planus which is known for being a side effect after receiving the Gardas... I was diagnosed with Lichen Planus which is known for being a side effect after receiving the Gardasil vaccine. More
2857080 50 M WI 09/05/2025 PNC20
 PFIZER\WYETH
 LN4932
Erythema, Lymphadenopathy, Malaise, Pain in extremity, Pyrexia Erythema, Lymphadenopathy, Malaise, Pain in extremity, Pyrexia
Malaise and feeling feverish on the next day, 9/3/2025. Redness, soreness and erythema on the righ... Malaise and feeling feverish on the next day, 9/3/2025. Redness, soreness and erythema on the right upper arm. There was a reactive lymph node that arose in the supraclavicular area on 9/4/2025, improved some by 9/5/2025, but still sore. As of office visit on 9/5/2025, improving trajectory on a predictable course, but not fully resolved. He will monitor symptoms and follow up if needed. More
2857081 42 F 09/05/2025 COVID19
 PFIZER\BIONTECH
 LN7302
Underdose Underdose
child dose was given to pt 0.3 ml child dose was given to pt 0.3 ml
2857082 85 M UT 09/05/2025 FLU3
 SANOFI PASTEUR
Balance disorder, Dizziness, Extra dose administered, Headache, Malaise Balance disorder, Dizziness, Extra dose administered, Headache, Malaise
Wife and patient intended to have flu and pneumonia vaccine. Patient had a flu shot, and I went to ... Wife and patient intended to have flu and pneumonia vaccine. Patient had a flu shot, and I went to give him his pneumonia shot, I accidentally picked up his wife's flu shot and gave him that. So, he got 2 flu shots by accident. Patient reported dizziness, loss of balance, sick and headache the first day after. The second day after, he said he started feeling better, but not as bad. Totally recovered the day after that. More
2857083 0.33 M CA 09/05/2025 PNC20
RV5
 PFIZER\WYETH
MERCK & CO. INC.
 HN2630
2003161
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event More
PT RECIEVED 2 EXPIRE VACCINES ON 9/3/25 THAT UNFORTUNATLY I DID NOT CHECH THE EXPERATION DATES WHEN ... PT RECIEVED 2 EXPIRE VACCINES ON 9/3/25 THAT UNFORTUNATLY I DID NOT CHECH THE EXPERATION DATES WHEN I PREPARED THE VACCINE BEFORE GIVEN. More
2857084 40 M 09/05/2025 COVID19
 PFIZER\BIONTECH
 LN7302
Underdose Underdose
pt was administered a child dose 0.3ml pt was administered a child dose 0.3ml
2857085 33 F NC 09/05/2025 COVID19
 PFIZER\BIONTECH
 GK1337
Exposure during pregnancy, Pericarditis, Pharyngitis streptococcal, Premature de... Exposure during pregnancy, Pericarditis, Pharyngitis streptococcal, Premature delivery More
Admitted into the hospital, following a diagnosis of strep throat, in December 2023. I was in my sec... Admitted into the hospital, following a diagnosis of strep throat, in December 2023. I was in my second trimester at that time. Diagnosed with pericarditis. The team was not able to determine a cause for the parent carditis, even after meeting with infectious disease to rule out rheumatic fever. Managed on steroids, which required insulin administration during pregnancy. Baby was born at 36 weeks, premature. More
✓
2857086 11 F FL 09/05/2025 MNP
MNP
TDAP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 X7R4Z
X7R4Z
3RE73
3RE73
Contusion, Epistaxis, Fatigue, Gastrooesophageal reflux disease, Gingival bleedi... Contusion, Epistaxis, Fatigue, Gastrooesophageal reflux disease, Gingival bleeding; Headache, Platelet count decreased, Purpura; Contusion, Epistaxis, Fatigue, Gastrooesophageal reflux disease, Gingival bleeding; Headache, Platelet count decreased, Purpura More
Purpura, large dark bruising located over body, headaches, acid reflux, fatigue, uncontrollable nose... Purpura, large dark bruising located over body, headaches, acid reflux, fatigue, uncontrollable nose bleeding, gum bleeding. Critical platelet levels. Started within 5 days with noticeable bruising and purpura. More
2857087 57 F NH 09/05/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 EY57A
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient was to receive Hep B injection. Patient was given Hep A injection. To date the patient has... Patient was to receive Hep B injection. Patient was given Hep A injection. To date the patient has had no adverse reactions. More
2857088 26 F GA 09/05/2025 UNK
 UNKNOWN MANUFACTURER
 h4k3s
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient was to receive Gardasil and received Boostrix instead. Patient was not experiencing any adve... Patient was to receive Gardasil and received Boostrix instead. Patient was not experiencing any adverse events. More
2857089 0.33 F MI 09/05/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 5g23d
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Four month vaccines were pulled , i pulled pediarix first and verified patient was not due for Hep B... Four month vaccines were pulled , i pulled pediarix first and verified patient was not due for Hep B but could have gotten the extra hep B but we don't do that in this office so i pulled the combo that had the two vaccines that she did need. Not realizing it was 4-6 years. I had vaccines double checked by another MA and went ahead with the vaccines. I was rushed to get to the next room for the provider to begin a procedure. It was noticed after the fact when our next four month shots arrived for immunizations. I called health Dept and was given the ok for safety and notified mother who stated understanding and thanks for advising. Patient had no adverse reaction or concerns no further appointment. More
2857090 44 M TX 09/05/2025 COVID19
 MODERNA
 B0021
Unevaluable event Unevaluable event
On 08/29/2025 presents to clinic requesting Covid 19 vaccine, Moderna (Spikevax) . Days before (poss... On 08/29/2025 presents to clinic requesting Covid 19 vaccine, Moderna (Spikevax) . Days before (possibly Tuesday 08/26/2025) was speaking to Chief nurse from the Bureau of Immunization and was told for to continue to give the 2024-25 Covid 19 until expiration date. As it states on package 2024-25. Then on 09/04/2025 the Immunization Bureau sends an email to take all Covid 19 2024-25 "off the shelves", to quarantine and do not use. More
2857091 46 F TX 09/05/2025 COVID19
 MODERNA
 B0021
Unevaluable event Unevaluable event
On 08/29/2025 patient present s to the clinic and request Covid 19 vaccine, Moderna (Spikevax 2024-2... On 08/29/2025 patient present s to the clinic and request Covid 19 vaccine, Moderna (Spikevax 2024-25). Days before per conversation with Chief Nurse of Immunization Bureau, states that we should still be offering Covid 19 vaccines 2024-25. To use until the expiration date, as we have not recieved the upcoming season 2025-26 yet. on 09/04/2025 an email is recieved from the Immunization Bureau with instructions to discontinue vaccines and quarantine all Covid 19 vaccine 2024-25. More
2857092 54 M CA 09/05/2025 PNC20
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 LN4929
3273H
Dyspnoea, Guillain-Barre syndrome, Hypoaesthesia, Paraesthesia; Dyspnoea, Guilla... Dyspnoea, Guillain-Barre syndrome, Hypoaesthesia, Paraesthesia; Dyspnoea, Guillain-Barre syndrome, Hypoaesthesia, Paraesthesia More
guillain barre syndrome shortness of breath tingling and numb guillain barre syndrome shortness of breath tingling and numb
2857093 70 M AZ 09/05/2025 COVID19
COVID19
 MODERNA
MODERNA
 017F21A
017F21A
Acoustic stimulation tests abnormal, Barotrauma, Deafness, Fatigue, Hearing aid ... Acoustic stimulation tests abnormal, Barotrauma, Deafness, Fatigue, Hearing aid user; Sinus disorder, Sleep deficit, Tinnitus More
I received the recommended COVID 19 Moderna vaccination booster shot on 10/26/2021. Approximately No... I received the recommended COVID 19 Moderna vaccination booster shot on 10/26/2021. Approximately November 10th through November 19th I experienced frequent, random episodes of ear barotrauma in one or both ears. On November 20, 2021 ear barotrauma in the right ear "popped", followed immediately with continuous tinnitus in both ears. Ear barotrauma stopped immediately with the onset of tinnitus. I required an emergency room visit on 11/29/21 for exhaustion / sleep deprivation caused by a long history of pollen allergies and recent onset of 24/7 tinnitus. Diagnosis stated "Sinus disease; Tinnitus, bilateral". Referral to ENT doctor by medical facility upon discharge. On 12/06/21 Ear, Nose and Throat physician. Dr. requested a hearing test from on-site audiologist which revealed significant hearing loss. The onset of continuous tinnitus was diagnosed at that time as possibly due to hearing loss and sudden occurrence considered abnormal. Tinnitus is 24/7 and has continued to this day. Hearing aids, 100mm of Trazdone, 5 mg of Melatonin and occasional prescribed use of Valium 5mg allow for adequate sleep. I may (or may not) have developed chronic onset of sudden, continuous tinnitus on November 20,2021. I accepted significant hearing loss as the cause of my sudden chronic tinnitus, but recent medical articles have caused me to question the exact cause. COVID-19 vaccination-related tinnitus is associated with pre-vaccination metabolic disorders More
✓
2857094 64 M TX 09/05/2025 COVID19
 MODERNA
 B0021
Unevaluable event Unevaluable event
On 08/29/2025 patient presents to clinic, requesting Covid 19 vaccine Moderna 2024-25 (Spikevax). O... On 08/29/2025 patient presents to clinic, requesting Covid 19 vaccine Moderna 2024-25 (Spikevax). On Tuesday 08/26/2025 after conversation with Bureau Chief Nurse, she stated that we should offering Covid 19 vaccines 2024-25 until the expiration dates, as we are still in 2025. On 09/4/2025 an email was recieved from Immunization Bureau to quarantine and discontinue all Covid 19 Vaccines immediately. Vaccines were picked up by Bureau staff around noon on 09/04/2025 to be returned to the manufacturer. More
2857095 4 M TN 09/05/2025 HIBV
 MERCK & CO. INC.
 Y013911
Extra dose administered, No adverse event Extra dose administered, No adverse event
HIB administered prior to updated shot record received/ no treatment needed HIB administered prior to updated shot record received/ no treatment needed
2857096 73 F WA 09/05/2025 PNC20
 PFIZER\WYETH
 ln4927
Fatigue, Impaired driving ability, Injection site swelling, Injection site warmt... Fatigue, Impaired driving ability, Injection site swelling, Injection site warmth, Nausea More
Arm started swelling near site of injection 2 to 3 hours after administration of Prevnar 20. Patient... Arm started swelling near site of injection 2 to 3 hours after administration of Prevnar 20. Patient felt fatigued and nauseated the day after immunization. Her arm continued to swell and became hot to the touch. She applied ice and warm compresses but no relief. Her arm was still swollen day 3 and she considered going to urgent care, but did not feel well enough to drive. The swelling in arm started decreasing on day 4 and she felt "back to normal" on day 5. The swelling was gone and she did not feel as fatigued More
2857097 4 M AL 09/05/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 7D2Y4
Expired product administered Expired product administered
Patient received an expired dose of Kinrix. Guidance was giving from the manufacture as to what step... Patient received an expired dose of Kinrix. Guidance was giving from the manufacture as to what step should be taken to administer the vaccine again. Parent was given guidance about the incident More
2857098 59 M FL 09/05/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.

Agitation, Anxiety, Depression, Disturbance in attention, Fear; Mania, Palpitati... Agitation, Anxiety, Depression, Disturbance in attention, Fear; Mania, Palpitations, Paranoia, Tachyphrenia More
Manic symptoms, agitation, paranoia, fear, depression, inability to concentrate, anxiety, racing tho... Manic symptoms, agitation, paranoia, fear, depression, inability to concentrate, anxiety, racing thoughts, heart racing. More
2857099 74 F CA 09/05/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 946908
Urticaria Urticaria
Pt presented to clinic with facial hives, while conducting pt assessment, pt began to develop furthe... Pt presented to clinic with facial hives, while conducting pt assessment, pt began to develop further hives on sternum. No c/o shortness of breath or other secondary effects related to allergic reaction. More
2857100 68 F AL 09/05/2025 FLU3
PNC20
 SANOFI PASTEUR
PFIZER\WYETH
 u8764bb
ln4927
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Patient had already received the Prevnar 20 vaccine on 11/7/22 so this was an unneeded duplicate. Re... Patient had already received the Prevnar 20 vaccine on 11/7/22 so this was an unneeded duplicate. Reached out to patient but have not heard back to hear if there were any adverse effects More
2857101 32 F NJ 09/05/2025 TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8673AA
U8673AA
Incorrect route of product administration, Injection site erythema, Injection si... Incorrect route of product administration, Injection site erythema, Injection site mass, Injection site pruritus, Injection site reaction; Injection site swelling, Skin exfoliation More
Nurse incorrectly administered injection as subcutaneous instead of intramuscularly. Injection site ... Nurse incorrectly administered injection as subcutaneous instead of intramuscularly. Injection site swelled over the course of the next few days with hard lump formation at injection site. Small redness initially presented around injection but rednesss continued to spread over the next few days and became very itchy and skin seemed to start to peel around injection site. More
2857102 62 F TX 09/05/2025 PNC21
TDAP
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS

Erythema, Urticaria; Erythema, Urticaria Erythema, Urticaria; Erythema, Urticaria
large red welt on left arm - unsure due to which vaccine, directed patient to benadryl but also dire... large red welt on left arm - unsure due to which vaccine, directed patient to benadryl but also directed her to draw a circle around it and if it got larger over the next 24 hours, to go to urgent care/er. More
2857103 72 F AZ 09/05/2025 FLU3
 SEQIRUS, INC.
 407242
Chest discomfort, Dizziness, Feeling hot Chest discomfort, Dizziness, Feeling hot
Patient said she felt dizzy, warm and her chest felt heavy following flu shot. Patient sat down on ... Patient said she felt dizzy, warm and her chest felt heavy following flu shot. Patient sat down on bench and after a few minutes felt better. Paramedics were called to check vitals, everything was normal according to them. More
2857104 2 M VA 09/05/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 FH4YR
Ecchymosis, Erythema, Inflammation, Skin warm Ecchymosis, Erythema, Inflammation, Skin warm
Central Ecchymosis, inflammation, hot to touch, with erythematous perimeter Central Ecchymosis, inflammation, hot to touch, with erythematous perimeter
2857105 4 F CA 09/05/2025 DTAPIPV
VARCEL
 SANOFI PASTEUR
MERCK & CO. INC.

Injection site reaction, Rash erythematous; Injection site reaction, Rash erythe... Injection site reaction, Rash erythematous; Injection site reaction, Rash erythematous More
Rash at injection site that is as large as a palm and red. Rash at injection site that is as large as a palm and red.
2857106 15 M 09/05/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 37r35
Inappropriate schedule of product administration Inappropriate schedule of product administration
given dose not needed 1 year interval given dose not needed 1 year interval
2857107 38 M CA 09/05/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 ew0170
ew0168
Immediate post-injection reaction, Tinnitus; Immediate post-injection reaction, ... Immediate post-injection reaction, Tinnitus; Immediate post-injection reaction, Tinnitus More
Immediately after getting the second vaccine injection, I started to experience Tinnitus in both ear... Immediately after getting the second vaccine injection, I started to experience Tinnitus in both ears. It began immediately after and has consistent since injection. More
✓
2857108 70 F 09/05/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 kr75k
Inappropriate schedule of product administration Inappropriate schedule of product administration
patient was given a second dose, 6 months after she received the 1st dose patient was given a second dose, 6 months after she received the 1st dose
2857109 24 F 09/05/2025 TDAP
 SANOFI PASTEUR
 u83538a
Hypoaesthesia Hypoaesthesia
patient felt numbness in her legs briefly for few hours next day after getting vaccine patient felt numbness in her legs briefly for few hours next day after getting vaccine
2857110 0.17 F GA 09/05/2025 DTAP
DTAP
DTAP
HIBV
HIBV
HIBV
PNC20
PNC20
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 47Y5M
47Y5M
47Y5M
4J452
4J452
4J452
HN5978
HN5978
HN5978
Chest X-ray, Cyanosis, Dissociation, Electroencephalogram abnormal, Intensive ca... Chest X-ray, Cyanosis, Dissociation, Electroencephalogram abnormal, Intensive care; Laboratory test, Lumbar puncture, Magnetic resonance imaging, Pallor, Partial seizures; Ultrasound head, Unresponsive to stimuli; Chest X-ray, Cyanosis, Dissociation, Electroencephalogram abnormal, Intensive care; Laboratory test, Lumbar puncture, Magnetic resonance imaging, Pallor, Partial seizures; Ultrasound head, Unresponsive to stimuli; Chest X-ray, Cyanosis, Dissociation, Electroencephalogram abnormal, Intensive care; Laboratory test, Lumbar puncture, Magnetic resonance imaging, Pallor, Partial seizures; Ultrasound head, Unresponsive to stimuli More
Within 72 hours after my daughter's two month appointment where she received these vaccinations... Within 72 hours after my daughter's two month appointment where she received these vaccinations, she had an episode in which her lips turned blue, skin pale, and she was unresponsive. She finally came to after about 30 seconds. She kept having these episodes and when she was 5 months old, we went to the ER and had to stay in the PICU. After many tests and an overnight EEG, they confirmed she was having focal seizures, concentrated in the right temporal lobe of her brain. Her focal seizures during this time were intense as she would zone out, lips blue, pale skin, and had tongue clicks. She is 15 months old now, and still has breakthrough seizures, while on her anti-seizure medication. More
✓
2857111 74 F NM 09/05/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Headache, Injection site erythema, Injection site induration, Injection site oed... Headache, Injection site erythema, Injection site induration, Injection site oedema, Injection site pain; Myalgia, Skin burning sensation More
Severe myalgia over entire body, headache, local reaction to injection site with redness and edema/... Severe myalgia over entire body, headache, local reaction to injection site with redness and edema/induration and pain, skin burning sensation over entire body More
2857112 61 F CA 09/05/2025 PNC20
PNC20
PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 LX4486
LX4486
LX4486
LX4486
Agranulocytosis, Autoimmune haemolytic anaemia, Basophil percentage decreased, B... Agranulocytosis, Autoimmune haemolytic anaemia, Basophil percentage decreased, Biopsy bone marrow abnormal, Bone marrow failure; Febrile neutropenia, Haematocrit decreased, Haemoglobin decreased, Marrow hyperplasia, Neutropenia; Neutrophil count decreased, Neutrophil percentage decreased, Pharyngitis, Plasmacytosis, Platelet count decreased; Pyrexia, Rash, Staphylococcal infection, Thrombocytopenia, White blood cell count decreased More
large rash on L arm 5 days post injection, then fever 7 days post, then presented to ER with severe ... large rash on L arm 5 days post injection, then fever 7 days post, then presented to ER with severe neutropenia/agranulocytosis (ANC=0), autoimmune hemolytic anemia, mild thrombocytopenia. Hospitalized for neutropenic fever, MRSA pharyngitis. bone marrow biopsy shows hypocellular marrow without malignancy. At time of this report still ANC of zero (7 days post initial diagnosis). Of note patient was on methimazole 2.5 mg BID at time of reaction, but had been on this for more than 5 years. Also was taking chinese medical mushroom extract (exact ingredients unknown). More
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2857113 28 F NC 09/05/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 Ew0167
Ew0167
Ew0167
Ew0167
Ew0167
Ew0167
Ew0167
ER8736
ER8736
ER8736
ER8736
ER8736
ER8736
ER8736
Abdominal distension, Abdominal pain upper, Alopecia, Anxiety, Aphasia; Arthriti... Abdominal distension, Abdominal pain upper, Alopecia, Anxiety, Aphasia; Arthritis, Brain fog, Cognitive disorder, Constipation, Diarrhoea; Drug hypersensitivity, Dyspnoea, Exercise tolerance decreased, Fatigue, Food allergy; Gait inability, Insomnia, Loss of personal independence in daily activities, Malabsorption, Malaise; Mobility decreased, Muscle injury, Myalgia, Nausea, Neuralgia; Nightmare, Palpitations, SARS-CoV-2 antibody test positive, Seizure, Temperature intolerance; Urticaria, Vertigo, Vision blurred; Abdominal distension, Abdominal pain upper, Alopecia, Anxiety, Aphasia; Arthritis, Brain fog, Cognitive disorder, Constipation, Diarrhoea; Drug hypersensitivity, Dyspnoea, Exercise tolerance decreased, Fatigue, Food allergy; Gait inability, Insomnia, Loss of personal independence in daily activities, Malabsorption, Malaise; Mobility decreased, Muscle injury, Myalgia, Nausea, Neuralgia; Nightmare, Palpitations, SARS-CoV-2 antibody test positive, Seizure, Temperature intolerance; Urticaria, Vertigo, Vision blurred More
First month after: breathlessness, inability to run or workout, brain fog, extreme anxiety out of no... First month after: breathlessness, inability to run or workout, brain fog, extreme anxiety out of no where, heart palpations, blurred vision, muscle tears, sore muscles. Then it got worse to the point I couldn't walk at all, for 8 months I couldn't talk or move, my husband had to bath me. Siezures, heart palpations, breathlessness, hot and cold intolerances, post exertional mylas, fatigue, hives, stomach pains, bloating, diarrhea, constipation, nausea, blurred vision, vertigo, nerve pain, new allergies to medications and food, arthritis, brain fog, insomnia, anxiety, night mares, hair loss, cognitive decline, body not absorbing nutrients properly More
✓
2857119 4 F OR 09/05/2025 DTAPIPV
DTAPIPV
 SANOFI PASTEUR
SANOFI PASTEUR
 U8383AB
U8383AB
Injection site erythema, Injection site movement impairment, Injection site pain... Injection site erythema, Injection site movement impairment, Injection site pain, Injection site rash, Injection site swelling; Injection site warmth, Local reaction More
Assessment & Plan Vaccine reaction, initial encounter Patient has experienced localized reaction... Assessment & Plan Vaccine reaction, initial encounter Patient has experienced localized reaction to vaccine administered to L thigh 2 days ago. Vaccines administered were MMR and Dtap/IPV. I suspect the reaction was to Dtap/IPV. Reassurance given that rash will likely subside and does not indicate an allergy to the vaccine. Coop compresses. VAERS report submitted. As needed follow up or if symptoms don't resolve in 3-5 days. SUBJECTIVE Patient is a 4 y.o. who is here today for a reaction to MMR or DTaP/IPV (Quadracel) vaccine. Done on 09/02/2025 Mother reports redness at the injection site following vaccine administration (around 3 pm x2 days ago). By the following morning, swelling and rash developed. At 9:00 AM the affected area measured approximately penny-to-nickel size, and by 4:00 PM had progressed to silver-dollar size. Since then, the reaction has spread from the injection site to involve the entire thigh, extending down toward the knee. Mother describes splotchy and streaking erythema, with the area warm to the touch. Patient is experiencing burning pain and has difficulty with movement. No history of prior vaccine reactions. Mother denies lethargy, increased fatigue, or other systemic symptoms. The reaction stemmed from the DTaP/IPV (Quadracel) injection. More
2857120 59 F TX 09/05/2025 COVID19
HEPAB
MMR
PNC21
RSV
TDAP
VARZOS
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 me6072
p2447
4015020
9292002
ln5463
793pt
3273h
Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia; In... Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia; Injection site pain, Malaise, Pyrexia More
per patient, developed severe pain at the injection sites, malaise and fever prompting a trip to the... per patient, developed severe pain at the injection sites, malaise and fever prompting a trip to the urgent care More
2857121 65 F CA 09/05/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 u8764cb
u8764cb
Contusion, Injected limb mobility decreased, Joint injury, Nerve injury, Periphe... Contusion, Injected limb mobility decreased, Joint injury, Nerve injury, Peripheral swelling; Product administered at inappropriate site More
IMZ was administered too high on the shoulder and hit the joint/nerve. Patient got bruises and swoll... IMZ was administered too high on the shoulder and hit the joint/nerve. Patient got bruises and swollen on her arm for a few days. patient still cannot lift her arm until after a week of injection More
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