๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ 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.

๐Ÿ“– Help & Search Guide

Column Icons Legend

๐Ÿ’€ Death
๐Ÿฅ Hospitalized
๐Ÿš‘ Emergency Room
โ™ฟ Disability
โš ๏ธ Life Threatening

How to Search

๐Ÿ’ก 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 "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ 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:

  • โœ… Early warning system for potential safety signals
  • โœ… Open and transparent - publicly accessible
  • โœ… Accepts all reports regardless of likelihood of causation
  • โœ… Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • โš ๏ธ Reports are unverified - not investigated before publication
  • โš ๏ธ Cannot determine if vaccine caused the event
  • โš ๏ธ Underreporting - not all adverse events are reported
  • โš ๏ธ Overreporting - coincidental events may be reported
  • โš ๏ธ 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?

โš ๏ธ 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
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2864227 41 F 10/08/2025 TDAP
SANOFI PASTEUR

Exposure during pregnancy, Injected limb mobility decreased, Loss of personal in... Exposure during pregnancy, Injected limb mobility decreased, Loss of personal independence in daily activities, Pain in extremity, Sleep disorder More
I don't know the specifics of the vaccine administered, but I received the TDAP vaccine as part... I don't know the specifics of the vaccine administered, but I received the TDAP vaccine as part of regular prenatal care. The vaccine made my arm unable to function normally for two weeks and included loss of mobility and strength to perform normal responsibilities. I also could not lay or sleep on the arm during the full two weeks that it was in pain. Primary care physician provided exercises to help strengthen the arm again and I used peppermint oil for pain relief only. No anti-inflammatories were used. My arm is finally back to normal almost 3 weeks later. More
2864228 59 F FL 10/08/2025 UNK
UNKNOWN MANUFACTURER

Erythema Erythema
Erythema Left arm ~ 10 cm Erythema Left arm ~ 10 cm
2864229 64 F OH 10/08/2025 FLU3
SANOFI PASTEUR
U8837CA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
RECEIVED HIGH DOSE PRIOR TO 65TH BIRTHDAY RECEIVED HIGH DOSE PRIOR TO 65TH BIRTHDAY
2864230 8 M IN 10/08/2025 COVID19
PFIZER\BIONTECH
MY9547
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
The patient received Pfizer COVID-19 vaccine for 12 years to 64 years instead of Pfizer COVID-19 vac... The patient received Pfizer COVID-19 vaccine for 12 years to 64 years instead of Pfizer COVID-19 vaccine for 5-11 years old. More
2864232 34 F FL 10/08/2025 UNK
UNK
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
9JC49
9JC49
Confusional state, Diarrhoea, Dizziness, Dyspnoea, Exposure during pregnancy; He... Confusional state, Diarrhoea, Dizziness, Dyspnoea, Exposure during pregnancy; Headache, Myalgia, Pyrexia More
Shortness of breath, fever, dizziness, confusion, left arm muscular pain, headache, diarrhea. I'... Shortness of breath, fever, dizziness, confusion, left arm muscular pain, headache, diarrhea. I'm 17 weeks pregnant with due date March 15 2026. More
2864233 16 F ND 10/08/2025 MENB
NOVARTIS VACCINES AND DIAGNOSTICS
CD44A
Erythema, Fatigue, Feeling abnormal, Limb discomfort, Somnolence Erythema, Fatigue, Feeling abnormal, Limb discomfort, Somnolence
Started 11am while child was in school. Described legs feeling like lead. and stated she didn't... Started 11am while child was in school. Described legs feeling like lead. and stated she didn't feel right, very tire.d Redness and spider webbing half way down arm. Got home from school around 3:30 slept until 6pm. Continued feeling heavy and tiring to move. Next day called doctor took in for appointment Continued spreading of red area to arm. No medications provided. Stayed home Thursday and Friday continued heavy feeling and tired. Saturday started moving around a little better not as tired. By Monday she was back to normal. More
2864234 40 M FL 10/08/2025 FLU3
GLAXOSMITHKLINE BIOLOGICALS
33CM4
Head discomfort, Headache, Hyperhidrosis, Hypoaesthesia Head discomfort, Headache, Hyperhidrosis, Hypoaesthesia
40-year-old male with a history of HTN, HLD, CKD, s/p renal and pancreas transplant Dec 2023- Clinic... 40-year-old male with a history of HTN, HLD, CKD, s/p renal and pancreas transplant Dec 2023- Clinic (tacrolimus), OSA, anemia, hyperparathryoidism, and DM1 (although states he's no longer on meds for DM) presents to the ED d/t diaphoresis and headache s/p flu vaccination that occured around 0745 this morning (1 hr 45 min ago). He describes headache as pressure and numbness across his forehead and both temples. No vision changes, dizziness, nausea, vomiting, or diarrhea. No CP or SOB. No swelling of lips/tongue. No difficulty swallowing. No rash. More
2864235 70 M OH 10/08/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
7503A
Extra dose administered, No adverse event Extra dose administered, No adverse event
NO ADVERSE REACTIONS NOTED, PATIENT GOT AN EXTRA DOSE OF SHINGRIX HERE, BECAUSE HE DID NOT KNOW HE G... NO ADVERSE REACTIONS NOTED, PATIENT GOT AN EXTRA DOSE OF SHINGRIX HERE, BECAUSE HE DID NOT KNOW HE GOT HIS FULL SERIES IN 2019, WAS DISCOVERED BY DOCTOR AT YEARLY PHYSICAL More
2864236 80 M MO 10/08/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
C9X3R
Dizziness, Nausea, Pyrexia, Vomiting Dizziness, Nausea, Pyrexia, Vomiting
PATIENT EXPERIENCED FEVER, DIZZINESS, NAUSEA AND VOMITING PATIENT EXPERIENCED FEVER, DIZZINESS, NAUSEA AND VOMITING
2864237 84 F ME 10/08/2025 FLU3
FLU3
SANOFI PASTEUR
SANOFI PASTEUR


Abdominal pain upper, Chills, Cough, Feeling cold, Headache; Pain in extremity, ... Abdominal pain upper, Chills, Cough, Feeling cold, Headache; Pain in extremity, Sneezing, Tremor More
Shivering and shacking, frezzing cold. I felt like (withheld) in the excosit. Last for 4 hours My bo... Shivering and shacking, frezzing cold. I felt like (withheld) in the excosit. Last for 4 hours My body was jusmping up and down, I had to wear mulitple layers including a coat. Coughing and sneezing every few seconds. Arm hurts. And stomach pain from the coughing. I now have a headache from the sneezing. More
2864238 40 F 10/08/2025 FLU3
FLU3
SANOFI PASTEUR
SANOFI PASTEUR


Arthralgia, Hypoaesthesia, Joint noise, Joint range of motion decreased, Musculo... Arthralgia, Hypoaesthesia, Joint noise, Joint range of motion decreased, Musculoskeletal stiffness; Pain, Paraesthesia, Sleep disorder More
It has been 7 days since my flu shot on 10/1/25. Since having my flu shot I have been experiencing t... It has been 7 days since my flu shot on 10/1/25. Since having my flu shot I have been experiencing tingling, numbness, stiffness, popping, limited ROM and pain in my left shoulder. When I try to move my arm out and stretch it, It is stiff and becomes irritated often causing twinges of pain in my shoulder area. My injection was given higher on my shoulder than I have ever had it before. The day of and the day after my shoulder was sore as to be expected, but it has gotten worse since then. I have been doing stretches, icing it, etc with no relief. I just wanted to make you aware that I feel it may have been the placement of my injection causing the issues. I have not lifted anything or done anything out of the ordinary for me. I hate to even bring it up, I was hoping for it to go away on its own, but it just hasn?t. I can't even sleep on my left side, so it was time to say something. I have not seen a medical professional for it. I am a nurse and have been trying to do some ROM exercises, stretching, NSAIDS, rice, with no relief. More
2864239 55 F NC 10/08/2025 FLU3
SANOFI PASTEUR
UT8829BA
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient not 65 or older and should not have received high dose influenza vaccine, should have been a... Patient not 65 or older and should not have received high dose influenza vaccine, should have been administered regular dose vaccine. No reported adverse effects at time of completing this form. More
2864240 81 M FL 10/08/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
bg5j4
Hot flush, Hyperhidrosis, Injected limb mobility decreased, Pain Hot flush, Hyperhidrosis, Injected limb mobility decreased, Pain
Patient received the RSV shot on 10/04 and reported adverse reactions on 10/08 that started 10/05 wh... Patient received the RSV shot on 10/04 and reported adverse reactions on 10/08 that started 10/05 which has continued to today. He describes unbearable pain when he tries to raise his left arm, could not get it higher than his chest. He also describes that he gets hot flashes at night where he wakes up drenched in sweat. He also had body aches the next day, but that has since resolved. He treats his pain with twice daily OTC Naproxen. More
2864241 73 F FL 10/08/2025 PNC20
PFIZER\WYETH
ma2523
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient did not report any actual adverse events; rather, the patient received this vaccine in error... Patient did not report any actual adverse events; rather, the patient received this vaccine in error. Apparently, the patient had received one dose of Prevnar20 in Dec. 2023 at a different medical facility. The pharmacist did not see documentation of receiving this vaccine when the patient came into the pharmacy on 10/2/25. More
2864242 59 F NC 10/08/2025 FLU3
SANOFI PASTEUR
UT8829BA
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient not 65 or older and should not have received high dose influenza vaccine, should have been a... Patient not 65 or older and should not have received high dose influenza vaccine, should have been administered regular dose vaccine. No reported adverse effects at time of completing this form. More
2864243 60 F SD 10/08/2025 FLU3
SEQIRUS, INC.
407272
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse affect. High dose given to person age 60. no adverse affect. High dose given to person age 60.
2864244 84 F NC 10/08/2025 PNC20
PFIZER\WYETH

Injection site erythema, Injection site pruritus Injection site erythema, Injection site pruritus
red and itchy at site and below site of injection red and itchy at site and below site of injection
2864245 53 F KS 10/08/2025 FLU3
SANOFI PASTEUR
ut8779ja
Pyrexia, Sleep disorder, Tachycardia Pyrexia, Sleep disorder, Tachycardia
Awakened around midnight with tachycardia - smart watch reported range of 100-150 sustained for 4 ho... Awakened around midnight with tachycardia - smart watch reported range of 100-150 sustained for 4 hours before going to ER. ER discovered I had spiked a fever of 101.8 in my sleep. IV fluids and antyi-pyretics in ER More
2864246 45 F NC 10/08/2025 FLU3
SANOFI PASTEUR
UT8829BA
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient not 65 or older and should not have received high dose influenza vaccine, should have been a... Patient not 65 or older and should not have received high dose influenza vaccine, should have been administered regular dose vaccine. No reported adverse effects at time of completing this form. More
2864247 84 F TX 10/08/2025 COVID19
PFIZER\BIONTECH
NA0738
Pain in extremity Pain in extremity
Sore arm Sore arm
2864249 77 F AL 10/08/2025 FLU3
SANOFI PASTEUR

Fatigue, Gait disturbance, Mobility decreased, Muscular weakness, Pain Fatigue, Gait disturbance, Mobility decreased, Muscular weakness, Pain
weakness inn legs, difficulty walking, could not roll over once in bed, general aches all over body,... weakness inn legs, difficulty walking, could not roll over once in bed, general aches all over body, extreme fatigue following day More
2864251 102 F CA 10/08/2025 COVID19
FLU3
PFIZER\BIONTECH
SANOFI PASTEUR
NA0587
U8883AA
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
PATIENT WAS GIVEN 2 DOSES OF FLUZONE. FIRST ADMINISTRATION DOSE (LOT # U8827AA) + DATE ON 9/18/25. S... PATIENT WAS GIVEN 2 DOSES OF FLUZONE. FIRST ADMINISTRATION DOSE (LOT # U8827AA) + DATE ON 9/18/25. SECOND DOSE OF FLUZONE GIVEN ON 10/7/25 More
2864252 93 F FL 10/08/2025 COVID19
FLU3
PFIZER\BIONTECH
SANOFI PASTEUR
NA4452
UT8781DA
Injection site erythema, Injection site pruritus, Injection site swelling, Injec... Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth; Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth More
Pt reported on 10/5/25 that she received her vaccine on 10/2/25. She reports her left arm at the inj... Pt reported on 10/5/25 that she received her vaccine on 10/2/25. She reports her left arm at the injection site being red, itchy, hot, and appears swelling/spreading. She denies any movement issues of the arm. She also was going to reach out to her Dr. (her primary doctor). More
2864253 58 F CT 10/08/2025 FLU3
SEQIRUS, INC.
406985
Oral pruritus, Pruritus, Throat irritation Oral pruritus, Pruritus, Throat irritation
per patient, received the vaccine approximately 1300. Started to experience symptoms around 1530- it... per patient, received the vaccine approximately 1300. Started to experience symptoms around 1530- itchy, scratchy throat, mouth, and body. More
2864257 77 F NC 10/08/2025 COVID19
FLU3
MODERNA
SEQIRUS, INC.
80777-04900-60
70461-0025-03
Back pain, Dizziness, Dyspnoea, Malaise; Back pain, Dizziness, Dyspnoea, Malaise Back pain, Dizziness, Dyspnoea, Malaise; Back pain, Dizziness, Dyspnoea, Malaise
Patient stated they felt ill, and light headed. Said they were short of breath and had back pain Patient stated they felt ill, and light headed. Said they were short of breath and had back pain
2864258 18 M TX 10/08/2025 FLU3
HEP
TDAP
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
40255
9YB4G
GC3N48
Extra dose administered; Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered; Extra dose administered
Patient had received the vaccines (Tdap and Hep B) one day earlier on 9/29/2025, prior to receiving ... Patient had received the vaccines (Tdap and Hep B) one day earlier on 9/29/2025, prior to receiving the same exact vaccines on 9/30/2025. Pt stated no vaccines within the last 4 weeks on documentation. More
2864259 28 M NY 10/08/2025 COVID19
COVID19
FLU3
FLU3
MODERNA
MODERNA
SEQIRUS, INC.
SEQIRUS, INC.
3052736
3052736
406997
406997
Chest X-ray normal, Chest pain, Electrocardiogram normal, Malaise, Neck pain; Py... Chest X-ray normal, Chest pain, Electrocardiogram normal, Malaise, Neck pain; Pyrexia, Troponin increased; Chest X-ray normal, Chest pain, Electrocardiogram normal, Malaise, Neck pain; Pyrexia, Troponin increased More
Pt developed fever and malaise evening of vaccination day, then over the next few days developed nec... Pt developed fever and malaise evening of vaccination day, then over the next few days developed neck and chest pain and presented to our ED on 10/9/2025. More
โœ“ โœ“
2864261 65 F AZ 10/08/2025 RSV
PFIZER\WYETH

Diplopia, Halo vision, Vision blurred Diplopia, Halo vision, Vision blurred
Sudden onset of blurred vision in right eye with double vision in the form of white halo above objec... Sudden onset of blurred vision in right eye with double vision in the form of white halo above objects viewed. More
2864262 81 F OH 10/08/2025 FLU3
SANOFI PASTEUR
U8855AA
Peripheral swelling, Rash, Rash pruritic, Sleep disorder Peripheral swelling, Rash, Rash pruritic, Sleep disorder
Patient woke up at Midnight following the vaccine with large, itchy bumps on the right forearm only.... Patient woke up at Midnight following the vaccine with large, itchy bumps on the right forearm only. The patient brought it to my attention today 10/08/2025. The bumps are still a pretty decent size (golf ball size) , but the patient stated the swelling has gone down. It is still itchy and she is taking an OTC antihistamine to help with that. Patient stated she believed it to be from the vaccine since it happened on the arm the vaccine was administered in and had never has a reaction to the flu vaccine prior. More
2864264 10 F WI 10/08/2025 FLU3
GLAXOSMITHKLINE BIOLOGICALS
4D255
Agitation, Dizziness, Vomiting Agitation, Dizziness, Vomiting
After receiving flu shot and going back to class patient became "worked up" per teacher, g... After receiving flu shot and going back to class patient became "worked up" per teacher, got dizzy and threw up. Parents were notified and child was sent home. More
2864265 1 F MI 10/08/2025 HIBV
VARCEL
MERCK & CO. INC.
MERCK & CO. INC.
Y016315
Y017915
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered More
Pt was given Beyfortus 100mg/mL injection instead of the PCV13 injection in error. Pt's mother ... Pt was given Beyfortus 100mg/mL injection instead of the PCV13 injection in error. Pt's mother was contacted immediately. No symptoms at this time. More
2864267 21 M NC 10/08/2025 FLU3
SANOFI PASTEUR
UT8858KA
Migraine, Nausea, Vision blurred, Vomiting Migraine, Nausea, Vision blurred, Vomiting
Blurry vision approximately 20-25 minutes following vaccination. Vision cleared and left sided migra... Blurry vision approximately 20-25 minutes following vaccination. Vision cleared and left sided migraine headache onset with nausea and vomiting. Sx lasted for approximately 1.5 hours before being evaluated at the clinic. More
2864268 0.17 M ND 10/08/2025 DTPPVHBHPB
PNC15
RV5
MSP VACCINE COMPANY
MERCK & CO. INC.
MERCK & CO. INC.
U8265aa
Z006429
2139673
Crying, Decreased appetite, Pyrexia; Crying, Decreased appetite, Pyrexia; Crying... Crying, Decreased appetite, Pyrexia; Crying, Decreased appetite, Pyrexia; Crying, Decreased appetite, Pyrexia More
Extreme crying 4 hours inconsolable, slept for about an hour, another few hours inconsolable, patter... Extreme crying 4 hours inconsolable, slept for about an hour, another few hours inconsolable, pattern continued through out night. Would not eat for over 12 hour. Fever around 101. Called ER, was told it was not necessary to bring him in. More
2864269 96 F GA 10/08/2025 COVID19
MODERNA
3052549
Injection site erythema, Injection site pruritus Injection site erythema, Injection site pruritus
ITCHING AND REDNESS AT THE INJECTION SITE. CLEARED ON DAY 5 ITCHING AND REDNESS AT THE INJECTION SITE. CLEARED ON DAY 5
2864271 63 M CA 10/08/2025 FLU3
SANOFI PASTEUR
UT8794CA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Pharmacist was at a clinic at assisted living facility and patient is 63 but was given a high dose s... Pharmacist was at a clinic at assisted living facility and patient is 63 but was given a high dose shot More
2864272 52 F CA 10/08/2025 FLU3
SANOFI PASTEUR
U8800CA
Flushing, Headache, Product administered to patient of inappropriate age Flushing, Headache, Product administered to patient of inappropriate age
52 year 52-year-old patient was administered a high-dose FluZone Influenza vaccine, when she should ... 52 year 52-year-old patient was administered a high-dose FluZone Influenza vaccine, when she should have been given the standard dose. Patient initially felt flushed, which resolved after 1 hour and also had a headache. More
2864274 76 F SC 10/08/2025 COVID19
FLU3
PFIZER\BIONTECH
SANOFI PASTEUR
NA0590
UT8781DA
Chills, Diarrhoea; Chills, Diarrhoea Chills, Diarrhoea; Chills, Diarrhoea
PATIENT HAD SEVERE DIARRHEA AND CHILLS ALL NIGHT BETWEEN 10/4/25 AND 10/5/25. SIDE EFFECTS RESOLVED... PATIENT HAD SEVERE DIARRHEA AND CHILLS ALL NIGHT BETWEEN 10/4/25 AND 10/5/25. SIDE EFFECTS RESOLVED ON THEIR OWN WITHOUT TREATMENT IN 24 HOURS. More
2864275 65 F MI 10/08/2025 FLU3
PNC15
SANOFI PASTEUR
MERCK & CO. INC.
407246
Z006889
Erythema, Inflammation, Skin weeping; Erythema, Inflammation, Skin weeping Erythema, Inflammation, Skin weeping; Erythema, Inflammation, Skin weeping
red inflamed arm with excaudate. Was given Hydrocortisone 2.5% topical and Mupirocin 2% topical red inflamed arm with excaudate. Was given Hydrocortisone 2.5% topical and Mupirocin 2% topical
2864276 13 M CT 10/08/2025 HPV9
MERCK & CO. INC.
Y018416
Condition aggravated, Generalised tonic-clonic seizure Condition aggravated, Generalised tonic-clonic seizure
Patient had grand mal seizure at home witnessed by his mother, lasting less than 1 minute. This occ... Patient had grand mal seizure at home witnessed by his mother, lasting less than 1 minute. This occurred at 5 am in the morning. Pt was stable otherwise, mother denied fever, rash, injection site pain. Neurology Dept called and updated pt's provider via nursing line so they can follow up with patient as needed. More
2864277 72 F OH 10/08/2025 COVID19
MODERNA

Rash, Urticaria Rash, Urticaria
Rash and hives on 9/27, treated initially with prednisone but 2 days later they were worse then rece... Rash and hives on 9/27, treated initially with prednisone but 2 days later they were worse then received dexamethasone injection and dexamethasone tabs for 5 days w/ improvement . Hives gone by10/3 More
2864278 62 F IA 10/08/2025 FLU3
SEQIRUS, INC.
407252
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Patient was to receive Fluarix as they are less than 65 years old. Patient was given Fluad by mistak... Patient was to receive Fluarix as they are less than 65 years old. Patient was given Fluad by mistake. Patient was informed as the mistake was discovered immediately. They were counseled on symptoms to expect and encouraged to call back if any adverse reactions develop. Patient did not have any questions or concerns at that time. More
2864279 74 F VA 10/08/2025 COVID19
FLU3
PFIZER\BIONTECH
SANOFI PASTEUR
NA4452
U8837CA
Body temperature increased, Dermal filler reaction, Lip swelling, Skin warm, Swe... Body temperature increased, Dermal filler reaction, Lip swelling, Skin warm, Swelling face; Body temperature increased, Dermal filler reaction, Lip swelling, Skin warm, Swelling face More
Patient called to state that the composite fillings in her face (checks, lips, and between the eyes)... Patient called to state that the composite fillings in her face (checks, lips, and between the eyes) had swollen and felt slightly hot to the touch. Had an elevated temperature a few hours following the vaccines but stated that was her normal expected reaction. More
2864280 10 F NJ 10/08/2025 COVID19
MODERNA
3052663
Headache, Incorrect dose administered, Injection site pain, Vomiting Headache, Incorrect dose administered, Injection site pain, Vomiting
Patient received Spikevax for 12+ instead of the Spikevax 3-11 year old. The pharmacist and pharmacy... Patient received Spikevax for 12+ instead of the Spikevax 3-11 year old. The pharmacist and pharmacy team was notified on Tuesday evening that the child received the wrong dose. We called the mother to inform them of incident and ask if the child was experiencing side effects or adverse reactions. Mother reported the child threw up on Sunday evening the day they received the vaccine, headache and sore arm at the injection site. More
2864281 73 M IN 10/08/2025 COVID19
COVID19
COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
MY9550
MY9550


Urticaria; Rash; Urticaria; Rash Urticaria; Rash; Urticaria; Rash
Patient walked into his Primary Care Providers office, with hives on upper arms, neck and face. Pro... Patient walked into his Primary Care Providers office, with hives on upper arms, neck and face. Provider gave order for Medrol 4mg dose pak. More
2864283 58 F MI 10/08/2025 FLU3
SEQIRUS, INC.
407255
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
No reaction. Was given high dose in error No reaction. Was given high dose in error
2864284 11 F AK 10/08/2025 DTAP
FLU3
HPV9
MNQ
GLAXOSMITHKLINE BIOLOGICALS
SEQIRUS, INC.
MERCK & CO. INC.
SANOFI PASTEUR
JF7DM
406989
Y015760
U8351BA
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered More
No adverse reactions noted. Infanrix was inadvertently administered instead of Boostrix. No adverse reactions noted. Infanrix was inadvertently administered instead of Boostrix.
2864286 71 M WV 10/08/2025 FLU3
SEQIRUS, INC.
948417
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient should have received the Fluad vaccination but received Flucelvax instead. No adverse react... Patient should have received the Fluad vaccination but received Flucelvax instead. No adverse reactions. More
2864287 63 F SC 10/08/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
3J2S2
Dry skin, Injection site erythema, Injection site pallor, Injection site reactio... Dry skin, Injection site erythema, Injection site pallor, Injection site reaction More
Patient came into our pharmacy for her second shingles shot (today 10/8/25). She has only ever recei... Patient came into our pharmacy for her second shingles shot (today 10/8/25). She has only ever received vaccines at our pharmacy so we do not know medical or other drug information on this person. When I was about to administer the second shot she said "wait until you see what the first one did to me" and I examined her arm to find a round slightly rough patch of white skin with a pink center. She said it didnt hurt or itch but it never went away. More
2864289 11 M VA 10/08/2025 FLU3
HPV9
MNQ
TDAP
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
7FY52
z008263
U8438AA
U8670BA
Arthralgia, Hypoaesthesia, Musculoskeletal stiffness, Paraesthesia, Tachycardia;... Arthralgia, Hypoaesthesia, Musculoskeletal stiffness, Paraesthesia, Tachycardia; Arthralgia, Hypoaesthesia, Musculoskeletal stiffness, Paraesthesia, Tachycardia; Arthralgia, Hypoaesthesia, Musculoskeletal stiffness, Paraesthesia, Tachycardia; Arthralgia, Hypoaesthesia, Musculoskeletal stiffness, Paraesthesia, Tachycardia More
Patient had full body muscle stiffness with shoulder pain and numbness/tingling of his right hand. ... Patient had full body muscle stiffness with shoulder pain and numbness/tingling of his right hand. It took 15 minutes for his muscles to relax and he was able to drink water and walk normally within 20 minutes. He had tachycardia and normal respirations. More
2864290 62 F IL 10/08/2025 FLU3
SANOFI PASTEUR
U8881DA
Injection site erythema, Injection site inflammation Injection site erythema, Injection site inflammation
redness and inflammation below injection site redness and inflammation below injection site