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
2824616 65 F 02/05/2025 PNC20
PFIZER\WYETH

Injection site erythema, Injection site pain Injection site erythema, Injection site pain
patient is describing tender, burning, and redness that is spreading to elbow after an inject of Pre... patient is describing tender, burning, and redness that is spreading to elbow after an inject of Prevnar 20 More
2824617 34 M TX 02/05/2025 COVID19
PFIZER\BIONTECH

Angina pectoris, Dyspnoea, Heart sounds abnormal, Malaise, Wheezing Angina pectoris, Dyspnoea, Heart sounds abnormal, Malaise, Wheezing
I received the COVID shot from Pfizer and ever since I have been having trouble catching my breath. ... I received the COVID shot from Pfizer and ever since I have been having trouble catching my breath. I also nearly "Died Suddenly" when my heart started hurting out of no where and made a thud. More
โœ“ โœ“ โœ“
2824618 F PA 02/05/2025 RV5
MERCK & CO. INC.

Developmental regression Developmental regression
After baby received first dose of rotavirus vaccine she stopped being able to roll front to back eve... After baby received first dose of rotavirus vaccine she stopped being able to roll front to back even though she was consistently able to do so prior. She also had a significant decrease in her babbling and cooing. We thought it was just a coincidence so opted to still get the second dose. She slowly regained her ability to roll again over that time period and also started rolling back to front. The babbling and cooing remained decreased but she did still do it. After the second dose of rotavirus on 1/20/25 she again stopped rolling. When doing tummy time she no longer rolled or even push up on her arms even though she consistently did so beforehand and very frequently. She would barely lift her head off the ground. She stopped reaching forward to grab toys and play while on her tummy. Arms would remain by her side like she couldn't lift them. She also completely stopped babbling and cooing. A week later and now she has started to roll both ways again but it seems more difficult for her like she's learning all over. The babbling and cooing has not returned. More
2824619 F 02/05/2025 FLUX
UNKNOWN MANUFACTURER

Axillary mass, Swelling, Tenderness Axillary mass, Swelling, Tenderness
A tender, large lump appeared under my left armpit after getting the flu vaccination in my left arm.... A tender, large lump appeared under my left armpit after getting the flu vaccination in my left arm. It's no longer tender and the swelling went down a couple days later. I just don't know if it's completely gone. More
2824620 F 02/05/2025 COVID19
COVID19
FLUX
FLUX
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER




Infection, Pain, Rash, Skin exfoliation, Skin laceration; Staphylococcal infecti... Infection, Pain, Rash, Skin exfoliation, Skin laceration; Staphylococcal infection; Infection, Pain, Rash, Skin exfoliation, Skin laceration; Staphylococcal infection More
patient reported 6 recent infections and was hospitalized for staph infection in january. rheumatolo... patient reported 6 recent infections and was hospitalized for staph infection in january. rheumatologist has referred her to infectious disease department. patient broke out in peeling skin on hands, got better in hospital, but the skin tears are back. patient has upcoming appointment with md, but there are no plans stop cosentyx because she has crippling pain without it. md discontinued prolia because she had 3 utis after starting prolia. patient reports she had flu and covid vaccines on 12/18/24; the rash started the next day. rash was so severe that she went to hospital, where they told her that she had staph infection. patient using triamcinolone. exact dates and length of stay of hospitalization unknown. More
โœ“
2824621 0.75 M OH 02/05/2025 FLU3
HEP
SANOFI PASTEUR
MERCK & CO. INC.
U8486AA
Y003449
Urticaria; Urticaria Urticaria; Urticaria
Hives < 48hrs after receiving Hepatitis B and Influenza vaccine. Hives < 48hrs after receiving Hepatitis B and Influenza vaccine.
2824685 77 M NM 02/05/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
5Y4TL
Injection site erythema, Injection site pain, Injection site reaction, Injection... Injection site erythema, Injection site pain, Injection site reaction, Injection site swelling More
Patient had a reaction on the injection site---redness , swelling and soreness were visible when pa... Patient had a reaction on the injection site---redness , swelling and soreness were visible when patient came in to report on 2/4/25 More
2824686 61 F NJ 02/05/2025 COVID19
MODERNA
Lot Number 013H
Bell's palsy, Magnetic resonance imaging spinal, Nerve conduction studies, ... Bell's palsy, Magnetic resonance imaging spinal, Nerve conduction studies, Small fibre neuropathy More
Small fiber Neuropathy developed . Treatment steroid with relief but relapse after stopping. Unable ... Small fiber Neuropathy developed . Treatment steroid with relief but relapse after stopping. Unable to tolerate Dulexetine. And higher doses of pregabalin. Taking Pregabalin 75 mg bid . Persistent symptoms. Developed Left Facial nerve palsy More
โœ“
2824687 16 M MI 02/05/2025 HEPA
HPV9
MENB
MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
Y009094
Y008843
LF5308
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
I accidentally gave patient the adult HEP A Vaccine instead of the children's HEP A Vaccine I accidentally gave patient the adult HEP A Vaccine instead of the children's HEP A Vaccine
2824688 76 F KY 02/05/2025 FLU3
RSV
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
U8524BA
35P2C
Acne, Injection site erythema, Injection site pruritus, Injection site warmth; A... Acne, Injection site erythema, Injection site pruritus, Injection site warmth; Acne, Injection site erythema, Injection site pruritus, Injection site warmth More
Patient states injection site turned red, warm to the touch, itching, and a white pimple formed. Patient states injection site turned red, warm to the touch, itching, and a white pimple formed.
2824689 0.5 M UT 02/05/2025 HIBV
SANOFI PASTEUR

No adverse event, Product preparation error No adverse event, Product preparation error
ActHIB was given without the diluent it was given with sterile diluent. Patient had no reaction. ActHIB was given without the diluent it was given with sterile diluent. Patient had no reaction.
2824690 69 M IN 02/05/2025 FLU3
SANOFI PASTEUR

Injection site pain, Injection site rash, Muscular weakness, Paraesthesia Injection site pain, Injection site rash, Muscular weakness, Paraesthesia
Pain and rash at injection site. Weakness in left hand and tingling in 4th and 5th fingers of left h... Pain and rash at injection site. Weakness in left hand and tingling in 4th and 5th fingers of left hand. More
2824691 9 F MO 02/05/2025 HPV9
MERCK & CO. INC.
Y014059
Loss of consciousness, Pallor Loss of consciousness, Pallor
@1650: mom called us into the room and said patient had fainted. Upon entering the room patient was ... @1650: mom called us into the room and said patient had fainted. Upon entering the room patient was sitting up, pale, answering questions appropriately. I asked mom if she had hit anything like her head or anything else and mom said no. We laid her down and elevated her feet and color returned to her cheeks. Lying VS: 77 HR, 98% O2 on RA, 90/56 blood pressure. When she sat up HR went up to 110 but quickly went down to <100bpm and O2 remained at 98%. We also gave her some apple juice. Within 5 minutes she said "I feel all better" and was alert, in no acute distress, respirations nonlabored, skin color normal for ethnicity. She hopped up got ready to leave and safely exited the clinic. Mom stated that Mom faints with vaccines as well. I did not clarify if she fully lost consciousness. I tried to call mom afterward and LMOM for her to call back. I will try to call her later this week to clarify this. Per the nurse she was clenching up during vaccine administration due to nerves and after the nurse left the room, mom called out and said "I need help in here, my daughter just passed out." 2/4/25 @1710: Mom called me immediately back and said patient fell, mom caught her and patient fully lost consciousness for about 30 seconds and then was coherent again. More
2824692 11 F PA 02/05/2025 HPV9
MERCK & CO. INC.

Inappropriate schedule of product administration Inappropriate schedule of product administration
Patient given immunization too soon after first dose (1 month instead of 6 months) Patient given immunization too soon after first dose (1 month instead of 6 months)
2824693 71 M GA 02/05/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
52Z52
Extra dose administered Extra dose administered
Patient was given a second dose of RSV vaccine. Previous dose was on 9/14/2023. Patient was given a second dose of RSV vaccine. Previous dose was on 9/14/2023.
2824694 1.08 M MA 02/05/2025 VARCEL
MERCK & CO. INC.

Dermatitis acneiform Dermatitis acneiform
Pimple like rash noticed aprox 8 days post injection of varicella and MMR. Nurse discussed this may ... Pimple like rash noticed aprox 8 days post injection of varicella and MMR. Nurse discussed this may be a reaction to the varicella vaccine and to avoid immunocompromised individuals. Pt was to monitor and call back with no improvement, new/worsening sxs or questions/concerns. More
2824695 1 M MI 02/05/2025 COVID19
PFIZER\BIONTECH
LN8272
No adverse event, Product storage error No adverse event, Product storage error
Dose given was reconstituted the previous day, so out of the 12 hour range. Dose may not be fully ef... Dose given was reconstituted the previous day, so out of the 12 hour range. Dose may not be fully effective. No adverse effects to patient. Mother of patient notified. More
2824696 0.75 F MI 02/05/2025 COVID19
PFIZER\BIONTECH
LN8272
No adverse event, Product storage error No adverse event, Product storage error
Dose given was reconstituted the previous day. So outside of the 12 hour manufacturer guideline. No ... Dose given was reconstituted the previous day. So outside of the 12 hour manufacturer guideline. No adverse effects to patient. Recommended that patient be re-dosed. Mother of patient notified. More
2824697 23 F GA 02/05/2025 HPV9
MERCK & CO. INC.
W014513
Expired product administered, No adverse event Expired product administered, No adverse event
Expired Gardasil vaccine was given to patient, patient has not reported any adverse events or side e... Expired Gardasil vaccine was given to patient, patient has not reported any adverse events or side effects. More
2824698 13 M KY 02/05/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
FC3181
FC3181
Anxiety, Electrocardiogram normal, Electroencephalogram normal, Fall, Fear; Magn... Anxiety, Electrocardiogram normal, Electroencephalogram normal, Fall, Fear; Magnetic resonance imaging normal, Magnetoencephalography, Paraesthesia, Scan with contrast normal, Seizure More
Extreme anxiety and fear not previously observed, seizures that became so common that he began havin... Extreme anxiety and fear not previously observed, seizures that became so common that he began having on a daily basis, and tingling of the left arm prior to these episodes. Currently on SSRI (celexa) and 3 seizure meds (Clobazam, Keppra, Oxcarbazepine). Also has frequent episodes of complete mental and body "freezing" where he will fall over. More
โœ“ โœ“ โœ“
2824699 40 M CO 02/05/2025 COVID19
PFIZER\BIONTECH
EW0168
Dermatitis atopic, Skin disorder Dermatitis atopic, Skin disorder
According to my dermatologist and primary care physician, something within the vaccine caused my ski... According to my dermatologist and primary care physician, something within the vaccine caused my skin barrier to break down. I have a type of super atopic dermatitis from head to toe that has not completely cleared since 5/20/21. I still have to manage it and will have to for the rest of my life by taking multiple bleach baths per week, using 3 to 5 cream/lotions, giving myself 4 shots per month of Nemluvio. More
โœ“
2824700 4 F 02/05/2025 DTAPIPV
SANOFI PASTEUR
U7838AA
Cellulitis, Erythema, Skin lesion Cellulitis, Erythema, Skin lesion
Cellulitis after Quadracel: Left thigh has erythematous raised lesion measuring 4.5 in by 4 inch Cel... Cellulitis after Quadracel: Left thigh has erythematous raised lesion measuring 4.5 in by 4 inch Cellulitis after Proqrad: Right thigh has erythematous raised lesion measuring 2.5 in by 2.5 in Worsening after 3 days and started of cephalexin More
2824701 60 F ID 02/05/2025 HPV9
MERCK & CO. INC.
Y008843
No adverse event, Product administered to patient of inappropriate age, Wrong pr... No adverse event, Product administered to patient of inappropriate age, Wrong product administered More
HPV given to patient over age of 45. Should have been given Prevnar 20. Patient notified at time ... HPV given to patient over age of 45. Should have been given Prevnar 20. Patient notified at time of visit with no adverse effects notified. More
2824702 72 F TX 02/05/2025 COVID19
COVID19
MODERNA
MODERNA
204J23A
204J23A
Atrial fibrillation, Blood test abnormal, Chest pain, Computerised tomogram thor... Atrial fibrillation, Blood test abnormal, Chest pain, Computerised tomogram thorax abnormal, Echocardiogram abnormal; Electrocardiogram, Pericarditis, Pleural effusion More
About 10 days after receiving the vaccine, I developed chest pains, especially lying down. About 14... About 10 days after receiving the vaccine, I developed chest pains, especially lying down. About 14 days later I was admitted to the ER and then to the IC with arterial fibrillation (which I had never had been diagnosed in yearly exams) and diagnosed also with pericarditis and pleural effusion. I was in out of the the hospital for a week, on oxygen for over a month, 24hrs a day, at home. I had in home nurse visitse for 3 months, physical therapy and am on blood thinners for the rest of my life, according my cardiologist and my primary care physician.. More
โœ“ โœ“ โœ“
2824703 46 F TX 02/05/2025 HEP
HEPA
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
4T39P
HR4RB
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
None None
2824704 41 F GA 02/05/2025 COVID19
MODERNA
8081561
Expired product administered Expired product administered
Administered vaccine past beyond use date Administered vaccine past beyond use date
2824705 60 M GA 02/05/2025 COVID19
FLU3
PNC20
MODERNA
SANOFI PASTEUR
PFIZER\WYETH
8081561
UT8514KA
LC1279
Expired product administered; Expired product administered; Expired product admi... Expired product administered; Expired product administered; Expired product administered More
Administered vaccine past beyond use date Administered vaccine past beyond use date
2824706 47 F IL 02/05/2025 COVID19
FLU3
MODERNA
SEQIRUS, INC.
8081260
388489
No adverse event, Product administered to patient of inappropriate age; No adver... No adverse event, Product administered to patient of inappropriate age; No adverse event, Product administered to patient of inappropriate age More
Patient was incorrectly given Fluad instead of Afluria given age <65 years without immunocompromi... Patient was incorrectly given Fluad instead of Afluria given age <65 years without immunocompromising condition. She received Fluad in addition to a moderna covid-19 booster vaccination. After 24 hours, patient experiencing a typical immune response with no adverse reactions. More
2824707 86 F PR 02/05/2025 FLU3
SEQIRUS, INC.
388482
Dermatitis, Eye inflammation, Inflammation, Injection site inflammation, Pyrexia Dermatitis, Eye inflammation, Inflammation, Injection site inflammation, Pyrexia
ON 02-01-25 PATIENT WAS VACCINATED , AND AFTER ARRIVING HOME EXPERIENCED A LIKE ANA ALLERGIC REACTIO... ON 02-01-25 PATIENT WAS VACCINATED , AND AFTER ARRIVING HOME EXPERIENCED A LIKE ANA ALLERGIC REACTION BUT AT THE TIME WASN'T TOO SERIUS, SHE HAD THE AREA OF THE VACCINATION INFLAMED A LITTLE BIT. THE NEXT DAY THE PATIENT WAS FEELING WORST THE NEXT DAY WITH INFLAMED EYES, INFLAMED ARMS AND FEVER. aSHE WENT TO TEH DOCTOR ON 02/04/25 AND HE PRESCRIPBED ANTIBIOTICS ( LEVOFLOXACIN ) AND TODAY 02/05/25 HE SEND TOBRADEX. PATIENT FELT MUCH BETTER TODAY AFTER ANTIBIOTICS PRESCRIBED YESTERDAY AND PHYSICIAN SAID THE POSSIBLE MAS A DERMATITIS. More
2824708 42 F FL 02/05/2025 HEP
DYNAVAX TECHNOLOGIES CORPORATION
944942
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
PATIENT RECEIVED THE SECOND DOSE OF THE VACCINE ON THE 25TH DAY INSTEAD OF THE REGULAR 30 DAYS AFTER... PATIENT RECEIVED THE SECOND DOSE OF THE VACCINE ON THE 25TH DAY INSTEAD OF THE REGULAR 30 DAYS AFTER FIRST DOSE. PATIENT HAS NO SYMPTOMS AND PATIENT CLAIMS TO BE IN PERFECT CONDITION More
2824709 67 F CT 02/05/2025 FLU3
SEQIRUS, INC.
946590
Extra dose administered Extra dose administered
The patient came in asking for a flu vaccine. We told them we did not have the high dose vaccine in ... The patient came in asking for a flu vaccine. We told them we did not have the high dose vaccine in stock we only had the regular dose. The patient asked when we would be getting more in, I told her we wouldn't be as the flu vaccine giving is ending. She said fine I will take the regular dose. She then came back in a few hours later saying she forgot she already had a flu vaccine, when I looked back she did receive the high dose flu vaccine (fluzone HD). More
2824710 40 M CA 02/05/2025 ANTH
IPV
MMR
TYP
EMERGENT BIOSOLUTIONS
SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
300215A
X1D141M
Y011484
X1A271M
Dysgeusia; Dysgeusia; Dysgeusia; Dysgeusia Dysgeusia; Dysgeusia; Dysgeusia; Dysgeusia
Patient complaint of change in taste in palette shortly after receiving Polio, Anthrax, Typhoid and... Patient complaint of change in taste in palette shortly after receiving Polio, Anthrax, Typhoid and MMR More
2824711 10 M MA 02/05/2025 COVID19
PFIZER\BIONTECH
LP1776
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Administered Covid 12+ to patient who is 10 years old Administered Covid 12+ to patient who is 10 years old
2824712 56 F CA 02/05/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
9R397
Vaccination site pain Vaccination site pain
Patient stated that she started getting pain on vaccine site a week after she had gotten the vaccine... Patient stated that she started getting pain on vaccine site a week after she had gotten the vaccine. The pain comes and goes. Pain just comes, nothing that she does different causes the pain. More
2824713 49 F OH 02/05/2025 UNK
UNKNOWN MANUFACTURER

Eye pain, Pain Eye pain, Pain
Pain in right eye, worse with movement of eye. Attempted to treat with ibuprofen, not effective. O... Pain in right eye, worse with movement of eye. Attempted to treat with ibuprofen, not effective. Ongoing pain, 21 hours thus far. More
2824714 79 F ND 02/05/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
GA99K
Cellulitis, Injection site erythema, Injection site pain, Injection site swellin... Cellulitis, Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth More
Arm on administration site was painful, swollen, red, and hot from shoulder to elbow. Started on 1/... Arm on administration site was painful, swollen, red, and hot from shoulder to elbow. Started on 1/31/25 evening and continued to spread further down arm past elbow through 2/4/25. Saw HCP on 2/4/25 afternoon. Prescriptions for cefelexin 500mg and benedryl. diagnosis of Cellulitis. Improvement noted with minimal redness still visible by 2/5/25 More
2824715 0.33 M TX 02/05/2025 UNK
UNKNOWN MANUFACTURER

Product administered to patient of inappropriate age Product administered to patient of inappropriate age
influenza vaccine administered to infant 4 months of age influenza vaccine administered to infant 4 months of age
2824716 0.25 F TN 02/05/2025 DTPPVHBHPB
PNC20
MSP VACCINE COMPANY
PFIZER\WYETH
U7899AA
LG5578
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
First dose given at 15 weeks 1 day of age First dose given at 15 weeks 1 day of age
2824717 7 F VA 02/05/2025 MMRV
MERCK & CO. INC.
Y012074
Inappropriate schedule of product administration Inappropriate schedule of product administration
administered varicella vaccine too soon from previous administration due to wrong documentation of f... administered varicella vaccine too soon from previous administration due to wrong documentation of first administration More
2824718 50 M 02/05/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
7ZM55
Injection site erythema, Injection site swelling, Injection site warmth Injection site erythema, Injection site swelling, Injection site warmth
Redness, swelling, and warm to touch around injection site and down to elbow of left arm Redness, swelling, and warm to touch around injection site and down to elbow of left arm
2824719 73 M MS 02/05/2025 COVID19
COVID19
MODERNA
MODERNA
3043156
3043156
COVID-19, Feeling abnormal, Injection site erythema, Injection site swelling, Pa... COVID-19, Feeling abnormal, Injection site erythema, Injection site swelling, Pain in extremity; Product storage error, SARS-CoV-2 test positive More
Patient stated on 2/5/25 he experienced injection site reaction of redness, swelling and had a sore ... Patient stated on 2/5/25 he experienced injection site reaction of redness, swelling and had a sore arm. Stated he felt bad for several days and tested positive with covid with a home test. Patient's vaccine was part of a temperature excursion as well. More
2824720 0.33 M GA 02/05/2025 HIBV
PNC13
MERCK & CO. INC.
PFIZER\WYETH
Y008355
LK6651
Lethargy, No adverse event, Pyrexia, Vomiting projectile; Lethargy, No adverse e... Lethargy, No adverse event, Pyrexia, Vomiting projectile; Lethargy, No adverse event, Pyrexia, Vomiting projectile More
Pt received pediarix, hib, and rota at his 2 month well check on 11/20/24. Within 24 hours pt experi... Pt received pediarix, hib, and rota at his 2 month well check on 11/20/24. Within 24 hours pt experienced high fever. Pt was given a Prevnar vaccine on 12/27/24 and did not have any adverse reaction. On 2/4/25 Pt was given Hib and Prevnar vaccines and within 8-12 hours had a high fever (102.0), lethargy, and projectile vomiting. More
2824721 2 F CA 02/05/2025 MNQ
NOVARTIS VACCINES AND DIAGNOSTICS
L7373
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Physician ordered Menveo 1-vial formulation for 2-year old patient in preparation for upcoming trave... Physician ordered Menveo 1-vial formulation for 2-year old patient in preparation for upcoming travel out of the country. Vaccine administered by LVN as ordered. Menveo 1-vial formulation is FDA-approved for ages 10-55 years. The prescribing information states "Safety and effectiveness of the one-vial presentation of MENVEO in children aged younger than 10 years have not been established. For children 2 months through 9 years of age, only the two-vial presentation is approved for use." The order in EMR reads "Meningococcal MCV40 (MENVEO) - 1 vial (10-55yr)". The vial states "10 years through 55 Years of Age". More
2824722 0.75 F NJ 02/05/2025 FLU3
SEQIRUS, INC.

Acne, Crying, Erythema, Pruritus Acne, Crying, Erythema, Pruritus
After we return from her visit I realized she wasn't herself. She was crying so I put her to be... After we return from her visit I realized she wasn't herself. She was crying so I put her to bed. In the night some minutes to 12, I realized she is itching. I switched the over head lights on and her entire body had pimples all over even her face and her eyes had red streaks in it like blood shots. I raised the concern to a friend and I called the doctor but was unable to get in contact, so I took pictures to show the doctor on her next visit. This is when the doctor advised me to contact VAERS and make a report. More
2824723 0.67 M CA 02/05/2025 MNQ
NOVARTIS VACCINES AND DIAGNOSTICS
L7373
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Physician ordered Menveo 1-vial formulation for 2-year old patient in preparation for upcoming trave... Physician ordered Menveo 1-vial formulation for 2-year old patient in preparation for upcoming travel out of the country. Vaccine administered by LVN as ordered. Menveo 1-vial formulation is FDA-approved for ages 10-55 years. The prescribing information states "Safety and effectiveness of the one-vial presentation of MENVEO in children aged younger than 10 years have not been established. For children 2 months through 9 years of age, only the two-vial presentation is approved for use." The order in record reads "Meningococcal MCV40 (MENVEO) - 1 vial (10-55yr)". The vial states "10 years through 55 Years of Age". More
2824724 0.25 F TN 02/05/2025 DTPPVHBHPB
PNC20
MSP VACCINE COMPANY
PFIZER\WYETH
U7899AA
LC5485
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
Rotarix dose 1 was given at 17 weeks 1 day of age. Should be given before 14 weeks and 6 days. Rotarix dose 1 was given at 17 weeks 1 day of age. Should be given before 14 weeks and 6 days.
2824725 27 M 02/05/2025 HEP
IPV
MMR
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
CT3Z7
X1D141M
Y005808
Dizziness, Hyperhidrosis, Nausea, Pallor; Dizziness, Hyperhidrosis, Nausea, Pall... Dizziness, Hyperhidrosis, Nausea, Pallor; Dizziness, Hyperhidrosis, Nausea, Pallor; Dizziness, Hyperhidrosis, Nausea, Pallor More
3:05 PM pt stated he felt dizzy, he looked pale, got diaphoretic, and felt nauseous. Treatment initi... 3:05 PM pt stated he felt dizzy, he looked pale, got diaphoretic, and felt nauseous. Treatment initiated right away by placing an ice pack on the back of his neck, smelling an alcohol pad, and fanning him with a fan. At 15:15 BP read 110/70, HR 64, Temperature 97.4. More
2824726 39 F WA 02/05/2025 COVID19
COVID19
FLU3
FLU3
MODERNA
MODERNA
SEQIRUS, INC.
SEQIRUS, INC.
942645384
942645384
A3254041285141
A3254041285141
Blood test normal, Condition aggravated, Decreased appetite, Drug screen positiv... Blood test normal, Condition aggravated, Decreased appetite, Drug screen positive, Insomnia; Loss of personal independence in daily activities, Mania, Patient restraint, Pressure of speech, Psychomotor hyperactivity; Blood test normal, Condition aggravated, Decreased appetite, Drug screen positive, Insomnia; Loss of personal independence in daily activities, Mania, Patient restraint, Pressure of speech, Psychomotor hyperactivity More
After injection on 01/04/2025 I did not have any major symptoms, where my family also got vaccinated... After injection on 01/04/2025 I did not have any major symptoms, where my family also got vaccinated that day they were recovering as if from a flu for a day but I did not have the same reaction. Instead on 01/06/2025 I began feeling manic, unable to sleep that night. By the next day (tues) I was having to stay home from normal activities. Wednesday things got worse and I was speaking rapidly, unable to stop moving. Still not sleeping. Thursday and friday I stopped eating and barely drinking. On Saturday morning my husband dragged me to the ER where I had to be restrained and sedated until I spent the next 3 weeks at hospital. More
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2824727 82 M NY 02/05/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS

Injection site pain, Limb discomfort Injection site pain, Limb discomfort
The Injection was more painful then I have ever received and I have been receiving injections for 82... The Injection was more painful then I have ever received and I have been receiving injections for 82 years. That evening about 6 hours later I started having pain in my left arm (injection arm). Pain was very painful I was thinking I am having a heart attack. Now 3 weeks later I am still having discomfort in my left arm. More
2824728 17 F UT 02/05/2025 VARCEL
VARCEL
MERCK & CO. INC.
MERCK & CO. INC.


Back pain, Burning sensation, Rash, Rash erythematous, Scab; Skin lesion Back pain, Burning sensation, Rash, Rash erythematous, Scab; Skin lesion
Presenting for a rash/burning and pain that has been present over the right side over her lower abdo... Presenting for a rash/burning and pain that has been present over the right side over her lower abdomen/hip for the past 5 days. States that the burning is quite severe. States that the lesions for showed up in her right upper inguinal region but she also had/has pain in her low back on the right side as well. States that they showed up as red bumps and have turned into scab like lesions at this point but still are quite painful. More