🏥 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 💀 🏥 🚑 ♿ ⚠️
2822671 0.67 F TX 01/24/2025 DTAPIPVHIB
HEP
PNC13
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 UK036A8
PE9G5
GD1168
Incorrect dose administered; Incorrect dose administered; Incorrect dose adminis... Incorrect dose administered; Incorrect dose administered; Incorrect dose administered More
Adult Hep B dose administered to pediatric patient instead of pediatric dose. No treatment needed. O... Adult Hep B dose administered to pediatric patient instead of pediatric dose. No treatment needed. Outcome N/A. More
2822672 69 M FL 01/24/2025 PNC20
 PFIZER\WYETH
 lc5482
Extra dose administered, No adverse event Extra dose administered, No adverse event
Not an adverse event- just a duplicate shot- patient already received this shot in the past 11/19/20... Not an adverse event- just a duplicate shot- patient already received this shot in the past 11/19/2023 More
2822673 1.5 M 01/24/2025 PNC20
 PFIZER\WYETH
Wrong product administered Wrong product administered
MD ordered the wrong vaccine and it was administered to patient. MD ordered the wrong vaccine and it was administered to patient.
2822674 1.5 F 01/24/2025 PNC20
 PFIZER\WYETH
Wrong product administered Wrong product administered
MD ordered the wrong vaccine and it was administered to patient. MD ordered the wrong vaccine and it was administered to patient.
2822675 7 M VA 01/24/2025 DTAP
IPV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 BH57H
W1B511M
Y015356
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; No adverse event, Product administered to patient of inappropriate age More
No adverse events - Dtap given to 7 year old patient instead of Tdap No adverse events - Dtap given to 7 year old patient instead of Tdap
2822676 66 F AL 01/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Facial paralysis Facial paralysis
Right side of mouth drooping Right side of mouth drooping
2822677 83 F MI 01/24/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
FLU3
FLU3
FLU3
FLU3
FLU3
FLU3
 NOVAVAX
NOVAVAX
NOVAVAX
NOVAVAX
NOVAVAX
NOVAVAX
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
 6024MF020
6024MF020
6024MF020
6024MF020
6024MF020
6024MF020
388489
388489
388489
388489
388489
388489
Acute respiratory failure, Areflexia, CSF culture negative, CSF glucose increase... Acute respiratory failure, Areflexia, CSF culture negative, CSF glucose increased, CSF lactate decreased; CSF protein increased, CSF red blood cell count positive, CSF white blood cell count negative, Clotting factor transfusion, Cytology abnormal; Cytomegalovirus test negative, Endotracheal intubation, Enterovirus test negative, Gram stain, Gram stain negative; Guillain-Barre syndrome, Herpes simplex test negative, Muscular weakness, Mycobacterium test negative, Plasmapheresis; Potassium hydroxide preparation negative, Quadriplegia, Toxic encephalopathy, Treponema test negative, Varicella virus test negative; West Nile virus test negative; Acute respiratory failure, Areflexia, CSF culture negative, CSF glucose increased, CSF lactate decreased; CSF protein increased, CSF red blood cell count positive, CSF white blood cell count negative, Clotting factor transfusion, Cytology abnormal; Cytomegalovirus test negative, Endotracheal intubation, Enterovirus test negative, Gram stain, Gram stain negative; Guillain-Barre syndrome, Herpes simplex test negative, Muscular weakness, Mycobacterium test negative, Plasmapheresis; Potassium hydroxide preparation negative, Quadriplegia, Toxic encephalopathy, Treponema test negative, Varicella virus test negative; West Nile virus test negative More
83 y.o. female with relevant past medical history of hypertension, hyperlipidemia and hypothyroidism... 83 y.o. female with relevant past medical history of hypertension, hyperlipidemia and hypothyroidism presented to an OSH on 12/26 with complaint of significant lower extremity weakness. Pt was found to have AIDP, acute respiratory failure (extubated 1/5), and acute toxic metabolic encephalopathy, now s/p plasmapheresis (completed on 1/15) and cryoprecipitate (1/16) now presenting with incomplete tetraplegia with LE much more affected than UE. Admitted to for AIDP on 1/17/2025. AIDP -consistent with GBS, especially given elevated CSF protein, absent DTRs and recent influenza and COVID vaccines about 1 month ago -CSF studies to date reviewed: -Protein 124.6, glucose 101 -Lactic acid 2.2 -WBC 1, RBC 1 -Gram stain no organisms, Cx NGTD -VDRL not detected -VZV, HSV, CMV, WNV, enterovirus PCR negative -KOH prep reveals no mycelia or yeast forms; ABF smear negative -Cytology revealed increased white cells with a few neutrophils, lymphocytes and many monocytes -Completed 5 sessions of plasmapheresis last on 1/15. More
✓
2822678 64 F KY 01/24/2025 TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8264AA
U8264AA
Arthralgia, Atrial fibrillation, Dizziness, Dyspnoea, Electrocardiogram; Heart r... Arthralgia, Atrial fibrillation, Dizziness, Dyspnoea, Electrocardiogram; Heart rate increased, Injection site pain, Malaise, Pain, Pain in extremity More
Patient had constant sore left arm with throbbing with shooting pains from the left elbow to the wri... Patient had constant sore left arm with throbbing with shooting pains from the left elbow to the wrist and fingers ("feels like a lightning bolt"), arm feels like it is bruised and aching ("like someone punched you in the arm that never stops"), sore all the way around her arm at the injection site (anterior and posterior), dizziness, went into Atrial Fibrillation on 12/8/2024, still has dizziness and at times has increased heart rate and shortness of air without any exertion, just feels unwell. More
2822679 58 F GA 01/24/2025 COVID19
 PFIZER\BIONTECH
 Fc3184, FE3594,
Computerised tomogram venography head, Macrocytosis, Venogram abnormal Computerised tomogram venography head, Macrocytosis, Venogram abnormal
Left transverse sinus, sigmoid sinus, and jugular vein show small caliber and intraluminal filling d... Left transverse sinus, sigmoid sinus, and jugular vein show small caliber and intraluminal filling defect noted consistent with chronic thrombus. More
✓ ✓
2822680 65 M MI 01/24/2025 COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 GJ2524
GJ2524
GJ2524
GJ2524
GJ2524
Atrial fibrillation, Brain natriuretic peptide increased, C-reactive protein inc... Atrial fibrillation, Brain natriuretic peptide increased, C-reactive protein increased, COVID-19, COVID-19 pneumonia; Cardiac failure acute, Cardiac failure congestive, Chest pain, Condition aggravated, Cough; Diabetic foot, Dyspnoea, Electrocardiogram abnormal, Gastrointestinal disorder, Hyperglycaemia; Hypocalcaemia, Hypoxia, Myocardial ischaemia, Pyrexia, Red blood cell sedimentation rate increased; Respiratory viral panel, SARS-CoV-2 test positive, Troponin increased, Viral infection More
BRIEF OVERVIEW: Admission Date: 1/14/2025 Discharge Date: Jan 16, 2025 Discharge Disposition: home ... BRIEF OVERVIEW: Admission Date: 1/14/2025 Discharge Date: Jan 16, 2025 Discharge Disposition: home health care svc DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypocalcemia [E83.51] Elevated C-reactive protein (CRP) [R79.82] Elevated sed rate [R70.0] Hypoxia [R09.02] Elevated troponin [R79.89] Atrial fibrillation with RVR [I48.91] Elevated brain natriuretic peptide (BNP) level [R79.89] Diabetic ulcer of toe of right foot associated with diabetes mellitus of other type, unspecified ulcer stage [E13.621, L97.519] Acute on chronic congestive heart failure, unspecified heart failure type [I50.9] Hyperglycemia due to diabetes mellitus [E11.65] Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] COVID [U07.1] HOSPITAL COURSE: Patient is a 67-year-old male history of diabetes, diabetic neuropathy, peripheral vascular disease status post left AKA, coronary artery disease, AFib on Xarelto, depression anxiety and chronic pain. Presents for chief complaint of cough shortness for breath chest pain. Admission EKGs chronic AFib without ST segment or T-wave changes. Troponins were noted to be elevated with negative delta likely related to demand ischemia from hypoxia. Patient was on 2 L at admission febrile. RVP was obtained and positive for COVID-19. Patient was started on remdesivir and Decadron for COVID treatment. Initially requiring supplemental oxygen titrated to room air. Patient was complete course of steroids at discharge. During stay patient was noted to have right 1st toe chronic wound. He was seen by wound care team without obvious signs of infection although some concern for long-term healing. Patient was not seen Cardiothoracic surgery in 3-4 years she will be referred on outpatient basis for further workup. We will follow up with wound care team and have home health for wound nursing. Patient was recurrent episodes of chest pain during his stay all associated with morning meals and self resolving. EKGs were obtained and normal at those times likely deemed related to viral syndrome versus GI based. Discharged to Home Health Services More
✓
2822681 63 F CO 01/24/2025 COVID19
COVID19
 MODERNA
MODERNA

Arthralgia, Axillary pain, Bundle branch block right, Electrocardiogram abnormal... Arthralgia, Axillary pain, Bundle branch block right, Electrocardiogram abnormal, Injection site mass; Ligament sprain, Pain in extremity, Rotator cuff syndrome, X-ray normal More
pt says her left arm became very sore and developed a lump around the injection site. The soreness s... pt says her left arm became very sore and developed a lump around the injection site. The soreness started to move into the armpit and down into the elbow. It continued to get worse so she went to Urgent Care. They did an Xray and EKG. Xray was negative. The EKG showed some right bundle branch block. She was told to follow up with cardiologist. She was referred to an Orthopedic doctor for a suspected shoulder sprain or rotator cuff injury. She went to Ortho Dr. She was given 2 cortisone shots in the left shoulder. She is suspected to have a torn rotator cuff that is possibily turning into a frozen shoulder and was prescribed physical therapy. She will start on Feb 5th. She is scheduled to have a MRI and will FU w/ Ortho Dr. on Jan 29th after MRI. More
✓
2822682 1.25 M ID 01/24/2025 FLUN3
 MEDIMMUNE VACCINES, INC.
 WL2006B
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Pt given Flumist 7 months to early. No actual adverse effects. Pt on 1 year 3 months. Pt given Flumist 7 months to early. No actual adverse effects. Pt on 1 year 3 months.
2822683 12 M NH 01/24/2025 FLU3
HPV9
 SANOFI PASTEUR
MERCK & CO. INC.
 5Z977
X024251
No adverse event; No adverse event No adverse event; No adverse event
There was no reaction to the vaccine There was no reaction to the vaccine
2822684 8 F IL 01/24/2025 COVID19
 MODERNA
 3044079
Chest pain, Electrocardiogram, Expired product administered Chest pain, Electrocardiogram, Expired product administered
Covid vaccine expired. Chest pain 2 minutes after receiving vaccine Covid vaccine expired. Chest pain 2 minutes after receiving vaccine
2822685 49 M MA 01/24/2025 COVID19
 NOVAVAX
CSF protein increased, Computerised tomogram, Hypoaesthesia, Magnetic resonance ... CSF protein increased, Computerised tomogram, Hypoaesthesia, Magnetic resonance imaging More
i started losing feeling in my arms and legs shortly after my covid vaccine i started losing feeling in my arms and legs shortly after my covid vaccine
✓ ✓
2822686 80 M MS 01/24/2025 PNC21
 MERCK & CO. INC.
 Y013009
Arthralgia, Cough, Malaise, Myalgia Arthralgia, Cough, Malaise, Myalgia
GENERAL MALAISE, COUGHING, WHOLE BODY MUSCLES AND JOINTS SORENESS. GENERAL MALAISE, COUGHING, WHOLE BODY MUSCLES AND JOINTS SORENESS.
2822687 0.17 M NV 01/24/2025 PNC20
 PFIZER\WYETH
Pyrexia, Supraventricular tachycardia Pyrexia, Supraventricular tachycardia
Patient received Prevnar 20 on Jan 14, 2025. On 1/15, patient had fever induced SVT requiring adeno... Patient received Prevnar 20 on Jan 14, 2025. On 1/15, patient had fever induced SVT requiring adenosine, acetaminophen, and ice packs. Once the fever came down, so did the HR More
✓
2822688 90 F MO 01/24/2025 PNC20
 PFIZER\WYETH
 GH4082
No adverse event No adverse event
No adverse events noted No adverse events noted
2822689 12 F CA 01/24/2025 HPV9
 MERCK & CO. INC.
 Y008640
Abdominal distension, Eczema, Eczema eyelids, Rash erythematous, Rash pruritic Abdominal distension, Eczema, Eczema eyelids, Rash erythematous, Rash pruritic
Came back home on 12/21/2024, received MMR#2 (MMR-II), Tdap (Adacel) and IPV#5 in left upper arm at ... Came back home on 12/21/2024, received MMR#2 (MMR-II), Tdap (Adacel) and IPV#5 in left upper arm at HC on 12/24/2024 without reaction. On 1/06/2025 received MCV (Menveo) and HPV (Gardasil 9) in left upper arm, developed swelling in left upper arm along with itchy red rash over shoulders, in folds of arms, wrists, over MCPs of hands, upper eyelids and flexural ankles. Patient started over-the-counter Benadryl 25mg tab oral and hydrocortisone 1% cream since 1/06 without relief. Constantly itching, picked red bumps over wrists. Never has had a history of eczema in the past. Examined by MD on 1/23/25 and placed on tacrolimus 0.03% ointment for eyelid eczema; triamcinolone acetonide 0.1% ointment for flexural eczema and hydroxyzine 25mg oral tab QID PRN itching More
2822690 0.33 M GA 01/24/2025 DTPPVHBHPB
PNC20
RV5
 MSP VACCINE COMPANY
PFIZER\WYETH
MERCK & CO. INC.
 U7921AA
LG5574
Y003754
Rash; Rash; Rash Rash; Rash; Rash
Child awakened the day after the vaccines with a rash compatable with erythema multiforme. Child awakened the day after the vaccines with a rash compatable with erythema multiforme.
2822692 21 F GA 01/24/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 N7CX5
N7CX5
Cough, Endotracheal intubation, Intensive care, Pallor, Throat tightness; Wheezi... Cough, Endotracheal intubation, Intensive care, Pallor, Throat tightness; Wheezing More
WITHIN MINUTES OF RECEIVING FLU VACCINE, EMPLOYEE DEVELOPED A COUGH, ASKED FOR WATER, NO RELIEF, DEV... WITHIN MINUTES OF RECEIVING FLU VACCINE, EMPLOYEE DEVELOPED A COUGH, ASKED FOR WATER, NO RELIEF, DEVELOPED AUDIBLE WHEEZING, CHEST AUSCULTAION BILAT WHEEZING ALL LOBES; EMPLOYEE COMPLAINED OF THROAT FEELING FEELING CONSTRICTING; COLOR PALE; EMPLOYEE HAD EPI-PEN WITH HER, GAVE IM RIGHT THIGH, CALLED EMS, TRANSPORTED TO ED. INTUBATED, ADMITTED OVERNIGHT TO INTENSIVE CARE. More
✓
2822693 8 M FL 01/24/2025 IPV
 SANOFI PASTEUR
 X1C891M
Immediate post-injection reaction, Injection site reaction, Rash papular Immediate post-injection reaction, Injection site reaction, Rash papular
Immediately following injection the injection site developed a raised round area 1 cm in diameter. W... Immediately following injection the injection site developed a raised round area 1 cm in diameter. Within 1-2 minutes a raised red rash developed from the injection site out to the side approximately and inch on each side and down the arm to the elbow. Within 10 minutes the rash diminished to about half the size and was no longer raised. More
2822694 32 F 01/24/2025 COVID19
 PFIZER\BIONTECH
Bacterial infection, Upper respiratory tract infection Bacterial infection, Upper respiratory tract infection
Several weeks after vaccination, developed upper respiratory tract infection (COVID-19 negative) whi... Several weeks after vaccination, developed upper respiratory tract infection (COVID-19 negative) which then developed into a secondary bacterial infection. Unlikely to be related to vaccination. More
2822695 68 M MA 01/24/2025 COVID19
COVID19
PNC20
 MODERNA
MODERNA
PFIZER\WYETH
 3043023
3042648
LK6650
Underdose; Underdose; Underdose Underdose; Underdose; Underdose
Patient given pediatric dose of vaccine instead of adult strength vaccine. Returned a few hours lat... Patient given pediatric dose of vaccine instead of adult strength vaccine. Returned a few hours later to receive the adult dose of vaccine (only -.25 to make it collectively a full dose) More
2822696 80 F GA 01/24/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 LM2216
UT8470BA
Tendon injury; Tendon injury Tendon injury; Tendon injury
Patient reports tendon tear in the left arm starting two weeks after receiving the Covid vaccine Patient reports tendon tear in the left arm starting two weeks after receiving the Covid vaccine
2822697 81 M OH 01/24/2025 COVID19
 MODERNA
 P-3043924
Mobility decreased, Pain in extremity Mobility decreased, Pain in extremity
relates that has had a reaction since day given. never reacted to a shot before. Denies redness, fev... relates that has had a reaction since day given. never reacted to a shot before. Denies redness, fever, illness relates Pain dsown arm is the reaction , DO NOT have full range of motion. Been since I received shot. More
2822698 61 M GA 01/24/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 3043391
388484
Dyspnoea, Myasthenia gravis; Dyspnoea, Myasthenia gravis Dyspnoea, Myasthenia gravis; Dyspnoea, Myasthenia gravis
After approximately 3 days, patient showed up to doctor's office complaining of difficulties br... After approximately 3 days, patient showed up to doctor's office complaining of difficulties breathing. He was diagnosed as having Myasthenia Gravis. He had no previous symptoms nor diagnoses of MG. It is unknown if the vaccine was a trigger, but given the disease mechanisms, it is possible that the vaccine(s) triggered an undiagnosed condition. More
✓
2822699 0.5 F 01/24/2025 DTAP
HIBV
RV5
 SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.


Aggression, Dyskinesia, Head banging, Strabismus; Aggression, Dyskinesia, Head b... Aggression, Dyskinesia, Head banging, Strabismus; Aggression, Dyskinesia, Head banging, Strabismus; Aggression, Dyskinesia, Head banging, Strabismus More
Baby started aggressively banging head on everything especially hard surfaces, began squinting eyes,... Baby started aggressively banging head on everything especially hard surfaces, began squinting eyes, and having whole body jerks More
✓
2822700 41 F PA 01/24/2025 COVID19
 MODERNA
Alopecia, Condition aggravated Alopecia, Condition aggravated
Significant hair loss Significant hair loss
2822701 10 F 01/24/2025 COVID19
 MODERNA
Erythema Erythema
Redness to arm 2 weeks later, measuring 30x20cm Redness to arm 2 weeks later, measuring 30x20cm
2822702 64 F FL 01/24/2025 UNK
 UNKNOWN MANUFACTURER
 388499
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
No adverse event took place but patient received vaccine for over 65 year old before reaching that a... No adverse event took place but patient received vaccine for over 65 year old before reaching that age. Patient is only 64 years and 9 month old. More
2822703 1 M MA 01/24/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 LP1776
LP1776
LP1776
LP1776
Incorrect dose administered, Pyrexia; Full blood count, Overdose, Product admini... Incorrect dose administered, Pyrexia; Full blood count, Overdose, Product administered to patient of inappropriate age, Pyrexia; Incorrect dose administered, Pyrexia; Full blood count, Overdose, Product administered to patient of inappropriate age, Pyrexia More
Patient was given a covid vaccine (Pfizer Comirnaty for age 12+) when he should have received the co... Patient was given a covid vaccine (Pfizer Comirnaty for age 12+) when he should have received the covid vaccine (Moderna for age 6m-11yr). Patient did develop a fever that night after receiving the wrong vaccine for his age. More
2822705 4 F MI 01/24/2025 DTAPIPVHIB
MMRV
 SANOFI PASTEUR
MERCK & CO. INC.
 UJ984AA
Y013573
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
Pt received incorrect vaccine, Quadracel ordered, but pentacel given which is not accurate product f... Pt received incorrect vaccine, Quadracel ordered, but pentacel given which is not accurate product for patient's need. More
2822706 3 F MA 01/24/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 LP1776
LP1776
LP1776
LP1776
Product administered to patient of inappropriate age, Pyrexia; Overdose, Product... Product administered to patient of inappropriate age, Pyrexia; Overdose, Product administered to patient of inappropriate age, Pyrexia; Product administered to patient of inappropriate age, Pyrexia; Overdose, Product administered to patient of inappropriate age, Pyrexia More
Patient was given a covid vaccine (Pfizer Comirnaty for age 12+) when she should have received the c... Patient was given a covid vaccine (Pfizer Comirnaty for age 12+) when she should have received the covid vaccine (Moderna for age 6m-11yr). Patient did develop a fever that night after receiving the wrong vaccine for her age. More
2822707 10 F 01/24/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Alopecia, Condition aggravated; Alopecia, Condition aggravated Alopecia, Condition aggravated; Alopecia, Condition aggravated
Excessive hair loss Excessive hair loss
2822708 11 F NV 01/24/2025 MNQ
TDAP
 NOVARTIS VACCINES AND DIAGNOSTICS
GLAXOSMITHKLINE BIOLOGICALS
 3E99M
M77CC
Head injury, Seizure like phenomena, Syncope; Head injury, Seizure like phenomen... Head injury, Seizure like phenomena, Syncope; Head injury, Seizure like phenomena, Syncope More
PATIENT HAD WHAT LOOKED LIKE A SEIZURE BEFORE FAINTING AND HITTING HER HEAD. PATIENT HAD WHAT LOOKED LIKE A SEIZURE BEFORE FAINTING AND HITTING HER HEAD.
2822709 10 F MI 01/24/2025 COVID19
 PFIZER\BIONTECH
 LN7302
Expired product administered Expired product administered
This vaccine was beyond use date. Vaccine was being stored in refrigerator between temperatures of 3... This vaccine was beyond use date. Vaccine was being stored in refrigerator between temperatures of 36-46 degrees Fahrenheit, which means this vaccine is good for 10 weeks after receiving it. Date would have been 12/25/2024 More
2822710 11 M MN 01/24/2025 MNQ
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
 7GF79
7GF79
Eschar, Injection site erythema, Injection site oedema, Injection site rash, Inj... Eschar, Injection site erythema, Injection site oedema, Injection site rash, Injection site reaction; Livedo reticularis, Sensitive skin More
Left deltoid superior aspect with small eschar and no local redness, inferior aspect of deltoid, sma... Left deltoid superior aspect with small eschar and no local redness, inferior aspect of deltoid, small eschar with local redness and mild edema, pink/violaceous irregular rash inferior to deltoid but congrunet with inferior injection site. Superficial tactile sensitivy but no significant induration, no soft tissue or bony defect. Distal to mid portion of upper arm is slightly pale lacey purplish/mottled area. Distal forearm and hand normal. Notes: MCV-4 appears to be the presumed trigger for this fixed local reaction. It's expected to diffuse in the next 3-4 days. May migrate with gravity. May treat locally with ice/heat if needed, may continue experience sensory sensitivity of skin until rash is resolved. Discussed okay to tentatively plan to repeat vaccine when due at 16 years. Fixed local reaction does not appear to be in the spectrum of allergy with risk of systemic allergy or dangerous consequences. Patient is uniquie in circumstances as his liklihood of reaction may be a reflection of the pooled immunoglobulin he gets for his hypogammaglobulinemia. May address with Immunologist if parents wish. VAERS report to be filed. More
2822711 27 F 01/24/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR

Arthralgia, Bone marrow oedema, Immediate post-injection reaction, Magnetic reso... Arthralgia, Bone marrow oedema, Immediate post-injection reaction, Magnetic resonance imaging joint; Arthralgia, Bone marrow oedema, Immediate post-injection reaction, Magnetic resonance imaging joint More
L shoulder pain immediately after vaccine administration and chronically for months following. L shoulder pain immediately after vaccine administration and chronically for months following.
2822712 32 F VA 01/24/2025 FLU3
 SANOFI PASTEUR
 UT8514KA
Extra dose administered, No adverse event Extra dose administered, No adverse event
The nursing assistant gave a second flu shot to this member. No adverse effects. The nursing assistant gave a second flu shot to this member. No adverse effects.
2822713 2 M TX 01/24/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 3RT93
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
No adverse reactions. No adverse reactions.
2822714 21 F WI 01/24/2025 HPV9
 MERCK & CO. INC.
 Y003462
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received 3rd dose of HPV, when only needed the 2 dose series. No symptoms or side effects no... Patient received 3rd dose of HPV, when only needed the 2 dose series. No symptoms or side effects noted. More
2822715 44 M KS 01/24/2025 FLU3
FLU3
FLU3
FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
 AW1620A
AW1620A
AW1620A
AW1620A
AW1620A
Arthralgia, Asthenia, Chest X-ray, Chest discomfort, Chest pain; Cold sweat, Dec... Arthralgia, Asthenia, Chest X-ray, Chest discomfort, Chest pain; Cold sweat, Decreased appetite, Dizziness, Electrocardiogram, Fatigue; Flushing, Full blood count, Influenza virus test, Insomnia, Metabolic function test; Nausea, Nervousness, Pallor, Respiratory syncytial virus test, SARS-CoV-2 test; Sluggishness, Syncope, Tinnitus, Troponin, Tunnel vision More
Patient presented to ER at outlying facility complaining of chest pain, vision changes (tunnel visio... Patient presented to ER at outlying facility complaining of chest pain, vision changes (tunnel vision), ears ringing, near syncope, dizziness, pale, clammy, flushing of skin, chest tightness, weak, sluggish, and fatigue. He was evaluated at ER on 1/16/25 and everything on exam reported to be benign. Patient has since followed up with us to be evaluated by his PCP on 1/17/25 and again 1/24/25 and is still continuing to have lingering symptoms, reporting lightheaded, joint pain, shaky, dizzy, nausea, decreased appetite, and difficulty sleeping. PCP Dr. is suspicious this is post influenza vaccination reaction with neurological involvement and encephalopathy. We will continue to follow up with patient and his symptoms. More
2822716 8 F OH 01/24/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3044210
U8531AA
Eye swelling, Pyrexia, Urticaria; Eye swelling, Pyrexia, Urticaria Eye swelling, Pyrexia, Urticaria; Eye swelling, Pyrexia, Urticaria
fever, facial hives and eye swelling approximately 5 minutes after vaccine administration. Patient g... fever, facial hives and eye swelling approximately 5 minutes after vaccine administration. Patient given Benadryl and Ibuprofen. Observed for 20 minutes after medication administration with resolution of facial hives and eye swelling. One hour later, fever resolved per parent report over the phone. More
2822717 52 F UT 01/24/2025 HEPAB
IPV
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 M4B34
X1D141M
Arthralgia, Mobility decreased, Pain; Arthralgia, Mobility decreased, Pain Arthralgia, Mobility decreased, Pain; Arthralgia, Mobility decreased, Pain
Pt complains of increasing pain and decreased movement of R shoulder, with symptoms starting to wors... Pt complains of increasing pain and decreased movement of R shoulder, with symptoms starting to worsen 48 hours after injection. No redness, swelling, or rash at site. States that it has been painful as she moves her shoulder from body and when she raises her arm above her head. More
2822718 64 F MT 01/24/2025 COVID19
 PFIZER\BIONTECH
 LM2222
Hyperhidrosis, Injection site pain, Nausea Hyperhidrosis, Injection site pain, Nausea
PT STATED THAT WITHIN ABOUT 2 HOURS AFTER RECEIVING THE SHINGRIX IMMUNIZATION, HER UPPER ARM STARTED... PT STATED THAT WITHIN ABOUT 2 HOURS AFTER RECEIVING THE SHINGRIX IMMUNIZATION, HER UPPER ARM STARTED HURTING A LOT ABOUT 2 INCHES BELOW THE AREA OF THE SHOT. SHE WAS ALSO SWEATING AND HAD SIGNIFICANT NAUSEA. More
2822719 F IN 01/24/2025 COVID19
 MODERNA
 3044143
Pyrexia, Vomiting Pyrexia, Vomiting
Well on the same day she vomited, had a fever I feel like that COVID 19 vaccine made her sick, and f... Well on the same day she vomited, had a fever I feel like that COVID 19 vaccine made her sick, and for me that's not right More
2822720 19 F IL 01/24/2025 MNQ
 SANOFI PASTEUR
 U8369AA
Induration, Injection site erythema, Injection site warmth, Pyrexia, Swelling Induration, Injection site erythema, Injection site warmth, Pyrexia, Swelling
induration, swelling, warmth and redness of injection site, fever up to 101F induration, swelling, warmth and redness of injection site, fever up to 101F
2822721 0.67 M CA 01/24/2025 COVID19
 PFIZER\BIONTECH
 ln8272
Underdose Underdose
During the administration of the Pfizer COVID-19 vaccine, it was noted that the vaccine was diluted ... During the administration of the Pfizer COVID-19 vaccine, it was noted that the vaccine was diluted with 1.8 mL of diluent instead of the recommended 1.1 mL. More
2822722 38 F CA 01/24/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 772YT
Dizziness, Dry skin Dizziness, Dry skin
At around 10:30 am on 01/24/2025 patient approached Team (PHN Team) - (RN, PHN and RN, PHN and requ... At around 10:30 am on 01/24/2025 patient approached Team (PHN Team) - (RN, PHN and RN, PHN and requested a Hepatitis A vaccine. RN, PHN reviewed patient eligibility and confirmed vaccine history in the Immunization Registry database. Patient denied having a history of allergies or adverse reactions to vaccines. Patient denied syncope after receiving vaccines in the past. At 10:55 am, RN, PHN administered Havrix (Lot # 772YT, Expiration date 9/23/2025) in the right deltoid, intramuscularly. At 11:00 am patient reported she ?felt dizzy?. Patient appeared sitting calmly in the chair, RN, PHN provided patient with a juice box. RN, PHN, offered to lie patient down on the yoga mat. Patient denied moving and requested to stay sitting. Patient began drinking the juice box. Patient's skin was dry and appropriate color for Ethinicy. At 11:05 am patient gave verbal consent for RN, PHN to measure vitals. Vital signs measured as follows: blood pressure 102/68 mm Hg, heart rate 75 beats per minute, respiratory rate 18 breaths per minute, oxygen saturation 98%. Patient stated she was "feeling better". At 11:08 am patient reported symptom had resolved completely. PHN, educated patient about risk for syncope with vaccinations. PHN, referred patient to primary care clinic for follow up and future vaccines. Patient stood up at 11:10 am to go to her appointment at clinic. Patient denied any return of symptoms and walked away with a steady gait and balance to the next resource tent. More
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