🏥 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 💀 🏥 🚑 ♿ ⚠️
2851839 78 M IA 07/30/2025 COVID19
 MODERNA
 3044202
Death Death
Resident expired Resident expired
✓
2851840 57 M GA 07/30/2025 COVID19
 MODERNA
Magnetic resonance imaging, Tendon rupture, X-ray Magnetic resonance imaging, Tendon rupture, X-ray
Quad rupture Quad rupture
2851841 1 M TX 07/30/2025 HEPA
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 22gp3
427554
y013349
Rash vesicular; Rash vesicular; Rash vesicular Rash vesicular; Rash vesicular; Rash vesicular
chickenpox like rash which developed 5-6 days post vaccine chickenpox like rash which developed 5-6 days post vaccine
2851842 40 F VT 07/30/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 X4494
Injection site erythema, Injection site pain, Injection site swelling, Urticaria Injection site erythema, Injection site pain, Injection site swelling, Urticaria
Swelling, redness, pain at vaccine site, the following day she developed hives at vaccine site which... Swelling, redness, pain at vaccine site, the following day she developed hives at vaccine site which progressed to total body hives. More
2851843 11 M KS 07/30/2025 MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
 AMAB064A
No adverse event, Product preparation issue No adverse event, Product preparation issue
Patient was given only the diluent liquid. Patient was not given the powder that was to be reconstit... Patient was given only the diluent liquid. Patient was not given the powder that was to be reconstituted with it. Patient has had no reaction to just the diluent. Patient is fully vaccinated according to the CDC with just the diluent in the U.S. Patient will need to be revaccinated if he plans to leave the country, specifically Africa. More
2851844 1 F PA 07/30/2025 HEPA
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 H3N97
Y015551
Z005233
Febrile convulsion, Pyrexia, Rash; Febrile convulsion, Pyrexia, Rash; Febrile co... Febrile convulsion, Pyrexia, Rash; Febrile convulsion, Pyrexia, Rash; Febrile convulsion, Pyrexia, Rash More
fever, rash, complex febrile seizure fever, rash, complex febrile seizure
2851845 30 F MD 07/30/2025 HPV9
 MERCK & CO. INC.
 Y013565
Exposure during pregnancy, No adverse event, Pregnancy test positive, Product us... Exposure during pregnancy, No adverse event, Pregnancy test positive, Product use issue More
On 7-28-25 Patient was scheduled at clinic for pap and HPV # 3 vaccine. The patient was interviewed ... On 7-28-25 Patient was scheduled at clinic for pap and HPV # 3 vaccine. The patient was interviewed by nurse, pregnancy test result was negative, vaccine administered (in right deltoid area with no reactions noted). Next, pt was sent to clinician where exam/pap was completed, that was when pt disclosed to the doctor that she did a home pregnancy test and and result was positive. Clinician immediately ordered a repeat pregnancy test, result positive. This is patient's first pregnancy, EDD is March 13, 2026 based on LMP 6-9-2025. More
2851846 26 F FL 07/30/2025 FLU3
 SANOFI PASTEUR
 TFAA2501
Chest discomfort, Electrocardiogram, Pain in jaw Chest discomfort, Electrocardiogram, Pain in jaw
pt contacted pharmacy to let them know she went to the ER because she had pressure on her chest. She... pt contacted pharmacy to let them know she went to the ER because she had pressure on her chest. She had jaw pain and could not her jaw. She was given EKG. BP 102/69, heart rate and temp was in normal range. She was discharged to home to follow up PCP. More
2851847 16 F IA 07/30/2025 MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
 AMVB064A
Product preparation issue Product preparation issue
received the liquid conjugate component only; received the liquid conjugate component only; This non... received the liquid conjugate component only; received the liquid conjugate component only; This non-serious case was reported by a nurse via call center representative and described the occurrence of inappropriate preparation of medication in a 16-year-old female patient who received Men ACWY-CRM NVS (Menveo) (batch number AMVB064A, expiry date 31-DEC-2025) for prophylaxis. On 08-JUL-2025, the patient received Menveo (intramuscular, left deltoid). On 08-JUL-2025, an unknown time after receiving Menveo, the patient experienced inappropriate preparation of medication (Verbatim: received the liquid conjugate component only) and inappropriate dose of vaccine administered (Verbatim: received the liquid conjugate component only). On 08-JUL-2025, the outcome of the inappropriate preparation of medication was not applicable. The outcome of the inappropriate dose of vaccine administered was not applicable. Additional Information: GSK Receipt Date: 17-JUL-2025 The reporter was a nurse who called to report that a female patient had received only the liquid conjugate component of Menveo in her left deltoid on 8-JUL-2025, which led to Inappropriate preparation of medication and Inappropriate dose of vaccine administered. All the information that was provided about this adverse event was reported.; Sender's Comments: US-GSK-US2025091770:same reporter, Different patient, 1 of 3 report US-GSK-US2025091796:same reporter, Different patient, 3 of 3 report More
2851848 0.33 M VA 07/30/2025 DTAPIPV
 SANOFI PASTEUR
 NA
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient was given Quadracel instead of Vaxelis at well child visit. Quadracel details were not docum... Patient was given Quadracel instead of Vaxelis at well child visit. Quadracel details were not documented. Patient returned 7/18/25 to receive Vaxelis. No noted side effects from either vaccine. More
2851849 1.17 M PA 07/30/2025 UNK
 UNKNOWN MANUFACTURER
Pyrexia Pyrexia
fevers, parents admin tylenol and motrin. fevers, parents admin tylenol and motrin.
2851850 16 F GA 07/30/2025 MENB
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
 GSKPX7E2
PMCU8351BA
Loss of consciousness; Loss of consciousness Loss of consciousness; Loss of consciousness
Pt passed out while walking toward the exit from the exam room hallway into the lobby. Her mother wa... Pt passed out while walking toward the exit from the exam room hallway into the lobby. Her mother was walking behind her and caught the patient and lowered her to the floor. Pt remained seated on the floor for 5-10 minutes while being given water and having a damp towel placed on her head. Pt was talking and smiling during this time. Pt denied dizziness and was moved to a chair where she sat for about 5 minutes before getting up and walking to the car with her mother. More
2851851 12 F AZ 07/30/2025 HPV9
MNQ
TDAP
 MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
 1965079
U7986AA
TD2FD
Syncope; Syncope; Syncope Syncope; Syncope; Syncope
Patient was given 3 vaccines during a routine exam and shortly after vaccines given, patient fainted... Patient was given 3 vaccines during a routine exam and shortly after vaccines given, patient fainted, vasovagal syncope More
2851852 22 F OH 07/30/2025 TDAP
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 PG3RP
YO17063
Injection site erythema, Injection site oedema, Injection site pain; Injection s... Injection site erythema, Injection site oedema, Injection site pain; Injection site erythema, Injection site oedema, Injection site pain More
Of note, the patient was here on 06/11/2025 (see note) and received a Tdap vaccine to the left delto... Of note, the patient was here on 06/11/2025 (see note) and received a Tdap vaccine to the left deltoid and a varicella vaccine to the posterior aspect of the left arm. Since then, the patient has noticed erythema, edema, and tenderness to the area More
2851854 89 F NC 07/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 2HJ99
Pruritus, Rash Pruritus, Rash
Received vaccine at 10am 7/29, started itching at 7pm 7/29 on legs, back and arms. Developed rashes ... Received vaccine at 10am 7/29, started itching at 7pm 7/29 on legs, back and arms. Developed rashes legs below the knees. Was seen at urgent care 7/30. Advised to use benadryl and oatmeal bath soak. More
2851855 30 M ID 07/30/2025 ANTH
ANTH
ANTH
TYP
TYP
TYP
 EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 300216A
300216A
300216A
X2A411
X2A411
X2A411
Back pain, Chills, Constipation, Dizziness, Dyspnoea; Dysuria, Feeling abnormal,... Back pain, Chills, Constipation, Dizziness, Dyspnoea; Dysuria, Feeling abnormal, Full blood count normal, Headache, Metabolic function test normal; Renal pain, Urine analysis normal, Vomiting; Back pain, Chills, Constipation, Dizziness, Dyspnoea; Dysuria, Feeling abnormal, Full blood count normal, Headache, Metabolic function test normal; Renal pain, Urine analysis normal, Vomiting More
Patient presents for adverse reaction to vaccine. Reports receiving both the Anthrax and Typhoid vac... Patient presents for adverse reaction to vaccine. Reports receiving both the Anthrax and Typhoid vaccine on 03 Jul 2025. He started feeling bad right away and reports low back pain since 04 Jul. Started having migraines since 06 Jul and had 2 episodes of emesis- bile and chills on 08 Jul. He states he doesn't get migraines but he assumed it was a migraine. Headache is currently 3/10. Reports consistent kidney pain and difficulty with urination and bowel movements. Also reports dizziness and mild difficulty breathing at times. More
2851856 1 F PA 07/30/2025 HEPA
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 H3N97
Y015551
Z005233
Pyrexia, Rash; Pyrexia, Rash; Pyrexia, Rash Pyrexia, Rash; Pyrexia, Rash; Pyrexia, Rash
fever and rash. parent admin tylenol and motrin fever and rash. parent admin tylenol and motrin
2851857 19 F OH 07/30/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 H4279
Loss of consciousness, Presyncope Loss of consciousness, Presyncope
vasovagal response, loss of consciousness, laid patient flat on floor, patient returned to conscious... vasovagal response, loss of consciousness, laid patient flat on floor, patient returned to consciousness after laying flat, patient evaluated, slowly raised to sitting position, waited an additional 10 minutes prior to standing position, patient left accompanied by mother More
2851858 36 F CA 07/30/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 FF2593
FF2593
FF2593
3203083
3203083
3203083
Arrhythmia, Atrial flutter, Endotracheal intubation, Laboratory test, Laryngeal ... Arrhythmia, Atrial flutter, Endotracheal intubation, Laboratory test, Laryngeal dyskinesia; Laryngomalacia, Loss of consciousness, Raynaud's phenomenon, Seizure, Tracheal dilation procedure; Tracheostomy; Arrhythmia, Atrial flutter, Endotracheal intubation, Laboratory test, Laryngeal dyskinesia; Laryngomalacia, Loss of consciousness, Raynaud's phenomenon, Seizure, Tracheal dilation procedure; Tracheostomy More
After the first vaccine in 10/2021 within weeks I started to have aflutter in my heart and passing o... After the first vaccine in 10/2021 within weeks I started to have aflutter in my heart and passing out at work. I had to be admitted to the hospital. I filled a workmans comp claim and was denied. I was forced to get the second vaccine as well and within a month I started to have raynauds syndrome in my hands and feet, heart arrythmias , seizures, adult onset laryngomalacia and paradoxical vocal fold motion disorder. I was hospitalized several times, told I was lying and drug seeking. I was intubated over 6 times and had to have multiple surgeries to open my airway. Due to the delayed care and medical malpractice I ended up with a tracheostomy for 9 months. I have had a couple surgeries since I got the trach out in 2023. The last surgery I had to dilate my airway was may 16th 2025. I still use oxygen at night and am fighting for social security. More
✓ ✓
2851859 52 F MO 07/30/2025 UNK
VARZOS
 UNKNOWN MANUFACTURER
GLAXOSMITHKLINE BIOLOGICALS
 t5d73
3273h
Neck pain, Pain in extremity, Pain in jaw, Tenderness; Neck pain, Pain in extrem... Neck pain, Pain in extremity, Pain in jaw, Tenderness; Neck pain, Pain in extremity, Pain in jaw, Tenderness More
Patient states was having pain in the left arm (even to the touch) a couple of days after shingrix a... Patient states was having pain in the left arm (even to the touch) a couple of days after shingrix and engerix were administered. Stated it started in the area of the vaccines but now has travelled up to her neck/jaw. No redness or rash indicated . patient states going to contact primary physician to be seen. More
2851860 34 F VA 07/30/2025 TDAP
 SANOFI PASTEUR
 U8564AA
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient received TDAP vaccine instead of intended HPV vaccine 2nd dose. Patient returned next day to... Patient received TDAP vaccine instead of intended HPV vaccine 2nd dose. Patient returned next day to receive correct vaccine. No adverse effects noted from either vaccine, unknown how long it has been since pt last had TDAP since pt was from out of state. More
2851861 07/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Inappropriate schedule of product administration Inappropriate schedule of product administration
Second dose was administered 46 days after the first Shingrix vaccine; This non-serious case was rep... Second dose was administered 46 days after the first Shingrix vaccine; This non-serious case was reported by a pharmacist via sales rep and described the occurrence of drug dose administration interval too short in a patient who received Herpes zoster (Shingrix) for prophylaxis. Concomitant products included Varicella zoster vaccine rgE (CHO) (Shingrix). On 16-JUL-2025, the patient received the 2nd dose of Shingrix (unknown deltoid). On 16-JUL-2025, an unknown time after receiving Shingrix, the patient experienced drug dose administration interval too short (Verbatim: Second dose was administered 46 days after the first Shingrix vaccine). The outcome of the drug dose administration interval too short was not applicable. Additional Information: GSK Receipt Date: 21-JUL-2025 The pharmacist reported that a patient was administered second dose of vaccine 46 days after the first dose of Shingrix vaccine which led to shortening of vaccination schedule. More
2851862 1 F OK 07/30/2025 HEPA
MMRV
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 L9R92
Y008885
Z003766
Extra dose administered, Pyrexia, Rash; Extra dose administered, Pyrexia, Rash; ... Extra dose administered, Pyrexia, Rash; Extra dose administered, Pyrexia, Rash; Extra dose administered, Pyrexia, Rash More
Patient began running fever on 7/26/2025 one day after receiving vaccinations (including 2 doses of... Patient began running fever on 7/26/2025 one day after receiving vaccinations (including 2 doses of Varicella given in error). Patient broke out in rash the morning of 7/28/2025, 3 days after receiving vaccinations, Patient was prescribed Prednisolone 10mg/5mL give 2.5 mL in AM with food, continue cetirizine. More
2851863 13 F VA 07/30/2025 HPV9
MNQ
TDAP
 MERCK & CO. INC.
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 X026668
U8493AA
CX4HL
Clonus, Crying, Eye movement disorder, Feeling hot, Nausea; Clonus, Crying, Eye ... Clonus, Crying, Eye movement disorder, Feeling hot, Nausea; Clonus, Crying, Eye movement disorder, Feeling hot, Nausea; Clonus, Crying, Eye movement disorder, Feeling hot, Nausea More
Patient into Health Department for required 7th grade vaccinations. TDAP administered first in LA, M... Patient into Health Department for required 7th grade vaccinations. TDAP administered first in LA, MCV-4 Quad administered next in LA, & HPV 9 administered last in RA. A few seconds after removal of needle from RA, patient complained of being hot, color turned ashen, then patient started heavy breathing, eyes rolled back and mild clonic response of upper and lower extremities was noted without loss of any bladder control. Clonic response lasted only several seconds then patient took very long deep breath and asked "what happened". Client was advised to put head between legs and take slow deep breaths. Ice pack was obtained and place on nape of neck. BP attempted immediately with electronic cuff, unable to initially read BP due to patient being upset, crying, and moving around. Patient calmed and and BP attempted again around 11:17 with a reading of 58/32, HR 71. Patient with c/o nausea but never did vomit. Client given apple juice to sip and fan obtained to provide cool air to patient. Patient's BP repeated at approximately 11:28 after patient had taken several sips of the juice, BP - 74/46, HR - 66. Patient continued to sit in chair with mother at her side. Patient began talking about her interest with color slowly returning to her skin and continuing to sip juice. At approximately 11:38, patient's color to skin had returned to close of that prior to vaccination. Patient stated feeling better with no c/o dizziness. Advised patient to slowly stand. BP 89/60, HR - 68. Patient denied any complaints at this time, other than "being tired". Color pink, vitals WNL. Patient ambulated out into lobby with mother and undersigned in attendance. Patient tol well. Client exited building with her mother & siblings at approximately 11:50 am. Mother was present during whole incident. More
2851864 12 M TX 07/30/2025 DTAP
MNQ
 GLAXOSMITHKLINE BIOLOGICALS
NOVARTIS VACCINES AND DIAGNOSTICS
 5KR3R
DL4YY
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
Nurse was to administer Tdap vaccine, per provider order. Pulled and administered DTap vaccine, and ... Nurse was to administer Tdap vaccine, per provider order. Pulled and administered DTap vaccine, and then realized she had given the incorrect vaccine upon documenting vaccine. Provider and parent was made aware. Call made to GSK to notify and request recommendation for further administration of tetanus vaccine. More
2851865 1 M 07/30/2025 MMR
 MERCK & CO. INC.
 Y013131
Papule, Rash vesicular Papule, Rash vesicular
Measles like rash across body, pink papules Measles like rash across body, pink papules
2851866 5 F MI 07/30/2025 DTPPVHBHPB
 MSP VACCINE COMPANY
 U7446AA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Vaccine error - Vaxelis given outside of recommended guideline. Vaccine error - Vaxelis given outside of recommended guideline.
2851867 1.25 F MI 07/30/2025 DTPPVHBHPB
 MSP VACCINE COMPANY
 U7788AA
Extra dose administered Extra dose administered
Vaccine error - gave Vaxelis as 4th dose. Vaccine error - gave Vaxelis as 4th dose.
2851868 2.83 M LA 07/30/2025 UNK
 UNKNOWN MANUFACTURER
Pyrexia Pyrexia
patient had low grade fevers starting that night that continued around 101-102 for 3 days then spike... patient had low grade fevers starting that night that continued around 101-102 for 3 days then spiked to 104.5 on day 3 after vaccine. This had happened after first dose as well, but was not reported to the office More
2851869 3 M MI 07/30/2025 DTPPVHBHPB
 MSP VACCINE COMPANY
 U7788AA
Extra dose administered Extra dose administered
Vaccine Error - Vaxelis given as dose 4 Vaccine Error - Vaxelis given as dose 4
2851870 12 F FL 07/30/2025 HPV9
MNQ
 MERCK & CO. INC.
SANOFI PASTEUR
 Y014510
U8494AA
Gait disturbance, Hemiparesis; Gait disturbance, Hemiparesis Gait disturbance, Hemiparesis; Gait disturbance, Hemiparesis
Dad reports the day after immunizations to administration to the left arm, had left sided weakness a... Dad reports the day after immunizations to administration to the left arm, had left sided weakness along with difficulties walking on the left leg. States lasted about a couple of days. Has no issues walking today in clinic. No numbness, tingling or pain. Unsure if administration played a role. No other symptoms or concerns. More
2851871 16 M FL 07/30/2025 MENB
MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
PFIZER\WYETH
 DD72H
LF5302
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Patient was accidently given Bexsero and Trumenba. Provider was made aware and contacted the family.... Patient was accidently given Bexsero and Trumenba. Provider was made aware and contacted the family. Provider also follow up with the family today. More
2851872 35 M MI 07/30/2025 HPV9
 MERCK & CO. INC.
 Z007667
Face injury, Fall, Loss of consciousness Face injury, Fall, Loss of consciousness
Patient presented to office for nurse visit for Tdap, MMR, Hep A and HPV. Received Tdap and Hep A i... Patient presented to office for nurse visit for Tdap, MMR, Hep A and HPV. Received Tdap and Hep A in right deltoid and MMR and Hep A in left deltoid without difficulty. VIS was given, and patient was informed to call with any questions or concerns. See imms/injections for more details. At 9:45 am pt passed out post HPV vaccine (last one given in left deltoid). Was sitting on the bed, as I was lying pt down, passed out and fell to his right side, landing face down first and hitting face down on the floor. Pt hit his nose and right side of cheek. Noticeable red marks seen on his nose and right cheek. Dr. and other MA's and staff were called in the room for help. BP was checked and it was high at first, pt laid on the flood for good 10-15 minutes, crackers and juice were given to help him recuperate. BP were checked a few times and were normal before patient left (see vitals for review). Per pt he felt good, just sore from fall, but was good to leave. More
2851873 12 F TX 07/30/2025 HPV9
MNQ
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
 Y015599
X7R4Z
Nervousness; Nervousness Nervousness; Nervousness
Pt was nervous for vaccines after giving vaccines patient lend back of the chair that's when we... Pt was nervous for vaccines after giving vaccines patient lend back of the chair that's when we gave the patients water took vitals, the vitals was stable patient stayed for 15 minutes for evaluation and was fine and left. The following vital sign readings: at 12:20 pm BP: 96/75 - HR: 69 ' SAT: 94%. At 12:35 pm : BP: 100/79 - HR: 82' - SAT: 99% Also notice the provider about above information. More
2851875 1.33 F MI 07/30/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK234AB
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient got pentacel vaccine instead of a daptacel vaccine on the left thigh and got a hib on the ... Patient got pentacel vaccine instead of a daptacel vaccine on the left thigh and got a hib on the right thigh. As soon as the error was noticed the manager was alerted. health department was called and notified of the situation, and they said no adverse reaction would occur. Patients' mom was notified, and she said the patient was normal but in case of any reaction, she would contact the clinic. More
2851876 18 F 07/30/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 JF7DM
Wrong product administered Wrong product administered
patient was given a a dose of Dtap Infanrix insead of Tdap Boostrix patient was given a a dose of Dtap Infanrix insead of Tdap Boostrix
2851877 18 F NJ 07/30/2025 MNQ
 SANOFI PASTEUR
 U8369BA
Fall, Loss of consciousness Fall, Loss of consciousness
Within 10 minutes of receiving the vaccine, patient lost her consciousness and fell to the ground. P... Within 10 minutes of receiving the vaccine, patient lost her consciousness and fell to the ground. Patient regained consciousness in a few seconds but refused EMS. After drinking some water and sat around for about 10 minutes, patient left on her own. More
2851878 75 F SD 07/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 2hj99
Rash Rash
patient reported that the first vaccine did not cause any issues, but the second dose caused a rash ... patient reported that the first vaccine did not cause any issues, but the second dose caused a rash to her face More
2851879 58 F AK 07/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3J2S2
Arthralgia, Feeling hot Arthralgia, Feeling hot
Right shoulder pain onset the afternoon on day of injection and persisting to present. Pain in ante... Right shoulder pain onset the afternoon on day of injection and persisting to present. Pain in anterolateral shoulder/detoid with overhead movements. No prior history of shoulder pain or injury. Treating with NSAIDs, avoid aggravating activities, PT. More
2851880 32 F KY 07/30/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 JANSSEN
JANSSEN
JANSSEN
JANSSEN
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 204A21A
204A21A
204A21A
204A21A
8000010
8000010
8000010
8000010
GJ5083
GJ5083
GJ5083
GJ5083
Acoustic stimulation tests, Balance disorder, Deafness unilateral, Dizziness, Dy... Acoustic stimulation tests, Balance disorder, Deafness unilateral, Dizziness, Dysstasia; Exposure during pregnancy, Glycosylated haemoglobin, Hypotension, Influenza, Magnetic resonance imaging; Photophobia, Respiratory tract infection viral, Sinusitis, Sudden hearing loss, Tinnitus; Vomiting; Acoustic stimulation tests, Balance disorder, Deafness unilateral, Dizziness, Dysstasia; Exposure during pregnancy, Glycosylated haemoglobin, Hypotension, Influenza, Magnetic resonance imaging; Photophobia, Respiratory tract infection viral, Sinusitis, Sudden hearing loss, Tinnitus; Vomiting; Acoustic stimulation tests, Balance disorder, Deafness unilateral, Dizziness, Dysstasia; Exposure during pregnancy, Glycosylated haemoglobin, Hypotension, Influenza, Magnetic resonance imaging; Photophobia, Respiratory tract infection viral, Sinusitis, Sudden hearing loss, Tinnitus; Vomiting More
By November 2022, I was in my 5th month of pregnancy and suddenly began experiencing severe vomiting... By November 2022, I was in my 5th month of pregnancy and suddenly began experiencing severe vomiting and debilitating dizziness that made it difficult to stand. They always associated it with my pregnancy and low blood pressure during this time. By April 2023, I realized I could not hear from my right ear. An auditory test showed a sudden hearing loss and as a result, tinnitus. Throughout 2024 and 2025, I experienced multiple flu episodes along with dizziness, vomiting, loss of balance, and light sensitivity. The diagnosis was sinusitis. In less than 6 months, I have undergone 3 treatments with antibiotics, and I continue to have relapses from viruses in the respiratory tract. More
✓
2851881 80 M FL 07/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 75323J
Injection site bruising, Injection site erythema, Injection site pruritus Injection site bruising, Injection site erythema, Injection site pruritus
Bruising, redness, itching at injection site Bruising, redness, itching at injection site
2851882 3 M NM 07/30/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 34MF9
Extra dose administered Extra dose administered
Pt is three and received vaccine rated for 4-6 years Pt is three and received vaccine rated for 4-6 years
2851883 17 F OR 07/30/2025 VARCEL
 MERCK & CO. INC.
 X024540
Rash, Rash papular Rash, Rash papular
Developed rash on hands about 10 days after receiving Varicella & MMR vaccines together, the ras... Developed rash on hands about 10 days after receiving Varicella & MMR vaccines together, the rash swells and hurts but doesn't itch much and by the time the family reported it to our clinic it was mostly resolving - the only reason they called to report it was because she's due for the second dose soon and they weren't sure if she should have it yet. More
2851884 18 F TN 07/30/2025 MNQ
 SANOFI PASTEUR
 U8558AA
Extra dose administered Extra dose administered
EXTRA MENINGOCOCCAL VACCINE GIVEN EXTRA MENINGOCOCCAL VACCINE GIVEN
2851885 82 M NY 07/30/2025 COVID19
COVID19
 MODERNA
MODERNA

Colonoscopy normal, Dyspnoea, Endoscopy normal, Fatigue, Haemoglobin decreased; ... Colonoscopy normal, Dyspnoea, Endoscopy normal, Fatigue, Haemoglobin decreased; Somnolence More
Excessive tiredness, could not walk more than 50 ft without having to stop and catch my breath. Slee... Excessive tiredness, could not walk more than 50 ft without having to stop and catch my breath. Sleepiness all the time. More
2851886 58 F IN 07/30/2025 PNC20
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS

Erythema, Pruritus; Erythema, Pruritus Erythema, Pruritus; Erythema, Pruritus
red circle from top of arm to arm pit, outline of circle. itchiness. 1 week later and is still red, ... red circle from top of arm to arm pit, outline of circle. itchiness. 1 week later and is still red, circle and itchy More
2851887 40 M 07/30/2025 TDAP
 UNKNOWN MANUFACTURER
 C3SB5
Herpes zoster, Rash, Rash vesicular Herpes zoster, Rash, Rash vesicular
Today (Monday) he has clusters of vesicles in the axilla, over his left biceps, and on his left post... Today (Monday) he has clusters of vesicles in the axilla, over his left biceps, and on his left posterior shoulder; Herpes zoster-diagnosed with shingles/ it's not really painful enough to be shingles; It could be folliculitis; began to develop a slightly painful, not itchy vesicular rash in his left axilla; slightly painful, not itchy vesicular rash in his left axilla; This non-serious case was reported by a physician via other manufacturer and described the occurrence of shingles in a 40-year-old male patient who received DTPa (Reduced antigen) (Tdap Vaccine) (batch number C3SB5) for prophylaxis. Co-suspect products included tuberculin ppd (Tubersol) solution for injection (batch number 83821) for tuberculin test. The patient's past medical history included exposure to communicable disease. On 06-MAY-2025, the patient received Tdap Vaccine (left deltoid) and Tubersol .1 ml. On 08-MAY-2025, 2 days after receiving Tdap Vaccine and Tubersol, the patient experienced shingles (Verbatim: Herpes zoster-diagnosed with shingles/ it's not really painful enough to be shingles), folliculitis (Verbatim: It could be folliculitis), vesicular rash (Verbatim: began to develop a slightly painful, not itchy vesicular rash in his left axilla) and axillary pain (Verbatim: slightly painful, not itchy vesicular rash in his left axilla). On 09-MAY-2025, the patient experienced blister (Verbatim: Today (Monday) he has clusters of vesicles in the axilla, over his left biceps, and on his left posterior shoulder). The outcome of the shingles, folliculitis, vesicular rash, axillary pain and blister were resolving. It was unknown if the reporter considered the shingles, folliculitis, vesicular rash, axillary pain and blister to be related to Tdap Vaccine and Tubersol. It was unknown if the company considered the shingles, folliculitis, vesicular rash, axillary pain and blister to be related to Tdap Vaccine and Tubersol. Additional Information: GSK Receipt Date: 01-JUL-2025 The physician reported that the patient started taking (Tubersol) tuberculin test, (once) via left forearm for Tuberculin test and received an unknown dose of suspect diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TD AP), via unknown route in the left deltoid for prophylactic vaccination (Immunization) and both with unknown strength and expiry date. The patient experienced slightly painful, not itchy vesicular rash in his left axilla. Today (Monday) on 09-MAY-2025, 3 days after, he had clusters of vesicles in the axilla, over his left biceps, and on his left posterior shoulder and diagnosed with shingles after treated with tuberculin test (Tubersol) and diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP). On 13-MA Y-2025 at 12:00 hours, 7 days 12 hours after, the patient developed diagnosed with shingles (herpes zoster). Reportedly, it could be folliculitis although he had no unusual exposure, it was not really painful enough to be shingles. It was not reported if the patient received a corrective treatment for both the events. At time of initial reporting, the outcome was not recovered or not resolved for the event rash vesicular and recovering for the events herpes zoster and rash. Additional information was received on 04-Jun-2025 from physician and update the outcome from ongoing to recovering for the event rash. More
2851888 0.33 M KS 07/30/2025 DTAPIPV
DTPPVHBHPB
HIBV
RV1
 GLAXOSMITHKLINE BIOLOGICALS
MSP VACCINE COMPANY
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS



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; Product administered to patient of inappropriate age More
On 2/7/25, My 4 month old infant was administered the Kinrix Vaccine at (withheld) Health Center in ... On 2/7/25, My 4 month old infant was administered the Kinrix Vaccine at (withheld) Health Center in (withheld state), despite it being approved for only chikdren ages 4-6 years. This is a serious vaccine administration error and not in accordance with CDC immunization guidelines for infants. The correct vaccines for a 4 month old were due , DTap , ipv, ETC. but instead Kinrix, a vaccine formulated for older children was given. The clinic has confirmed the error and I am monitoring my child closely for any side effects. I am submitting this report to ensure the event is documented as part of national vaccine safety efforts. More
2851889 11 F WA 07/30/2025 HPV9
 MERCK & CO. INC.
 Z002903
No adverse event, Scratch No adverse event, Scratch
Tip of needle grazed patients arm resulting in a small dot of blood. Patient stayed seated for 10 mi... Tip of needle grazed patients arm resulting in a small dot of blood. Patient stayed seated for 10 minutes and when I checked on her, she expressed feeling well with no symptoms of illness or other reaction. A band-aide was placed on arm, covering both vaccine site and small needle scratch. Event was reported to covering provider and clinic supervisor. Patient left with mother with no further issues. More
2851890 07/30/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
Suspected vaccination failure; shingles on scalp; This serious case was reported by a consumer via i... Suspected vaccination failure; shingles on scalp; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: shingles on scalp). The outcome of the vaccination failure and shingles were not reported. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine. The company considered the vaccination failure to be unrelated to Shingles vaccine. It was unknown if the company considered the shingles to be related to Shingles vaccine. Additional Information: GSK Receipt Date: 22-JUL-2025 This case was reported by a patient via interactive digital media. The patient got the vaccine and knew that he/she got shingles on his/her scalp. This case was considered as suspected vaccination failure as details regarding completion of primary vaccination schedule, time to onset for shingles and laboratory confirmation regarding shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK Shingles vaccine. More
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