🏥 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 💀 🏥 🚑 ♿ ⚠️
2866505 3 F CA 10/16/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3052553
UT8802NA
Dysgeusia, Nausea, Regurgitation, Respiratory tract congestion, Vomiting; Dysgeu... Dysgeusia, Nausea, Regurgitation, Respiratory tract congestion, Vomiting; Dysgeusia, Nausea, Regurgitation, Respiratory tract congestion, Vomiting More
Unclear if related to vaccine. One day after vaccine, had nausea all day with one episode of vomitin... Unclear if related to vaccine. One day after vaccine, had nausea all day with one episode of vomiting. Since then, has been experiencing reflux symptoms (regurgitation, sour taste in mouth, nausea, congestion). More
2866506 70 F GA 10/16/2025 FLU3
PNC20
 SANOFI PASTEUR
PFIZER\WYETH
 UT8781DA
LX4482
Diarrhoea, Dyspnoea, Nausea, Vomiting; Diarrhoea, Dyspnoea, Nausea, Vomiting Diarrhoea, Dyspnoea, Nausea, Vomiting; Diarrhoea, Dyspnoea, Nausea, Vomiting
Patient called a couple hours after she returned home from receiving the vaccines saying she was nau... Patient called a couple hours after she returned home from receiving the vaccines saying she was nauseous and vomiting. She also said she was having trouble taking deep breaths. The pharmacist advised the patient to seek emergency care if she was having difficulty breathing. Patient attempted to take benadryl. Patient had husband with her. Pharmacist advised patient to seek medical treatment immediately. Pharmacist also advised patient to notify her doctor. Pharmacist called patient back to check on the patient and she had also began to have diarrhea. The patient indicated her breathing had returned to normal. Patient had previously had flu vaccines routinely in the last several years with no issue. More
2866507 36 M NJ 10/16/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 088d21a
088d21a
088d21a
088d21a
Biopsy bone marrow abnormal, Cardiac stress test, Chemotherapy, Computerised tom... Biopsy bone marrow abnormal, Cardiac stress test, Chemotherapy, Computerised tomogram, Essential thrombocythaemia; Full blood count increased, Genetic testing, Haematological malignancy, Laboratory test, Magnetic resonance imaging; Platelet count increased, Scan, Skin discolouration, Thrombosis, Whole body scan; X-ray More
A short summary, prior to 2021 I was a healthy very fit 37 year old. It was recommended and mandated... A short summary, prior to 2021 I was a healthy very fit 37 year old. It was recommended and mandated by my physician to get vaccinated. I reluctantly complied. I was given Moderna Shortly, after the shot, I started getting symptoms, such as purple feet, blood clots, elevated, platelet, and blood cell counts. Number reaching 1.1m for platelets. It took several months and years to finally be diagnosed. I went to foot doctors, cardiologist, rheumatologist, hematologist, oncologist, sports medicine doctors, I had every type of scan and test you could do. Finally, I was diagnosed with essential thrombocytosis. Essential meaning unknown. I did genetic testing and gave fingernail clippings, and it was confirmed that I was not born with this genetic disorder. It was something that was mutated. I have an identical, twin brother with the same DNA and he did not receive the Moderna Covid shot. He is perfectly fine. I am now on a chemotherapy drug for life, blood thinner, and additional medication to control the condition. I have been diagnosed with blood cancer. I went to (withheld) Cancer care with the extensive testing from Sloan Kettering. I had two bone marrow biopsies, confirming my diagnosis. Although it is tough to diagnose because I do not have the typical positive markers there are between three disorders, but they are leaning more towards the one listed, although we could go either way. They haven?t seen cases like this the numbers just don?t make sense compared to the testing. I?ve spent the last several years testing my blood anywhere from Daly, weekly monthly. my out-of-pocket expenses have been astronomical the time and impact this has had on me and my family has been detrimental. I have all medical records, pictures, and a timeline, confirming all of these statements. I am looking for guidance and help. Thank you , More
✓ ✓ ✓
2866508 78 F FL 10/16/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 my9550
ut8781da
Blood pressure increased, Confusional state, Echocardiogram normal, Positron emi... Blood pressure increased, Confusional state, Echocardiogram normal, Positron emission tomogram normal; Blood pressure increased, Confusional state, Echocardiogram normal, Positron emission tomogram normal More
Patient received 2 shots on Friday. Went to hospital Sunday night. Was discharged Tuesday. Patient r... Patient received 2 shots on Friday. Went to hospital Sunday night. Was discharged Tuesday. Patient reported increase in blood pressure and confusion. She states they did a stroke work up, ECHO cardiogram, and PET Scan. All of which came back normal. She states the doctors don't know what caused the problem or what the problem was, but noted having the vaccines was the only event out of routine. More
✓
2866509 76 M SC 10/16/2025 FLU3
 SANOFI PASTEUR
 u8855da
Joint swelling, Urticaria Joint swelling, Urticaria
Patient reported hives on arms, legs, and trunk. No hives on face or neck. Hives did not itch, burn ... Patient reported hives on arms, legs, and trunk. No hives on face or neck. Hives did not itch, burn and were not painful. No fever. No pain no itch. Ankles swollen but resolved within 12 hours. Patient went to urgent care and received a 5 day course of prednisone to resolve hives. More
2866510 72 M AL 10/16/2025 PNC20
 PFIZER\WYETH
 MA2523
Extra dose administered Extra dose administered
Patient was mistakenly given a second Prevnar 20 vaccine two years after the original first dose was... Patient was mistakenly given a second Prevnar 20 vaccine two years after the original first dose was given. More
2866511 44 F HI 10/16/2025 FLU3
 SANOFI PASTEUR
 UT8826LA
Asthenia, Pain in extremity Asthenia, Pain in extremity
Left arm pain; subjective weakness. persistent x 2 weeks Left arm pain; subjective weakness. persistent x 2 weeks
2866512 41 F CA 10/16/2025 COVID19
 MODERNA
Contusion, Immediate post-injection reaction, Muscle spasms, Pain in extremity, ... Contusion, Immediate post-injection reaction, Muscle spasms, Pain in extremity, Skin burning sensation More
Immediately the next day I had a burning skin all over my. Pain shooting up my legs, leg cramps , br... Immediately the next day I had a burning skin all over my. Pain shooting up my legs, leg cramps , bruises , I am going to do a brain mri and 3 different spinal mris More
2866516 F VA 10/16/2025 FLU3
 SEQIRUS, INC.
 AY5590A
Urticaria Urticaria
Urticaria to upper body: arms, trunk, chest, neck about 30 minutes after vaccine administration. Pat... Urticaria to upper body: arms, trunk, chest, neck about 30 minutes after vaccine administration. Patient to 50mg Benedryl which alleviated symptoms within 45 minutes. More
2867316 85 F IL 10/16/2025 FLU3
PNC20
 SEQIRUS, INC.
PFIZER\WYETH
 409493
MA2505
Arthralgia, Feeling hot, Injection site pruritus, Joint swelling; Arthralgia, Fe... Arthralgia, Feeling hot, Injection site pruritus, Joint swelling; Arthralgia, Feeling hot, Injection site pruritus, Joint swelling More
Patient called to complain of significant swelling and soreness on shoulder, half way down to elbow ... Patient called to complain of significant swelling and soreness on shoulder, half way down to elbow 3 days after receiving immunization. Complained of feeling hot (did not take temp to verify fever). 3 days after injection patient said no longer hurts but was still experiencing itching at injection site. Patient received Fluad and Prevnar in the right deltoid. More
2865872 70 M WA 10/15/2025 COVID19
PPV
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Dizziness, Fatigue, SARS-CoV-2 test; Dizziness, Fatigue, SARS-CoV-2 test Dizziness, Fatigue, SARS-CoV-2 test; Dizziness, Fatigue, SARS-CoV-2 test
dizziness; lot of fatigue; Initial information received on 26-Sep-2025 (both processed together) reg... dizziness; lot of fatigue; Initial information received on 26-Sep-2025 (both processed together) regarding an unsolicited valid non-serious case received from Patient This case involves a 70 years old male patient (12.954 cm and 84.09 kg) who experienced lot of fatigue and dizziness after receiving vaccines NVX-COV2373 (original) adjuvanted vaccine [nuvaxovid] and Pneumococcal vaccine. The patient's past vaccination(s) included RSV VACCINE for Respiratory syncytial virus (RSV) immunisation and VARICELLA ZOSTER VACCINE for immunization on unknown date, Janssen Covid vaccine on 25-Oct-2021 and Novavax on 12-Oct-2023 for covid-19 immunization and other shots. The patient's son and his wife had COVID-19 (family history). The patient's past medical treatment(s) was not provided. On unknown date in 2023, patient had SARS-CoV-2 test using home test kit sent by the Department of Health which resulted as positive. On 24-Sep-2025, the patient received a Dose 2 at 0.5 mL dose of suspect NVX-COV2373 (original) adjuvanted vaccine injection (strength and lot number not reported) via unknown route in the left arm for covid-19 immunization and suspect Pneumococcal vaccine not produced by Sanofi Pasteur (strength, formulation, dose and lot number not reported) via unknown route in the left arm with 2-4 inches apart for prophylactic vaccination. Information on batch number and expiry date corresponding to the one at time of event occurrence was requested. On unknown date In Sep-2025 the patient had lot fatigue (Fatigue) and dizziness (approximately few days: latency). Patient was reported that felt quite ill about a day and a half, but now totally fine and felt much better. Action taken: Not applicable. It was not reported if the patient received a corrective treatment for the events (fatigue, dizziness). At time of reporting, the outcome was Recovered / Resolved on an unknown date in September 2025 for both events. More
2865876 1.5 M ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
was administered post temperature excursion that left the product not suitable for use. Vaccine wa... was administered post temperature excursion that left the product not suitable for use. Vaccine was used at a flu clinic post excursion due to human error with no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 6 months old male patient who was administered INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE [FLUZONE] post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5 ml dose of suspect INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE Suspension for injection (lot U8827AA, Expiry date: 30-Jun-2026, strength: standard) via unknown route in right arm as immunization and was administered post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event (product storage error; latency: same day) Reason: refrigerator temperature knob was accidentality turned down Max temperature reached: 25.7F DEGREES Duration: 4 hours and 17 minutes Previous Excursion? No Human error? Y Administered post excursion? Yes Does extended stability data cover the excursion? NO Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865877 4 M ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
was administered post temperature excursion that left the product not suitable for use. Vaccine wa... was administered post temperature excursion that left the product not suitable for use. Vaccine was used at a flu clinic post excursion due to human error with no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 years old male patient who was administered INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE [FLUZONE] post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5 ml of suspect INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE Suspension for injection (lot U8827AA, Expiry date: 30-Jun-2026, strength: standard) via unknown route in the right arm as immunization and was administered post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event (product storage error: latency: same day) Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865878 15 F ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
refg temp knob was accidentality turned downMax temperature reached: 25.7F Duration: 4 h17 with no a... refg temp knob was accidentality turned downMax temperature reached: 25.7F Duration: 4 h17 with no ae; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 15 years old female patient received Influenza USP Trival A-B Subvirion No Preservative Vaccine [Fluzone that had a temperature excursion where the refrigerator temperature knob was accidentally turned downmax temperature reached: 25.7f duration: 4 h17 with no ae (adverse event). The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025 the patient received a dose of 0.5ml of suspect Influenza USP Trival A-B Subvirion No Preservative Vaccine Suspension for injection (lot U8827AA and expiry date-30-Jun-2026) via intramuscular route in the right arm for Immunization that had a temperature excursion where the refrigerator temperature knob was accidentally turned down max temperature reached: 25.7f duration: 4 h17 with no ae (product storage error) (unknown latency). Reportedly- extended stability data does not cover the excursion, human error was involved (temperature knob was accidentality turned down), The product was administered. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865879 3 M ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
was administered post temperature excursion that left the product not suitable for use. Vaccine wa... was administered post temperature excursion that left the product not suitable for use. Vaccine was used at a flu clinic post excursion due to human error with no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 3 years old male patient who experienced was administered INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE [FLUZONE] post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5 ml dose of suspect INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE Suspension for injection (lot U8827AA, Expiry date: 30-Jun-2026, strength: standard) via unknown route in the left arm as immunization and was administered post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event (product storage error; latency: same day) Reason: refrigerator temperature knob was accidentality turned down Max temperature reached: 25.7F DEGREES Duration: 4 hours and 17 minutes Previous Excursion? No Human error? Y Administered post-excursion? Yes Does extended stability data cover the excursion? NO Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865880 10 F ID 10/15/2025 FLU3
FLU3
FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 U8827AA
U8827AA
U8827AA
U8827AA
No adverse event, Product storage error; No adverse event, Product storage error... No adverse event, Product storage error; No adverse event, Product storage error; No adverse event, Product storage error; No adverse event, Product storage error More
patient received Fluzone which was exposed to temperature excursion due to refrigerator temperature ... patient received Fluzone which was exposed to temperature excursion due to refrigerator temperature knob was accidentality turned down and Max temperature reached: 25.7 degree Fahrenheit for 4 hours and 17 minutes with no adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case was linked to US-SA-2025SA301769. This case involves a 10 years old female patient who received Influenza Usp Trival A-B Subvirion No Preservative Vaccine [Fluzone] which was exposed to temperature excursion due to refrigerator temperature knob was accidentality turned down and maximum temperature reached was 25.7 degree Fahrenheit for 4 hours and 17 minutes with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5ml dose of suspect Influenza Usp Trival A-B Subvirion No Preservative Vaccine (once), Suspension for injection, Strength Standard, lot U8827AA and expiry date 30-Jun-2026 for immunisation, which was exposed to temperature excursion due to refrigerator temperature knob was accidentality turned down and maximum temperature reached was 25.7 degree Fahrenheit for 4 hours and 17 minutes with no adverse event (product storage error) (Latency Same day). Reportedly, this excursion occurred due to a human error, extended stability data did not cover the excursion. Vaccine did not had any previous excursion. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.; Sender's Comments: US-SA-2025SA301769: More
2865881 8 F ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
was administered post temperature excursion that left the product not suitable for use. Vaccine wa... was administered post temperature excursion that left the product not suitable for use. Vaccine was used at a flu clinic post excursion due to human error with no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 8 years old female patient who was administered INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE [FLUZONE] post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5 ml dose of suspect INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE Suspension for injection (lot U8827AA, Expiry date: 30-Jun-2026) via unknown route in the right arm as immunization and was administered post temperature excursion that left the product not suitable for use. vaccine was used at a flu clinic post excursion due to human error with no reported adverse event (product storage error; latency: same day) Reason: refrigerator temperature knob was accidentality turned down Max temperature reached: 25.7F DEGREES Duration: 4 hours and 17 minutes Previous Excursion? No Human error? Y Administered post-excursion? Yes Does extended stability data cover the excursion? NO Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865882 9 M ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
temperature excursion: temperature reached: 25.7 f degrees duration: 4 hours and 17 minutes with no ... temperature excursion: temperature reached: 25.7 f degrees duration: 4 hours and 17 minutes with no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 9 years old male patient who was administered to Influenza Usp Trival A-B Subvirion No Preservative Vaccine [Fluzone] which had temperature excursion: temperature reached: 25.7 F degrees duration: 4 hours and 17 minutes with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5mL of suspect Influenza Usp Trival A-B Subvirion No Preservative Vaccine, Suspension for injection (lot U8827AA, expiry date 30-Jun-2026, frequency once and strength standard) via intradermal route in the right arm for Immunisation and temperature excursion: temperature reached: 25.7 f degrees duration: 4 hours and 17 minutes with no reported adverse event (product storage error). Reportedly, human error occurred as refrigerator temperature knob was accidentality turned down. There was no Previous Excursion and administered post-excursion. The extended stability data did not cover the excursion. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865883 6 M ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
fluzone np that was administered post temperature excursion, refrigerator temperature knob was accid... fluzone np that was administered post temperature excursion, refrigerator temperature knob was accidentality turned down, temperature reached: 25.7f wih no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case was linked to US-SA-2025SA301769. This case involves a 6 years old male patient who received Influenza Usp Trival A-B Subvirion No Preservative Vaccine [Fluzone] which was exposed to temperature excursion due to refrigerator temperature knob was accidentality turned down and maximum temperature reached was 25.7 degree Fahrenheit for 4 hours and 17 minutes with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5ml dose of suspect Influenza Usp Trival A-B Subvirion No Preservative Vaccine (once), Suspension for injection, Strength Standard, lot U8827AA and expiry date 30-Jun-2026 via unknown route into Right arm for immunisation, which was exposed to temperature excursion due to refrigerator temperature knob was accidentality turned down and maximum temperature reached was 25.7 degree Fahrenheit for 4 hours and 17 minutes with no adverse event (product storage error) (Latency Same day). Reportedly, this excursion occurred due to a human error, extended stability data did not cover the excursion. Vaccine did not have any previous excursion. Action taken : Not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.; Sender's Comments: US-SA-2025SA301769: More
2865884 10 F ID 10/15/2025 FLU3
 SANOFI PASTEUR
 U8827AA
No adverse event, Product storage error No adverse event, Product storage error
refrigerator temperature knob was accidentality turned down temperature reached: 25.7f degrees 4 hou... refrigerator temperature knob was accidentality turned down temperature reached: 25.7f degrees 4 hours and 17 minutes human error? y administered post-excursion with no ae; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 10 years old female patient and refrigerator temperature knob was accidentality turned down temperature reached: 25.7f degrees 4 hours and 17 minutes human error? y administered post-excursion with no ae for vaccine INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE [FLUZONE] The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 07-Oct-2025, the patient received 0.5 ml dose of suspect INFLUENZA USP TRIVAL A-B SUBVIRION NO PRESERVATIVE VACCINE Suspension for injection (lot U8827AA, Expiry date: 30-Jul-2026, strength: standard) via unknown route in the left arm as immunization and refrigerator temperature knob was accidentality turned down temperature reached: 25.7f degrees 4 hours and 17 minutes human error? y administered post-excursion with no ae (product storage error) (latency: same day) FLUZONE NP that was administered post temperature excursion that left the product not suitable for use. Vaccine was used at a flu clinic post excursion previous Excursion? No Does extended stability data cover the excursion? NO Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.; Sender's Comments: US-SA-2025SA301769: More
2865886 0.25 F TX 10/15/2025 FLU3
 SANOFI PASTEUR
 UT8770JA
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
gave a 3-and-a-half-month-old patient a FLUZONE NP with no adverse event; Initial information receiv... gave a 3-and-a-half-month-old patient a FLUZONE NP with no adverse event; Initial information received on 09-Oct-2025 regarding an unsolicited valid non-serious case received from other health professional. This case involves 3 and a half months old female patient who received a influenza USP trival A-B subvirion NO preservative vaccine [Fluzone] with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 08-Oct-2025, the patient received dose 1 of 0.5 ml of suspect influenza USP trival A-B subvirion NO preservative vaccine Suspension for injection of standard strength with lot UT8770JA and expiry date 30-Jun-2026 via intramuscular route in the right thigh for Influenza (Influenza immunisation) with no adverse event (product administered to patient of inappropriate age) (Latency same day). Reportedly, reporter mentioned that she gave a 3-and-a-half-month-old patient a fluzone NP, which they are not supposed to get until 6 months Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865887 PA 10/15/2025 FLU3
 SANOFI PASTEUR
No adverse event, Wrong product administered No adverse event, Wrong product administered
inappropriate use due to administration of wrong vaccine to a patient with no reported adverse event... inappropriate use due to administration of wrong vaccine to a patient with no reported adverse event; Initial information received on 09-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a patient with unknown age and gender who was administered to Influenza Usp Trival A-B Subvirion No Preservative Vaccine [Fluzone] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect Influenza Usp Trival A-B Subvirion No Preservative Vaccine, Suspension for injection (lot number, expiry date and strength not reported) via unknown route in unknown administration site for Influenza and it was inappropriately used due to administration of wrong vaccine to a patient with no reported adverse event (wrong product administered) (latency same day). Information on the batch number was requested corresponding to the one at time of event occurrence. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2865918 F 10/15/2025 COVID19
 UNKNOWN MANUFACTURER
Chills, Fatigue, Feeling cold, Tremor Chills, Fatigue, Feeling cold, Tremor
I got really, really cold; I was shaking though; I was shivering and my teeth were chattering; I was... I got really, really cold; I was shaking though; I was shivering and my teeth were chattering; I was tired from it. I mean, it tired me out; Initial information received on 02-Oct-2025 regarding an unsolicited valid non-serious case received from patient This case involves a 68 years old female patient who got really, really cold, shivering and my teeth were chattering, shaking though, and tired from it which means it tired her out after receiving NVX-COV2705 (omicron JN.1) adjuvanted vaccine [Novavax Covid-19 Vaccine, Adjuvanted]. The patient's past medical history included Pain in extremity and Feeling cold on unknown date and COVID-19 in Aug-2024 The patient's past medical treatment included Paxlovid in 2024 for covid. The patient's past vaccination(s) included moderna for covid-19 immunization. The patient's past family history was not provided. At the time of the event, the patient had ongoing Neoplasm malignant. On an unknown date, the patient received unknown dose number of suspect NVX-COV2705 (omicron JN.1) adjuvanted vaccine Injection (with unknown dose and lot number, strength and expiry date) via unknown route in unknown administration site for covid-19 immunization. On an unknown date the patient reported that she got really, really cold (feeling cold), had shivering her teeth were chattering (chills), had shaking though (tremor), and was tired from it. She mean, it tired her out (fatigue) (unknown latency). It was reported that "patient had a strong reaction that evening and what happened was patient got really, really cold, really cold. Patient put on sweats and a heavy bathrobe, and we turned the electric blanket on in the bed, and patient was shaking though, Patient was shivering, and her teeth were chattering, and patient was just really, really, really cold and patient got into bed with lots of blankets and the electric blanket, and her husband laid down with me and held me. Patient was shivering, she was really shivering, and it was over in 40 minutes, done, no more reaction and she was tired from it. She means, it tired her out. She went to be the next day, perfectly fine. No, no hangover and nothing. But she did have a past 40 minutes of, you know, shivering and teeth chattering and feeling really, really cold. So, she wants to have another Novavax. It's been 13 months since she had COVID and Paxlovid and it's been years since she had my last Novavax. I sort of feel, and she don't know, but she sort of think that my reaction was so strong because she had had COVID and Paxlovid only eight weeks before. She not a medical person, but she pretty sure she read in places that having had COVID before getting a vaccine can increase your reaction. She would like to know if you think that it's possible that getting the vaccine so close to having been ill with COVID and, you know, probably having a lot of antibodies in me from both Paxlovid and COVID caused the extreme reaction that occurred, and she say extreme, it was worse than the other reactions, but it only lasted for 40 minutes, we timed it. So, that's what she asking about. Before you go any further, she already talked to my doctor. Her doctor is useless because she said she's never heard of anyone getting chills from a vaccine. You know, that was not a helpful thing because Moderna, Pfizer, and Novavax, they all say you can get chills. And she think being cold is a chill, but nobody will tell her if that's chills, what she went through. Did she go through chills" Action taken: Not applicable. It was not reported if the patient received corrective treatment for the events. She put on sweats and a heavy bathrobe, and turned the electric blanket on in the bed. At time of reporting, the outcome was Recovered / Resolved on an unknown date for all events. More
2865920 0.17 M 10/15/2025 PNC20
RV1
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS

Pyrexia; Pyrexia Pyrexia; Pyrexia
101.6 fever in a 2 month old 101.6 fever in a 2 month old
2865980 43 F SC 10/15/2025 FLU3
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 9cc9k
f9k3l
Injection site erythema, Injection site nodule, Injection site warmth, Pruritus;... Injection site erythema, Injection site nodule, Injection site warmth, Pruritus; Injection site erythema, Injection site nodule, Injection site warmth, Pruritus More
Tdap and flu received-erythema, skin warm, knot at injection site post vaccine. continued itching-ta... Tdap and flu received-erythema, skin warm, knot at injection site post vaccine. continued itching-taking benadryl More
2865982 0.42 M IN 10/15/2025 PNC20
RV5
VARCEL
 PFIZER\WYETH
MERCK & CO. INC.
MERCK & CO. INC.
 lx2498
2117042
z004455
Wrong product administered; Wrong product administered; Wrong product administer... Wrong product administered; Wrong product administered; Wrong product administered More
Dr ordered Vaxelis on 10/14/25. I grabbed Varivax in error and administered instead of Vaxelis. Dr w... Dr ordered Vaxelis on 10/14/25. I grabbed Varivax in error and administered instead of Vaxelis. Dr was immediately notified, along with all supervisors. Poison control was called, and consulted with their Head of Infectious DIsease. Parents were notified and asked to watch for any high fever or rash. More
2865983 0.58 M MI 10/15/2025 DTAPIPV
PNC20
RV5
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.
 93H32
MA2502
Y011797
Fatigue, Irritability, Product administered to patient of inappropriate age; Fat... Fatigue, Irritability, Product administered to patient of inappropriate age; Fatigue, Irritability, Product administered to patient of inappropriate age; Fatigue, Irritability, Product administered to patient of inappropriate age More
Pt received Kinrix, not appropriate for age. Parent states pt did not seem any different other than ... Pt received Kinrix, not appropriate for age. Parent states pt did not seem any different other than the typical fatigue and slight fussiness following vaccine administration. More
2865984 64 10/15/2025 FLU3
 SANOFI PASTEUR
 U8800DA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
PATIENT IS 64 YOF WHO RECEIVED HIGH DOSE FLUE VACCINE INSTEAD OF REGUALR DOSE. PROVIDER CONTACTED PA... PATIENT IS 64 YOF WHO RECEIVED HIGH DOSE FLUE VACCINE INSTEAD OF REGUALR DOSE. PROVIDER CONTACTED PATIENT DIRECTLY AFTER TO INFORM THEM OF INCIDENT AND THAT THERE WOULD BE NO HARM. More
2865986 63 F FL 10/15/2025 FLU3
 SANOFI PASTEUR
 u8823ba
Contusion Contusion
Extreme Brusing Extreme Brusing
2865987 12 F VA 10/15/2025 COVID19
 MODERNA
 8146545
Headache, Pain, Pyrexia, Vomiting Headache, Pain, Pyrexia, Vomiting
Fever to 105+, headache, multiple episodes of vomiting, body aches. Symptoms develop approx 12 hour... Fever to 105+, headache, multiple episodes of vomiting, body aches. Symptoms develop approx 12 hours after the vaccine and remained severe for about 12 hours. Was still achy at 48 hours after the vaccine but no longer vomiting or having fever. Exam was normal at 48 hours. More
2865988 48 F MI 10/15/2025 FLU3
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8881BA
U8620BA
Pain in extremity, Sleep disorder; Pain in extremity, Sleep disorder Pain in extremity, Sleep disorder; Pain in extremity, Sleep disorder
Patient received vaccines on 9/30/25. Patient stated that she did not have any pain for 3 days, stat... Patient received vaccines on 9/30/25. Patient stated that she did not have any pain for 3 days, states that she woke up in the middle of the night and her left arm was in pain. States that she knows that the Tdap is painful and just figured that is what is was from. States by 10/14/25 the pain had not subsided so she decided to come in and have it checked out. She was trying to document through CDC but she needed information regarding the vaccine to do so. Patient has had left shoulder pain since before 2023. Had x-rays done on 2/20/23 for left shoulder pain. And also had already had right shoulder surgery. Hx of recurring acute left shoulder pain. More
2865990 0.17 F MI 10/15/2025 DTAPIPV
PNC20
RV5
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.
 93H32
MA2502
Y011797
Decreased appetite, Injection site erythema, Injection site induration, Irritabi... Decreased appetite, Injection site erythema, Injection site induration, Irritability; Decreased appetite, Injection site erythema, Injection site induration, Irritability; Decreased appetite, Injection site erythema, Injection site induration, Irritability More
Pt seen in office 10/3/2025, there was left thigh redness, hard lump under the skin. Pt was reported... Pt seen in office 10/3/2025, there was left thigh redness, hard lump under the skin. Pt was reported fussier than normal, not wanting to eat or latch on. Pt seen 10/9/2025 in office - eating normally per mom. Lump on left thigh smaller, still present. More
2865991 58 M MO 10/15/2025 FLU3
PNC20
 SEQIRUS, INC.
PFIZER\WYETH
 Ax5812A
MA2488
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Two doses of Afluria and Prevnar 20 vaccines were administered to the same patient by two different ... Two doses of Afluria and Prevnar 20 vaccines were administered to the same patient by two different pharmacists on the same day at the vaccine clinic at a nursing home. One pharmacist administered the vaccines on the left deltoid, and the other did it on the right deltoid. There were two of the same consent form were given to both pharmacists by two different nurses at that facility. More
2865992 62 F NC 10/15/2025 COVID19
 MODERNA
Influenza like illness, Pain, Pain in extremity Influenza like illness, Pain, Pain in extremity
Moderna shot given at clinic claiming old location By the time I got home within 1 or 2 hours I fel... Moderna shot given at clinic claiming old location By the time I got home within 1 or 2 hours I felt flu like symptoms severe pain in my arm body aching went to bed had flu about a week arm severely sore over 2 months and I told nurse when I got shot number 2 More
2865993 93 F OH 10/15/2025 FLU3
 SEQIRUS, INC.
 407259
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received a second dose of 2025/26 Fluad. No adverse reactions noted at this time. Patient received a second dose of 2025/26 Fluad. No adverse reactions noted at this time.
2865995 50 M WA 10/15/2025 FLU3
 SANOFI PASTEUR
 AX5589A
Pharyngeal swelling, Swelling face, Urticaria Pharyngeal swelling, Swelling face, Urticaria
Patient reports hives, facial and throat swelling in evening of 10/08/2025. Pt. did not request med... Patient reports hives, facial and throat swelling in evening of 10/08/2025. Pt. did not request medical until following morning. Pt. seen at 0700 on 10/09/2025 by medical. Hives were present at that time with no respiratory difficulty , swelling etc. More
2865996 13 F VA 10/15/2025 CHIK
CHIK
CHIK
CHIK
FLU3
FLU3
FLU3
FLU3
 BAVARIAN NORDIC
BAVARIAN NORDIC
BAVARIAN NORDIC
BAVARIAN NORDIC
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 MY9547
MY9547
MY9547
MY9547
407004
407004
407004
407004
Blood alcohol normal, Blood thyroid stimulating hormone normal, Computerised tom... Blood alcohol normal, Blood thyroid stimulating hormone normal, Computerised tomogram head normal, Computerised tomogram thorax normal, Differential white blood cell count normal; Drug screen negative, Dyspnoea, Fibrin D dimer increased, Full blood count normal, Head injury; Headache, Human chorionic gonadotropin negative, Loss of consciousness, Metabolic function test normal, Pain; Retching, Troponin normal, Urine analysis normal; Blood alcohol normal, Blood thyroid stimulating hormone normal, Computerised tomogram head normal, Computerised tomogram thorax normal, Differential white blood cell count normal; Drug screen negative, Dyspnoea, Fibrin D dimer increased, Full blood count normal, Head injury; Headache, Human chorionic gonadotropin negative, Loss of consciousness, Metabolic function test normal, Pain; Retching, Troponin normal, Urine analysis normal More
Patient experienced headache and achiness evening of 10/13/25 and took some Tylenol. Headache worsen... Patient experienced headache and achiness evening of 10/13/25 and took some Tylenol. Headache worsened and became short of breath. Patient then passed out and when awakened began dry heaving. She then went to bathroom and passed out again hitting head on door. Parents called 911 and was taken to ER . More
2865997 68 F MO 10/15/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 JS74H
No adverse event No adverse event
patient reported no adverse symptoms or signs. patient plans to get re-vaccinated with the correct v... patient reported no adverse symptoms or signs. patient plans to get re-vaccinated with the correct vaccination (fluad). More
2865998 58 M TN 10/15/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.

Bell's palsy, Ear discomfort, Eyelid function disorder, Hypoaesthesia, Orop... Bell's palsy, Ear discomfort, Eyelid function disorder, Hypoaesthesia, Oropharyngeal pain; Upper-airway cough syndrome More
After the injection i was feeling fine, Serveral hours after the vaccine i was having issues with dr... After the injection i was feeling fine, Serveral hours after the vaccine i was having issues with drainage in my neck, The next morning i had a sore throat from the drainage this lasted till saturday sunday. Monday i started having alot of pressure on my right side especially my ear. On tuesday i woke up and the right side of my face was numb and my wife noticed that i could not shut my eye. They put him on steriods for 9 days and his eye has to be shut so it dosent get try he is supposed to return to the doctor on tuesday. When we went to the doctor yesterday they said they think its bells palsay. They have him on predisone 10mg. His limbs and every are okay so they said he didn't have a stroke and he goes back on tuesday to check this. More
2865999 49 F 10/15/2025 FLU3
 SANOFI PASTEUR
 UT8779NA
Pain in extremity Pain in extremity
ARM IS SORE ARM IS SORE
2866000 66 F MA 10/15/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA4452
Headache, Malaise, Pain, Rash, Rash pruritic; Headache, Malaise, Pain, Rash, Ras... Headache, Malaise, Pain, Rash, Rash pruritic; Headache, Malaise, Pain, Rash, Rash pruritic More
I got a flu vaccine (*) and a Pfizer Covid vaccine on Monday morning 10/13 and developed an itchy r... I got a flu vaccine (*) and a Pfizer Covid vaccine on Monday morning 10/13 and developed an itchy rash on both legs overnight on Wednesday (i.e. after midnight on Tuesday, early Wed morning 10/15). I also have a non-itchy rash on my arms. I felt lousy the day after the shot, achy and had a headache but no fever. *NOTE the type/brand of flu vaccines was not labeled in the vaccine record but I assume I got the over-65 shot) More
2866001 10 F MI 10/15/2025 COVID19
 MODERNA
 3052741
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
None None
2866002 33 F GA 10/15/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 0
0
Biopsy kidney, Blood test, Computerised tomogram, Genetic testing, Glomeruloneph... Biopsy kidney, Blood test, Computerised tomogram, Genetic testing, Glomerulonephritis minimal lesion; Nephrotic syndrome, Urine analysis, X-ray More
Minimal chance disease with nephrotic syndrome Minimal chance disease with nephrotic syndrome
✓ ✓ ✓
2866005 4 F VA 10/15/2025 DTAPIPV
MMRV
 SANOFI PASTEUR
MERCK & CO. INC.
 U8209CB
Z008587
Injection site rash, Pyrexia, Rash, Varicella, Viral test positive; Injection si... Injection site rash, Pyrexia, Rash, Varicella, Viral test positive; Injection site rash, Pyrexia, Rash, Varicella, Viral test positive More
Patient was seen for her 4 year well check on 09/10/2025 and was given her 4-year vaccines that incl... Patient was seen for her 4 year well check on 09/10/2025 and was given her 4-year vaccines that included the MMRV. Mother contacted the office on 09/29/2025 stating that patient had developed a nickel size rash around the injection site. Advised to apply hydrocortisone cream to are to help with the reaction and to contact the office with any other changes or concerns. On October 5th patient started with fever and rash. Patient took her to the Emergency room where they determined that patient had vaccine-induced chicken pox from the MMRV vaccine. Patient was discharged home with Acyclovir. On October 7th patient started with fever again and rapid spreading of rash and parents returned to the Emergency Room where she was admitted until the rash was no longer spreading and the fever was resolved. Patient was discharged on 10/13/2025. More
✓
2866006 1.58 M NY 10/15/2025 PNC20
 PFIZER\WYETH
 LX2496
Wrong product administered Wrong product administered
Patient received a dose of pneumococcal 20 instead of Hepatitis A. As soon as LPN realized, she info... Patient received a dose of pneumococcal 20 instead of Hepatitis A. As soon as LPN realized, she informed RN and provider. Provider then notified mother. More
2866007 42 F TX 10/15/2025 FLU3
 SANOFI PASTEUR
Rash, Urticaria Rash, Urticaria
I broke out in a Rash or Hives all over my arms, hips, upper legs, and lower legs I broke out in a Rash or Hives all over my arms, hips, upper legs, and lower legs
2866008 67 F VA 10/15/2025 FLU3
 SEQIRUS, INC.
 407271
Abdominal pain, Back pain, Burning sensation, Urticaria Abdominal pain, Back pain, Burning sensation, Urticaria
Patient developed trace hives on arms and chest, burning all over body, abdominal and back pain with... Patient developed trace hives on arms and chest, burning all over body, abdominal and back pain with 2-5minutes after receiving flu vaccine. Benadryl 50mg IM was given for symptoms. Patient was taken to emergency department for further evaluation. More
2866009 70 F MT 10/15/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3052734
UT8794CA
Urticaria; Urticaria Urticaria; Urticaria
Hives all over body. Hives all over body.
2866011 39 M IN 10/15/2025 COVID19
 JANSSEN
Computerised tomogram, Kidney fibrosis, Magnetic resonance imaging, Renal vein t... Computerised tomogram, Kidney fibrosis, Magnetic resonance imaging, Renal vein thrombosis More
5 months later blood clot formed in my right kidney, the medical center has all the records. Permane... 5 months later blood clot formed in my right kidney, the medical center has all the records. Permanente scarring in my right Kidney. More
✓
2866013 3 F OR 10/15/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA0846
U8881AA
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
Pfizer COVID for ages 5-11 was accidentally given to the patient. Pfizer COVID for ages 5-11 was accidentally given to the patient.
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