🏥 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 💀 🏥 🚑 ♿ ⚠️
2867287 TX 10/20/2025 FLU3
 SANOFI PASTEUR
Extra dose administered, No adverse event Extra dose administered, No adverse event
Administered with (0.5 ml) and then again inadvertently administered with 1.0 ml of fluzone, with no... Administered with (0.5 ml) and then again inadvertently administered with 1.0 ml of fluzone, with no reported adverse event.; Initial information received on 15-Oct-2025 regarding an unsolicited valid non-serious case received from other health professional. This case involves an unknown age and gender patient who was administered with (0.5 ml) and then again inadvertently administered with 1.0 ml of 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 was administered with 0.5 ml and then inadvertently administered with 1ml (once) dose of suspect Influenza Usp Trival A-B Subvirion No Preservative Vaccine, Suspension for injection (lot number, expiry date: not reported) via unknown route in unknown administration site for Influenza (Influenza immunisation), with no reported adverse event (extra dose administered) (latency: same day). It was reported, "Caller stated that a medical assistant (MA) administered the Fluzone vaccine (0.5mL) to a patient. Then another MA came in and administered an additional FLUZONE dose. The patient got 1.0 mL of FLUZONE." Information on batch number and expiration date corresponding to the one at time of event occurrence was requested. 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. More
2867288 57 PA 10/20/2025 FLU3
 SANOFI PASTEUR
 U8862AA
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
FLUZONE HD was given to a 57 year old patient with no adverse event; Initial information received on... FLUZONE HD was given to a 57 year old patient with no adverse event; Initial information received on 16-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 57 years old and unknown gender patient who received INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE [FLUZONE HD] with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 16-Oct-2025, the patient received a dose 0.5 ml of suspect INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE, Suspension for injection in pre-filled syringe (strength high, lot U8862AA and expiry 30-Jun-2026) with no adverse event (product administered to patient of inappropriate age) (latency same day) via intramuscular route in the right deltoid for Influenza. Reportedly:- Nurse was instructed by their clinical service department to contact us because the FLUZONE HD was given to a 57 y/o patient which is not the recommended age. She wanted to make sure that there's no harm on the patient and if there are immediate actions to be taken 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
2867290 M 10/20/2025 FLU3
 SANOFI PASTEUR
No adverse event, Underdose No adverse event, Underdose
patient not receiving a full dose/a drop of FLUBLOK came out before or after the needle was pulled o... patient not receiving a full dose/a drop of FLUBLOK came out before or after the needle was pulled out with no reported adverse event; Initial information received on 16-Oct-2025 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age male patient who did not receiving a full dose of Influenza Trivalent Recombinant Vaccine [Flublok] due to a drop of vaccine came out before or after the needle was pulled out 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 Trivalent Recombinant Vaccine, Solution for injection,(unknown strength and expiry date) lot number not reported via unknown route in unknown administration site for influenza immunisation, but a drop of vaccine came out before or after the needle was pulled out with no reported adverse event (incorrect dose administered) (latency same day). It was reported, "Patient said that they were not able to get the full dose and wanted to get another dose". 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
2867291 M MI 10/20/2025 UNK
 UNKNOWN MANUFACTURER
 407252
Device leakage, Underdose Device leakage, Underdose
The total dose was not administered; There was a leakage between the insertion of the needle with th... The total dose was not administered; There was a leakage between the insertion of the needle with the syringe.; This spontaneous case initially received on 07-Oct-2025, was reported by a health professional and concerns an elderly male patient. Administration of company suspect drug: On 07-Oct-2025, the patient received Fluad (TIV) for Flu prevention, Dose regimen: 0.5 ml, route of administration: not reported, Anatomical location: Not reported, Lot number: 407252. No additional suspect drugs. Adverse reactions/events and outcomes: On an unknown date, the patient experienced The total dose was not administered (outcome: Unknown), There was a leakage between the insertion of the needle with the syringe. (outcome: Unknown). A pharmacist reported that a Fluad vaccine (LOT: 407252, EXP: 05-May-2026) vaccine was given to a patient and the total dose was not administered. Pharmacist informed that during administration there was a leakage between the insertion of the needle with the syringe. The defect was noticed while the pharmacist was administering the vaccine, as it leaked from the connection point between the needle and the syringe. After administration, the pharmacist observed the vaccine dripping, indicating that only a partial dose had been administered. The plunger was depressed during the injection, and pharmacist stated that the shield was put back in place after pulling out the needle from the patient. The leak was specifically located at the needle insertion point with the syringe. There were no visible signs of damage on the syringe. Details regarding the needle used, its manufacturer or model, whether it was tightly attached, or if any attempts were made to tighten or replace it, remain unknown. It is also unknown whether a complaint sample was obtained or if there are any signs of damage on the needle. A picture of the complaint sample has not yet been provided and should be obtained. No information is available regarding treatment measures, outcome of the event, concomitant medications, or the patient's medical history. The patient was not hospitalized. Fluad (TIV) action taken: Not Applicable Reporter's assessment: The reporter did not provide the seriousness and causality of the events.; Reporter's Comments: The events are not related due to nature of event (special situation) More
2867304 74 M IL 10/20/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 030L20A
011M20A
067F21A
037A22B
030G22B
3031417
Death, Glioblastoma; Death, Glioblastoma; Death, Glioblastoma; Death, Glioblasto... Death, Glioblastoma; Death, Glioblastoma; Death, Glioblastoma; Death, Glioblastoma; Death, Glioblastoma; Death, Glioblastoma More
Patient was pressured, coerced, and fooled into taking six Government funded (through withheld name)... Patient was pressured, coerced, and fooled into taking six Government funded (through withheld name) Moderna C-19 ModRNA bioweapon shots from Jan 2021 to Dec 2023. Patient was diagnosed with a sudden and aggressive turbo cancer - Grade 4 Glioblastoma on May 22, 2024 and died Oct 21, 2024. (5 months). The bioweapon shots caused or greatly contributed to his sudden death. More
✓ ✓
2867305 18 F AZ 10/20/2025 COVID19
FLU3
HEPA
MENB
MNQ
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
 3052550
37KF3
3255P
49M9N
U8599AA
Syncope; Syncope; Syncope; Syncope; Syncope Syncope; Syncope; Syncope; Syncope; Syncope
Client requested 6 immunizations; states she needs them for her clinical rotation, shortly as I was ... Client requested 6 immunizations; states she needs them for her clinical rotation, shortly as I was getting ready to administer the last IZ (HPV) she had a full syncopal episode; I called employee and she came in to assist, client did not hit her head, cold compresses applied to her back and forehead, tang X 2 glasses were given crackers also given; last injection was given, client was escorted to a room with an exam table and was observed for 45 min ; no more syncopal episodes, tolerated tang and water well, blood pressure monitored, discharged to home without any complaints, client states she feels fine Blood pressure: 1505: 100/64: 1510: 110/80; 1530: 110/80 More
2867306 35 F CA 10/20/2025 COVID19
 PFIZER\BIONTECH
 NA0590
Vestibular neuronitis Vestibular neuronitis
Vestibular Neuritis Vestibular Neuritis
2781106 33 F FL 10/19/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 301558
3230BD
3230BD & 301558
Biopsy gingival, Blood test, Gingival discomfort, Lichen planus; Biopsy gingival... Biopsy gingival, Blood test, Gingival discomfort, Lichen planus; Biopsy gingival, Blood test, Gingival discomfort, Lichen planus; Lichen planus, Malaise, Mental disorder More
Lichen Planus (cutaneous & mucosal)- autoimmune disorder due T-helper 1 (Th1) & spike protei... Lichen Planus (cutaneous & mucosal)- autoimmune disorder due T-helper 1 (Th1) & spike protein. Within 3 months after vaccine my gums were flared up, after several rounds of steroids (oral & solution), oral surgeon performed a biopsy which then confirmed Oral Lichen Planus. Then it spread on to the rest of my skin & private parts. Years of trying different medicine, treatments, red light therapy, the only thing that will keep it controlled is Methotrexate weekly which the side effects are terrible. Currently looking into CellCept. A lot of natural life style changes such as Gluten Free diet to help with the inflammation. I have to live with this for the rest of my life! More
2866820 69 M CA 10/19/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 EN6200
EN6208
Pulmonary thrombosis; Pulmonary thrombosis Pulmonary thrombosis; Pulmonary thrombosis
Sudden onset of chest pain with blood clots diagnoised, initially and originating in the lung. NOT... Sudden onset of chest pain with blood clots diagnoised, initially and originating in the lung. NOT THE LEGS. DR. SAYS THEY DON'T KNOW THE CAUSE OF THE BLIOD CLOTS. More
2866821 70 M PA 10/19/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 En62020
Er8733
Pain in extremity; Pain in extremity Pain in extremity; Pain in extremity
Complaints of pain in arm Complaints of pain in arm
✓
2866822 44 M ME 10/19/2025 COVID19
 PFIZER\BIONTECH
 EN6205
Arrhythmia, Cerebrovascular accident, Magnetic resonance imaging, Transient isch... Arrhythmia, Cerebrovascular accident, Magnetic resonance imaging, Transient ischaemic attack More
Stroke/TIA and heart rhythm issues Stroke/TIA and heart rhythm issues
✓
2866823 77 F MA 10/19/2025 COVID19
 MODERNA
Arthralgia, Back pain, Malaise, Muscular weakness, Scan Arthralgia, Back pain, Malaise, Muscular weakness, Scan
Every booster in the past 4 years has made me very ill. I have been left with serious arthritis pain... Every booster in the past 4 years has made me very ill. I have been left with serious arthritis pain in my back and other joints, also mustle weakness, all of which has gotten progressively worse with each vaccine and was not a problem before More
✓
2866824 33 M VA 10/19/2025 COVID19
 MODERNA
Chills, Headache Chills, Headache
Intense chills and throbbing headache for a period of 24 hours. Intense chills and throbbing headache for a period of 24 hours.
2866825 54 F 10/19/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.

Oral herpes; Oral herpes Oral herpes; Oral herpes
cold sore on bottom lip cold sore on bottom lip
2866826 65 M AL 10/19/2025 COVID19
FLU3
PNC20
 PFIZER\BIONTECH
SANOFI PASTEUR
PFIZER\WYETH
 NA4457
ut8781DA
LP4947
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event More
The patient was administered prevnar 20 outside of treatment guidelines. The last prevnar 20 dose ad... The patient was administered prevnar 20 outside of treatment guidelines. The last prevnar 20 dose administered was 10/6/2023. The patient's primary care physician instructed him to get an additional dose. The patient is experiencing no side effects. More
2866827 78 F NM 10/19/2025 FLU3
FLU3
RSV
RSV
 SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH



Chest pain, Chills, Cough, Fatigue, Headache; Pain, Pyrexia; Chest pain, Chills,... Chest pain, Chills, Cough, Fatigue, Headache; Pain, Pyrexia; Chest pain, Chills, Cough, Fatigue, Headache; Pain, Pyrexia More
Fever, aches, chills, headache, fatigue, chest pain with slight cough. I don?t know which flu or rav... Fever, aches, chills, headache, fatigue, chest pain with slight cough. I don?t know which flu or raven vaccine I received as the pharmacy gave me no information. More
2866828 13 M AZ 10/19/2025 FLU3
 SANOFI PASTEUR
 tfaa2547
Loss of consciousness, Presyncope Loss of consciousness, Presyncope
Patient received flublok and passed out within 5-10 minutes . Paramedics came to access him and pare... Patient received flublok and passed out within 5-10 minutes . Paramedics came to access him and parents decided to have him evaluated at hospital. More
2866829 75 F FL 10/19/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Arthralgia, Muscular weakness, Musculoskeletal stiffness Arthralgia, Muscular weakness, Musculoskeletal stiffness
Weeks 4 to present (week 6) ; Muscle weakness around knees, and leg stiffness, especially when walki... Weeks 4 to present (week 6) ; Muscle weakness around knees, and leg stiffness, especially when walking. Burning inside knee joints (diminished around 5th week). More
2866830 90 F MN 10/19/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA0589
U8862CA
Contusion, Haemorrhage; Contusion, Haemorrhage Contusion, Haemorrhage; Contusion, Haemorrhage
Local bruising and bleeding that resolved on its own. Local bruising and bleeding that resolved on its own.
2866831 73 F IL 10/19/2025 RSV
 PFIZER\WYETH
 MD5462
Injection site erythema Injection site erythema
REDNESS AT SITE OF INJECTION REDNESS AT SITE OF INJECTION
2866832 71 F MD 10/19/2025 FLU3
PNC21
 SANOFI PASTEUR
MERCK & CO. INC.
 UT8763EA
2009661
Injection site erythema, Injection site pruritus, Injection site swelling; Injec... Injection site erythema, Injection site pruritus, Injection site swelling; Injection site erythema, Injection site pruritus, Injection site swelling More
Per patient: is experiencing local itching, swelling, redness on the right arm near injection sites.... Per patient: is experiencing local itching, swelling, redness on the right arm near injection sites. Counseled to use cold compress, antihistamines, and follow up with doctor today or tomorrow if no improvement. More
2866833 74 F 10/19/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.
 NA0738
407245
Injection site erythema, Injection site pruritus; Injection site erythema, Injec... Injection site erythema, Injection site pruritus; Injection site erythema, Injection site pruritus More
Patient received both vaccines in left arm on 10/16/25. On 10/18/25, she removed bandages from her a... Patient received both vaccines in left arm on 10/16/25. On 10/18/25, she removed bandages from her arm and noticed redness at the injection site. She also stated there was itching around the injection sites. She said she used an antihistamine and it seemed to help with redness and itching. More
2866834 58 F AZ 10/19/2025 FLU3
 SEQIRUS, INC.
 AX5586 C
Arthralgia, Injected limb mobility decreased, Nausea, Pain in extremity, Sleep d... Arthralgia, Injected limb mobility decreased, Nausea, Pain in extremity, Sleep disorder More
About 2 days after I received the flu shot my arm was real sore and could barely move it. Today is ... About 2 days after I received the flu shot my arm was real sore and could barely move it. Today is 10/19/2025 (12 days later) and my arm hurts so bad that is literally makes me sick to my stomach, I can not lift it and can barely move it. My arm - from elbow to shoulder has to basically stay against my side then I am able to move at least my arm below the elbow to my hand. Going to sleep at night is the worst. I went to the ER at medical facility on 10/15/2025. and saw PA, with a diagnosis of Should joint pain - left. At ER I received a Toradol shot for the pain. I also received Ibuprofen 600MG tablet, Lidocaine 5% Topical patch, and Menthol/Methyl Salicy (10-15%) CRM 85GM. This treatment did not work as I still feel a lot of pain in my shoulder area and it is goin on 4 days from this treatment. More
2866835 73 F FL 10/19/2025 COVID19
 MODERNA
Mobility decreased, Pain in extremity, Pyrexia Mobility decreased, Pain in extremity, Pyrexia
My arm was so painful up into the shoulder. for approximately 48 hours. Have had many vaccines but n... My arm was so painful up into the shoulder. for approximately 48 hours. Have had many vaccines but never a reaction like this. Could not lift my arm, Slight fever of 99.8 More
2866837 43 F IN 10/19/2025 FLU3
 SANOFI PASTEUR
Injection site pain Injection site pain
Having pain at injection site that has lasted for over too weeks. Patient describing it as excruciat... Having pain at injection site that has lasted for over too weeks. Patient describing it as excruciating More
2866838 73 M NE 10/19/2025 RSV
 PFIZER\WYETH
Burning sensation, Chest pain, Hypoaesthesia, Inflammation, Monoplegia Burning sensation, Chest pain, Hypoaesthesia, Inflammation, Monoplegia
Per patient, he had burning sensation and paralysis of the leg, chest pain under the skin, inflammat... Per patient, he had burning sensation and paralysis of the leg, chest pain under the skin, inflammation of the whole body, numbness of the muscles. More
2866839 66 F MD 10/19/2025 COVID19
 MODERNA
Photopsia, Visual impairment Photopsia, Visual impairment
Flashes of light in right eye, what appeared to be wisps of smoke also in right eye, usually in the ... Flashes of light in right eye, what appeared to be wisps of smoke also in right eye, usually in the morning and evening More
2866840 40 F IN 10/19/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA0590
U8837AA
No adverse event; No adverse event No adverse event; No adverse event
None noted at time of injection; none expected, since patient received higher dose of flu vaccine sh... None noted at time of injection; none expected, since patient received higher dose of flu vaccine she was already scheduled to receive; followed up with patient on 10/19/25 and she reported that "nothing out of the ordinary" happened after receiving the vaccine More
2866841 7 F MI 10/19/2025 COVID19
COVID19
 MODERNA
MODERNA

Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
The patient received two pediatric Spikevax COVID-19 vaccinations, the patient was okay and the gua... The patient received two pediatric Spikevax COVID-19 vaccinations, the patient was okay and the guardians are aware. Guardian present was (mother). Guardians were counseled to monitor for adverse reactions. Pediatrician will be notified. More
2866842 73 F IN 10/19/2025 FLU3
 SEQIRUS, INC.
 407266
Injection site bruising, Injection site erythema, Injection site pain, Injection... Injection site bruising, Injection site erythema, Injection site pain, Injection site swelling More
red and blue at injection site (bruise), pain and swelling at injection site red and blue at injection site (bruise), pain and swelling at injection site
2866843 34 M CA 10/19/2025 HPV9
 MERCK & CO. INC.
 2002437
Extra dose administered Extra dose administered
duplicated vaccine was given in error. Pharmacist should be checking patient's database histor... duplicated vaccine was given in error. Pharmacist should be checking patient's database history prior to giving a vaccine. In this case, patient already completed the 3-dose series for HPV. More
2866844 74 M WA 10/19/2025 COVID19
COVID19
FLU3
FLU3
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\BIONTECH
PFIZER\BIONTECH
 NA0589
NA0589
UT8763HA
UT8763HA
Vision blurred; Vision blurred; Vision blurred; Vision blurred; Vision blurred; ... Vision blurred; Vision blurred; Vision blurred; Vision blurred; Vision blurred; Vision blurred More
Patient reported having blurred vision since the morning after vaccination. (vaccine done on 10/16/2... Patient reported having blurred vision since the morning after vaccination. (vaccine done on 10/16/25). More
2866845 60 M FL 10/19/2025 HEP
MMR
TDAP
VARCEL
 DYNAVAX TECHNOLOGIES CORPORATION
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 945662
Y014096
Y3Z9P
Y014181
Malaise, Pain in extremity; Malaise, Pain in extremity; Malaise, Pain in extremi... Malaise, Pain in extremity; Malaise, Pain in extremity; Malaise, Pain in extremity; Malaise, Pain in extremity More
THE PATIENT CAME BACK TO THE PHARMACY WANT TO GET FLU VACCINE, THEY MENTION THAT THE RIGHT ARM STILL... THE PATIENT CAME BACK TO THE PHARMACY WANT TO GET FLU VACCINE, THEY MENTION THAT THE RIGHT ARM STILL HURT (JOINT PAIN) AND NUMBNESS ON THE FINGERS. THEY WERE VERY SICK AFTER HAVING THE SHOTS. THEY TOOK ACEMINOPHEN FOR 2 DAYS. More
2866846 74 F MI 10/19/2025 FLU3
FLU3
 SANOFI PASTEUR
SEQIRUS, INC.
 U8862EA
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
PATINET HAS NOT REPORTED ANY ADVERSE EVENTS. PATIENT CAME TO THE PHARAMCY TO TALK TO THE PHARMACIST ... PATINET HAS NOT REPORTED ANY ADVERSE EVENTS. PATIENT CAME TO THE PHARAMCY TO TALK TO THE PHARMACIST ABOUTH THE DOUBLE DOSES SHE REVEIVED. More
2866847 57 F NC 10/19/2025 FLU3
 SANOFI PASTEUR
 u8864ca
Erythema, Mobility decreased, Skin swelling Erythema, Mobility decreased, Skin swelling
The patient stated that she had a reaction after receiving the Flublok vaccine yesterday, She had a ... The patient stated that she had a reaction after receiving the Flublok vaccine yesterday, She had a red raised area on the back of her neck and the middle of her back. The skin was so swollen on the back of her neck that she could not tilt her head back. The area on her neck reminded me of an insect bite. She stated the swelling had gone down from last night and she was now able to tilt her head back. She stated she would let her provider know about the reaction during her next appointment. More
2866849 51 F NH 10/19/2025 FLU3
 SANOFI PASTEUR
 U8863BA
Cellulitis, Injection site erythema, Injection site swelling, Injection site war... Cellulitis, Injection site erythema, Injection site swelling, Injection site warmth More
PATIENT STATED THAT SHE RECEIVED THE VACCINE LAST SATURDAY 10/11/25 AND ON MONDAY HER LEFT ARM UNDER... PATIENT STATED THAT SHE RECEIVED THE VACCINE LAST SATURDAY 10/11/25 AND ON MONDAY HER LEFT ARM UNDER THE INJECTION SITE BECAME RED, SWOLLEN AND HOT TO THE TOUCH. SHE WENT TO SEE HER PHYSICIAN ON THURSDAY 10/16/25 AND WAS DIAGNOSED WITH CELLULITIS. SHE CAME TO THE PHARMACY TODAY REPORTING THE INCIDENT AND STATED THAT THE ANTIBIOTICS DID NOT SEEM TO BE WORKING. THE ARM WAS STILL VISIBLY SWOLLEN AND RED TODAY. More
2866851 80 F FL 10/19/2025 PNC20
 PFIZER\WYETH
 ma2502
Back pain Back pain
Patient called on 10-18-25 to complain of nagging constant pain on her lower back (kidney area) sinc... Patient called on 10-18-25 to complain of nagging constant pain on her lower back (kidney area) since she got her pneumonia shot. She communicated with her PCP, she is waiting to hear back from PCP. More
2866852 30 F MA 10/19/2025 COVID19
FLU3
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
 3052741
73BN2
Abdominal pain, Diarrhoea, Fatigue, Pain; Abdominal pain, Diarrhoea, Fatigue, Pa... Abdominal pain, Diarrhoea, Fatigue, Pain; Abdominal pain, Diarrhoea, Fatigue, Pain More
Abdominal pain, diarrhea, body aches, fatigue Abdominal pain, diarrhea, body aches, fatigue
2866854 39 M FL 10/19/2025 FLU3
 SANOFI PASTEUR
 U8832AA
Injected limb mobility decreased, Pain in extremity Injected limb mobility decreased, Pain in extremity
PATIENT CALLED THE PHARMACY ON 10/19/25 AND REPORTED THAT HIS ARM HAS BEEN SORE WITH LIMITED MOBILIT... PATIENT CALLED THE PHARMACY ON 10/19/25 AND REPORTED THAT HIS ARM HAS BEEN SORE WITH LIMITED MOBILITY SINCE THE TIME THE VACCINE WAS ADMINISTERED ON 10/16/25. HE SAID THAT HE IS UNABLE TO MOVE HIS LEFT ARM ABOVE THE LEVEL OF HIS SHOULDER. HE REPORTS THAT HE BELIEVES THE VACCINE WAS ADMINISTERED TOO HIGH ON THE SHOULDER. More
2866855 77 F FL 10/19/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 f4ac3
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient was mistakenly given an additional dose of Arexvy(only indicated for 1 dose) on 10/17/2025. ... Patient was mistakenly given an additional dose of Arexvy(only indicated for 1 dose) on 10/17/2025. Patient received original dose on 9/24/2024. Spoke with patient and explained to her what happened and what to look out for, as well as how to report if anything arises on 10/19/2025. Patient reports no side effects/issues whatsoever and is doing perfectly fine. More
2866856 82 F NM 10/19/2025 FLU3
TDAP
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 ut8820ba
94kg2
Mobility decreased; Mobility decreased Mobility decreased; Mobility decreased
82 you female received two vaccine on 10-18-25 around 3pm. administration went smoothly. Patients h... 82 you female received two vaccine on 10-18-25 around 3pm. administration went smoothly. Patients husband called me 930 am the next am around 1030am. He said that she had had two vaccines the day before and this am she cannot get out of bed. He said that her oxygen was 88. I recommended that she see a doctor, that he needs or I need to call EMS. I talked with patient later around 3pm and she said she was heading to the ER. More
2866857 26 F UT 10/19/2025 FLUN3
 MEDIMMUNE VACCINES, INC.
Bell's palsy, Blood test, Electrocardiogram, Magnetic resonance imaging, Ne... Bell's palsy, Blood test, Electrocardiogram, Magnetic resonance imaging, Neurological symptom More
Showed signs of stroke and was diagnosed with bells palsy Showed signs of stroke and was diagnosed with bells palsy
2866858 4 M CO 10/19/2025 DTAPIPV
DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 4L454
4L454
Crying, Diarrhoea, Gait inability, Insomnia, Nausea; Pyrexia, Screaming Crying, Diarrhoea, Gait inability, Insomnia, Nausea; Pyrexia, Screaming
Spike in fever to 104, screaming, crying, unable to walk, unable to sleep, nausea, diarrhea - sympto... Spike in fever to 104, screaming, crying, unable to walk, unable to sleep, nausea, diarrhea - symptoms started around 6pm (approximately 3 hours after the vaccine) and continued all evening and then intermittently for the next 48hr More
✓
2866860 70 F VA 10/19/2025 COVID19
COVID19
 MODERNA
MODERNA

Chills, Fatigue, Headache, Muscular weakness, Pyrexia; Vomiting Chills, Fatigue, Headache, Muscular weakness, Pyrexia; Vomiting
within 4 hours of injection, violent vomitting, high fever, chills, muscle weakness, wobbly legs, ti... within 4 hours of injection, violent vomitting, high fever, chills, muscle weakness, wobbly legs, tiredness, splitting headache More
2866908 60 F FL 10/19/2025 FLU3
 SANOFI PASTEUR
 U8832AA
Extra dose administered Extra dose administered
Patient received two doses of the 2025-2026 Flublok. First dose was given on 07/29/25 and second dos... Patient received two doses of the 2025-2026 Flublok. First dose was given on 07/29/25 and second dose was given on 10/10/25. More
2866909 72 F CA 10/19/2025 FLU3
 SANOFI PASTEUR
 ut8794ca
Nausea, Pain Nausea, Pain
pt states has a fever of 99, body aches, and nausea feeling on Friday (the day after the vaccines) a... pt states has a fever of 99, body aches, and nausea feeling on Friday (the day after the vaccines) and continues. she states she is feeling better today. will follow up with people on monday or tuesday More
2866910 69 F OR 10/19/2025 FLU3
 SANOFI PASTEUR
 U8764CB
Vision blurred Vision blurred
blurred vision of right eye blurred vision of right eye
2866911 65 F AZ 10/19/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 3EG9B
3EG9B
Chest discomfort, Dyspnoea, Eye swelling, Facial pain, Migraine; Pain of skin, R... Chest discomfort, Dyspnoea, Eye swelling, Facial pain, Migraine; Pain of skin, Rash More
Pt developed a migraine at 12:30 am (10/11/2025) followed by right eye swelling. She reported it wen... Pt developed a migraine at 12:30 am (10/11/2025) followed by right eye swelling. She reported it went away by the next day but returned on 10/14 Tuesday with migraine, Right side face hurt along eye brow/scalp area. 10/15/2025 Pt reported SOB with chest pressure that resolved. 10/17/2025 Pt reported to ER tests completed to evaluate brain tumor progression/change and eye evaluated. 10/18 Pt reported to pharmacist at 5:42pm that rash developed and possible shingles outbreak. 10/19 rx for Valtrex filled More
2866912 12 F OR 10/19/2025 FLU3
 SEQIRUS, INC.
 406996
Feeling hot, Flushing, Hyperventilation Feeling hot, Flushing, Hyperventilation
Patient was flushed and hot and hyperventilating after receiving the vaccine. Starting having sympto... Patient was flushed and hot and hyperventilating after receiving the vaccine. Starting having symptoms several minutes after administration of her vaccine and after watching her mother get vaccinated. Patient drank some water, denied needed emergency assistance. Patients symptoms improved with deep breaths in and out. After sitting outside of the vaccine room symptoms improved. Patient left pharmacy without medical intervention. Prior to patient leaving, pharmacist offered to take patient's blood pressure, father declined for patient. More
2866914 51 M CA 10/19/2025 COVID19
 MODERNA
 3052671
Rash Rash
Patient had rash ever since received the vaccine weeks ago. Patient had rash ever since received the vaccine weeks ago.
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