๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ Privacy & Data Disclaimer

About This Site

This is a public data browser for the Vaccine Adverse Event Reporting System (VAERS). By using this site, you acknowledge and agree to the following:

Data Source & Accuracy

  • Public Data: All data displayed comes from the publicly available VAERS database maintained by the CDC and FDA.
  • No Verification: VAERS accepts all reports without verifying medical accuracy. Reports do not prove causation between vaccines and adverse events.
  • Anyone Can Report: Healthcare providers, patients, family members, and anyone else can submit reports to VAERS.
  • Research Purpose: This data is for transparency, research, and monitoring vaccine safety signals only.

Your Privacy

  • No Personal Data Collection: This site does not collect, store, or track any personal information about visitors.
  • No Cookies: We do not use cookies except for remembering that you've seen this disclaimer (stored locally in your browser).
  • No Analytics: We do not use Google Analytics or any other tracking services.
  • Search Privacy: Your searches and filters are not logged or stored on our servers.
  • Public Data Only: The VAERS data shown here is already public and contains no personally identifiable information.

Medical Disclaimer

  • Not Medical Advice: This tool is for informational purposes only and does not provide medical advice.
  • Consult Healthcare Providers: Always consult qualified healthcare professionals for medical decisions.
  • No Liability: We are not responsible for decisions made based on this data.

Data Interpretation

  • The presence of a report does not mean the vaccine caused the adverse event.
  • Coincidental events are often reported (e.g., a heart attack that happened to occur after vaccination).
  • Serious adverse events must be reported by law, even if unrelated to the vaccine.
  • The database is useful for detecting safety signals that require further investigation.

๐Ÿ“– Help & Search Guide

Column Icons Legend

๐Ÿ’€ Death
๐Ÿฅ Hospitalized
๐Ÿš‘ Emergency Room
โ™ฟ Disability
โš ๏ธ Life Threatening

How to Search

๐Ÿ’ก Search Tips:
  • Select Year: Choose a specific year OR "All Years" to search across all data
  • All Years requires filters: When searching all years, you must select at least one filter (lot number, vaccine type, outcome, etc.) for performance
  • Lot number tracking: Use "All Years" + Lot Number to track lots across multiple years
  • Combine filters: Use multiple filters together to narrow results (e.g., Age + Vaccine Type + Death)
  • VAERS ID: Search for specific report by ID number
  • Age: Enter exact age (e.g., 25) or decimal (e.g., 0.5 for 6 months)
  • State: Enter 2-letter state code (e.g., CA, NY, TX)
  • Vaccine Type: Search partial names (e.g., "COVID19", "FLU", "HPV")
  • Manufacturer: Search by company (e.g., "PFIZER", "MODERNA")
  • Lot Number: Search specific vaccine lot (works great with "All Years")
  • Symptoms: Search for any symptom keyword (e.g., "fever", "rash")
  • Death/Hospitalized: Filter to only show cases with these outcomes

Understanding the Data

  • Reports are unverified: VAERS accepts all reports without medical verification
  • Not proof of causation: A report does not mean the vaccine caused the event
  • Anyone can report: Healthcare providers, patients, and family members can submit reports
  • Multiple vaccines: One report may list multiple vaccines given at the same time
  • Blank fields: Not all fields are required, so some data may be missing

Using the Table

  • Sort columns: Click column headers (ID, Age, Sex, Date, Died) to sort
  • Expand text: Click "More" to see full narrative or symptom text
  • Navigate pages: Use pagination controls at top and bottom of table
  • Export results: Click "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ VAERS Vaccine Data Browser is an independent, third-party data browser for publicly available VAERS (Vaccine Adverse Event Reporting System) data.

Important: This site is NOT affiliated with, endorsed by, or operated by the CDC, FDA, or any government agency. We are an independent service that makes public VAERS data easier to search and analyze.

What is VAERS?

VAERS (Vaccine Adverse Event Reporting System) is a national early warning system established in 1990 to detect possible safety problems with vaccines. It's co-managed by the CDC (Centers for Disease Control and Prevention) and FDA (Food and Drug Administration).

VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination.

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

  • Publicly available - Published by the CDC/FDA on their official website
  • De-identified - Contains no personally identifiable information (names, addresses, contact info removed)
  • Legally accessible - Available to researchers, media, and the general public under FOIA (Freedom of Information Act)
  • Not protected health information - Once de-identified and published by the government, it's no longer covered by HIPAA restrictions

This site displays the same public data available at vaers.hhs.gov/data.

Why does this site exist?

We believe in transparency and public access to health data. While the CDC/FDA provide VAERS data, their official site:

  • Is difficult to search and filter
  • Requires downloading large CSV files and technical knowledge
  • Is not user-friendly for the average person

This independent site makes the same publicly available data easier to search, filter, and understand for researchers, journalists, healthcare workers, and concerned citizens.

Where does the data come from?

All data is downloaded directly from the official CDC/FDA VAERS website at vaers.hhs.gov/data.

The data is:

  • Publicly released by the CDC/FDA every week
  • Available as downloadable CSV files
  • Imported into this site's database for easier searching
  • Displayed exactly as provided (no modifications or filtering)

This site does not collect, modify, or add to the official VAERS data.

My vaccine lot number matches one with deaths/serious events - should I be worried?

Important context:

  • VAERS reports do NOT prove causation - A report means an event occurred after vaccination, but doesn't mean the vaccine caused it
  • Anyone can report - Reports are not verified for medical accuracy before being published
  • Coincidences happen - When millions of people get vaccinated, some will experience unrelated medical events afterward
  • Large lot numbers - Popular vaccines may have hundreds of thousands of doses from one lot number
  • More vaccinations = more reports - Lots used widely will naturally have more reports

What to do:

  • Don't panic - VAERS data requires expert analysis to interpret
  • Talk to your doctor if you have concerns
  • Check official CDC/FDA safety communications for genuine safety signals
  • Remember: billions of vaccine doses have been safely administered

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

  • โœ… Early warning system for potential safety signals
  • โœ… Open and transparent - publicly accessible
  • โœ… Accepts all reports regardless of likelihood of causation
  • โœ… Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • โš ๏ธ Reports are unverified - not investigated before publication
  • โš ๏ธ Cannot determine if vaccine caused the event
  • โš ๏ธ Underreporting - not all adverse events are reported
  • โš ๏ธ Overreporting - coincidental events may be reported
  • โš ๏ธ Incomplete data - not all fields are required

Bottom line: VAERS is an important tool for safety monitoring, but individual reports should not be used as proof that a vaccine caused harm.

What are "adverse events"?

An adverse event is any undesirable health occurrence that happens after vaccination, including:

  • Common reactions: Sore arm, mild fever, fatigue (usually expected)
  • Serious events: Hospitalization, disability, life-threatening illness, death
  • Coincidental events: Medical conditions that would have occurred anyway

Important: An adverse event doesn't mean the vaccine caused it - only that it occurred after vaccination. Many reported events are coincidental or unrelated.

Why are some lot numbers listed multiple times?

This is normal and expected! A person may receive multiple doses of the same vaccine from the same lot number:

  • COVID vaccines require 2-3 doses
  • HPV, Hepatitis B, and other vaccines have multi-dose schedules
  • Each dose is recorded as a separate entry

Example: Person receives Pfizer COVID dose 1 (lot ABC123) and dose 2 (lot ABC123) - lot ABC123 appears twice in their report.

How often is this data updated?

The CDC/FDA releases new VAERS data every Friday. This site is typically updated:

  • Weekly or bi-weekly for recent data
  • Check the available years to see what data is currently loaded
  • During updates, the site may be in maintenance mode temporarily

Where can I learn more?

โš ๏ธ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2853662 74 F CA 08/11/2025 FLU3
 SANOFI PASTEUR
 U8764BB
Contusion, Muscle swelling, Pain in extremity, Paraesthesia, Tenderness Contusion, Muscle swelling, Pain in extremity, Paraesthesia, Tenderness
Arm pain, swollen deltoid, bruising and tenderness, tingling down the arm Arm pain, swollen deltoid, bruising and tenderness, tingling down the arm
2853663 59 F GA 08/11/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 793pt
Angioedema Angioedema
angioedema, symptoms of anaphylaxis. Patient went to ER for treatment and received steroid therapy. angioedema, symptoms of anaphylaxis. Patient went to ER for treatment and received steroid therapy.
2853664 4 M MI 08/11/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 9k34m
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
To this providers knowledge there has been no adverse effect to the patient. This provider spoke wit... To this providers knowledge there has been no adverse effect to the patient. This provider spoke with patient's father who reported no ill effects. Patient was incorrectly administered a full dose of the adult engerix-B (20mcg/1ml) instead of the pediatric dose of 10mcg/0.5ml More
2853685 33 F MT 08/11/2025 MMRV
 MERCK & CO. INC.
 Y019530
No adverse event, Wrong product administered No adverse event, Wrong product administered
Client received an MMRV vaccine, rather than an MMR vaccine. There were NO side effects or untoward ... Client received an MMRV vaccine, rather than an MMR vaccine. There were NO side effects or untoward symptoms noted. More
2853686 88 M FL 08/11/2025 FLU3
 SANOFI PASTEUR
 U8764CB
Rash, Rash papular Rash, Rash papular
SMALL RED RAISED DOTS APPEARED ON THE TOP OF BOTH THIGHS THE NEXT DAY - NO ITCHING SMALL RED RAISED DOTS APPEARED ON THE TOP OF BOTH THIGHS THE NEXT DAY - NO ITCHING
2853687 56 F SC 08/11/2025 HEPAB
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 az2a3
lk6651
Rash, Rash erythematous, Rash pruritic; Rash, Rash erythematous, Rash pruritic Rash, Rash erythematous, Rash pruritic; Rash, Rash erythematous, Rash pruritic
Itchy red bumps on the forearm went away when the patient took Claritin Itchy red bumps on the forearm went away when the patient took Claritin
2853688 21 F IN 08/11/2025 TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8503AA
U8503AA
Anxiety, Blindness, Confusional state, Dizziness, Hyperhidrosis; Loss of conscio... Anxiety, Blindness, Confusional state, Dizziness, Hyperhidrosis; Loss of consciousness, Nausea, Pallor, Urinary incontinence More
DONOR LOST VISION, INCONINENT OF BLADDER, PALLOR, LOC <30 SECONDS, ANXIETY, CONFUSION, SWEATY, DI... DONOR LOST VISION, INCONINENT OF BLADDER, PALLOR, LOC <30 SECONDS, ANXIETY, CONFUSION, SWEATY, DIZZINESS. DONOR SISTER ALERTED STAFF THAT THE DONOR PASSED OUT AND HAD INCONTENENCE OF BLADDER. DONOR WAS CONFUSED AS TO WHERE SHE WAS. DONOR HAD NAUSEA THAT SUBSIDED. DONOR HAD REACTION THAT OCCURED APPROXIMATELY 8 MINUTES AFTER INJECTION WAS ADMINISTERED. DONOR FULLY RECOVERED WITHIN 20 MINUTES. DONOR WAS GIVEN CRACKERS AND A GATORADE. DONOR HAD LOW BP INITIALLY DURING THE REACTION, THEN CAME UP TO WLN AFTER DRINKING GATORADE. More
2853689 40 M FL 08/11/2025 FLU3
TDAP
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 TFAA2502
KR75K
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Patient received a double dose of Boostrix. First dose on 2/21/2025 and second dose on 8/5/2025. Patient received a double dose of Boostrix. First dose on 2/21/2025 and second dose on 8/5/2025.
2853690 29 F AK 08/11/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Injection site mass, Perioral dermatitis, Rash, Rash macular Injection site mass, Perioral dermatitis, Rash, Rash macular
Hard knot under the skin directly under the injection site, and macular rash on face, spreading to p... Hard knot under the skin directly under the injection site, and macular rash on face, spreading to perioral area. More
2853691 16 F IN 08/11/2025 FLU3
MMR
MNQ
 SEQIRUS, INC.
MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
 406986
Y015022
9549B
Syncope; Syncope; Syncope Syncope; Syncope; Syncope
Patient syncope Patient syncope
2853692 50 F OR 08/11/2025 TDAP
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 9JT4S
PJ353
Rash; Rash Rash; Rash
Patient came back after a few days to let us know that she developed a rash on her leg the day after... Patient came back after a few days to let us know that she developed a rash on her leg the day after getting vaccinated. More
2853693 63 F TX 08/11/2025 PNC13
PNC13
PNC13
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH


Abscess, Arthralgia, Blood test, Burning sensation, Chills; Hyperhidrosis, Mobil... Abscess, Arthralgia, Blood test, Burning sensation, Chills; Hyperhidrosis, Mobility decreased, Pain, Pain in extremity, Ultrasound scan abnormal; White blood cell count increased More
Initial soreness for 2 or 3 days , then severe pain, burning, aching of upper arm/shoulder, unable ... Initial soreness for 2 or 3 days , then severe pain, burning, aching of upper arm/shoulder, unable to move arm , shaking chills , sweating , teeth chattering. Tylenol gave no relief , tried ibuprofen , helped some initially then that did not offer any relief from the pain. Went back to Dr office, prescribed prednisone pak and keflex antibiotics. More
โœ“
2853694 0.33 M NC 08/11/2025 DTAPHEPBIP
HIBV
PNC20
RV5
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.



Culture stool positive, Haematochezia, Mucous stools, Ultrasound scan normal; Cu... Culture stool positive, Haematochezia, Mucous stools, Ultrasound scan normal; Culture stool positive, Haematochezia, Mucous stools, Ultrasound scan normal; Culture stool positive, Haematochezia, Mucous stools, Ultrasound scan normal; Culture stool positive, Haematochezia, Mucous stools, Ultrasound scan normal More
Vaccines administered wed. Baby slept a lot day 2. Acted normal. Large amount of bloody mucous stool... Vaccines administered wed. Baby slept a lot day 2. Acted normal. Large amount of bloody mucous stool in diaper Sunday at 6 pm. Called on call peds at 615. Sent doc pic and they elected to send us to the ER. Arrived at ER around 715 pm. Took vitals and took us back to a room. Baby appeared fine. Notified he had just received vaccines Wednesday several times. Tested stool. Confirmed blood in stool. Ordered ultrasound. Waited almost 2 hours for ultrasound. Doc received normal note from radiology. Given discharge notes and sent home by 11:30 pm More
2853702 2.17 F RI 08/11/2025 MMRV
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
 Y014437
Y011018
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
N/A N/A
2853453 20 F TX 08/10/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Continuous glucose monitoring, Diarrhoea, Eczema, Feeding disorder, Insomnia; Lo... Continuous glucose monitoring, Diarrhoea, Eczema, Feeding disorder, Insomnia; Loss of consciousness, Pancreatic disorder, Type 1 diabetes mellitus, Vomiting More
in September 2022, i ate a bag of M&Ms and started violently puking, diarrheaing, and passing ou... in September 2022, i ate a bag of M&Ms and started violently puking, diarrheaing, and passing out. because i had not received a diagnosis yet, i thought it was normal. in February 2024, i was diagnosed with type one diabetes. my pancreas is now dead and i have to take insulin shots and constantly monitor my sugar (i cant eat, i cant sleep, years are taken off my life). in addition to this, i have also developed eczema. More
โœ“ โœ“
2853454 9 F TX 08/10/2025 HEP
HEPA
HPV9
IPV
MMRV
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
 3N2ND
DN273
Y010656
Y1A212M
Z003308
U8274AA
Dizziness, Pallor, Vision blurred; Dizziness, Pallor, Vision blurred; Dizziness,... Dizziness, Pallor, Vision blurred; Dizziness, Pallor, Vision blurred; Dizziness, Pallor, Vision blurred; Dizziness, Pallor, Vision blurred; Dizziness, Pallor, Vision blurred; Dizziness, Pallor, Vision blurred More
Patient Presentation & Pre-Vaccination Assessment: Patient presented accompanied by mother and s... Patient Presentation & Pre-Vaccination Assessment: Patient presented accompanied by mother and sister for immunizations. Full name and date of birth were verified. Screening for allergies to medications, vaccines, or foods, as well as any underlying medical conditions or contraindications, was negative per the mother. Last food intake was breakfast. After reviewing the patient?s vaccination record, it was determined that 7 vaccines were due: Hepatitis A, Hepatitis B, HPV, Polio, MMRV, and Tdap (6 injections total). The mother was informed of the vaccines, potential adverse reactions, and provided with Vaccine Information Statements. She verbalized understanding and signed informed consent. Vaccination Administration: Vaccines were administered as indicated. The patient appeared anxious prior to vaccination. Adverse Event: Approximately 3 minutes post-vaccination, the patient reported dizziness. Legs were elevated, and an alcohol pad was provided for inhalation. Symptoms improved, and the patient reported feeling better. At 14:41, the patient again reported dizziness and was observed to be pale. Legs were elevated. Vital signs: BP 78/66 mmHg, HR 50 bpm, SpO2 100%, RR 20/min, Temp 97.6๏ฟฝF. The patient stated, ?I no longer see blurry; I feel better.? Repeat vitals at 14:50: BP 78/62 mmHg, HR 73 bpm, SpO2 98%, RR 20/min, Temp 97.6๏ฟฝF. Monitoring & Outcome: Patient was monitored for 22 minutes. At 15:02, vitals were: BP 92/62 mmHg, HR 75 bpm, SpO2 100%, RR 19/min, Temp 98.6๏ฟฝF. She was alert, conscious, oriented, with normal skin color restored. She was instructed to lower her legs slowly and remain seated under observation. Monitored for an additional 15 minutes, during which she was given food and drink. The patient ambulated from the area without complications, accompanied by her parents and sister. More
2853455 61 M 08/10/2025 COVID19
 PFIZER\BIONTECH
Cardiac disorder, Carotid endarterectomy, Cerebrovascular accident, Inflammation Cardiac disorder, Carotid endarterectomy, Cerebrovascular accident, Inflammation
Heart disease, stroke, carotid surgery, flammatory complications. Heart disease, stroke, carotid surgery, flammatory complications.
โœ“ โœ“
2853456 70 F FL 08/10/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR

Blood glucose increased, Chills, Condition aggravated, Continuous glucose monito... Blood glucose increased, Chills, Condition aggravated, Continuous glucose monitoring, Headache; Myalgia, Type 2 diabetes mellitus More
With the headache, muscle aches, and chills my blood sugar has been consistently higher than usual w... With the headache, muscle aches, and chills my blood sugar has been consistently higher than usual with extreme highs with food More
2853457 35 F NY 08/10/2025 RSV
RSV
RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 5H777
5H777
Exposure during pregnancy, Fatigue, Malaise, Pain in extremity, Product use issu... Exposure during pregnancy, Fatigue, Malaise, Pain in extremity, Product use issue; Exposure during pregnancy, Product use issue, Wrong product administered; Exposure during pregnancy, Fatigue, Malaise, Pain in extremity, Product use issue; Exposure during pregnancy, Product use issue, Wrong product administered More
I received the RSV vaccine while 32 weeks and 5 Days pregnant. My due date is 9/27/2025. I had my fi... I received the RSV vaccine while 32 weeks and 5 Days pregnant. My due date is 9/27/2025. I had my first baby on 11/13/2023 (due date 11/10/2023) at 7 pounds and 13 ounces. On 8/82025 I started to feel unwell with body aches and general exhaustion. I am feeling fine now on 8/10/2025 with just minor soreness on my arm. My understanding is that this vaccine is not approved for pregnant women. More
2853458 84 M MO 08/10/2025 FLU3
 SANOFI PASTEUR
Chills, Headache, Malaise, Myalgia, Pyrexia Chills, Headache, Malaise, Myalgia, Pyrexia
Chills, low headache, minor muscle ache, low temperature, general malaise Chills, low headache, minor muscle ache, low temperature, general malaise
2853459 69 M WI 08/10/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Chills, Hyperhidrosis, Pyrexia Chills, Hyperhidrosis, Pyrexia
Sweating chills slight fever Sweating chills slight fever
2853460 6 F TX 08/10/2025 DTAPIPV
HEPA
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 52D72
DN273
Z008501
Dizziness; Dizziness; Dizziness Dizziness; Dizziness; Dizziness
Patient Presentation & Pre-Vaccination Assessment: Patient presented accompanied by her parents ... Patient Presentation & Pre-Vaccination Assessment: Patient presented accompanied by her parents and sister for immunizations. Full name and date of birth were verified. Screening for allergies to medications, vaccines, or foods, as well as any underlying medical conditions or contraindications, was negative per the mother. Last food intake was breakfast. The patient appeared slightly anxious after observing her sister experience dizziness earlier during vaccination. She was reassured and encouraged to remain calm. After reviewing the patient?s vaccination record, it was determined that 5 vaccines were due: Hepatitis A, DTaP?Polio, and MMRV (3 injections total). The mother was informed of the vaccines and potential adverse reactions, and was provided with Vaccine Information Statements in (withheld). She verbalized understanding and signed informed consent. Vaccination Administration: Vaccines were administered as indicated. Adverse Event: At 15:30, immediately after vaccine administration, the patient reported feeling dizzy. She was placed in a supine position with legs elevated, and an alcohol pad was provided for inhalation. The patient was not pale and did not lose consciousness. Initial vital signs: BP 90/72 mmHg, HR 105 bpm, SpO2 99%, RR 31/min, Temp 97.1๏ฟฝF. She was monitored for 15 minutes, during which she reported feeling better, though she appeared apprehensive. Monitoring & Outcome: At 15:40, vital signs were: BP 98/76 mmHg, HR 100 bpm, SpO2 99%, RR 20/min, Temp 97.7๏ฟฝF. The patient was alert, conscious, oriented, and conversing with her parents. She was instructed to remain seated under observation. After an additional 5 minutes of monitoring, the patient ambulated from the area without complications, accompanied by her parents and sister. More
2853461 55 F GA 08/10/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 2NG23
Condition aggravated, Seizure Condition aggravated, Seizure
The immunizer stated that the patient started to have a seizure about 7-110 minutes after the flu sh... The immunizer stated that the patient started to have a seizure about 7-110 minutes after the flu shot was given. It last less than 1 minute. She stayed in the immunization room for about 20 minutes with the store manager. PT stated that she has a history of seizures and wasn't sure it was related to vaccine. More
2853462 80 F FL 08/10/2025 PNC20
 PFIZER\WYETH
 LP4947
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received Prevnar 20 on 8/9/25. We didn't catch that she has already received Prevnar 20... Patient received Prevnar 20 on 8/9/25. We didn't catch that she has already received Prevnar 20 on 7/26/24. Spoke with patient and she said that she hasn't had any side effects except for soreness in the arm. More
2853463 80 F MA 08/10/2025 COVID19
 MODERNA
Fatigue Fatigue
my husband and I have received all Moderna Covid Shots - we never got covid - the problem is we are ... my husband and I have received all Moderna Covid Shots - we never got covid - the problem is we are both physically exhausted all the time started about a year ago and we wanted to know if this could be a long term side effect of all the shots More
2853464 23 F KY 08/10/2025 FLU3
 SANOFI PASTEUR
Guillain-Barre syndrome, Lumbar puncture Guillain-Barre syndrome, Lumbar puncture
Guillaine Barre Syndrome Guillaine Barre Syndrome
โœ“ โœ“
2853465 89 F FL 08/10/2025 FLU3
RSV
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 u8764bb
bg5j4
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
Patient had previously received RSV (Arexvy) on 9/28/23. Per patient, she did not experience any a... Patient had previously received RSV (Arexvy) on 9/28/23. Per patient, she did not experience any adverse effects. More
2853466 93 M FL 08/10/2025 FLU3
RSV
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 u8764bb
bg5j4
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
Patient had previously received RSV (Arexvy) on 9/28/23. Per patient, he did not experience any ad... Patient had previously received RSV (Arexvy) on 9/28/23. Per patient, he did not experience any adverse effects. More
2853467 66 M PR 08/10/2025 FLU3
TDAP
VARZOS
 SEQIRUS, INC.
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS


Erythema, Inflammation; Erythema, Inflammation; Erythema, Inflammation Erythema, Inflammation; Erythema, Inflammation; Erythema, Inflammation
THIS WAS THE VACCINE THAT CAUSED AN ADVERSE REACTION. WITH RED AND INFLAMED AREA. THIS WAS THE VACCINE THAT CAUSED AN ADVERSE REACTION. WITH RED AND INFLAMED AREA.
2853468 71 M FL 08/10/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 bg5j4
Extra dose administered Extra dose administered
pt had apparently already received 2 doses several years ago. got yet a 3rd dose when only 1 dose is... pt had apparently already received 2 doses several years ago. got yet a 3rd dose when only 1 dose is required More
2853469 70 F FL 08/10/2025 PNC21
 MERCK & CO. INC.
 Z004302
Fatigue, Injection site erythema, Injection site rash, Injection site warmth, Ma... Fatigue, Injection site erythema, Injection site rash, Injection site warmth, Malaise More
THE PATIENT EXPERIENCED SEVERE FATIGUE AND MALAISE. SHE HAD A RASH THAT EXTENDED FROM THE INJECTIION... THE PATIENT EXPERIENCED SEVERE FATIGUE AND MALAISE. SHE HAD A RASH THAT EXTENDED FROM THE INJECTIION SITE TO HER ELBOW. IT WAS RED AND WARM TO THE TOUCH. More
2853470 12 F OH 08/10/2025 MNQ
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8438AA
U8620AA
Dizziness, Mydriasis, Vision blurred; Dizziness, Mydriasis, Vision blurred Dizziness, Mydriasis, Vision blurred; Dizziness, Mydriasis, Vision blurred
Dizziness, blurred vision, dilated pupils Dizziness, blurred vision, dilated pupils
2853471 60 F FL 08/10/2025 FLU3
PNC21
 SANOFI PASTEUR
MERCK & CO. INC.
 U8823CA
Z004302
Fatigue, Injection site rash, Injection site warmth, Malaise, Mobility decreased... Fatigue, Injection site rash, Injection site warmth, Malaise, Mobility decreased; Fatigue, Injection site rash, Injection site warmth, Malaise, Mobility decreased More
THE PATIENT EXPERIENCED SEVERE MALAISE AND FATIGE. SHE COULD NOT GET OUT OF THE BED FOR 2 DAYS. SHE ... THE PATIENT EXPERIENCED SEVERE MALAISE AND FATIGE. SHE COULD NOT GET OUT OF THE BED FOR 2 DAYS. SHE SLSO HAD A HUGE RASH ON HER LET ARM AT THE INJECTION SITE AND SURROUNDING AREA. IT WAS HOT TO THE TOUCH More
2853472 46 F ID 08/10/2025 HEP
 MERCK & CO. INC.
 P-Y004552
Underdose Underdose
patient was given Hep B 19 yrs only (0.5ml). The appropriate dosage for patients 20 years and older ... patient was given Hep B 19 yrs only (0.5ml). The appropriate dosage for patients 20 years and older is 1 mL. The 0.5mL dose is considered invalid More
2853473 76 F FL 08/10/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Facial pain, Fatigue, Malaise, Mobility decreased, Pyrexia; Rash, Skin discolour... Facial pain, Fatigue, Malaise, Mobility decreased, Pyrexia; Rash, Skin discolouration, Tenderness, Tremor More
THE PATIENT EXPERIENCED SEVERE MALAISE AND FATIGUE FOR 2 DAYS. SHE COULD NOT LIFT EITHER ARM. SHE HA... THE PATIENT EXPERIENCED SEVERE MALAISE AND FATIGUE FOR 2 DAYS. SHE COULD NOT LIFT EITHER ARM. SHE HAD FEVER, THE SHAKES, AND RIGHT SIDE FACE PAIN THAT WAS PAINFUL TO TOUCH. SHE ALSO HAD A PURPLISH RASH ON HER FACE AS WELL. More
2853474 74 F FL 08/10/2025 RSV
 PFIZER\WYETH
 HY1813
Extra dose administered Extra dose administered
PATIENT ALREADY RECEIVED THIS VACCINE BACK IN 2023 PATIENT ALREADY RECEIVED THIS VACCINE BACK IN 2023
2853475 12 M TX 08/10/2025 FLU3
MNQ
 SANOFI PASTEUR
NOVARTIS VACCINES AND DIAGNOSTICS
 U8823CA
AMVB072A
Anaphylactic reaction, Hypopnoea, Loss of consciousness, Urticaria; Anaphylactic... Anaphylactic reaction, Hypopnoea, Loss of consciousness, Urticaria; Anaphylactic reaction, Hypopnoea, Loss of consciousness, Urticaria More
Patient was administered the above vaccinations and within a few minutes, patient developed anaphyla... Patient was administered the above vaccinations and within a few minutes, patient developed anaphylactic reaction which includes shallow breathing, hives and unconscious. I administered Epipen to the right thigh and within a few seconds, patient breathing was better and consciousness returned. More
2853498 17 F VA 08/10/2025 FLU3
HPV9
MNQ
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 39R9B
Y012921
U8361AA
9JT4S
Dizziness, Feeling hot; Dizziness, Feeling hot; Dizziness, Feeling hot; Dizzines... Dizziness, Feeling hot; Dizziness, Feeling hot; Dizziness, Feeling hot; Dizziness, Feeling hot More
PATIENT SCHEDULED 4 VACCINATIONS. THE PATIENT WAS IMMUNIZED FIRST WITH FLUARIX AND THEN GARDASIL. AF... PATIENT SCHEDULED 4 VACCINATIONS. THE PATIENT WAS IMMUNIZED FIRST WITH FLUARIX AND THEN GARDASIL. AFTER GARDASIL SHE FELT LIGHTHEADED AND OVERHEATED. THE IMMUNIZING INTER CALLED ME (RPH) INTO THE ROOM AND THE PATIENT APPEARED TO BE ON THE VERGE OF SYNCOPE BUT STATED SHE WAS JUST VERY AFRAID OF NEEDLES. SHE WAS GIVEN WATER AND PAPER TOWELS TO WIPE HER FACE. PATIENT AND HER PARENTS DECLINED OFFER TO CALL EMS. RECOMMENDED THE PATIENT NOT GET THE OTHER 2 VACCINATIONS (MENINGITIS AND TDAP) AT THIS TIME, BUT THE PATIENT STATED SHE FELT BETTER AFTER DRINKING WATER AND RESTING FOR 15 MINUTES AND PATIENT/PARENTS DECIDED TO CONTINUE WITH THE IMMUNIZATIONS. PATIENT REMAINED SEATED FOR 30 MINTUES WITH NO FURTHER ADVERSE EFFECTS. More
2853499 68 M TX 08/10/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FK9896
FK9896
Abdominal distension, Biopsy colon abnormal, Blood test abnormal, Colitis micros... Abdominal distension, Biopsy colon abnormal, Blood test abnormal, Colitis microscopic, Colonoscopy abnormal; Diarrhoea, Flatulence, Immunodeficiency common variable More
1. Severe recurring diarrhea, gas, bloating - diagnosed by Dr. 06/28/2022 via colonoscopy and biopsy... 1. Severe recurring diarrhea, gas, bloating - diagnosed by Dr. 06/28/2022 via colonoscopy and biopsy; no previous history prior to COVID-19 vaccines; treated with budesonide, temporary relief only; condition worsened - treated with prednisone 10mg starting 12/2022 with some relief; recurring episodes of severe diarrhea treated with prednisione to current date. 2. Immune system no longer protective - CVID diagnosed 1/12/2024 by Dr.; no previous history prior to COVID-19 vaccines; currently treated with subcutaneous infusion of HyQvia. More
2853500 51 F 08/10/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 NR4T5
Rash Rash
Largest rash on opposite shoulder, elbow-to-wrist Largest rash on opposite shoulder, elbow-to-wrist
2853409 VA 08/09/2025 MMRV
 MERCK & CO. INC.
 Z003309
No adverse event, Product storage error No adverse event, Product storage error
No symptoms or side effects were reported by HCP; HCP reporting that a patient received a dose of im... No symptoms or side effects were reported by HCP; HCP reporting that a patient received a dose of improperly stored PROQUAD. Reference TE case #02843001. HCP reported that she did not know the date the excursion occurred, but knows the PROQUAD was administered following the excursion. HCP reported; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 14-Jul-2025, the patient was vaccinated with an improperly storage dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), (lot #Z003309, expiration date: 21-Jul-2026) 0.5 mL, for prophylaxis, diluted with sterile diluent (MERCK STERILE DILUENT), 0.5 mL (indication, expiration date, and lot # were not reported). Temperature excursion occurred at 52.2 F; timeframe was unknown (Product storage error). No symptoms or side effects were reported. More
2853410 M NJ 08/09/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.

Chills, Fatigue, Headache, Injection site pruritus, Injection site rash; Injecti... Chills, Fatigue, Headache, Injection site pruritus, Injection site rash; Injection site swelling, Pain in extremity More
On 7/29/25 he did not have a rash any longer, and today 7/30, it is back and stronger than it was an... On 7/29/25 he did not have a rash any longer, and today 7/30, it is back and stronger than it was and it is itching, at the same spot, around the inject site. Right arm.; On 7/29/25 he did not have a rash any longer, and today 7/30, it is back and stronger than it was and it is itching, at the same spot, around the inject site. Right arm.; Initially his arm was sore for a couple days; Headache; Fatigue; chills; slight rash around the injection site; a little swollen around injection site; This spontaneous report was received from a Consumer or other non health professional and refers to a 69-year-old male patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant medications included Rosuvastatin calcium (CRESTOR). On 25-Jul-2025, the patient was vaccinated with a dose of Pneumococcal 21-valent Conjugate Vaccine Injection (CAPVAXIVE) in Right Arm (strength, dose, dose number, route, lot # and expiration date were not reported) as vaccination. On 25-Jul-2025, the patient had initially his arm sore for a couple days (vaccination site pain) with chills, fatigue, headache, a little swollen (Vaccination site swelling) and a slight rash around the injection site ( Vaccination site rash). On 29-JUL-2025, the patient recovered from the vaccination site rash, however on 30-Jul-2025, the rash back and stronger (Vaccination site rash) than it was and it is itching at the same spot, around the inject site (Right arm) (Vaccination site pruritus). It was mentione that the patient did not Sought Medical Attention and not received treatment. At the reporting time, the patient had not recovered from Headache, vaccination site pain, Fatigue, chills, Vaccination site swelling, Vaccination site pruritus and Vaccination site rash (onset date: 30-Jul-2025). The causal relationship between all adverse events and Pneumococcal 21-valent Conjugate Vaccine Injection (CAPVAXIVE) was not provided. More
2853412 0.67 F VA 08/09/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 yN2X2
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
8-month-old patient accidentally received a dose of Kinrix; 8-month-old patient accidentally receive... 8-month-old patient accidentally received a dose of Kinrix; 8-month-old patient accidentally received a dose of Kinrix as their third IPV and DTaP series; This non-serious case was reported by a nurse via call center representative and described the occurrence of inappropriate age at vaccine administration in a 8-month-old female patient who received DTPa-IPV (Kinrix) (batch number yN2X2, expiry date 01-OCT-2026) for prophylaxis. On 14-JUL-2025, the patient received Kinrix. On 14-JUL-2025, an unknown time after receiving Kinrix, the patient experienced inappropriate age at vaccine administration (Verbatim: 8-month-old patient accidentally received a dose of Kinrix) and inappropriate schedule of vaccine administered (Verbatim: 8-month-old patient accidentally received a dose of Kinrix as their third IPV and DTaP series). The outcome of the inappropriate age at vaccine administration and inappropriate schedule of vaccine administered were not applicable. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 17-JUL-2025 A nurse called in to report that an 8-month-old patient accidentally received a dose of Kinrix as their third IPV and DTaP series, which led to an inappropriate age at vaccine administration and inappropriate schedule of vaccine administered. They stated the first two doses were with Pediarix. The vaccine administration facility was the same as primary reporter. More
2853413 08/09/2025 COVID19
 PFIZER\BIONTECH
COVID-19, Drug ineffective COVID-19, Drug ineffective
the following year, patient did get COVID and got pretty sick with it even though they did get vacci... the following year, patient did get COVID and got pretty sick with it even though they did get vaccinated; the following year, patient did get COVID and got pretty sick with it even though they did get vaccinated; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A 69-year-old patient received BNT162b2 (COMIRNATY NOS), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2024, outcome "unknown" and all described as "the following year, patient did get COVID and got pretty sick with it even though they did get vaccinated". The clinical course was reported as follows: Patient was a teacher working in a fitness facility and they felt vulnerable. The patient didn't know if they should get another dose before school started or wait until the new version was available, but that might be after school started. The patient asked if they could get another dose every 6 months. Two years ago, the patient's superintendent urged them to get vaccinated before they came to school because of the likelihood of a surge with kids coming back into the classroom. The following year, patient did get COVID and got pretty sick with it even though they did get vaccinated. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2853426 11 F IL 08/09/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Bell's palsy, Hypoaesthesia; Bell's palsy, Hypoaesthesia Bell's palsy, Hypoaesthesia; Bell's palsy, Hypoaesthesia
Diagnosed with Bell's Pasly. Numbness on right side of face Diagnosed with Bell's Pasly. Numbness on right side of face
2853427 0.33 M OK 08/09/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
Death, Pyrexia Death, Pyrexia
Fever, 2 days later death occurred Fever, 2 days later death occurred
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2853428 42 F WA 08/09/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Brain fog, COVID-19, Dizziness, Fatigue, Heart rate decreased; Malaise, Nausea, ... Brain fog, COVID-19, Dizziness, Fatigue, Heart rate decreased; Malaise, Nausea, Oxygen saturation decreased, Pain, Pyrexia More
Fell ill - high fever. Extremely body aches, dizziness, extremely fatigue, nausea, brain fog and ext... Fell ill - high fever. Extremely body aches, dizziness, extremely fatigue, nausea, brain fog and extreme pain, ended up in the ER after a week from getting the vaccine. They claimed it was because I caught covid. O2 levels dropped to 86. Heart rate dropped to 38. Fever 104. More
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2853429 0.33 M TX 08/09/2025 DTAPHEPBIP
DTAPHEPBIP
HIBV
HIBV
PNC20
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
PFIZER\WYETH
 TE499
TE499
35FA4
35FA4
LP4948
LP4948
C-reactive protein, Computerised tomogram head, Cyanosis, Electrocardiogram, Ful... C-reactive protein, Computerised tomogram head, Cyanosis, Electrocardiogram, Full blood count; Hypotonic-hyporesponsive episode, Metabolic function test, Pallor, Procalcitonin; C-reactive protein, Computerised tomogram head, Cyanosis, Electrocardiogram, Full blood count; Hypotonic-hyporesponsive episode, Metabolic function test, Pallor, Procalcitonin; C-reactive protein, Computerised tomogram head, Cyanosis, Electrocardiogram, Full blood count; Hypotonic-hyporesponsive episode, Metabolic function test, Pallor, Procalcitonin More
Hypotonic-Hyporesponsive episode - patient went limp, pale and blue color of the face lasting about ... Hypotonic-Hyporesponsive episode - patient went limp, pale and blue color of the face lasting about 4 minutes More
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2853430 61 F GA 08/09/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 LM2211
TFAA2434
Pain in extremity; Pain in extremity Pain in extremity; Pain in extremity
THe patient reported that she has been having pain in her arms since last October. She states she is... THe patient reported that she has been having pain in her arms since last October. She states she is unable to lift more than 15 pounds and that her arms fall asleep often. More
2853431 31 F WA 08/09/2025 COVID19
COVID19
COVID19
COVID19
MMR
MMR
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER





Menstruation delayed; Menstruation delayed; Menstruation delayed; Menstruation d... Menstruation delayed; Menstruation delayed; Menstruation delayed; Menstruation delayed; Menstruation delayed; Menstruation delayed More
Missed period 10+ days, no pregnancy. Unusual as it is always on time. Missed period 10+ days, no pregnancy. Unusual as it is always on time.
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