🏥 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 💀 🏥 🚑 ♿ ⚠️
2864910 48 F MI 10/10/2025 UNK
 UNKNOWN MANUFACTURER
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Gave a HD Fluzone vaccine to patient who was <65 years of age. Gave a HD Fluzone vaccine to patient who was <65 years of age.
2864911 29 F OH 10/10/2025 COVID19
 MODERNA
 3052731
Arthralgia, Immediate post-injection reaction, Mobility decreased Arthralgia, Immediate post-injection reaction, Mobility decreased
Patient came to see NP at clinic with complaints of left shoulder loss of motion and severe pain aft... Patient came to see NP at clinic with complaints of left shoulder loss of motion and severe pain after flu and COVID-19 vaccines on 10/6/25 at Pharmacy. This was her first time reporting the incident. Patent states immediately the higher injection felt wrong and caused a shooting pain anteriorly into her shoulder joint. She then began to have severe pain that night and in the morning could not move her shoulder. Patient only has full ROM from the elbow down. Patient denies any other injury to her shoulder or previous injury/surgery. More
2864912 63 F PA 10/10/2025 COVID19
FLU3
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
 3052581
N9CS2
Contusion, Injected limb mobility decreased, Pain in extremity; Contusion, Injec... Contusion, Injected limb mobility decreased, Pain in extremity; Contusion, Injected limb mobility decreased, Pain in extremity More
Pt called to explain that her right arm, the one the COVID shot was in, is bruised and achy. Some li... Pt called to explain that her right arm, the one the COVID shot was in, is bruised and achy. Some limited ROM, can raise above shoulder but not above head. Had previous shot years ago given by a pharmacist that was in her bursa, this "does not feel like that". She has taken ibuprofen with some relief. Encouraged her to keep me informed of the evolution of this event. No complaints on L arm where Flu was. Did explain that we sometimes see inflammation with the COVID shot, but to follow up with PCP as needed and that I would file this report. More
2864915 27 F 10/10/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Exposure during pregnancy, Product use issue Exposure during pregnancy, Product use issue
Patient presented to pharmacy for RSV vaccine. It 34 weeks pregnant. Pharmacist looked up guidelines... Patient presented to pharmacy for RSV vaccine. It 34 weeks pregnant. Pharmacist looked up guidelines for RSV vaccine and confirmed it can be administered between 32-36 weeks, but did not realize that only Abrysvo is indicated in pregnancy (NOT Arexvy). Pharmacy only stocks Arexvy. Patient received a dose. 3 days later, pharmacist realized the error. Contacted patient and patient's OB/Gyn . Patient is being monitored but no noted signs of adverse events. Prior to vaccination, patient was already scheduled for an induction at 37 weeks. More
2864916 70 F MI 10/10/2025 COVID19
 MODERNA
 3052154
Erythema, Pruritus, Skin warm, Swelling Erythema, Pruritus, Skin warm, Swelling
Swollen, red, painful, hot to touch, itchy Swollen, red, painful, hot to touch, itchy
2864917 30 F MI 10/10/2025 COVID19
COVID19
 MODERNA
MODERNA
 O44A21A
O44A21A
Blood test, Cerebrovascular accident, Computerised tomogram, Contrast echocardio... Blood test, Cerebrovascular accident, Computerised tomogram, Contrast echocardiogram, Echocardiogram; Magnetic resonance imaging, Transient ischaemic attack More
Stroke, TIA Stroke, TIA
✓ ✓
2864918 66 F GA 10/10/2025 FLU3
PNC21
 SANOFI PASTEUR
MERCK & CO. INC.
 U8859BA
Z009681
Pruritus, Pyrexia; Pruritus, Pyrexia Pruritus, Pyrexia; Pruritus, Pyrexia
Patient received flu and pneumonia vaccinations on 10/8/25 in the late afternoon. She presented to ... Patient received flu and pneumonia vaccinations on 10/8/25 in the late afternoon. She presented to the pharmacy on 10/10 with complaint of fever that began the evening of vaccination, and itching that began the following evening. Patient showed area of itching, no rash present. Itching located around the waist and moving down the legs. The patient had been taking fever reducer and loratadine. More
2864919 73 M PA 10/10/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 na4457
u8862ba
Loss of consciousness; Loss of consciousness Loss of consciousness; Loss of consciousness
patient sat for a while and felt okay then as leaving passed out patient sat for a while and felt okay then as leaving passed out
2864921 72 F NC 10/10/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 3052296
407247
Skin discolouration; Skin discolouration Skin discolouration; Skin discolouration
RED YELLOWISH PATCH PROBABLY DUE TO PATIENT IS ON ASPIRIN RED YELLOWISH PATCH PROBABLY DUE TO PATIENT IS ON ASPIRIN
2864922 90 F MN 10/10/2025 FLU3
 SEQIRUS, INC.
 407248
Contusion, Feeling hot, Pain Contusion, Feeling hot, Pain
Patient presented to clinic with excessive bruising, sore, warmth. Treatment - warm compresses Patient presented to clinic with excessive bruising, sore, warmth. Treatment - warm compresses
2864923 25 F TX 10/10/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 PK9C5
Exposure during pregnancy Exposure during pregnancy
patient is G2P0101 that is 33 weeks and 4 days gestation when she presented to the PCP office with a... patient is G2P0101 that is 33 weeks and 4 days gestation when she presented to the PCP office with a letter from her OB/GYN provider requesting for patient to receive the RSV vaccine, her first baby was born at 32 weeks by C-section due to a complete placenta abruption, patient's due date for this current pregnancy is 11-22-25. More
2864925 58 M CA 10/10/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 94j5e
Erythema, Feeling hot, Peripheral swelling Erythema, Feeling hot, Peripheral swelling
Patient received 2nd Shingrix vaccine on 10/1/25. He came in the morning of 10/10/25, to let us know... Patient received 2nd Shingrix vaccine on 10/1/25. He came in the morning of 10/10/25, to let us know that on the night of 10/10/25, saying that on the night of 10/1/25, he experienced a red, warm swollen band across the arm. He called his primary care physician, who said it's not normal, to let pharmacy know so they could document it. Patient said he didn't experience any other symptoms (fever, sweating, spreading rash, etc). The rash lasted 4-5 days, gradually going down. More
2864928 3 F CO 10/10/2025 DTAPHEPBIP
FLU3
HIBV
MMR
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 TE499
F4A7R
Z603263
4F9T5
LX4486
Injection site pain, Pyrexia; Injection site pain, Pyrexia; Injection site pain,... Injection site pain, Pyrexia; Injection site pain, Pyrexia; Injection site pain, Pyrexia; Injection site pain, Pyrexia; Injection site pain, Pyrexia More
Father of child states that pt had a little bit of fever and her legs are sore but no other symptoms... Father of child states that pt had a little bit of fever and her legs are sore but no other symptoms. More
2864929 27 M CO 10/10/2025 FLU3
 SANOFI PASTEUR
 u8848AA
Throat tightness Throat tightness
Throat tightening and DIB he received the flu shot. @ 600. Given Cterizine, Epi pen, orders for p... Throat tightening and DIB he received the flu shot. @ 600. Given Cterizine, Epi pen, orders for prednisone. Discharge home with medicines More
2864930 72 M CT 10/10/2025 FLU3
FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
 409166
409166
409166
Blood creatinine normal, Blood pH normal, Brain natriuretic peptide normal, Ches... Blood creatinine normal, Blood pH normal, Brain natriuretic peptide normal, Chest X-ray normal, Condition aggravated; Dyspnoea, Electrocardiogram normal, Haemoglobin decreased, Influenza virus test negative, Liver function test normal; PCO2 increased, Platelet count decreased, Troponin normal, White blood cell count normal More
Per local ER notes: ... Per local ER notes: 72yom with PMHx including HTN, HLD, OSA, CVA, anxiety, asthma/O2 dependent COPD (2.5 L), atrial fibrillation on Eliquis presents for evaluation of shortness of breath Patient states he had a flu shot yesterday and feels his breathing worsened a few hours after he received it EMS reports patient was 89% on his baseline 2.5 L upon their arrival, improved SpO2 when O2 increased to 3 L Patient reports dyspnea on exertion and chronic cough that is unchanged No associated chest pain and denies fever/chills More
2864931 80 M PA 10/10/2025 FLU3
 SANOFI PASTEUR
 U8862ba
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Red at the site of injection, swelling at injection site. Red at the site of injection, swelling at injection site.
2864932 71 F KY 10/10/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.
 na0587
407267
Chills, Cold sweat, Pain; Chills, Cold sweat, Pain Chills, Cold sweat, Pain; Chills, Cold sweat, Pain
Per patient - chills, body ache, cold sweats Per patient - chills, body ache, cold sweats
2864934 46 M CO 10/10/2025 FLU3
 SANOFI PASTEUR
 U8848AA
Cough, Dysphagia, Dyspnoea Cough, Dysphagia, Dyspnoea
per client- i received the fllu vaccine and about 30 minutes or so later , he was back in his offic... per client- i received the fllu vaccine and about 30 minutes or so later , he was back in his office and started to notice that is was difficulet to swallow, developed a dry cough and was hard to breath. I took 50 mg of benadryl and a full dose of my albuteraol inhaler. does not have asthma His co-workers instructed him to return to the flu rodeo, no symptoms noted at that time. More
2864935 48 F SC 10/10/2025 FLU3
 SANOFI PASTEUR
 U8832aa
Eye swelling, Peripheral swelling, Pyrexia, Swelling face, Urticaria Eye swelling, Peripheral swelling, Pyrexia, Swelling face, Urticaria
Patient Stated: A few hours after vaccine had a fever; next day 10/08/25 notice small hives and swe... Patient Stated: A few hours after vaccine had a fever; next day 10/08/25 notice small hives and swelling of face and hands (mild); took Ibuprofen and chewable Benadryl; notice that the hives and swelling was improving (getting better); On Thursday reported to nurse at school who contacted me asap 10/09/25; Only notice small amount swelling around one eye on 10/09/25; Did not have to seek medical assistance; She definitely felt everything was resolving by evening 10/09/25 More
2864936 19 F OH 10/10/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 3J9G4
Expired product administered Expired product administered
a vaccine for Havrix, the Hep A vaccine, it was expired on 30-Aug-2025 and it was given to a patient... a vaccine for Havrix, the Hep A vaccine, it was expired on 30-Aug-2025 and it was given to a patient; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 19-year-old female patient who received HAV (Havrix) (batch number 3J9G4, expiry date 30-AUG-2025) for prophylaxis. On 23-SEP-2025, the patient received Havrix. On 23-SEP-2025, an unknown time after receiving Havrix, the patient experienced expired vaccine used (Verbatim: a vaccine for Havrix, the Hep A vaccine, it was expired on 30-Aug-2025 and it was given to a patient). The outcome of the expired vaccine used was 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: 23-SEP-2025 A Primary care supervisor had a vaccine for Havrix, the Hepatitis A vaccine, it was expired on 30th August 2025, and it was given to a patient on 23rd September 2025 which led to expired vaccine used. More
2864938 11 M IN 10/10/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 3052579
407002
Injection site pain, Injection site swelling, Urticaria; Injection site pain, In... Injection site pain, Injection site swelling, Urticaria; Injection site pain, Injection site swelling, Urticaria More
Administered vaccines around 12:30 pm on 10/10/2025, and further concerns for hives around 18:00. Ar... Administered vaccines around 12:30 pm on 10/10/2025, and further concerns for hives around 18:00. Arm had a little bit of swelling around the site of injection and was complaining of pain. Received a dose of diphenhydramine and cortisone cream around 23:30 pm. Hives have resolved as of the morning of 10/11/2025. More
2864939 54 M AL 10/10/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EW0175
EW0175
FC3184
FC3184
Anosmia, Asthenia, Asthma, Lethargy, Nasal polypectomy; Nasal polyps, Rhinitis, ... Anosmia, Asthenia, Asthma, Lethargy, Nasal polypectomy; Nasal polyps, Rhinitis, Sleep apnoea syndrome, Supraventricular tachycardia, Tinnitus; Anosmia, Asthenia, Asthma, Lethargy, Nasal polypectomy; Nasal polyps, Rhinitis, Sleep apnoea syndrome, Supraventricular tachycardia, Tinnitus More
The second shot listed in item 17 was given on 8/31/2021 1/1/2022 Tinnitus, ongoing with no relief ... The second shot listed in item 17 was given on 8/31/2021 1/1/2022 Tinnitus, ongoing with no relief 3/13/2022 SVT diagnosis, a single 12 hour episode 8/10/2022 Sleep apnea diagnosis, ongoing 3/2023 Loss of smell, partially recovered 7/2025 after Dr treatment 4/2023 Nasal polyp/rhinitis diagnosis, surgery fro polyps, onigoing rhinitis issues affecting sinuses and lungs/breathing 4/2023 Asthma diagnosis, Nucala medication has greatly improved situation. Still reduced energy and lethargic however. More
2864940 9 F RI 10/10/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 F4A7R
Rash, Rash pruritic, Urticaria Rash, Rash pruritic, Urticaria
rash that developed the day after flu vaccine. Rash was on stomach/back/chest. Not itchy. Was due to... rash that developed the day after flu vaccine. Rash was on stomach/back/chest. Not itchy. Was due to be seen yesterday but cancelled appt b/c rash resolved. Rash returned after playing outside yesterday. Rash was on neck, face, stomach, back. Was itchy. Gave Benadryl with improvement but no resolution. Had welts last night as Benaryl wore off. Today, rash was present. Still itchy today.Denies fever. referred to Allergy recommended take certrizine and if still itching to call and will prescribe prednisone More
2864941 54 F NV 10/10/2025 COVID19
 PFIZER\BIONTECH
 NA0846
Underdose Underdose
Patient was inadvertently given pediatric dose of Comirnaty COVID vaccine instead of adult dose. Patient was inadvertently given pediatric dose of Comirnaty COVID vaccine instead of adult dose.
2864942 8 F CA 10/10/2025 HPV9
MNQ
TDAP
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
GLAXOSMITHKLINE BIOLOGICALS
 Y018297
AH7Z3
37R35
No adverse event, Product administered to patient of inappropriate age; No adver... No adverse event, Product administered to patient of inappropriate age; No adverse event, Product administered to patient of inappropriate age; No adverse event, Product administered to patient of inappropriate age More
VACCINES ADMINISTERED TO SOON FOR PATIENTS AGE, PER MOM PT HAS NOT HAD ANY SIDE EFFECTS. VACCINES ADMINISTERED TO SOON FOR PATIENTS AGE, PER MOM PT HAS NOT HAD ANY SIDE EFFECTS.
2864943 21 F PA 10/10/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 3052835
407007
Loss of consciousness, Pallor; Loss of consciousness, Pallor Loss of consciousness, Pallor; Loss of consciousness, Pallor
Patient passed out for about 25 seconds, about two minutes after the injection. She was seated in ou... Patient passed out for about 25 seconds, about two minutes after the injection. She was seated in our hearing aid department right outside the counseling room where she was vaccinated. Her blood pressure was 90/53. She was given ice packs to put on her neck. She was feeling better and gaining more color in her face after about 10 minutes, and left. Her mother reported that she had eaten prior to getting both her vaccines. More
2864944 82 F LA 10/10/2025 PNC20
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 LN4931
94J5E
Rash; Rash Rash; Rash
RASH UNDER AND AROUND RIGHT ARM RASH UNDER AND AROUND RIGHT ARM
2864945 27 F IN 10/10/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
Injection site rash, Rash, Rash erythematous, Rash pruritic Injection site rash, Rash, Rash erythematous, Rash pruritic
I developed an allergic reaction that began as small red bumps around the vaccination site and has s... I developed an allergic reaction that began as small red bumps around the vaccination site and has since spread across my body. The rash is very itchy and has not improved over the past week. I was seen by provider at the Student Health Center, who prescribed a steroid and an antihistamine, but the symptoms have not subsided. More
2864946 76 M OH 10/10/2025 COVID19
PNC21
 PFIZER\BIONTECH
MERCK & CO. INC.
 MY9547
Z003579
Dizziness, Injection site bruising, Injection site reaction; Dizziness, Injectio... Dizziness, Injection site bruising, Injection site reaction; Dizziness, Injection site bruising, Injection site reaction More
Patient received Capvaxive and Comirnaty on 9/18/25 both in the right arm. He presented to the pharm... Patient received Capvaxive and Comirnaty on 9/18/25 both in the right arm. He presented to the pharmacy today saying on 9/19/25 he started to develop dark bruising and blood pooling underneath skin. He had a large area near injection site of bruising and blood underneath skin but also had another large area just below his elbow. It appeared to be some sort of vasculitis reaction. The reaction was pretty extensive throughout his arm. I asked about any other symptoms he was having and he originally said no but after questioning did say he has felt a little dizzy. I looked at patient's other arm and no reaction. I asked if he was ever told about having a clotting disorder and he said no. He said he thinks the reaction is improving. I told him I highly recommend he call his PCP today and follow up with them. I also called his PCP myself to let them know. I spoke to a receptionist and let her know all the details. Patient had received only pfizer vaccines in the past and this was his 7th covid pfizer vaccine More
2864947 48 F IN 10/10/2025 FLU3
 SANOFI PASTEUR
 U8881BA
Arthralgia, Pain, Pain in extremity, Swelling, Tenderness Arthralgia, Pain, Pain in extremity, Swelling, Tenderness
10/3/25 received vaccine. developed pain to left arm, radiates to left clavicle. reported to Employe... 10/3/25 received vaccine. developed pain to left arm, radiates to left clavicle. reported to Employee Health on 10/8/25 with c/o left arm/clavicle pain. also had swelling/raised area to left clavicle that was painful to touch. no redness, no fever. Sent to Occupational Health for evaluation. More
2864949 78 F CA 10/10/2025 FLU3
 SEQIRUS, INC.
 407244
Back pain, Chest pain, Hyperhidrosis Back pain, Chest pain, Hyperhidrosis
Result type: Oncology Office/Clinic Note Result date: October 10, 2025 9:10 PDT Result status: Modif... Result type: Oncology Office/Clinic Note Result date: October 10, 2025 9:10 PDT Result status: Modified Result title: Flu vaccine reaction Performed by: MD on October 10, 2025 9:43 PDT Verified by: MD on October 10, 2025 9:43 PDT Encounter info: HemOnc, Ambulatory PCA, 10/10/2025 - * Final Report * Document Contains Addenda pt in clinic for Flu vaccine @ 0855, ( Fluad Influeza Vaccine,Adjuvanted) NDC# 70461-025-04/lot# 407244/ Exp. 2026 APR23 within minutes after administering flu vaccine (Left Deltoid, IM) to pt, pt complained of chest pain down center of back down to her tailbone, severe chest pain w/ forehead hyperhidrosis. Dr. was advised and present, Rapid Response was called at 0900 a.m, vitals were taken at 0901 a.m., L arm with BP 165/72 O2 sat. 99% HR 85 Rapid Response Team arrived and pt was transported to E.R for further evaluation Signature Line Electronically Signed By: MD On 10/10/25 09:43 Co Signature By: Modify Signature By: MA On 10/10/25 09:27 Addendum by MA on October 10, 2025 9:50 PDT (Verified) Correction Vaccine administered Right Deltoid, IM Signature Line Electronically Signed By: MA On 10/10/25 09:51 Co Signature By: Modify Signature By: MA On 10/10/25 09:50 More
2864950 23 F NE 10/10/2025 FLU3
RSV
 SEQIRUS, INC.
PFIZER\WYETH
 407981
LL8391
Injury associated with device; Injury associated with device Injury associated with device; Injury associated with device
Patient is an employee at our pharmacy and had a needlestick injury to her left index finger. Patient is an employee at our pharmacy and had a needlestick injury to her left index finger.
2864952 81 F WI 10/10/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 g2ha7
Dyspnoea, Fatigue, Headache, Myalgia, Nausea Dyspnoea, Fatigue, Headache, Myalgia, Nausea
fatigue, myalgia, headache, nausea, dyspnea fatigue, myalgia, headache, nausea, dyspnea
2864953 19 F IA 10/10/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 9KC4M
Incorrect dose administered Incorrect dose administered
Engerix-B adult dose administration in a 19-year-old patient; Engerix-B adult dose administration in... Engerix-B adult dose administration in a 19-year-old patient; Engerix-B adult dose administration in a 19-year-old patient; This non-serious case was reported by a other health professional via call center representative and described the occurrence of adult product administered to child in a 19-year-old female patient who received HBV (Engerix B adult) (batch number 9KC4M, expiry date 05-SEP-2027) for prophylaxis. On an unknown date, the patient received Engerix B adult. On an unknown date, an unknown time after receiving Engerix B adult, the patient experienced adult product administered to child (Verbatim: Engerix-B adult dose administration in a 19-year-old patient) and overdose (Verbatim: Engerix-B adult dose administration in a 19-year-old patient). The outcome of the adult product administered to child and overdose 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: 23-SEP-2025 A health care provider asked if it was ok to administer an adult dose to a 19-year-old patient which led to overdose and adult product administration to child. More
2864954 29 F TN 10/10/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 2NG23
Extra dose administered Extra dose administered
Pt was given second dose of influenza within a month's time. Vaccine was not completely reconci... Pt was given second dose of influenza within a month's time. Vaccine was not completely reconciled and was entered after given. More
2864955 87 M KY 10/10/2025 FLU3
 SEQIRUS, INC.
 407271
Immediate post-injection reaction, Injection site bruising, Injection site haemo... Immediate post-injection reaction, Injection site bruising, Injection site haemorrhage, Injection site swelling More
Immediately after giving vaccine, the patient formed a bump at the site of vaccination and it bled a... Immediately after giving vaccine, the patient formed a bump at the site of vaccination and it bled and began to bruise. Patient reported that they bruise very easily normally. Upon rubbing the bump it began to go down. Kept patient in the pharmacy to monitor for over 30 minutes and the patient had no complaints and did not feel off or sick at all. The patient reported that they felt completely fine multiple times. The patient had a doctor's appointment coming up the following week and I recommended to the patient to have the doctor check out the area and to also seek medical attention if the bump has not gone away within 2 days. More
2864958 14 M CO 10/10/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.
 NA0590
948414
Crying, Facial pain, Fall, Head injury; Crying, Facial pain, Fall, Head injury Crying, Facial pain, Fall, Head injury; Crying, Facial pain, Fall, Head injury
Patient walked into vaccination room , pleasant with no issues . Patient received 2 vaccines admini... Patient walked into vaccination room , pleasant with no issues . Patient received 2 vaccines administered by pharmacy technician. Technician stated patient had no issues with receiving vaccines, said thank you, walked out of the room ok. Patient took about 10 steps and fell down, hitting their head on a bar on the stand. Pt was aware, breathing, crying, face hurt, speaking while laying on floor. EMS was called and patient was transported to the hospital. More
2864959 83 M OH 10/10/2025 FLU3
 SEQIRUS, INC.
 407246
Extra dose administered Extra dose administered
There is no true adverse event that occurred here. I am filling out this report because the Patient ... There is no true adverse event that occurred here. I am filling out this report because the Patient came to the pharmacy requesting a shingles and RSV vaccine but instead received a flu shot, Which he has already received this year elsewhere. This is to report the duplication of administration of a flu shot. More
2864960 81 M NC 10/10/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
PNC21
PNC21
PNC21
PNC21
PNC21
PNC21
PNC21
PNC21
PNC21
PNC21
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.



















Ammonia normal, Aspartate aminotransferase increased, Blood creatine phosphokina... Ammonia normal, Aspartate aminotransferase increased, Blood creatine phosphokinase MB increased, Blood creatine phosphokinase increased, Blood creatinine increased; Blood culture negative, Blood ethanol normal, Blood glucose normal, Blood lactic acid normal, Blood magnesium normal; Blood sodium decreased, Blood thyroid stimulating hormone increased, Chest X-ray normal, Computerised tomogram head normal, Computerised tomogram neck normal; Confusional state, Drug screen negative, Electrocardiogram normal, Full blood count, Gait inability; Glycosylated haemoglobin normal, Haematocrit normal, Haemoglobin normal, International normalised ratio normal, Lymphocyte count normal; Magnetic resonance imaging head normal, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume increased; Metabolic function test, N-terminal prohormone brain natriuretic peptide increased, Neutrophil count normal, Platelet count decreased, Procalcitonin increased; Protein urine present, Prothrombin time prolonged, Pyrexia, Red blood cell count normal, Red cell distribution width increased; Respiratory pathogen panel, Troponin T increased, Urinary occult blood positive, Urine ketone body present, White blood cell count normal; White blood cells urine negative; Ammonia normal, Aspartate aminotransferase increased, Blood creatine phosphokinase MB increased, Blood creatine phosphokinase increased, Blood creatinine increased; Blood culture negative, Blood ethanol normal, Blood glucose normal, Blood lactic acid normal, Blood magnesium normal; Blood sodium decreased, Blood thyroid stimulating hormone increased, Chest X-ray normal, Computerised tomogram head normal, Computerised tomogram neck normal; Confusional state, Drug screen negative, Electrocardiogram normal, Full blood count, Gait inability; Glycosylated haemoglobin normal, Haematocrit normal, Haemoglobin normal, International normalised ratio normal, Lymphocyte count normal; Magnetic resonance imaging head normal, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal, Mean platelet volume increased; Metabolic function test, N-terminal prohormone brain natriuretic peptide increased, Neutrophil count normal, Platelet count decreased, Procalcitonin increased; Protein urine present, Prothrombin time prolonged, Pyrexia, Red blood cell count normal, Red cell distribution width increased; Respiratory pathogen panel, Troponin T increased, Urinary occult blood positive, Urine ketone body present, White blood cell count normal; White blood cells urine negative More
Fever, marked confusion, inability to walk Hydration in hospital; released in stable condition afte... Fever, marked confusion, inability to walk Hydration in hospital; released in stable condition after one overnight in the hospital More
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2864961 1 F PR 10/10/2025 HEPA
HIBV
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 L4EA4
UK231AA
Z008195
Injection site pain; Injection site pain; Injection site pain Injection site pain; Injection site pain; Injection site pain
A family member of the patient reported taking her to her pediatrician because the child was complai... A family member of the patient reported taking her to her pediatrician because the child was complaining of leg pain. Muscle myalgia. The treatment was not specified, but the pediatrician indicated that the child should wait approximately 7-8 months before receiving any further vaccinations. More
2864963 57 F CA 10/10/2025 FLU3
 SANOFI PASTEUR
 UT8858JA
Headache, Stress, Vomiting Headache, Stress, Vomiting
Healthcare worker informed Employee Health Services of having severe headaches 2 hours after receivi... Healthcare worker informed Employee Health Services of having severe headaches 2 hours after receiving the influenza vaccines (medication error-received 2 doses in one visit). Stated she vomited x1 and had some stress related to the headaches. More
2864964 9 F OR 10/10/2025 COVID19
 MODERNA
 8146545
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
Adult COVID vaccine given to a pediatric patient in error. Contacting manufacture as well. At this t... Adult COVID vaccine given to a pediatric patient in error. Contacting manufacture as well. At this time, patient has not reported any side effects from dose. More
2864965 63 F SC 10/10/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 na0589
u8832ca
Erythema, Pyrexia, Swelling; Erythema, Pyrexia, Swelling Erythema, Pyrexia, Swelling; Erythema, Pyrexia, Swelling
redness, swelling and fever redness, swelling and fever
2864966 79 M MI 10/10/2025 FLU3
 SEQIRUS, INC.
 407252
Device connection issue, No adverse event, Underdose Device connection issue, No adverse event, Underdose
NO ADVERSE EVENT, BUT WHEN GIVING SHOT, SOME LEAKED OUT BETWEEN NEEDLE AND SYRINGE SO NOW INVALID DO... NO ADVERSE EVENT, BUT WHEN GIVING SHOT, SOME LEAKED OUT BETWEEN NEEDLE AND SYRINGE SO NOW INVALID DOSE AND NEEDS TO BE REPEATED More
2864967 77 M WI 10/10/2025 COVID19
RSV
 MODERNA
PFIZER\WYETH
 3052669
ln5464
Blood glucose increased, Condition aggravated, Delirium, Diabetes mellitus; Bloo... Blood glucose increased, Condition aggravated, Delirium, Diabetes mellitus; Blood glucose increased, Condition aggravated, Delirium, Diabetes mellitus More
Pt reports that evening experiencing high blood sugar (self measured) and then delirious over the co... Pt reports that evening experiencing high blood sugar (self measured) and then delirious over the course of 1-2 days that made his family concerned and he did not want to leave bed until 10/9 afternoon More
2864969 23 F IA 10/10/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 93NL9
Blood glucose normal, Dizziness, Headache, Nausea Blood glucose normal, Dizziness, Headache, Nausea
Pt felt nauseous, dizzy and had a headache 10 minutes after getting the vaccine. 50mg of Benadryl wa... Pt felt nauseous, dizzy and had a headache 10 minutes after getting the vaccine. 50mg of Benadryl was given and she slowly felt better over the next hour. More
2864970 37 M FL 10/10/2025 COVID19
 MODERNA
 070H21A
Burning sensation, Inflammation, Joint noise, Sleep disorder, Tinnitus Burning sensation, Inflammation, Joint noise, Sleep disorder, Tinnitus
I have tinnitus it?s been coming and going for years now but only after having the COVID-19 vaccine.... I have tinnitus it?s been coming and going for years now but only after having the COVID-19 vaccine. Now It seems here to stay. I have had some success making the tinnitus go away by dry-fasting for days at a time. The tinnitus can go away from months - but then out of now where come back and stay for months. I had the tinnitus diagnosed by a specialist Sep 19 2022 - but it doesn't matter. They don't fix anything. I also had an ACL surgery two years before the vaccine that was fine, but after the COVID-19 vaccine my knee is often inflamed, and shows signs of chondromalacia. I had the Chondromalacia first diagnosed Nov 3, 2021 - but it doesn't matter either the specialist doesn't fix anything. My knee is much better now today which I attribute to my dry fasting. I can pretty much do a squat down now without hearing tearing gristly noises. There is an audible noise when I straighten my leg but at least I am not kept up at night by a burning knee cap anymore. My knee used to burn so bad I couldn't sleep at night. I did not have any of these problems until after I had the COVID-19 vaccine. I also got the booster shot the Moderna booster shot. Seems (withheld) found 1000x variance in mRNA degradation rates - it might still be making spike protein in me (withheld link) - (withheld country) finds 30% increase in cancer in just the first year after vaccines (withheld like) (withheld name) university finds the mRNA is reverse transcribed into the nucleus as cDNA (withheld link) - which would describe why (withheld name) finds S-protein being produced greater than 2 years after having taken the vaccine (withheld link) "Detectable S1 was found in participants' 348 plasma ranging from 26 to 709 days from the most recent known exposure" which would explain why I may still being inflamed internally by S1. The booster shot was on 12/18/2021 More
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2864971 67 F NC 10/10/2025 COVID19
FLU3
HEPAB
 PFIZER\BIONTECH
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 NA0589
U8832DA
AZ2A3
Dizziness; Dizziness; Dizziness Dizziness; Dizziness; Dizziness
PATIENT FELT DIZZY AND LIGHT HEADED AFTER SHOTS. SHE HAD TO LAY DOWN ON BENCH. PATIENT WAS GIVEN WAT... PATIENT FELT DIZZY AND LIGHT HEADED AFTER SHOTS. SHE HAD TO LAY DOWN ON BENCH. PATIENT WAS GIVEN WATER AND ICE PACK. AFTER ROUGHLY 30 MINUTES PATIENT WAS STARTING TO FEEL BETTER. More
2864972 78 F MA 10/10/2025 COVID19
 PFIZER\BIONTECH
 NA4452
Extra dose administered, Feeling hot Extra dose administered, Feeling hot
On the morning of September 30, 2025, the patient received a dose of the Cominarty (Pfizer-BioNTech)... On the morning of September 30, 2025, the patient received a dose of the Cominarty (Pfizer-BioNTech) COVID-19 vaccine during a vaccine clinic held at her assisted living facility. The patient had requested the vaccine and did not recall having already received a dose earlier in the month. It was later discovered that the patient had previously received a Cominarty COVID-19 vaccine at her primary care provider's office on September 7, 2025. Due to the patient's mild dementia, she was unable to recall the earlier vaccineation, and a second dose was inadvertently administered within the same month. Following the administration of the second dose, the patient did reported feeling mildly feverish. However, multiple temperature checks revealed no measurable fever, and the patient remained clinically stable. Per nursing staff at nursing home, the patient did not exhibit any severe symptoms and continues to do well. This report is being submitted out of an abundance of caution due to the administration of an additional dose within a short interval. More
2864973 17 F CA 10/10/2025 MENB
MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
PFIZER\WYETH
 DD72H
Interchange of vaccine products; Interchange of vaccine products Interchange of vaccine products; Interchange of vaccine products
Interchangeability/Dosing Schedule (BEXSERO 1st dose, TRUMEMBA 2nd dose); This non-serious case was ... Interchangeability/Dosing Schedule (BEXSERO 1st dose, TRUMEMBA 2nd dose); This non-serious case was reported by a nurse via call center representative and described the occurrence of interchange of vaccine products in a 17-year-old female patient who received Men B NVS (Bexsero) (batch number DD72H) for prophylaxis. Co-suspect products included Meningococcal vaccine B rfHbpA/fHbpB (Trumenba) for prophylaxis. On 10-FEB-2025, the patient received the 1st dose of Bexsero. On 18-SEP-2025, the patient received the 2nd dose of Trumenba. On an unknown date, an unknown time after receiving Bexsero and Trumenba, the patient experienced interchange of vaccine products (Verbatim: Interchangeability/Dosing Schedule (BEXSERO 1st dose, TRUMEMBA 2nd dose)). The outcome of the interchange of vaccine products was 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: 23-SEP-2025 The first dose administered was Bexsero and received a Trumenba dose afterwards. The reporter asked how long do they have to wait to complete the series with Bexsero? The reporter consented to follow up. More
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