🏥 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 💀 🏥 🚑 ♿ ⚠️
2872275 85 F GA 11/12/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 ut8781da
ut8781da
Dysstasia, Fall, Fractured coccyx, Intensive care, Lumbar vertebral fracture; Mo... Dysstasia, Fall, Fractured coccyx, Intensive care, Lumbar vertebral fracture; Mobility decreased, Multiple organ dysfunction syndrome, Muscular weakness, Musculoskeletal stiffness More
Reported by daughter [withheld name] 11-5@530PM; After receiving flu shot, left arm became super sti... Reported by daughter [withheld name] 11-5@530PM; After receiving flu shot, left arm became super stiff and could not move finger(s) (did not clarify which finger(s)) Used heat, ice, and APAP, Reports MD told her to continue with the heat, ice and APAP, possible pinched nerve. Still did not help. Then daughter reports patient could not move arm and she fell out of chair when trying to get up because her arm was too weak. She fractured her tail bone and L1 spine. All organs then went into trauma, was in [withheld name] hospital ICU for 10 days then transferred to the trauma floor where she is currently. Muscle relaxer prescribed and picked up, steroid dose pack also later prescribed but not picked up, MRI scheduled for 11-5. On 11-10, [withheld daughter's name] reports, MRI not done because of pacemaker. Still in hospital. More
✓
2872278 3 M IN 11/12/2025 FLU3
 SANOFI PASTEUR
 UT8770MA
Injection site reaction, Rash erythematous, Rash pruritic Injection site reaction, Rash erythematous, Rash pruritic
From patient's chart on morning of 10/29, per Triage RN: "Per mom red itchy rash appeared ... From patient's chart on morning of 10/29, per Triage RN: "Per mom red itchy rash appeared on bilateral thighs starting that evening of 10/27. Mom stated the rash became worse, spreading across thighs, but is now improving today. Mom did not given any otc medications for the rash or symptoms. Mom would like this reported and would like to know how to proceed for further flu vaccinations. " More
2872283 70 F 11/12/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA4459
U8874AA
Muscle spasms, Muscular weakness, Paraesthesia; Muscle spasms, Muscular weakness... Muscle spasms, Muscular weakness, Paraesthesia; Muscle spasms, Muscular weakness, Paraesthesia More
Severe muscle cramps/spasms in legs during sleep. Tingling sensation in legs during day but no spasm... Severe muscle cramps/spasms in legs during sleep. Tingling sensation in legs during day but no spasms. Spasms started night of vaccination and have continued through today with little improvement. She also experienced significant muscle weakness in left biceps. She has had spasm relief with double muscle relaxers More
2872285 76 F VA 11/12/2025 FLU3
FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR


Chills, Disorientation, Dizziness, Feeding disorder, Feeling abnormal; Hyperhidr... Chills, Disorientation, Dizziness, Feeding disorder, Feeling abnormal; Hyperhidrosis, Malaise, Nausea, Pain, Pain in extremity; Pyrexia, Tremor, Visual impairment More
pt says about three hours after the vaccine, her arm was sore and her entire body started hurting, a... pt says about three hours after the vaccine, her arm was sore and her entire body started hurting, aching, nauseated and shaking. She had chills and fever. These symptoms lasted about three hours. She was disoriented and felt bad all over. She was not able to eat anything. She took Tylenol and went to bed. The next day she was still dizzy, achy and not feeling well with a low grade fever. Her eyes felt like they are jiggling where she was not able to read. After waking up she would be soaking wet from sweat. Today, she is still shaky but recovering slowly. More
2872286 56 F IL 11/12/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 ZE423
Asthenia, Chills, Dizziness, Nausea, Tremor Asthenia, Chills, Dizziness, Nausea, Tremor
"10/31/25 at around 0330 started to feel weak, lightheaded, dizzy, nauseous and chilled with un... "10/31/25 at around 0330 started to feel weak, lightheaded, dizzy, nauseous and chilled with uncontrollable shaking. Temp 37.8 c. Sent home around 0600 with above symptoms." More
2872287 47 F OH 11/12/2025 FLU3
 SEQIRUS, INC.
 409109
Arthralgia, Asthenia Arthralgia, Asthenia
Persistent pain and weakness of the left shoulder for greater than four weeks. Patient reports vacci... Persistent pain and weakness of the left shoulder for greater than four weeks. Patient reports vaccine administered in the left shoulder joint space as opposed to left deltoid. Seen by Employee Health and referred to orthopedic surgery shoulder specialist for further evaluation. No imaging available at the time of event reporting, but physical exam consistent with neurologic or left shoulder musculoskeletal pathology possibly related to vaccine injection. More
2872288 18 F AZ 11/12/2025 COVID19
UNK
UNK
UNK
UNK
UNK
UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 3052550
Y1A212M
B4J4B
5EF45
Y015599
Z004246
Z00342
U8599AA
Underdose; Underdose; Underdose; Underdose; Underdose; Underdose; Underdose; Und... Underdose; Underdose; Underdose; Underdose; Underdose; Underdose; Underdose; Underdose More
wrong dose, pediatric v. adult wrong dose, pediatric v. adult
2872290 75 M MI 11/12/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 UT8763EA
UT8763EA
Abdominal pain, Back pain, Chills, Headache, Nausea; Neck pain Abdominal pain, Back pain, Chills, Headache, Nausea; Neck pain
chills, headache, neck and back pain, abdominal pain, nausea for 2 weeks after vaccination. chills, headache, neck and back pain, abdominal pain, nausea for 2 weeks after vaccination.
2872296 66 M NY 11/12/2025 COVID19
 MODERNA
Dizziness, Hypotension, Loss of consciousness Dizziness, Hypotension, Loss of consciousness
Low blood pressure, dizziness, passed out momentarily. Felt exactly like I did when I tested positiv... Low blood pressure, dizziness, passed out momentarily. Felt exactly like I did when I tested positive for Covid 4 months ago. Slept and rested for 4 hours and felt fine. Blood pressure and Oxygen returned to normal More
2872298 9 F MI 11/12/2025 FLU3
 SEQIRUS, INC.
 410514
Injection site erythema, Injection site swelling, Injection site warmth Injection site erythema, Injection site swelling, Injection site warmth
Patient reported having a swollen left deltoid that was red and warm to the touch. Patient reported having a swollen left deltoid that was red and warm to the touch.
2872299 51 F OH 11/12/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EW0168
EW0168
EW0168
EW0168
EW0168
EW0168
EW0168
FC3184
FC3184
FC3184
FC3184
FC3184
FC3184
FC3184
EW0169
EW0169
EW0169
EW0169
EW0169
EW0169
EW0169
FC3184
FC3184
FC3184
FC3184
FC3184
FC3184
FC3184
Arrhythmia, Arthritis, Blood pressure fluctuation, Condition aggravated, Depress... Arrhythmia, Arthritis, Blood pressure fluctuation, Condition aggravated, Depression; Dizziness, Exostosis, Fibrous histiocytoma, Guttate psoriasis, Headache; Hepatic cirrhosis, Hepatic steatosis, Immune system disorder, Inflammation, Malabsorption; Malnutrition, Mast cell activation syndrome, Migraine, Nervous system disorder, Osteoporosis; Pain, Pancreatic failure, Postural orthostatic tachycardia syndrome, Psoriatic arthropathy, Pustular psoriasis; Rosacea, SARS-CoV-2 antibody test positive, Seborrhoeic keratosis, Small fibre neuropathy, Spinal pain; Spinal stenosis, Stenosis, Tachycardia, Thyroid neoplasm, Weight decreased; Arrhythmia, Arthritis, Blood pressure fluctuation, Condition aggravated, Depression; Dizziness, Exostosis, Fibrous histiocytoma, Guttate psoriasis, Headache; Hepatic cirrhosis, Hepatic steatosis, Immune system disorder, Inflammation, Malabsorption; Malnutrition, Mast cell activation syndrome, Migraine, Nervous system disorder, Osteoporosis; Pain, Pancreatic failure, Postural orthostatic tachycardia syndrome, Psoriatic arthropathy, Pustular psoriasis; Rosacea, SARS-CoV-2 antibody test positive, Seborrhoeic keratosis, Small fibre neuropathy, Spinal pain; Spinal stenosis, Stenosis, Tachycardia, Thyroid neoplasm, Weight decreased; Arrhythmia, Arthritis, Blood pressure fluctuation, Condition aggravated, Depression; Dizziness, Exostosis, Fibrous histiocytoma, Guttate psoriasis, Headache; Hepatic cirrhosis, Hepatic steatosis, Immune system disorder, Inflammation, Malabsorption; Malnutrition, Mast cell activation syndrome, Migraine, Nervous system disorder, Osteoporosis; Pain, Pancreatic failure, Postural orthostatic tachycardia syndrome, Psoriatic arthropathy, Pustular psoriasis; Rosacea, SARS-CoV-2 antibody test positive, Seborrhoeic keratosis, Small fibre neuropathy, Spinal pain; Spinal stenosis, Stenosis, Tachycardia, Thyroid neoplasm, Weight decreased; Arrhythmia, Arthritis, Blood pressure fluctuation, Condition aggravated, Depression; Dizziness, Exostosis, Fibrous histiocytoma, Guttate psoriasis, Headache; Hepatic cirrhosis, Hepatic steatosis, Immune system disorder, Inflammation, Malabsorption; Malnutrition, Mast cell activation syndrome, Migraine, Nervous system disorder, Osteoporosis; Pain, Pancreatic failure, Postural orthostatic tachycardia syndrome, Psoriatic arthropathy, Pustular psoriasis; Rosacea, SARS-CoV-2 antibody test positive, Seborrhoeic keratosis, Small fibre neuropathy, Spinal pain; Spinal stenosis, Stenosis, Tachycardia, Thyroid neoplasm, Weight decreased More
CHRONIC MIGRAINE 4 years. Small Cell neuropathy. Arrhythmia, tachycardia and BP fluctuation, pain. ... CHRONIC MIGRAINE 4 years. Small Cell neuropathy. Arrhythmia, tachycardia and BP fluctuation, pain. POTS. Dizzy. Neurological dysfunction. Spine pain stenosis, spurs, arthritis, inflammation. Malabsorption/malnutrition. Thyroid tumor. Dermatofibroma. Immune-related production of seborrheic keratosis, rosacea and guttate and pustular Psoriasis. Psoriatic arthritis, stenosis, osteoporosis. GI conditions MAST CELL, pancreatic insufficiency, cirrhosis of the liver, fatty liver. Total body system dysfunction, one Rheumatogist referring to it as my VAIDS. Prior to 2021, I was a full-time exercise instruction/personal trainer and competitive runner who could bench my body weight of 125. Now, I can't keep 109 lbs on. HEALTHY ATHLETE. I sought HUMIRA for life-long psoriasis, no intention of getting vaccinated for COVID 3 months later. Mandated to get shot for freedom of movement about the country. The next day, my brain felt that something foreign entered the body and the headache began. I already had the 12/2022 arthritis appointment for the HUMIRA, when the spine pain was unbearable. They immediately started a study to see if I had Anklosing Splondy. I did not. My case was dropped. I was mistreated and lied to for years. Gaslit and deceived, I gave up. My mental health declined and out of frustration, I committed myself to mental health care. They could not find anything to explain my pain and 250 symptoms and it was declared depression was never the culprit, and they dropped my care again, after a brief session of talk therapy. I had no idea there was a SARS SPIKE antigen test already available when I was in Clinic, to determine if the SARS SPIKE ANTIBODY was present, and causing these problems. Labs detected SARS, even though I was not sick, and they never mentioned it. Clinic LIED TO ME, DENIED ME THE AVAILABLE TESTING, and worse, follow-up through infectious disease, doubled down and said the SPIKE Antigen did not exist, therefore no test for imaginary culprits exist. I complained to the hospital. They disciplined the doctor. I left for Dr and finally got a diagnosis of SARS SPIKE ANTIGEN causing mal-absorption. FOUR YEARS OF 100's of doctor visits FINALLY I have PROOF! And the statue was up 3 years ago. The imbalance of micronutrients combines with autoimmunity, and illness like this doesn't even show up for 4 years, if you began as healthy as I did. I have revolving health issues in every single organ and cell that blood can reach. I am blood injured, and to "repair" it, my blood is compromised with a foreign man-made protein, called SARS SPIKE antigen, and a body programmed to attack it's own healthy tissues as well. More
✓
2872301 39 F OH 11/12/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 U8881CA
U8881CA
Cough, Dyspnoea, Hypertension, Palatal oedema, Tachycardia; Urticaria Cough, Dyspnoea, Hypertension, Palatal oedema, Tachycardia; Urticaria
Cough, SOB, Uvula edema, hives, tachycardic, hypertensive Cough, SOB, Uvula edema, hives, tachycardic, hypertensive
2872304 34 F OH 11/12/2025 FLU3
 SANOFI PASTEUR
 U8881CA
Anxiety, Dyspnoea, Lip oedema, Urticaria Anxiety, Dyspnoea, Lip oedema, Urticaria
Hives, SOB, anxiety, lip edema code called epi given transferred to Hospital for elevated adult care... Hives, SOB, anxiety, lip edema code called epi given transferred to Hospital for elevated adult care released later the same day. More
2872307 61 F MD 11/12/2025 COVID19
FLU3
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
 na0590
9fg5m
Injection site induration, Injection site pruritus, Pain in extremity; Injection... Injection site induration, Injection site pruritus, Pain in extremity; Injection site induration, Injection site pruritus, Pain in extremity More
pt reports a very sore arm more than usual from previous flu vaccines and itching at the site of inj... pt reports a very sore arm more than usual from previous flu vaccines and itching at the site of injection, as well as the skin around the injection site becoming harden More
2872308 33 M MO 11/12/2025 FLU3
 SANOFI PASTEUR
 UT8836JA
Head injury, Loss of consciousness, Syncope, Tenderness Head injury, Loss of consciousness, Syncope, Tenderness
Patient passed out in restroom about 5 minutes after sitting after immunization. He fainted and hit... Patient passed out in restroom about 5 minutes after sitting after immunization. He fainted and hit his head on the floor of the restroom. RN checked his blood pressure and Dr. checked the back of his head. There were no cuts on his head, just sore to the touch. He sat for about 15 more minutes before getting up. Dr. examined him before allowing him to get up. More
2872309 20 F NE 11/12/2025 FLU3
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 P394K
P394K
Bursitis, Impaired work ability, Muscle strain, Pain in extremity, Rotator cuff ... Bursitis, Impaired work ability, Muscle strain, Pain in extremity, Rotator cuff syndrome; Sleep disorder, X-ray limb More
11/3/2025: Patient called to report that she has a sore left arm since getting the influenza vaccina... 11/3/2025: Patient called to report that she has a sore left arm since getting the influenza vaccination, stating "around two-weeks ago". Date of dose confirmed to be 10/21/2025. Patient stated, "I started getting sore after the shot and thought it was getting better however it has become worse". She further stated, "It's to the point where I can't sleep on that side and it hurts when I move it'. She reports taking Advil and using ice to treat the discomfort". Advised to complete Injury report. Recommended to see medical provider. Advised to present to Employee Health to review claim process. acknowledged understanding. Since the appointment with her PCP she stated "being referred to an orthpaedist due to concern of a torn rotator cuff from the vaccine, a rare condition". She reports getting an X-ray of the shoulder with the physician ordering an MRI and PT. She indicated she can return to work with restrictions, with no lifting using the left arm and with a lifting restriction of no more than 20#, right arm. On 11/6/2025, patient called, stating, "I've seen the orthopaedic doctor and I do not have a torn rotator cuff'. She further stated, "I have bursitis of the left bicep, strained deltoid and shoulder impingement". In addition, she stated, "I'll be starting PT and learned that I can return to work and can lift as long as there is no discomfort". She is working with the Employee Health Case Management Team. More
2872310 76 F CA 11/12/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA4452
UT8794DA
Arthralgia; Arthralgia Arthralgia; Arthralgia
Shoulder pain. treatment: Physical therapy and Tylenol Shoulder pain. treatment: Physical therapy and Tylenol
2872316 73 F OH 11/12/2025 COVID19
 MODERNA
 3053648
Contusion Contusion
5 DAYS AFTER RECEIVING THE VACCINE THE PATIENT STOPPED BY THE PHARMACY TO SHOW US A LARGE BRUISE ON ... 5 DAYS AFTER RECEIVING THE VACCINE THE PATIENT STOPPED BY THE PHARMACY TO SHOW US A LARGE BRUISE ON HER ARM. More
2872317 75 F 11/12/2025 COVID19
COVID19
FLU3
FLU3
 MODERNA
MODERNA
SEQIRUS, INC.
SEQIRUS, INC.
 3053669
3053669
407273
407273
Balance disorder, Chills, Eye pain, Fatigue, Headache; Hyperhidrosis, Pain, Trem... Balance disorder, Chills, Eye pain, Fatigue, Headache; Hyperhidrosis, Pain, Tremor; Balance disorder, Chills, Eye pain, Fatigue, Headache; Hyperhidrosis, Pain, Tremor More
Chills, uncontrolled shaking, sever headache, body aches, unsteady on her feet. everything was a &qu... Chills, uncontrolled shaking, sever headache, body aches, unsteady on her feet. everything was a " jumble" sweating, eye pain, fatigue More
2872318 12 M AL 11/12/2025 UNK
 UNKNOWN MANUFACTURER
Injection site erythema Injection site erythema
pt had TDAP vaccination given elsewhere at (withheld), presented to clinic with erythema to injecti... pt had TDAP vaccination given elsewhere at (withheld), presented to clinic with erythema to injection site More
2872319 83 M IA 11/12/2025 FLU3
 SEQIRUS, INC.
 407255
Mobility decreased, Pain in extremity Mobility decreased, Pain in extremity
Patient received the fluad vaccine on his right arm and he reported having a sore arm, unable to lif... Patient received the fluad vaccine on his right arm and he reported having a sore arm, unable to lift his arm. When he called he was advised to use Tylenol for the pain. Patient reports using Tylenol and tried hot and cold packs but did not get relief from the pain. On 11/11/2025 he went to seek medical help and was prescribed Prednisone and Tizanidine for the pain. He is currently taking these meds and was intructed to let us if the meds help More
2872320 73 M IL 11/12/2025 COVID19
COVID19
VARZOS
VARZOS
 PFIZER\BIONTECH
PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 lc4370
lc4370
d243k
d243k
Diplopia, Dysphagia, Extra dose administered, Eyelid ptosis, Mastication disorde... Diplopia, Dysphagia, Extra dose administered, Eyelid ptosis, Mastication disorder; Myasthenia gravis; Diplopia, Dysphagia, Extra dose administered, Eyelid ptosis, Mastication disorder; Myasthenia gravis More
Diplopia, sagging right eyelid, difficulty chewing and swallowing food which began days after receiv... Diplopia, sagging right eyelid, difficulty chewing and swallowing food which began days after receiving both injections of covid and shingrix in the same arm. notably this was the patients third Shingrix vaccine as the pharmacist messed up and/or stated that the illinois vaccine database said that he said not already received his second Shingrix years prior (which he had records of). Patient was evaluated by neurology and ophthalmology and was found to have Myasthenia Gravis. Now on Mestinon; occasionally requires prednisone for flares. More
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2872323 74 M IL 11/12/2025 FLU3
 SANOFI PASTEUR
 u8874ba
Dysphagia, Eyelid ptosis, Facial paresis, Speech disorder Dysphagia, Eyelid ptosis, Facial paresis, Speech disorder
Patient is noticing that he is having an increased difficulty speaking, swallowing, smiling, worse l... Patient is noticing that he is having an increased difficulty speaking, swallowing, smiling, worse lid drooping More
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2872328 52 F MD 11/12/2025 COVID19
 PFIZER\BIONTECH
 na4457
Wrong product administered Wrong product administered
fluarix ordered. Comirnaty given due to pharmacist misreading consent form (horizontal layout- box c... fluarix ordered. Comirnaty given due to pharmacist misreading consent form (horizontal layout- box checked for flu to right of covid - misread as covid checkmark More
2872329 5 M VA 11/12/2025 DTAPHEPBIP
HEPA
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 5J7EF
L4EA4
Y017205
Cough, Eye swelling, Lacrimation increased, Rash macular, Throat irritation; Cou... Cough, Eye swelling, Lacrimation increased, Rash macular, Throat irritation; Cough, Eye swelling, Lacrimation increased, Rash macular, Throat irritation; Cough, Eye swelling, Lacrimation increased, Rash macular, Throat irritation More
Child returned to clinic approx 10 minutes later with eye swollen, watery, red splotches on face; c/... Child returned to clinic approx 10 minutes later with eye swollen, watery, red splotches on face; c/o itchy throat, cough, received Epipen Jr and taken to ER via squad More
2872330 3 M MI 11/12/2025 COVID19
 PFIZER\BIONTECH
 NA0846
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Patient was given Pfizer covid vaccine for 5-11 years old at the age of 3 years and 11 months. Patient was given Pfizer covid vaccine for 5-11 years old at the age of 3 years and 11 months.
2872331 58 F WI 11/12/2025 FLU3
FLU3
PNC20
PNC20
 SEQIRUS, INC.
SEQIRUS, INC.
PFIZER\WYETH
PFIZER\WYETH
 AX4605A
AX4605A
MA2505
MA2505
Chills, Injection site cellulitis, Injection site erythema, Injection site pain,... Chills, Injection site cellulitis, Injection site erythema, Injection site pain, Injection site swelling; Injection site warmth, Pain, Pyrexia; Chills, Injection site cellulitis, Injection site erythema, Injection site pain, Injection site swelling; Injection site warmth, Pain, Pyrexia More
Patient had localized redness start at the injection site approximately 24 hours following injection... Patient had localized redness start at the injection site approximately 24 hours following injection. The pain and swelling progressed to encompass her entire upper left arm with coinciding fever and chills. The area of the left upper arm was evaluated 11/12/2025, area is tender and hot to touch; patient continues to have body aches. More
2872332 86 F SD 11/12/2025 FLU3
 SANOFI PASTEUR
 u8874aa
Pain in extremity Pain in extremity
Patient stated that her arm was extremely sore afterwards for almost a week. She said that the arm ... Patient stated that her arm was extremely sore afterwards for almost a week. She said that the arm never swelled up or was red. She said that she used ice packs but nothing seemed to help. With time, the pain lessened. More
2872333 78 F OR 11/12/2025 COVID19
 MODERNA
 3052581
Vision blurred Vision blurred
approximately 3 hours after receiving the vaccine, the patient reports having vision changes that im... approximately 3 hours after receiving the vaccine, the patient reports having vision changes that impaired her reading ability then caused more pronounced blurred vision for several hours. She said it then resolved over the next few hours and she did not at that time seek medical treatment. More
2872334 44 F TX 11/12/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 UT8826KA
UT8826KA
Asthenia, Headache, Joint swelling, Lip swelling, Pain; Peripheral swelling, Swe... Asthenia, Headache, Joint swelling, Lip swelling, Pain; Peripheral swelling, Swelling face More
Reports waking up with : swelling of the face-yes, lips-yes, arm-yes, and hands-yes, and weakness-y... Reports waking up with : swelling of the face-yes, lips-yes, arm-yes, and hands-yes, and weakness-yes. Weakness is generalized body with aches and headache. More
2872335 5 M MN 11/12/2025 FLU3
 SANOFI PASTEUR
 UT8802MA
Extra dose administered Extra dose administered
Booster was given 09/29/2025 & was on schedule 11/10/25 for just COVID & received another ex... Booster was given 09/29/2025 & was on schedule 11/10/25 for just COVID & received another extra Booster dose of Influenza Vaccine. More
2872338 73 M NV 11/12/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR

Erythema, Induration, Limb mass, Myalgia, Peripheral swelling; Pruritus, Skin wa... Erythema, Induration, Limb mass, Myalgia, Peripheral swelling; Pruritus, Skin warm, Tenderness More
By the following morning after the injection. Arm swelled, red, hot, muscular pain, painful to pres... By the following morning after the injection. Arm swelled, red, hot, muscular pain, painful to pressure/touch expanded to 3.5 inches in diameter. Raised about 0.5 inches, Became a hard mass that remained hard, painful, and red and of that size for approximately 7 days. Then slowly went down and away over the next 4 days. In that 4 day period the site was itchy and remained itchy days after the swelling, hardness, and redness went away. More
2872340 16 M IN 11/12/2025 FLU3
MENB
MNQ
 SANOFI PASTEUR
PFIZER\WYETH
SANOFI PASTEUR
 UT8779NA
LL0641
u8438aa
Blood glucose normal, Musculoskeletal stiffness, Tremor; Blood glucose normal, M... Blood glucose normal, Musculoskeletal stiffness, Tremor; Blood glucose normal, Musculoskeletal stiffness, Tremor; Blood glucose normal, Musculoskeletal stiffness, Tremor More
During vaccination, patient was sitting upright in chair. Nurse administered vaccines and while admi... During vaccination, patient was sitting upright in chair. Nurse administered vaccines and while administering, patient slumped over and then tightened-body and shook upper extremities for 1-2 seconds. BP 100/62, BS 118, RR16. Normal cardiac and neuro exam, A&O x 3 and acting per usual. No significant fatigue but had pt drink an apple juice and lay down on exam table. Patient reports that he has drank water today and at a chicken burrito for lunch. More
2872341 92 M IA 11/12/2025 FLU3
 SANOFI PASTEUR
 U8862CA
Extra dose administered Extra dose administered
Patient had received an influenza vaccine at his assisted living facility on 10/21/2025. His daught... Patient had received an influenza vaccine at his assisted living facility on 10/21/2025. His daughter did not know this and scheduled him for an appointment at our pharmacy. Medicare did not flag the claim as a duplicate so we administered the vaccine. The daughter called back after returning him to the facility to ask why we didn't know he had already received the vaccine. It is not policy to check the vaccine registry for influenza vaccines if the insurance accepts the claim. The patient is currently feeling fine and not experiencing any side effects. More
2872342 68 F HI 11/12/2025 FLU3
 SANOFI PASTEUR
 U8830AA
Injection site erythema, Injection site pruritus, Injection site rash, Injection... Injection site erythema, Injection site pruritus, Injection site rash, Injection site reaction, Urticaria More
C/O itching and rash to left upper arm. Observed on site left upper arm with welt/redness covering a... C/O itching and rash to left upper arm. Observed on site left upper arm with welt/redness covering about 70-80% of upper arm. Patient denies pain, skin intact, no other concerns More
2872343 74 M OH 11/12/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
 407274
407274
Alcohol use, Computerised tomogram head normal, Confusional state, Disorientatio... Alcohol use, Computerised tomogram head normal, Confusional state, Disorientation, Magnetic resonance imaging head normal; Scan with contrast normal More
He had the vaccine at 1:15 pm on 11/3/25. That night, he took a Trazodone 150 mg and had a glass of ... He had the vaccine at 1:15 pm on 11/3/25. That night, he took a Trazodone 150 mg and had a glass of wine before bed. Around 10:30 pm, he was noted to be disorientated, confused. He was taken to the ER and admitted. Testing was negative and returned to normal cognitiion by 5 am. Hospitalization for 1 day at [withheld] Hospital, [withheld city, state]. More
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2872345 86 F OH 11/12/2025 FLU3
FLU3
FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 U8862CA
U8862CA
U8862CA
U8862CA
Asthenia, Atrial fibrillation, Blood calcium, Blood lactic acid, Blood magnesium... Asthenia, Atrial fibrillation, Blood calcium, Blood lactic acid, Blood magnesium; Catheterisation cardiac normal, Chest X-ray, Computerised tomogram heart, Dyspnoea, Echocardiogram abnormal; Ejection fraction decreased, Electrocardiogram, Endotracheal intubation, Full blood count, Metabolic function test; Pulseless electrical activity, Resuscitation, Troponin, Ventricular hypokinesia, Wearable defibrillator therapy More
On October 27, 2025, the day after her influenza vaccine, she developed sudden onset shortness of br... On October 27, 2025, the day after her influenza vaccine, she developed sudden onset shortness of breath and severe weakness without other symptoms. She was intubated at the scene. Was transported to the ER and prior to arrival arrested in the Ambulance with PEA rhythm. Had 2 rounds of epinephrine with CPR with recovery of rhythm. She was able to be extubated on 10/28/2025. Left heart cath showed no acute findings of CAD. Echo showed EF 20-25% with global hypokinesis. Previous echo 1/12/2023 showed EF 55-60% with normal LV function. She also developed atrial fib on 10/30. Currently back to baseline on breathing but is scheduled to get a pacemaker and defibrillator. She is currently wearing a lifevest until then and is on amiodarone. More
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2872346 61 F UT 11/12/2025 COVID19
TDAP
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
 3052784
H4K3S
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
Tdap given in error when influenza was requested. Patient has had severe reactions to tetanus toxoid... Tdap given in error when influenza was requested. Patient has had severe reactions to tetanus toxoid in the past so will monitor and follow up with us if there are concerns. More
2872347 53 M UT 11/12/2025 COVID19
TDAP
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
 3052784
H4K3S
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
Tdap given in error when influenza was requested. Patient notified and will follow up if any adverse... Tdap given in error when influenza was requested. Patient notified and will follow up if any adverse affects from the error and will seek influenza dose More
2872349 69 F IL 11/12/2025 FLU3
 SANOFI PASTEUR
 u8874aa
Haematoma, Induration, Swelling, Ultrasound scan abnormal Haematoma, Induration, Swelling, Ultrasound scan abnormal
diagnosed with hematoma on 11/11/25 post ultrasound and physician office visit. Swelling and hardnes... diagnosed with hematoma on 11/11/25 post ultrasound and physician office visit. Swelling and hardness developed two days post vaccination on or around 10/19/25. No pain, no blood clots. More
2872353 26 F OK 11/12/2025 FLU3
HPV9
 SEQIRUS, INC.
MERCK & CO. INC.
 407005
1998828
Injection site pain, Pain; Injection site pain, Pain Injection site pain, Pain; Injection site pain, Pain
Right arm pain starting on 11/11/25 (2 weeks post vaccination) at injection site. Both vaccines were... Right arm pain starting on 11/11/25 (2 weeks post vaccination) at injection site. Both vaccines were given in the right arm, therefore both vaccines reported. Client states pain has worsened today and is worse with movement. Client states there is no visible redness or swelling at injection site. Client advised to monitor pain and seek evaluation from physician if no improvement. VAERS report made per patient's request. More
2872356 12 F IL 11/12/2025 COVID19
FLU3
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS
 B0021
FH4YR
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event More
The Covid vaccine that was administered to the patient was expired (expiration date 09/14/2025). No ... The Covid vaccine that was administered to the patient was expired (expiration date 09/14/2025). No adverse event at this time. More
2872365 11/12/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Systemic lupus erythematosus Systemic lupus erythematosus
patient contracted lupus after shingles shot; This serious case was reported by a consumer via inter... patient contracted lupus after shingles shot; This serious case was reported by a consumer via interactive digital media and described the occurrence of systemic lupus erythematosus in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced systemic lupus erythematosus (Verbatim: patient contracted lupus after shingles shot) (serious criteria GSK medically significant). The outcome of the systemic lupus erythematosus was not reported. It was unknown if the reporter considered the systemic lupus erythematosus to be related to Shingles vaccine. The company considered the systemic lupus erythematosus to be unrelated to Shingles vaccine. Additional Information: GSK Receipt Date: 06-NOV-2025 The batch number was not provided and a request for this information has been made.; Sender's Comments: A case of Systemic lupus erythematosus, unknown time after receiving Shingles vaccine, in a patient. Based on the available information a?possible causality that the event was caused by the GSK product cannot be ascertained. Consent for further follow-up has not been received. More
2872372 11/12/2025 FLUX
 UNKNOWN MANUFACTURER
 UNK
Malaise Malaise
got a flu shot I'm sick for a week or two; This non-serious case was reported by a consumer via... got a flu shot I'm sick for a week or two; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of sickness in a patient who received Flu unspecified (Flu vaccine) for prophylaxis. On an unknown date, the patient received Flu vaccine. On an unknown date, an unknown time after receiving Flu vaccine, the patient experienced sickness (Verbatim: got a flu shot I'm sick for a week or two). The outcome of the sickness was not reported. It was unknown if the reporter considered the sickness to be related to Flu vaccine. It was unknown if the company considered the sickness to be related to Flu vaccine. Additional Information: GSK receipt date: 28-OCT-2025 The batch number was not provided, and we are unable to contact the reporter. More
2872381 IN 11/12/2025 FLU3
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 UNK
UNK
Product storage error; Product storage error Product storage error; Product storage error
Administration of flulaval after a temperature excursion; Administration boostrix after a temperatur... Administration of flulaval after a temperature excursion; Administration boostrix after a temperature excursion; This non-serious case was reported by a other health professional via call center representative and described the occurrence of incorrect storage of drug in an unspecified number of patients who received Flu Seasonal TIV Quebec (FluLaval 2025-2026 season) for prophylaxis. Co-suspect products included DTPa (Reduced antigen) (Boostrix) for prophylaxis. On an unknown date, the patient received FluLaval 2025-2026 season and Boostrix. On an unknown date, an unknown time after receiving FluLaval 2025-2026 season and not applicable after receiving Boostrix, the patient experienced incorrect storage of drug (Verbatim: Administration of flulaval after a temperature excursion) and incorrect storage of drug (Verbatim: Administration boostrix after a temperature excursion). The outcome of the incorrect storage of drug and incorrect storage of drug 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: 03-NOV-2025 The reporter reported a temperature for FluLaval and Boostrix. According to reporter, during all October the vaccines had been exposed to low temperatures, the lowest being 29.3-degree F. According to reporter, the exposure was of 14 hours every day, and she did not know the exact number of days the vaccines were exposed to low temperatures. Reporter mentioned that an unknown number of doses of these two vaccines were administered to an unknown number of patients after the temperature excursions. The reporter consented to follow up. The batch number was not provided upon follow up with the reporter. More
2872385 24 F VA 11/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 B5NJ9
Exposure during pregnancy, Product use issue, Wrong product administered Exposure during pregnancy, Product use issue, Wrong product administered
pregnant patient got a dose of AREXVY instead of Abrysvo; Vaccine maladministration; patient got a d... pregnant patient got a dose of AREXVY instead of Abrysvo; Vaccine maladministration; patient got a dose of AREXVY instead of Abrysvo; This non-serious prospective pregnancy case was reported by a pharmacist via call center representative and described the occurrence of vaccine exposure during pregnancy in a 24-year-old female patient who received RSVPreF3 adjuvanted (Arexvy) (batch number B5NJ9, expiry date 05-DEC-2026) for prophylaxis. Co-suspect products included RSV vaccine prot. subunit PreF 2v (Abrysvo) for prophylaxis. On 06-NOV-2025, the patient received Arexvy. On an unknown date, the patient received Abrysvo. On 06-NOV-2025, an unknown time after receiving Arexvy and an unknown time after receiving Abrysvo, the patient experienced vaccine exposure during pregnancy (Verbatim: pregnant patient got a dose of AREXVY instead of Abrysvo), wrong vaccine administered (Verbatim: Vaccine maladministration) and product use in unapproved population (Verbatim: patient got a dose of AREXVY instead of Abrysvo). The outcome of the vaccine exposure during pregnancy, wrong vaccine administered and product use in unapproved population were not applicable. Pregnancy exposure: Pregnancy Exposure (Arexvy): Trimester unknown Pregnancy Exposure (Abrysvo): Trimester unknown Pregnancy Outcome: Pregnancy was ongoing Additional Information: GSK Receipt Date: 10-Nov-2025 The reporter reported on 10th November 2025, that a pregnant patient got a dose of Arexvy instead of Abrysvo (RSV vaccine approved by the FDA for pregnant patients) back on 6th November 2025. The reporter wanted to know what the steps are or guidance after this incident. More
2872390 F NY 11/12/2025 COVID19
 MODERNA
Diarrhoea, Maternal exposure during breast feeding, Nausea, Oropharyngeal pain, ... Diarrhoea, Maternal exposure during breast feeding, Nausea, Oropharyngeal pain, Pyrexia More
breastfeeding; sore throats; diarrhea; fevers; queasy; This spontaneous case was reported by a consu... breastfeeding; sore throats; diarrhea; fevers; queasy; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL PAIN (sore throats), DIARRHOEA (diarrhea), PYREXIA (fevers), NAUSEA (queasy) and MATERNAL EXPOSURE DURING BREAST FEEDING (breastfeeding) in a female patient of an unknown age who received mRNA-1273.251 (Spikevax LP.8.1 PFS) for COVID-19 prophylaxis. Co-suspect product included Pre-filled Syringe injection for COVID-19 prophylaxis. No Medical History information was reported. On 31-Oct-2025, the patient received dose of mRNA-1273.251 (Spikevax LP.8.1 PFS) (Intramuscular use) 1 dosage form. On an unknown date, the patient started Pre-filled Syringe (unknown route) at an unspecified dose. In 2025, the patient experienced OROPHARYNGEAL PAIN (sore throats), DIARRHOEA (diarrhea), PYREXIA (fevers) and NAUSEA (queasy). On 31-Oct-2025, after starting mRNA-1273.251 (Spikevax LP.8.1 PFS), the patient experienced MATERNAL EXPOSURE DURING BREAST FEEDING (breastfeeding). On 31-Oct-2025, MATERNAL EXPOSURE DURING BREAST FEEDING (breastfeeding) had resolved. At the time of the report, OROPHARYNGEAL PAIN (sore throats), DIARRHOEA (diarrhea), PYREXIA (fevers) and NAUSEA (queasy) outcome was unknown. No concomitant medications were provided. The patient had the vaccine and had fever, which was expected. However, the patient had sore throats, which was not expected. She had a light vomiting. She felt queasy. She was breastfeeding. It was unknown if the patient experienced any additional symptoms/events. There were no additional lab data/result available. No treatment medication was provided. This case was linked to US-MODERNATX, INC.-MOD-2025-790823, US-MODERNATX, INC.-MOD-2025-790841 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2025-790823:Master case (Husband case) US-MODERNATX, INC.-MOD-2025-790841:Child case More
2872391 11/12/2025 COVID19
 MODERNA
Death Death
Three of my neighbors are dead thanks to your vax; This spontaneous case was reported by a non-healt... Three of my neighbors are dead thanks to your vax; This spontaneous case was reported by a non-health professional and describes the occurrence of DEATH (Three of my neighbors are dead thanks to your vax) in a patient of an unknown age and gender who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (unknown route) 1 dosage form. Death occurred on an unknown date The cause of death was not reported. It is unknown if an autopsy was performed. This case was for 2nd patient out of 3 patients. Concomitant medications were not reported. Reporter had not administered the moderna vaccine. It was reported that the individual expresses intense dissatisfaction with the COVID vaccine, attributing the deaths of three neighbors because of the vaccine. It was unknown if the patient experienced any additional symptoms/events. Treatment information was not reported. This case was linked to US-MODERNATX, INC.-MOD-2025-790961 (E2B Linked Report).; Reporter's Comments: The benefit-risk relationship of product is not affected by this report.; Sender's Comments: US-MODERNATX, INC.-MOD-2025-790961:Patient 2; Reported Cause(s) of Death: Three of my neighbors are dead thanks to your vax More
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2872392 89 M 11/12/2025 COVID19
 MODERNA
Fatigue, Heart rate, Heart rate increased, Pain Fatigue, Heart rate, Heart rate increased, Pain
rapid heart rate; hurts; tires; This spontaneous case was reported by a consumer and describes the o... rapid heart rate; hurts; tires; This spontaneous case was reported by a consumer and describes the occurrence of HEART RATE INCREASED (rapid heart rate), PAIN (hurts) and FATIGUE (tires) in an 89-year-old male patient who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. The patient's past medical history included Coronary bypass. Previously administered products included for Product used for unknown indication: Moderna COVID-19 vaccine (Patient had received several Moderna Covid vaccines with no problems.). Past adverse reactions to the above products included No adverse effect with Moderna COVID-19 vaccine. Concurrent medical conditions included Cardiac disorder NOS and Artificial cardiac pacemaker user. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced HEART RATE INCREASED (rapid heart rate), PAIN (hurts) and FATIGUE (tires). At the time of the report, HEART RATE INCREASED (rapid heart rate) outcome was unknown and PAIN (hurts) and FATIGUE (tires) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Heart rate: increased. No concomitant medication was reported. Patient had a heart bypass and have a pacemaker. He was tired and hurt for a day or 2 afterward. Patient recently had cardioversion and heart ablation to slow down his pulse rate for a pre-existing cardiac condition, which did succeed in slowing down the heart rate. It was unknown if the patient experienced any additional symptoms/events. Reporter did not allow further contact More
2872393 M CO 11/12/2025 COVID19
 MODERNA
Infection Infection
infection related symptoms; This spontaneous case was reported by a consumer and describes the occur... infection related symptoms; This spontaneous case was reported by a consumer and describes the occurrence of INFECTION (infection related symptoms) in a male patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. In 2023, the patient experienced INFECTION (infection related symptoms). In 2024, INFECTION (infection related symptoms) had resolved. Concomitant medications were not reported. It was reported that in 2023, after struggling to find medical treatment post-COVID-19 booster, the sender became homeless. By fall 2024, patient's infection symptoms vanished, coinciding with the start of telepathic experiences. Patient became homeless in 2023 after failing to find medical treatment for an infection that began shortly after a Covid19 booster shot. In the fall of 2024, the infection related symptoms vanished. It was unknown if the patient experienced any additional symptoms/events. Treatment information was not reported. More
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