🏥 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 💀 🏥 🚑 ♿ ⚠️
2868180 28 F OH 10/24/2025 FLU3
 SEQIRUS, INC.
Immediate post-injection reaction, Mobility decreased, Pain, Product administere... Immediate post-injection reaction, Mobility decreased, Pain, Product administered at inappropriate site More
Vaccine given too high causing immediate pain and discomfort. Patient unable to lift arm up beyond 9... Vaccine given too high causing immediate pain and discomfort. Patient unable to lift arm up beyond 90 degrees without pain. More
2868181 30 F LA 10/24/2025 UNK
UNK
FLU3
FLU3
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
SEQIRUS, INC.
SEQIRUS, INC.
 409413
409413
409413
409413
Pruritus, Rash; Rash, Rash pruritic; Pruritus, Rash; Rash, Rash pruritic Pruritus, Rash; Rash, Rash pruritic; Pruritus, Rash; Rash, Rash pruritic
REPORTS SHE DEVELOPED FULL BODY RASH/ITCHING SEVERAL HOURS POST VACCINE. HAS NOT SOUGHT MEDICAL EVA... REPORTS SHE DEVELOPED FULL BODY RASH/ITCHING SEVERAL HOURS POST VACCINE. HAS NOT SOUGHT MEDICAL EVALUATION. HAS BEEN TREATING WITH OTC ANTIHISTAMINES. More
2868187 82 F 10/24/2025 FLU3
 SEQIRUS, INC.
 407272
Injection site reaction, Rash erythematous Injection site reaction, Rash erythematous
red rash around injections site. pt has managed with benadryl and ice packs. pt thinks the adhesi... red rash around injections site. pt has managed with benadryl and ice packs. pt thinks the adhesive from the inject safe bandage may be the cause, but we are unsure. More
2868188 58 M NV 10/24/2025 COVID19
PNC21
 MODERNA
MERCK & CO. INC.
 3052155
Injection site pruritus, Injection site reaction, Injection site swelling, Urtic... Injection site pruritus, Injection site reaction, Injection site swelling, Urticaria; Injection site pruritus, Injection site reaction, Injection site swelling, Urticaria More
PT RECEIVED 2 VACCINES ON THE LEFT ARM, CAPVAXIVE AND MNEXSPIKE. HE STATED THAT INJECTION SITE REACT... PT RECEIVED 2 VACCINES ON THE LEFT ARM, CAPVAXIVE AND MNEXSPIKE. HE STATED THAT INJECTION SITE REACTION STARTED HAPPENING ON SATURDAY AND SLOWLY PROGRESSED. HE CAME IN TO THE PHARMACY ON THURSDAY, 10/23/25 TO REPORT THE REACTION. HE PRESENTED WITH ITCHING, SWELLING, WELTS ON THE LEFT ARM. HE WAS ADVICED BY PHARMACIST TO SEE A PROVIDER FOR FURTHER CARE. More
2868189 4 M NY 10/24/2025 DTAPIPV
FLU3
MMRV
 SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
 U8623AA
U8881CA
Z011680
Injection site erythema, Injection site swelling, Injection site vesicles; Injec... Injection site erythema, Injection site swelling, Injection site vesicles; Injection site erythema, Injection site swelling, Injection site vesicles; Injection site erythema, Injection site swelling, Injection site vesicles More
patient had vaccines given at 4 yr visit on 10/21/25. He received 3 vaccines, listed above. On 10/23... patient had vaccines given at 4 yr visit on 10/21/25. He received 3 vaccines, listed above. On 10/23/25 mom noted redness and swelling which was thought to be a normal local reaction. Today, patient had increased redness and swelling with blistering on a large portion of arm. Looks cellulitic. Started on oral antibiotics (Keflex). More
2868193 52 F IA 10/24/2025 COVID19
 PFIZER\BIONTECH
 MY9550
Injection site mass, Injection site pain Injection site mass, Injection site pain
Injection into right arm has been hurting since day of injection and have lump where vaccine was giv... Injection into right arm has been hurting since day of injection and have lump where vaccine was given at. More
2868194 77 F IN 10/24/2025 FLU3
 SANOFI PASTEUR
 U8837DA
Rash, Rash erythematous, Rash papular Rash, Rash erythematous, Rash papular
Patient reported hive like rash. Red raised spots starting at elbow of right arm and down to hand. ... Patient reported hive like rash. Red raised spots starting at elbow of right arm and down to hand. Later appearing over body. More
2868195 70 F NV 10/24/2025 FLU3
 SANOFI PASTEUR
 U8800AA
Pyrexia Pyrexia
PATIENT SPIKED UP A FEVER THE DAY AFTER VACCINATION OF >103 AND REMAINED ELEVATED FOR SEVERAL DAY... PATIENT SPIKED UP A FEVER THE DAY AFTER VACCINATION OF >103 AND REMAINED ELEVATED FOR SEVERAL DAYS REQUIRING DOCTORS' VISITS. More
2868196 M 10/24/2025 COVID19
 MODERNA
COVID-19, Diabetes mellitus, Discomfort, Fall, SARS-CoV-2 test COVID-19, Diabetes mellitus, Discomfort, Fall, SARS-CoV-2 test
he had diabetes prior to contracting COVID-19; got a moderate case of Covid; I fell down once; had s... he had diabetes prior to contracting COVID-19; got a moderate case of Covid; I fell down once; had some discomfort/general discomfort; This spontaneous case was reported by a consumer and describes the occurrence of DIABETES MELLITUS (he had diabetes prior to contracting COVID-19) in an elderly male patient who received mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Atrial fibrillation. In October 2024, the patient received dose of mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) (Intramuscular use) 1 dosage form. On 10-Apr-2025, the patient experienced COVID-19 (got a moderate case of Covid). In April 2025, the patient experienced FALL (I fell down once). In 2025, the patient experienced DISCOMFORT (had some discomfort/general discomfort). On an unknown date, the patient experienced DIABETES MELLITUS (he had diabetes prior to contracting COVID-19) (seriousness criterion medically significant). In April 2025, FALL (I fell down once) had resolved with sequelae, COVID-19 (got a moderate case of Covid) had resolved. In 2025, DISCOMFORT (had some discomfort/general discomfort) had resolved. At the time of the report, DIABETES MELLITUS (he had diabetes prior to contracting COVID-19) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 10-Apr-2025, SARS-CoV-2 test: confirmed COVID. The patient's current age was reported as 78 years. No concomitant medications were reported. The patient had received all the covid vaccines since they came out. On 10-Apr-2025, he got a moderate case of Covid which was confirmed by testing in a walk-in clinic. He was moderately sick, was not very weak, but he got sore throat, soreness in the ears and nose, and sinus-like infection symptoms, and he fell once he got really weak when bent over to something that happened one time. But he had no fever or anything. It took him about a week to get over it. He had some general discomfort lasting about 7 to 10 days but did not experience any fever, lungs, or chest involvement. He had diabetes prior to contracting COVID-19. He was not able to confirm if the diabetes was pre-existing before any covid vaccine or newly diagnosed. His doctor advised him to take the new injection because he received the regular Spikevax last year in October 2024 and got COVID in April, so 6 months passed, but the doctor wanted him to take the new one, the MNEXSPIKE, the new one (0.2 mg or less dose). It was unknown if the patient experienced any additional symptoms/events. No treatment information was provided. This case was linked to US-MODERNATX, INC.-MOD-2025-790310 (E2B Linked Report). This case was linked to MOD-2021-020830 (Patient Link). Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 15-Oct-2025: Live follow-up received contains significant information included event added, narrative updated, and reference numbers were added. On 15-Oct-2025: Live follow-up received contains non-significant information included narrative updated, and reference numbers were added.; Reporter's Comments: Concurrent medical conditions Atrial fibrillation is a contributor for event fall. .In view of the long non-suggestive onset latency the causality of the events discomfort and fall was assessed as not related to the vaccine. The benefit -risk relationship of product is not affected by this report.; Sender's Comments: US-MODERNATX, INC.-MOD-2025-790310:reporter mentioned "I've known someone More
2868197 M AL 10/24/2025 FLU3
FLU3
FLU3
FLU3
FLU3
FLU3
FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR



U8800AA
U8800AA
U8800AA
U8800AA
Arthralgia, Headache, Neck pain, Skin warm, Skull X-ray; X-ray; Arthralgia, Arth... Arthralgia, Headache, Neck pain, Skin warm, Skull X-ray; X-ray; Arthralgia, Arthritis, Mobility decreased, Myalgia, Neck pain; Scan abnormal, Skin warm; Arthralgia, Headache, Neck pain, Skin warm, Skull X-ray; X-ray; Arthralgia, Arthritis, Mobility decreased, Myalgia, Neck pain; Scan abnormal, Skin warm More
Sore Shoulder / Soreness in Neck / Soreness & Warmth in rear skull Sore Shoulder / Soreness in Neck / Soreness & Warmth in rear skull
2868198 76 M TX 10/24/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Atrial fibrillation, Blood test, Computerised tomogram, Electrocardiogram, Pulmo... Atrial fibrillation, Blood test, Computerised tomogram, Electrocardiogram, Pulmonary embolism; Pulmonary pain, X-ray More
On 10/3/2025, one week after getting the Covid shot, I had intense pain in my right lung when sleepi... On 10/3/2025, one week after getting the Covid shot, I had intense pain in my right lung when sleeping. Went to the Emergency Room at (withheld name) University Hospital in (withheld city, state). Was quickly diagnosed as being in AFib with a blood clot in both the right and left lung. After numerous tests and drug treatments in the ER, I was admitted to the hospital where I remained until being released on 10/5/2025. I have had appointments with a primary care doctor and hematologist since, with future appointments with these doctors and a cardiologist. I have never previously been diagnosed with AFib or blood clots. More
✓ ✓
2868201 62 F GA 10/24/2025 FLU3
 SANOFI PASTEUR
 TFAA2501
Rash Rash
The skin rashes (papules) start from bilateral legs after about three week of Flublok vaccination. t... The skin rashes (papules) start from bilateral legs after about three week of Flublok vaccination. then the rashes spread to bilateral tighes and strat on bilateral forearms also after 6 week of vaciination. More
2868202 77 F OH 10/24/2025 FLU3
 SEQIRUS, INC.
 407269
Arthralgia, Mobility decreased Arthralgia, Mobility decreased
Patient states is having pain in shoulder joint; having trouble moving arm; spoke with patient 10/24... Patient states is having pain in shoulder joint; having trouble moving arm; spoke with patient 10/24/25 who states pain is getting better and it is no longer progressing down her arm. More
2868204 93 M GA 10/24/2025 COVID19
 PFIZER\BIONTECH
 LP1780
Desmoid tumour Desmoid tumour
sudden onset growth on chest wall sudden onset growth on chest wall
✓
2868205 81 M OH 10/24/2025 FLU3
 SEQIRUS, INC.
 407269
Arthralgia, Mobility decreased Arthralgia, Mobility decreased
Patient states is having pain in shoulder joint; having trouble moving arm; spoke with patient 10/24... Patient states is having pain in shoulder joint; having trouble moving arm; spoke with patient 10/24/25 who states pain is getting better and it is no longer progressing down her arm. More
2868207 5 M AZ 10/24/2025 MMRV
MMRV
 MERCK & CO. INC.
MERCK & CO. INC.

Bruxism, Cyanosis, Eye movement disorder, Febrile convulsion, Hypopnoea; Mobilit... Bruxism, Cyanosis, Eye movement disorder, Febrile convulsion, Hypopnoea; Mobility decreased, Musculoskeletal stiffness, Pyrexia, Somnolence More
Child slept all day and then ran a fever. I gave him 5 ml of Motrin around 5pm, and before 5:11pm he... Child slept all day and then ran a fever. I gave him 5 ml of Motrin around 5pm, and before 5:11pm he froze, teeth clenched, eyes open looking to left, stiff unable to move, white skin fingers, finger tips blue, lips violet and shallow limited breaths by 5:19pm EMTs arrive. More
2868208 65 F MD 10/24/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 JS74H
Pruritus, Rash Pruritus, Rash
Patient started itching and developed rash on their other arm, not the arm where the injection occur... Patient started itching and developed rash on their other arm, not the arm where the injection occurred. Around 6AM patient took 2 Benadryl and the itching began to subside. at 2PM the next day they were still experiencing a little itchiness, but it was mostly gone. More
2868209 75 F IN 10/24/2025 FLU3
 SANOFI PASTEUR
 u8823da
Unresponsive to stimuli Unresponsive to stimuli
1414 influenza vaccine given. 1425 patient unresponsive. UF off, rinsed back, 500ml saline admin, 02... 1414 influenza vaccine given. 1425 patient unresponsive. UF off, rinsed back, 500ml saline admin, 02 6 L, trendelenburg, Epi 0.3mg given L thigh IM. Benadryl 50mg IVP given, 125mg Solumedrol IVP given. 1426 Patient responsive. Notified PA, Dtr and DO. Added Influenza vaccine as an allergy. More
2868210 26 F OH 10/24/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 JE74J
Arthralgia, Pain Arthralgia, Pain
Patient states having pain in shoulder joint when moving it Patient states having pain in shoulder joint when moving it
2868211 81 F CT 10/24/2025 COVID19
 PFIZER\BIONTECH
 NA0587
Rash, Rash maculo-papular Rash, Rash maculo-papular
Maculopapular rash on chest below rib cage - located on both sides Maculopapular rash on chest below rib cage - located on both sides
2868212 70 M LA 10/24/2025 FLU3
PPV
 SANOFI PASTEUR
MERCK & CO. INC.
 U8830CA
Z004034
Injection site erythema, Injection site pruritus; Injection site erythema, Injec... Injection site erythema, Injection site pruritus; Injection site erythema, Injection site pruritus More
Patient's wife reported that there was a large red area around the site of injections. It remai... Patient's wife reported that there was a large red area around the site of injections. It remained for about 3 days. Patient's wife stated that he complained of itching. The reaction was localized to the injection sites. The patient's wife wanted to report the reaction. More
2868214 70 F 10/24/2025 COVID19
 MODERNA
Food allergy Food allergy
Diagnosed with alpha gal syndrome/Red meat allergy/Allergy to artificial red dye; This spontaneous c... Diagnosed with alpha gal syndrome/Red meat allergy/Allergy to artificial red dye; This spontaneous case was reported by a consumer and describes the occurrence of FOOD ALLERGY (Diagnosed with alpha gal syndrome/Red meat allergy/Allergy to artificial red dye) in a 70-year-old female patient 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 June 2024, the patient experienced FOOD ALLERGY (Diagnosed with alpha gal syndrome/Red meat allergy/Allergy to artificial red dye). At the time of the report, FOOD ALLERGY (Diagnosed with alpha gal syndrome/Red meat allergy/Allergy to artificial red dye) outcome was unknown. Concomitant medication use information was not provided by reporter. No relevant medical history (vaccines within the past 4 weeks, medical conditions) was reported. The reporter did not remember if the patient had any vaccines within the past 4 weeks from previous vaccines. The patient had been getting them when they first said we could get them; the patient was on the vaccine bandwagon early. The most recent vaccine was in October of 2024. The patient was diagnosed with alpha-gal syndrome in late June 2024. The patient had been taking Moderna shots before her diagnosis, "whenever they first said we could get them," and has had a vaccine since her diagnosis in October 2024, which was the most recent vaccine. Before the alpha-gal diagnosis, many vaccines were available since 2020. The patient had always had the Moderna COVID-19 vaccine in the past and had never had any trouble. It was reported that the shots were risky for people with alpha-gal syndrome. Sometimes it was called a red meat allergy, but it went further than that. The alpha-gal syndrome included allergies to any dairy products, "also some weird ones that pop up such as kerogen, could not be in it (the vaccine)," any mammal-related by-products like whey or gel, or gelatin. The reporter also mentioned that the patient had an allergy to artificial red dye as well. It was unknown if the patient experienced any additional symptoms/events. Treatment medication use information was not provided by reporter. More
2868216 76 M WI 10/24/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3052034
U8862BA
Hyperhidrosis, Vomiting; Hyperhidrosis, Vomiting Hyperhidrosis, Vomiting; Hyperhidrosis, Vomiting
Patient stated that night, early next morning he experience Profuse Sweating & Vomiting. This la... Patient stated that night, early next morning he experience Profuse Sweating & Vomiting. This lasted the night and into mid morning the next day. Patient felt better (Back to Normal) in 3 days. More
2868217 53 F NY 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868218 4 F OH 10/24/2025 FLU3
 SANOFI PASTEUR
 U8889CA
Erythema, Feeling hot Erythema, Feeling hot
Large Local Reaction about 24 hours later - erythema and warmth, measuring 12 x 13 cm Large Local Reaction about 24 hours later - erythema and warmth, measuring 12 x 13 cm
2868219 73 M FL 10/24/2025 FLU3
 SANOFI PASTEUR
 u8859da
Cough, Laryngitis, Rhinorrhoea Cough, Laryngitis, Rhinorrhoea
Spouse reported 48 hours after vaccine, Patient developed a cough, runny nose, laryngitis that has l... Spouse reported 48 hours after vaccine, Patient developed a cough, runny nose, laryngitis that has lasted until today, 10/24/2025 but with lesser effects. Pt is using saltwater gargle and OTC cough meds. PCP not notified. Patient is doing better. Spouse is a retired nurse and wanted to report since Patient had conjunctivitis "years ago" from a flu shot. More
2868220 57 F 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868221 39 M 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868222 48 M 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868224 39 F MN 10/24/2025 FLU3
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 LT9HP
LT9HP
Extra dose administered, Wrong product administered; Extra dose administered, Wr... Extra dose administered, Wrong product administered; Extra dose administered, Wrong product administered More
Patient was accidentally given two flu shots. She was supposed to receive one flu shot and one covid... Patient was accidentally given two flu shots. She was supposed to receive one flu shot and one covid shot. She was called and informed of the mistake shortly after she left. More
2868225 42 M NY 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868226 26 F NY 10/24/2025 FLU3
 SANOFI PASTEUR
Erythema, Pruritus, Swelling Erythema, Pruritus, Swelling
Swelling, itching, redness Swelling, itching, redness
2868227 77 F OR 10/24/2025 FLU3
 SANOFI PASTEUR
 U8764BB
Malaise, Peripheral swelling Malaise, Peripheral swelling
Patient said she often gets some side effects due to her mastocytosis after receiving vaccines. Afte... Patient said she often gets some side effects due to her mastocytosis after receiving vaccines. After she received the vaccine, she went home and said that her arm became very swollen, from the elbow to the shoulder, and she had malaise. The symptoms went away however, and she did not see her doctor for the issue. More
2868228 40 F OH 10/24/2025 FLU3
 SANOFI PASTEUR
 U8830BA
No adverse event No adverse event
No adverse events reported by patient No adverse events reported by patient
2868229 14 M OH 10/24/2025 FLU3
 SANOFI PASTEUR
 U8830BA
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
No adverse events reported by patient No adverse events reported by patient
2868230 47 M 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868231 10 M OH 10/24/2025 FLU3
 SANOFI PASTEUR
 U8830BA
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
No adverse events reported by patient No adverse events reported by patient
2868232 77 F 10/24/2025 COVID19
 MODERNA
Electrocardiogram, Vaccination site pain Electrocardiogram, Vaccination site pain
"little tenderness" on her arm after receiving Spikevax; This spontaneous case was reporte... "little tenderness" on her arm after receiving Spikevax; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN ("little tenderness" on her arm after receiving Spikevax) in a 77-year-old female patient who received mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) for COVID-19 prophylaxis. Concurrent medical conditions included Peripheral vascular disease NOS (Patient had vascular disease. Patient saw a vein doctor, a vascular doctor every 3 months), Anemia (mildly anemic), Arthritis (had a very bad case of arthritis.) and Heartbeats premature (extra heartbeats). On 30-Oct-2024, the patient received dose of mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) (Intramuscular use) 1 dosage form. On 30-Oct-2024, after starting mRNA-1273.712 (SPIKEVAX 2024-2025 PFS), the patient experienced VACCINATION SITE PAIN ("little tenderness" on her arm after receiving Spikevax). At the time of the report, VACCINATION SITE PAIN ("little tenderness" on her arm after receiving Spikevax) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Electrocardiogram: come back good o arrhythmias. No other vaccines were given within the past 4 weeks. The patient was not on any medication for it because sometimes the EKGs come back good or with arrhythmias, but the doctor had not put her on any medications because, like, the patient comes and goes with it. It was unknown if the patient experienced any additional symptoms/events. No treatment medication was reported. Reported causality not provided. More
2868233 58 F 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
EXPIRED VACCINE GIVEN EXPIRED VACCINE GIVEN
2868234 84 M MN 10/24/2025 COVID19
 MODERNA
COVID-19, SARS-CoV-2 test positive COVID-19, SARS-CoV-2 test positive
Hospitalization related to COVID 19 following completion of primary vaccine series Hospitalization related to COVID 19 following completion of primary vaccine series
✓
2868235 37 F MN 10/24/2025 FLU3
 SEQIRUS, INC.
 948414
Extra dose administered Extra dose administered
Patient received a second dose of the current flu vaccine, #1 9/2025 and today 10/14/25 Patient received a second dose of the current flu vaccine, #1 9/2025 and today 10/14/25
2868236 47 M 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
expired vaccine expired vaccine
2868237 4 F MA 10/24/2025 COVID19
 MODERNA
 3052579
Bell's palsy, Facial paralysis, Hypoaesthesia Bell's palsy, Facial paralysis, Hypoaesthesia
Bells Palsy of L Face (L-sided droop, numbness) about 18 hours after administering vaccine - self-r... Bells Palsy of L Face (L-sided droop, numbness) about 18 hours after administering vaccine - self-resolving. Seen at Hospital , no further work-up. More
2868238 35 F 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
expired vaccine expired vaccine
2868239 34 F NC 10/24/2025 UNK
 UNKNOWN MANUFACTURER
 33CM4
Arthralgia, Injected limb mobility decreased, Pain, Product administered at inap... Arthralgia, Injected limb mobility decreased, Pain, Product administered at inappropriate site, X-ray More
Injection was given high on right arm, near acromion process. Pain in shoulder joint began a few hou... Injection was given high on right arm, near acromion process. Pain in shoulder joint began a few hours post injection and has persisted 15 days. Persistent pain at rest with high intensity pain with certain movements. Limited use and range of motion in right arm due to pain. More
2868240 22 F 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
expired vaccine expired vaccine
2868241 84 M CA 10/24/2025 COVID19
 MODERNA
 Unk
Arthropathy Arthropathy
Left elbow bursa Left elbow bursa
2868242 65 F SC 10/24/2025 COVID19
FLU3
PNC21
 MODERNA
SANOFI PASTEUR
MERCK & CO. INC.
 3051995
U8859DA
z009681
Arthralgia, Ear pain, Pain; Arthralgia, Ear pain, Pain; Arthralgia, Ear pain, Pa... Arthralgia, Ear pain, Pain; Arthralgia, Ear pain, Pain; Arthralgia, Ear pain, Pain More
Patient called on 10/24 complaining of complications in the right shoulder due to a vaccine (Fluzone... Patient called on 10/24 complaining of complications in the right shoulder due to a vaccine (Fluzone HD) administrated on 10/01. Patients described it as a major shoulder pain in the tip of right arm, also mentioned pain is radiating towards the collar bone and all the way up to the right ear. Patient also added that it's feeling better now but still feeling pain in the shoulder. pt will consult with her PCP and update us. More
2868243 58 F AZ 10/24/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 JS74H
Pain in extremity, Tenderness, Ultrasound Doppler normal Pain in extremity, Tenderness, Ultrasound Doppler normal
EE complained of left lower leg pain and tenderness on the evening after vaccine was administered. S... EE complained of left lower leg pain and tenderness on the evening after vaccine was administered. She took Tylenol for pain and applied ice packs. Saw her PCP on 10/21/2025 and an US of her LLE was done with negative DVT. Symptoms are improving now More
2868244 46 M 10/24/2025 FLU3
 SEQIRUS, INC.
 AW1670B
Expired product administered Expired product administered
expired vaccine expired vaccine
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