🏥 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 💀 🏥 🚑 ♿ ⚠️
2865456 45 M CA 10/13/2025 PNC21
 MERCK & CO. INC.
 Z003579
Hypoaesthesia, Injection site erythema, Injection site swelling, Paraesthesia, R... Hypoaesthesia, Injection site erythema, Injection site swelling, Paraesthesia, Rash More
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Numbness ... Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: PATIENT DESCRIBES HAVING NUMBNESS OF MIDDLE FINGER AFTER RECEIVING VACCINE AND RASH ABOUT 2 INCHES X 2 INCHES, HE REACHED OUT TO MEDICAL PROVIDER WHICH SUGGESTED TO GO TO URGENT CARE. PATIENT STATES HE WILL GO TO URGENT CARE TO BE SEEN AND FOLLOW UP WITH PHARMACY DEPENDING ON RESULTS More
2865457 89 F NY 10/13/2025 COVID19
 UNKNOWN MANUFACTURER
 3052734
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling More
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Inject... Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2865459 55 F MO 10/13/2025 COVID19-2
COVID19-2
 PFIZER\BIONTECH
PFIZER\BIONTECH
 my9548
my9548
Arthralgia, Injection site bruising, Injection site pain, Joint injury, Joint st... Arthralgia, Injection site bruising, Injection site pain, Joint injury, Joint stiffness; Product administered at inappropriate site More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Shoulder Joint I... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Shoulder Joint Injury (prolonged pain, tingling, etc.)-Medium, Systemic: joint stiffness, given too high in the arm-Medium, Systemic: Joint Pain-Medium, Additional Details: shot was given too high in the arm More
2865460 62 F FL 10/13/2025 FLU3
 SANOFI PASTEUR
 U8832AA
Injection site bruising, Injection site swelling Injection site bruising, Injection site swelling
THE PATIENTS SIGNIFICANT OTHER REPORTED THE PATIENT HAD A BRUISED SWOLLEN ARM. HE SHOWED ME A PICTU... THE PATIENTS SIGNIFICANT OTHER REPORTED THE PATIENT HAD A BRUISED SWOLLEN ARM. HE SHOWED ME A PICTURE AND IT WAS A BRUISE THE SIZE OF A GOLF BALL IN THE ARM WHERE SHE HAD RECEIVED THE VACCINE. More
2865461 81 F NY 10/13/2025 FLU3
 SANOFI PASTEUR
 U8855DA
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
patient experienced swelling and redness on left bicep, far below where the vaccine was given patient experienced swelling and redness on left bicep, far below where the vaccine was given
2865462 42 F KS 10/13/2025 COVID19
 MODERNA
 3052663
Erythema, Pain in extremity, Peripheral swelling, Tenderness Erythema, Pain in extremity, Peripheral swelling, Tenderness
1.5 hours after injection her arm was sore and swollen and it was red and tender. 1.5 hours after injection her arm was sore and swollen and it was red and tender.
2865463 38 F NY 10/13/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.

Chest X-ray abnormal, Chest pain, Cough, Dyspnoea, Fibrin D dimer increased; Pne... Chest X-ray abnormal, Chest pain, Cough, Dyspnoea, Fibrin D dimer increased; Pneumonia, Pyrexia More
Cough, Difficulty breathing (SOB), chest pain, fever and was diagnosed with Pneumonia. Cough, Difficulty breathing (SOB), chest pain, fever and was diagnosed with Pneumonia.
✓
2865465 62 M MN 10/13/2025 COVID19
COVID19
FLU3
FLU3
 PFIZER\BIONTECH
PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
 00069-2528-10
00069-2528-10
49281-0725-10
49281-0725-10
Abdominal pain, Chills, Fatigue, Headache, Hyperhidrosis; Nausea, Pain; Abdomina... Abdominal pain, Chills, Fatigue, Headache, Hyperhidrosis; Nausea, Pain; Abdominal pain, Chills, Fatigue, Headache, Hyperhidrosis; Nausea, Pain More
Sudden onset during the night of abdominal cramping and intense pain. Sweating, chills, nausea. Fol... Sudden onset during the night of abdominal cramping and intense pain. Sweating, chills, nausea. Followed by headache, body aches. Symptoms continued for 48 hours including fatigue and the headache. More
2865466 9 F MN 10/13/2025 COVID19
 MODERNA
 3052581
Wrong product administered Wrong product administered
Patient (child) received the incorrect vaccine. She received Moderna 12+ Covid vaccine rather than t... Patient (child) received the incorrect vaccine. She received Moderna 12+ Covid vaccine rather than the consented Flu vaccine for a 9 year old. More
2865467 88 F 10/13/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 EC2R9
Injection site pruritus, Injection site swelling, Injection site warmth Injection site pruritus, Injection site swelling, Injection site warmth
Patient stated was doing fine until day 6 post vaccine...woke up with itching and swelling at the in... Patient stated was doing fine until day 6 post vaccine...woke up with itching and swelling at the injection site. Per patient report also felt warm to the touch. Patient got OTC Benadryl and also applied an ice pack. Symptoms resolved within 12 hours. No further complaints at this time. More
2865468 75 M NC 10/13/2025 FLU3
 SANOFI PASTEUR
 UT8781DA
Arthralgia, Injected limb mobility decreased Arthralgia, Injected limb mobility decreased
Patient reported to pharmacy on 10/13/25 that he was experiencing pain in his left shoulder and inab... Patient reported to pharmacy on 10/13/25 that he was experiencing pain in his left shoulder and inability to raise his arm above the shoulder level following his vaccine on 9/25/25. Patient went to a physician who administered a steroid injection to mitigate the pain and inflammation. Patient suspected bursitis due to vaccine administration in the bursa sac, but no official diagnosis was disclosed. More
2865469 2 F MA 10/13/2025 COVID19
 PFIZER\BIONTECH
 NA0846
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
None None
2865471 17 M OR 10/13/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 F4A7R
Rash, Rash erythematous Rash, Rash erythematous
Approximately 8 hours after vaccination, a mild full body rash (described as red bumps) was noted. I... Approximately 8 hours after vaccination, a mild full body rash (described as red bumps) was noted. It had resolved by the next morning. More
2865472 82 F MI 10/13/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 u8837ba
u8837ba
Body temperature increased, Diarrhoea, Hypotension, Nausea, Use of accessory res... Body temperature increased, Diarrhoea, Hypotension, Nausea, Use of accessory respiratory muscles; Vomiting More
rec'd flu vaccine 10/10/2025 on day shift, on midnight shift developed temp, n/v/d- was given i... rec'd flu vaccine 10/10/2025 on day shift, on midnight shift developed temp, n/v/d- was given im promethazine and tylenol suppository with some reduction in sx. Started on IV fluids 10/11/25 and was noted that vomiting had resolved and she was also taking oral fluids and was more alert/responsive. She pulled out her IV and declined transfer to hospital and wished to remain no code/no hospitalization for her advance directives. 10/12/25 she was noted to again have a temp on midnight shift along with hypotension and use of accessory muscles for breathing - NP was contacted and gave orders for PO morphine and ativan for comfort. More
✓
2865473 38 M TN 10/13/2025 COVID19
FLU3
 NOVAVAX
SANOFI PASTEUR
 6315MF002C
U8832CA
Fall, Head injury, Syncope; Fall, Head injury, Syncope Fall, Head injury, Syncope; Fall, Head injury, Syncope
After patient had 2 vaccines above. He was looking ok and walking away from the pharmacy. He left th... After patient had 2 vaccines above. He was looking ok and walking away from the pharmacy. He left the pharmacy and then he came back and complained that he have the fainting and was sitting in the booth. He then felt to the ground and hit his head in the booth. The whole process was happening in around 10-15 minutes. More
2865474 49 F AZ 10/13/2025 COVID19
 PFIZER\BIONTECH
Memory impairment Memory impairment
memory issues memory issues
2865476 F 10/13/2025 VARZOS
VARZOS
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 UNK
UNK
Herpes zoster, Vaccination failure; Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure; Herpes zoster, Vaccination failure
Suspected vaccination failure; Shingles; had shingles since 2019; This serious case was reported by ... Suspected vaccination failure; Shingles; had shingles since 2019; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a adult female patient who received Herpes zoster (Shingles vaccine) for prophylaxis. Co-suspect products included Herpes zoster (Shingles vaccine) for prophylaxis. Concurrent medical conditions included shingles. On an unknown date, the patient received the 2nd dose of Shingles vaccine and the 1st dose of Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine and Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant), shingles (Verbatim: Shingles) and drug use for unapproved indication (Verbatim: had shingles since 2019). The outcome of the vaccination failure was not reported and the outcome of the shingles was unknown and the outcome of the drug use for unapproved indication was not applicable. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine and Shingles vaccine. The company considered the vaccination failure to be unrelated to Shingles vaccine and Shingles vaccine. It was unknown if the company considered the shingles to be related to Shingles vaccine and Shingles vaccine. Additional Information: GSK Receipt Date: 06-OCT-2025 This case was reported by a patient via interactive digital media. Patient had shingles since 2019. Patient could not take the prescription because patient was allergic to it. Patient's doctor took off the prescription patient was still going through it and had the 2 shots for it. This case was considered as suspected vaccination failure as details regarding time to onset for shingles and laboratory confirmation regarding shingles were unknown at the time of reporting. The batch number was not provided, and we are unable to contact the reporter.; Sender's Comments: A case of Vaccination failure, an unknown time after receiving Shingles vaccine (dose 1 and dose 2), in a female 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. The company has assessed that it is unlikely that event Product use in unapproved indication was caused by vaccine Shingles vaccine (dose 1 and dose 2). More
2865478 87 M IA 10/13/2025 COVID19
 MODERNA
 3046732
Death Death
resident passed away resident passed away
✓
2865479 59 F VA 10/13/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
Injection site erythema, Injection site nodule, Injection site warmth Injection site erythema, Injection site nodule, Injection site warmth
Nodule under vaccination injection site. Scattered redness and warmth on right arm. Extends to top... Nodule under vaccination injection site. Scattered redness and warmth on right arm. Extends to top of the shoulder. Normal range or motion demonstrated by Employee. More
2865480 83 M CA 10/13/2025 COVID19
 PFIZER\BIONTECH
 NA4452
Arthralgia, Joint contracture, Mobility decreased Arthralgia, Joint contracture, Mobility decreased
At around 1:00am on 10/12, the fingers on my left hand seized in a rigid curl along with excruciatin... At around 1:00am on 10/12, the fingers on my left hand seized in a rigid curl along with excruciating pain in all finger joints. This continued until 6:00am on 10/12 after which the symptoms slowly began to dissipate. More or less returning to a normal condition at around 7:00 on 10/13. More
2865481 54 F MO 10/13/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 7FY52
Injection site erythema, Injection site pruritus, Injection site warmth, Product... Injection site erythema, Injection site pruritus, Injection site warmth, Product administered at inappropriate site More
Received the injection in the morning and did not notice an adverse reactions. the injection was gi... Received the injection in the morning and did not notice an adverse reactions. the injection was given about 2 inches above and to the side of her left elbow. When she went home after her shift about 11 hours later, a family member noticed redness above her left elbow. The area was also warm. Employee began to notice the area was itchy. The daughter drew a circle around the area to check for spreading. The next day the redness had spread and the itchiness remained. The following day 10-12-2025 a co-worker told her to take "allergy medication." She reports she did have allergy medication and does not know the name. She took the medication once yesterday. Today the area is slightly itchy and measures 100mm tall starting at the elbow and 70mm wide. Patient delined any medical care. More
2865482 20 M FL 10/13/2025 COVID19
 PFIZER\BIONTECH
Oropharyngeal pain, Pyrexia, Throat irritation Oropharyngeal pain, Pyrexia, Throat irritation
Site mild infection, very sore muscle aches all over. Fever of 101 to 102 even after taking tylenol.... Site mild infection, very sore muscle aches all over. Fever of 101 to 102 even after taking tylenol. Sore itchy throat More
2865483 5 M IN 10/13/2025 COVID19
HPV9
 MODERNA
MERCK & CO. INC.
 3052859
Y015560
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
Pt received the above vaccines outside of the age indication. There were two patients with the same ... Pt received the above vaccines outside of the age indication. There were two patients with the same first name in our office at the same time. When the patient presented to the vaccinator, patient's dad confirmed that the DOB, first and last name written on the consent form were correct for his child. Once the incident was identified, Lead Nurse called and informed the patient's father of the incident and that VAERS would be completed. More
2865484 58 F CA 10/13/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3052583
U8832AA
Face oedema, Urticaria; Face oedema, Urticaria Face oedema, Urticaria; Face oedema, Urticaria
Facial Edema and hives all over body Facial Edema and hives all over body
2865485 79 F MO 10/13/2025 COVID19
 PFIZER\BIONTECH
 NA0587
Bone pain, Mobility decreased Bone pain, Mobility decreased
Patient said that her bones in her whole body hurt but specifically the bones in her neck, back, and... Patient said that her bones in her whole body hurt but specifically the bones in her neck, back, and arms hurt. She stated that the shot "kept me in my chair all day long". She also stated that she has never had a reaction to any vaccine before including the COVID shot. More
2865486 66 F PA 10/13/2025 FLU3
 SEQIRUS, INC.
 407272
Dizziness postural, Malaise Dizziness postural, Malaise
Patient called to report dizziness upon sitting up and moving around. Overall not feeling well. Pati... Patient called to report dizziness upon sitting up and moving around. Overall not feeling well. Patient is of smaller weight (about 100 lbs). More
2865487 30 F MO 10/13/2025 FLU3
FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
 406999
406999
406999
Blood pressure increased, Chills, Computerised tomogram normal, Ear discomfort, ... Blood pressure increased, Chills, Computerised tomogram normal, Ear discomfort, Fatigue; Headache, Migraine, Myalgia, Oropharyngeal erythema, Oropharyngeal pain; Pyrexia, Streptococcus test negative More
Events: sore/red throat, migraine causing high blood pressure (first even migraine I've had), c... Events: sore/red throat, migraine causing high blood pressure (first even migraine I've had), chills, fatigue, fever, muscle aches, ear pressure. Treatment: on 10/10 I saw my PCP for a strep test since my throat was so sore (test was negative). On 10/11 I woke up with an excruciating headache that led to my first ever migraine that did not resolve with tylenol/ibuprofen. I went to the ER due to having a headache/migraine for approximately 17 hours, as well as high blood pressure. At the ER I receive a CT scan (no issues found on it) and multiple medicines (including narcotics) in an IV. which finally helped lower by blood pressure more and mostly (but not completely) relieved my migraine. A couple of hours after discharging home, the migraine came back for approximately 6 hours. More
2865488 58 F NY 10/13/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 C9X3r
C9X3r
Chills, Erythema, Eye swelling, Facial discomfort, Fatigue; Headache, Hypoaesthe... Chills, Erythema, Eye swelling, Facial discomfort, Fatigue; Headache, Hypoaesthesia, Ocular hyperaemia, Pain More
Patient received vaccine on Wednesday 10/8. Early on Thursday morning patient had mild symptoms incl... Patient received vaccine on Wednesday 10/8. Early on Thursday morning patient had mild symptoms including feeling tired and mild body aches. Later in the afternoon on Thursday, patient started to notice chills and a headache. When patient woke up on Thursday she noticed that her left eye was red and swollen. Throughout the day the redness then spread from her eye to her cheek and the left side of her face became numb. She was seen at an urgent care on Friday and was given a course of prednisone. Patient was contacted on Monday and reported her symptoms greatly improved although she still reported a little redness and slight pressure in her face. More
2865489 42 F NC 10/13/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 NA0589
NA0589
Back pain, Injection site erythema, Injection site pain, Injection site pruritus... Back pain, Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling; Injection site warmth, Neck pain, Pain in extremity, Paraesthesia, Paraesthesia oral More
The injection site arm soreness came back. But I also felt it on the right side of my neck, right u... The injection site arm soreness came back. But I also felt it on the right side of my neck, right upper back, and area between neck and right shoulder. I looked and saw it was puffy, raised, red, and hurt when touched as well. It also itched some and was hot and later warm to the touch. The soreness eventually left but it was still puffy. Later the soreness came back, the hurt as well. It was tingling in that area, and my lips were tingling some too. It was now pink and still raised, puffy, just not as thick/high up. The tingling did not last long. It is no longer red or pink. But it is still slightly warm to the touch. It is also still sore, puffy, and raised. More
2865490 68 F ID 10/13/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.

Erythema, Peripheral swelling, Skin warm; Erythema, Peripheral swelling, Skin wa... Erythema, Peripheral swelling, Skin warm; Erythema, Peripheral swelling, Skin warm More
Redness, warmth, and swelling in upper arm Redness, warmth, and swelling in upper arm
2865493 20 F AR 10/13/2025 FLU3
 SANOFI PASTEUR
 U8764CB
Product administered to patient of inappropriate age, Wrong product administered Product administered to patient of inappropriate age, Wrong product administered
Patient received high dose flu vaccine instead of regular flu vaccine Patient received high dose flu vaccine instead of regular flu vaccine
2865494 0.67 M IL 10/13/2025 COVID19
 PFIZER\BIONTECH
 MY9548
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient is an 8 month old infant that was administered the Comirnaty Covid vaccine (12 years old+) i... Patient is an 8 month old infant that was administered the Comirnaty Covid vaccine (12 years old+) instead of the Moderna Spikevax that is intended for patients 6 months-11 years old. Patient did not exhibit any adverse side effects after injection and did not show and adverse side effects 48 hours later. Parents are aware, and have been monitoring infant at home. More
2865495 12 F MI 10/13/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 5XA2J
Wrong product administered Wrong product administered
Patient had not been seen for 3 years and was behind on routine vaccination. An error was made by th... Patient had not been seen for 3 years and was behind on routine vaccination. An error was made by the Medical Assistant on what was needed for patient to be caught up, was given Men B vaccine by mistake. More
2865496 57 F AR 10/13/2025 FLU3
 SANOFI PASTEUR
 U8764CB
Product administered to patient of inappropriate age, Wrong product administered Product administered to patient of inappropriate age, Wrong product administered
High dose flu shot was administered instead of regular flu shot High dose flu shot was administered instead of regular flu shot
2865497 68 M PA 10/13/2025 FLU3
 SEQIRUS, INC.
 407263
Confusional state, Depressed level of consciousness, Disturbance in attention, R... Confusional state, Depressed level of consciousness, Disturbance in attention, Restlessness, Somnolence More
Pt called the pharmacy the day after the influenza vaccine was administered complaining of restlessn... Pt called the pharmacy the day after the influenza vaccine was administered complaining of restlessness, confusion, sleepiness. He stated that he wasn't alert and couldn't focus on a television show like he normally does. More
2865498 58 M AR 10/13/2025 FLU3
 SANOFI PASTEUR
 U8764CB
Product administered to patient of inappropriate age, Wrong product administered Product administered to patient of inappropriate age, Wrong product administered
Patient received high dose flu shot when they should have received the regular flu shot Patient received high dose flu shot when they should have received the regular flu shot
2865499 68 F FL 10/13/2025 PNC20
 PFIZER\WYETH
Oropharyngeal discomfort, Pruritus Oropharyngeal discomfort, Pruritus
Patient developed generalized ithcing and throat discomfort after vaccines. Required medrol dose pac... Patient developed generalized ithcing and throat discomfort after vaccines. Required medrol dose pack More
2865500 76 F PA 10/13/2025 FLU3
 SEQIRUS, INC.
 407263
Palpitations, Sleep disorder Palpitations, Sleep disorder
Pt reported that the night after the vaccine she was awakened by her heart racing fast. She was unab... Pt reported that the night after the vaccine she was awakened by her heart racing fast. She was unable to go back to sleep. Since that evening she hasn't experienced any other side effects. Of note, this was her first flu vaccine in a "long time", probably 30 years. More
2865501 63 M CA 10/13/2025 COVID19
 NOVAVAX
 6315MF001C
Erythema Erythema
Patient got a Novavax vaccine on the left arm. This is his first time getting Novavax. No reaction d... Patient got a Novavax vaccine on the left arm. This is his first time getting Novavax. No reaction during the administration. Patient notice redness later and it spread all the way to the right side of the body. No itching or burning sensation. He came back a week later to notify the pharmacy. The redness is lessen according to the patient. I advised the patient to take anti-histamine OTC and follow up with his primary care on Monday. More
2865502 39 F CA 10/13/2025 UNK
 UNKNOWN MANUFACTURER
Pharyngeal swelling, Swelling face Pharyngeal swelling, Swelling face
swelling of face/ throat according to patient after receiving Pfizer Covid 19 vaccine on 09/25/2025 swelling of face/ throat according to patient after receiving Pfizer Covid 19 vaccine on 09/25/2025
2865503 82 F CO 10/13/2025 COVID19
 MODERNA
 3052734
Blister, Oral mucosal blistering Blister, Oral mucosal blistering
Patient got blisters on lips and surrounding mouth areas. She had it for few days. Patient got blisters on lips and surrounding mouth areas. She had it for few days.
2865504 0.33 M FL 10/13/2025 DTAPHEPBIP
HIBV
PNC20
RV1
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 9C295 PRIVATE
C47XX PVT
LX4486 PVT
J757K
Diarrhoea; Diarrhoea; Diarrhoea; Diarrhoea Diarrhoea; Diarrhoea; Diarrhoea; Diarrhoea
Pt developed diarrhea for 2 weeks. Pt developed diarrhea for 2 weeks.
2865505 18 F VT 10/13/2025 COVID19
 MODERNA
 3052736
Loss of consciousness, Syncope Loss of consciousness, Syncope
Syncope. Patient lost consciousness for a brief moment after receiving the vaccine a few minutes pri... Syncope. Patient lost consciousness for a brief moment after receiving the vaccine a few minutes prior. More
2865506 76 F NY 10/13/2025 COVID19
FLU3
HEPAB
 MODERNA
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 3052034
U8862BA
AZ2A3
Dizziness, Tinnitus; Dizziness, Tinnitus; Dizziness, Tinnitus Dizziness, Tinnitus; Dizziness, Tinnitus; Dizziness, Tinnitus
Pt received three vaccines and then left pharmacy to do some shopping. About 30 minutes later she re... Pt received three vaccines and then left pharmacy to do some shopping. About 30 minutes later she returned to the pharmacy with complaints of dizziness and light headedness. She took a seat on a bench in front of the pharmacy and was given a bottle of water. The patient later complained of her hearing sounding "like I am in a tunnel." She sat there for over 30 minutes sipping on the water until she felt bottle which at that time she had also finished the water bottle. She then left the pharmacy and said she was going to eat something. More
2865508 11 F IL 10/13/2025 MNQ
 SANOFI PASTEUR
 u8645aa
Dizziness, Dyspnoea, Loss of consciousness, Pallor, Syncope Dizziness, Dyspnoea, Loss of consciousness, Pallor, Syncope
Pt received this vaccine on right arm along with boostrix on the left arm. Pt was initially fine and... Pt received this vaccine on right arm along with boostrix on the left arm. Pt was initially fine and was sitting on chair as her father was getting his vaccine. While her father was getting vaccinated the pt felt dizzy and fainted. After coming to she looked pale and out of breath. 911 was called More
2865509 89 M NC 10/13/2025 FLU3
 SANOFI PASTEUR
 UT8804AA
Extra dose administered, No adverse event Extra dose administered, No adverse event
THERE WERE NO ADVERSE EVENTS. PATIENT RECEIVED A FLU SHOT THROUGH THE CLINIC 10/8/2025 THAT WAS NOT ... THERE WERE NO ADVERSE EVENTS. PATIENT RECEIVED A FLU SHOT THROUGH THE CLINIC 10/8/2025 THAT WAS NOT DOCUMENTED CORRECTLY. PATIENT RECEIVED TWO FLU SHOTS IN ONE WEEK. More
2865510 13 F PA 10/13/2025 FLU3
 SANOFI PASTEUR
 UT8792L
Rash, Rash erythematous, Rash maculo-papular Rash, Rash erythematous, Rash maculo-papular
diffuse erythematous maculopapular rash head to toe diffuse erythematous maculopapular rash head to toe
2865511 89 F MT 10/13/2025 COVID19
 MODERNA
 B0020
Hypoaesthesia Hypoaesthesia
Numbness of bilateral feet and legs ongoing Numbness of bilateral feet and legs ongoing
2865512 2 F CT 10/13/2025 FLU3
 SEQIRUS, INC.
 406989
Injection site erythema, Injection site swelling, Injection site warmth, Pyrexia Injection site erythema, Injection site swelling, Injection site warmth, Pyrexia
on 10/7/25 redness and swelling noted to left thigh, in area of injection. Red area measured 12cm x ... on 10/7/25 redness and swelling noted to left thigh, in area of injection. Red area measured 12cm x 6cm, area soft and warm to touch. Fever of 103. On 10/8/25, red area noted to be larger, measuring 20cm x 10cm. Swelling increased, left thigh circumference 30cm, right thigh circumference 26.5cm. Area soft and warm to touch. Fever of 101. More
2865513 7 M CO 10/13/2025 FLU3
 SANOFI PASTEUR
 tfaa2547
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient should have gotten Fluzone due to being under 9 years old. Was mistakenly given Flublok for ... Patient should have gotten Fluzone due to being under 9 years old. Was mistakenly given Flublok for ages 9 and up. Reported to family, family has not noted any issues or adverse events to this point. More
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