🏥 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 💀 🏥 🚑 ♿ ⚠️
2844172 F WI 06/06/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Blood test, COVID-19, Drug ineffective, Influenza A virus test, Influenza B viru... Blood test, COVID-19, Drug ineffective, Influenza A virus test, Influenza B virus test; Respiratory syncytial virus test, SARS-CoV-2 test More
covid; covid; This is a spontaneous report received from a Physician from medical information team, ... covid; covid; This is a spontaneous report received from a Physician from medical information team, Program ID. An 80-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2025, outcome "recovering" and all described as "covid". The event "covid" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (2025) Unknown results; Influenza A virus test: (2025) Unknown results; Influenza B virus test: (2025) Unknown results; Respiratory syncytial virus test: (2025) Unknown results; SARS-CoV-2 test: (2025) Positive, notes: 3rd or 4th day tested positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: It was the first time both reporter (husband) and his wife (the patient) had COVID since the beginning of the year. 3rd or 4th day, tested positive. They were put on Paxlovid and symptoms went absolutely away progressively. 5 days when they were on it, nasal drainage was much less, and it was putrid and coughing started to clear quite a bit. After 5th day, it was like a reticence of the disease and it was worse that they have ever had and next 2 or 3 days it was progressively worse and worse and worse. At time of report, week after that, and they seem to be doing well.; Sender's Comments: Vaccine efficacy varies from person to person and is subject to many other factors. The association between the event lack of effect (COVID-19) with COMIRNATY (2024-2025 FORMULA can not be fully excluded. More
2844173 66 F LA 06/06/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 HH7595
HH7595
COVID-19; COVID-19, Vaccination failure; COVID-19; COVID-19, Vaccination failure COVID-19; COVID-19, Vaccination failure; COVID-19; COVID-19, Vaccination failure
She got COVID after the vaccine; This is a spontaneous report received from a Consumer or other non ... She got COVID after the vaccine; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 68-year-old female patient received BNT162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), on 03Oct2023 as dose 1, single (Lot number: HH7595) at the age of 66 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), administration date: Mar2021, when the patient was 64 years old, for COVID-19 Immunization; Bnt162b2 (DOSE 2, SINGLE), administration date: Mar2021, when the patient was 64 years old, for COVID-19 Immunization; Bnt162b2 (DOSE 3 (BOOSTER), SINGLE), administration date: Sep2021, when the patient was 64 years old, for COVID-19 Immunization; Bnt162b2 (DOSE 4 (BOOSTER), SINGLE), administration date: Apr2022, when the patient was 65 years old, for COVID-19 Immunization; Bnt162b2;bnt162b2 omi ba.4-5 (DOSE 5 (BOOSTER), SINGLE), administration date: Sep2022, when the patient was 65 years old, for COVID-19 Immunization; Bnt162b2;bnt162b2 omi ba.4-5 (DOSE 6 (BOOSTER), SINGLE), administration date: Apr2023, when the patient was 66 years old, for COVID-19 Immunization. The following information was reported: COVID-19 (non-serious) with onset 2025, outcome "unknown", described as "She got COVID after the vaccine". Additional information:Other Products: No. The patient did not had prior vaccination within 4 weeks. She got COVID after the vaccine and was just prescribed Paxlovid and wanted to get some help with paying for Paxlovid. More
2844174 81 F CA 06/06/2025 COVID19
 PFIZER\BIONTECH
COVID-19, Drug ineffective COVID-19, Drug ineffective
her last vaccination was Feb, and now she got COVID; her last vaccination was Feb, and now she got C... her last vaccination was Feb, and now she got COVID; her last vaccination was Feb, and now she got COVID; This is a spontaneous report received from a Consumer or other non HCP, Program ID. An 81-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), in Feb2025 as dose 1, single (Batch/Lot number: unknown) at the age of 81 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2025, outcome "unknown" and all described as "her last vaccination was Feb, and now she got COVID". Therapeutic measures were taken as a result of covid-19. Clinical course information: During an inbound call for financial assistance, the reporter stated that the patient was diagnosed with COVID and received a prescription for Paxlovid. The patient just got Pfizer vaccinated in Feb. When asked for confirmation regarding the patient vaccination in Feb the reporter started her last vaccination was Feb, and now she got COVID. It's unfortunate. The patient has been on Paxlovid before, and then had gotten COVID, have they changed the formula, is it what are the chances specifically of that happening again after you have been on it once. The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received. More
2844175 06/06/2025 COVID19
 PFIZER\BIONTECH
Vaccination site pain Vaccination site pain
still to this day have a pain where the shot was administered; This is a spontaneous report received... still to this day have a pain where the shot was administered; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 71-year-old patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), on 01Apr2025 as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Comirnaty (Primary immunization series complete), for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 2025, outcome "unknown", described as "still to this day have a pain where the shot was administered". The event "still to this day have a pain where the shot was administered" required physician office visit. Additional information: The patient went to the Doctor and it could be two things, a reaction to drug or the pharmacist hit a nerve. The patient stated that all his/her COVID shots where Pfizer and until now have had no issues. The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received. More
2844176 58 F NY 06/06/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 elo142
elo142
el9261
el9261
Angiogram, Angiogram cerebral, Atrial fibrillation, Atrial septal defect, Comput... Angiogram, Angiogram cerebral, Atrial fibrillation, Atrial septal defect, Computerised tomogram; Craniotomy, Echocardiogram, Electrocardiogram, Haemorrhagic stroke, Magnetic resonance imaging; Angiogram, Angiogram cerebral, Atrial fibrillation, Atrial septal defect, Computerised tomogram; Craniotomy, Echocardiogram, Electrocardiogram, Haemorrhagic stroke, Magnetic resonance imaging More
I had a hemorrhagic stroke on 8/18/24 , with craniotomy that same day. Since it was a cryptic stro... I had a hemorrhagic stroke on 8/18/24 , with craniotomy that same day. Since it was a cryptic stroke, I had further testing, which revealed AFib & PFO ( they don't think the PFO was the cause of the stroke). While I'm at the age where AFib can occur - I can't prove that the vaccines caused it - BUT you can't prove that the vaccine didn't cause it. More
✓ ✓
2844177 16 F DE 06/06/2025 MENB
MNQ
 PFIZER\WYETH
SANOFI PASTEUR
 LF5302
U8493AA
Injection site bruising, Injection site erythema, Injection site swelling; Injec... Injection site bruising, Injection site erythema, Injection site swelling; Injection site bruising, Injection site erythema, Injection site swelling More
Developed redness, swelling, bruising about 48h after injection. 2.5cm area of redness and swelling... Developed redness, swelling, bruising about 48h after injection. 2.5cm area of redness and swelling. Seen in office 6/6/25 and symptoms were improving. Low concern for ongoing infection. More
2844178 5 M PA 06/06/2025 DTAPIPV
 SANOFI PASTEUR
 U7838AA
Erythema, Peripheral swelling, Skin warm Erythema, Peripheral swelling, Skin warm
Parent reported immunization reaction in arm Quadracel was administered. The arm was swollen, red, a... Parent reported immunization reaction in arm Quadracel was administered. The arm was swollen, red, and hot to touch. More
2844179 5 F AL 06/06/2025 DTAP
HEP
IPV
MMRV
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 3CA03C3
7NX57

Y008787
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event More
There was no adverse reaction. Pt. received vaccines on 4/22/2025 and then again on 5/30/2025 (fat... There was no adverse reaction. Pt. received vaccines on 4/22/2025 and then again on 5/30/2025 (father brought in child). After the vaccines were given on 5/30/2025 the mother called the clinic wanted to know why more shots were given when she was told she was up to date with vaccines. Our record showed these vaccines were due. Mother was asked to bring in her vaccine record and when vaccines were entered into database patient was up to date after the 7/19/2024 vaccines. Child received vaccines on 4/22/2025 that were not needed. Mother did not report any adverse reaction and mother was informed that child was indeed up to date. More
2844180 4 F PA 06/06/2025 DTAPIPV
 SANOFI PASTEUR
 U7838AA
Erythema, Peripheral swelling, Skin warm Erythema, Peripheral swelling, Skin warm
Parent reported immunization reaction in arm Quadracel was administered. The arm was swollen, red, a... Parent reported immunization reaction in arm Quadracel was administered. The arm was swollen, red, and hot to touch. More
2844181 5 F PA 06/06/2025 DTAPIPV
 SANOFI PASTEUR
 U7838AA
Erythema, Peripheral swelling, Skin warm Erythema, Peripheral swelling, Skin warm
Parent reported immunization reaction in arm Quadracel was administered. The arm was swollen, red, a... Parent reported immunization reaction in arm Quadracel was administered. The arm was swollen, red, and hot to touch. More
2844182 3 F 06/06/2025 MMRV
 MERCK & CO. INC.
 Z005150
Erythema multiforme, Urticaria Erythema multiforme, Urticaria
Patient developed a hive rash at night on the 31st. Received MMR/V 2 days prior (Given early for tra... Patient developed a hive rash at night on the 31st. Received MMR/V 2 days prior (Given early for travel). However, she was also on Amoxicillin and that finished 2 days prior as well. The hives progressed to an erythema multiforme rash. She never developed a fever. More
2844183 7 F GA 06/06/2025 MMR
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
 Y005808
Y011019
Chest pain, Crying, Panic reaction; Chest pain, Crying, Panic reaction Chest pain, Crying, Panic reaction; Chest pain, Crying, Panic reaction
Patient described feeling chest pains after receiving the MMR and Varicella vaccines. She felt panic... Patient described feeling chest pains after receiving the MMR and Varicella vaccines. She felt panicked and was crying and seeking comfort with her mother. Symptoms lasted for about an hour and then resolved. More
2844184 5 F AL 06/06/2025 DTAP
HEP
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 3CA03C3
7NX57
No adverse event, Vaccination error; No adverse event, Vaccination error No adverse event, Vaccination error; No adverse event, Vaccination error
There was NO adverse reaction to vaccinations administered. Doses that were not needed were administ... There was NO adverse reaction to vaccinations administered. Doses that were not needed were administered due to incorrect immunization records that were entered into database by clerical staff. More
2844185 1 F AL 06/06/2025 MMR
MMR
VARCEL
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 Y020516
Y020516
Y017061
Y017061
Blister, Faeces discoloured, Fatigue, Rash, Rash erythematous; Rash macular; Bli... Blister, Faeces discoloured, Fatigue, Rash, Rash erythematous; Rash macular; Blister, Faeces discoloured, Fatigue, Rash, Rash erythematous; Rash macular More
MOP states the child woke up and had a red, macular rash on her face, that progressed down her body ... MOP states the child woke up and had a red, macular rash on her face, that progressed down her body through out the morning. Pt was not scratching. MOP also states pt is "not herself" and fatigued with yellow poop. Mother says the child has not exhibited this color before. There are 2 blisters on patient's fingers, but MOP suggests its probably from teething, since patient has been chewing on her fingers. no recent change in diet or activities. More
2844186 12 M WI 06/06/2025 HPV9
MNQ
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
 y010466
x4t99
Injection site erythema; Injection site erythema Injection site erythema; Injection site erythema
Hi, patient had 2 shots on Monday, one in each shoulder. His right shoulder is red and he said it fe... Hi, patient had 2 shots on Monday, one in each shoulder. His right shoulder is red and he said it feels like sunburn. His left is normal. He wasn't in the sun. I don't know which shot went into which arm. Other than that he's been behaving normally. More
2844187 44 F WA 06/06/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH

Fatigue, Injection site pain, Injection site rash, Injection site swelling, Inje... Fatigue, Injection site pain, Injection site rash, Injection site swelling, Injection site warmth; Pain More
Fatigue/body aches at 24-48 hours, increasing injection site pain/swelling/heat for 3-4 days, hive l... Fatigue/body aches at 24-48 hours, increasing injection site pain/swelling/heat for 3-4 days, hive like rash on injected shoulder at 60hrs post injection More
2844188 2 F 06/06/2025 HIBV
 GLAXOSMITHKLINE BIOLOGICALS
 APSA3
Incorrect route of product administration Incorrect route of product administration
Administered subcutaneously instead of intramuscularly Administered subcutaneously instead of intramuscularly
2844189 51 F MN 06/06/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 Z002626
Z002626
Contusion, Erythema, Full blood count normal, Headache, Pain; Peripheral swellin... Contusion, Erythema, Full blood count normal, Headache, Pain; Peripheral swelling, Pruritus, Skin warm More
Patient had headache and body aches the day after the vaccine. his arm then appeared red, swollen, w... Patient had headache and body aches the day after the vaccine. his arm then appeared red, swollen, warm, and itchy. When he came in for appt there was noticeable symptoms. Outlined the redness in skin marker. The next day it was out of the markings and a noticeable bruise has formed by the redness NOT by the injection site. Blood test was done to see if patient had an elevated WBC, he did not. This vaccine has been added to pts allergy list. Prednisone was given to help with symptoms. More
2844190 3 F NY 06/06/2025 DTAP
HIBV
PNC20
 SANOFI PASTEUR
MERCK & CO. INC.
PFIZER\WYETH
 3CA55C1
UK328AA
MF0415
Erythema, Rash; Erythema, Rash; Erythema, Rash Erythema, Rash; Erythema, Rash; Erythema, Rash
Woke up with bright red blotch on left cheek and left earlobe. Arms and back covered in rash. Woke up with bright red blotch on left cheek and left earlobe. Arms and back covered in rash.
2844191 23 F TX 06/06/2025 COVID19
 MODERNA
 052E21Q
Chest pain, Electrocardiogram abnormal, Electrocardiogram ambulatory abnormal, P... Chest pain, Electrocardiogram abnormal, Electrocardiogram ambulatory abnormal, Palpitations, Ventricular extrasystoles More
Chest pain with palpitations Chest pain with palpitations
2844192 48 F KY 06/06/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 053E21A
053E21A
053E21A
078C21A
078C21A
078C21A
Angiogram, Arrhythmia, Bradycardia, Echocardiogram, Electrocardiogram; Electroca... Angiogram, Arrhythmia, Bradycardia, Echocardiogram, Electrocardiogram; Electrocardiogram ambulatory, Implantable cardiac monitor insertion, Supraventricular extrasystoles, Tachycardia, Ultrasound scan; Ventricular extrasystoles; Angiogram, Arrhythmia, Bradycardia, Echocardiogram, Electrocardiogram; Electrocardiogram ambulatory, Implantable cardiac monitor insertion, Supraventricular extrasystoles, Tachycardia, Ultrasound scan; Ventricular extrasystoles More
Heart arrhythmia, PVC?s, PAC?s, tachycardia, bradycardia Heart arrhythmia, PVC?s, PAC?s, tachycardia, bradycardia
✓ ✓
2844193 57 F OH 06/06/2025 TYP
TYP
UNK
UNK
UNK
UNK
 BERNA BIOTECH, LTD.
BERNA BIOTECH, LTD.
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER





Arthralgia, C-reactive protein, Mobility decreased, Neck pain, Polymyalgia rheum... Arthralgia, C-reactive protein, Mobility decreased, Neck pain, Polymyalgia rheumatica; Red blood cell sedimentation rate; Arthralgia, C-reactive protein, Mobility decreased, Neck pain, Polymyalgia rheumatica; Red blood cell sedimentation rate; Arthralgia, C-reactive protein, Mobility decreased, Neck pain, Polymyalgia rheumatica; Red blood cell sedimentation rate More
Dec 13th day of injections; mild joint pain began on Dec 17th; Typhoid fever pills completed on Dec ... Dec 13th day of injections; mild joint pain began on Dec 17th; Typhoid fever pills completed on Dec 20; Dec 26th moderate joint pain of knees and hips after riding in car for 2 hours; Jan 14, 2024 neck and shoulder pain began (moderate); knee, hip, neck and shoulder pain continue to worsen throughout Jan and early Feb 2024; Feb 10th, woke up and could not get out of bed without assistance; diagnosed with PMR March 18, 2024 More
✓
2844194 17 M GA 06/06/2025 MNQ
 SANOFI PASTEUR
 U8361AA
Hyperhidrosis, Hypotension, Syncope Hyperhidrosis, Hypotension, Syncope
Pt. initially tolerated injection well but had a syncopal episode around 11:08 am. Pt. sat in a chai... Pt. initially tolerated injection well but had a syncopal episode around 11:08 am. Pt. sat in a chair right before episode and mother kept him in the chair. No fall occurred. Pt. was initially sweaty, and BP was low, but it increased within a few minutes. Instructed parent and child to report episode to healthcare facility when future vaccines are received, so they can make accommodations in case this was a vagal episode. More
2844195 48 F TN 06/06/2025 COVID19
 MODERNA
Photopsia, Retinal detachment, Vitreous detachment Photopsia, Retinal detachment, Vitreous detachment
On April 9, 2021, the vitreous in my left eye detached at approximately 9:30 PM CST. This event was ... On April 9, 2021, the vitreous in my left eye detached at approximately 9:30 PM CST. This event was very obvious to me as I was sitting in a dark room at the time it happened. I saw a series of bright, white flashes in the corner of my eye, which subsided within a couple of minutes. More
✓
2844196 31 F OK 06/06/2025 HEP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 T5D73
EB499
Hypoaesthesia, Malaise, Nausea, Syncope, Tinnitus; Hypoaesthesia, Malaise, Nause... Hypoaesthesia, Malaise, Nausea, Syncope, Tinnitus; Hypoaesthesia, Malaise, Nausea, Syncope, Tinnitus More
Hep B administered IM in right deltoid; pt tolerated well. TDaP administered IM in left deltoid; aft... Hep B administered IM in right deltoid; pt tolerated well. TDaP administered IM in left deltoid; after administration complete, pt states, "I don't feel well", and had syncope episode. Patient regained consciousness and reports ringing in her ears, numb hands, and nausea. Facility code blue arrived and took pt blood pressure and O2 sats and transferred by wheel chair to same day clinic for observation. More
2844197 31 M 06/06/2025 HEP
MMR
VARCEL
 DYNAVAX TECHNOLOGIES CORPORATION
MERCK & CO. INC.
MERCK & CO. INC.
 947931
Y020517
Y017062
No adverse event; No adverse event; No adverse event No adverse event; No adverse event; No adverse event
There have been no adverse reactions There have been no adverse reactions
2844198 11 F NC 06/06/2025 HPV9
MNQ
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
 Y012921
DL4YY
Injection site induration, Pain in extremity; Injection site induration, Pain in... Injection site induration, Pain in extremity; Injection site induration, Pain in extremity More
Left arm is hard from the shoulder down to the elbow. Painful to lift arm. Left arm is hard from the shoulder down to the elbow. Painful to lift arm.
2844199 69 M PA 06/06/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3273H
Circumstance or information capable of leading to medication error Circumstance or information capable of leading to medication error
Had to stick pt twice. Pt flinched on first stick. Removed needle and replaced with new needle and s... Had to stick pt twice. Pt flinched on first stick. Removed needle and replaced with new needle and stuck patient again approximately 1 inch away then pushed vaccine in. More
2844200 17 M NC 06/06/2025 MNQ
VARCEL
 NOVARTIS VACCINES AND DIAGNOSTICS
MERCK & CO. INC.
 EK7DG
Y014511
Cough, Dyspnoea, Throat clearing, Throat tightness, Urticaria; Cough, Dyspnoea, ... Cough, Dyspnoea, Throat clearing, Throat tightness, Urticaria; Cough, Dyspnoea, Throat clearing, Throat tightness, Urticaria More
Patient's father brought him back to the office about 30 minutes after he left. He had hives on... Patient's father brought him back to the office about 30 minutes after he left. He had hives on bilateral arms, face, neck, chest, and back. Patient was coughing and trying to clear his throat. He stated his throat felt tight and he was SOB. Patient was sent straight to the ED. Patient was given Zyrtec, Epi, Famotidine, and Solu-Medrol. More
2844201 F WI 06/06/2025 HEP
 MERCK & CO. INC.
 7006341601
Expired product administered Expired product administered
Patient was given Hep V vaccine and the vaccine was expired. Patient was given Hep V vaccine and the vaccine was expired.
2844202 61 F TX 06/06/2025 PNC21
 MERCK & CO. INC.
Injection site cellulitis, Injection site rash, Injection site swelling, Injecti... Injection site cellulitis, Injection site rash, Injection site swelling, Injection site warmth, Rash erythematous More
Patient reports that a rash appeared on left arm the day after the vaccine (located directly below t... Patient reports that a rash appeared on left arm the day after the vaccine (located directly below the site of the injection on her left arm) but that she wasn't immediately concerned. Reports the rash was flat and seem to improve until yesterday when it got larger, hot to touch, and much more swollen. Exam demonstrated erythematous rash 3" x 5," hot to touch, and swollen, without abscess. Patient treated for cellulitis at site. Rx provided for Cephalexin 500mg every 6 hours for 10 days. Patient picked up the medication today (6/6/2025) More
2844203 80 F 06/06/2025 RSV
 PFIZER\WYETH
Pain in extremity, Rash erythematous, Skin warm Pain in extremity, Rash erythematous, Skin warm
RED RASH LARGER THAN 2 INCHES. PAIN IN ARM. SKIN HOT TO TOUCH. LASTED FOR AT LEAST 5 DAYS. RED RASH LARGER THAN 2 INCHES. PAIN IN ARM. SKIN HOT TO TOUCH. LASTED FOR AT LEAST 5 DAYS.
2844204 8 M TX 06/06/2025 YF
 SANOFI PASTEUR
 uk137aa
Incorrect route of product administration, No adverse event Incorrect route of product administration, No adverse event
No adverse reaction reported yet. Immunization was administered unintentionally into intramuscular ... No adverse reaction reported yet. Immunization was administered unintentionally into intramuscular route. More
2844205 11 F AZ 06/06/2025 HPV9
 MERCK & CO. INC.
 Y005835
Fall Fall
Patient fell upon trying to stand after receiving HPV vaccine Patient fell upon trying to stand after receiving HPV vaccine
2844207 39 F NJ 06/06/2025 COVID19
 MODERNA
 0321321A
Impaired work ability, Pain, Pericarditis Impaired work ability, Pain, Pericarditis
Pericarditis, repeated hospitalization, steroid myopathy in legs, chronic pain, disability from work Pericarditis, repeated hospitalization, steroid myopathy in legs, chronic pain, disability from work
✓ ✓
2844208 56 F CT 06/06/2025 VARCEL
 MERCK & CO. INC.
 Y013347
Extra dose administered Extra dose administered
Varicella was administered in error. Colleague came to clinic for administration of MMR dose #2. Col... Varicella was administered in error. Colleague came to clinic for administration of MMR dose #2. Colleague has a history of Varicella positive titer and reports no allergy to Varicella. Colleague was educated on potential adverse reaction and at this time denies any adverse reactions. Colleague was administered MMR #2 on opposite arm within the hour of receiving Varicella. More
2844209 11 F ME 06/06/2025 HPV9
MENB
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
 W011321
2RF2X
No adverse event, Product administered to patient of inappropriate age; No adver... No adverse event, Product administered to patient of inappropriate age; No adverse event, Product administered to patient of inappropriate age More
Pt did not have an adverse reaction that we know of, however vaccine was given before the age it is ... Pt did not have an adverse reaction that we know of, however vaccine was given before the age it is indicated. More
2844210 55 F CT 06/06/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 D4J9L
D4J9L
Asthenia, Feeling abnormal, Formication, Paraesthesia, Sensory disturbance; Slee... Asthenia, Feeling abnormal, Formication, Paraesthesia, Sensory disturbance; Sleep disorder, Tremor More
On April 12, I was given the Tdap injection at pharmacy. After receiving it, I felt a strange sensa... On April 12, I was given the Tdap injection at pharmacy. After receiving it, I felt a strange sensation on the left arms. I felt something crawling moving inside as if the medicine started working giving me small popping sensations. I thought this was normal and that the injection was working for me. But these crawling popping feelings continued to move day by day to different areas and I thought it was the medicine still doing the job. On June 1, during the night these sensations continue stronger from the mid section down. So the lower body started shaking uncontrollably for 5 to 10 seconds and I thought nothing of it the next day as I didn't feel it. I have been with little energy pushing myself day in and day out. On the night of 6/5/25 I didn't feel my left leg but then the sensation left quickly while the right had lots of tingling. I am not sleeping well either as these little popping feelings continue waking me up. Some days I feel great and some days I feel terrible. I just want to get better. More
2844211 4 F MI 06/06/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 4L454
Injection site erythema, Injection site swelling, Pain, Pyrexia Injection site erythema, Injection site swelling, Pain, Pyrexia
24 HRS POST VACCINATION, LOW GRADE FEVER, PAIN, REDNESS AND SWELLING AT INJECTION SITE. PAIN AND RE... 24 HRS POST VACCINATION, LOW GRADE FEVER, PAIN, REDNESS AND SWELLING AT INJECTION SITE. PAIN AND REDNESS CONTINUED FOR 3 DAYS. More
2844212 45 F MN 06/06/2025 COVID19
 MODERNA
 Not noted in my
Chronic fatigue syndrome, Impaired work ability, Loss of personal independence i... Chronic fatigue syndrome, Impaired work ability, Loss of personal independence in daily activities, Postural orthostatic tachycardia syndrome More
Started with POTS symptoms and ME/CFS between 12/1/23 and 12/4/23 that escalated to having to be out... Started with POTS symptoms and ME/CFS between 12/1/23 and 12/4/23 that escalated to having to be out of work, inability to work full time, and marked functional decline. More
✓
2844213 51 F CA 06/06/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 X72D2
Blister, Erythema Blister, Erythema
Small red fluid filled blisters on L wrist and R thigh Small red fluid filled blisters on L wrist and R thigh
2844214 58 F NH 06/06/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 9L944
Product preparation issue Product preparation issue
Pt received the diluent only, the powder was not reconstituted. Pt received the diluent only, the powder was not reconstituted.
2844215 16 F FL 06/06/2025 HPV9
TDAP
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 MSD X022735
SKB X449Y
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
These 2 vaccines were given in error to patient. They were meant to be given to her sister and were... These 2 vaccines were given in error to patient. They were meant to be given to her sister and were incorrectly administered to her. She did not need these vaccines. She completed the 2 vaccines for HPV (dose 1 : 11/8/22, dose 2: 11/10/23) prior to age 15 which means she did not need a 3rd dose. She completed her TDAP series 6/5/19 and did not need this extra TDAP vaccine. We are concerned about adverse long term or short term effects of being given the wrong vaccines. Also, the doctor's office needs to be reported due to their gross errors in administering the wrong vaccines to our children. More
2844216 52 F MN 06/06/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 037K204
061M20A
003J212A
AS7168B
Death; Death; Death; Death Death; Death; Death; Death
Patient expired 6/5/2025. Patient expired 6/5/2025.
✓
2844217 11 F FL 06/06/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 SKB DD72H
Wrong patient Wrong patient
This vaccine was given in error to patient. Her 16 year old sister was supposed to receive this vac... This vaccine was given in error to patient. Her 16 year old sister was supposed to receive this vaccine and the medical assistant made a gross error in administering this vaccine to the wrong child. This vaccine should not have been administered to a healthy 11 year old with no pre-existing health concerns or need for Men B vaccine. Another form was filled out for her sister, since she received the vaccines meant for patient. More
2844218 11 M AZ 06/06/2025 COVID19
 PFIZER\BIONTECH
 LN7302
Expired product administered Expired product administered
Vaccine administered past beyond use date of 5/13/25. Vaccine administered past beyond use date of 5/13/25.
2844219 66 M GA 06/06/2025 COVID19
 PFIZER\BIONTECH
 MD3414
Rash Rash
Pityriasis rosea-like rash on front and back torso, not painful or itchy. Started with small outbrea... Pityriasis rosea-like rash on front and back torso, not painful or itchy. Started with small outbreak and progressed to entire area as described. More
2844220 3 F AK 06/06/2025 DTAP
HEPA
MMR
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 9kb9g
j4k4x
y013131
Injection site erythema, Injection site induration, Injection site pain; Injecti... Injection site erythema, Injection site induration, Injection site pain; Injection site erythema, Injection site induration, Injection site pain; Injection site erythema, Injection site induration, Injection site pain More
Patients mom called to mention that the site of the injection was hard and red and that she was comp... Patients mom called to mention that the site of the injection was hard and red and that she was complaining of it hurting. She noticed it the Thursday after the vaccine and called Friday 6/6/25 to ask us about it. She drew a circle around it on Wednesday to see if it kept spreading and it did so she called. We informed her that it is a normal reaction, and to use tyelenol, ice it, to not let her touch the area and to watch her fever. If she were to spke a fever or it was to get worse over the weekend to go to urgent care as our clinic is not open on the weekend. More
2844221 9 F AZ 06/06/2025 COVID19
 PFIZER\BIONTECH
 LN7302
Expired product administered Expired product administered
Vaccine administered past beyond use date of 5/13/25. No known adverse event reported. Vaccine administered past beyond use date of 5/13/25. No known adverse event reported.
2844222 67 F OH 06/06/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Arthralgia, Dysstasia, Headache, Mobility decreased, Pain in extremity; Spinal p... Arthralgia, Dysstasia, Headache, Mobility decreased, Pain in extremity; Spinal pain More
Extreme pain in both hips, middle to lower back along spine, pain down both legs. Have never had it ... Extreme pain in both hips, middle to lower back along spine, pain down both legs. Have never had it this bad, not due to exercise or housework. On a pain scale, it was a 9 out of 10. Extreme difficulty moving, needed help getting out of chair. Also headaches started about the same time, 1 and a half to 2 days after shot. Took acetaminophen around the clock, and medical marijuana at evening. Neither helped to relieve the pain. It lasted a good 48 hours, finally felt some relief. Still sore but manageable. Different from arthritis and over worked joint pains I've had. Didn't see a physician. More
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