🏥 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 💀 🏥 🚑 ♿ ⚠️
2801016 U LA 10/22/2024 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
EL9262
Neuralgia; Chest pain, Pain in extremity Neuralgia; Chest pain, Pain in extremity
nerve pain; This is a spontaneous report received from a Consumer or other non HCP from medical info... nerve pain; This is a spontaneous report received from a Consumer or other non HCP from medical information team, Program ID:. A patient (age and gender not provided) received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), in 2024 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: NEURALGIA (non-serious) with onset 2024, outcome "not recovered", described as "nerve pain". Additional information: Patient had been having nerve pain since taking the COVID 19 vaccine. Patient was wondering if others have had the same problems, and what, if any, treatment had helped. The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received. More
2791539 63 F FL 09/18/2024 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
TDAP
TDAP
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 lm2215
lm2215
LM2215
LM2215
Lm2215
Lm2215
X357E
X357E
Flushing, Hyperhidrosis, Injection site erythema, Pustule, Rash; Pustule, Urtica... Flushing, Hyperhidrosis, Injection site erythema, Pustule, Rash; Pustule, Urticaria; Flushing, Hyperhidrosis, Injection site erythema, Pustule, Rash; Pustule, Urticaria; Pustule, Rash, Rash pustular, Scar, Skin discolouration; Urticaria; Pustule, Rash, Rash pustular, Scar, Skin discolouration; Urticaria More
Site: Redness at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Mild, Systemic: Flushed /... Site: Redness at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: patient had postules on her body, Other Vaccines: VaccineTypeBrand: boostrix; Manufacturer: glaxo smithkline; LotNumber: x357e; Route: intramuscular; BodySite: left arm; Dose: ; VaxDate: UNKNOWN More
2819366 29 F KY 01/03/2025 UNK
UNK
UNK
UNK
FLU3
FLU3
TDAP
TDAP
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
SANOFI PASTEUR
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS



TFAA2426
TFAA2426
3RE73
3RE73
Chills, Exposure during pregnancy, Headache, Pain, Pyrexia; Diarrhoea, Headache,... Chills, Exposure during pregnancy, Headache, Pain, Pyrexia; Diarrhoea, Headache, Pyrexia, Vision blurred, Vomiting; Chills, Exposure during pregnancy, Headache, Pain, Pyrexia; Diarrhoea, Headache, Pyrexia, Vision blurred, Vomiting; Chills, Exposure during pregnancy, Headache, Pain, Pyrexia; Diarrhoea, Headache, Pyrexia, Vision blurred, Vomiting; Chills, Exposure during pregnancy, Headache, Pain, Pyrexia; Diarrhoea, Headache, Pyrexia, Vision blurred, Vomiting More
I am currently 7 months pregnant. My estimate due date is 3-18-2025. My symptoms started about 12 ho... I am currently 7 months pregnant. My estimate due date is 3-18-2025. My symptoms started about 12 hours after receiving the flu vaccine and a Tdap booster. I?m unsure of the brands. I had a low grade fever, extreme aches and extreme chills, and severe headache. I initially took 1 500 mg Tylenol but the symptoms continued for 12 more hours. I took the next dose of Tylenol (1000 mg) and the symptoms subsided until it was time for the next dose of Tylenol I started getting a fever, chills and aches again. I took more 500 mg Tylenol and the symptoms subsided again after 1 hour. More
2819367 66 M TN 01/03/2025 PNC20
 PFIZER\WYETH
 lg5577
No adverse event No adverse event
No adverse events noted. No adverse events noted.
2819368 0.33 M KS 01/03/2025 DTAPHEPBIP
DTAPHEPBIP
IPV
IPV
UNK
UNK
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER





Behaviour disorder, Blood test, Febrile convulsion, Lethargy, Pyrexia; Speech di... Behaviour disorder, Blood test, Febrile convulsion, Lethargy, Pyrexia; Speech disorder developmental, Strabismus; Behaviour disorder, Blood test, Febrile convulsion, Lethargy, Pyrexia; Speech disorder developmental, Strabismus; Behaviour disorder, Blood test, Febrile convulsion, Lethargy, Pyrexia; Speech disorder developmental, Strabismus More
Extremely high fever, emergency room visit, lethargic movements on day of given vaccines. Later, ext... Extremely high fever, emergency room visit, lethargic movements on day of given vaccines. Later, extremely delayed speech, left eye crossed, febrile seizures, ADHD like behavior. More
✓
2818934 0.25 M 01/02/2025 DTAPHEPBIP
DTAPHEPBIP
DTAPHEPBIP
HIBV
HIBV
HIBV
MMR
MMR
MMR
PNC13
PNC13
PNC13
RV1
RV1
RV1
UNK
UNK
UNK
VARCEL
VARCEL
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; ... Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing; Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing; Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing; Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing; Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing; Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing; Chest X-ray normal, Cough, Croup infectious, Dyspnoea, Full blood count normal; Influenza, Influenza A virus test positive, Laryngitis, Nasal congestion, Pyrexia; Respiratory failure, Respiratory syncytial virus test negative, Vomiting, Wheezing More
Influenza A; This 20-month-old male subject was enrolled in a Study to Assess the Safety and Immunog... Influenza A; This 20-month-old male subject was enrolled in a Study to Assess the Safety and Immunogenicity of GSK Meningococcal Group B Vaccine and 13-valent Pneumococcal Vaccine when Administered Concomitantly with Routine Vaccines to Healthy Infants. The subject received the 4th dose of Bexsero vs Placebo (intramuscular) on 16-JUL-2019, for prophylaxis. The subject received the 4th dose of DTPa-HBV-IPV (intramuscular) on 16-JUL-2019, for prophylaxis. The subject received the 2nd dose of Rotarix lyophilized formulation (intramuscular) on 17-OCT-2018, for prophylaxis. The subject received the 3rd dose of Hiberix (intramuscular) on 21-DEC-2018, for prophylaxis. The subject received the 1st dose of M-M-R II (intramuscular) on 16-JUL-2019, for prophylaxis. The subject received the 1st dose of Varivax (intramuscular) on 16-JUL-2019, for prophylaxis. Co-suspect products included PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) for prophylaxis. Concomitant products included montelukast sodium (Singulair). On 07-MAR-2020, 235 days after receiving Bexsero vs Placebo, DTPa-HBV-IPV, M-M-R II and Varivax, 507 days after receiving Rotarix lyophilized formulation and 442 days after receiving Hiberix, the subject developed severe - grade 3 influenza a virus infection (Verbatim: Influenza A). Serious criteria included hospitalization. The subject was treated with cetirizine hydrochloride (Zyrtec), amoxicillin, salbutamol (Albuterol), prednisolone, oseltamivir phosphate (Tamiflu) and paracetamol (Tylenol). The outcome of influenza a virus infection was resolved on 20-MAR-2020. Relevant Tests: On 07-MAR-2020 RSV test performed result showed negative. On 11-MAR-2020 RSV test performed result showed negative. On 15-MAR-2020 Chest x-ray showed negative. On 15-MAR-2020 CBC showed negative. On 15-MAR-2020 Flu A showed Positive.. The investigator considered that there was no reasonable possibility that the influenza a virus infection may have been caused by Bexsero vs Placebo, DTPa-HBV-IPV, Rotarix lyophilized formulation, Hiberix, M-M-R II and Varivax. Other possible cause(s) of the influenza a virus infection included DTPa-HBV-IPV vaccine PRE-FILLED SYRINGE DEVICE and Rotavirus vaccine ORAL APPLICATOR DEVICE. The company considered that there was no reasonable possibility that the influenza a virus infection may have been caused by Bexsero vs Placebo, DTPa-HBV-IPV, Rotarix lyophilized formulation, Hiberix, M-M-R II and Varivax. Linked case(s) involving the same subject: US2019200424 GSK Receipt Date: 17-MAR-2020, 24-MAR-2020, 30-MAR-2020, 02-APR-2020, 08-APR-2020, 24-APR-2020, 27-APR-2020, 28-OCT-2020, 12-NOV-2020, 14-DEC-2020, 08-APR-2021, 22-APR-2021, 26-APR-2021, 04-MAY-2021. Subject admitted for Respiratory Failure. Mom stated the subject began having shortness of breath on 15Mar2020 at 9:00 a.m. She treated with Albuterol. subject did not improve so she took him to the hospital. The subject was admitted that night. subject was positive for Flu A. subject was discharged 19Mar2020. Prior to admission, the subject was seen by the Primary care physician on 07Mar2020 and diagnosed with acute obstructive laryngitis (croup) and cough. Also complained of fever, vomiting and difficulty breathing. subject was prescribed Prednisolone and Amoxicillin. subject was seen by Primary care physician on 11Mar2020 for cough, fever, nasal congestion, shortness of breath and wheezing. subject was continuing the Amoxicillin. The PI reviewed the medical record and determined that the SAE term should be Influenza A and not respiratory distress. The respiratory distress was caused by the Influenza A. Follow-up information received on 30-DEC-2024, 31-DEC-2024 Summary of changes: Dose, unit, frequency for medication Singulair, Zyrtec were updated, drug name for Albuterol 0.083 percent was updated and narrative updated.; Sender's Comments: A case of influenza, 235 days after receiving the 4th dose of Bexsero vs Placebo, the 4th dose of DTPa-HBV-IPV, 1st dose of M-M-R II and the 1st dose of Varivax, 442 days after receiving the 3rd dose of Hiberix and 507 days after receiving the 2nd dose of Rotarix lyophilized formulation , in a 20-month-old male subject. Report is inconsistent with causal relation to the vaccine product, considering implausible time to onset, absence of biological plausibility and alternative etiology (On 15-MAR-2020 Flu A showed Positive). US-GLAXOSMITHKLINE-US2019200424: More
✓
2818938 11 M PA 01/02/2025 HPV9
HPV9
HPV9
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.


Eye movement disorder, Immediate post-injection reaction, Injection site rash, M... Eye movement disorder, Immediate post-injection reaction, Injection site rash, Malaise, Pallor; Palpitations, Posture abnormal, Pyrexia, Rash, Unresponsive to stimuli; Vomiting More
My 11 year old son is NOT allergic to bakers yeast or latex received the gardesil vaccine and within... My 11 year old son is NOT allergic to bakers yeast or latex received the gardesil vaccine and within seconds his eyes rolled back he slumped in the chair he was unresponsive and started seizing. He developed an immediate rush from his injection site to his wrist, racing heart beat, pale white complexion and high temperature. His doctor pulled his sweatshirt off pant legs up put ice packs on him and gave him benadryl. An hour later he was ok enough to come home but was still not feeling great and threw up a lot. More
2818941 F AZ 01/02/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR

Bronchitis, Chills, Cough, Eye swelling, Ocular hyperaemia; Oropharyngeal pain, ... Bronchitis, Chills, Cough, Eye swelling, Ocular hyperaemia; Oropharyngeal pain, Pyrexia More
I received the Fluzone High-Dose Triv 2024-25 on Monday 12/09/2024 thru my Pharmacy. 24 hours later,... I received the Fluzone High-Dose Triv 2024-25 on Monday 12/09/2024 thru my Pharmacy. 24 hours later, I started to have chills, slight fever, coughing, and a sore throat. By Thurs, the 12th , my eyes were swollen and bloodshot and the coughing had gotten worse. By Monday, the 16th the cough had turned into bronchitis and the eyes were still red. I ended up having to going to my NP to seek treatment for my coughing and red eyes. I was given a Z pak and drops for my eyes all of which took care of the problem. I had gotten flu shots for years and never had this kind of reation to them. More
2818943 51 F 01/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Lymphadenopathy, Pain, Vaginal ulceration Lymphadenopathy, Pain, Vaginal ulceration
Had second dose shingles vaccination 12/13/24. On 12/23/24, began developing vaginal sores and swoll... Had second dose shingles vaccination 12/13/24. On 12/23/24, began developing vaginal sores and swollen lymph nodes in the groin area. Only occurred on left side of body. Sores remain today but are not as painful and seem to be healing. More
2818944 52 F 01/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 4H79Y
Gastrointestinal disorder Gastrointestinal disorder
Gastro intestinal issues after 2nd Shingles Vaccine. Shingrix. Gastro intestinal issues after 2nd Shingles Vaccine. Shingrix.
2818945 48 M IL 01/02/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 PAA165969
PAA165969
Arthralgia, Back pain, Blood creatine increased, Dry eye, Fatigue; Hypertension,... Arthralgia, Back pain, Blood creatine increased, Dry eye, Fatigue; Hypertension, Inflammation, Red blood cell sedimentation rate, Urine analysis More
Fatigue Creatine Protein High Inflammation Sed Rate Inflammation High Blood Messure Joint pain / Ba... Fatigue Creatine Protein High Inflammation Sed Rate Inflammation High Blood Messure Joint pain / Back Pain Dry Eyes Sar Total Spike More
2818946 72 F IL 01/02/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EM9810
EM9810
EM9810
Back pain, Bronchitis chronic, C-reactive protein increased, Dry eye, Fatigue; F... Back pain, Bronchitis chronic, C-reactive protein increased, Dry eye, Fatigue; Fibrin D dimer increased, Haemoglobin decreased, Hypertension, Inflammation, Red blood cell sedimentation rate abnormal; Urinary tract infection, Urine analysis More
Chronic Bronchitis Fatigue UTI's D- Dimer Elevated Joint Pain ... Chronic Bronchitis Fatigue UTI's D- Dimer Elevated Joint Pain C Reactive Protein High Dry Eyes Hemoglobin Low Back Pain Inflamation Sed-Rate Inflamation High Blood pressure More
2818993 1 M DC 01/02/2025 FLU3
MMR
PNC20
VARCEL
 SANOFI PASTEUR
MERCK & CO. INC.
PFIZER\WYETH
MERCK & CO. INC.



Product lot number issue; Product lot number issue; Product lot number issue; Pr... Product lot number issue; Product lot number issue; Product lot number issue; Product lot number issue More
Pt was due for HIB and PCV at time of visit. HIB lot number was documented under PCV20 order. Unable... Pt was due for HIB and PCV at time of visit. HIB lot number was documented under PCV20 order. Unable to determine if pt received either or both vaccines at visit. More
2818994 56 M FL 01/02/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 58160-0823-11
58160-0823-11
Burning sensation, Chills, Headache, Injection site erythema, Injection site pai... Burning sensation, Chills, Headache, Injection site erythema, Injection site pain; Neuralgia, Pain, Pruritus, Pyrexia More
First 24 hours: fever, chills, headache, body ache; injection site pain/redness. Next five days/ongo... First 24 hours: fever, chills, headache, body ache; injection site pain/redness. Next five days/ongoing: nerve pain/itching/burning over all of body; injection site pain/redness. More
2818995 70 M FL 01/02/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
patient received second dose of vaccine patient received second dose of vaccine
2818996 4 F OH 01/02/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 U8009AB
Injection site erythema, Irritability, Pyrexia, Urticaria Injection site erythema, Irritability, Pyrexia, Urticaria
Vaccine given 12/23. Fussy and fever to 101 F within 48 hours. Hives around injection site started... Vaccine given 12/23. Fussy and fever to 101 F within 48 hours. Hives around injection site started 12/28. Mom giving oral benadryl and topical hydrocortisone cream 1% several times a day but the hives have been recurrent. More
2818997 11 M 01/02/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 ES49H
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
The resident under the supervison of an attending staff provider ordered the Men B vaccine in error ... The resident under the supervison of an attending staff provider ordered the Men B vaccine in error and the MA who administered this vaccine is newer and did not catch the error before administration. More
2818998 70 F FL 01/02/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
patient received second dose of rsv patient received second dose of rsv
2818999 78 F LA 01/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Urticaria Urticaria
hives hives
2819000 0.25 F TX 01/02/2025 UNK
 UNKNOWN MANUFACTURER
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Vaccine error, given to a 3 month old Vaccine error, given to a 3 month old
2819001 4 M IN 01/02/2025 DTAPIPV
MMRV
 SANOFI PASTEUR
MERCK & CO. INC.
 U8209CB
Y014438
Induration, Necrosis; Induration, Necrosis Induration, Necrosis; Induration, Necrosis
Timeframe within the first 24 hours with severe pain and induration without necrosis. This is consi... Timeframe within the first 24 hours with severe pain and induration without necrosis. This is consistent with an Arthus reaction. The primary intervention to be made is to defer subsequent Tetanus-Diphtheria vaccinations for 10 years in order to limit likelihood of recurrence. More
2819002 25 F MS 01/02/2025 COVID19
HPV9
 PFIZER\BIONTECH
MERCK & CO. INC.

Ageusia, Dry eye, Hypoaesthesia oral; Ageusia, Dry eye, Hypoaesthesia oral Ageusia, Dry eye, Hypoaesthesia oral; Ageusia, Dry eye, Hypoaesthesia oral
Dry eyes, no taste, numb lips and tongue. Mouth seems to have a slight droop delay when puckering up... Dry eyes, no taste, numb lips and tongue. Mouth seems to have a slight droop delay when puckering up. No treatment at the moment but appointment has been scheduled for further testing. More
2819003 55 F GA 01/02/2025 COVID19
 MODERNA
 B0001
COVID-19, Pain in extremity, SARS-CoV-2 test COVID-19, Pain in extremity, SARS-CoV-2 test
I had no adverse reactions to the injection other than a sore arm for a day or two. However, I beca... I had no adverse reactions to the injection other than a sore arm for a day or two. However, I became ill with COVID on 12/29/2024 which was within 2 months of vaccination. More
2819004 88 F FL 01/02/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient had no reaction, it was a duplicate therapy. Patient received the arexvy vaccine on 12/22/20... Patient had no reaction, it was a duplicate therapy. Patient received the arexvy vaccine on 12/22/2023 and received another arexvy vaccine on 12/31/2024. Patient's state shot records did not have the vaccine reported on 12/22/2023. More
2819005 72 M CO 01/02/2025 FLU3
 SANOFI PASTEUR
 U8519EA
Extra dose administered, No adverse event, Wrong product administered Extra dose administered, No adverse event, Wrong product administered
Pt given high-dose flu instead of intended covid vaccine. No adverse reaction. Had already been give... Pt given high-dose flu instead of intended covid vaccine. No adverse reaction. Had already been given annual flu shot on 11/29/24. More
2819006 60 F CT 01/02/2025 FLU3
FLU3
RSV
RSV
 SEQIRUS, INC.
SEQIRUS, INC.
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 388532
388532
D7953
D7953
Blood test, Dizziness, Headache, Malaise, Rash; Sneezing, Urticaria; Blood test,... Blood test, Dizziness, Headache, Malaise, Rash; Sneezing, Urticaria; Blood test, Dizziness, Headache, Malaise, Rash; Sneezing, Urticaria More
COULDNT STOP SNEEZING, WELTS AND RASHES, FEELING SICK, DIZZINESS,TERRIBLE HEADACHES, ALL THE TIME COULDNT STOP SNEEZING, WELTS AND RASHES, FEELING SICK, DIZZINESS,TERRIBLE HEADACHES, ALL THE TIME
2819007 1.08 F WI 01/02/2025 COVID19
 PFIZER\BIONTECH
 4S5YG
Product preparation issue Product preparation issue
Patient was given 0.3mLs of the UNDILUTED Covid -19 6m-<5yr vaccine in their left vastus laterali... Patient was given 0.3mLs of the UNDILUTED Covid -19 6m-<5yr vaccine in their left vastus lateralis. More
2819008 64 M ID 01/02/2025 VARCEL
 MERCK & CO. INC.
 Merk & Co
Inappropriate schedule of product administration Inappropriate schedule of product administration
Patient received Varicella Vaccination 6 days after receiving MMR vaccine. Patient received Varicella Vaccination 6 days after receiving MMR vaccine.
2819009 92 F KY 01/02/2025 COVID19
 PFIZER\BIONTECH
 LM2224
Death Death
Resident expired Resident expired
✓
2819010 26 F PA 01/02/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 K9XL5
Arthralgia, Joint range of motion decreased Arthralgia, Joint range of motion decreased
Shoulder pain, decreased range of motion, needing PT treatments Shoulder pain, decreased range of motion, needing PT treatments
2819011 84 F AL 01/02/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
Patient received a duplicate Arexvy shot. Last dose was given 12/13/23 at our location but our syst... Patient received a duplicate Arexvy shot. Last dose was given 12/13/23 at our location but our system did not stop this duplicate fill. I called and spoke with the patient and she was not aware she had the shot back in 2023. She was very understanding. More
2819012 94 F IA 01/02/2025 COVID19
 MODERNA
 3043332
Death Death
Death Death
✓
2819013 43 M IL 01/02/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 COVID 19 COMIRN
flu/sh
Catheterisation cardiac, Chest pain, Dyspnoea, Electrocardiogram abnormal, Myoca... Catheterisation cardiac, Chest pain, Dyspnoea, Electrocardiogram abnormal, Myocardial infarction; Catheterisation cardiac, Chest pain, Dyspnoea, Electrocardiogram abnormal, Myocardial infarction More
Once I can home from my vaccination on 12/19/24 about an hour later my chest started to hurt. I was ... Once I can home from my vaccination on 12/19/24 about an hour later my chest started to hurt. I was getting shortage of breath and chest pain. More
✓ ✓
2819014 76 M NH 01/02/2025 COVID19
COVID19
 MODERNA
MODERNA

Agraphia, Amnesia, Aphasia, Balance disorder, Blood test; Dysgraphia, Magnetic r... Agraphia, Amnesia, Aphasia, Balance disorder, Blood test; Dysgraphia, Magnetic resonance imaging, Reading disorder More
Could no longer spell, read, use computer, difficulty writing, remembering, loss of ability to put t... Could no longer spell, read, use computer, difficulty writing, remembering, loss of ability to put thoughts into words, balance issues. More
✓
2819016 73 M MD 01/02/2025 UNK
 UNKNOWN MANUFACTURER
Blood test, Inflammation, Mobility decreased, Pain, X-ray Blood test, Inflammation, Mobility decreased, Pain, X-ray
pt says a couple of days after the flu vaccine he was stepping of a boat onto a dock and he felt a t... pt says a couple of days after the flu vaccine he was stepping of a boat onto a dock and he felt a twinge in his hip area that went down both sides of his legs but stopped before reaching his knees. It began to progress after the next few days moving up his body towards his torso and both arms, wrist, hands and neck. He was tolerating it dealing with other family matters. He contacted his physician and he was prescribed methopredisone. This medicine helped with the pain from the inflammation he was having from the vaccine. A couple of days after the medicine was out of his system he was back to where he could barely move. His doctor prescribed more steroids. He scheduled an appt with a Rheumotologist Dr. on 11/25/24. He had labs and xrays. He has not received his evaluations from the results on his test until he has a follow up appt. He is not any better at this time. More
2819017 0.25 F TX 01/02/2025 IPV
 SANOFI PASTEUR
 X1D141M
Pallor, Vomiting Pallor, Vomiting
No events occured in clinic. Parents called clinic to report that baby had turned pale and vomited ... No events occured in clinic. Parents called clinic to report that baby had turned pale and vomited x1 approximately 0930 the morning of the vaccine. Infant was at home. No respiratory distress reported. Approximately 1 hour after administration of vaccine. Advised to bring infant in to assess. Infant brought back to clinic at approximately 1040 am on 1/2/25. Exam was WNL, respirations were noted to be even and unlabored at time of exam. Injection site without redness or swelling. VS Stable. More
2819018 2 F MO 01/02/2025 COVID19
 PFIZER\BIONTECH
 LN6739
No adverse event, Product preparation issue No adverse event, Product preparation issue
After administering the vaccine, I realized it had not yet been diluted with saline as we are suppos... After administering the vaccine, I realized it had not yet been diluted with saline as we are supposed to for the 6mo-4yr vial. The mother of the patient was contacted, the physician was notified, and a hospital report was made. No adverse reaction from the patient at this time. More
2819019 1.75 F VI 01/02/2025 HIBV
 SANOFI PASTEUR
 UK008AA
Expired product administered Expired product administered
Gave an expired vaccine. Exp. date 12/31/2024 Gave an expired vaccine. Exp. date 12/31/2024
2819020 18 F MI 01/02/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 yy37b
Incorrect dose administered Incorrect dose administered
Patient is under the age 19 and should have been given the pediatric dose vaccine but was given the ... Patient is under the age 19 and should have been given the pediatric dose vaccine but was given the adult dose More
2819021 35 F MN 01/02/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 EL3246
EL9262
Cough, Oropharyngeal pain, Respiratory tract congestion, SARS-CoV-2 test; Cough,... Cough, Oropharyngeal pain, Respiratory tract congestion, SARS-CoV-2 test; Cough, Oropharyngeal pain, Respiratory tract congestion, SARS-CoV-2 test More
Cough x1 month, congestion, sore throat Cough x1 month, congestion, sore throat
2819022 12 F 01/02/2025 MNP
 PFIZER\WYETH
 LJ0077
Unevaluable event Unevaluable event
None None
2819023 1.25 M MI 01/02/2025 DTAP
FLU3
HEPA
 SANOFI PASTEUR
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 3CA25C1
U8518BA
YA11643
Inappropriate schedule of product administration, No adverse event; Inappropriat... Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event More
Patient was mistakenly given Hepatitis A vaccine before it was due. No adverse affects for patient. Patient was mistakenly given Hepatitis A vaccine before it was due. No adverse affects for patient.
2819024 11 F 01/02/2025 MNP
 PFIZER\WYETH
 LJ0077
Unevaluable event Unevaluable event
None None
2819025 76 F MA 01/02/2025 RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 49H4G
49H4G
Catheterisation cardiac normal, Chest X-ray, Dyspnoea, Echocardiogram normal, El... Catheterisation cardiac normal, Chest X-ray, Dyspnoea, Echocardiogram normal, Electrocardiogram; Exercise tolerance decreased, Feeling abnormal, Myocardial necrosis marker More
Shortness of breath resulting in being unable to exercise ( 2x weekly one mile swimmer) could not co... Shortness of breath resulting in being unable to exercise ( 2x weekly one mile swimmer) could not complete 5 laps! Also walking any distance, normal housework ?all an extreme effort. Just did not feel ?right? or like myself. Went to urgent care on November 8th, sent to ER. After a whole day of EKG, chest x-ray, bloodwork to check heart enzymes, I was released and told to go to a cardiologist within 72 hours. More
2819026 10 F IA 01/02/2025 UNK
 UNKNOWN MANUFACTURER
No adverse event No adverse event
There was no adverse event There was no adverse event
2819027 12 M 01/02/2025 MNP
 PFIZER\WYETH
 LJ0077
Unevaluable event Unevaluable event
none none
2819028 11 F 01/02/2025 MNP
 PFIZER\WYETH
 LJ0077
Unevaluable event Unevaluable event
None None
2819029 43 F NJ 01/02/2025 TDAP
 SANOFI PASTEUR
Erythema, Inflammation, Pain in extremity, Peripheral swelling, Pyrexia Erythema, Inflammation, Pain in extremity, Peripheral swelling, Pyrexia
On the day following the injection, my left hand became red, swollen, and painful, accompanied by a ... On the day following the injection, my left hand became red, swollen, and painful, accompanied by a fever. By the third day, the entire left hand was painful, with a deep red, circular swelling and a yellowish center, along with persistent fever. I took ibuprofen and Tylenol to manage the pain and inflammation. After consulting my physician, I was advised to monitor the symptoms for two more days, continue the pain medication, and consider antibiotics if necessary. More
2819030 1.17 M VT 01/02/2025 HEPA
HIBV
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 5JA57
UK025AA
No adverse event, Product preparation issue; No adverse event, Product preparati... No adverse event, Product preparation issue; No adverse event, Product preparation issue More
The child may have only received diluent instead of HIB reconstituted with diluent. There were three... The child may have only received diluent instead of HIB reconstituted with diluent. There were three patients of which may have been affected. Two received appropriately prepared HIB vaccines and one received diluent. It is unclear which patient of the three received only diluent. No adverse reactions have occurred since the time of administration. The dose is planned to be repeated during the child's 18 month visit to ensure proper vaccination, and the child will be monitored for any reactions at that time. Parents have been notified and expressed understanding of the situation and have no further concerns. More
2819031 15 M 01/02/2025 MNP
 PFIZER\WYETH
 LJ0077
Unevaluable event Unevaluable event
none none
📋 Privacy Policy & Data Disclaimer