🏥 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 💀 🏥 🚑 ♿ ⚠️
2823409 1 M PA 01/28/2025 MMRV
 MERCK & CO. INC.
 Y010247
Rash, Rash vesicular, Varicella virus test positive Rash, Rash vesicular, Varicella virus test positive
Vesicular rash from R pubic/groin down R lateral thigh to knee Vesicular rash from R pubic/groin down R lateral thigh to knee
2822894 1.25 U PA 01/27/2025 MMR
 MERCK & CO. INC.
 Y010046
No adverse event, Syringe issue No adverse event, Syringe issue
caller unsure if patient received full amount of dose as some of the diluent leaked out due to the s... caller unsure if patient received full amount of dose as some of the diluent leaked out due to the suction; syringe experienced suction when twisting the needle onto the hub of syringe causing cap; caller unsure if patient received full amount of dose as some of the diluent leaked out due to the suction; device fluid leak; no adverse event; This spontaneous report was received from registered nurse and refers to a 15-month-old. patient of unknown gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On an unknown date, the patient started therapy with measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live (M-M-R II) injection, lot #Y010046, expiration date: 29-MAY-2026, administered for prophylaxis (strength, and route of administration were not provided), status albumin- rHA; and sterile diluent (BAXTER STERILE DILUENT) solution for injection/infusion, lot #1973242, expiration date: 17-FEB-2026 (strength, route of administration, and indication were not provided). On an unknown date, the sterile diluent syringe experienced suction when twisting the needle onto the hub of syringe causing cap of syringe to pop off. The nurse reported that a dose of M-M-R-II was administered to a patient that was reconstituted using the defective sterile diluent syringe and caller unsure if patient received full amount of dose as some of the diluent leaked out due to the suction. No adverse events reported. More
2822895 U 01/27/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Malaise Malaise
I got sick; This non-serious case was reported by a consumer via interactive digital media and descr... I got sick; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of sickness in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced sickness (Verbatim: I got sick). The outcome of the sickness was not reported. It was unknown if the reporter considered the sickness to be related to Shingles vaccine. It was unknown if the company considered the sickness to be related to Shingles vaccine. Additional Information: GSK Receipt Date: 07-JAN-2025 This case was reported by a patient via interactive digital media. The patient got sick after his/her shingles shot but it was nothing compared to getting actual shingles. More
2822896 U 01/27/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
Suspected vaccination failure; the vaccination didn't stop it for me; This serious case was rep... Suspected vaccination failure; the vaccination didn't stop it for me; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: the vaccination didn't stop it for me). The outcome of the vaccination failure and shingles were not reported. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine. The company considered the vaccination failure and shingles to be unrelated to Shingles vaccine. Additional Information: GSK Receipt Date: 13-JAN-2025 This case was reported by a patient via interactive digital media. The patient reported that the vaccination did not stop it for him/her. This case was considered as suspected vaccination failure as details regarding completion of primary vaccination schedule, time to onset for shingles and laboratory confirmation regarding shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding the completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK Shingles vaccine. Herpes zoster is an unlisted event which is considered unrelated to GSK Shingles vaccine. More
2822897 M VA 01/27/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Incomplete course of vaccination Incomplete course of vaccination
received first dose of shingles vaccine January 18th 2024; This non-serious case was reported by a c... received first dose of shingles vaccine January 18th 2024; This non-serious case was reported by a consumer via call center representative and described the occurrence of incomplete course of vaccination in a 55-year-old male patient who received Herpes zoster (Shingles vaccine) for prophylaxis. Previously administered products included Shingles vaccine (Patient received first dose on 18-JAN-2024). On an unknown date, the patient did not receive the 2nd dose of Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced incomplete course of vaccination (Verbatim: received first dose of shingles vaccine January 18th 2024). The outcome of the incomplete course of vaccination was unknown. Additional Information: GSK Receipt Date: 03-JAN-2025 Patient received first dose of shingles vaccine brand, lot number and expiration date was unknown on January 18th 2024 and he forgot to get the second dose 6 months later. Till the time of reporting the patient did not receive second dose of Shingles vaccine which led to incomplete course of vaccination. More
2822898 F CO 01/27/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incomplete course of vaccination Incomplete course of vaccination
Inappropriate schedule of vaccine; This non-serious case was reported by a pharmacist via call cente... Inappropriate schedule of vaccine; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of incomplete course of vaccination in a adult female patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (first dose of Shingrix about 2.5 years ago). On an unknown date, the patient did not receive the 2nd dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced incomplete course of vaccination (Verbatim: Inappropriate schedule of vaccine). The outcome of the incomplete course of vaccination was unknown. Additional Information: GSK Receipt Date: 06-JAN-2025 Till the time of reporting the patient had not received the second dose of Shingrix, which led to incomplete course of vaccination. The reporter asked what were the recommendations as to if she should receive her second dose since it's way outside of the 2 to 6 month window. The reporter consented to follow up. More
2822899 F PA 01/27/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 2345B
Incorrect dose administered Incorrect dose administered
0.5mL of an adult Havrix dose to a 16 year old female patient; This non-serious case was reported by... 0.5mL of an adult Havrix dose to a 16 year old female patient; This non-serious case was reported by a other health professional via call center representative and described the occurrence of adult product administered to child in a 16-year-old female patient who received HAV (Havrix adult) (batch number 2345B, expiry date 02-FEB-2026) for prophylaxis. On 02-DEC-2024, the patient received the 2nd dose of Havrix adult. On 02-DEC-2024, an unknown time after receiving Havrix adult, the patient experienced adult product administered to child (Verbatim: 0.5mL of an adult Havrix dose to a 16 year old female patient). The outcome of the adult product administered to child was unknown. Additional Information: GSK receipt date: 08-JAN-2025 The physician reported that 0.5mL of an adult Havrix dose to a 16 year old female patient because they did not stock the pediatric formulation in the office, which led to adult product administered to child. More
2822900 U NM 01/27/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incomplete course of vaccination Incomplete course of vaccination
no second dose was administered; This non-serious case was reported by a pharmacist via call center ... no second dose was administered; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of incomplete course of vaccination in a patient who received HAB (Twinrix) for prophylaxis. Previously administered products included Twinrix (received 1st dose of Twinrix vaccine on March 2024). On an unknown date, the patient did not receive Twinrix. On an unknown date, an unknown time after receiving Twinrix, the patient experienced incomplete course of vaccination (Verbatim: no second dose was administered). The outcome of the incomplete course of vaccination was unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 10-JAN-2025 The Healthcare professional reported on the day of reporting, 10th January 2025 that a patient received the first dose of Twinrix on March 2024 and had not received the second dose. The reporter was called to made clinical decision, no second dose was administered at the moment of the call yet. Till the time of reporting, the patient did not receive 2nd dose of Twinrix, which led to incomplete course of vaccination. More
2822908 27 M CA 01/27/2025 ANTH
 EMERGENT BIOSOLUTIONS
Injection site erythema, Injection site induration, Injection site swelling Injection site erythema, Injection site induration, Injection site swelling
Large local reaction at injection site, characterized by firm swelling >6 cm and mild erythema, n... Large local reaction at injection site, characterized by firm swelling >6 cm and mild erythema, no pain. Resolved with conservative care over 3 days. Refer to DHA IHD More
2822915 U MI 01/27/2025 HIBV
 GLAXOSMITHKLINE BIOLOGICALS
Expired product administered Expired product administered
expired dose administered; This non-serious case was reported by a other health professional via cal... expired dose administered; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a patient who received Hib (Hiberix) (expiry date 14-DEC-2024) for prophylaxis. On 16-DEC-2024, the patient received Hiberix. On 16-DEC-2024, an unknown time after receiving Hiberix, the patient experienced expired vaccine used (Verbatim: expired dose administered). The outcome of the expired vaccine used was unknown. Additional Information: GSK receipt date: 09-JAN-2025 The reporter reported that the patient was administered Hiberix two days after expiration date which led to, expired vaccine used. The health care professional did not had patient details or lot number of the suspect. More
2822918 72 M MA 01/27/2025 FLU3
RSV
 SEQIRUS, INC.
PFIZER\WYETH
 388493
KD0161
Mobility decreased, Pain; Mobility decreased, Pain Mobility decreased, Pain; Mobility decreased, Pain
Patient came to pharmacy on 1/24/25 complaining that from the day after he received the RSV (abrysvo... Patient came to pharmacy on 1/24/25 complaining that from the day after he received the RSV (abrysvo) vacine he has experienced pain and has not been able to raise his arm above shoulder height. Patient will be visiting primary MD in the coming weeks. Patient states that the pain has not resolved. More
2822971 80 M IA 01/27/2025 COVID19
 MODERNA
 3043159
Death Death
Death Death
✓
2822972 12 F IN 01/27/2025 PNC13
 PFIZER\WYETH
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Swollen, red and painful shoulder at sight of injection Swollen, red and painful shoulder at sight of injection
2822973 11 F MI 01/27/2025 FLU4
FLU4
 SANOFI PASTEUR
SANOFI PASTEUR
 ut8408ja
ut8408ja
Blood glucose decreased, Chills, Dizziness, Fatigue, Flushing; Hyperhidrosis, Le... Blood glucose decreased, Chills, Dizziness, Fatigue, Flushing; Hyperhidrosis, Lethargy More
Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mil... Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: patient was 11 years upon questioning her she indicated that she did not have breakfast or anything to eat prior to receiving the flu shot , ems arrived and upon taking the patient glucose level it was trending low 68 , patient was instructed by ems to have some orange juice and some crackers patient received some at the pharmacy and was feeling better after, Other Vaccines: VaccineTypeBrand: Fluzone; Manufacturer: sanofi; LotNumber: ut8408ja; Route: im; BodySite: left deltoid; Dose: ; VaxDate: UNKNOWN More
2822974 71 M IN 01/27/2025 RSV
 PFIZER\WYETH
 hn8090
Hypoaesthesia, Paraesthesia, Walking aid user Hypoaesthesia, Paraesthesia, Walking aid user
Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial a... Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Additional Details: pt spent time in hospital numb & tingly in both legs and feet-worse in right leg. using a walker now but hoping to recover More
✓
2822975 36 F FL 01/27/2025 HPV9
 MERCK & CO. INC.
 y007197
Loss of consciousness, Nausea, Syncope, Unresponsive to stimuli Loss of consciousness, Nausea, Syncope, Unresponsive to stimuli
Systemic: Fainting / Unresponsive-Mild, Systemic: pt fainted about 3 minutes after shot and recovere... Systemic: Fainting / Unresponsive-Mild, Systemic: pt fainted about 3 minutes after shot and recovered quickly with water and fan air-Mild, Systemic: Nausea-Mild, Additional Details: Patient past out after being administered 2 vaccines shingles and Gardasil in the same arm left deltoid, by tech. After administration she was packing up and fainted. We help her up and she recovered quickly, and asked what happened and she felt like vomitting. We provided her with water and a fan to cool due to wet clothing. I asked if she could be pregnant she stated no. She laid on the floor for a 10minutes, then left and I called and about 2 hours after and she states she is ok., Other Vaccines: VaccineTypeBrand: shingrix; Manufacturer: gsk; LotNumber: 4h79y; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 01/18/2025 More
2822976 85 F CT 01/27/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 LN4P2
Atrial fibrillation, Tachycardia Atrial fibrillation, Tachycardia
Systemic: Patient experienced atrial fibrillation-Medium, Systemic: Tachycardia-Medium, Additional D... Systemic: Patient experienced atrial fibrillation-Medium, Systemic: Tachycardia-Medium, Additional Details: Patient called to report that she experienced AFib and tachycardia (110 bpm at rest) and wanted to know if it was associated with the RSV vaccine she received 1 day prior. The event was resolved by the patient when she took an extra dose of metoprolol and diazepam. She contacted the pharmacy after the event. The pharmacist recommended that she follows-up with her cardiologist (who she has an appointment with next month) on the next business day. More
2822977 56 F NM 01/27/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 74nc9
Cellulitis, Injection site erythema, Injection site pain Cellulitis, Injection site erythema, Injection site pain
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Additional Details: Pat... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Additional Details: Patient stated she works in the ER department and physician there said she got cellulitis from vaccine. Injections was given vaccine intramuscularly. I explained to her its common to develop rash and redness at injection site with shingrix vaccine. It looked like a normal reaction to vaccine site. Patient was not seeking compensation just thought we should be aware of situation., Other Vaccines: VaccineTypeBrand: prevnar 20; Manufacturer: wyeth/pfizer; LotNumber: lp8151; Route: intramuscular; BodySite: left arm; Dose: ; VaxDate: UNKNOWN More
2822978 69 F TX 01/27/2025 RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 x4ea5
x4ea5
Injection site bruising, Injection site erythema, Injection site induration, Inj... Injection site bruising, Injection site erythema, Injection site induration, Injection site inflammation, Injection site pain; Injection site pruritus, Injection site scab, Injection site swelling More
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injec... Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: patient presented on 01/19/2025 with wound that was scabbed over. patient stated that it progressed from red inflamed bruised knot to open sore to scabbed over, Other Vaccines: VaccineTypeBrand: singrix; Manufacturer: glaxo; LotNumber: kb2yt; Route: im; BodySite: left deltoid; Dose: ; VaxDate: UNKNOWN More
2822979 55 F NJ 01/27/2025 FLUC4
FLUC4
 SEQIRUS, INC.
SEQIRUS, INC.
 946635
946635
Dermatitis allergic, Injection site erythema, Injection site pruritus, Injection... Dermatitis allergic, Injection site erythema, Injection site pruritus, Injection site swelling, Pruritus; Rash More
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at In... Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash Generalized-Mild, Other Vaccines: VaccineTypeBrand: Flucelvax; Manufacturer: sequiris; LotNumber: 946635; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 01/11/2025, VaccineTypeBrand: Pfizer Covid 19 2024-2025; Manufacturer: pfizer; LotNumber: lp1780; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 01/11/2025 More
2822980 81 F FL 01/27/2025 FLU4
 SANOFI PASTEUR
 u8532ca
Injection site bruising, Injection site pain, Injection site swelling Injection site bruising, Injection site pain, Injection site swelling
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Inje... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2822981 37 F AZ 01/27/2025 HPV9
HPV9
 MERCK & CO. INC.
MERCK & CO. INC.
 y013712
y013712
Asthenia, Fatigue, Injection site erythema, Injection site pain, Injection site ... Asthenia, Fatigue, Injection site erythema, Injection site pain, Injection site pruritus; Injection site swelling, Lethargy More
Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection ... Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Mild, Systemic: Exhaustion / Lethargy-Severe, Systemic: Weakness-Severe More
2822982 45 F FL 01/27/2025 COVID19-2
 PFIZER\BIONTECH
 lp1780
Lymphadenopathy Lymphadenopathy
Systemic: Lymph Node Swelling-Mild Systemic: Lymph Node Swelling-Mild
2822983 64 F CA 01/27/2025 COVID19
 MODERNA
 0000
Dizziness, Fatigue, Lethargy Dizziness, Fatigue, Lethargy
Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium
2822984 61 F MD 01/27/2025 COVID19
 PFIZER\BIONTECH
 0000
Chills, Pain, Pyrexia Chills, Pain, Pyrexia
Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Fever-Medium Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Fever-Medium
2822985 70 M MI 01/27/2025 COVID19
 MODERNA
 0000
Rash Rash
Systemic: Allergic: Rash Generalized-Medium Systemic: Allergic: Rash Generalized-Medium
2822986 64 F VA 01/27/2025 PNC20
 PFIZER\WYETH
 LP8151
Injection site pain Injection site pain
Site: Pain at Injection Site-Mild Site: Pain at Injection Site-Mild
2822987 36 M IL 01/27/2025 COVID19
 MODERNA
 7654321
Myocardial infarction Myocardial infarction
Systemic: Not Covid, vaccine unknown. Per patent's Cardiologist, he cannot take any vaccines d... Systemic: Not Covid, vaccine unknown. Per patent's Cardiologist, he cannot take any vaccines due to heart complications from previous vaccines.-Severe, Systemic: Heart Attack-Severe More
2822988 75 M MN 01/27/2025 PNC21
 MERCK & CO. INC.
 Y013009
Asthenia, Injection site erythema, Nausea Asthenia, Injection site erythema, Nausea
Site: Redness at Injection Site-Medium, Systemic: weakness and nausea-Medium, Systemic: Nausea-Mediu... Site: Redness at Injection Site-Medium, Systemic: weakness and nausea-Medium, Systemic: Nausea-Medium, Systemic: Weakness-Medium, Additional Details: Patient received Arexy and Capvaxive in the left deltoid on 1/18/25 at 3:49pm. Patient denies ever having soreness, tenderness or pain. Sunday night, 1/19/25, patient says he began to feel weakness and nausea, of which worsened by Monday, 1/20/25. Went to the doctor on Tuesday, 1/21/25, and diagnosed with redness of the arm and potential cellulitis. Being treated with cephalexin for 5 days starting afternoon of 1/21/25., Other Vaccines: VaccineTypeBrand: Arexvy; Manufacturer: GSK; LotNumber: 4BN95; Route: IM; BodySite: left arm; Dose: 1; VaxDate: 01/18/2025 More
2822989 37 M NY 01/27/2025 FLUC4
 SEQIRUS, INC.
 946636
Injection site bruising, Injection site pain, Injection site swelling Injection site bruising, Injection site pain, Injection site swelling
Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Swelling at Inje... Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe More
2822991 80 F PA 01/27/2025 COVID19
 MODERNA
 10232024
Fatigue, Lethargy, Pain, Pyrexia Fatigue, Lethargy, Pain, Pyrexia
Systemic: Body Aches Generalized-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fever-Mil... Systemic: Body Aches Generalized-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fever-Mild More
2822992 76 F TX 01/27/2025 COVID19
COVID19
 MODERNA
MODERNA
 3043823
3043823
Back pain, Blood pressure increased, Dizziness, Dyspnoea, Hyperventilation; Musc... Back pain, Blood pressure increased, Dizziness, Dyspnoea, Hyperventilation; Muscle spasms, Muscle tightness, Pain More
Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Body Aches Generalized-Severe, Systemic: ... Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Patient had muscle spasms ans tightness below the waist, lower back pain, elevated blood pressure-Severe, Systemic: Hyperventilation-Medium, Additional Details: Muscle Spasms below the waist, back pain, elevated blood pressure, breathing heavy, light headed, Other Vaccines: VaccineTypeBrand: moderna; Manufacturer: moderna; LotNumber: 3043823; Route: Intramuscular; BodySite: Left Deltoid; Dose: 4; VaxDate: 01/22/2025 More
2822993 67 F PA 01/27/2025 COVID19
 PFIZER\BIONTECH
 LM7786
Pruritus Pruritus
Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Genera... Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Additional Details: Pt has received initial vaccines and all booster doses (all pfizer) and reported ongoing full body itchiness since administration date of latest vaccine (10/18/24). has seen PCP and dermatologist, has tried topical creams and oral medications to stop itching with no improvement More
2822994 19 M CA 01/27/2025 FLUC4
 SEQIRUS, INC.
 946619
Dizziness, Pallor, Pyrexia Dizziness, Pallor, Pyrexia
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fever-Mild, Additional Details: Patient experi... Systemic: Dizziness / Lightheadness-Medium, Systemic: Fever-Mild, Additional Details: Patient experienced dizziness, fever, and his skin turned pale. He sat more than 15 minutes until he felt better and left. He did not want to call 911. More
2822995 66 F MI 01/27/2025 COVID19
COVID19
 MODERNA
MODERNA
 0000
0000
Asthenia, Fatigue, Headache, Lethargy, Pain; Pyrexia Asthenia, Fatigue, Headache, Lethargy, Pain; Pyrexia
Systemic: Body Aches Generalized-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Med... Systemic: Body Aches Generalized-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Headache-Medium, Systemic: Weakness-Medium More
2822996 54 F FL 01/27/2025 COVID19
 PFIZER\BIONTECH
 0000
Chills, Fatigue, Lethargy Chills, Fatigue, Lethargy
Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium
2822997 61 M CA 01/27/2025 COVID19
COVID19
 MODERNA
MODERNA
 022J21A
022J21A
Angina pectoris, Chest pain, Fatigue, Lethargy, Palpitations; Tachycardia Angina pectoris, Chest pain, Fatigue, Lethargy, Palpitations; Tachycardia
Systemic: Exhaustion / Lethargy-Medium, Systemic: Tachycardia-Medium, Additional Details: PATIENT RE... Systemic: Exhaustion / Lethargy-Medium, Systemic: Tachycardia-Medium, Additional Details: PATIENT REPORTS HAVING HEART/CHEAT PAIN, PALPITATIONS, AND EXAUHSTION W/IN 2 DAYS OF COVAX. HE WENT TO THE ER AS A RESULT. & HAS SINCE DECIDED NOT TO GET VACCINATED FOR COVID. More
2822998 52 F RI 01/27/2025 FLUR4
 PROTEIN SCIENCES CORPORATION
 U8432AA
Trigeminal neuralgia Trigeminal neuralgia
Systemic: Neurological Disorder (diagnosed by MD)-Medium, Additional Details: Patient reports experi... Systemic: Neurological Disorder (diagnosed by MD)-Medium, Additional Details: Patient reports experiencing left-sided facial neuralgia 10-15 minutes post-vaccination. Most symptomatic, throughout the first week post-vaccination. Continued on/off for two months post-vaccination. Patient received full work-up for stroke/TIA with neurologist. Neurologist confirmed no neurological deficits indicative of stroke/TIA; informed patient to contact pharmacy as believes neuralgia a result of vaccine-related adverse event. More
2822999 49 F TX 01/27/2025 COVID19
COVID19
 MODERNA
MODERNA

Antinuclear antibody, Differential white blood cell count, Full blood count, Ras... Antinuclear antibody, Differential white blood cell count, Full blood count, Rash, Swelling face; Urticaria More
Rash/hives, facial swelling Rash/hives, facial swelling
2823000 19 F IN 01/27/2025 MENB
MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
 3L339
3L339
Blood iron abnormal, Dizziness, Electrocardiogram, Full blood count normal, Head... Blood iron abnormal, Dizziness, Electrocardiogram, Full blood count normal, Headache; Insomnia, Nausea, Paraesthesia, Presyncope More
12 hours post vaccine administration- vasovagal/near syncope episode, headache, nausea, dizziness, l... 12 hours post vaccine administration- vasovagal/near syncope episode, headache, nausea, dizziness, lightheadedness, trouble sleeping and intermittent "pins and needles feeling in hands and feet" More
2823001 61 M WI 01/27/2025 SMALLMNK
SMALLMNK
 BAVARIAN NORDIC
BAVARIAN NORDIC
 96867
96867
Arthralgia, Fatigue, Injection site erythema, Injection site induration, Injecti... Arthralgia, Fatigue, Injection site erythema, Injection site induration, Injection site pain; Injection site pruritus, Injection site warmth, Myalgia More
Pt has occupational risk of exposure to orthopoxviruses as individual who directly handle cultures o... Pt has occupational risk of exposure to orthopoxviruses as individual who directly handle cultures or animals contaminated or infected with monkeypox virus. Jynneos booster given on 1/22/25 to left arm is noted to be red, indurated and slight warmness to area where vaccine was given. Redness measures 20 x 10 cm. Induration is 14cm long. Pt notes that he experienced joint pain, myalgia, and fatigue following Jynneos injection that improved on 1/23/25 evening. Pt notes injection site was itchy. Pt notes injection site caused a dull ache pain in the center of the induration. Discomfort was up to 6/10 on pain scale. Pt notes pain on 1/24/25 is much better at a 1-2/10. More
2823002 67 M 01/27/2025 COVID19
 MODERNA
 3043332
Expired product administered Expired product administered
After Pt was vaccinated i noticed there was no Beyond Use date label from when vaccine was thawed. P... After Pt was vaccinated i noticed there was no Beyond Use date label from when vaccine was thawed. Per Manufacturer and CDC there is a 60 day Beyond use date after being thawed. I followed with contacting our supply and figured it was delivered on 25 Nov 2024 and that because no one knew when it was that that it was 60 days from that date. I then called our med safety pharmacist and she followed up with the manufacturer which they advised to revaccinate. More
2823003 31 M WA 01/27/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 B2451V1B
Extra dose administered Extra dose administered
Patient had already received 3 doses and should not have received this dose Patient had already received 3 doses and should not have received this dose
2823004 22 F 01/27/2025 COVID19
 MODERNA
 3043332
Expired product administered Expired product administered
After Pt was vaccinated i noticed there was no Beyond Use date label from when vaccine was thawed. P... After Pt was vaccinated i noticed there was no Beyond Use date label from when vaccine was thawed. Per Manufacturer and CDC there is a 60 day Beyond use date after being thawed. I followed with contacting our supply and figured it was delivered on 25 Nov 2024 and that because no one knew when it was that that it was 60 days from that date. I then called our med safety pharmacist and she followed up with the manufacturer which they advised to revaccinate. Pt is 26 weeks pregnant and estimated delivery date is 24 Feb 2025. More
2823005 41 F SC 01/27/2025 COVID19
 MODERNA
Hysterectomy, Menstrual disorder, Ultrasound scan abnormal, Uterine leiomyoma Hysterectomy, Menstrual disorder, Ultrasound scan abnormal, Uterine leiomyoma
I started having menstral issues and developed 5 large uterine fibroids. As a result, my uterus had ... I started having menstral issues and developed 5 large uterine fibroids. As a result, my uterus had to be removed More
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2823006 4 F NH 01/27/2025 DTAPIPV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 T343J
Y008280
Expired product administered; Expired product administered Expired product administered; Expired product administered
Patient was administered two vaccines at her well child exam today on 1/27/27 of Kinrix and Proquad.... Patient was administered two vaccines at her well child exam today on 1/27/27 of Kinrix and Proquad. Both the Registered Nurse and Medical assistant verified the date of the vaccines with the impression todays date was 1/25/25. After administration, the kinrix vaccine was discovered to be expired. The patients provider APRN and the patient's father were informed. More
2823007 72 F SC 01/27/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255t2
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received 2 RSV vaccines unknowingly. Received first on 09/29/2023 and second 01/23/2025. Has... Patient received 2 RSV vaccines unknowingly. Received first on 09/29/2023 and second 01/23/2025. Has not experienced any side effects so far. More
2823008 39 F VA 01/27/2025 UNK
 UNKNOWN MANUFACTURER
Mobility decreased, Pain in extremity Mobility decreased, Pain in extremity
The day after getting the flu shot my arm was more sore than typical. It continued to get worse unti... The day after getting the flu shot my arm was more sore than typical. It continued to get worse until I began to notice that my movement was more limited. It got to the point that I could not raise my arm more than about 10%. More
2823009 80 F FL 01/27/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received duplication vaccine 14 months apart with NO adverse event or symptoms. Patient received duplication vaccine 14 months apart with NO adverse event or symptoms.
2823010 71 F MA 01/27/2025 FLU3
 SEQIRUS, INC.
 388462
Urticaria Urticaria
About 4 hours (7:00 pm). after the shot, I developed hives. They gradually increased until they wer... About 4 hours (7:00 pm). after the shot, I developed hives. They gradually increased until they were everywhere except my feet and my head. They went away about 5:00 am the next morning. However, they returned the next evening (same places) and then the second round also went away about 7:00 the next morning. This time, they didn't return. My question is whether or not I should get a flu shot next year. More
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