๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ 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.

๐Ÿ“– Help & Search Guide

Column Icons Legend

๐Ÿ’€ Death
๐Ÿฅ Hospitalized
๐Ÿš‘ Emergency Room
โ™ฟ Disability
โš ๏ธ Life Threatening

How to Search

๐Ÿ’ก 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 "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ 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:

  • โœ… Early warning system for potential safety signals
  • โœ… Open and transparent - publicly accessible
  • โœ… Accepts all reports regardless of likelihood of causation
  • โœ… Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • โš ๏ธ Reports are unverified - not investigated before publication
  • โš ๏ธ Cannot determine if vaccine caused the event
  • โš ๏ธ Underreporting - not all adverse events are reported
  • โš ๏ธ Overreporting - coincidental events may be reported
  • โš ๏ธ 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?

โš ๏ธ 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
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2836001 69 F AZ 04/14/2025 COVID19
 PFIZER\BIONTECH
 LN0590
Arthralgia, Musculoskeletal stiffness Arthralgia, Musculoskeletal stiffness
Patient reported severe right shoulder pain and stiffness from the evening of vaccination and contin... Patient reported severe right shoulder pain and stiffness from the evening of vaccination and continuing for 2 days. More
2836002 65 F NC 04/14/2025 TDAP
 SANOFI PASTEUR
 U8015AA
Arthralgia, Mobility decreased, X-ray limb Arthralgia, Mobility decreased, X-ray limb
R shoulder pain and decreased ROM since a few days afterwards. Obtained R shoulder XR due to pain an... R shoulder pain and decreased ROM since a few days afterwards. Obtained R shoulder XR due to pain and difficulty w/ ROM. Impression above (no acute findings). I will refer her to PT to help with her pain and ROM improvement. More
2836003 17 M NV 04/14/2025 JEV1
YF
 INTERCELL AG
SANOFI PASTEUR
 JEV23K07E
UK134AA
Dizziness, Nausea, Pallor; Dizziness, Nausea, Pallor Dizziness, Nausea, Pallor; Dizziness, Nausea, Pallor
After administration client complained of lightheadedness. Became very pale and complained of nausea... After administration client complained of lightheadedness. Became very pale and complained of nausea. Elevated feet, ice pack to back of neck, water and lollipop. BP 79/40, pulse 56, O2 98%. Symptoms resolved in a couple of minutes. No vomiting. Skin tone returned to normal. BP 101/65 and pulse 55. No LOC More
2836004 54 F PR 04/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 MG5S9
Injection site erythema, Injection site swelling, Pruritus Injection site erythema, Injection site swelling, Pruritus
Patients refers left arm is red and swollen at the vaccination administration site. Doctor prescribe... Patients refers left arm is red and swollen at the vaccination administration site. Doctor prescribes antibiotic and for pruritus More
2836005 16 F TN 04/14/2025 FLU3
 SANOFI PASTEUR
 UT8488KA
Extra dose administered Extra dose administered
PATIENT HAD BEEN A FLU VACCINE FOR THIS FLU SEASON 12/2024 PATIENT HAD BEEN A FLU VACCINE FOR THIS FLU SEASON 12/2024
2836006 13 M 04/14/2025 COVID19
 PFIZER\BIONTECH
Pyrexia Pyrexia
low grade fever low grade fever
2836007 72 M MN 04/14/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 032M20A
032M20A
027B21A
027B21A
FL3209
FL3209
GH9697
GH9697
HF9300
HF9300
Cough, Decreased appetite, Diarrhoea, Nasal congestion, Upper respiratory tract ... Cough, Decreased appetite, Diarrhoea, Nasal congestion, Upper respiratory tract congestion; Viral test; Cough, Decreased appetite, Diarrhoea, Nasal congestion, Upper respiratory tract congestion; Viral test; Cough, Decreased appetite, Diarrhoea, Nasal congestion, Upper respiratory tract congestion; Viral test; Cough, Decreased appetite, Diarrhoea, Nasal congestion, Upper respiratory tract congestion; Viral test; Cough, Decreased appetite, Diarrhoea, Nasal congestion, Upper respiratory tract congestion; Viral test More
Upper respiratory congestion, nasal congestion, cough, loose stools, loss of appetite Upper respiratory congestion, nasal congestion, cough, loose stools, loss of appetite
2836008 60 M VA 04/14/2025 PNC20
 PFIZER\WYETH
 lx4484
Extra dose administered Extra dose administered
Patient forgot he got the prevnar shot and was given a second one in the same day Patient forgot he got the prevnar shot and was given a second one in the same day
2836009 0.25 M NJ 04/14/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 2H2S9
Incorrect dose administered Incorrect dose administered
Vaccine given too soon. Pt is only 3 months old. Vaccine is for 6 months and up Vaccine given too soon. Pt is only 3 months old. Vaccine is for 6 months and up
2836011 75 F PA 04/14/2025 COVID19
 MODERNA
 3043335
Limb mass, Peripheral swelling Limb mass, Peripheral swelling
swelling from elbow to shoulder occurred day following vaccine and continued until the next saturday... swelling from elbow to shoulder occurred day following vaccine and continued until the next saturday. Small lump remains on arm More
2836012 28 F MN 04/14/2025 COVID19
 JANSSEN
 203A21A
Dizziness, Fatigue, Pain, Respiratory tract congestion, Viral test Dizziness, Fatigue, Pain, Respiratory tract congestion, Viral test
Body aches, exhaustion, dizzy, congestion Body aches, exhaustion, dizzy, congestion
2836013 59 F NY 04/14/2025 MMR
 MERCK & CO. INC.
Flushing, Hyperhidrosis, Palpitations, Pruritus, Throat irritation Flushing, Hyperhidrosis, Palpitations, Pruritus, Throat irritation
I got flushed, face got sweaty, heart raced, body and throat got itchy. I got flushed, face got sweaty, heart raced, body and throat got itchy.
2836014 1 F WI 04/14/2025 MMRV
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
 Y013572
Y010045
Extra dose administered, Pyrexia; Extra dose administered, Pyrexia Extra dose administered, Pyrexia; Extra dose administered, Pyrexia
Orders for patient vaccination were to receive MMR II vaccine. Medical Assistant prepared and admini... Orders for patient vaccination were to receive MMR II vaccine. Medical Assistant prepared and administered Proquad. Patient also received a separate varicella (Varivax) vaccine. Patient reported fever following vaccination with no other symptoms. More
2836015 68 M TX 04/14/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
 HK6938
HK6938
Biopsy skin, Biopsy skin abnormal, Injection site pruritus, Injection site react... Biopsy skin, Biopsy skin abnormal, Injection site pruritus, Injection site reaction, Injection site swelling; Micrographic skin surgery, Skin lesion, Squamous cell carcinoma More
After the vaccine, pt had an itchy raised bump at the site of injection. He followed up to the clini... After the vaccine, pt had an itchy raised bump at the site of injection. He followed up to the clinic one month later, on 10-29-2024. He was treated for possible infection of injection site and was treated with Bactrim DS 800 mg-160 mg tablet 1 tablet every 12 hours for 7 days. Lesion did not heal/resolve so he was referred to dermatologist. Biopsy was taken of the raised lesion and came back positive for squamous cell carcinoma at the injection site. More
2836016 18 F OH 04/14/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 DD72H
Injection site swelling, Neck pain, Oedema peripheral, Pain in extremity Injection site swelling, Neck pain, Oedema peripheral, Pain in extremity
arm was sore all day, before bed started Edema of left upper arm Pt noted to have mild dema of L upp... arm was sore all day, before bed started Edema of left upper arm Pt noted to have mild dema of L upper extremity after Bexsero dose #2. Advised pt she has completed this series, no further doses are needed. Pt with swelling of L upper bicep area. Pt with pain/soreness in L arm and myalgias going into L side of neck. More
2836017 24 F ID 04/14/2025 MMRV
 MERCK & CO. INC.
 Y018161
No adverse event, Underdose No adverse event, Underdose
Patient was given a children's MMR vaccination. No adverse reactions occurred. Patient informed... Patient was given a children's MMR vaccination. No adverse reactions occurred. Patient informed of error. More
2836018 8 M UT 04/14/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 34MF9
Extra dose administered, Injection site erythema, Injection site swelling, Produ... Extra dose administered, Injection site erythema, Injection site swelling, Product administered to patient of inappropriate age More
Pt came in for an MA visit for vaccines and brought the pt's vaccination record. The vaccinatio... Pt came in for an MA visit for vaccines and brought the pt's vaccination record. The vaccination and database was reviewed by both me and another MA. My vaccine preparation was double checked by another MA. We administered the Kinrix vaccine. Pt tolerated it without complaint. I later realized that the pt had already received 4 doses of the polio vaccine and both me and the other MA missed it when reviewing the vaccination record. The state was notified and their response was "The child should not have received Kinrix as it is only licensed through 6 years of age. However, the Dtap can be considered valid so revaccination does not need to occur. The extra IPV dose should not harm the patient but it should be reported to VAERS as an administration error. " I notified the pt's mother of the vaccine error, additional polio vaccine, the pt's mother said "thank you for letting me know" she spoke in a calm voice, expressed no concerns about the extra polio dose. She did say the pt's arm, at the vaccine site, did have swelling and redness, she reported that she "put potatoes on it" and the pt's arm "went back to normal on" 4/13/25. After that, pt's mother had no further questions More
2836019 21 M VA 04/14/2025 COVID19
 PFIZER\BIONTECH
 md3414
Rash Rash
patient started having rash on hands and arm near injection site about 5 minutes after vaccination .... patient started having rash on hands and arm near injection site about 5 minutes after vaccination . Patient was given 2 tablets of benadryl and improved about 5-10 minutes (patient stayed in pharmacy extra 30 minutes) More
2836020 24 M 04/14/2025 HEP
HPV9
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 MD9SL
Y013712
Erythema, Injection site pain; Erythema, Injection site pain Erythema, Injection site pain; Erythema, Injection site pain
Localized redness at right arm, pain in right deltoid. Localized redness at right arm, pain in right deltoid.
2836021 5 F IA 04/14/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 34MF9
Erythema, Muscle swelling, Skin warm Erythema, Muscle swelling, Skin warm
Redness, swelling, warmth of deltoid muscle aprox. within 24 hours of vaccine. Conservative treatmen... Redness, swelling, warmth of deltoid muscle aprox. within 24 hours of vaccine. Conservative treatment with cold packs and tylenol More
2836022 25 F SC 04/14/2025 MMR
 MERCK & CO. INC.
 y014096
Product preparation error Product preparation error
Vaccine diluted with MedQuadfi (Sanofi) instead of Sterile Diluent. Vaccine diluted with MedQuadfi (Sanofi) instead of Sterile Diluent.
2836023 55 F FL 04/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 mg5s9
Injection site swelling, Pyrexia Injection site swelling, Pyrexia
pt called stating her arm injection site was swollen and fever on Sat 4/12, but it is getting better... pt called stating her arm injection site was swollen and fever on Sat 4/12, but it is getting better. More
2836024 85 F FL 04/14/2025 PNC20
 PFIZER\WYETH
 LJ5281
Extra dose administered, No adverse event Extra dose administered, No adverse event
Gave unneeded duplicate Prevnar 20 on this date. Patient came into Pharmacy with a MD note to get it... Gave unneeded duplicate Prevnar 20 on this date. Patient came into Pharmacy with a MD note to get it done. However, she did not mention that she had already gotten it last year. No adverse effects noted by patient due to this vaccine. More
2836025 19 F SC 04/14/2025 MMR
 MERCK & CO. INC.
 y014096
Product preparation error Product preparation error
MMRII accidentally diluted with MenQuadfi (Sanofi) instead of actual diluent. MMRII accidentally diluted with MenQuadfi (Sanofi) instead of actual diluent.
2836026 44 M OR 04/14/2025 COVID19
FLU3
PNC20
 MODERNA
SANOFI PASTEUR
PFIZER\WYETH
 B0005

LG5574
No adverse event, Product storage error; No adverse event, Product storage error... No adverse event, Product storage error; No adverse event, Product storage error; No adverse event, Product storage error More
No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained vi... No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained viable after the excursion per Moderna. More
2836027 53 F OR 04/14/2025 COVID19
 MODERNA
 B0005
No adverse event, Product storage error No adverse event, Product storage error
No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained vi... No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained viable after the excursion per Moderna. More
2836028 63 F CO 04/14/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 AK334
Dry throat, Feeling jittery, Palpitations, Skin warm Dry throat, Feeling jittery, Palpitations, Skin warm
Pt triaged for reaction reporting hot face, palpitations, resting heart rate of 101 lasting 20 minut... Pt triaged for reaction reporting hot face, palpitations, resting heart rate of 101 lasting 20 minutes, jittery feeling, throat feeling dry. Pt reports symptoms are completely resolved now. More
2836029 1 F IL 04/14/2025 HIBV
MMRV
PNC20
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
MERCK & CO. INC.
 Y006393
Y017206
LG5574
Y015101
Extra dose administered; Extra dose administered; Extra dose administered; Extra... Extra dose administered; Extra dose administered; Extra dose administered; Extra dose administered More
Patient received both Proquad and Varivax vaccine during 12 month well child exam visit on 3/18/2025... Patient received both Proquad and Varivax vaccine during 12 month well child exam visit on 3/18/2025. Multiple attempts have been made to contact parents to follow-up on child's health status and ensure child had not developed any adverse effects post vaccinations. Clinical team was unsuccessful in contacting the parents despite making several attempts. Child has a scheduled appointment on June 26, 2025 for a 15 month old well child exam and team will ensure to obtain correct contact information as well as confirm if child had any adverse effects. More
2836030 14 F KY 04/14/2025 HEPA
MENB
MNQ
 GLAXOSMITHKLINE BIOLOGICALS
NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
 TF27T
A2JX7
U8271AC
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered More
On 12/16/2024, Pt was to receive Meningococcal conjugate quadrivalent (MenACWY-TT) as part of routin... On 12/16/2024, Pt was to receive Meningococcal conjugate quadrivalent (MenACWY-TT) as part of routine vaccinations. However, Meningococcal B (Bexsero) vaccine was given in place of MenACWY-TT vaccine in error. Upon realizing error, clinic nurse informed nurse supervisor. Pt's guardian/parent was informed of the error and need to administer correct Meningococcal vaccine (MenACWY-TT) discussed. Pt's mother verbalized understanding. Pt was then given correct Meningococcal (MenACWY-TT) vaccine. Pt had no adverse reaction to vaccines given, VAERS report being completed due to recommendation from CDC regarding immunization error. More
2836031 30 F IL 04/14/2025 HPV9
 MERCK & CO. INC.
 Y000206
Extra dose administered, No adverse event Extra dose administered, No adverse event
Client was administered two doses of newest formulation of Gardasil 9 vaccine despite having a full ... Client was administered two doses of newest formulation of Gardasil 9 vaccine despite having a full series of the quadrivalent formula completed with 3 doses. Quadrivalent series was administered on 04/25/2007, 07/30/2007 and 08/24/2011. Client did not and has not reported any adverse events following the two recent doses administered on 02/07/2025 and 03/12/2025. Client will not have any additional doses administered any longer as current ACIP and CDC guidelines do not advise on this. More
2836032 55 F OR 04/14/2025 COVID19
 MODERNA
 B0005
No adverse event, Product storage error No adverse event, Product storage error
No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained vi... No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained viable after the excursion per Moderna. More
2836033 34 M OR 04/14/2025 COVID19
FLU3
PNC20
 MODERNA
SEQIRUS, INC.
PFIZER\WYETH
 B0005
391417
LG5574
No adverse event, Product storage error; No adverse event, Product storage error... No adverse event, Product storage error; No adverse event, Product storage error; No adverse event, Product storage error More
No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained vi... No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained viable after the excursion per Moderna. More
2836034 41 M OR 04/14/2025 COVID19
PNC20
 MODERNA
PFIZER\WYETH
 B0005
LG5574
No adverse event, Product storage error; No adverse event, Product storage error No adverse event, Product storage error; No adverse event, Product storage error
No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained vi... No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained viable after the excursion per Moderna. More
2836035 50 F OR 04/14/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 B0005
391417
No adverse event, Product storage error; No adverse event, Product storage error No adverse event, Product storage error; No adverse event, Product storage error
No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained vi... No adverse event reported. Reporting per Moderna after a temperature excursion, vaccine remained viable after the excursion per Moderna. More
2836036 51 F SC 04/14/2025 HEPAB
PNC21
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 M4834
Y019158
7KD58
Blood pressure decreased, Palpitations; Blood pressure decreased, Palpitations; ... Blood pressure decreased, Palpitations; Blood pressure decreased, Palpitations; Blood pressure decreased, Palpitations More
Soon after vaccination but already at home blood pressure went down and the heart started racing Soon after vaccination but already at home blood pressure went down and the heart started racing
โœ“
2836037 52 F OH 04/14/2025 PNC21
VARZOS
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 Y019157
47N3Y
Injection site erythema, Injection site rash, Injection site warmth, Pain in ext... Injection site erythema, Injection site rash, Injection site warmth, Pain in extremity, Pyrexia; Injection site erythema, Injection site rash, Injection site warmth, Pain in extremity, Pyrexia More
Arm soreness and fever of 101๏ฟฝF began a few hours after injection and continued for about 48 hours... Arm soreness and fever of 101๏ฟฝF began a few hours after injection and continued for about 48 hours. Then a 2 inch x 5 inch red, warm "rash" about 4 inches below injection site appeared about 48 hours after injection. This "rash" does remain painful and when it gets warm begins to itch--five days post injection. "Rash" does not appear to be spreading. More
2836038 70 F WA 04/14/2025 COVID19
 PFIZER\BIONTECH
 LM2221
Blood test normal, Urticaria Blood test normal, Urticaria
I received the Covid 19 Shot around 11: 00 AM on 10-31-24 and by 3:PM the same day I had large blotc... I received the Covid 19 Shot around 11: 00 AM on 10-31-24 and by 3:PM the same day I had large blotchy hives all over my torso front and back. I have continuously had the same hives since then. Sometimes they are on my legs and arms. Most recently they have been on my legs and torso. I have never had hives before and never had a reaction to Pfizer Covid shots until this one. More
2836039 31 F CA 04/14/2025 HEP
HEP
HEP
MMR
MMR
MMR
TDAP
TDAP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 TP2F9
TP2F9
TP2F9
X027903
X027903
X027903
4799G
4799G
4799G
Cluster headache, Dyspnoea, Dyspnoea exertional, Fatigue, Insomnia; Nausea, Nigh... Cluster headache, Dyspnoea, Dyspnoea exertional, Fatigue, Insomnia; Nausea, Night sweats, Rash, Rash erythematous, Rash papular; Rash pruritic, Rash vesicular, Tachycardia, Tenderness; Cluster headache, Dyspnoea, Dyspnoea exertional, Fatigue, Insomnia; Nausea, Night sweats, Rash, Rash erythematous, Rash papular; Rash pruritic, Rash vesicular, Tachycardia, Tenderness; Cluster headache, Dyspnoea, Dyspnoea exertional, Fatigue, Insomnia; Nausea, Night sweats, Rash, Rash erythematous, Rash papular; Rash pruritic, Rash vesicular, Tachycardia, Tenderness More
Onset of cluster headache, night sweats, nausea, fatigue, and insomnia approximately 1 week followin... Onset of cluster headache, night sweats, nausea, fatigue, and insomnia approximately 1 week following vaccine and lasting about 1 month total. Felt harder to breathe for a few weeks, different from usual asthma symptoms. Some tachycardia and dyspnea with exertion. Onset of rash on right hand - swollen red itchy bumps over dorsal hand first 3 digits from 2 weeks post vaccine lasting 2 weeks. Some partially vesicular in appearance and painful to touch. Widespread but milder rash over face, trunk, and arms starting 10 days after vaccines and lasting about 2 days. Not itchy. More
2836040 16 M KY 04/14/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 52N4S
Injection site erythema, Injection site pain, Injection site warmth, Joint swell... Injection site erythema, Injection site pain, Injection site warmth, Joint swelling More
Developed redness and swelling at injection site on the evening after. Has still been painful, swoll... Developed redness and swelling at injection site on the evening after. Has still been painful, swollen. Parent has noticed increasing redness on surface of skin, and area is warm to touch. More
2836043 41 F CA 04/14/2025 FLU3
VARCEL
 SEQIRUS, INC.
MERCK & CO. INC.
 946615
Y014511
Disorientation, Injection site erythema, Injection site pruritus; Disorientation... Disorientation, Injection site erythema, Injection site pruritus; Disorientation, Injection site erythema, Injection site pruritus More
Redness and itchiness, right arm, where Varicella was given a day after. Pt reports feeling disorien... Redness and itchiness, right arm, where Varicella was given a day after. Pt reports feeling disoriented 3 days after administration of vaccine. More
2835912 81 M TN 04/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 47N3Y
Bell's palsy Bell's palsy
Patient was diagnosed and given treatment for Bell's palsy on 4/13/2025. Valtrex 1 gram, t ta... Patient was diagnosed and given treatment for Bell's palsy on 4/13/2025. Valtrex 1 gram, t tablet TID for 7 days; prednisone 20 mg 3 tablets QD for 7 days More
2835913 71 M FL 04/13/2025 PNC20
 PFIZER\WYETH
 LX4482
No adverse event No adverse event
pt did not have any symptoms since he got the vaccine pt did not have any symptoms since he got the vaccine
2835914 18 F FL 04/13/2025 HEPA
MNQ
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 3j9g4
u8437aa
Immediate post-injection reaction, Seizure; Immediate post-injection reaction, S... Immediate post-injection reaction, Seizure; Immediate post-injection reaction, Seizure More
Patient received Havrix vaccine first, in the left arm, then Menquadfi second in the right arm. Imme... Patient received Havrix vaccine first, in the left arm, then Menquadfi second in the right arm. Immediately after the Menquadfi vaccine was administered, patient started having a seizure. Seizure lasted less than a few minutes, 911 was called, fire department arrived first. Vitals were 86/53 bp and heart rate 60. Patient was taken by ambulance to ER. Patient was alert and able to answer questions. No physical trauma noted. More
2835915 74 M CA 04/13/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 088D21A
088D21A
030M20A
030M20A
029620A
029620A
Cancer surgery, Condition aggravated, Immediate post-injection reaction, Influen... Cancer surgery, Condition aggravated, Immediate post-injection reaction, Influenza like illness, Radiotherapy; Recurrent cancer; Cancer surgery, Condition aggravated, Immediate post-injection reaction, Influenza like illness, Radiotherapy; Recurrent cancer; Cancer surgery, Condition aggravated, Immediate post-injection reaction, Influenza like illness, Radiotherapy; Recurrent cancer More
Flu- like symptoms immediately following injections, RECURRENT CANCER at the same site that was trea... Flu- like symptoms immediately following injections, RECURRENT CANCER at the same site that was treated with radiation in 1995. TURBO CANCER after 26 years of remission. More
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2835916 59 F WA 04/13/2025 COVID19
COVID19
 JANSSEN
JANSSEN
 203A21A
203A21A
Computerised tomogram, Condition aggravated, Echocardiogram, Electrocardiogram, ... Computerised tomogram, Condition aggravated, Echocardiogram, Electrocardiogram, Herpes simplex; Pericarditis More
Pericarditis, recurring starting in November 2021 went ER. Again in 2022, unsure of month, ER tr... Pericarditis, recurring starting in November 2021 went ER. Again in 2022, unsure of month, ER treatment. In November of 2023 ER treatment and hospitalization for 4 days. Other adverse effects include severe worsening of herpes simplex 2 symptoms in frequency, duration and severity. 3 hours after vaccine taken herpes symptoms broke out did not go away for one month additionally since taking the vaccine in 2021 I have had 10 herpes breakouts whereas I had only had 11 instances of herpes breakouts since I first contracted it in 1987. More
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2835917 69 F MA 04/13/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 PFIZERFF2590
PFIZERFF2590
PFIZERFF2590
Abdominal pain, Abdominal pain upper, Antinuclear antibody positive, Biopsy skin... Abdominal pain, Abdominal pain upper, Antinuclear antibody positive, Biopsy skin, Blood test; Computerised tomogram abdomen, Constipation, Dehydration, General physical health deterioration, Large intestinal obstruction; Neurolysis, Pain, Small fibre neuropathy, Ultrasound abdomen, Weight decreased More
I never felt OK after the PFIZER Booster. My condition deteriorated weekly, monthly, now 3.5 years a... I never felt OK after the PFIZER Booster. My condition deteriorated weekly, monthly, now 3.5 years after the shot. Pain all over turned out to be small fiber neuropathy. My stomach started hurting and I've seen many doctors as recently as April 5, 2025; another CT scan. I can't eat with out horrible pain and I'm 111 lbs, down from 140 prior to she booster. I'm a different woman since that booster at pharmacy. I an always dehydrated. Constipation and now the report says my Colon is collapsed. I'll be seeing a GI doctor. More
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2835918 39 F CO 04/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 47n3y
Wrong product administered Wrong product administered
Patient received the wrong vaccine. Patient was to receive the MMR vaccine, instead she received Shi... Patient received the wrong vaccine. Patient was to receive the MMR vaccine, instead she received Shingrix. More
2835919 23 M NY 04/13/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 FJ6369
FJ6369
FJ6369
Back pain, Chemotherapy, Coma, Constipation, Death; Impaired work ability, Magne... Back pain, Chemotherapy, Coma, Constipation, Death; Impaired work ability, Magnetic resonance imaging spinal abnormal, Malignant neoplasm of spinal cord, Metastases to central nervous system, Mobility decreased; Peroneal nerve palsy, Radiotherapy, Seizure, Tumour excision, Urinary retention More
Injection received February 2022. Patient had extreme back pain through December 2022, leaving emplo... Injection received February 2022. Patient had extreme back pain through December 2022, leaving employment 1/5/2023. Suffered Drop Foot and limited mobility 1/18/2023. Sent to emergency room due to lack of ability to urinate or have bowel movements 1/23/2023. Resulting MRI revealed tumor of the spine. Surgery to remove tumor took place 1/31/2023. Standard of care chemotherapy and radiation took place, followed by inpatient acute rehabilitation. A clinical trial for trial medication ONC201 was started to assist in stopping the cancer. Seizures began 8/31/2024, resulting in Coma for about 5 days. Patient passed away from metastasis to brain 10/15/2024. More
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2835920 75 M TX 04/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 99Y4J
Brain fog, Fatigue, Pain in extremity Brain fog, Fatigue, Pain in extremity
Patient stated he became disoriented with fog brain and very fatigued, arm was sore for 2 weeks Patient stated he became disoriented with fog brain and very fatigued, arm was sore for 2 weeks
2835921 49 F NY 04/13/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FJ6369
FJ6369
Asthenia, Back pain, Epstein-Barr virus infection, Epstein-Barr virus test posit... Asthenia, Back pain, Epstein-Barr virus infection, Epstein-Barr virus test positive, Fatigue; Malaise, Migraine, Pyrexia, Syncope, Throat irritation More
Received booster vaccination 2/10/2022. Didn't feel well with migraine headaches, overall weakn... Received booster vaccination 2/10/2022. Didn't feel well with migraine headaches, overall weakness and fatigue since injection. Back pain, feverish feeling and throat irritation resulted in urgent care visit June 2023. Bloodwork confirmed reactivation of Epstein-Barr Virus with high serology levels. Suffered syncope with collapse 7/13/2023, with no known cause. Symptoms from EBV persist to date of this report. More
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