🏥 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 💀 🏥 🚑 ♿ ⚠️
2834026 40 F FL 04/02/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 EW0181
EW0181
Inflammation, Injected limb mobility decreased, Injection site reaction, Insomni... Inflammation, Injected limb mobility decreased, Injection site reaction, Insomnia, Muscle spasms; Vaccination site pain More
Few days after the second Covid vaccine I started with occasional cramping pain on the vaccine site... Few days after the second Covid vaccine I started with occasional cramping pain on the vaccine site but I didn?t really pay much attention to it because it will come and go. Also because I had suffer from pain due to the degenerative disc disease and why I didn?t go to see my doctor sooner however, this was a different kind of pain and in a rare area for me but thought it would go away. As the months , years have gone on the pain is now always there. I have range of motion issues , and can?t sleep, raise, or move the left arm as I used to. I went to my doctor for unbearable pain since is just getting worst . She found inflammation and range of motion issues but dismissed my concern and timeframe given since the first episode. More
✓
2834027 0.17 M WA 04/02/2025 IPV
PNC20
RV5
 SANOFI PASTEUR
PFIZER\WYETH
MERCK & CO. INC.
 W1C751M
HN5980
2032347
Product storage error; Product storage error; Product storage error Product storage error; Product storage error; Product storage error
Patient was administered a polio vaccine that had been in a excursion and should have been disposed ... Patient was administered a polio vaccine that had been in a excursion and should have been disposed of. This vaccine is not as effective, and patient will need a extra polio. Patient mother was advised and stated understanding. More
2834028 77 M 04/02/2025 CHIK
CHIK
JEV1
JEV1
TYP
TYP
 VALNEVA USA, INC.
VALNEVA USA, INC.
INTERCELL AG
INTERCELL AG
SANOFI PASTEUR
SANOFI PASTEUR
 24B011
24B011
JEV23K07E
JEV23K07E
W1A991M
W1A991M
Abdominal pain upper, Blood test normal, Dizziness, Electrocardiogram normal, Ni... Abdominal pain upper, Blood test normal, Dizziness, Electrocardiogram normal, Night sweats; Pyrexia, SARS-CoV-2 test negative, Syncope, X-ray normal; Abdominal pain upper, Blood test normal, Dizziness, Electrocardiogram normal, Night sweats; Pyrexia, SARS-CoV-2 test negative, Syncope, X-ray normal; Abdominal pain upper, Blood test normal, Dizziness, Electrocardiogram normal, Night sweats; Pyrexia, SARS-CoV-2 test negative, Syncope, X-ray normal More
Client has hx of vocal cord cancer but has been in remission for 8 years now. Stated that he had no ... Client has hx of vocal cord cancer but has been in remission for 8 years now. Stated that he had no concerns during the appointment. Timeline: 3/18 -- received Typhim, Ixiaro and Ixchiq 3/20 to 3/24 -- client experienced stomach cramps 3/28 -- client felt feverish (did not take temperature) and experienced night sweats 3/29 -- Client was out walking, felt dizzy and fainted around 4am. Client continued feeling dizzy by 7am. Consulted with PCP who recommended that the client go to ER. Wife took husband to the ER by 10am. EKG, blood work and xrays were done -- all tests were WNL. All symptoms resolved since then. Note: Covid tests all came back negative. More
2834029 72 M KS 04/02/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Respiratory syncytial virus infection Respiratory syncytial virus infection
Became ill with RSV Became ill with RSV
2834030 5 F OH 04/02/2025 DTAP
IPV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 9KB9G
W1C831M
Y012341
Hyperhidrosis, Pallor; Hyperhidrosis, Pallor; Hyperhidrosis, Pallor Hyperhidrosis, Pallor; Hyperhidrosis, Pallor; Hyperhidrosis, Pallor
Patient stayed in facility x 10 minutes after vaccinations given, became pale and diaphoretic. Alert... Patient stayed in facility x 10 minutes after vaccinations given, became pale and diaphoretic. Alert and oriented. Patient talking and making eye contact. Juice given. Refused cool cloth and crackers. Guardians state patient did not eat breakfast, "she had a couple cookies." Instructed guardians to have patient eat breakfast after leaving facility, and seek medical attention if needed. Guardians verbalized understanding of all information provided. Patient stayed another 10 minutes and skin w/d/pale pink. Alert and oriented, making eye contact, talking and smiling. Ambulated out of facility with guardians and a steady gait. Called for follow up approximately 1 hour and 20 minutes later and spoke to guardian, who states that patient is doing well. states that patient ate breakfast and is currently laying down watching cartoons. denies any further issues/concerns with patient. Instructed to seek medical attention if needed and she verbalized understanding of all information provided. More
2834031 65 F WI 04/02/2025 COVID19
RSV
 PFIZER\BIONTECH
PFIZER\WYETH

Rash, Skin warm, Swelling; Rash, Skin warm, Swelling Rash, Skin warm, Swelling; Rash, Skin warm, Swelling
Swollen, painful expanding rash, hot to the touch. Swollen, painful expanding rash, hot to the touch.
2834032 25 F TX 04/02/2025 COVID19
HEP
VARCEL
 MODERNA
DYNAVAX TECHNOLOGIES CORPORATION
MERCK & CO. INC.
 8081596
945660
y013348
Dizziness, Nausea; Dizziness, Nausea; Dizziness, Nausea Dizziness, Nausea; Dizziness, Nausea; Dizziness, Nausea
Dizziness, lightheadedness, nausea, Dizziness, lightheadedness, nausea,
2834033 23 F OK 04/02/2025 COVID19
 MODERNA
Anaphylactic reaction Anaphylactic reaction
Anaphylaxis Anaphylaxis
✓
2834034 64 M WV 04/02/2025 FLU3
 SEQIRUS, INC.
 388490
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Pt was given Fluad, he was 64 years and 10 month at the time. It is indicated for age 65 and up. T... Pt was given Fluad, he was 64 years and 10 month at the time. It is indicated for age 65 and up. There was no clinical adverse reaction. More
2834035 3 M CA 04/02/2025 DTAPHEPBIP
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 9D25P
Y015991
Pyrexia, Rash; Pyrexia, Rash Pyrexia, Rash; Pyrexia, Rash
Rah and Fever Rah and Fever
2834037 1.67 M UT 04/02/2025 DTAP
HEPA
HIBV
VARCEL
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 3CA03C3
C24B9
UK170AB
Y013073
No adverse event, Product preparation issue; No adverse event, Product preparati... No adverse event, Product preparation issue; No adverse event, Product preparation issue; No adverse event, Product preparation issue; No adverse event, Product preparation issue More
Injection was given of diluent without the Hib vaccination mixed in, no adverse effects noted, patie... Injection was given of diluent without the Hib vaccination mixed in, no adverse effects noted, patient rescheduled for Hib vaccination More
2834038 50 F FL 04/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 47n3y
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Patient present with injection reaction symptoms including pain at injection site, redness, pain and... Patient present with injection reaction symptoms including pain at injection site, redness, pain and swelling only around injection site. Patient was advised to get Benadryl, apply compression stockings and ice the area; waiting on resolution of symptoms More
2834039 52 F PA 04/02/2025 PNC21
 MERCK & CO. INC.
 Y011819
Injection site erythema, Injection site pruritus, Injection site swelling Injection site erythema, Injection site pruritus, Injection site swelling
PATIENT EXPERIENCED REDNESS, SWELLING, AND ITCHING JUST BELOW INJECTION SITE. TREATING WITH COLD COM... PATIENT EXPERIENCED REDNESS, SWELLING, AND ITCHING JUST BELOW INJECTION SITE. TREATING WITH COLD COMPRESS, IBUPROFEN, BENADRYL More
2834040 64 M MN 04/02/2025 COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 031A21A
041B21A
033F21A
014H22A
3043335
Death; Death; Death; Death; Death Death; Death; Death; Death; Death
Patient expired on 3/31/2025. Patient expired on 3/31/2025.
✓
2834041 73 F MI 04/02/2025 MMRV
 MERCK & CO. INC.
 Y012076
Wrong product administered Wrong product administered
was inadvertently given MMRV (Proquad) versus MMR. was inadvertently given MMRV (Proquad) versus MMR.
2834042 70 M MI 04/02/2025 MMRV
 MERCK & CO. INC.
 Y012076
Wrong product administered Wrong product administered
was inadvertently given MMRV (Proquad) versus MMR. was inadvertently given MMRV (Proquad) versus MMR.
2834043 60 F MT 04/02/2025 DTAP
 SANOFI PASTEUR
 47Y5M
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
No adverse symptoms stated by patient. No adverse symptoms stated by patient.
2834044 77 M IA 04/02/2025 COVID19
 MODERNA
 8081260
Fatigue, Flushing, Parosmia, Somnolence Fatigue, Flushing, Parosmia, Somnolence
Lingering Bad smell, Fatigue, Increased Sleeping, Flushed Face Lingering Bad smell, Fatigue, Increased Sleeping, Flushed Face
2834045 57 F NY 04/02/2025 PNC20
 PFIZER\WYETH
 LJ5280
Rash Rash
RASH STARTED 03/27/2027, 2X5 INCHES . SPOKE TO DOCTOR 04/02/2025 PATIENT IS USING TYLENOL 500MG Q4H,... RASH STARTED 03/27/2027, 2X5 INCHES . SPOKE TO DOCTOR 04/02/2025 PATIENT IS USING TYLENOL 500MG Q4H, AQUAPHOR, HYDROCORTISIONE CREAM AND BENADRYL. More
2834046 64 F FL 04/02/2025 PNC20
 PFIZER\WYETH
 L6651
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient had no sign or symptoms of any adverse event. However, patient got the Prevnar 20 vaccine Ja... Patient had no sign or symptoms of any adverse event. However, patient got the Prevnar 20 vaccine January 29 2024 and then got a second dose, which is not in the guidelines, on 4-1-25 More
2834047 61 M MA 04/02/2025 PNC21
 MERCK & CO. INC.
 Y019158
Injection site cellulitis Injection site cellulitis
cellulitis of injection site cellulitis of injection site
2834048 50 M MN 04/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 MG5S9
Product preparation error Product preparation error
mixed with Merck diluent 0006-4175-89 mixed with Merck diluent 0006-4175-89
2834049 86 F NY 04/02/2025 PNC21
 MERCK & CO. INC.
 Y019157
Dizziness, Injection site erythema, Injection site swelling, Pain in extremity, ... Dizziness, Injection site erythema, Injection site swelling, Pain in extremity, Pruritus More
Redness, minor swelling at injection site, itchiness, lightheadedness. All side effects manifested ... Redness, minor swelling at injection site, itchiness, lightheadedness. All side effects manifested 4 days after vaccine administration, only side effect following administration was minor sore arm which subsided after a day. More
2834050 62 F CA 04/02/2025 PNC20
 PFIZER\WYETH
 LK665
Erythema, Local reaction, Pruritus, Skin swelling Erythema, Local reaction, Pruritus, Skin swelling
Localized skin reaction with redness, mild swelling, itching Localized skin reaction with redness, mild swelling, itching
2834051 1.5 F NC 04/02/2025 IPV
 SANOFI PASTEUR
Blood test, Culture, Pyrexia, Respiratory pathogen panel Blood test, Culture, Pyrexia, Respiratory pathogen panel
Fever started within 24 hours. Fever of 105 persisted for 5 days leading to 2 emergency room visits ... Fever started within 24 hours. Fever of 105 persisted for 5 days leading to 2 emergency room visits and one pediatrician visit. More
2834052 29 F AK 04/02/2025 ANTH
ANTH
ANTH
 EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
 300215A
300215A
300215A
Arthralgia, Decreased appetite, Fatigue, Headache, Hypersomnia; Immediate post-i... Arthralgia, Decreased appetite, Fatigue, Headache, Hypersomnia; Immediate post-injection reaction, Impaired work ability, Injection site pain, Nausea, Pain in extremity; Rhinorrhoea More
Pain at the injection site started immediately and lasted four days. Pain approximately 6 inches bel... Pain at the injection site started immediately and lasted four days. Pain approximately 6 inches below the injection site started approximately 30 minutes after injection and lasted 3 days. Pain in right forearm and wrist started 30 minutes after injection and lasted three days. Extreme fatigue started the evening of 7Mar, approximately 8 hours after injection, and lasted 3 days. On the fourth day, fatigue improved to moderate and lasted an additional 10 days. Headache started the day after injection and lasted two days. On day three after injection, patient started experiencing very mild symptoms of infection, such as increased nasal discharge. On day 13, patient experience sudden onset nausea. Patient thought she was going to throw up multiple times and ended up having to leave work mid-morning. On day 14, the nausea had improved to mild, and patient was able to return to work. For all mild symptoms, patient just endured and did her best to keep working. For all moderate-to-severe symptoms, patient slept a lot. During the first few days after injection, patient was sleeping 9+ hours each night, taking 4+ hours naps each day, and still felt exhausted. During nausea episode, patient went home and slept for 5-6 hours, felt too nauseous to eat anything, and went to bed early that night. More
2834053 3 M OK 04/02/2025 DTAP
 SANOFI PASTEUR
 3CA25C1
Poor quality sleep, Pruritus, Rash, Skin warm, Streptococcus test negative Poor quality sleep, Pruritus, Rash, Skin warm, Streptococcus test negative
Mother took patient to ED on 3/31/2025 and reported rash with onset 3/29/2025 in evening. Rash bega... Mother took patient to ED on 3/31/2025 and reported rash with onset 3/29/2025 in evening. Rash began on face and spread. Mother reports patient felt warm, and was itchy and not sleeping well. No rash to injection site. Mother did not treat with any topical or oral meds. No history of similar episodes. Per ED record "SLAPPED CHEEK APPEARANCE NO RASH ON PALMS OR SOLES BLANCHES TO PRESSURE MORBILLIFORM APPEARANCE NO MACULOPAPULAR RASH APPEARANCE" More
2834054 18 M MA 04/02/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
Chills, Headache, Nausea, Pain in extremity, Vomiting Chills, Headache, Nausea, Pain in extremity, Vomiting
C/o arm soreness. This morning, he had a slight headache. He went to school. Headache/ chills. N... C/o arm soreness. This morning, he had a slight headache. He went to school. Headache/ chills. Normal lunch. Rested all afternoon. Still have headache. Chills went away. No temp. Up at 5 pm, ate a pear cup. 15-20 minutes later, vomited twice. Still nauseated. No sore throat. More
2834055 58 F MO 04/02/2025 PNC20
 PFIZER\WYETH
 LX2497
Injection site pain, Injection site swelling Injection site pain, Injection site swelling
Day after vaccination, patient reported pain and swelling at left deltoid (injection site) up to col... Day after vaccination, patient reported pain and swelling at left deltoid (injection site) up to collarbone/neck. More
2834056 77 M AK 04/02/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 8081260
8081260
8081260
Anisocytosis, Blood disorder, Neutropenia, Neutrophil count decreased, Platelet ... Anisocytosis, Blood disorder, Neutropenia, Neutrophil count decreased, Platelet count decreased; Poikilocytosis, Pyrexia, Red blood cell acanthocytes present, Red blood cell schistocytes, Red blood cell spherocytes; Red blood cell target cells present, Thrombocytopenia More
fever up to 101.5 F that night x 48 hrs; fever up to 101.5 F that night x 48 hrs;
2834057 22 M FL 04/02/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 4N222
Incorrect route of product administration Incorrect route of product administration
pt was given the vaccine IM instead of subQ (no issues reported yet but wanted to document wrong adm... pt was given the vaccine IM instead of subQ (no issues reported yet but wanted to document wrong administration) More
2834058 17 F LA 04/02/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 B4J4B
Injection site erythema, Injection site pain, Injection site warmth Injection site erythema, Injection site pain, Injection site warmth
3 inch area of erythema at injection site. Red, warm and tender. 3 inch area of erythema at injection site. Red, warm and tender.
2834059 79 F TN 04/02/2025 PNC21
 MERCK & CO. INC.
 Y011819
Injection site bruising, Injection site erythema, Injection site swelling Injection site bruising, Injection site erythema, Injection site swelling
Adverse Event: redness, swelling, and bruising of the upper right arm, Treatment: antibiotic course ... Adverse Event: redness, swelling, and bruising of the upper right arm, Treatment: antibiotic course given by provider, Outcome: patient to have follow up with provider next week to determine outcome More
2834060 18 F OR 04/02/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 MD9SL
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
None. He received Adult formulation instead of pediatric formulation None. He received Adult formulation instead of pediatric formulation
2834061 32 F NJ 04/02/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 ER8736
ER8736
ER8736
Amnesia, Autoimmune disorder, Blood test, Brain fog, Computerised tomogram; Cyst... Amnesia, Autoimmune disorder, Blood test, Brain fog, Computerised tomogram; Cystitis noninfective, Electroencephalogram, Epilepsy, Inflammation, Magnetic resonance imaging; Orthostatic hypotension, Pain, Seizure, X-ray limb More
I was diagnosed with seizures after struggling with brain fog and memory loss, I recieved an eeg. I ... I was diagnosed with seizures after struggling with brain fog and memory loss, I recieved an eeg. I have been having countless symptoms so I started getting tested looking for different things and eventually found I have an auto immune disease I am currently undergoing testing. I have also been struggling with inflammation throughout my body, fingers, toes, bladder. I am in pain daily from this issue. I am undergoing testing to specifically diagnosed this as well I had an xray today 4/2/25 of my hands at hospital. I am waiting for the results. I am currently seeking medical help from mostly doctors, I see a urologist, endocrinologist, rheumatologist and am beginning PT next week. I am doing what I can to manage my symptoms. I also take medication for the seizures, orthostatic hypo tension, and inflammation. More
✓ ✓
2834062 12 F CA 04/02/2025 HPV9
 MERCK & CO. INC.
 z002580
Dizziness Dizziness
Patient went to the parking lot after vaccine administration at 334p and felt faint and lightheaded,... Patient went to the parking lot after vaccine administration at 334p and felt faint and lightheaded, Patient sat down on bench, brought up to pediatrics in wheel chair at 343p. Patient states feeling better with juice and crackers. Vitals taken. Dr. checked patient, patient in stable condition. Dr. gave the ok to discharge. More
2834063 67 F TX 04/02/2025 HEP
PNC21
TDAP
 DYNAVAX TECHNOLOGIES CORPORATION
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 944942
Y013009
L5229
Injection site erythema, Injection site warmth; Injection site erythema, Injecti... Injection site erythema, Injection site warmth; Injection site erythema, Injection site warmth; Injection site erythema, Injection site warmth More
Patient started getting redness on the left arm at the site of injection on Saturday 3/29/25, 2 days... Patient started getting redness on the left arm at the site of injection on Saturday 3/29/25, 2 days after injection. Patient then started getting warmth at the site of the localized redness at site of injection starting on Tuesday 4/1/25, 5 days after injection. Patient did not take anything for self treatment. Patient reported to the pharmacy on Wednesday 4/2/25 and was counseled to apply cold compress, take an antihistamine, and anti-inflammatory over the counter and monitor for improvement. If symptoms getting worse and not better, patient was counseled to contact VAERS, the pharmacy, and/or seek urgent care treatment. More
2834064 16 M AL 04/02/2025 FLU3
 SEQIRUS, INC.
 946623
Asthenia, Chest discomfort, Dizziness Asthenia, Chest discomfort, Dizziness
About 10 minutes after vaccination, the patient felt faint and was helped to the floor by mother. He... About 10 minutes after vaccination, the patient felt faint and was helped to the floor by mother. He was responsive but felt weak. Mentioned having a tight feeling in chest but no problems breathing or swallowing. I was about to administer an Epi-Pen when he mentioned that he was feeling better and I helped him sit up and wait for the EMT's to arrive. They checked him out and his mother said he was feeling back to normal. More
2834065 18 F PA 04/02/2025 MENB
 PFIZER\WYETH
 FN5547
Crying, Headache, Pain in extremity, Sleep disorder Crying, Headache, Pain in extremity, Sleep disorder
Approximately 15-30 minutes after the shot, unberable pain in arm, and thunderclap headache that was... Approximately 15-30 minutes after the shot, unberable pain in arm, and thunderclap headache that was excruciatingly painful, couldn't get off the floor or stop sobbing. Ended up with a sore arms for moths and was unable to apply pressure on sleep on the side due to arm pain. More
2834066 52 F CA 04/02/2025 VARZOS
VARZOS
VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 5y4tl
5y4tl
5Y4TL
5Y4TL
Lacrimation increased, Lip pruritus, Oral discomfort; Oral mucosal blistering, O... Lacrimation increased, Lip pruritus, Oral discomfort; Oral mucosal blistering, Oral pain, Oral pruritus; Lacrimation increased, Lip pruritus, Oral discomfort; Oral mucosal blistering, Oral pain, Oral pruritus More
pt claims symptoms started several days after administration. "itchy and burning upper lip and... pt claims symptoms started several days after administration. "itchy and burning upper lip and watery eyes sever for first week". pt also states that these symptoms have been continuous til present 04/02/2025, albeit less severe. More
2834071 0.5 M ID 04/02/2025 DTAPHEPBIP
DTAPIPV
PNC20
RV5
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.
 5YB7L
Y49B2
LC5484
Y005877
Wrong product administered; Wrong product administered; Wrong product administer... Wrong product administered; Wrong product administered; Wrong product administered; Wrong product administered More
Kinrix vaccine inadvertently given at 6 mo. visit. Family was notified. The flu vaccine was intended... Kinrix vaccine inadvertently given at 6 mo. visit. Family was notified. The flu vaccine was intended, Kinrix and flu vaccine have the same color band & were stored in close proximity to one another. More
2833898 29 M NY 04/01/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.

Allergy test negative, Choking, Quality of life decreased, Skin test negative, S... Allergy test negative, Choking, Quality of life decreased, Skin test negative, Sleep disorder; Sleep study normal, Stress, Suffocation feeling, Throat clearing, Throat tightness More
I don?t have the exact flu shot on hand, it?s in my work record. Just not accessible at this time. C... I don?t have the exact flu shot on hand, it?s in my work record. Just not accessible at this time. Can provide at later date.Within one week of receiving the influenza vaccine, I began experiencing sudden episodes of choking and a sensation of throat constriction, particularly at night while lying on my back. The feeling is intense and causes me to forcibly swallow and reposition my throat to regain normal breathing. These symptoms have persisted for over 8 years and have significantly affected my sleep, stress levels, and quality of life. Multiple ENT evaluations, allergy tests (both skin and blood), and sleep studies have failed to identify a mechanical cause. No nasal polyps or sleep apnea were found. Sinus surgery was suggested without confidence of resolution. No other changes in lifestyle, medication, or exposure occurred around the time of the vaccine. This event remains unexplained by conventional testing and has not resolved since onset. More
2833899 1.08 F KY 04/01/2025 MMRV
 MERCK & CO. INC.
 Y004115
Pyrexia, Rash papular, Rhinorrhoea Pyrexia, Rash papular, Rhinorrhoea
Fever, runny nose, and raised rash. Child experienced symptoms over the course of a week. Fever, runny nose, and raised rash. Child experienced symptoms over the course of a week.
2833902 68 F DC 04/01/2025 FLU3
 SANOFI PASTEUR
 UT8470DA
Lip swelling Lip swelling
Reported Symptoms: 10024570:LIP SWELLING; Narrative: A 69 yo female whose PMH included sleep apnea, ... Reported Symptoms: 10024570:LIP SWELLING; Narrative: A 69 yo female whose PMH included sleep apnea, lipoma, chronic headache, memory impairment, chronic PTSD, DM, Chronic back pain, HTN, OA of knee, IBS, exposure to potentially hazardous substance, venous insufficiency of leg and asthma. On December 3, 2024, PCC physician reported the patient had a historical ADR of trivalent PF Influenza vaccine induced lower lip swelling for which she sought a non facility Emergency Room visit and received IV BENADRYL, famotidine and solumedrol treatment. No swelling of tongue and patient oropharynx with no difficulty breathing were documented per Dec 3, record summary. The patient was discharged with three days supply of oral prednisone, famotidine and benadryl. Other Relevant HX: Other: LIP SWELLING More
2833903 74 M FL 04/01/2025 COVID19
 PFIZER\BIONTECH
 LM7786
Chills, Dyspnoea, Hypersensitivity, Malaise, Tremor Chills, Dyspnoea, Hypersensitivity, Malaise, Tremor
Reported Symptoms: 10008531:CHILLS; 10013963:DYSPNEA; 10025482:MALAISE; Narrative: Per ADR entry: &q... Reported Symptoms: 10008531:CHILLS; 10013963:DYSPNEA; 10025482:MALAISE; Narrative: Per ADR entry: "Patient reports an allergic reaction to COVID-vaccine. Shaky slightly short of breath malaise and felt better after taking Benadryl and meloxicam." Patient reached out via secure messaging as noted 1/24/2025, "I had some kind of allergic reaction to the covid shot. it didn't happen until around 4am, so a 12 hour delay...I say allergic reaction because after about an hour and a half of this I took one Loratadine pill. it seemed to make it all go away." Other Relevant HX: Other chills, malaise, dyspnea More
2833904 63 M KY 04/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 75GZ7
Extra dose administered, No adverse event Extra dose administered, No adverse event
Reported Symptoms: 10027091:MEDICATION ERROR; 10064366: EXTRA DOSE ADMINISTERED; Narrative: No adver... Reported Symptoms: 10027091:MEDICATION ERROR; 10064366: EXTRA DOSE ADMINISTERED; Narrative: No adverse event occurred from patient receiving an extra vaccine of Shingrix in error. Patient was fully vaccinated (had received 2 doses of vaccine previously). Reporting to VAERS for information. Other Relevant HX: Other: EXTRA DOSE GIVEN IN ERROR More
2833905 23 F IL 04/01/2025 COVID19
COVID19
 MODERNA
MODERNA
 3042648
3042648
Injection site erythema, Injection site mass, Injection site pruritus, Injection... Injection site erythema, Injection site mass, Injection site pruritus, Injection site rash, Injection site swelling; Injection site warmth, Pyrexia More
Reported Symptoms: 10016558:Fever; 10037844:RASH; Narrative: Pt is a 24 female with PMH of anxiety ... Reported Symptoms: 10016558:Fever; 10037844:RASH; Narrative: Pt is a 24 female with PMH of anxiety disorder, ovarian cysts, and vitamin b12 deficiency. Pt received both a Covid and influenza vaccine on 11/01/2024. Pt developed a rash and a fever that same night. Her right arm (where she received the Covid vaccine) was red, swollen, and warm to the touch. After four days of worsening symptoms, the patient went to the ER on 11/5/24 after a new lump developed at the sight and the sight was now itching. Patient received clindamycin for 5 days and the rash resolved. Other Relevant HX: Pt is a 24 yo female with PMH of anxiety disorder, ovarian cysts, and vitamin b12 deficiency. Pt received both a Covid vaccine and influenza vaccine on 11/01/24. Pt developed a rash and a fever that same night. Her right arm (where she received the Covid vaccine) was red, swollen, and warm to the touch. After four days of worsening symptoms, the patient wen to the ER on 11/5/24 after a new lump developed at the sight and the sight was now itching. Patient received clindamycin for 5 days and the rash resolved. Other: RASH; FEVER More
2833906 67 M IL 04/01/2025 COVID19
 MODERNA
 3042648
Headache, Somnolence Headache, Somnolence
Reported Symptoms: 10013649:DROWSINESS; 10019211:HEADACHE; 10039897:SEDATION; Narrative: Patient is ... Reported Symptoms: 10013649:DROWSINESS; 10019211:HEADACHE; 10039897:SEDATION; Narrative: Patient is 67 YOM w/ PMH of bladder cancer, tobacco use, DM, and OSA received covid booster. Reported drowsiness and headache after vaccination that eventually subsided. Other Relevant HX: N/a Other: DROWSY; HEADACHE More
2833907 M DC 04/01/2025 COVID19
 PFIZER\BIONTECH
Eczema Eczema
Reported Symptoms: 10014184:ECZEMA; Narrative: A 44yo male with PMH which included Obesity, TBI, Ten... Reported Symptoms: 10014184:ECZEMA; Narrative: A 44yo male with PMH which included Obesity, TBI, Tendonitis, PTSD, Lumbago, Herpes, Cervicalgia, Abnormal Liver Function test and Exposure to potentially hazardous substance. Per January 24, 2025, Nursing note, the patient presented alert and oriented x 3 for his annual appointment. During the visit the patient refused COVID-19 (MODERNA), MRNA, LNP-S, PF, 50 MCG/0.5ml, (Ages 12+ years). The patient refused all immunization(s) in the Covid-19 group due to hx of Covid-19 vaccine induced allergic reaction of Eczema on hands. Other Relevant HX: Other: ECZEMA. More
2833908 F CA 04/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 5RK5T
Rash Rash
Reported Symptoms: 10037844:RASH; Narrative: Other Relevant HX: The patient was newly started on esc... Reported Symptoms: 10037844:RASH; Narrative: Other Relevant HX: The patient was newly started on escitalopram the day after the vaccine. When the rash occurred, the patient was told to stop the escitalopram. However, she later reported she never stopped escitalopram, and the rash went away. Thus she thinks the rash was due to the vaccine. Other: More
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