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
2833819 79 F CA 03/31/2025 PPV
MERCK & CO. INC.
X022827
Injected limb mobility decreased, Injection site erythema, Injection site pain, ... Injected limb mobility decreased, Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling More
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Inject... Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: difficulty bending arm-Medium, Additional Details: Pt received Pneumovax 23 vaccine yesterday afternoon. Pt came to pharmacy this morning to report adverse effects of moderate arm pain, itchiness, swelling, and difficulty bending arm. More
2833820 30 F TX 03/31/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
X3M3D
Injection site erythema, Injection site rash, Lymph node pain, Lymphadenopathy, ... Injection site erythema, Injection site rash, Lymph node pain, Lymphadenopathy, Rash More
Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)... Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Lymph Node Swelling-Severe, Additional Details: rash around injection site and one-sided lymph node swelling. pain in axillary lymph nodes More
2833821 62 F WI 03/31/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
354m3
Injection site bruising, Injection site erythema, Injection site pain, Injection... Injection site bruising, Injection site erythema, Injection site pain, Injection site swelling More
Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Medium, Site: Redness at Injec... Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Additional Details: Patient is unsure about getting second vaccine and will talk to primary care before getting but she showed pharmacist photo of the vaccine site and it was extreamly red and swollen and brusing also present - more so than normal vacccine reaction site- Patient works at a doctor office and their MD (not her primary care) glanced at it when it occured and stated it looked like a cellilutis reaction due to infection at the site. went away after 3 days though More
2833822 41 F HI 03/31/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
XXPN4
Syncope, Unresponsive to stimuli Syncope, Unresponsive to stimuli
Systemic: Fainting / Unresponsive-Mild, Additional Details: cUSTOMER CAM INFOR VACCINES. aFTER ADMIN... Systemic: Fainting / Unresponsive-Mild, Additional Details: cUSTOMER CAM INFOR VACCINES. aFTER ADMINISTERED CUSTOMER FELT FINE. wHEN GETTING UP CUSTOMER FAINTED I THEN CAUGHT HER. sHE HAD NO INJURIES AND EMS CHECKED HER OUT. CUSTOMER WAS FINE GOT UP AND LEFT. , Other Vaccines: VaccineTypeBrand: BOOSTRIX; Manufacturer: GSK; LotNumber: 39LB7; Route: IM; BodySite: LEFT DELTOID; Dose: 1; VaxDate: 03/23/2025 More
2833823 61 F NC 03/31/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
xx9n4
Injection site pain, Muscle spasms Injection site pain, Muscle spasms
Site: Pain at Injection Site-Medium, Additional Details: muscle was spasming in right arm Site: Pain at Injection Site-Medium, Additional Details: muscle was spasming in right arm
2833824 59 F FL 03/31/2025 TDAP
GLAXOSMITHKLINE BIOLOGICALS
xn575
Injection site erythema Injection site erythema
Site: Redness at Injection Site-Medium, Other Vaccines: VaccineTypeBrand: prevnar 20; Manufacturer:... Site: Redness at Injection Site-Medium, Other Vaccines: VaccineTypeBrand: prevnar 20; Manufacturer: pfizer; LotNumber: lx4483; Route: im; BodySite: right detoid; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: fluzone trivalent 2024-2025; Manufacturer: sanofi; LotNumber: UT8485LA; Route: IM; BodySite: left detoid; Dose: ; VaxDate: UNKNOWN More
2833825 64 F FL 03/31/2025 PNC21
MERCK & CO. INC.
y019158
Injection site bruising, Injection site erythema, Injection site pain, Injection... Injection site bruising, Injection site erythema, Injection site pain, Injection site swelling More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Severe, Site: Redness at Injec... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2833826 60 F IN 03/31/2025 PNC21
MERCK & CO. INC.
Y013009
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling, Pruritus More
Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Inject... Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Additional Details: Unknown what medication was given in the ER -- pt did get medrol dosepak filled from pharmacy after ER visit More
2833827 59 F MI 03/31/2025 PNC21
MERCK & CO. INC.
y019157
Dermatitis allergic, Injection site erythema, Injection site swelling, Injection... Dermatitis allergic, Injection site erythema, Injection site swelling, Injection site warmth More
Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Ras... Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Additional Details: area swollen and red, hot to the touch. Counselled to ice and start benadryl and discuss with dr if any further issues. More
2833828 20 F FL 03/31/2025 MENB
NOVARTIS VACCINES AND DIAGNOSTICS
77KA5
Dizziness, Syncope, Unresponsive to stimuli Dizziness, Syncope, Unresponsive to stimuli
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Additional Detai... Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient felt lightheaded/dizzy after receiving the vaccine. She felt faint but she was response and communicating with me the whole time. I offered to call 911 multiple times but patient insisted that she did not want us to call 911. She wanted to lie down for a few minutes. After a few minutes, she had some water and a granola bar and she felt better. I advised her to stay seated for a few more minutes which she did. She had indicated "no" on the fainting question on the consent form. More
2833829 67 F NY 03/31/2025 PNC21
PNC21
MERCK & CO. INC.
MERCK & CO. INC.
y019157
y019157
Arthralgia, Fatigue, Injection site erythema, Injection site pain, Lethargy; Ras... Arthralgia, Fatigue, Injection site erythema, Injection site pain, Lethargy; Rash More
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Ras... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Exhaustion / Lethargy-Mild, Systemic: Joint Pain-Medium, Additional Details: Patient presented back to the pharmacy 5 days after innoculation with Capvaxive with pain in shoulder and a 4 inch rash down her arm. I suggested she see her provider and take benadryl for the rash and advil/tylenol for the pain, Other Vaccines: VaccineTypeBrand: Shingles- Shingrix; Manufacturer: Glaxosmithkline; LotNumber: 55th4; Route: IM; BodySite: left arm; Dose: 1; VaxDate: 02/28/2025 More
2833830 40 F NY 03/31/2025 FLU4
FLU4
FLU4
FLU3
FLU3
FLU3
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
u8518ca
u8518ca
u8518ca
U8518CA
U8518CA
U8518CA
Hypoaesthesia, Injection site bruising, Injection site erythema, Injection site ... Hypoaesthesia, Injection site bruising, Injection site erythema, Injection site haemorrhage, Injection site hypoaesthesia; Injection site pain, Injection site swelling; Hypoaesthesia, Injection site bruising, Injection site haemorrhage, Injection site hypoaesthesia; Hypoaesthesia, Injection site bruising, Injection site erythema, Injection site haemorrhage, Injection site hypoaesthesia; Injection site pain, Injection site swelling; Hypoaesthesia, Injection site bruising, Injection site haemorrhage, Injection site hypoaesthesia More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injec... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: Patient noticed excessive bleeding and numbness in the area, Other Vaccines: VaccineTypeBrand: Fluzone; Manufacturer: sanofi; LotNumber: u8518ca; Route: IM; BodySite: Left Arm; Dose: ; VaxDate: UNKNOWN More
2833831 49 F FL 03/31/2025 HEPAB
HEPAB
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
4ds4n
4ds4n
Arthralgia, Flushing, Hyperhidrosis, Injection site bruising, Injection site ery... Arthralgia, Flushing, Hyperhidrosis, Injection site bruising, Injection site erythema; Injection site pain, Injection site swelling, Nausea More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injec... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Joint Pain-Mild, Systemic: Nausea-Mild More
2833832 63 F RI 03/31/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
y7rz7
Injection site pain Injection site pain
Site: Pain at Injection Site-Mild, Additional Details: pt reports months later she just feels tender... Site: Pain at Injection Site-Mild, Additional Details: pt reports months later she just feels tender and still feels the spot and on occasion it still bothers her at the site of injection More
2833833 72 F NJ 03/31/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
55th4
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Mild, Site: Swelling at Injecti... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild More
2833834 32 F CA 03/31/2025 TDAP
GLAXOSMITHKLINE BIOLOGICALS
PG3RP
Asthenia, Hypoaesthesia, Hyporesponsive to stimuli, Muscular weakness, Speech di... Asthenia, Hypoaesthesia, Hyporesponsive to stimuli, Muscular weakness, Speech disorder More
Systemic: MUSCLE WEAKNESS, NUMBNESS OF ARMS-Severe, Systemic: Numbness (specify: facial area, extrem... Systemic: MUSCLE WEAKNESS, NUMBNESS OF ARMS-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Weakness-Severe, Additional Details: NUMBNESS OF ARM. WAS ABLE TO SIP WATER AND BREATH NORMALLY THROUGH NOSE. HAVING HARD TIME TO TALK. WAS CONSCIOUS AND ANSWERED SLOWLY. PT WAS ON WHEELCHAIR WHEN CAME IN BUT SHE WAS ABLE TO WALK TO VACCINE ROOM More
2833835 80 M MN 03/31/2025 COVID19
PFIZER\BIONTECH
LM7786
Injection site swelling, Peripheral swelling Injection site swelling, Peripheral swelling
Site: Swelling at Injection Site-Mild, Additional Details: patient had a swelling in arm. had patien... Site: Swelling at Injection Site-Mild, Additional Details: patient had a swelling in arm. had patient wait for 20-25 minutes and ice the site. patient said the site recovered by time he got home (called at 5pm and got shot around noon) More
2833836 35 F FL 03/31/2025 PNC21
MERCK & CO. INC.
Y019158
Injection site erythema, Injection site pain, Injection site swelling, Injection... Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth More
Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injec... Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Additional Details: patient called 3/26/2025 complaining that her injection arm was still swollen, red, hot and burning sensation that started later in the day after receiving her vaccine and has continued for 5 days so far and seems to be getting worse with no relief. She is following up with urgent care or her physician. More
2833837 69 F IL 03/31/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
55th4
Blood disorder, Deep vein thrombosis, Injection site pain Blood disorder, Deep vein thrombosis, Injection site pain
Site: Pain at Injection Site-Mild, Systemic: Blood Disorder (diagnosed by MD)-Severe, Additional De... Site: Pain at Injection Site-Mild, Systemic: Blood Disorder (diagnosed by MD)-Severe, Additional Details: dvt, Other Vaccines: VaccineTypeBrand: abrysvo; Manufacturer: pfizer; LotNumber: kd0161; Route: im; BodySite: right arm; Dose: ; VaxDate: UNKNOWN More
โœ“
2833838 54 M CT 03/31/2025 PNC21
MERCK & CO. INC.
y019157
Injection site erythema, Injection site pain Injection site erythema, Injection site pain
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium
2833839 50 M NY 03/31/2025 TDAP
GLAXOSMITHKLINE BIOLOGICALS
L5229
Injection site erythema, Injection site pruritus, Injection site swelling Injection site erythema, Injection site pruritus, Injection site swelling
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 More
2833840 33 F FL 03/31/2025 MMR
MMR
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
955E2
955E2
Asthenia, Confusional state, Dizziness, Dyspnoea, Headache; Nausea, Syncope, Unr... Asthenia, Confusional state, Dizziness, Dyspnoea, Headache; Nausea, Syncope, Unresponsive to stimuli More
Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Light... Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Headache-Mild, Systemic: Nausea-Mild, Systemic: Weakness-Mild, Other Vaccines: VaccineTypeBrand: Boostrix; Manufacturer: Glaxosmith; LotNumber: Dy3K7; Route: im; BodySite: LEFT; Dose: 1; VaxDate: 03/26/2025, VaccineTypeBrand: Heplisav b; Manufacturer: Zb Dynavax; LotNumber: 945659; Route: im; BodySite: Right; Dose: 1; VaxDate: 03/26/2025, VaccineTypeBrand: Flucevax; Manufacturer: Zb Sequirus; LotNumber: 946636; Route: im; BodySite: Right; Dose: 1; VaxDate: 03/26/2025 More
2833841 23 F CA 03/31/2025 HEP
HEP
DYNAVAX TECHNOLOGIES CORPORATION
DYNAVAX TECHNOLOGIES CORPORATION
945663
945663
Asthenia, Dehydration, Fatigue, Influenza like illness, Lethargy; Nausea, Vomiti... Asthenia, Dehydration, Fatigue, Influenza like illness, Lethargy; Nausea, Vomiting More
Systemic: Exhaustion / Lethargy-Severe, Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Systemic... Systemic: Exhaustion / Lethargy-Severe, Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Systemic: Weakness-Severe, Additional Details: Mom of pt called complaining that pt had severe nausea/ vomiting and flu like symptoms. Unable to keep down food/ liquids and so dehydrated and pt is a diabetic so had to end up going to the hospital More
2833842 72 F PA 03/31/2025 RSV
RSV
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
49H4G
49H4G
Injection site erythema, Injection site induration, Injection site oedema, Injec... Injection site erythema, Injection site induration, Injection site oedema, Injection site pain, Injection site pruritus; Injection site swelling More
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Inject... 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 experienced pain, redness and edema of right arm (down to elbow). The arm was also hard to the touch. , Other Vaccines: VaccineTypeBrand: pneumo conjugate (Prevnar 20); Manufacturer: Pfizer; LotNumber: LJ5284; Route: intramuscular; BodySite: arm, side unknown; Dose: ; VaxDate: UNKNOWN More
2833843 30 M CA 03/31/2025 COVID19
MODERNA
3043391
Syncope, Unresponsive to stimuli Syncope, Unresponsive to stimuli
Systemic: Fainting / Unresponsive-Medium Systemic: Fainting / Unresponsive-Medium
2833844 61 F NY 03/31/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
xx9n4
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Other Vaccines: VaccineTypeBrand: twinrx; Manufacturer: ; LotNumber: m4b34; Route: IM; BodySite: left delt; Dose: 1; VaxDate: 03/02/2025, VaccineTypeBrand: prevnar20; Manufacturer: ; LotNumber: lx2497; Route: IM; BodySite: right delt; Dose: 1; VaxDate: 03/02/2025 More
2833845 75 M MO 03/31/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
49h4g
Fear, Hallucination, Injection site pain, Insomnia Fear, Hallucination, Injection site pain, Insomnia
Site: Pain at Injection Site-Mild, Systemic: hallucinations-Medium, Additional Details: patient stat... Site: Pain at Injection Site-Mild, Systemic: hallucinations-Medium, Additional Details: patient stated he experienced hallucinations after receiving the vaccine- the vaccine was given 3-26-25 12:41pm and patient started hallucinations from 2am to 5am the next morning. He stated that they were very severe and he could not sleep and was terrified. Patient came in today 3-28-25 and stated that the hallucinations went away and only lasted for 3-4 hours and he was able to sleep last night 3-27-25. More
2833846 77 F IL 03/31/2025 DTAPIPVHIB
SANOFI PASTEUR
UK043AA
Wrong product administered Wrong product administered
Pt given pentacel in error Pt given pentacel in error
2833847 52 F PA 03/31/2025 COVID19
MODERNA
025lz1b
Tinnitus Tinnitus
About 3-4 weeks after Moderna booster for Covid,( J&J done in 2021 with no issues, I developed s... About 3-4 weeks after Moderna booster for Covid,( J&J done in 2021 with no issues, I developed severe left ear tinnitus and moderate right ear tinnitus. It is acute and doesn?t ease up. More
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2833848 7 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given 1 month expired vaccine. Scheduled for revaccination. Patient given 1 month expired vaccine. Scheduled for revaccination.
2833849 2 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient administered expired vaccine (5 days). Provider will decide whether to revaccinate Patient administered expired vaccine (5 days). Provider will decide whether to revaccinate
2833850 2 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient administered 5 day expired vaccine. Revaccination to be determined by provider Patient administered 5 day expired vaccine. Revaccination to be determined by provider
2833851 41 F UT 03/31/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
LP1776
LP1776
Dyspnoea, Euphoric mood, Fatigue, Flushing, Injection site discomfort; Pain in e... Dyspnoea, Euphoric mood, Fatigue, Flushing, Injection site discomfort; Pain in extremity More
WAITED FOR 15 MINUTES IN CAR. RETURNED TO CLINIC SINCE EXPERIENCING SHORTNESS OF BREATH, FLUSHED FAC... WAITED FOR 15 MINUTES IN CAR. RETURNED TO CLINIC SINCE EXPERIENCING SHORTNESS OF BREATH, FLUSHED FACE, FEELING LIKE HIGH. STATED ARM WITH VACCINATION FEELING TIGHT FROM INJECTION SITE TO FOREARM. HAD CLIENT DRINK FLUID. OFFERED BENADRYL. DECLINED. BLOOD PRESSURE, PULSE, AND O2 SATS MONITORED FOR ABOUT 30 MINUTES. HAD CLIENT RECLINE AND REST IN A CHAIR IN ROOM. REASSURED. ENCOURAGED TO SEE PCP OR GO TO URGENT CARE IF CONTINUE TO EXPERIENCE SYMPTOMS. More
2833852 5 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient was administered expired vaccine. Scheduled for revaccination Patient was administered expired vaccine. Scheduled for revaccination
2833853 31 M UT 03/31/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS

Wrong product administered Wrong product administered
Incorrect vaccine administration Incorrect vaccine administration
2833854 6 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given expired vaccine. Will revaccinate, Patient given expired vaccine. Will revaccinate,
2833855 F TX 03/31/2025 DTAPHEPBIP
HIBV
PNC20
RV5
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.




Eye movement disorder, Lethargy, Nausea, Somnolence, Vomiting projectile; Eye mo... Eye movement disorder, Lethargy, Nausea, Somnolence, Vomiting projectile; Eye movement disorder, Lethargy, Nausea, Somnolence, Vomiting projectile; Eye movement disorder, Lethargy, Nausea, Somnolence, Vomiting projectile; Eye movement disorder, Lethargy, Nausea, Somnolence, Vomiting projectile More
She received four vaccinations at her six-month appointment, including the rotavirus vaccine, Pediar... She received four vaccinations at her six-month appointment, including the rotavirus vaccine, Pediarix (a combination of tetanus, hepatitis B, and polio), Hib for haemophilus influenza type B, and Prevnar for strep pneumo. Approximately four to five hours post-vaccination, she became lethargic, with her eyes rolling back and difficulty waking up, and experienced projectile vomiting. These symptoms persisted until about eight to twelve hours after the vaccinations. She was taken to the emergency room, where she received Zofran for nausea, and the vomiting subsided by the evening. There was no recollection of fever or diarrhea accompanying the vomiting, and she did not require IV fluids. The caregiver could not recall if she had a fever during the reaction, although she typically runs a low-grade fever after vaccinations. More
2833856 8 M 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given expired vaccine. Will reschedule for repeat dose. Patient given expired vaccine. Will reschedule for repeat dose.
2833857 0.58 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient received expired vaccine. (5 days expired) Provider to determine revaccination. Patient received expired vaccine. (5 days expired) Provider to determine revaccination.
2833858 0.5 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given 5 day expired vaccine. Provider to determine revaccination Patient given 5 day expired vaccine. Provider to determine revaccination
2833859 10 M CT 03/31/2025 VARCEL
MERCK & CO. INC.
Y011015
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Patient med record reviewed, mom reports having additional documentation not presented. Vaccine dos... Patient med record reviewed, mom reports having additional documentation not presented. Vaccine dose given too soon. No adverse reaction noted. Discussed with mom to monitor for any adverse effects and follow up. More
2833860 7 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given expired vaccine. Revaccination scheduled Patient given expired vaccine. Revaccination scheduled
2833861 6 F 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given expired vaccine. Revaccination scheduled Patient given expired vaccine. Revaccination scheduled
2833862 8 M 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient given expired vaccine. (7 days) Recommend revaccination. Patient given expired vaccine. (7 days) Recommend revaccination.
2833863 8 M CT 03/31/2025 HEPA
VARCEL
MERCK & CO. INC.
MERCK & CO. INC.
Y013120
Y011015
Inappropriate schedule of product administration, No adverse event; Inappropriat... Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event More
Not sufficient time between dose. No apparent Rx noted. immunization record reviewed, mom reports ha... Not sufficient time between dose. No apparent Rx noted. immunization record reviewed, mom reports having additional documents not turned in for review. Dose administered and upon follow up noted patient already received the vaccine previously. Denies any symptoms at time of visit. Discussed with Mom. No treatment required at this time. More
2833864 68 M WA 03/31/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
A5T73
Injection site erythema, Injection site warmth, Rash, Rash papular, Skin warm Injection site erythema, Injection site warmth, Rash, Rash papular, Skin warm
The day after the shot he had a red, warm area the size of a baseball at the injection site. He als... The day after the shot he had a red, warm area the size of a baseball at the injection site. He also had a "rash" raised, warm area on his upper left chest area. More
2833865 4 M 03/31/2025 COVID19
PFIZER\BIONTECH

Expired product administered Expired product administered
Patient received expired vaccine. Provider to determine revaccination. Patient received expired vaccine. Provider to determine revaccination.
2833866 70 F FL 03/31/2025 COVID19
MODERNA
3042645
Chills, Headache, Pain, Photophobia, Pyrexia Chills, Headache, Pain, Photophobia, Pyrexia
Sensitive to light, fever, chills, body aches, headache Sensitive to light, fever, chills, body aches, headache
2833867 42 F FL 03/31/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
4N222
Incorrect route of product administration Incorrect route of product administration
The vaccine was administered IM vs SQ The vaccine was administered IM vs SQ
2833868 11 M TX 03/31/2025 HPV9
MNQ
TDAP
MERCK & CO. INC.
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
y010466
u8256ba
x449y
Disturbance in attention, Pruritus, Rash, Skin irritation, Urticaria; Disturbanc... Disturbance in attention, Pruritus, Rash, Skin irritation, Urticaria; Disturbance in attention, Pruritus, Rash, Skin irritation, Urticaria; Disturbance in attention, Pruritus, Rash, Skin irritation, Urticaria More
Mother reports that student developed what appeared to be urticaria on the patient's arms the m... Mother reports that student developed what appeared to be urticaria on the patient's arms the morning after the vaccine. Mother reports that student is consistently itching and complaining of irritation. School nurse contacted mother today because patient could not focus in class. Mother still reports that the rash is spreading. denies rash on face. denies SOB. denies facial swelling, trouble swallowing, or swelling of the tongue. denies nausea, diarrhea, or vomiting. mother reports that student was given "ointment" at school but was unaware. School nurse confirms urticaria and denies patient receiving ointment at school. More