🏥 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 💀 🏥 🚑 ♿ ⚠️
2831430 49 F FL 03/14/2025 RAB
RAB
 SANOFI PASTEUR
SANOFI PASTEUR
 X1B611M
X1B611M
Asthenia, Chills, Decreased appetite, Fatigue, Headache; Influenza virus test ne... Asthenia, Chills, Decreased appetite, Fatigue, Headache; Influenza virus test negative, Laboratory test normal, Pyrexia, Vomiting More
The donor disclosed that on 02/20/25 after the Rabies immunization was received, later that night sh... The donor disclosed that on 02/20/25 after the Rabies immunization was received, later that night she started having low fever (100.1 C), chills, loss of appetite, fatigue, weakness and headache. She stated that the following day, she had the same symptoms and vomiting. Donor then went to an Urgent Care to seek medical attention. There she was prescribed Tylenol for the symptoms and was tested for Influenza and respiratory infections with negative results. Symptoms describe above persisted for 3 days. More
2831431 71 M FL 03/14/2025 PNC20
 PFIZER\WYETH
 LK6650
Extra dose administered Extra dose administered
PATIENT RECEIEVED VACCINE IN 2024. VACCINE GIVEN IN 2025 WAS NOT NEEDED PATIENT RECEIEVED VACCINE IN 2024. VACCINE GIVEN IN 2025 WAS NOT NEEDED
2831433 68 F AR 03/14/2025 COVID19
 MODERNA
 204G23A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831434 56 M AR 03/14/2025 COVID19
 MODERNA
 033H21A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831435 76 M AR 03/14/2025 COVID19
 PFIZER\BIONTECH
 HG4589
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831437 66 F AR 03/14/2025 COVID19
 MODERNA
 002C21A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831438 14 F IL 03/14/2025 HPV9
 MERCK & CO. INC.
 Y018398
Syncope Syncope
Patient fainted after receiving HPV vaccine. Patient fainted after receiving HPV vaccine.
2831439 37 F TX 03/14/2025 FLU3
 SEQIRUS, INC.
 946598
Immediate post-injection reaction, Injection site pain, Joint range of motion de... Immediate post-injection reaction, Injection site pain, Joint range of motion decreased, Joint stiffness, Product administered at inappropriate site More
At time of injection, there was more pain that past experiences. Noticed that injector placed bandai... At time of injection, there was more pain that past experiences. Noticed that injector placed bandaid very high on top of shoulder after injection. Soreness was immediate and progressively got worse with pain during any movement, stiffness of joint, loss of range of motion. OTC medications were taken to ease pain. This continued for 2 months with no improvement of symptoms. Saw an orthopedic surgeon that gave one dose of steroid injection into joint. This relieved pain for 2 weeks. Pain returned after that and has not improved. Pain continues with passive movement. Pain during sleep. Unable to lay on left shoulder due to pain. More
2831440 76 M AR 03/14/2025 COVID19
 MODERNA
 013F21A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831441 62 M AR 03/14/2025 COVID19
 MODERNA
 056A22A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831442 72 F FL 03/14/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 FP4554
FP4554
FP4554
Aspiration bone marrow, Blood iron, Blood uric acid, Full blood count, Janus kin... Aspiration bone marrow, Blood iron, Blood uric acid, Full blood count, Janus kinase 2 mutation; Metabolic function test, Platelet count increased, Serum ferritin, Thrombocytopenia; Gene mutation identification test positive, Janus kinase 2 mutation, Platelet count, Platelet count increased, Thrombocytopenia; Aspiration bone marrow, Blood iron, Blood uric acid, Full blood count, Janus kinase 2 mutation; Metabolic function test, Platelet count increased, Serum ferritin, Thrombocytopenia; Gene mutation identification test positive, Janus kinase 2 mutation, Platelet count, Platelet count increased, Thrombocytopenia More
Exactly a year after my fourth covid vaccine my platelet count started to increase. In April, 2024,... Exactly a year after my fourth covid vaccine my platelet count started to increase. In April, 2024, I was diagnosed with essential thrombocytopenia and in May 2024 I tested positive for the JAK 2 gene. More
2831443 1.25 F PA 03/14/2025 MMR
 MERCK & CO. INC.
Heart rate decreased, Irritability, Pain of skin, Pyrexia, Rash Heart rate decreased, Irritability, Pain of skin, Pyrexia, Rash
Fever of 103.5 for 3 days, full body rash for 4 days, cranky and irritable, skin hurt to touch, lowe... Fever of 103.5 for 3 days, full body rash for 4 days, cranky and irritable, skin hurt to touch, lower heart rate when sleeping More
2831444 33 F MA 03/14/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 FF2593
FF2593
FF2593
Anxiety, C-reactive protein increased, Chest discomfort, Colitis ulcerative, Con... Anxiety, C-reactive protein increased, Chest discomfort, Colitis ulcerative, Condition aggravated; Heart rate increased, Injection site pain, Lymphocyte percentage decreased, Neutrophil count increased, Neutrophil percentage increased; Palpitations, Platelet count normal, Red blood cell sedimentation rate increased, White blood cell count increased More
I began having chest pressure daily starting on the day of vaccination (10/14/21) along with palpita... I began having chest pressure daily starting on the day of vaccination (10/14/21) along with palpitations. It lasted for about 10 minute intervals and caused anxiety and elevated heart rate. I also had multiple flare ups of my ulcerative colitis that was well controlled prior to this vaccination. One of these flares required hospitalization on March 3rd, 2024. My labs from 3/4/2024 included a CRP of 137, ESR of 40, WBC of 15.9, Neutrophils 85.3, Neutrophils absolute 13.59, Lymphocytes 7.9. on 3/6/24 my platelets were 389. All of these numbers showing a high level of systemic inflammation in my body. I still get chest pressure and palpitations at least occurring once a month since vaccination. Also, I have chronic pain in my left arm from my shoulder to my elbow in the same arm I was vaccinated in. This still occurs today, and is constant 3/10 pain. I get no relief from analgesics. More
2831445 26 F MI 03/14/2025 HEP
HEP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 Y004552
Y004552
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
No adverse symptoms noted at time of administration. No adverse symptoms noted at time of administration.
2831446 74 M FL 03/14/2025 PNC20
 PFIZER\WYETH
 lk6650
Extra dose administered Extra dose administered
none, but duplicate vaccine last given 03/14/2023 none, but duplicate vaccine last given 03/14/2023
2831447 54 M CA 03/14/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 K2BB7
K2BB7
Headache, Hyperhidrosis, Injection site pain, Presyncope, Unresponsive to stimul... Headache, Hyperhidrosis, Injection site pain, Presyncope, Unresponsive to stimuli; Vision blurred More
Patient reported pain upon injection of dissolved Shingrix liquid in the vaccine room and I had him ... Patient reported pain upon injection of dissolved Shingrix liquid in the vaccine room and I had him report to the consultation window for information on the booster date and observation. As I discussed the date range for 2-6 months he closed his eyes, leaned toward the consultation window and did not respond to verbal greeting. I ran out to him and had him sit down. I asked if he had breakfast and drank water today. He reported he had had breakfast but had not drank water for 1-2 days, just coffee that made him void. The blood pressure cuff from the vaccine room did not produce a value upon 3 attempts so a floor wrist BP monitor was utilized which also did not show a value. I told him there was sweat on his brow. He called his wife and she said she would come. I asked her to bring a BG monitor because his BP could be low, his BP was being measures and he could be having an allergic reaction. A bottle of water was given with 2 Hershey kiss candies.. Patient reported a lump in his throat, no chest, arm or neck pain, blurring vision and a headache. Paramedics were called. After the second water bottle was given with more chocolate I called his wife again. She was headed to the hospital, per her text but we notified her that we were still waiting for the paramedics. She said she would come to the pharmacy When the paramedics arrived I reported his symptoms with him. He was verbal, conscious. alert and oriented. This headache and blurred vision were improving and he was able to open his eyes again. Paramedics reported low BP about 70/50 and normal BG about 120. Paramedics had his care under control so I returned to the pharmacy for the care of other patients. Patient left with the paramedics. Called MD office spoke with medical assistant. Noted if he wants the 2nd Shringx vaccine and it is determined to not be an allergic reaction, he should get it at the MD office rather than the pharmacy. 6:20PM Called ER. He had been discharged. He did not answer his cell phone but ER released wife's cell phone. She said he is home and fine. It was a vasovagal reaction (suspected). More
2831448 17 F VA 03/14/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 945656
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Hepsilav B administered. Upon documentation of Hepsilav , flagged that should only be used in 18 yea... Hepsilav B administered. Upon documentation of Hepsilav , flagged that should only be used in 18 years and older adults. Discussed with provider and practice manager. Provider notified patient. Practice manager notified parent (mother). More
2831449 22 M TX 03/14/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
Bursitis, Pain, Swelling Bursitis, Pain, Swelling
Two days after the MMR 1 Vaccine was administered, Bursitis began developing in the right arm. Over ... Two days after the MMR 1 Vaccine was administered, Bursitis began developing in the right arm. Over the next two days, the Bursitis increased in pain and swelling. More
2831450 72 F 03/14/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 LM2215
U8499DA
Mobility decreased; Mobility decreased Mobility decreased; Mobility decreased
patient states she is unable to move her LEFT arm appropriately. patient states she is unable to move her LEFT arm appropriately.
2831452 4 F OH 03/14/2025 MMR
 MERCK & CO. INC.
Vomiting Vomiting
Vomiting twice morning after getting vaccine Vomiting twice morning after getting vaccine
2831453 0.5 M MI 03/14/2025 DTPPVHBHPB
PNC20
RV5
 MSP VACCINE COMPANY
PFIZER\WYETH
MERCK & CO. INC.
 U7921AA
LG5574
2073367
Injection site nodule; Injection site nodule; Injection site nodule Injection site nodule; Injection site nodule; Injection site nodule
Patient has had no previous reactions to vaccines. Left leg had localized small hard nodule within 1... Patient has had no previous reactions to vaccines. Left leg had localized small hard nodule within 1.5 hours of Vaxelis. Right leg had localized small hard nodule within 4 hours of PCV20. Patient was sore. Normal vaccine reactions except patient has not had this previously occur and has received the same vaccines in the past but with different lot numbers. More
2831454 62 M FL 03/14/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 JB27A
Extra dose administered, No adverse event Extra dose administered, No adverse event
Pharmacy administered a second RSV vaccine because patient did not remember previously receiving on ... Pharmacy administered a second RSV vaccine because patient did not remember previously receiving on in September 2023. Patient has two shot records and confirmed both are his (current address and previous address) and pharmacy only pulled up his older one at time of administration. Patient has not experienced any adverse events and says he feels fine. More
2831455 40 M MN 03/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Arthritis Arthritis
Severe, completely debilitating, polyarticular inflammatory arthritis that was resistant to high do... Severe, completely debilitating, polyarticular inflammatory arthritis that was resistant to high dose NSAIDs and steroids. Has lasted >2 weeks. He has been on dexamethasone 6mg 2x daily with gradual improvement in symptoms. More
2831456 29 F PA 03/14/2025 TDAP
 SANOFI PASTEUR
 2CA61C1
Wrong product administered Wrong product administered
Administration error in that this employee was given TDap vaccine instead of her second Hepatitis B ... Administration error in that this employee was given TDap vaccine instead of her second Hepatitis B vaccine. Nurse administering the vaccine, noted it after she administered it. had last dose of TDAp in 2022. More
2831457 5 M TX 03/14/2025 DTAPIPV
HEPA
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 42Y93
TF27T
Y014435
Extra dose administered, Nausea, No adverse event; Extra dose administered, Naus... Extra dose administered, Nausea, No adverse event; Extra dose administered, Nausea, No adverse event; Extra dose administered, Nausea, No adverse event More
patient did not have any Adverse events but was given 3 doses of DTAP-IPV (KINRIX) and MMRV (PROQUAD... patient did not have any Adverse events but was given 3 doses of DTAP-IPV (KINRIX) and MMRV (PROQUAD). Second dose was given on 10/09/2024 and third dose given on 03/11/2025. Mother to patient is worried about any reactions. Patient has not had any adverse reactions at this time. Patient was diagnosed with influenza on 03/10/2024. No severe symptoms were ongoing at the time of vaccine. patient was prescribed Ondansetron was prescribed for nausea. We have informed mom we will report the extra vaccination. There are no adverse events at this time from the vaccines given. More
2831458 54 F AZ 03/14/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
Mobility decreased, Shoulder injury related to vaccine administration Mobility decreased, Shoulder injury related to vaccine administration
SIRVA within 24 hours of injection; treated initially w NSAIDs. Unable to move arm at 48 hours so e... SIRVA within 24 hours of injection; treated initially w NSAIDs. Unable to move arm at 48 hours so escalated to prednisolone 30mg daily x 5 days More
2831459 84 F AR 03/14/2025 COVID19
 MODERNA
 022N20A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831460 1.42 M AZ 03/14/2025 MMR
MMR
 MERCK & CO. INC.
MERCK & CO. INC.
 R035701
R035701
Attention deficit hyperactivity disorder, Autism spectrum disorder, Fine motor d... Attention deficit hyperactivity disorder, Autism spectrum disorder, Fine motor delay, Gross motor delay, Laboratory test; Pyrexia More
Fevers of 106 degrees. Taken to 3 ERs, (admitted for 11 days). Currently having ADHD symptomology,... Fevers of 106 degrees. Taken to 3 ERs, (admitted for 11 days). Currently having ADHD symptomology, delays in fine motor and gross motor skills, and some austistic features. More
✓ ✓
2831461 79 M AR 03/14/2025 COVID19
 MODERNA
 3043030
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831462 63 M TN 03/14/2025 PNC20
 PFIZER\WYETH
 LC5482
Extra dose administered Extra dose administered
Patient insurance alerted to a duplicate paid claim from 02/01/2023 for prevnar 20. Patient didn... Patient insurance alerted to a duplicate paid claim from 02/01/2023 for prevnar 20. Patient didn't remember receiving in the past but accidentally got a second dose of vaccine. More
2831463 84 F AR 03/14/2025 COVID19
 MODERNA
 061F22A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831464 40 M AR 03/14/2025 COVID19
 MODERNA
 066H21A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831465 64 F AR 03/14/2025 COVID19
 MODERNA
 45J21A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831466 3 M MI 03/14/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 TF27T
Inappropriate schedule of product administration Inappropriate schedule of product administration
Vaccine given to early. Vaccine given to early.
2831467 0.75 F AR 03/14/2025 COVID19
 PFIZER\BIONTECH
 LN8272
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831468 82 F AR 03/14/2025 COVID19
 MODERNA
 060F22A
COVID-19 COVID-19
covid infection with hospitalization after vaccination covid infection with hospitalization after vaccination
2831469 68 F 03/14/2025 PNC20
TDAP
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS

Extra dose administered, No adverse event, Wrong patient; Extra dose administere... Extra dose administered, No adverse event, Wrong patient; Extra dose administered, No adverse event, Wrong patient More
This patient was given the Prevnar20 and Boostrix vaccine under the account of another person who ha... This patient was given the Prevnar20 and Boostrix vaccine under the account of another person who has a very similar name. The vaccines were processed and given under the wrong patient's profile. The patient who received the vaccines was actually due for the Boostrix vaccine but not for the Prevnar20 because she has already received it. The mistake was realized when we recommended these vaccines to a patient. The patient stated that she had already received a few weeks prior. We could not find it on her profile since it was processed for the wrong patient with a similar name. After investigating, we were able to locate the consent form that showed we gave the vaccines to the incorrect patient. The patient was advised and informed of the mistake. Has not experienced any adverse reactions. More
2831470 70 F MI 03/14/2025 FLU3
 SANOFI PASTEUR
 UT8437BA
Extra dose administered Extra dose administered
Client received 24/25 high dose trivalent flu vaccine at pharmacy on 8/20/24. Client to this clinic ... Client received 24/25 high dose trivalent flu vaccine at pharmacy on 8/20/24. Client to this clinic on 9/19/24 for 2nd vaccination. 2nd dose of vaccine was given without knowledge of receiving the first dose on 8/20/24. More
2831472 17 M ME 03/14/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 4T93R
Incorrect dose administered Incorrect dose administered
CLIENT IS A 17-YEAR-OLD MALE. HE RECEIVED A 1.0 CC ADULT DOSE OF HEPATITIS A VACCAINE RATHER THAN T... CLIENT IS A 17-YEAR-OLD MALE. HE RECEIVED A 1.0 CC ADULT DOSE OF HEPATITIS A VACCAINE RATHER THAN THE 0.5CC HEPATITIS A CHILD DOSE More
2831473 19 F 03/14/2025 HEP
 MERCK & CO. INC.
 Y018229
Incorrect dose administered Incorrect dose administered
Pt given one 1mL dose of Hep b instead of 0.5mL dose. Pt given one 1mL dose of Hep b instead of 0.5mL dose.
2831474 11 M MI 03/14/2025 MENB
 PFIZER\WYETH
 GF4143
Wrong product administered Wrong product administered
Patient was given menB when he was supposed to get MenQuadValent. Patient is going to be scheduled f... Patient was given menB when he was supposed to get MenQuadValent. Patient is going to be scheduled for the correct vaccine. More
2831475 67 F AL 03/14/2025 PNC20
 PFIZER\WYETH
 LG5579
Extra dose administered, No adverse event Extra dose administered, No adverse event
No adverse event occurred pt feels fine. Pt had previously received a shot on 9/29/22. No adverse event occurred pt feels fine. Pt had previously received a shot on 9/29/22.
2831476 1.25 M MD 03/14/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 P224H
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient given 3rd dose of seasonal influenza vaccine in error, only required 2 doses of vaccination ... Patient given 3rd dose of seasonal influenza vaccine in error, only required 2 doses of vaccination for 2024-2025 season as this was the patient's first time receiving the flu vaccine. No known adverse effects/side effects from erroneous administration. More
2831477 63 M 03/14/2025 PNC21
 MERCK & CO. INC.
 Y011819
Extra dose administered, No adverse event Extra dose administered, No adverse event
Pt received CAPVAXIVE on Feb. 13th 2025. Pt received second dosing of CAPVAXIVE on MArch 14th 2025. ... Pt received CAPVAXIVE on Feb. 13th 2025. Pt received second dosing of CAPVAXIVE on MArch 14th 2025. CAPVAXIVE is a one time dose. Medical team and pt were alerted. Pt was notified and pt denied any adverse reaction or symptoms. Pt was told to contact medical team if adverse reactions occured. Pt verbalized understanding. More
2831478 59 F MA 03/14/2025 PNC20
 PFIZER\WYETH
 LX4483
Injection site erythema, Injection site pain, Injection site warmth Injection site erythema, Injection site pain, Injection site warmth
States it feels hot, it's red, painful to move and itchy. Redness has spread all the way around... States it feels hot, it's red, painful to move and itchy. Redness has spread all the way around underarm More
2831479 38 F ME 03/14/2025 UNK
 UNKNOWN MANUFACTURER
 Y011637
Burning sensation Burning sensation
patient experiencing a burning sensation all over the body. patient experiencing a burning sensation all over the body.
2831480 1.25 M 03/14/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UJ984AA
Expired product administered Expired product administered
The vaccine that was given is expired The vaccine that was given is expired
2831481 56 F MI 03/14/2025 HEP
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 3X937
LX4483
Injection site erythema, Injection site swelling, Pruritus, Rash; Injection site... Injection site erythema, Injection site swelling, Pruritus, Rash; Injection site erythema, Injection site swelling, Pruritus, Rash More
Patient was here for an appointment on 3/10/25 when vaccines were received. Patient stated that MA g... Patient was here for an appointment on 3/10/25 when vaccines were received. Patient stated that MA gave both into the same arm. Patient started itching this morning and noticed redness on arm. When I came to check on the reaction, patient has redness and swelling at injection site and all arm inside of arm down to her elbow. No fever, shortness of breath. Explained to her that this is a common reaction but gave another VIS sheet and discussed extreme reactions to contact doctor. More
2831482 17 F WA 03/14/2025 MENB
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
 3L339
U8370AA
Injection site erythema, Injection site nodule, Injection site warmth; Injection... Injection site erythema, Injection site nodule, Injection site warmth; Injection site erythema, Injection site nodule, Injection site warmth More
Patient reported first noticed on Wednesday, 3/12, firm nodule on RT shoulder/deltoid with surroundi... Patient reported first noticed on Wednesday, 3/12, firm nodule on RT shoulder/deltoid with surrounding warmth and minor redness. Today (3/14/25) redness and warmth have resolved. RT firm nodule not tender or painful. Full active ROM without pain or tenderness. No s/sx of infection. Recommend warm compresses to site and f/u on Monday (3/17) if not continuing to improve. More
2831483 72 F NY 03/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Influenza like illness, Rash, Rash macular Influenza like illness, Rash, Rash macular
pt felt flu like symptoms for 24 hours and then today noticed diffuse macular rash to chest, abdomen... pt felt flu like symptoms for 24 hours and then today noticed diffuse macular rash to chest, abdomen and back More
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