🏥 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 💀 🏥 🚑 ♿ ⚠️
2821251 86 M IA 01/16/2025 COVID19
 MODERNA
 3043159
Death Death
Death Death
✓
2821252 42 F FL 01/16/2025 PPV
PPV
PPV
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.


Hypersensitivity, Immediate post-injection reaction, Injection site erythema, In... Hypersensitivity, Immediate post-injection reaction, Injection site erythema, Injection site inflammation, Injection site pain; Injection site pruritus, Injection site reaction, Injection site swelling, Injection site warmth, Skin tightness; Urticaria More
Injection site was red and itchy immediately after injection. Hydrocortisone cream was applied to th... Injection site was red and itchy immediately after injection. Hydrocortisone cream was applied to the site and the itching was relieved. As the day progressed, the injection site and surrounding tissue started to swell, eventually resulting in a welt approximately 4 inches wide and 2 inches long. The area was warm, painful to the touch, and felt swollen/the skin felt tight. As the welt grew, the welt itself was white/pale with a red border. (I have a series of pictures that I'm happy to share if that would be helpful). At 3:10pm, the welt's border was traced with permanent marker to monitor its spread. Approximately 5pm, an ice pack was applied to the area as an attempt to reduce the inflammation with no success. No signs of anaphylaxis were present, but an urgent care visit was scheduled. Per the urgent care provider, this was a localized allergic reaction. A steroid shot was injected and prescriptions for Pepcid, Zyrtec, and a Medrol dose pack were provided. More
2821253 35 F AR 01/16/2025 COVID19
 PFIZER\BIONTECH
Autoimmune thyroiditis, Hypothyroidism, Rheumatoid arthritis Autoimmune thyroiditis, Hypothyroidism, Rheumatoid arthritis
Autoimmune response resulting in rheumatoid arthritis, hypothyroidism, hashimotos. Autoimmune response resulting in rheumatoid arthritis, hypothyroidism, hashimotos.
2821254 88 M MI 01/16/2025 COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
 208E23A2
208E23A2
208E23A2
Bacteraemia, Bladder hypertrophy, Blood creatinine increased, COVID-19, Chest X-... Bacteraemia, Bladder hypertrophy, Blood creatinine increased, COVID-19, Chest X-ray normal; Computerised tomogram abdomen abnormal, Dysuria, Klebsiella test positive, Malaise, Nausea; Sepsis, Ureterolithiasis, Urinary tract infection, Vomiting More
DATE OF ADMISSION: 1/7/2025 DATE OF DISCHARGE: 1/12/25 Discharge Diagnoses: Sepsis secondary to UTI... DATE OF ADMISSION: 1/7/2025 DATE OF DISCHARGE: 1/12/25 Discharge Diagnoses: Sepsis secondary to UTI with bacteremia and COVID-19 - Blood cultures growing Klebsiella - Urine culture growing Klebsiella - CT A/P 1/7 right distal ureter stone measuring 6 mm unchanged from July 2024 and with no hydronephrosis. Diffusely thickened bladder wall. - Given no chest imaging findings of COVID-19 pneumonia and no hypoxia, the patient does not qualify for steroids. - Received 5 days of IV Rocephin while hospitalized. I will prescribe Keflex on discharge to complete a 14 day course of antibiotics. Atrial fibrillation//severe aortic stenosis//HTN - TTE 9/2023: EF 70-75%, severe aortic stenosis - Unsure why he is not on anticoagulation. It looks like he was started on Eliquis in October 2023, but was discontinued at some point for which I can not find any documentation. - Resume home Lasix and Norvasc CKD 3 - Baseline creatinine appears to be around 1.4 Hospital Course: 89-year-old male with past history of severe aortic stenosis, CKD 3, CVA, hypertension, and AFib. Patient was admitted 01/08 after presenting with symptoms malaise, dysuria and nausea/vomiting. Patient was found to COVID-19 as well as a UTI. He was started on IV Rocephin. His urine and blood cultures were positive for Klebsiella. Over the course of his hospital stay, his clinical picture has improved. He is stable for discharge back to his long-term care facility on oral antibiotics. More
✓
2821255 88 M FL 01/16/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255T2
Extra dose administered Extra dose administered
Patient mistakenly received a second dose of Arexvy. He received his original dose on 1/9/24 and a ... Patient mistakenly received a second dose of Arexvy. He received his original dose on 1/9/24 and a second dose on 1/15/25. More
2821256 73 M MI 01/16/2025 COVID19
COVID19
 MODERNA
MODERNA
 AS7146B
AS7146B
COVID-19, Computerised tomogram thorax abnormal, Deep vein thrombosis, Pain in e... COVID-19, Computerised tomogram thorax abnormal, Deep vein thrombosis, Pain in extremity, Peripheral swelling; Pulmonary embolism, SARS-CoV-2 test positive, Scan with contrast abnormal, Ultrasound Doppler abnormal More
DATE OF ADMISSION: 1/10/2025 DATE OF DISCHARGE: 01/12/2025 Discharge Diagnoses: Acute PE/LLE DVT i... DATE OF ADMISSION: 1/10/2025 DATE OF DISCHARGE: 01/12/2025 Discharge Diagnoses: Acute PE/LLE DVT in the setting of COVID-19 infection - U/S LLE 1/10: Acute appearing extensive occlusive DVT in the left lower extremity. - CTA chest 1/10: Acute right PE suspected. - I personally discussed with IR who recommends medical management with anticoagulation given no clot extension above the inguinal ligament - Was on heparin drip while hospitalized and will switch to therapeutic Eliquis on discharge. Chronic HFrEF//HTN - Continue home aspirin, statin, Coreg - Continue home Invokana, Repatha, Lasix, lisinopril, and Aldactone for now - Unsure why he is on digoxin as I can not find any documented diagnoses associated with this. T2DM with A1c 8.8% Hospital Course: 76-year-old male with past medical history of hypertension, T2DM, and HFrEF. Patient was admitted 01/10 for acute left lower extremity DVT and acute PE after presenting with symptoms of left leg pain and swelling. Patient was also found to be positive for COVID-19. Patient was started on a heparin drip with subsequent improvement in his symptoms. He is stable for discharge home on oral anticoagulation. More
✓
2821257 75 F SC 01/16/2025 FLU3
 SANOFI PASTEUR
 U8532CA
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
She arrived to office to make us aware of an area of redness and swelling that surrounds the injecti... She arrived to office to make us aware of an area of redness and swelling that surrounds the injection site. Area covers most of the patients upper arm. She denied any pain or discomfort . She also refused to be seen by the physician assistant, stating she has never had that reaction before and just wanted to make us aware. Encouraged to use a cold compress and to continue to monitor the area for increased swelling or pain. She denied any fever, chills, sob, chest pain or throat discomfort as well. ER precautions were given in the event of any worsening or ongoing symptoms. Verbalized understanding of instructions. ***on this form it is marked patient died but it will not allow me to uncheck the box*** More
2821258 86 F MI 01/16/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 058H21A
058H21A
058H21A
058H21A
Acute respiratory failure, Bowel obstruction surgery, COVID-19, COVID-19 pneumon... Acute respiratory failure, Bowel obstruction surgery, COVID-19, COVID-19 pneumonia, Chronic obstructive pulmonary disease; Condition aggravated, Confusional state, Death, Enema administration, Intestinal dilatation; Pneumonia staphylococcal, Positive airway pressure therapy, Respiratory distress, SARS-CoV-2 test positive, Staphylococcal bacteraemia; Suicidal ideation More
BRIEF OVERVIEW: Discharge Provider: MD Primary Care Physician at Discharge: NP Admission Date: 1/5/2... BRIEF OVERVIEW: Discharge Provider: MD Primary Care Physician at Discharge: NP Admission Date: 1/5/2025 Discharge Disposition: Deceased DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Suicidal ideation [R45.851] Acute on chronic respiratory failure (HCC) [J96.20] Chronic obstructive pulmonary disease with (acute) exacerbation (HCC) [J44.1] Pneumonia due to infectious organism, unspecified laterality, unspecified part of lung [J18.9] Lab test positive for detection of COVID-19 virus [U07.1] HOSPITAL COURSE: 89-year-old female was brought in from nursing facility for respiratory distress, acute on chronic respiratory failure, and was found to have COVID-19 pneumonia complicated by MRSA pneumoniae and MRSA bacteremia. On admission patient also had questionable suicidal ideation, as she was trying to wrap around tubing of oxygen around her neck to get attention from the staff in the nursing facility. There was 1 day when patient tried to similar behavior while in the hospital trying to wrap IV tubing around her neck. Patient was also evaluated by Psychiatry and social worker and had tele sitter in the room. Due to COVID-19, MRSA pneumoniae and MRSA bacteremia, patient is received treatment with remdesivir, vancomycin. Initially she had some improvement over a few days, however later Respiratory distress and confusion worsened. Patient was also found to have severely distended large bowel, required enemas, surgery was following. After discussion with POA decision was made to transition to comfort care in the evening on 1/11/25. BiPAP was eventually removed on 01/12/2025 and patient expired peacefully on 01/13/2025. More
✓ ✓
2821259 44 F 01/16/2025 RAB
RAB
 SANOFI PASTEUR
SANOFI PASTEUR
 X1B761M
X1B761M
Chest X-ray, Hypoaesthesia, Inflammation, Laboratory test, Magnetic resonance im... Chest X-ray, Hypoaesthesia, Inflammation, Laboratory test, Magnetic resonance imaging head; Magnetic resonance imaging spinal, Neck pain, Paraesthesia More
Today she had her second rabies vaccine for pre-exposure at 09:30. After the vaccine at around 12pm ... Today she had her second rabies vaccine for pre-exposure at 09:30. After the vaccine at around 12pm she starting having numbness and tingling in her face on the left side of her face and into her left hand. She denies and throat, tongue or lip swelling, no difficulty breathing. Patient reports recent long illness of lingering URI symptoms with cough and nausea. Treatment : Benadryl 25mg given orally with no change of symptoms , 30mg IM toradol and 10mg cyclobenzaprine orally in attempt to decrease local inflammation - patient had decreased neck pain after but numbness persisted. Dr., neurologist, agreed to come evaluate patient. More
2821260 42 F IL 01/16/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 8080797
8080797
8080797
8080797
Abnormal loss of weight, Allergy test positive, Blood immunoglobulin G decreased... Abnormal loss of weight, Allergy test positive, Blood immunoglobulin G decreased, Brain fog, Diarrhoea; Eye pruritus, Fatigue, Full blood count, Malaise, Mechanical urticaria; Milk allergy, Ocular hyperaemia, Pruritus, Rash, Tryptase; Urticaria, Vitamin D deficiency, White blood cell count decreased More
Intense full body itching, rashes, dermatographia, and hives that rotate in location and began two d... Intense full body itching, rashes, dermatographia, and hives that rotate in location and began two days after vaccine (10/23/24) and have not resolved despite aggressive antihistamine therapy and topical steroid cream. Accompanied by intermittent itchy, red eyes. Severe diarrhea with unintended weight loss, generalized fatigue and malaise, brain fog. More
2821261 1.25 M TX 01/16/2025 TDAP
 SANOFI PASTEUR
 U8252AA
No adverse event No adverse event
PT HAD NO ADVERSE REACTIONS TO Tdap VACCINE PT HAD NO ADVERSE REACTIONS TO Tdap VACCINE
2821263 75 M NJ 01/16/2025 MENB
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
 DD72H
3E99M
Oropharyngeal pain, Pain in extremity; Oropharyngeal pain, Pain in extremity Oropharyngeal pain, Pain in extremity; Oropharyngeal pain, Pain in extremity
patient states that approximately 4 hours after vaccine administration on 01/15/25 he developed a so... patient states that approximately 4 hours after vaccine administration on 01/15/25 he developed a sore throat. He also mentioned sore arms but has gMG and this is not uncommon. No other symptoms More
2821264 42 F NE 01/16/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Asthenia, Back pain, Fatigue, Headache, Malaise; Myalgia, Neck pain, Pain, Pain ... Asthenia, Back pain, Fatigue, Headache, Malaise; Myalgia, Neck pain, Pain, Pain in extremity, Sleep disorder More
All over muscle pain, headaches, fatigue, weakness, exhaustion, malaise, back pain, neck pain, leg p... All over muscle pain, headaches, fatigue, weakness, exhaustion, malaise, back pain, neck pain, leg pain. Inability to sleep due to pain. Trouble sitting at work all day due to all over pain. More
2821265 60 M OH 01/16/2025 COVID19
 PFIZER\BIONTECH
 FD0810
Paraesthesia Paraesthesia
Since the third shot I have had paresthesia in my right arm . Worse in the right shoulder radiating... Since the third shot I have had paresthesia in my right arm . Worse in the right shoulder radiating from my elbow to my right side of my chin More
2821266 80 F GA 01/16/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
Gave patient 2 doses of Arexvy first dose was given in 2023 outside of guidelines. Gave patient 2 doses of Arexvy first dose was given in 2023 outside of guidelines.
2821267 14 F 01/16/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 GJ5342
GJ5342
Blood electrolytes normal, Blood test normal, Cyanosis, Faeces discoloured, Leth... Blood electrolytes normal, Blood test normal, Cyanosis, Faeces discoloured, Lethargy; Magnetic resonance imaging normal, Vomiting, X-ray normal More
Per chart review patient had 3rd vaccine on 10/20/2022 and had an influenza vaccine on the same day.... Per chart review patient had 3rd vaccine on 10/20/2022 and had an influenza vaccine on the same day. On 10/21/2022 patient was seen in ER for a 5-minute episode of turning blue in the lips with no apnea and was saturating 92% by EMS. She also had 6 episodes of nonbloody nonbilious emesis with dark-colored stools. She denies any shortness of breath, cough or other symptoms.Patient received work up to confirm there was no issue with her VP shunt. MRI as well as an x-ray to check for positioning and function. Both of these results have come back as normal and we have reached out to our neurosurgery colleagues and they do not recommend any further work-up or treatment at this time. We also looked at your blood samples and blood electrolytes and so far all of these labs have remained normal. The ER concluded that: Although we do not have a reason for why she became lethargic, and blue earlier today we have ruled out any emergent causes that may be of concern and require immediate intervention. Unclear evidence if episode directly related to COVID vaccine. More
2821268 5 M 01/16/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR

No adverse event, Underdose; No adverse event, Underdose No adverse event, Underdose; No adverse event, Underdose
Incorrect dose of Covid-19 administered. Client was 5 at time of administration but received the 6-m... Incorrect dose of Covid-19 administered. Client was 5 at time of administration but received the 6-month to 4-year-old dose (yellow top vial, 3 mcg/0.3 mL) instead of the 5 to 11-year-old dose (blue top vial, 10 mcg/0.3 mL). Notified client's mom who did not state any adverse reactions to incorrect dose. Relayed the recommendation for child to receive the correct dose for his age. More
2821270 76 M PA 01/16/2025 RSV
 PFIZER\WYETH
 ln5464
Extra dose administered Extra dose administered
Patient didn't recall getting an RSV vaccine prior to today. System was down so we were unable... Patient didn't recall getting an RSV vaccine prior to today. System was down so we were unable to verify via that site. Learned after the fact that patient had received the vaccine a year ago. More
2821271 32 F VT 01/16/2025 VARCEL
 MERCK & CO. INC.
 x017490
Labelled drug-drug interaction issue, No adverse event Labelled drug-drug interaction issue, No adverse event
This person called on 1/7/25 and requested two vaccines urgently before her physical on 1/9/25. She ... This person called on 1/7/25 and requested two vaccines urgently before her physical on 1/9/25. She was fluent in language. The person said she did not have any vaccine records but was told by agency she needed these vaccines(Polio and Varicella) prior to her physical. She filled out all the required paperwork, including the screening form. She marked "no" to any vaccines in the prior month. I tried to look her up in our vaccine registry but she had not been entered yet. I administered the Varicella and IPV. During the 15 minute waiting peroid I entered the vaccines into the registry. I printed her a few copies and told her that all vaccines she received would automatically go into the registry. This is when she pulled out a vaccine from the local free clinic and I took it to enter those vaccines later. When I reviewed those vaccines after she left, I found that she had received MMR on 1/6/25. Seeing this, I knew that the Varicella I just gave her was invalid. I have spoken to her twice since this date and there are no side effects or reactions. The patient is aware of the error and that she will need to be revaccinated with the Varicella because that dose was invalid. More
2821272 13 F IL 01/16/2025 COVID19
UNK
 PFIZER\BIONTECH
UNKNOWN MANUFACTURER

Fatigue, Lymphadenopathy, Pain; Fatigue, Lymphadenopathy, Pain Fatigue, Lymphadenopathy, Pain; Fatigue, Lymphadenopathy, Pain
Swelling of 3 separate lymph nodes on same side (left) as flu and Covid vaccines which were administ... Swelling of 3 separate lymph nodes on same side (left) as flu and Covid vaccines which were administered one 1/13/25. Causing moderate-severe pain and extreme levels of fatigue. More
2821273 13 M PR 01/16/2025 COVID19
FLU3
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
 LN0589
A555J
Abdominal pain, Dizziness, Pyrexia; Abdominal pain, Dizziness, Pyrexia Abdominal pain, Dizziness, Pyrexia; Abdominal pain, Dizziness, Pyrexia
Mother refers that the teen was dizzy, has a fever and abdominal pain. Mother refers that the teen was dizzy, has a fever and abdominal pain.
2821275 32 M NJ 01/16/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 058E21A
058E21A
058E21A
058E21A
Affect lability, Amyotrophic lateral sclerosis, Asthenia, Electromyogram, Hypoae... Affect lability, Amyotrophic lateral sclerosis, Asthenia, Electromyogram, Hypoaesthesia; Insomnia, Joint range of motion decreased, Magnetic resonance imaging abnormal, Metabolic function test, Mobility decreased; Muscle atrophy, Muscle contractions involuntary, Muscular weakness, Musculoskeletal stiffness, Pain; Paraesthesia, Restlessness More
The night after receiving my first dose of the Moderna Vaccine I couldn't sleep and was restles... The night after receiving my first dose of the Moderna Vaccine I couldn't sleep and was restless, when I woke I couldn't tern my neck. My muscles were essentially seized. I had numbness and tingling throughout my body but mostly in my left side. It was painful to attempt to move. I had very little movement of my left hand. Virtually no strength in my grip. I was "frozen." I went to the medical department at my work, They sent me/approved/agreed that I should see a orthopedic specialist because it appeared to be an issue with my neck. A couple days later I was seen by Dr. He took an MRI, prescribed Percocet, and physical therapy. I attended physical therapy for about a 2 months (oct/nov 2021). The numbness/tingling /pain subsided. I remained weaker than I had been prior to the vaccination. I stopped going to physical therapy believing I could live with my altered strength. Over the course of the next year and a half I felt increasing weakness in my left arm. I consistently saw my strength decrease, and a fair amount of muscle wasting in my left hand. In the spring of 2023 I noticed my entire body was experiencing muscle fasciculations and I could now feel left leg weakness. It also became I apparent I had been suffering from pseudobulbar affect. In June of 2023 I got an MRI, and was diagnosed with ALS. Since then I have been treated by clinic and currently I am at the second clinic. More
✓ ✓
2821276 69 F TN 01/16/2025 RSV
 PFIZER\WYETH
 LN5502
Rash, Rash erythematous, Rash pruritic, Skin warm Rash, Rash erythematous, Rash pruritic, Skin warm
Patient reports about 24 hours after vaccination, she developed a rash on the left side of her clavi... Patient reports about 24 hours after vaccination, she developed a rash on the left side of her clavicle spreading up her neck and around to the front. The rash is red, slightly warmer and itchy per the patient. The next day (following allergy shots) the rash was worsening. She has treated it with hydrocortisone with some relief. I advised that she take diphenhydramine for about 24 hours, If the symptoms worsen or do not go away with the anti-histamines, I advised seeking medical care for assessment and treatment, and requested to be informed if that is the course of action she has to take. More
2821277 6 M KY 01/16/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 4LM54
Extra dose administered Extra dose administered
Patient received a dose in October of 2024 and received an extra dose today. Patient received a dose in October of 2024 and received an extra dose today.
2821278 55 F TN 01/16/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 4G95T
Injection site swelling, Pain in extremity, Peripheral swelling, Skin warm Injection site swelling, Pain in extremity, Peripheral swelling, Skin warm
Pt. reports the night of the vaccine her arm swelled to the size of a golf ball, and was very painfu... Pt. reports the night of the vaccine her arm swelled to the size of a golf ball, and was very painful, and warm to touch. Pt. also reports her left arm continued to swell from her shoulder to her elbow, and remained swollen for 2 weeks. More
2821279 86 F WI 01/16/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Injection site erythema Injection site erythema
9cm by 10cm erythematous area around vaccine injection site 9cm by 10cm erythematous area around vaccine injection site
2821280 0.17 M MI 01/16/2025 HIBV
 GLAXOSMITHKLINE BIOLOGICALS
 FE9HZ
Product preparation issue Product preparation issue
Pt was in office for appt and was given three injections for vaccinations. When charting these vacci... Pt was in office for appt and was given three injections for vaccinations. When charting these vaccinations two of these were confirmed but the third vaccine given was just the normal saline as it was not reconstituted correctly by this RN. Dr. and pts mother aware. More
2821281 37 M NY 01/16/2025 COVID19
 MODERNA
 8058492
Cardiac failure, Laboratory test, Ventricular assist device insertion Cardiac failure, Laboratory test, Ventricular assist device insertion
Extended hospitalization following immunization, treated for heart failure and an LVAD was implanted... Extended hospitalization following immunization, treated for heart failure and an LVAD was implanted to sustain heart function and blood circulation. Hospitalization was for a duration of 2 month from admission to release with LVAD. More
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2821282 70 M FL 01/16/2025 RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Muscle spasms, Nasopharyngeal swab, Oropharyngeal pain, Productive cough, Sputum... Muscle spasms, Nasopharyngeal swab, Oropharyngeal pain, Productive cough, Sputum discoloured; Upper respiratory tract infection More
Muscle cramps the same night, then soar throat and upper respiratory infection starting 2 days after... Muscle cramps the same night, then soar throat and upper respiratory infection starting 2 days after vaccination. Persistent Green Pflem producing cough. More
2821283 13 M HI 01/16/2025 HPV9
 MERCK & CO. INC.
 X024251
Erythema, Fatigue, Gait disturbance, Hypoaesthesia, Peripheral swelling Erythema, Fatigue, Gait disturbance, Hypoaesthesia, Peripheral swelling
fatigue several hours after injection received 1/14/2025. upon awakening day after injection 1/15/... fatigue several hours after injection received 1/14/2025. upon awakening day after injection 1/15/2025 had numbness of both hands and feet (difficulty walking) with swelling sans erythema of hands all symptoms resolved by 1800 on 1/15/2025 More
2821284 5 M WI 01/16/2025 COVID19
 MODERNA
 3044186
No adverse event No adverse event
Nothing happened Nothing happened
2821285 34 F MD 01/16/2025 COVID19
 PFIZER\BIONTECH
Dizziness Dizziness
Patient stated that she felt light headed the morning after the vaccine and may have fainted. She sa... Patient stated that she felt light headed the morning after the vaccine and may have fainted. She said that happens when she is dehydrated also but was concerned that it could also be the vaccine More
2821286 25 F VA 01/16/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 332H7
Extra dose administered, No adverse event Extra dose administered, No adverse event
Client received 3 flu shots in 1 season. Client did not recall receiving. No symptoms or side effect... Client received 3 flu shots in 1 season. Client did not recall receiving. No symptoms or side effects were noted. More
2821287 4 F AR 01/16/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 Y49BZ
Injection site erythema, Injection site pruritus, Injection site swelling, Injec... Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth More
Progressively worsening red, warm, swollen injection site (6.25cmx9.25cm) with complaints of itching Progressively worsening red, warm, swollen injection site (6.25cmx9.25cm) with complaints of itching
2821288 81 M CA 01/16/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 LN0588
LN0588
Injection site erythema, Injection site pain, Injection site swelling, Injection... Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth, Pyrexia; Rash, Urticaria More
low grade fever for 48 hours, local inflammatory response at vaccine site (warmth, redness, swelling... low grade fever for 48 hours, local inflammatory response at vaccine site (warmth, redness, swelling, pain), hives for 2 days, residual rash for 7 days More
2821289 65 F PA 01/16/2025 RSV
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 52z52
4H79Y
Glaucoma, Headache, Lacrimation increased, Photosensitivity reaction, Uveitis; G... Glaucoma, Headache, Lacrimation increased, Photosensitivity reaction, Uveitis; Glaucoma, Headache, Lacrimation increased, Photosensitivity reaction, Uveitis More
Patient stated she had a severe headache that moved to her eye. photosensitivity, and watery eyes. C... Patient stated she had a severe headache that moved to her eye. photosensitivity, and watery eyes. Called emergency eye line and earliest she could be seen was 12/31/2024. She was diagnosed with uveitis which has now progressed into her being treated for glaucoma. More
2821290 65 F ND 01/16/2025 PNC20
 PFIZER\WYETH
Erythema, Mobility decreased, Pain in extremity, Skin warm Erythema, Mobility decreased, Pain in extremity, Skin warm
Patient received Prevnar vaccination at pharmacy, I do not have lot number, would have to contact th... Patient received Prevnar vaccination at pharmacy, I do not have lot number, would have to contact them for this. Patient developed redness, warmth, and pain with limitations on range of motion in the right arm that extended and spread down the arm and onto the elbow joint. There was no local inflammation noted. More
2821291 64 F MA 01/16/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 ER8727
ER8727
Arthralgia, Computerised tomogram, Full blood count, Gait disturbance, Gait inab... Arthralgia, Computerised tomogram, Full blood count, Gait disturbance, Gait inability; Magnetic resonance imaging, Pain in extremity, Walking aid user, X-ray More
Within 3 days of receiving my second vaccine I could not walk without a cane. I began having pain w... Within 3 days of receiving my second vaccine I could not walk without a cane. I began having pain which began in my right hip/leg and which is now in both legs from hip to feet . I can no longer walk and went from a cane to a rollator and now heading to a wheelchair! More
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2821292 64 M GA 01/16/2025 TDAP
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 SKBLX494
SKB45N42
Condition aggravated, Seizure; Condition aggravated, Seizure Condition aggravated, Seizure; Condition aggravated, Seizure
Both vaccines were administered to same arm (LEFT deltoid) per pt request d/t the right arm being hi... Both vaccines were administered to same arm (LEFT deltoid) per pt request d/t the right arm being his "bowling arm." Pt remained in reclined position until he sat upright in reclining chair and began to seize at 13:37. RN, CNM and employee were called to Lab for assistance. Pt put back into reclining position and BP cuff/O2 probe applied, VS obtained. At this point, pt was able to state that he seizes when "he gets shots." Pt states his last seizure was when he"got shots last." 1340 - 78/43 HR62 O2 95%; 1343 - 89/55 HR66 95%; 1344 - HR65 97%; 1345 - 96/62 HR64 92%. 1347- EMS arrived; Pt very responsive, answering questions appropriately, pt adamantly refuses EMS services/transport to hospital and signed Medical Transportation Refusal Form. 1348 - 98/62 HR67 95%. EMS left and pt was wheeled via wheelchair to waiting area to meet his escort home (a friend). Pt got out of wheelchair and walked to vehicle without complications. More
2821293 73 F PA 01/16/2025 COVID19
VARZOS
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
 LM2224
BP74J
Confusional state, Injection site reaction, Pyrexia; Confusional state, Injectio... Confusional state, Injection site reaction, Pyrexia; Confusional state, Injection site reaction, Pyrexia More
Patient came to the pharmacy 2 days after the vaccinations. She said that the evening of the vaccina... Patient came to the pharmacy 2 days after the vaccinations. She said that the evening of the vaccinations she got a large injection reaction on her right arm where she was given the Shingrix. She also complained of a fever and mental confusion. Patient's husband took her to the ER and the ER doctor said the reaction was bad, but "normal" for vaccinations. He was more concerned about the mental confusion and a possibility of a stroke in progress. Patient did not want to stay in the hospital and left. ER doctor did not give the patient anything to treat the vaccination reaction. The patient went to her PCP days later for the same complaints. The family doctor told her that she was having a severe systemic reaction to the vaccine and never to get the 2nd dose in the series and to alert us (the pharmacy that gave her the vaccine). More
2821294 18 F NC 01/16/2025 FLU3
MNQ
 SEQIRUS, INC.
SANOFI PASTEUR
 946638
U8351CA
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 known adverse event at this time; Reporting that an additional dose (#3) of the Meningococcal AC... No known adverse event at this time; Reporting that an additional dose (#3) of the Meningococcal ACWY vaccine was given with a complete documentation of the 2-dose series. More
2821295 73 F SC 01/16/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255t2
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient had Arexvy on 10/27/2023 but came in to get another dose of Arexvy on 01/15/2025. None of th... Patient had Arexvy on 10/27/2023 but came in to get another dose of Arexvy on 01/15/2025. None of the adverse effects has been reported. Notified patient of error and counseled on potential adverse events. More
2821296 58 F VA 01/16/2025 PNC20
PNC20
PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 LG5577
LG5577
Injection site erythema, Injection site swelling; Injection site erythema, Injec... Injection site erythema, Injection site swelling; Injection site erythema, Injection site swelling, Injection site warmth, Pain, Pyrexia; Injection site erythema, Injection site swelling; Injection site erythema, Injection site swelling, Injection site warmth, Pain, Pyrexia More
Patient reports to our pharmacy today 01/16/2025 at 4pm. Patient states she received a Prevnar 20 va... Patient reports to our pharmacy today 01/16/2025 at 4pm. Patient states she received a Prevnar 20 vaccine on 01/09/2025 and developed an injection site reaction characterized by redness and swelling extending down from the injection site. The patient observed the redness progressively increasing in size over the next few days. However, she reports that the symptoms are now improving, with the redness starting to diminish. Reaction appears to be resolving without further intervention. Patient hasn't taken any otc medication or anything to relieve it. She feels it getting better day by day and reports no struggle with daily activities. I advised patient to monitor affected area for any signs of worsening or systemic symptoms (fever, chills, etc). If redness or swelling persists or worsens, the patient should seek medical evaluation. More
2821297 21 F OH 01/16/2025 UNK
 UNKNOWN MANUFACTURER
Echocardiogram, Myocarditis Echocardiogram, Myocarditis
myocarditis diagnosed 12/14/2024 myocarditis diagnosed 12/14/2024
2821298 12 M MI 01/16/2025 FLU3
 SANOFI PASTEUR
 UT8648MA
Unevaluable event Unevaluable event
None None
2821299 60 F RI 01/16/2025 TDAP
 SANOFI PASTEUR
 U8122AA
Cellulitis, Erythema, Swelling Cellulitis, Erythema, Swelling
Severe erythema, swelling, ?cellulitis Severe erythema, swelling, ?cellulitis
2821300 65 F NC 01/16/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 Y013009
Y013009
Headache, Injection site erythema, Injection site inflammation, Injection site p... Headache, Injection site erythema, Injection site inflammation, Injection site pain, Injection site pruritus; Injection site warmth More
INJECTION SITE SORENESS, REDNESS, ITCHING, INFLAMMATION, HOT TO TOUCH AND A HEADACHE THAT LASTED ALL... INJECTION SITE SORENESS, REDNESS, ITCHING, INFLAMMATION, HOT TO TOUCH AND A HEADACHE THAT LASTED ALL DAY THE NEXT DAY More
2821301 37 F TX 01/16/2025 HPV9
 MERCK & CO. INC.
 Y013712
Limb discomfort, Mobility decreased, Pain in extremity, Peripheral swelling Limb discomfort, Mobility decreased, Pain in extremity, Peripheral swelling
The patient reported a reaction to the HPV vaccine, which resulted in swelling and persistent pain i... The patient reported a reaction to the HPV vaccine, which resulted in swelling and persistent pain in her arm. The patient reported that the pain was so severe that it feels like she is holding a weight and it has been difficult for her to lift her arm. More
2821302 50 F AZ 01/16/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Erythema, Pain, Swelling Erythema, Pain, Swelling
Major swelling on 4th day, redness, major soreness Major swelling on 4th day, redness, major soreness
2821303 10 F AS 01/16/2025 FLU3
FLU3
TDAP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
 J245K
J245K
U7983AA
U7983AA
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered More
Pt was to be given Havrix and Flulaval at 01/16/2025 appt. Though Havrix was documented in our vacci... Pt was to be given Havrix and Flulaval at 01/16/2025 appt. Though Havrix was documented in our vaccine log, along with flulaval, Tdap was pulled & given to the pt. along with Flulaval. Provider ordering the vaccinations was immediately notified along with the nurse manager & the medical director. With the assistance of our facilities interpreter, the mistake was descriped to the pt and her father. Both understood the error. Pt & father will make a new appt to receive the Havarix vaccine. Pt left our clinic with no adverse side effects. More
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