🏥 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 💀 🏥 🚑 ♿ ⚠️
2832841 1.33 M GA 03/24/2025 PNC20
 PFIZER\WYETH
 LJ5283
Full blood count normal, Hyporesponsive to stimuli, Lethargy, Metabolic function... Full blood count normal, Hyporesponsive to stimuli, Lethargy, Metabolic function test normal More
Approximately 4 days after he received his vaccine back in January 7, patient had episode of letharg... Approximately 4 days after he received his vaccine back in January 7, patient had episode of lethargy and decreased responsiveness. Lethargy lasted for approximately 24 hours. She did not contact us about that specifically but the emergency room doctor told her that this felt to be an adverse reaction to the vaccine that he had received. More
2832842 0.42 F ND 03/24/2025 DTPPVHBHPB
PNC20
RV1
 MSP VACCINE COMPANY
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 U7969AA
LK6651
2032352
Pyrexia, Rash; Pyrexia, Rash; Pyrexia, Rash Pyrexia, Rash; Pyrexia, Rash; Pyrexia, Rash
Mother called the next day with reports of baby having a rash on chest area extending up to neck are... Mother called the next day with reports of baby having a rash on chest area extending up to neck area and a fever More
2832843 47 F GA 03/24/2025 HEP
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 92NK25
X022411
X006980
Extra dose administered; Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered; Extra dose administered
PATIENT WAS GIVEN AN ADDITIONAL DOSE OF HEPATITIS B PATIENT WAS GIVEN AN ADDITIONAL DOSE OF HEPATITIS B
2832844 1.33 M OK 03/24/2025 DTAPHEPBIP
 GLAXOSMITHKLINE BIOLOGICALS
Pyrexia, Rash Pyrexia, Rash
Rash and high fever Rash and high fever
2832845 80 F FL 03/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 51hwnhk4ct
Herpes zoster, Nerve compression, Pain in extremity Herpes zoster, Nerve compression, Pain in extremity
Patient next day went to ER because of pain in arm (doctors thought pinched nerve) and after a week ... Patient next day went to ER because of pain in arm (doctors thought pinched nerve) and after a week developed shingles More
2832846 64 F AL 03/24/2025 PNC20
 PFIZER\WYETH
 lj5284
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient was given a second shot when current CDC recommendations include only one, no side effects Patient was given a second shot when current CDC recommendations include only one, no side effects
2832847 16 F GA 03/24/2025 MENB
MNQ
 PFIZER\WYETH
SANOFI PASTEUR
 LF5302
U8256BA
Erythema, Oedema peripheral, Pain in extremity; Erythema, Oedema peripheral, Pai... Erythema, Oedema peripheral, Pain in extremity; Erythema, Oedema peripheral, Pain in extremity More
Reaction recorded by facility. Left arm erythema, mild edema, and pain. One other note, but I am una... Reaction recorded by facility. Left arm erythema, mild edema, and pain. One other note, but I am unable to read the healthcare workers handwriting. More
2832849 34 F ME 03/24/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EW0153
EW0153
EW0176
EW0176
Caesarean section, Carpal tunnel syndrome, Duchenne muscular dystrophy gene carr... Caesarean section, Carpal tunnel syndrome, Duchenne muscular dystrophy gene carrier, Exposure during pregnancy, Food aversion; Gene mutation identification test positive, Induced labour, Nausea, Neonatal disorder, Sleep paralysis; Caesarean section, Carpal tunnel syndrome, Duchenne muscular dystrophy gene carrier, Exposure during pregnancy, Food aversion; Gene mutation identification test positive, Induced labour, Nausea, Neonatal disorder, Sleep paralysis More
Mom conceived on 4/17/21 and delivered at 39 weeks. Mom experienced carpal tunnel, food aversions, s... Mom conceived on 4/17/21 and delivered at 39 weeks. Mom experienced carpal tunnel, food aversions, sleep paralysis, and nausea during pregnancy. Labor was induced and began and ended in an emergency c-section. Baby was 6lbs9oz at birth. Baby was delayed with sitting independently (11 months) and walking (19 months) and is still unable to jump or run at 3yrs3mos. He requires assistance moving up and down stairs. He was diagnosed with Duchenne muscular dystrophy on 10/23/24, with an exon deletion of 3-44. Mom was diagnosed as a carrier of the same mutation on 11/14/24. Maternal grandmother tested negative. More
✓ ✓ ✓
2832850 71 M CA 03/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Magnetic resonance imaging normal, Transient ischaemic attack Magnetic resonance imaging normal, Transient ischaemic attack
1 hour after receiving the vaccination, I had a TIA (transient ischemic attack.) 1 hour after receiving the vaccination, I had a TIA (transient ischemic attack.)
2832851 37 F WI 03/24/2025 HPV9
 MERCK & CO. INC.
 1967338
Arthralgia, Burning sensation Arthralgia, Burning sensation
Pt reports ongoing shoulder pain since the vaccine was administered, which has not dissipated over t... Pt reports ongoing shoulder pain since the vaccine was administered, which has not dissipated over time. States it "burned excruciatingly" when administered but she wasn't sure if that was normal for HPV vaccine, as this was her first dose. States she recalls thinking at the time that it was administered very high up on her arm. States pain is not debilitating, but that its significant enough to wake her up at night and affects ability to do certain activities. Pt was treated with lidocaine patch and Medrol Dosepack steroids, with some relief. Pt has been evaluated and treated in Physical therapy, starting 9/3/24. Rates pain between a 1-7 at it's best/worst. PT describes as "pain along rotator cuff referral pattern, does not go to or past elbow. Abduction more painful than flexion. Abduction pain at shoulder height and above." More
2832852 70 F NC 03/24/2025 FLU3
 SANOFI PASTEUR
 U8489DA
Urticaria Urticaria
Patient had hives that were unrelieved by benadryl. Patient reported that she had a reaction in past... Patient had hives that were unrelieved by benadryl. Patient reported that she had a reaction in past to flu vaccine, but did not attribute reaction to vaccine at that time so was not on her record. Provider gave atarax 25mg tablet and a decadron shot 10mg. More
2832853 39 M NJ 03/24/2025 COVID19
COVID19
 MODERNA
MODERNA
 037C21A
037C21A
Asthenia, Cold sweat, Cold-stimulus headache, Electric shock sensation, Influenz... Asthenia, Cold sweat, Cold-stimulus headache, Electric shock sensation, Influenza like illness; Small fibre neuropathy More
Ice Cream headache and shocking sensation to my nervous system. Cold sweats and weakness. Ice Cream headache and shocking sensation to my nervous system. Cold sweats and weakness.
2832854 29 M ME 03/24/2025 COVID19
 PFIZER\BIONTECH
Addison's disease, Adrenocortical insufficiency acute Addison's disease, Adrenocortical insufficiency acute
Addison disease from Pfizer vaccine was hospitalized for 11 days with addisonion crisis from Addison disease from Pfizer vaccine was hospitalized for 11 days with addisonion crisis from
✓
2832855 F NY 03/24/2025 PNC21
 MERCK & CO. INC.
Asthenia, Fatigue, Nausea, Pyrexia, Vomiting Asthenia, Fatigue, Nausea, Pyrexia, Vomiting
HCP calling on behalf of their wife to report after receiving CAPVAXIVE, their wife experienced naus... HCP calling on behalf of their wife to report after receiving CAPVAXIVE, their wife experienced nausea, vomiting, fatigue, weakness and a fever. Caller states their wife received the PNEUMOVA23 in 2017 and had similar reactions but is unsure if they; HCP calling on behalf of their wife to report after receiving CAPVAXIVE, their wife experienced nausea, vomiting, fatigue, weakness and a fever. Caller states their wife received the PNEUMOVA23 in 2017 and had similar reactions but is unsure if they; HCP calling on behalf of their wife to report after receiving CAPVAXIVE, their wife experienced nausea, vomiting, fatigue, weakness and a fever. Caller states their wife received the PNEUMOVA23 in 2017 and had similar reactions but is unsure if they; HCP calling on behalf of their wife to report after receiving CAPVAXIVE, their wife experienced nausea, vomiting, fatigue, weakness and a fever. Caller states their wife received the PNEUMOVA23 in 2017 and had similar reactions but is unsure if they; HCP calling on behalf of their wife to report after receiving CAPVAXIVE, their wife experienced nausea, vomiting, fatigue, weakness and a fever. Caller states their wife received the PNEUMOVA23 in 2017 and had similar reactions but is unsure if they; This spontaneous report was received from a physician and refers to a 74-year-old female patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 07-Mar-2025, the patient started therapy with Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE), dose number 1, administered by Intramuscular route (lot # and expiration date were not reported) for routine vaccination. On 07-Mar-2025, the patient experienced nausea, vomiting, fatigue, weakness (asthenia) and a fever (pyrexia). At the reporting time, the patient had not recovered from the events. The causal relationship between the events and Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE) was unknown. More
2832856 4 F CA 03/24/2025 DTAPIPV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 4L454
Y018157
Injection site erythema, Injection site swelling, Injection site warmth; Injecti... Injection site erythema, Injection site swelling, Injection site warmth; Injection site erythema, Injection site swelling, Injection site warmth More
Redness, swelling about 2 in diameter to Right thigh, warmth to touch. Redness, swelling about 2 in diameter to Right thigh, warmth to touch.
2832857 8 M CA 03/24/2025 DTAP
 SANOFI PASTEUR
 3CA25C1
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
No adverse event occurred. On 3/20/25, the patient (8 years old) had appointment at 4:30 PM, and was... No adverse event occurred. On 3/20/25, the patient (8 years old) had appointment at 4:30 PM, and was brought in by his mother to receive vaccines. The mother did not know which vaccines her child needed, but brought in a form from the patient's school with a list of required vaccines, as well as the patient's vaccination record. The pharmacist reviewed the list and vaccination record, and determined that the patient had not yet received the 5th dose of Daptacel (DTaP). The school-required vaccines also indicated that the patient needed a 5th dose of DTaP. The pharmacist informed the patient's mother that he would be receiving Daptacel, and proceeded to check-in the patient and prepare the vaccine. The patient received the Daptacel vaccine 0.5 mL intramuscularly in the left deltoid. After the patient and his mother left, the pharmacy clerk attempted to complete the appointment. However, she was not able to select Daptacel as the product used. On the following day, 3/21/25, the pharmacist opened a ticket to see why we were not able to select the vaccine. informed us that we were not able to select Daptacel because it is only indicated for patients ages 6 months to 6 years old. After reviewing CDC guidelines, the pharmacist determined that the patient was actually indicated for Tdap, and should have received Adacel or Boostrix, instead of Daptacel. However, CDC guidelines also state that Daptacel is still valid for a patient in his age group, and that the patient can then receive a booster of Adacel or Boostrix once he turns 11 years old. The pharmacist called the patient?s mother using the telephone interpreter service (the patient?s mother only speaks Spanish). The pharmacist informed the patient?s mother of the mistake, and the patient?s mother was understanding and said ?Okay.? The pharmacist also received the patient?s PCP information from his mother and informed the PCP office of the mistake. For error prevention in the future, the pharmacist will thoroughly check CDC guidelines and age recommendations, and will not administer vaccines unless they are indicated for the patient?s age group. More
2832858 4 F MA 03/24/2025 MMRV
 MERCK & CO. INC.
 Y014435
Pyrexia, Vomiting Pyrexia, Vomiting
Fever and vomiting Fever and vomiting
2832859 28 F WA 03/24/2025 VARCEL
 MERCK & CO. INC.
 Y013348
Inappropriate schedule of product administration Inappropriate schedule of product administration
Varicella vaccine given on 3/18/2025 did not realize that patient was already given the MMR 3/01/202... Varicella vaccine given on 3/18/2025 did not realize that patient was already given the MMR 3/01/2025 More
2832860 56 F NM 03/24/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.

Asthenia, Burning sensation, Dry mouth, Dysphagia, Lymphadenopathy; Renal cancer Asthenia, Burning sensation, Dry mouth, Dysphagia, Lymphadenopathy; Renal cancer
Burning going through right and the up the left. I let the nurse know who stated it was normal and i... Burning going through right and the up the left. I let the nurse know who stated it was normal and i waited in the room for 15 mins. I took a sip of water and i could no swallow. After 15 min i was fine. I went home and an hour later i felt weak in the knees and then i felt like i could not swallow again and my husband took me to the ER. And then everything started to feel better but the doctor stated my lymphoid was swollen which is might be the reason i can not swallow. And he told me to do a follow. My mouth felt super dry and i started having crustiest on the outside of my mouth. More
2832861 0.17 M TX 03/24/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 L5229
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient was given Boostrix at 2 months of age instead of Vaxelis vaccine. Patient did not show any s... Patient was given Boostrix at 2 months of age instead of Vaxelis vaccine. Patient did not show any signs or symptoms of adverse reaction at time of administration. Patient was discharged from clinic after being observed and cleared by Dr. More
2832862 52 M OR 03/24/2025 MMR
 MERCK & CO. INC.
Erythema, Oedema peripheral, Tenderness Erythema, Oedema peripheral, Tenderness
Swelling and redness, approximately 7 cm in size, were reported in the left armpit, the same side as... Swelling and redness, approximately 7 cm in size, were reported in the left armpit, the same side as the MMR vaccine administration (03/19/25) . The individual also experienced pain when touched, with symptoms beginning on the same day as the vaccine More
2832863 50 M CA 03/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 pc5y3
Rash Rash
Patient reported a painful rash that developed the next day that has gotten smaller in size and pain... Patient reported a painful rash that developed the next day that has gotten smaller in size and pain as the days progressed. More
2832864 28 F GA 03/24/2025 COVID19
 MODERNA
Electrocardiogram, Pericarditis Electrocardiogram, Pericarditis
Pericarditis, treated with ibuprofen outpatient, no symptoms after 5 days Pericarditis, treated with ibuprofen outpatient, no symptoms after 5 days
2832866 63 M MI 03/24/2025 COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 LP1780
LP1780
LP1780
LP1780
LP1780
Blood bicarbonate increased, Blood electrolytes, Blood lactic acid, Blood pH dec... Blood bicarbonate increased, Blood electrolytes, Blood lactic acid, Blood pH decreased, Brain natriuretic peptide increased; Carbon dioxide increased, Chronic obstructive pulmonary disease, Condition aggravated, Cough, Diastolic dysfunction; Dyspnoea, Echocardiogram abnormal, Ejection fraction decreased, Heart failure with reduced ejection fraction, Hypercapnia; Hypoxia, Intensive care, Obstructive sleep apnoea syndrome, PCO2 increased, Positive airway pressure therapy; Respiratory distress, Tachycardia, Tachypnoea, Ventricular hypokinesia, Viral myocarditis More
Patient experienced new onset diagnosis, "it looks like viral myocarditis" and was hospita... Patient experienced new onset diagnosis, "it looks like viral myocarditis" and was hospitalized in the ICU for this. The timing is related to receipt of his COVID vaccine on 3/14/2025, but onset of symptoms started before the vaccine. It is unknown whether there is any causality since patient has had respiratory symptoms for approximately 2 weeks, and received the vaccine during his worsening respiratory symptoms. The cough and SOB may have been related to myocarditis prior to receiving the vaccine, due to recent suspected viral illness. The timing of the vaccine vs. viral exposure with sick contact clouds the picture. Patient also has longstanding 40py history of smoking and was diagnosed with a COPD exacerbation, and likely OSA. The heart failure with EF 11% is NYHA Class IV, Stage C, new onset. More details from H&P: "63 y.o. year-old male with unknown past medical history who presented with shortness of breath. Patient has not seen a physician in many years and has not been on any medications at home. Patient states that he was in his usual state of health up until 2 weeks ago when he developed had a cough. He states that his granddaughter was also sick with similar symptoms around the same time. He states that he received COVID-19 vaccine on 3/16 and since then has been having symptoms of cough and shortness of breath. He states that shortness of breath has been getting progressively worse and so he came to the ED for further evaluation. In the ED, patient was noted to be tachycardic, tachypneic and hypoxic with SpO2 of 53 on room air. He was subsequently started on 5 L of oxygen via nasal cannula. Electrolytes showed elevated CO2 consistent with chronic CO2 retention. ABG showed pH 7.26, pCO2 85.7, HCO3 38.5, lactate 0.7. Patient was started on breathing treatments. She was called due to respiratory distress and patient was transferred to the ICU. In ICU patient was started on BiPAP. Further evaluation with echocardiogram showed patient has EF of 11% with global LV hypokinesis and grade 2 diastolic dysfunction. Cardiology has been consulted for management of heart failure with severely reduced EF. Patient denies any family history of cardiac events. Brother, mother and Sister all died from lung cancer. He does state he gets chest pain and shortness of breath with any physical exertion fro the last 3 months. He also endorses snoring and feeling not well rested after sleeping." More
✓ ✓
2832867 4 F WA 03/24/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK017AA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Pt received the vaccine Pentacel in error instead of Quadracel that was needed for their age/Vaccina... Pt received the vaccine Pentacel in error instead of Quadracel that was needed for their age/Vaccination requirement. Verified with DOH that patient does not need repeated Dtap/IPV d/t the timing of the vaccine being out of age range recommendation for vaccine. More
2832868 10 M IN 03/24/2025 HPV9
 MERCK & CO. INC.
 HPV9
No adverse event No adverse event
none none
2832869 4 M IN 03/24/2025 MMRV
MMRV
 MERCK & CO. INC.
MERCK & CO. INC.
 Y013576
Y013576
Disorientation, Malaise, Poor quality sleep, Pyrexia, Screaming; Skin warm, Star... Disorientation, Malaise, Poor quality sleep, Pyrexia, Screaming; Skin warm, Staring, Streptococcus test negative, Tremor More
On 3-22-25 he had a fever and possible febrile seizure. He slept poorly on Friday. On Saturday at f... On 3-22-25 he had a fever and possible febrile seizure. He slept poorly on Friday. On Saturday at family members house mother suspected he wasn't feeling good and a bit warm. However that nigh he woke up 45 mins later somewhat disoriented. First thing mom noted that his hands started to shake. He then had his whole body was shaking. He then had a high pitched scream. Father picked him up and he continued to have some shaking. Eyes were staring blankly. No LOC. He did not pee himself, he is potty trained. All in all the shaking was < 5 mins. No vomiting. No color change. He was seen in the office and well appearing. He had a normal neurological exam. Family was advised to watch for future events. More
2832870 20 F MA 03/24/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
Pharyngeal swelling, Pruritus, Swelling, Swelling face Pharyngeal swelling, Pruritus, Swelling, Swelling face
Swollen face & neck/throat & itchiness were the symptoms. I went to urgent care and was pres... Swollen face & neck/throat & itchiness were the symptoms. I went to urgent care and was prescribed over the counter Benadryl & and EpiPen & prednisone More
2832871 70 M CA 03/24/2025 COVID19
 MODERNA
 3044069
Heart rate irregular, Hypopnoea, Pallor, Sepsis Heart rate irregular, Hypopnoea, Pallor, Sepsis
RESIDENT NOTED WITH CHANGE IN CONDITION EVENT ON 3/22/2025 1330- OXYGEN SATURATION @85% ON 2L OXYGE... RESIDENT NOTED WITH CHANGE IN CONDITION EVENT ON 3/22/2025 1330- OXYGEN SATURATION @85% ON 2L OXYGEN VIA NASAL CANNULA, SHALLOW RESPIRATONS, SKIN COLOR NOTED TO BE PALE. VITAL SIGNS: BP 117/66, P 121 (IRREGULAR), RR 12, T 97.2, SPO2 85% VIA 2L NC, BS 191. NON-REBREATHER MASK PLACED ON RESIDENT WITH O2 SATURATION AT 100%. MD NOTIFIED WITH ORDER TO TRANSFER RESIDENT TO HOSPITAL FOR FURTHER EVALUATION, RESIDENT TRANSFERRED TO HOSPITAL WITH DX OF SEPSIS. More
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2832872 69 F NY 03/24/2025 VARZOS
VARZOS
VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 NDC: 58160-0823
NDC: 58160-0823
UNK
UNK
Aphonia, Condition aggravated, Eyelid discolouration, Swelling of eyelid, Tinnit... Aphonia, Condition aggravated, Eyelid discolouration, Swelling of eyelid, Tinnitus; Aphonia, Erythema, Eye swelling, Eyelid oedema, Ocular hyperaemia; Aphonia, Condition aggravated, Eyelid discolouration, Swelling of eyelid, Tinnitus; Aphonia, Erythema, Eye swelling, Eyelid oedema, Ocular hyperaemia More
Both eyelids swollen and discolored; total loss of voice. Was advised to take 25mg diphenhydramine a... Both eyelids swollen and discolored; total loss of voice. Was advised to take 25mg diphenhydramine and 10mg Zyrtec. In ER was given 40mg prednisone PO and observed for several hours. Was discharged when voice started to return. Sent home on diphenhydramine 50mg PO q6h x 1week, Zyrtec 10mg q24h x 1 month, prednisone 50mg q24h x 5 additional days, famotidine 20mg q24h. Personal MD recommended using diphenhydramine PRN instead of q6h. Also recommended continuing prednisone 10mg q24h for 1 month following the 5 days of 50mg. Advised to continue the Zyrtec and famotidine for that month. Since then tinnitus is louder. More
2832873 60 F CA 03/24/2025 TDAP
VARZOS
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 3CA30C1
H97H2
Injection site erythema, Injection site swelling; Injection site erythema, Injec... Injection site erythema, Injection site swelling; Injection site erythema, Injection site swelling More
Redness, swelling at injection site Redness, swelling at injection site
2832874 85 F CA 03/24/2025 COVID19
 MODERNA
 3044069
Hypopnoea, Oedema peripheral, Pallor, Respiratory failure, Use of accessory resp... Hypopnoea, Oedema peripheral, Pallor, Respiratory failure, Use of accessory respiratory muscles More
ON 3/23/2025 @1830 RESIDENT NOTED WITH SHALLOW RESPIRATIONS W/ USE OF ACCESSORY MUSCLES. VS: BP 134/... ON 3/23/2025 @1830 RESIDENT NOTED WITH SHALLOW RESPIRATIONS W/ USE OF ACCESSORY MUSCLES. VS: BP 134/93, P 60 REGULAR, RR 12, T 97.3 SPO2 100% ON 2L VIA NON-REBREATHER MASK, PALE SKIN, RESIDENT NOTED WITH +1 BILATERAL EDEMA TO LEGS. MD NOTIFIED WITH ORDER TO TRANSFER TO HOSPITAL FOR FURTHER EVALUATION. DX OF RESPIRATORY FAILURE @ HOSPITAL. More
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2832875 0.25 F MI 03/24/2025 RV1
 GLAXOSMITHKLINE BIOLOGICALS
 FJ442
Inappropriate schedule of product administration Inappropriate schedule of product administration
Patient was started on immunization series 5 days outside of schedule guidelines. Patient was started on immunization series 5 days outside of schedule guidelines.
2832876 18 F MI 03/24/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 24PL5
Extra dose administered Extra dose administered
Patient was given another flu shot, she was given one initially 10/17/2024 Patient was given another flu shot, she was given one initially 10/17/2024
2832877 77 F ID 03/24/2025 COVID19
PPV
TDAP
TYP
 PFIZER\BIONTECH
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
 LN0591
LG5575
U8339BA
X1A271M
Extra dose administered; Extra dose administered; Extra dose administered; Extra... Extra dose administered; Extra dose administered; Extra dose administered; Extra dose administered More
CLIENT HAD RECEIVED THE SAME VACCINE PREVIOUSLY ON 09/23/2024, THIS WASN'T SEEN IN HER CHART OF... CLIENT HAD RECEIVED THE SAME VACCINE PREVIOUSLY ON 09/23/2024, THIS WASN'T SEEN IN HER CHART OF PREVIOUS RECORDS AND INADVERTANTLY GIVEN A SECOND TIME More
2832878 0.5 F GA 03/24/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 J4k4X
No adverse event, Wrong patient No adverse event, Wrong patient
No adverse events. Will be monitoring the baby. This baby, who is 6 months old, inadvertently rece... No adverse events. Will be monitoring the baby. This baby, who is 6 months old, inadvertently received Hep A, which was meant for another child. The was baby is doing well. Baby was supposed to receive Pediarix PCV & HIB. Instead, she received Hep A DTaP PCV. More
2832879 57 F MO 03/24/2025 VARZOS
VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 94SE2
94SE2
94SE2
Blood thyroid stimulating hormone, Diarrhoea, Feeling cold, Full blood count, Gl... Blood thyroid stimulating hormone, Diarrhoea, Feeling cold, Full blood count, Glycosylated haemoglobin; Hallucination, Headache, Lumbar puncture, Metabolic function test, Pyrexia; Vitamin D, Vomiting More
Reports fever, vomiting, diarrhea, headache, and hallucinations about 5 hours after injection. Needi... Reports fever, vomiting, diarrhea, headache, and hallucinations about 5 hours after injection. Needing several blankets to be warm. Her husband reported "she was talking to things that weren't there." More
2832880 14 F CA 03/24/2025 HPV9
 MERCK & CO. INC.
 Y008119
Anxiety, Dyskinesia, Fear, Tremor Anxiety, Dyskinesia, Fear, Tremor
tremors, vibration in the body, shaking, anxiety, fear, uncontrollable body movements, tremors, vibration in the body, shaking, anxiety, fear, uncontrollable body movements,
2832882 29 F PA 03/24/2025 FLU3
 SANOFI PASTEUR
 U8515CA
Nausea Nausea
Slight nausea Slight nausea
2832883 54 M WA 03/24/2025 PNC20
 PFIZER\WYETH
 LJ5284
Headache, Sinus congestion Headache, Sinus congestion
Patient claiming Sinus congestion; Headache when lay down after immunization, especially when he lay... Patient claiming Sinus congestion; Headache when lay down after immunization, especially when he lays down; Recommended using cetirizine for a week, but no improvement per patient at the moment More
2832884 1 F TX 03/24/2025 HEPA
MMR
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 Y008483
Y013132
Y014868
Infant irritability, Injection site erythema, Injection site pruritus, Rash; Inf... Infant irritability, Injection site erythema, Injection site pruritus, Rash; Infant irritability, Injection site erythema, Injection site pruritus, Rash; Infant irritability, Injection site erythema, Injection site pruritus, Rash More
Patient developed redness and itching around the vaccine sites within 5 minutes of injection. She wa... Patient developed redness and itching around the vaccine sites within 5 minutes of injection. She was more irritable than she typically is following vaccines. The reaction was limited to ~ 4 inches around the injection site. Patient was treated with oral Benadryl in office and monitored for 30 minutes with improvement in itching, fussiness, and rash. More
2832885 4 M AZ 03/24/2025 DTAPIPV
DTAPIPV
MMRV
MMRV
 SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.
 U7838AA
U7838AA
X025093
X025093
Injection site erythema, Injection site induration, Injection site reaction, Inj... Injection site erythema, Injection site induration, Injection site reaction, Injection site swelling, Injection site warmth; Musculoskeletal stiffness; Injection site erythema, Injection site induration, Injection site reaction, Injection site swelling, Injection site warmth; Musculoskeletal stiffness More
He received 2 shots one in each arm on Friday 3/14/25. The right arm started showing symptoms on Sat... He received 2 shots one in each arm on Friday 3/14/25. The right arm started showing symptoms on Saturday 3/15/25 around 8pm. His right arm had swollen tremendously from his shoulder to his elbow. His skin was hot and red, stiff, and when you touched his arm it was completely hard. More
2832886 0.33 F OR 03/24/2025 RV5
 MERCK & CO. INC.
 Y005877
Vomiting Vomiting
patient vomiting during administering. patient vomiting during administering.
2832887 63 M NJ 03/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 74NC9
Abdominal pain, Injection site erythema, Rash Abdominal pain, Injection site erythema, Rash
Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Abdom... Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Abdominal Pain-Medium, Additional Details: Redness at Injection Site of injection More
2832888 83 F IL 03/24/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 24m94
Injection site bruising, Injection site erythema, Injection site pain, Injection... Injection site bruising, Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling More
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injec... Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Other Vaccines: VaccineTypeBrand: pneumovax; Manufacturer: merck; LotNumber: y016291; Route: im; BodySite: left deltoid; Dose: ; VaxDate: UNKNOWN More
2832889 55 F AL 03/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 ts525
Asthenia, Headache, Injection site pain, Nausea, Pain Asthenia, Headache, Injection site pain, Nausea, Pain
Site: Pain at Injection Site-Mild, Systemic: Nausea-Mild, Systemic: Weakness-Mild, Additional Detail... Site: Pain at Injection Site-Mild, Systemic: Nausea-Mild, Systemic: Weakness-Mild, Additional Details: pt says she felt nauseated, sore, and someone was standing on her head., Other Vaccines: VaccineTypeBrand: hepslav b; Manufacturer: dynax; LotNumber: 945662; Route: im; BodySite: left; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: boostrix; Manufacturer: glaskosmith cline; LotNumber: 7kd5d; Route: im; BodySite: left; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: capvaxine; Manufacturer: merck; LotNumber: y013009; Route: im; BodySite: left; Dose: ; VaxDate: UNKNOWN More
2832890 72 F PA 03/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7349L
Injection site erythema, Injection site pruritus, Pruritus, Rash Injection site erythema, Injection site pruritus, Pruritus, Rash
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Allergic: Itch... Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Additional Details: Patient said it was onl mild. her arm is still red at the site of the injection but she reported tat it's getting better and 1 advised her to use benadryl and talk to her doctor. and to call 911 if symptoms are getting worse More
2832891 58 F PA 03/24/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 xx9n4
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-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection... Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild More
2832892 60 F CA 03/24/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 y019158
y019158
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site rash, Injection site swelling; Rash, Skin warm, Tenderness More
Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Medium, Site: Redness at Injectio... Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Additional Details: Pt received vaccine on Monday 3/10/2025, came in today Sunday 3/16 and showed rash to pharmacist. Pt said it started on 3/11 Tuesday and it has improved but the rash was from her injection site all the way down the arm. Pt states her arm is tender and warm. Pt has been taking Benadryl which has helped a little. Pharmacist recommended the pt to go seek medical attention at the ER or Urgent Care to make sure it is not cellulitis. Pt states she will think about it. More
2832893 58 M CA 03/24/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 y019158
y019158
Asthenia, Dizziness, Headache, Injection site erythema, Injection site pain; Inj... Asthenia, Dizziness, Headache, Injection site erythema, Injection site pain; Injection site pruritus, Injection site swelling, Myalgia, Pain 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: Body Aches Generalized-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: muscle pain and bodyweakness-Medium, Systemic: Headache-Medium, Systemic: Weakness-Medium More
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