๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ Privacy & Data Disclaimer

About This Site

This is a public data browser for the Vaccine Adverse Event Reporting System (VAERS). By using this site, you acknowledge and agree to the following:

Data Source & Accuracy

  • Public Data: All data displayed comes from the publicly available VAERS database maintained by the CDC and FDA.
  • No Verification: VAERS accepts all reports without verifying medical accuracy. Reports do not prove causation between vaccines and adverse events.
  • Anyone Can Report: Healthcare providers, patients, family members, and anyone else can submit reports to VAERS.
  • Research Purpose: This data is for transparency, research, and monitoring vaccine safety signals only.

Your Privacy

  • No Personal Data Collection: This site does not collect, store, or track any personal information about visitors.
  • No Cookies: We do not use cookies except for remembering that you've seen this disclaimer (stored locally in your browser).
  • No Analytics: We do not use Google Analytics or any other tracking services.
  • Search Privacy: Your searches and filters are not logged or stored on our servers.
  • Public Data Only: The VAERS data shown here is already public and contains no personally identifiable information.

Medical Disclaimer

  • Not Medical Advice: This tool is for informational purposes only and does not provide medical advice.
  • Consult Healthcare Providers: Always consult qualified healthcare professionals for medical decisions.
  • No Liability: We are not responsible for decisions made based on this data.

Data Interpretation

  • The presence of a report does not mean the vaccine caused the adverse event.
  • Coincidental events are often reported (e.g., a heart attack that happened to occur after vaccination).
  • Serious adverse events must be reported by law, even if unrelated to the vaccine.
  • The database is useful for detecting safety signals that require further investigation.

๐Ÿ“– Help & Search Guide

Column Icons Legend

๐Ÿ’€ Death
๐Ÿฅ Hospitalized
๐Ÿš‘ Emergency Room
โ™ฟ Disability
โš ๏ธ Life Threatening

How to Search

๐Ÿ’ก Search Tips:
  • Select Year: Choose a specific year OR "All Years" to search across all data
  • All Years requires filters: When searching all years, you must select at least one filter (lot number, vaccine type, outcome, etc.) for performance
  • Lot number tracking: Use "All Years" + Lot Number to track lots across multiple years
  • Combine filters: Use multiple filters together to narrow results (e.g., Age + Vaccine Type + Death)
  • VAERS ID: Search for specific report by ID number
  • Age: Enter exact age (e.g., 25) or decimal (e.g., 0.5 for 6 months)
  • State: Enter 2-letter state code (e.g., CA, NY, TX)
  • Vaccine Type: Search partial names (e.g., "COVID19", "FLU", "HPV")
  • Manufacturer: Search by company (e.g., "PFIZER", "MODERNA")
  • Lot Number: Search specific vaccine lot (works great with "All Years")
  • Symptoms: Search for any symptom keyword (e.g., "fever", "rash")
  • Death/Hospitalized: Filter to only show cases with these outcomes

Understanding the Data

  • Reports are unverified: VAERS accepts all reports without medical verification
  • Not proof of causation: A report does not mean the vaccine caused the event
  • Anyone can report: Healthcare providers, patients, and family members can submit reports
  • Multiple vaccines: One report may list multiple vaccines given at the same time
  • Blank fields: Not all fields are required, so some data may be missing

Using the Table

  • Sort columns: Click column headers (ID, Age, Sex, Date, Died) to sort
  • Expand text: Click "More" to see full narrative or symptom text
  • Navigate pages: Use pagination controls at top and bottom of table
  • Export results: Click "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ VAERS Vaccine Data Browser is an independent, third-party data browser for publicly available VAERS (Vaccine Adverse Event Reporting System) data.

Important: This site is NOT affiliated with, endorsed by, or operated by the CDC, FDA, or any government agency. We are an independent service that makes public VAERS data easier to search and analyze.

What is VAERS?

VAERS (Vaccine Adverse Event Reporting System) is a national early warning system established in 1990 to detect possible safety problems with vaccines. It's co-managed by the CDC (Centers for Disease Control and Prevention) and FDA (Food and Drug Administration).

VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination.

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

  • Publicly available - Published by the CDC/FDA on their official website
  • De-identified - Contains no personally identifiable information (names, addresses, contact info removed)
  • Legally accessible - Available to researchers, media, and the general public under FOIA (Freedom of Information Act)
  • Not protected health information - Once de-identified and published by the government, it's no longer covered by HIPAA restrictions

This site displays the same public data available at vaers.hhs.gov/data.

Why does this site exist?

We believe in transparency and public access to health data. While the CDC/FDA provide VAERS data, their official site:

  • Is difficult to search and filter
  • Requires downloading large CSV files and technical knowledge
  • Is not user-friendly for the average person

This independent site makes the same publicly available data easier to search, filter, and understand for researchers, journalists, healthcare workers, and concerned citizens.

Where does the data come from?

All data is downloaded directly from the official CDC/FDA VAERS website at vaers.hhs.gov/data.

The data is:

  • Publicly released by the CDC/FDA every week
  • Available as downloadable CSV files
  • Imported into this site's database for easier searching
  • Displayed exactly as provided (no modifications or filtering)

This site does not collect, modify, or add to the official VAERS data.

My vaccine lot number matches one with deaths/serious events - should I be worried?

Important context:

  • VAERS reports do NOT prove causation - A report means an event occurred after vaccination, but doesn't mean the vaccine caused it
  • Anyone can report - Reports are not verified for medical accuracy before being published
  • Coincidences happen - When millions of people get vaccinated, some will experience unrelated medical events afterward
  • Large lot numbers - Popular vaccines may have hundreds of thousands of doses from one lot number
  • More vaccinations = more reports - Lots used widely will naturally have more reports

What to do:

  • Don't panic - VAERS data requires expert analysis to interpret
  • Talk to your doctor if you have concerns
  • Check official CDC/FDA safety communications for genuine safety signals
  • Remember: billions of vaccine doses have been safely administered

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

  • โœ… Early warning system for potential safety signals
  • โœ… Open and transparent - publicly accessible
  • โœ… Accepts all reports regardless of likelihood of causation
  • โœ… Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • โš ๏ธ Reports are unverified - not investigated before publication
  • โš ๏ธ Cannot determine if vaccine caused the event
  • โš ๏ธ Underreporting - not all adverse events are reported
  • โš ๏ธ Overreporting - coincidental events may be reported
  • โš ๏ธ Incomplete data - not all fields are required

Bottom line: VAERS is an important tool for safety monitoring, but individual reports should not be used as proof that a vaccine caused harm.

What are "adverse events"?

An adverse event is any undesirable health occurrence that happens after vaccination, including:

  • Common reactions: Sore arm, mild fever, fatigue (usually expected)
  • Serious events: Hospitalization, disability, life-threatening illness, death
  • Coincidental events: Medical conditions that would have occurred anyway

Important: An adverse event doesn't mean the vaccine caused it - only that it occurred after vaccination. Many reported events are coincidental or unrelated.

Why are some lot numbers listed multiple times?

This is normal and expected! A person may receive multiple doses of the same vaccine from the same lot number:

  • COVID vaccines require 2-3 doses
  • HPV, Hepatitis B, and other vaccines have multi-dose schedules
  • Each dose is recorded as a separate entry

Example: Person receives Pfizer COVID dose 1 (lot ABC123) and dose 2 (lot ABC123) - lot ABC123 appears twice in their report.

How often is this data updated?

The CDC/FDA releases new VAERS data every Friday. This site is typically updated:

  • Weekly or bi-weekly for recent data
  • Check the available years to see what data is currently loaded
  • During updates, the site may be in maintenance mode temporarily

Where can I learn more?

โš ๏ธ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2830361 77 M FL 03/10/2025 COVID19
COVID19
MODERNA
MODERNA
8081564
8081564
Condition aggravated, Crepitations, Death, Dyspnoea, Guillain-Barre syndrome; Ox... Condition aggravated, Crepitations, Death, Dyspnoea, Guillain-Barre syndrome; Oxygen saturation decreased, Respiratory distress, Wheezing More
Reported Symptoms: 10038687:RESPIRATORY DISTRESS: Narrative: This was a hospice patient that had a ... Reported Symptoms: 10038687:RESPIRATORY DISTRESS: Narrative: This was a hospice patient that had a history of Guillain Barre to other vaccinations, CHF , permanent AF, CKD stage 3, colon cancer s/p colostomy. Healthcare surraogate agreed for the patient to receive the COVID-19 booster "In an attempt to minimize or prevent the risks of getting covid-19, and its potential complications. Patient presented with dyspnea and low oxygen saturations the following day. Patient had wheezes and crackles but was in minimal distress. Patient was admitted for further follow-up and due to poor prognosis found during adult was transferred to hospice where patient experienced worsening Guillain Barre deemed to be due to COVID vaccine. Patient passed away 12 days after receiving vaccine. Other Relevant HX: Other: Respiratory distress - History of Guillain Barre More
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2830362 64 M OH 03/10/2025 COVID19
PFIZER\BIONTECH
LM2224
Pruritus, Urticaria Pruritus, Urticaria
Reported Symptoms: 10037087:PRURITUS; 10046735:URTICARIA; Narrative: Other Relevant HX: Other: URTIC... Reported Symptoms: 10037087:PRURITUS; 10046735:URTICARIA; Narrative: Other Relevant HX: Other: URTICARIA; PRURITUS More
2830363 M DC 03/10/2025 COVID19
PFIZER\BIONTECH

Dyspnoea Dyspnoea
Reported Symptoms: 10013963:DYSPNEA; Narrative: A 49 yo male with PM.H of GERD, Carcinoma of Thyroid... Reported Symptoms: 10013963:DYSPNEA; Narrative: A 49 yo male with PM.H of GERD, Carcinoma of Thyroid (status post thyroidectomy), Lumbar Radiculopathy, Hypothyroidism, Barrett's Esophagus and Exposure to potentially hazardous substance. On October 02, 2024, PCC RN reported the patient had a historical ADR of Covid-1, 9 vaccine induced Dyspnea. No other information was provided regarding treatment or the vaccine i.e. vaccine Mfg., lot #, Expiration date, where and who administered the vaccine, what time and when it occurred etc.) However the Med. Center indicated the patient received Pfizer Covid-19 Vaccine, Mrna, LPN-S, Pf, 30mcg/0.3ml on April 1 2021@9:00 and April 22, 2021@9:00AM. Both vaccines administered IM to R. deltoid and without complication. Administered by RN on the one in April 1, 2021 and by RN on the one on April 22, 2021. Other Relevant HX: Other DYSPNEA More
2830364 77 M FL 03/10/2025 COVID19
MODERNA
8081564
Injection site pain Injection site pain
Reported symptoms: 10022086:INJECTION SITE PAIN; Narrative: Went to ED for injection site pain 12 ho... Reported symptoms: 10022086:INJECTION SITE PAIN; Narrative: Went to ED for injection site pain 12 hours after COVID-19 vaccine administration. Given dexamethasone IM and diphenhydramine in ED. Discharged with prednisone. Other Relevant HX: Patient received the Moderna COVID-19 vaccine 5 times since 2021. Other: Injection site pain More
2830365 84 M IL 03/10/2025 FLU3
FLU3
FLU3
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
UT8470DA
UT8470DA
UT8470DA
Asthenia, C-reactive protein increased, Cardiomegaly, Chest X-ray abnormal, Comp... Asthenia, C-reactive protein increased, Cardiomegaly, Chest X-ray abnormal, Computerised tomogram abdomen abnormal; Dyspnoea exertional, Echocardiogram, Echocardiogram normal, Fatigue, Pericardial drainage; Pericardial effusion, Pericarditis, Red blood cell sedimentation rate increased, Troponin I increased More
Reported Symptoms: 10013966:DYSPNEA EXERTIONAL; 10016256:FATIGUE; 10034484:PERICARDITIS; 10047862:WE... Reported Symptoms: 10013966:DYSPNEA EXERTIONAL; 10016256:FATIGUE; 10034484:PERICARDITIS; 10047862:WEAKNESS; Narrative: 84M w/ PMH of CAD s/p multiple PCIs (last 2019), HTN, HLD, thoracoabdominal aortic aneurysm, and COPD presenting to the ED 11/5/24 d/t pericarditis, generalized weakness/fatigue, and DOE post flu vaccine (10/15/24). CT A/P showed moderate pericardial effusion. Was admitted for further management, where pt had pericardiocentesis procedure 11/6/24. Was started on colchicine and aspirin at discharge 11/9/24. Other Relevant HX: Other: pericarditis, weakness, fatigue, dyspnea on exertion More
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2830366 M DC 03/10/2025 FLUX
UNKNOWN MANUFACTURER

Rash Rash
Reported Symptoms: 10037844:RASH; Narrative: A 78yo male with PMH of PTSD who presented for initial ... Reported Symptoms: 10037844:RASH; Narrative: A 78yo male with PMH of PTSD who presented for initial Psychiatric visit by phone on Nov. 26, 2024, was reported with a historical ADR of influenza vaccine induced rash by the clinic physician. The MD's report included a note " remote history via application". No other detailed information regarding the vaccine, severity, including where and by who it was administered, was provided. Other Relevant HX: Other: RASH More
2830367 86 M SC 03/10/2025 FLU3
RSV
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
U8515BA
C499C
Diarrhoea, Pain, Tremor, Vomiting; Diarrhoea, Pain, Tremor, Vomiting Diarrhoea, Pain, Tremor, Vomiting; Diarrhoea, Pain, Tremor, Vomiting
Reported Symptoms: 10000424:ACHE; 10012727:DIARRHEA; 10040527:SHAKINESS; 10047700;VOMITING; Narrativ... Reported Symptoms: 10000424:ACHE; 10012727:DIARRHEA; 10040527:SHAKINESS; 10047700;VOMITING; Narrative: Pt reported vomiting, body aches, shaking, and diarrhea post vaccine administration of influenza and RSV vaccines. Other Relevant HX: DN, HTN, insomnia, Parkinson's Disease, CKD, hearing loss, exposure to hazardous chemical, tinnitus, vitamin d deficiency, hyperlipidemia, GERD, lower back pain, Hx of coronary artery bypass grafting, Hx of squamous cell carcinoma of skin Other: shaking; body aches More
2830368 77 M FL 03/10/2025 COVID19
MODERNA

Dermatitis Dermatitis
Reported Systems: 10012431:DERMATITIS; 10037844:RASH; Narrative: Other Relevant HX: Covid-19 booste... Reported Systems: 10012431:DERMATITIS; 10037844:RASH; Narrative: Other Relevant HX: Covid-19 booster vaccine; no previous reactions reported Other: DERMATITIS More
2830369 M DC 03/10/2025 FLUX
UNKNOWN MANUFACTURER

Urticaria Urticaria
Reporter Symptoms: 10046735: URTICARIA; Narrative: A 58 yo male with PMH of HTN, OA, HLD, Asthma, Rh... Reporter Symptoms: 10046735: URTICARIA; Narrative: A 58 yo male with PMH of HTN, OA, HLD, Asthma, Rhinitis, GERD, Dry Eyes, OSA and Sarcoidosis, who on Nov 8, 2024, presented as a new patient via Tele Health. The PCC physician reported the patient had a historical ADR of influenza vaccine induced urticaria classified as moderate. No other detailed information regarding the vaccine, (i.e. Mfr., Exp. date, lot#, reaction treatment, where and by who it was administered) was provided. Other Relevant HX: Other: URTICARIA More
2830370 52 M WV 03/10/2025 PNC20
PFIZER\WYETH
LG5575
Arthralgia, Myalgia Arthralgia, Myalgia
Reported Symptoms: 10003239:ARTHRALGIA; 10028322:MUSCLE PAIN; Narrative: Other relevant HX: Other MU... Reported Symptoms: 10003239:ARTHRALGIA; 10028322:MUSCLE PAIN; Narrative: Other relevant HX: Other MUSCLE PAIN More
2830371 48 M PA 03/10/2025 COVID19
PFIZER\BIONTECH

Neuropathy peripheral Neuropathy peripheral
Reporter Symptoms: 100292328:NEUROPATHY; Narrative: Other Relevant HX: Other: Neuropathy Reporter Symptoms: 100292328:NEUROPATHY; Narrative: Other Relevant HX: Other: Neuropathy
2830372 M OH 03/10/2025 FLU3
SANOFI PASTEUR
UT8437DA
Pruritus Pruritus
Reported Symptoms: 10037087:PRURITIS; Narrative: Other Relevant HX: PRURITIS Reported Symptoms: 10037087:PRURITIS; Narrative: Other Relevant HX: PRURITIS
2830373 57 F CA 03/10/2025 COVID19
COVID19
MODERNA
MODERNA
038B21A
038B21A
Arthralgia, Drug hypersensitivity, Headache, Impaired work ability, Injection si... Arthralgia, Drug hypersensitivity, Headache, Impaired work ability, Injection site warmth; Pain, Pyrexia, Tenderness More
Very tired, low grade fever of 99.9 F, body aches, slight headache, slightly upset stomach. To bed a... Very tired, low grade fever of 99.9 F, body aches, slight headache, slightly upset stomach. To bed at 12:40pm. Slept off and on all afternoon/evening. Two Aleve at midnight for body aches and headache. Slept off and on till 11am next day. Aleve again at 8am. Advil the remainder of day and next day. Body aches still on Monday. Stayed home from work and in bed all day. Feeling better. Used heating pad for achy hips on Monday. Slept well on Monday evening. Noticed red arm about the size of a fist in the shot area. Tender area to sleep on, but not too uncomfortable. Went to work on Tuesday but left after an hour and a half. Shared my story with co-worker and touched arm. Warm to the touch and had not noticed before. Resting on Tuesday and napped for a short time. More
2830374 73 M WA 03/10/2025 COVID19
PFIZER\BIONTECH

Pityriasis rosea Pityriasis rosea
Developed pityriasis rosea rash on trunk within 48 hours of vaccination. Herald patch erupted first ... Developed pityriasis rosea rash on trunk within 48 hours of vaccination. Herald patch erupted first then spread over trunk over the first 2-3 days. More
2830432 42 F CA 03/10/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH


Diplopia, Headache, Night blindness; Diplopia, Headache, Night blindness Diplopia, Headache, Night blindness; Diplopia, Headache, Night blindness
Occular headaches, severe double vision in right eye, severe impaired vision at night Occular headaches, severe double vision in right eye, severe impaired vision at night
โœ“
2830433 39 F CA 03/10/2025 COVID19
JANSSEN
N/A
Cyst, Discomfort, Tenderness Cyst, Discomfort, Tenderness
Massive lump with fluid inside. Pain and uncomfortable at touch Massive lump with fluid inside. Pain and uncomfortable at touch
โœ“
2830434 74 F FL 03/10/2025 TDAP
GLAXOSMITHKLINE BIOLOGICALS
L5229
Injection site erythema, Injection site pruritus, Injection site swelling, Injec... Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth More
warm ,red and swelling, itching, around injection site, extending about 3-4 inches. patient reported... warm ,red and swelling, itching, around injection site, extending about 3-4 inches. patient reported to pharmacy on 1 week later and at that time it was getting better. More
2830435 4 F IN 03/10/2025 DTAPIPV
MMRV
SANOFI PASTEUR
MERCK & CO. INC.
U8209CB
Y014438
Cellulitis, Pain, Skin lesion; Cellulitis, Pain, Skin lesion Cellulitis, Pain, Skin lesion; Cellulitis, Pain, Skin lesion
Patient got vaccines on 3/4/25 and they called our office on 3/6/25 to report it. After observation,... Patient got vaccines on 3/4/25 and they called our office on 3/6/25 to report it. After observation, the patient was given Cephalexin 250 mg/5mL to treat for cellulitis due to concern on examination and pression of lesion with pain. Patient was advised to go to ER or return to clinic with anything worsens. More
2830436 2 F PA 03/10/2025 FLU3
HEPA
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
AE2J&
DN273
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
Additional doses give no adverse reaction Additional doses give no adverse reaction
2830437 70 M FL 03/10/2025 PNC20
PFIZER\WYETH
lk6650
Erythema, Peripheral swelling, Pruritus Erythema, Peripheral swelling, Pruritus
pt reports that starting 03/5 or 03/06, he started having swelling, redness and itching on the arm t... pt reports that starting 03/5 or 03/06, he started having swelling, redness and itching on the arm that he received the vaccine in. He started to apply Benadryl gel to the area, and it helped with the itching, but it continued to spread and swell. Pt presented to the pharmacy 03/09 with redness and swelling from the bicep area to below the elbow on the left arm. Recommend pt see a doctor to rule out cellulitis More
2830438 10 M NC 03/10/2025 COVID19
COVID19
MODERNA
MODERNA
3043023
3043023
Feeling abnormal, Headache, Injection site pain, Pain in extremity, Pruritus; Py... Feeling abnormal, Headache, Injection site pain, Pain in extremity, Pruritus; Pyrexia, Rash More
At 5:00 am 3/5/25, patient told mom he felt bad with headache, mild aching in legs, and itching on h... At 5:00 am 3/5/25, patient told mom he felt bad with headache, mild aching in legs, and itching on his arms and shoulders. Left arm was sore at injection site. Mom noticed a rash said he had a fever and brought him into the clinic. Provider saw patient and determined adverse reaction to Moderna Covid vaccine administered 3/4/25: pityriasis rosea- like rash to arms, upper torso, and face: Dose Benadryl 12.5mg/5mL 5mL po given at 9:20 am in the office. 10:07 am patient reported itching had improved. Mom was instructed to continue benedryl for rash/itching and tylenol for fever/aches. In addition, prescription given for Loratadine 10 mg once daily for at 2 weeks. and TCA 0.1% cream twice daily to localized itchy spots only. More
2830439 53 F FL 03/10/2025 PNC20
PFIZER\WYETH
LK6650
Unevaluable event Unevaluable event
patient requested after asking if she had vaccine for above patient requested after asking if she had vaccine for above
2830440 75 F MN 03/10/2025 RSV
PFIZER\WYETH
kd0161
Impetigo, Injection site infection, Injection site pruritus, Injection site swel... Impetigo, Injection site infection, Injection site pruritus, Injection site swelling, Product administered at inappropriate site More
patient noticed itching/swelling at site went to urgent care and was given keflex for skin infection... patient noticed itching/swelling at site went to urgent care and was given keflex for skin infection due to shot. physician at time of visit said shot was given way too low. More
2830441 12 M MN 03/10/2025 MNQ
NOVARTIS VACCINES AND DIAGNOSTICS
AMXBO44A
Product preparation issue Product preparation issue
Inadvertently administered only the liquid conjugate component without the reconstituted powder Inadvertently administered only the liquid conjugate component without the reconstituted powder
2830442 33 F 03/10/2025 VARCEL
VARCEL
MERCK & CO. INC.
MERCK & CO. INC.


Chest discomfort, Dyspnoea, Hyperhidrosis, Lip swelling, Nausea; Swelling of eye... Chest discomfort, Dyspnoea, Hyperhidrosis, Lip swelling, Nausea; Swelling of eyelid More
1206 pt received Varicella virus vaccine into left upper back arm at 1230 pm pt demonstrated an alle... 1206 pt received Varicella virus vaccine into left upper back arm at 1230 pm pt demonstrated an allergic reaction to the vaccine, c/o nausea, sob and chest discomfort, lips swollen and eye lids swollen, pt noted to be diaphoretic pt alert and oriented x 3 during event episode, provider at bedside IV access placed pt received Benadryl 25 mg IV x 2 , and a bolus of L/R 500 cc than L/R at 125 cc/hr to a total volume of 900cc LR, v/s/s, O2 Sat 97-100 % on RA ,, EKG done Sinus Tachycardia, at 1400 pt states she is feeling much better and feels her symptoms are resolving and slept to 1545, sinus tach resolved , heart rate 70, pt denies sob, chest discomfort and nausea, pt discharged to home by provider More
2830443 74 F CO 03/10/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
025J20-2A
025J20-2A
029L20A
029L20A
037F21A
037F21A
Asthenia, Blood test, Computerised tomogram head, Computerised tomogram thorax, ... Asthenia, Blood test, Computerised tomogram head, Computerised tomogram thorax, Diplopia; Magnetic resonance imaging head, Muscular weakness, Myasthenia gravis; Asthenia, Blood test, Computerised tomogram head, Computerised tomogram thorax, Diplopia; Magnetic resonance imaging head, Muscular weakness, Myasthenia gravis; Asthenia, Blood test, Computerised tomogram head, Computerised tomogram thorax, Diplopia; Magnetic resonance imaging head, Muscular weakness, Myasthenia gravis More
Myasthenia Gravis....Diplopia, muscle weakness Symptoms started December 2024. Diagnosis March 6 2... Myasthenia Gravis....Diplopia, muscle weakness Symptoms started December 2024. Diagnosis March 6 2025 by Neurologist Dr Started pyRIDostigmine 60mg for weakness and double vision and infusion will be started once approved by insurance More
โœ“
2830444 62 M NY 03/10/2025 UNK
UNKNOWN MANUFACTURER
80777-0102-93
Cardiac arrest, Death Cardiac arrest, Death
Patient had a fatal cardiac arrest on February 14, 2024 Patient had a fatal cardiac arrest on February 14, 2024
โœ“
2830445 71 M MD 03/10/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
74NC9
Hypotension, Syncope Hypotension, Syncope
PATIENT WAS GIVEN VACCINE AT 9:30 AM AND THEN AT AROUND 7 PM FAINTED AT HOME. HE THEN FAINTED THE N... PATIENT WAS GIVEN VACCINE AT 9:30 AM AND THEN AT AROUND 7 PM FAINTED AT HOME. HE THEN FAINTED THE NEXT MORNING. HE SAID THIS WAS UNUSUAL BUT HE CALLED HIS DOCTOR AND THEY TOLD HIM TO HYDRATE BECAUSE HIS BLOOD PRESSURE WAS LOW More
2830446 73 F KY 03/10/2025 PNC21
TDAP
VARZOS
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
Y011819
XN575
74NC9
Unevaluable event; Unevaluable event; Unevaluable event Unevaluable event; Unevaluable event; Unevaluable event
State Board of Pharmacy Inspector reported to Market Director that it was reported to them that the ... State Board of Pharmacy Inspector reported to Market Director that it was reported to them that the patient visited an emergency department on the evening of the day the vaccines were administered. This is all the information that was given so far. More
2830447 35 F FL 03/10/2025 COVID19
MODERNA
028L20A
Deep vein thrombosis, Laboratory test, Ultrasound Doppler abnormal Deep vein thrombosis, Laboratory test, Ultrasound Doppler abnormal
Acute deep vein thrombosis (DVT) of axillary vein of left upper extremity Acute deep vein thrombosis (DVT) of axillary vein of left upper extremity
โœ“ โœ“ โœ“
2830448 88 M NJ 03/10/2025 DTAP
SANOFI PASTEUR
3CA25C1
No adverse event, Underdose No adverse event, Underdose
Patient was given a DTAP injection instead of a TDAP. patient came in for a wound on finger and need... Patient was given a DTAP injection instead of a TDAP. patient came in for a wound on finger and needed a booster per doctor's request. After speaking the Sanofi and confirming there is no harm to an 88-yr old getting a pediatric dose of DTAP. Patient has not had any complaints or side effects of the vaccine. patient was notified by provider. No further actions are needed in regard to the patient. More
2830449 62 F MI 03/10/2025 COVID19
COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
GH9702
GH9702
GH9702
Acute respiratory failure, COVID-19, Calcium ionised, Chronic obstructive pulmon... Acute respiratory failure, COVID-19, Calcium ionised, Chronic obstructive pulmonary disease, Computerised tomogram thorax abnormal; Condition aggravated, Dyspnoea, Glycosylated haemoglobin increased, Leukocytosis, Lung opacity; Pneumonia, Respiratory failure, Vitamin D More
Discharge Summary MD (Physician) ? General Medicine BRIEF OVERVIEW: Admission Date: 2/21/2025 Discha... Discharge Summary MD (Physician) ? General Medicine BRIEF OVERVIEW: Admission Date: 2/21/2025 Discharge Date: 2/27/2025 Discharge Disposition: Home without services Active Issues Requiring Follow-up: COPD DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Mixed metabolic and respiratory acidosis of newborn [P84] Pneumonia due to infectious organism, unspecified laterality, unspecified part of lung [J18.9] Acute on chronic hypoxic respiratory failure [J96.21] Acute on chronic respiratory failure [J96.20] HOSPITAL COURSE: 64 y.o. female with a history of COPD on 1.5-2 L nasal cannula at baseline, OSA, morbid obesity, and Crohn's disease who presented for increased shortness of breath and dyspnea. Acute on chronic hypoxic respiratory failure - resolved COPD Exacerbation - improving Leukocytosis Recent COVID-19 infection - On Chronic 1.5-2L of O2 at home but now requiring HFNC. O2 supplementation PRN w/ goal O2 saturation 88-92% - CT chest notable for extensive multifocal airspace disease - Remdesivir - Levaquin, metronidazole, vancomycin - Oral dexamethasone - Symbicort - Continued home montelukast - Albuterol PRN - Supportive care Hypertension - Continue home amlodipine - Home losartan increased from 25 to 50 mg; continue Hyperglycemia in the setting of steroid use Type II Diabetes, not on long term insulin - HbA1c 7.2 - Held home oral diabetic medications - Lantus 34U - Basal bolus insulin - Carb Control Diet History of CVA - Continued ASA, statin GAD - Continued BuSpar - Held trazodone - PRN Atarax Chronic low back pain Glaucoma - Continued eye drops Hyponatremia, mild - stable Hypocalcemia - resolved - Checked ionized calcium - Checked vitamin D History of Crohns Does not appear to be on immunomodulating therapy - Continued Bentyl Vertigo - PRN meclizine Microcytic anemia Morbid obesity CONSULTS / RECOMMENDATION: IP CONSULT TO NUTRITION Discharged to Home. More
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2830450 71 F MI 03/10/2025 COVID19
COVID19
COVID19
MODERNA
MODERNA
MODERNA
8080473
8080473
8080473
Abdominal X-ray, Abdominal pain, Blood lactic acid increased, COVID-19, Computer... Abdominal X-ray, Abdominal pain, Blood lactic acid increased, COVID-19, Computerised tomogram abdomen abnormal; Nausea, Patient isolation, SARS-CoV-2 test positive, Scan with contrast normal, Vomiting; X-ray normal More
Name: Medical Record #: Age: 71 y.o. DOB: 4/X/19XX Admit date: 3/2/2025 Discharge date: 3-5-25 A... Name: Medical Record #: Age: 71 y.o. DOB: 4/X/19XX Admit date: 3/2/2025 Discharge date: 3-5-25 Admitting Physician: MD Attending Physician at the Time of Discharge: MD Primary Care Physician: MD Reason for Admission: Small bowel obstruction Brief Summary of Hospital Stay: 71 year old female admitted with abdominal pain, nausea, and vomiting. Abdominal surgical history includes cholecystectomy, sleeve gastrectomy (2014) with a recent medical history of positive Covid (2-27-25). CT abd/pel were concerning for possible small bowel obstruction and possible pneumatosis intestinalis of jejunal loops. Laboratory studies were significant for lactic acid of 2.7. Patient was admitted and a gastrografin challenge was completed - no evidence of fecal impaction with oral contrast within the colon and distal ileum. A clear liquid diet was started and tolerated. Zosyn 4.5 g IV was ordered due to the concern of pneumatosis intestinalis. That was discontinued on hospital day #2. Patient was in isolation due to her recent Covid status but ambulated in room, completed her own self care without difficulty. Abdominal pain, nausea, and vomiting subsided. As patient is a bariatric patient, diet and behaviors were discussed. Patient has not been to the bariatric clinic for several years. Patient agreed to return to get her dietary choices back on track. By hospital day #2, patient tolerated full liquids with diet advancement. There was no return of abdominal pain, nausea, or vomiting. It was determined that patient was stable for discharge home. More
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2830451 63 F MI 03/10/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
EW0171
EW0171
Ankle fracture, Open reduction of fracture, Pain in extremity, Procedural pain, ... Ankle fracture, Open reduction of fracture, Pain in extremity, Procedural pain, Radiotherapy; Syncope, Wheelchair user More
Name: Medical Record #: Age: 67 y.o. DOB: 11/X/19XX Admit date: 3/3/2025 Discharge date: 3/5/... Name: Medical Record #: Age: 67 y.o. DOB: 11/X/19XX Admit date: 3/3/2025 Discharge date: 3/5/2025 Admitting Physician: MD Attending Physician at the Time of Discharge: DO Primary Care Physician: PAC Reason for Admission: Right trimalleolar fracture Hospital Course: Patient is a 67 YO F with PMHx of stage I vulvar cancer, type 2 diabetes mellitus, hypertension, chronic obstructive pulmonary disease, CKD 3, chronic pain/fibromyalgia who presents after syncopal event with right leg pain and found to have unstable right trimalleolar fracture, status post ORIF on 3/4 by Dr. Post operative pain was difficult to control, but on the day of discharge she was well controlled with oxycodone 10 mg every 3 hours. She received radiation therapy in the hospital. She and her husband refused placement as she is essentially wheelchair-bound at baseline, following surgery was nonweightbearing right lower extremity on day of discharge. She was discharged home with home healthcare services on 3/5/2025 More
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2830452 58 F 03/10/2025 COVID19
MODERNA

Inflammation, Joint swelling, Muscle atrophy, Pain Inflammation, Joint swelling, Muscle atrophy, Pain
Joint swelling, pain, inflammation. Right arm and right shoulder muscle breakdown, muscle loss. Pt w... Joint swelling, pain, inflammation. Right arm and right shoulder muscle breakdown, muscle loss. Pt was prescribed Methotrexate, Humira, prednisone, then Rinvoq. More
2830453 69 M MI 03/10/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
HG6396
HG6396
Amnesia, Blood glucose normal, Cerebral haemorrhage, Disorientation, Fall; Fatig... Amnesia, Blood glucose normal, Cerebral haemorrhage, Disorientation, Fall; Fatigue, Glycosylated haemoglobin normal, Headache, Subdural haematoma More
Name: Date of Birth: 6/XX/19XX (Age: 70 y.o.) Date of Admission: 3/5/2025 Date of Discharge: 3/9... Name: Date of Birth: 6/XX/19XX (Age: 70 y.o.) Date of Admission: 3/5/2025 Date of Discharge: 3/9/2025 Consultants: neurology, neurosurgery Intern/Resident: n/a Hospital Course by Discharge Diagnoses: Intraparenchymal Hemorrhage and Subdural Hematoma -involving left frontal lobe, left tentorium and right lateral ventricle -appreciate neurosurgery input, no surgical intervention planned, keep systolic bp<150 -cont to hold any asa or ac at this time until resolved on serial imaging -stable for dc home per PT/OT recs, home therapy -f/u ct head ordered by neurosurgery Diabetes Mellitus -carb restrict, on ssi, glucose relatively controlled -cont home meds which includes jardiance, A1c 6.6 History of Substance Abuse -h/o endocarditis -mod-severe tricuspid regurg -cont home methadone Hypertension -increase valsartan, cont home spironolactone, resume home amlodipine Hyperlipidemia -cont statin Anxiety/Depression -cont citalopram, buspirone BPH-cont tamsulosin Tobacco Use -counsel cessation, nicotine patch Microcytosis without Anemia -fe studies normal, likely beta thalassemia Brief Admission History/Reason for Admission: Per H&P: 70 y.o.male with PMHx of alcohol abuse, opiate abuse, MDD, diabetes type 2, BPH, hypertension, osteoporosis who presented to the hospital overnight after an unwitnessed fall at home. His daughter, who is present for exam, states that she and her sister were with him and heard a loud thud around 2:00am. They went to check on their dad and he was on the ground in the bathroom. He does not recall the events of the fall or if he experienced any presyncopal symptoms. He is still unsure what occurred. He complains of a headache and is tired and slightly altered to orientation at this time, but denise any troubles with speech, hearing, numbness or weakness in his extremities or other focal neurologic deficits. He does not take ASA or other anticoagulation. Discharged to Home. More
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2830454 16 M 03/10/2025 FLU3
MENB
MNQ
GLAXOSMITHKLINE BIOLOGICALS
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
ae2j7
dd72h

Arthralgia, Shoulder injury related to vaccine administration; Arthralgia, Shoul... Arthralgia, Shoulder injury related to vaccine administration; Arthralgia, Shoulder injury related to vaccine administration; Arthralgia, Shoulder injury related to vaccine administration More
Pain in both shoulders after vaccines, right worse than left. SIRVA Pain in both shoulders after vaccines, right worse than left. SIRVA
2830455 66 F IL 03/10/2025 FLU3
RSV
SEQIRUS, INC.
PFIZER\WYETH
388490
LG9828
Asthenia, Dizziness, Heart rate irregular; Asthenia, Dizziness, Heart rate irreg... Asthenia, Dizziness, Heart rate irregular; Asthenia, Dizziness, Heart rate irregular More
66 with notable PMH of HIV and HSV received flu vax (>65) in right delt and RSV vax in left delt ... 66 with notable PMH of HIV and HSV received flu vax (>65) in right delt and RSV vax in left delt at internal medicine clinic. pt had received flu vaccine prior (last admin documented in 2020), however this was pt's first time receiving 65+ vax. this was also first time receiving RSV vax. after vaccine administration, pt reported feeling dizzy and weak, and RRT was called and pt was transported to ED. Pt reported that her partner had some sort of viral illness prior to visit, but reported feeling well in ED other than body aches. Pt was admitted for observation and ultimately diagnosed with HRV. No notable events occurred during admission and pt was discharged the next day More
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2830456 0.33 M IA 03/10/2025 FLU3
SANOFI PASTEUR
UT8468MA
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
REPORT BEING SUBMITTED ON THE DAY THE VACCINE WAS GIVEN, NO IMMEDIATE SYMPTOMS. PARENT OF PATIENT WA... REPORT BEING SUBMITTED ON THE DAY THE VACCINE WAS GIVEN, NO IMMEDIATE SYMPTOMS. PARENT OF PATIENT WAS GIVEN A INFORMATIONAL SHEET AND ASKED TO CONTACT OUR OFFICE OR TAKE PATIENT TO ER IF SYMPTOMS WERE SEVERE. NO TREATMENT NECESSARY AT THIS TIME. More
2830457 53 F WI 03/10/2025 PNC20
PFIZER\WYETH
LK6651
Diarrhoea, Nausea, Palpitations, Vomiting Diarrhoea, Nausea, Palpitations, Vomiting
Diarrhea, nausea, vomiting, palpitations Diarrhea, nausea, vomiting, palpitations
2830458 12 F WA 03/10/2025 COVID19
PFIZER\BIONTECH
EW0196
Anisomastia, Micromastia Anisomastia, Micromastia
The covid vaccination was given in the left arm and the left breast is significantly smaller than th... The covid vaccination was given in the left arm and the left breast is significantly smaller than the right breast. will need surgery to increase the size. has been seen by OBGYN. micromastia to the left breast. More
2830459 66 M MO 03/10/2025 COVID19
MODERNA
3043333
Rash, Seborrhoeic dermatitis Rash, Seborrhoeic dermatitis
Two different skin rashes appeared on legs, torso and face. One was Seborrheic Dermatitis and the o... Two different skin rashes appeared on legs, torso and face. One was Seborrheic Dermatitis and the other was not explained. Rashes began on 12/13/2024 and has not gone away as of 3/10/2025. More
2830460 13 F CO 03/10/2025 HEP
GLAXOSMITHKLINE BIOLOGICALS
92NK2
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient was given an adult dose of the Hepatitis B vaccine. No adverse events reported. Patient was given an adult dose of the Hepatitis B vaccine. No adverse events reported.
2830461 0.67 F UT 03/10/2025 FLU3
SANOFI PASTEUR
U8518DA
Extra dose administered Extra dose administered
Patient was brought into clinic on 12/23/2024 to receive booster flu vaccination and flu vaccination... Patient was brought into clinic on 12/23/2024 to receive booster flu vaccination and flu vaccination was administered that day. The flu vaccination was not documented into clinic system as being administered. Patient was brought in for an appointment on 02/18/2025 and was administered another flu vaccination dose because the dose on 12/23/2024 was not documented and it looked like patient still needed flu booster vaccination. Patient received a total of 3 flu vaccinations. Patient has been reported to be doing fine and displayed no side effects on 03/05/2025. More
2830462 61 F WI 03/10/2025 PNC21
MERCK & CO. INC.
Y013009
Injection site erythema, Injection site warmth, Lethargy, Pain, Pyrexia Injection site erythema, Injection site warmth, Lethargy, Pain, Pyrexia
Patient developed red warm circular area around the injection site approximately 1 day after receivi... Patient developed red warm circular area around the injection site approximately 1 day after receiving the vaccine. He also became lethargic and mild fever/body aches temporarily the day following. He is continuing to have redness around injection site 2 days post vaccination. More
2830463 60 M MI 03/10/2025 FLU3
GLAXOSMITHKLINE BIOLOGICALS
9h5j5
Unevaluable event Unevaluable event
10 years prior he good stomach pains from a flu vaccine. 10 years prior he good stomach pains from a flu vaccine.
2830464 61 F WA 03/10/2025 RSV
PFIZER\WYETH
LN5491
Injection site erythema, Injection site pain, Injection site pruritus Injection site erythema, Injection site pain, Injection site pruritus
5 days post vaccine. Itchy, raised & red area at inj site with soreness. 5 days post vaccine. Itchy, raised & red area at inj site with soreness.
2830465 46 M TN 03/10/2025 HEPA
HPV9
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
z27pb
y007322
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
given out of age range given out of age range
2830466 26 M CA 03/10/2025 DTAP
SANOFI PASTEUR

Injection site pain Injection site pain
Severe pain in shoulder where vaccination was given Severe pain in shoulder where vaccination was given
2830467 59 M NY 03/10/2025 PNC21
MERCK & CO. INC.
yo13009
Injection site cellulitis, Injection site erythema, Injection site swelling Injection site cellulitis, Injection site erythema, Injection site swelling
cellulitis (severe redness and swelling) around inject site. prescriber put the patient on doxycycli... cellulitis (severe redness and swelling) around inject site. prescriber put the patient on doxycycline on 3/10/2025 More