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
2831630 85 F FL 03/16/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 JB27A
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received a second dose of an RSV vaccine, first dose was administered in Jan. 2024. Pharmacy... Patient received a second dose of an RSV vaccine, first dose was administered in Jan. 2024. Pharmacy corporate team notified the store about the duplication. Pt has been notified, nothing to report to us at this time no issues at all. More
2831631 55 F OK 03/16/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 354m3
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
patient stated sore, red, and swollen arm at site of injection patient stated sore, red, and swollen arm at site of injection
2831632 0.33 M GU 03/16/2025 DTAPHEPBIP
HIBV
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
PFIZER\WYETH
 B532G
Y013470
LK6650
Death, Intensive care, Resuscitation, Unresponsive to stimuli; Death, Intensive ... Death, Intensive care, Resuscitation, Unresponsive to stimuli; Death, Intensive care, Resuscitation, Unresponsive to stimuli; Death, Intensive care, Resuscitation, Unresponsive to stimuli More
Infant was found at home unresponsive around 1900 on March 13, 2025, father began CPR and infant was... Infant was found at home unresponsive around 1900 on March 13, 2025, father began CPR and infant was brought to nearest hospital where the infant was then stabilized for transfer to a facility with an available pediatric provider. Infant slowly declined and was no longer responsive to treatments in ICU. Infant was pronounced deceased March 14, 2025 at 0814. More
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2831652 28 M IN 03/16/2025 COVID19
 PFIZER\BIONTECH
Arthralgia, Injection site erythema Arthralgia, Injection site erythema
Crepitus at injection site- popping started to occur with any movement in right arm. This popping wa... Crepitus at injection site- popping started to occur with any movement in right arm. This popping was frequent when performing circular cleaning motions with shoulder or any circular motion at the shoulder joint. This popping decreased over a span of 2 years but transitioned to pain in the shoulder joint. Popping still presently happening in shoulder in 2025 More
2831653 15 M GU 03/16/2025 HEPA
HPV9
MNQ
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
SANOFI PASTEUR
MERCK & CO. INC.
 T5727
1957405
U7996AA
Y011015
Generalised tonic-clonic seizure; Generalised tonic-clonic seizure; Generalised ... Generalised tonic-clonic seizure; Generalised tonic-clonic seizure; Generalised tonic-clonic seizure; Generalised tonic-clonic seizure More
Patient experienced a seizure approximately 2-3 minutes following receiving vaccines while I was att... Patient experienced a seizure approximately 2-3 minutes following receiving vaccines while I was attempted to place a tuberculin skin test. I did not inject the tuberculin because he started to seize. Patient had a first time witnessed seizure lasting 10-15 seconds. Seizure was tonic clonic. He did not experience any post-ictal symptoms. Patient's vitals were normal following seizure. He reported that he felt normal following seizure. EMS was called and patient was transferred to the emergency department for evaluation. More
2831566 55 F 03/15/2025 UNK
VARCEL
 UNKNOWN MANUFACTURER
MERCK & CO. INC.

Contraindication to vaccination, Injection site nodule, Pyrexia; Contraindicatio... Contraindication to vaccination, Injection site nodule, Pyrexia; Contraindication to vaccination, Injection site nodule, Pyrexia More
E-mail received in the Contact Center mailbox on 19FEB2025 at 1:07 PM ET forwarded from Merck emplo... E-mail received in the Contact Center mailbox on 19FEB2025 at 1:07 PM ET forwarded from Merck employee with the subject line " FW: Correspondence from Sanofi 2025SA021994" reporting a AE for VARICELLA ZOSTER VACCINE LIVE VARICELLA VACCINE" (se; Pyrexia; Contraindicated product administered; This spontaneous report was received from a consumer referring to a 55-year-old female patient. Information regarding the patient's concurrent conditions, medical history, or concomitant medications was not provided. On 20-JAN-2025, the patient was vaccinated with varicella zoster vaccine live, manufacturer unknown, administered in the left arm (dose, route of administration, lot number and expiration date was not reported), it was reported as contraindicated product administered. On 21-JAN-2025 the patient developed a knot on her left arm at the injection site (injection site mass) (latency 5 months approximately) following the first dose of Varicella zoster vaccine live. On the same date, body temperature was measured and showed 101.2 (units not provided) (Pyrexia). At the time of the reporting the outcome of the events was unknown. The causal relationship between the events occurred and the suspect vaccine was not reported. More
2831571 F 03/15/2025 MMR
MMR
VARCEL
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.



Antibody test negative; Antibody test negative; Antibody test negative; Antibody... Antibody test negative; Antibody test negative; Antibody test negative; Antibody test negative More
Customer called asking about the need for re-vaccination for MMR and VARIVAX. Customer said she was ... Customer called asking about the need for re-vaccination for MMR and VARIVAX. Customer said she was re-vaccinated for VARIVAX in 2020 or 2021 for a job. She had a "blood test" recently and it shows that she "does not have immunity" for either VARIVAX; This spontaneous report was received from a consumer referring to herself, a female patient of unknown age. The patient's pertinent medical history, concurrent conditions, previous drug reactions or allergies and concomitant medications were not reported. On an unknown date (reported as in 2020 or 2021), the patient was re-vaccinated for a job, with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) and with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), (doses, routes of administration, anatomical sites of injection, lot numbers and expiration dates were not reported); both vaccines administered for prophylaxis. On unknown date (reported as recently), the patient took a blood test and it showed that she didn't have immunity for either Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX) or Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) (Antibody test negative). At the time of the reporting, the outcome of the event was unknown. The causal relationship between the event and the suspect therapies was not provided. More
2831572 M SC 03/15/2025 VARCEL
 MERCK & CO. INC.
 Y010045
Product storage error Product storage error
VARIVAX administered after temperature excursion; This spontaneous report was received from a Pharma... VARIVAX administered after temperature excursion; This spontaneous report was received from a Pharmacist and refers to a male patient of unknown age. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 07-Feb-2025, the patient was vaccinated with an improperly stored dose of Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX) 0.5 ml, intramuscular, lot #Y010045, expiration date: 29-May-2026 (strength, dose number and anatomical location were not provided) which was reconstituted with sterile diluent (MERCK STERILE DILUENT) (strength, dose, lot number and expiration date were not provided) for prophylaxis The temperature excursion was in 54.9๏ฟฝF, for 1 hour 30 minutes and there was no previous temperature excursion. More
2831580 50 F WI 03/15/2025 COVID19
 MODERNA
 Unknown
Rash Rash
Rash to race, neck and shoulders Rash to race, neck and shoulders
2831581 68 M TX 03/15/2025 COVID19
 PFIZER\BIONTECH
Death, Heart rate increased Death, Heart rate increased
rapid unexplained heartbeat which then caused death rapid unexplained heartbeat which then caused death
โœ“ โœ“
2831582 45 F MI 03/15/2025 COVID19
COVID19
COVID19
COVID19
 JANSSEN
JANSSEN
JANSSEN
JANSSEN



Back pain, Biopsy, Blood iron decreased, Blood test, Cartilage atrophy; Culture,... Back pain, Biopsy, Blood iron decreased, Blood test, Cartilage atrophy; Culture, Fatigue, Fungal infection, Laboratory test, Migraine; Nasal septum disorder, Oral disorder, Oral mucosal blistering, Oropharyngeal blistering, Parosmia; Skin lesion, Throat lesion More
Covid lesions blisters in on mouth throat nose lost cartilage and septum extremely low iron having i... Covid lesions blisters in on mouth throat nose lost cartilage and septum extremely low iron having injections constant yeast infections causing lesions all over body extreme exhaustion and back pain and migraine.. phantom smells cigarette cat urine and has. More
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2831583 63 F PA 03/15/2025 PNC21
 MERCK & CO. INC.
 Y019158
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling More
5 days after vaccine, developed pain, redness, swelling and pruritus at the injection site. Lesion w... 5 days after vaccine, developed pain, redness, swelling and pruritus at the injection site. Lesion was circular, approximately 4 inches in diameter, raised, red and warm. No systemic symptoms. Resolved in 2 days. More
2831584 87 F 03/15/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received a second RSV vaccination; pt did not report any adverse effects due to this duplica... Patient received a second RSV vaccination; pt did not report any adverse effects due to this duplication More
2831585 69 M OH 03/15/2025 PPV
 MERCK & CO. INC.
Injection site cellulitis Injection site cellulitis
cellulitis at injection site cellulitis at injection site
2831586 47 M AR 03/15/2025 COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 GJ3274
GJ3274
GJ3274
GJ3274
GJ3274
Abnormal loss of weight, Arthralgia, Axonal neuropathy, Balance disorder, Biopsy... Abnormal loss of weight, Arthralgia, Axonal neuropathy, Balance disorder, Biopsy muscle; Concussion, Condition aggravated, Demyelination, Electromyogram abnormal, Fall; Hypoaesthesia, Immunoglobulin therapy, Large fibre neuropathy, Lumbar puncture, Lumbar radiculopathy; Lumbosacral radiculoplexus neuropathy, Multiple fractures, Muscular weakness, Nerve conduction studies abnormal, Neuropathy peripheral; Pain in extremity, Walking aid user, Wheelchair user More
On Febr. 10, 2023, I was walking a tour at Cemetery and my left leg felt wobbly. By May 2023 I was e... On Febr. 10, 2023, I was walking a tour at Cemetery and my left leg felt wobbly. By May 2023 I was experiencing pain in left leg. On Sept. 16, 2023, I was falling down because my left knee was buckling. Between Sept. 2023 and April 2024, I fell approximately 75 times, despite using crutches. I have been under a doctor's care since Oct. 2023. I had a second covid vaccine in Jan. 2024. On Feb. 1, 2024, the pain and weakness started in my right leg and I started falling by my right leg buckling, too. I have been in a wheelchair since April 2024 and have suffered five broken bones and a concussion from my falls. I did not get an accurate diagnosis until October 2024. I live in (redacted). My neurologist in (redacted) sent me to a another state, neurologist named Dr. In Aug. 2024, he suspected that I had "a diabetic radiculoplexopathy." He further noted in these notes: "Lack of response to IVIG argues against CIDP despite mild demyelinating features seen on NCS. In context of diabetes may represent diabetic radiculoplexus neuropathy. Currently with severe functionally limiting weakness affecting both lower extremities." He scheduled me for further testing. After further testing, Dr. believed that I had a diabetic radiculoplexus neuropathy. He noted on October 1, 2024: "Most consistent with diabetic radiculoplexus neuropathy. . . . I suspect his overall presentation is most consistent with diabetic radiculoplexus neuropathy." Dr. referred me to the neurology department at specialty clinic "for opinion on the current symptoms." Dr. instructed me in October 2024 to consider not getting further covid vaccinations. I underwent further testing and examination at specialty clinic in Nov. and Dec. 2024, under the direction of Dr., a world-renowned neurologist and the former dean of the specialty clinic medical school. After reviewing the new objective data from the tests conducted at clinic, he noted: "I reviewed patient's electrophysiological studies today. They clearly show changes most compatible with diabetes associated radicular plexus neuropathies in the lower limbs superimposed on a more generalized mild peripheral neuropathy." He diagnosed me as follows: "As in my addendum from November 29th, the electrophysiologic findings are suggestive of a large fiber, axonal more than demyelinating peripheral neuropathy with superimposed bilateral L3-L5 radiculopathies, without paraspinal muscle involvement. Clinically, this fits best with bilateral lumbosacral radiculoplexus neuropathy. Given that this presented in association with 45 lb weight loss (unintentional), moderately severe hip an anterior thigh pain, followed by the progression of weakness in the left leg, this is most compatible with a diabetes associated lumbosacral radiculoplexus neuropathy. In addition, the right leg developed pain and numbness months after the left leg, at the same time as the left leg stabilized. If we put this together with the electrophysiological findings, I think we can be confident of the diagnosis." More
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2831587 59 M FL 03/15/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 L5229
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Patient received a second dose of Boostrix within the 10-year recommendation time on accident. The p... Patient received a second dose of Boostrix within the 10-year recommendation time on accident. The patient did not report any signs or symptoms. More
2831588 82 F PA 03/15/2025 RSV
 PFIZER\WYETH
 LG9828
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient was given a duplicate RSV vaccine on 3/12/25 (original 2023). Patient has not reported any a... Patient was given a duplicate RSV vaccine on 3/12/25 (original 2023). Patient has not reported any adverse reactions to the shot or health events related to receiving the vaccine. More
2831589 16 F PA 03/15/2025 MENB
MENB
MNQ
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
SANOFI PASTEUR
 77KA5
77KA5
U8369AA
U8369AA
Injection site cellulitis, Injection site erythema, Injection site rash, Injecti... Injection site cellulitis, Injection site erythema, Injection site rash, Injection site warmth, Pain in extremity; Tenderness; Injection site cellulitis, Injection site erythema, Injection site rash, Injection site warmth, Pain in extremity; Tenderness More
Both shots administered in left arm after injection site was wiped with alcohol swab. Significant p... Both shots administered in left arm after injection site was wiped with alcohol swab. Significant pain started in left arm <5 hours after shot; Advil provided around 8pm due to pain. Pain continued on Friday, March 16th. Advil administered around 6am, Alieve around 11am, and Tylenol around 3pm. Touching/bumping arm caused significantly more pain. Rash, that was swollen, pink, and hot to the touch noted on arm around 8pm approximately 2cm below the injection site. Circle drawn around the rash. Saturday, March 15th 8am pain persisted, rash was red, hot to the touch, very tender, and slightly outside circle drawn the night before. Contacted PCP. PCP visit on March 15th at 11am, diagnosed with cellulitis. Rash measured approximately 8cm x 6cm. Oral cephalexin prescribed. More
2831590 60 M MN 03/15/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 A2J35
Rash, Rash morbilliform, Rash pruritic Rash, Rash morbilliform, Rash pruritic
About 10 days after the MMR vaccine I developed a rash on my arms, torso, and legs. The rash looked... About 10 days after the MMR vaccine I developed a rash on my arms, torso, and legs. The rash looked like measles bumps but it itched significantly. I was able to manage with hydrocortisone and it is almost completely gone. More
2831591 68 F CT 03/15/2025 RSV
RSV
 PFIZER\WYETH
PFIZER\WYETH

Arthralgia, Asthenia, Dizziness, Headache, Myalgia; Nausea, Tinnitus Arthralgia, Asthenia, Dizziness, Headache, Myalgia; Nausea, Tinnitus
Headache, nausea, muscle & join pain, weakness, dizziness, ringing in the ears. Headache, nausea, muscle & join pain, weakness, dizziness, ringing in the ears.
2831592 79 M CA 03/15/2025 COVID19
 PFIZER\BIONTECH
Haematuria, Lichen planus Haematuria, Lichen planus
Lichen Planus and intermittent hematuria Lichen Planus and intermittent hematuria
2831593 71 M NV 03/15/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
 LJ5283
LJ5283
Hypoaesthesia, Hypoaesthesia oral, Injection site pain, Loss of personal indepen... Hypoaesthesia, Hypoaesthesia oral, Injection site pain, Loss of personal independence in daily activities, Muscle spasms; Pain in extremity, Tenderness More
The patient has been experiencing sharp pain on the injection site (upper right arm) after he receiv... The patient has been experiencing sharp pain on the injection site (upper right arm) after he received Prevnar 20 on 01/24/2025. He complained the pain was spreading through the whole arm, and he experienced numbness, muscle spasms, sensitive sensation on his right arm. The adverse reaction causes the challenge for the patient to perform daily activities. The patient has been using ibuprofen and lidocaine patch to relieve the symptoms. More
2831594 74 M NY 03/15/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 EN6206
EN6206
Balance disorder, Computerised tomogram, Delayed dark adaptation, Delayed light ... Balance disorder, Computerised tomogram, Delayed dark adaptation, Delayed light adaptation, Dizziness; Magnetic resonance imaging, Vertigo, X-ray More
Severe vertigo for 2 days then consistent dizziness, off balance, trouble when going from dark to li... Severe vertigo for 2 days then consistent dizziness, off balance, trouble when going from dark to light or light to dark. It has been 4 years with no change. Have seen neurosurgeons, , ENT, chiropractors, acupuncturist. More
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2831595 57 F CA 03/15/2025 UNK
 UNKNOWN MANUFACTURER
Mobility decreased, Pain, Sleep disorder Mobility decreased, Pain, Sleep disorder
Today is March 15th, I have had persistently difficulty moving my arm, raising my right arm or lifti... Today is March 15th, I have had persistently difficulty moving my arm, raising my right arm or lifting it without pain. This includes sleep. No swelling or red streaks. It has been reported to my doctor and I have an appointment with a NP on March 17th. More
2831596 77 M FL 03/15/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 f4ac3
Extra dose administered, Pain in extremity Extra dose administered, Pain in extremity
Patient had previously gotten the RSV vaccine in 11/6/2024. This was a 2nd dose which is not current... Patient had previously gotten the RSV vaccine in 11/6/2024. This was a 2nd dose which is not currently recommended by CDC. Patient did not report any side effects other than a sore arm. More
2831597 87 F CA 03/15/2025 PNC20
TDAP
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 LK6651
XN575
Erythema, Rash, Skin warm; Erythema, Rash, Skin warm Erythema, Rash, Skin warm; Erythema, Rash, Skin warm
Rash on arm, redness, warmth Rash on arm, redness, warmth
2831598 77 F FL 03/15/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 f4ac3
Extra dose administered, Pain in extremity Extra dose administered, Pain in extremity
Patient had previously gotten the RSV vaccine in 11/6/2024. This was a 2nd dose which is not current... Patient had previously gotten the RSV vaccine in 11/6/2024. This was a 2nd dose which is not currently recommended by CDC. Patient reported sore arm. More
2831599 78 F FL 03/15/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 jb27a
Burning sensation Burning sensation
pt said her arm felt like it was on fire for a couple of hrs after the vaccine pt said her arm felt like it was on fire for a couple of hrs after the vaccine
2831600 62 F NC 03/15/2025 PNC21
 MERCK & CO. INC.
 Y011819
Injection site erythema, Injection site pain, Injection site warmth, Skin infect... Injection site erythema, Injection site pain, Injection site warmth, Skin infection More
Patient stated she went to the doctor with an injection site reaction approximately 5 days after rec... Patient stated she went to the doctor with an injection site reaction approximately 5 days after receiving the vaccine. She was having pain, warmth, and redness at the injection site. She was diagnosed with a skin infection. She was put on antibiotics for the infection. More
2831601 53 F AL 03/15/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 x72d2
Erythema, Pain in extremity, Skin warm Erythema, Pain in extremity, Skin warm
Patient has red, warm to touch, sore arm for the past few days. Patient has red, warm to touch, sore arm for the past few days.
2831602 12 F MD 03/15/2025 DTAP
DTAP
MNQ
MNQ
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR



Erythema multiforme, Rash, Rash erythematous, Rash papular, Rash pruritic; Skin ... Erythema multiforme, Rash, Rash erythematous, Rash papular, Rash pruritic; Skin lesion; Erythema multiforme, Rash, Rash erythematous, Rash papular, Rash pruritic; Skin lesion More
Rash began on 2/26 on palms of hands, red papules. Target lesions developed at day 3 spread to arms ... Rash began on 2/26 on palms of hands, red papules. Target lesions developed at day 3 spread to arms and legs. Very itchy. Erythema Multiforme minor diagnosis on 3/2/2025. Started on prednisone. More
2831603 36 M AR 03/15/2025 MMR
 MERCK & CO. INC.
 Y013131
Bell's palsy, Visual acuity tests Bell's palsy, Visual acuity tests
Bell's Palsy. High dose steroids for 7 days and valtrex 1 gm tid for 7 days. Treatment ongoing... Bell's Palsy. High dose steroids for 7 days and valtrex 1 gm tid for 7 days. Treatment ongoing. More
2831604 52 F CA 03/15/2025 COVID19
 PFIZER\BIONTECH
 EWO151
Acoustic stimulation tests abnormal, Hypoacusis, Pyrexia, Tinnitus Acoustic stimulation tests abnormal, Hypoacusis, Pyrexia, Tinnitus
Tinnitus began suddenly the evening of my first Pfizer Covid-19 vaccination dose. I also had 100-102... Tinnitus began suddenly the evening of my first Pfizer Covid-19 vaccination dose. I also had 100-102 degree fever for 4-5 days following vaccination and subsequent doses/boosters. More
2831605 75 F CO 03/15/2025 RSV
 PFIZER\WYETH
 HM9854
Fatigue, Nasal congestion, Pain Fatigue, Nasal congestion, Pain
March 14, I started feeling achy in the afternoon and nasal congestion. March 15 all day achy all o... March 14, I started feeling achy in the afternoon and nasal congestion. March 15 all day achy all over and fatigue. More
2831606 91 M FL 03/15/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered, No adverse event Extra dose administered, No adverse event
patient received the vaccine twice , on 09/26/2024 and on 03/14/2025 . pt has no symptoms or side ef... patient received the vaccine twice , on 09/26/2024 and on 03/14/2025 . pt has no symptoms or side effects to the vaccine More
2831607 70 M AL 03/15/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered Extra dose administered
Patient received a duplication in doses of Boostrix. One dose given on 3/10/25 and an additional dos... Patient received a duplication in doses of Boostrix. One dose given on 3/10/25 and an additional dose on 3/12/25 More
2831608 36 M 03/15/2025 UNK
 UNKNOWN MANUFACTURER
Muscle discomfort Muscle discomfort
The muscle in the arm started to feel strange & no one addressed it The muscle in the arm started to feel strange & no one addressed it
2831609 48 F CA 03/15/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 LN0588
LN0588
Arthralgia, Asthenia, Hypoaesthesia, Mobility decreased, Musculoskeletal stiffne... Arthralgia, Asthenia, Hypoaesthesia, Mobility decreased, Musculoskeletal stiffness; Myalgia, Odynophagia, Paraesthesia, Rash More
sudden onset of severe Myalgias and stiff neck starting in neck, shoulders, and arms descending over... sudden onset of severe Myalgias and stiff neck starting in neck, shoulders, and arms descending over time to the hips. Neck was so stiff that it was painful to swallow.. The neck stiffness resolved over a few days, but the severe shoulder and arm pain continued for at least a week. Weakness was such that it was difficult to turn over in bed; Noticed Rash that covered at least arms and torso the next morning after onset of the myalgias (although didn't check whole body for rash). Tingling in arms and hands throughout the week. Hands started going numb every night during that week and continued going numb every night for months. The numbness in hands continues to happen at night while sleeping (as of today 3/15.2025). More
2831660 71 F ID 03/15/2025 PNC20
 PFIZER\WYETH
 LK6655
Injection site oedema, Injection site warmth Injection site oedema, Injection site warmth
Patient presented to UC with the reaction. Patient presented with edema to the immunization site wit... Patient presented to UC with the reaction. Patient presented with edema to the immunization site with warmth. More
2831361 CA 03/14/2025 MMR
MMR
 MERCK & CO. INC.
MERCK & CO. INC.
 X004346
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event More
no adverse event; Expired vaccine used; Information has been received from Business Partner/CRO on 1... no adverse event; Expired vaccine used; Information has been received from Business Partner/CRO on 12-Feb-2025. This spontaneous report was received from a/an Other health professional and refers to a(n) patient of unknown age and gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On an unknown date, the patient started therapy with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II), (lot #X004346, expiration date: 08-Feb-2025) (0.5ml SQ),. On an unknown date, the patient started therapy with sterile diluent (MERCK STERILE DILUENT), (lot # and expiration date were not reported). The patient started therapy with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II), for the treatment of prophylaxis. The patient started therapy with sterile diluent (MERCK STERILE DILUENT), for the treatment of prophylaxis. On 12-Feb-2025, the patient experienced Expired vaccine used. On an unknown date, the patient experienced no adverse event. At the reporting time, the outcome of Expired vaccine used was unknown. The action taken with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live was reported as not applicable. More
2831379 24 F TN 03/14/2025 TDAP
 SANOFI PASTEUR
 u8274aa
Exposure during pregnancy, Inappropriate schedule of product administration Exposure during pregnancy, Inappropriate schedule of product administration
There were two patients that were pregnancy. First patient was 28 week and the next patient was 23 w... There were two patients that were pregnancy. First patient was 28 week and the next patient was 23 weeks and 5 days. MA was notified to give the 28 weeks patient a TDAP but the MA was gave the 23 weeks and 5 day patient the TDAP. Patient was notified about the vaccine and was given a VIS SHEET as well. More
2831380 24 F CA 03/14/2025 MMR
MMR
MMR
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 KH2BD
KH2BD
KH2BD
Coma, Decreased appetite, Fatigue, Glossodynia, Headache; Heart rate increased, ... Coma, Decreased appetite, Fatigue, Glossodynia, Headache; Heart rate increased, Lymph node pain, Lymphadenopathy, Nausea, Oropharyngeal pain; Pyrexia, Stomatitis, Vision blurred More
Day 14 (onset of symptoms): Developed swollen and painful lymph nodes (primarily in left groin and a... Day 14 (onset of symptoms): Developed swollen and painful lymph nodes (primarily in left groin and abdominal area, some in neck and collarbone). ? Day 15-16 (worsening symptoms): ? Low-grade fever (persisting for over 24 hours). ? Fatigue and loss of appetite, worsened by waves of sudden, intense nausea. ? Vomiting, causing a heart rate spike to 155 bpm ? Blurred vision in the left eye (same side as the vaccine), lasting an entire day and unresponsive to hydration/rest. ? Pressure headache behind the eyes, improved with Tylenol. ? Sore throat likely due to swollen lymph nodes. ? Mouth sores on the left side, on tongue and soft palate More
2831382 0.67 F MA 03/14/2025 DTAPHEPBIP
 GLAXOSMITHKLINE BIOLOGICALS
 2G273
Injection site erythema Injection site erythema
Redness at injection site with 1.5 induration. Redness at injection site with 1.5 induration.
2831422 51 F OH 03/14/2025 COVID19
VARZOS
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
 LN0591
93KK4
Diarrhoea, Fatigue, Muscular weakness, Myalgia; Diarrhoea, Fatigue, Muscular wea... Diarrhoea, Fatigue, Muscular weakness, Myalgia; Diarrhoea, Fatigue, Muscular weakness, Myalgia More
Severe muscle soreness, muscle weakness, diarrhea, severe fatigue Severe muscle soreness, muscle weakness, diarrhea, severe fatigue
2831423 49 F SC 03/14/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 LM2219
LM2219
LM2219
LM2219
LM2219
LM2219
Arthralgia, Immediate post-injection reaction, Injected limb mobility decreased,... Arthralgia, Immediate post-injection reaction, Injected limb mobility decreased, X-ray limb; Arthralgia, Magnetic resonance imaging abnormal, Mobility decreased, Pain, Tendon disorder; Tendon rupture; Arthralgia, Immediate post-injection reaction, Injected limb mobility decreased, X-ray limb; Arthralgia, Magnetic resonance imaging abnormal, Mobility decreased, Pain, Tendon disorder; Tendon rupture More
Covid vaccine administered 09/12/24 into left deltoid by RPh per Vaccine Admin Record. PER 10/29/2... Covid vaccine administered 09/12/24 into left deltoid by RPh per Vaccine Admin Record. PER 10/29/2024 CHART NOTE: "She also reports a new onset of left lateral shoulder pain that began immediately after receiving a COVID-vaccine 7 weeks ago that she feels was placed too high. This pain is constant aggravated by overhead activities on the left side." PER 2/18/25 CHART NOTE: "possible component of subacromial impingement and suspected partial thickness rotator cuff tear significant improvement after left subacromial steroid injection 10/29/2024 with recurrence of symptoms." More
2831424 35 M VA 03/14/2025 FLU3
 SANOFI PASTEUR
 UT8514KA
Extra dose administered Extra dose administered
Member was given an extra dose of the Influenza vaccine on 3/13/25. Member is a new patient with cl... Member was given an extra dose of the Influenza vaccine on 3/13/25. Member is a new patient with clinic/facility and came in asking for a Flu shot. After releasing the available order in our system and giving the member the vaccine, I realized that the member had already received the Influenza vaccine outside of our facility on 2/5/25 (found after reviewing outside records in his medical record). Member received numerous vaccines outside of our facility on 2/5/25. More
2831425 16 F DE 03/14/2025 MNQ
 SANOFI PASTEUR
 u7594aa
Expired product administered Expired product administered
Patient was given vaccine on 3/13/25 but vaccine had expired on 3/4/25 Patient was given vaccine on 3/13/25 but vaccine had expired on 3/4/25
2831426 90 M FL 03/14/2025 PNC20
 PFIZER\WYETH
 LK6650
Extra dose administered Extra dose administered
Patient received vaccine in 2024, patient was given unnecessary additional dose of vaccine in 2025 Patient received vaccine in 2024, patient was given unnecessary additional dose of vaccine in 2025
2831427 4 M PA 03/14/2025 HEPA
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 TF27T
Y008790
Urticaria; Urticaria Urticaria; Urticaria
urticaria urticaria
2831428 76 M IA 03/14/2025 COVID19
 MODERNA
 3043159
Cerebrovascular accident, Death, Dysphagia Cerebrovascular accident, Death, Dysphagia
Passed away while on hospice care for diagnosis: Dyphasia following CVA Passed away while on hospice care for diagnosis: Dyphasia following CVA
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