πŸ₯ VAERS Vaccine Data Browser

πŸ”’ 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.

πŸ“– Help & Search Guide

Column Icons Legend

πŸ’€ Death
πŸ₯ Hospitalized
πŸš‘ Emergency Room
β™Ώ Disability
⚠️ Life Threatening

How to Search

πŸ’‘ 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 "πŸ“₯ Export CSV" to download filtered data (max 10,000 records)

πŸ’‘ Frequently Asked Questions (FAQ)

What is this site?

πŸ₯ 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:

  • βœ… Early warning system for potential safety signals
  • βœ… Open and transparent - publicly accessible
  • βœ… Accepts all reports regardless of likelihood of causation
  • βœ… 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
πŸ”„ Reset πŸ“₯ Export CSV
ID Age Sex State Date β–Ό Onset Days Vaccine Manufacturer Lot # Symptoms Narrative πŸ’€ πŸ₯ πŸš‘ β™Ώ ⚠️
2828818 55 F IL 02/28/2025 PNC21
VARZOS
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 Y019157
N77J2
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
Patient had an injection site reaction in both arms - redness, swelling and warm to the touch, still... Patient had an injection site reaction in both arms - redness, swelling and warm to the touch, still present 48 hours after vaccination More
2828819 31 M CO 02/28/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Antinuclear antibody increased, Fatigue, Hypoaesthesia, Hypoaesthesia oral, Inso... Antinuclear antibody increased, Fatigue, Hypoaesthesia, Hypoaesthesia oral, Insomnia; Muscle fatigue, Paraesthesia More
Upon the second dose of the vaccine, I shortly thereafter started experiencing a feeling of numbness... Upon the second dose of the vaccine, I shortly thereafter started experiencing a feeling of numbness with pins and needles feeling in the hands,arms,feet, and legs. The intensity would vary, and it could alternate between pins and needles or numbness or feeling of the body part "falling asleep." I also experience muscle fatigue and general fatigue. At that time, and for many months afterwards I would also have trouble sleeping and I would sometimes feel like I'm having an adrenaline rush during sleep and wake up. I would also have a feeling of numbness in the tongue or mouth, primarily during sleep, which had gone away over time. More
2828820 0.5 M NC 02/28/2025 FLU3
PNC20
RV5
UNK
 SANOFI PASTEUR
PFIZER\WYETH
MERCK & CO. INC.
UNKNOWN MANUFACTURER



Urticaria; Urticaria; Urticaria; Urticaria Urticaria; Urticaria; Urticaria; Urticaria
Day after vaccines given patient developed urticaria on his bilateral lower extremities. Recommend t... Day after vaccines given patient developed urticaria on his bilateral lower extremities. Recommend treatment with zyrtec and to contact his allergist as well. More
2828821 60 M LA 02/28/2025 CHIK
CHIK
IPV
IPV
YF
YF
CHIK
CHIK
IPV
IPV
YF
YF
 VALNEVA USA, INC.
VALNEVA USA, INC.
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
VALNEVA USA, INC.
VALNEVA USA, INC.
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR





24B011
24B011
X1C891M
X1C891M
UK050AA
UK050AA
Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea; Arthra... Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea; Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea; Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea; Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea; Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea; Arthralgia, Dyspnoea, Joint swelling, Palpitations; Arthralgia, Dyspnoea More
Arthralgia, ankles, knees and swollen joints (ankles). Shortness of breath, heart palpitations Arthralgia, ankles, knees and swollen joints (ankles). Shortness of breath, heart palpitations
2828822 78 F FL 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient inadvertently given an extra dose of Shingrix vaccine. No adverse reaction noted upon patie... Patient inadvertently given an extra dose of Shingrix vaccine. No adverse reaction noted upon patient leaving clinic More
2828823 12 F MO 02/28/2025 HPV9
MNQ
TDAP
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
GLAXOSMITHKLINE BIOLOGICALS
 Y014510
9M2R7
9429J
Erythema, Feeling hot, Swelling; Erythema, Feeling hot, Swelling; Erythema, Feel... Erythema, Feeling hot, Swelling; Erythema, Feeling hot, Swelling; Erythema, Feeling hot, Swelling More
Redness, warmth, and swelling noted 5 days later Redness, warmth, and swelling noted 5 days later
2828824 74 F SC 02/28/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
 LJ5283
LJ5283
Cough, Headache, Injection site erythema, Injection site pruritus, Injection sit... Cough, Headache, Injection site erythema, Injection site pruritus, Injection site swelling; Rhinorrhoea More
Patient received the vaccine on Monday morning, 02/24/2025. On Thursday morning, 02/27/2025, patient... Patient received the vaccine on Monday morning, 02/24/2025. On Thursday morning, 02/27/2025, patient stated that the vaccine site on her left arm was red and swollen, the area also has some itchiness. She also endorses running nose, dry cough, and headaches that started on the morning of 02/27/2025. More
2828825 79 M FL 02/28/2025 TD
VARZOS
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS

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
Patient inadvertently given an extra doe of Shingrix vaccine. No adverse reaction noted upon patien... Patient inadvertently given an extra doe of Shingrix vaccine. No adverse reaction noted upon patient leaving clinic More
2828826 76 F NY 02/28/2025 COVID19
COVID19
 MODERNA
MODERNA

Abdominal pain upper, Dizziness, Dyspepsia, Gastrooesophageal reflux disease, Na... Abdominal pain upper, Dizziness, Dyspepsia, Gastrooesophageal reflux disease, Nausea; Vomiting More
Stomach pain.acid reflux, nausea, vomiting, heartburn, feeling faint, dizzy, lightheaded, all starte... Stomach pain.acid reflux, nausea, vomiting, heartburn, feeling faint, dizzy, lightheaded, all started one day after shot for 5-6 days. Made appt with gastroenterologist but appt was 2 months away More
2828827 60 M MT 02/28/2025 PNC20
 PFIZER\WYETH
 HR3906
Extra dose administered Extra dose administered
Patient received extra dose of prevnar 20 Patient received extra dose of prevnar 20
2828828 1.25 F WI 02/28/2025 DTAP
FLU3
HIBV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 223Y9
4LM54
Y011267
Febrile convulsion, Pyrexia, Vomiting; Febrile convulsion, Pyrexia, Vomiting; Fe... Febrile convulsion, Pyrexia, Vomiting; Febrile convulsion, Pyrexia, Vomiting; Febrile convulsion, Pyrexia, Vomiting More
Fever same night of vaccines to 102F tmax. Then this am febrile seizure questioned, but notably no ... Fever same night of vaccines to 102F tmax. Then this am febrile seizure questioned, but notably no post-ictal phase. Having some emesis last night too, not today. More
2828830 7 F MI 02/28/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 Y97N7
Inappropriate schedule of product administration Inappropriate schedule of product administration
None None
2828832 57 F SD 02/28/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 016B21A
016B21A
016B21A
016B21A
Abdominal distension, Affective disorder, Blood glucose fluctuation, Blood press... Abdominal distension, Affective disorder, Blood glucose fluctuation, Blood pressure fluctuation, Body temperature fluctuation; Change of bowel habit, Dizziness, Dysphagia, Dyspnoea, Gastrointestinal disorder; Gene mutation identification test, Metabolic disorder, Muscle spasms, Palpitations, Temperature intolerance; Vagus nerve disorder More
NEUROLOGICAL IMPAIRMENTS- *Muscle cramps in hands, feet, legs. *heart palpitations followed by epi... NEUROLOGICAL IMPAIRMENTS- *Muscle cramps in hands, feet, legs. *heart palpitations followed by episode of dysfunctional vagus nerve activity *dizziness *blood pressure dysregulation *heart palpitations*digestiv/bloate issues *mood (heightened emotions- sadder, softer emotions, i.e.- being overly touched by stories and events *swallowing issues,*shortness of breath, difficulty with *blood glucose dysregulation*body temp dysregulation *laying on the side creates palpitation at SA Node area of the heart related to VN *Fasting blood glucose *Change in bowel movements *turning/tilting head and neck, laying down with chin on the chest can create uncomfortable VN response *sensitive and sometimes unbareable to hot weather.* Poor metabolization of Prescription and OTC drugs *VN reactions/issues while initially laying down to fall asleep, palpitation and alarming increase in BP causing veins to appear on face & top of hands. *On Oct. '24, cardiologist referral to Neurologist -alcohol consumption- More
2828833 93 M PA 02/28/2025 COVID19
 MODERNA
 8081260
Antimicrobial susceptibility test resistant, Death, Septic shock Antimicrobial susceptibility test resistant, Death, Septic shock
Nursing home facility communicated to the Pharmacy about death of the patient due to Septic shock an... Nursing home facility communicated to the Pharmacy about death of the patient due to Septic shock and ESBL present in urine on 02/27/2025. The findings were shared with the pharmacy on 02/28/2025. More
βœ“
2828834 4 F OK 02/28/2025 DTAPIPV
DTAPIPV
MMRV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 3RT93
3RT93
Y008885
Y008885
Decreased appetite, Ear infection, Flushing, Headache, Injection site erythema; ... Decreased appetite, Ear infection, Flushing, Headache, Injection site erythema; Injection site reaction, Pyrexia, Rash macular, Skin burning sensation; Decreased appetite, Ear infection, Flushing, Headache, Injection site erythema; Injection site reaction, Pyrexia, Rash macular, Skin burning sensation More
Mother of patient reports patient started running fever on 2/26/25 around 3PM - patient is flushed a... Mother of patient reports patient started running fever on 2/26/25 around 3PM - patient is flushed and complaining of headache. Patient's skin was burning up. Mother of patient did not measure temp, but medicated with Tylenol. Fever improved. At midnight patient was "super hot" again. Mom gave more Tylenol and fever responds. 2/27/25 mother of patient reports patient's left thigh is bright red and blotchy. Mother of patient reports that patient is taking fluids and voiding, but appetite is decreased. Advised mother of patient it is not uncommon to have fever after vaccines, may continue with Tylenol every 4 hours, may alternate with Motrin every 3 hours if not responding well to Tylenol alone. Recommended measuring temp with recheck after 1 hour to ensure response to medication. Mother of patient denies any other rash. Advised to push fluids to prevent dehydration. Mother of patient reports the highest patient's temperature has been is 103.6. Pt.'s left thigh has mild redness on 2/28/25 in office. Pt. has been diagnosed with an ear infection on 2/28/25 in physician's office. More
2828835 77 M 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 9R397
Dry skin, Pruritus, Rash, Urticaria Dry skin, Pruritus, Rash, Urticaria
Patient stated that he broke out in itchy hives on his arms and back. This started 3 days after gett... Patient stated that he broke out in itchy hives on his arms and back. This started 3 days after getting the vaccine and he still has the rash on his back today (2/28/25). He doesn't recall changing anything in that period of time like soap, detergent, shampoo, taking any other new medications, or anything else new. He has gone to his dermatologist, and they stated that they believe it could just be dry skin because it is the winter, but the patient believes it is from the vaccine. The dermatologist suggested that this could be from the wood stove the patient has in the house, but the patient has been using the wood stove all winter and hasn't changed the type of wood used in it. The patient is going back to the dermatologist to get a full body exam to see if there is any other cause from it. More
2828836 81 F CO 02/28/2025 PNC21
 MERCK & CO. INC.
 y013009
Unevaluable event Unevaluable event
adviced pt to ice and take benadryl adviced pt to ice and take benadryl
2828837 8 M CA 02/28/2025 FLU3
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 FJ47R
FJ47R
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
No adverse reaction No adverse reaction
2828838 69 M AL 02/28/2025 PNC20
 PFIZER\WYETH
Extra dose administered Extra dose administered
patient came to get vaccinations our vaccination system did not reflect a prevnar 20 being received ... patient came to get vaccinations our vaccination system did not reflect a prevnar 20 being received already and patient stated they also did not remember getting one. we gave the vaccination per patient request and now it appears they also got one in 2023. patient is fine. More
2828839 8 F NJ 02/28/2025 FLU3
IPV
MMRV
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
 AE2J7
X1D141M
Y016876
U8274AA
Rash; Rash; Rash; Rash Rash; Rash; Rash; Rash
Mother reported that the child developed a rash on her chest, belly, and back post vaccination. Per ... Mother reported that the child developed a rash on her chest, belly, and back post vaccination. Per mom- the rash does not itch or hurt the child and the child is feeling ok. Alerted DON and county epi- following case per state guidelines. More
2828840 4 M TX 02/28/2025 COVID19
COVID19
COVID19
DTAPIPV
DTAPIPV
DTAPIPV
 JANSSEN
JANSSEN
JANSSEN
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 Y013577
Y013577
Y013577
U7908AA
U7908AA
U7908AA
Cough, Dyspnoea, Erythema, Hypersensitivity, Influenza virus test negative; Inje... Cough, Dyspnoea, Erythema, Hypersensitivity, Influenza virus test negative; Injection site erythema, Joint swelling, Pyrexia, Respiratory tract congestion, SARS-CoV-2 test negative; Streptococcus test negative; Cough, Dyspnoea, Erythema, Hypersensitivity, Influenza virus test negative; Injection site erythema, Joint swelling, Pyrexia, Respiratory tract congestion, SARS-CoV-2 test negative; Streptococcus test negative More
Patient received his 4 yr vaccines (proquad and quadracel) on Tuesday at 5:00 PM, on Friday around 8... Patient received his 4 yr vaccines (proquad and quadracel) on Tuesday at 5:00 PM, on Friday around 8:00 PM he started with fever. His temp was about 103, parents thought it could be from vaccines. He continued with the fever overnight. The following day he was red all over and had redness to one of his vaccine sites. He started getting swollen that morning (Saturday) before 12:00. He never had any trouble breathing. His body also had a lot of little bumps all over, then the following day (Sunday) the swelling got worse. Monday mom took him to urgent care (we were closed for holiday) Monday and they thought he was having an allergic reaction. The swelling was no worse between Sunday to Monday and it may have gotten a little better. They had been giving benadryl once a day, but are not sure if it made a significant difference. At urgent care, provider mentioned his throat was very swollen but mother says they did not notice any difference in his voice, throat clearing, or mouth itchiness. The fever was improving by Monday as well but did not go away completely until Thursday. He had fever through Wednesday. Urgent care gave him steroid to bring the swelling down, then they also gave him amoxicillin for a possible ear infection (but they said it was mild - he had had clear fluid in his ear on the day of his WCC and has recurrent AOM), but it was switched to cefdinir on Wed when mother followed up in urgent care because he she told them he has had a lot of AOM failures. He did well with that antibiotic and will finish it today (10th day). After the initial sx Friday - Monday, the following Tuesday - Friday he had congestion and cough like "he had a normal cold" that finally resolved on their own. More
2828841 38 F IL 02/28/2025 COVID19
 PFIZER\BIONTECH
 LM7786
Injection site erythema, Injection site pruritus, Injection site swelling, Injec... Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth More
Patient has 2"x 2" raised, red injection site reaction. Hot to touch and itchy. Still itch... Patient has 2"x 2" raised, red injection site reaction. Hot to touch and itchy. Still itching and red on day 2 (2/28/25). Counseled the patient to use antihistamine by mouth or benadryl and/or hydrocortisone cream topically as needed for the redness and itching. More
2828842 51 F VA 02/28/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 ER8732
ER8732
Arthritis, Back pain, COVID-19, Fluid retention, Magnetic resonance imaging abno... Arthritis, Back pain, COVID-19, Fluid retention, Magnetic resonance imaging abnormal; Malaise, Palpitations More
After i got that vaccine something happened. I started catching Covid too many times , i have had it... After i got that vaccine something happened. I started catching Covid too many times , i have had it 5 times and i didnt feel right, i didnt feel the same. I started getting back pain i thought it was kidney but it wasn't. They sent me to Hospital to get an MRI. The hospital called me and said i had stage 3 arthritis in my hips. Next week i have to see an Orthopedic doctor. My body is retaining fluid and i have to take meds to get it to get out and it makes my heart palpitate. I had to start cholesterol pills. More
2828843 77 F WV 02/28/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 ak334
Pain in extremity Pain in extremity
Pt reported having leg pain the evening after the vaccine until now (4 days later) until it became u... Pt reported having leg pain the evening after the vaccine until now (4 days later) until it became unbearable and she was brought to the clinic and referred to the ER More
2828844 65 M WI 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7ZM55
Erythema, Pain in extremity, Peripheral swelling Erythema, Pain in extremity, Peripheral swelling
Patient experienced redness, swelling, and pain in vaccinated arm. He has been using a cold compres... Patient experienced redness, swelling, and pain in vaccinated arm. He has been using a cold compress and OTC pain reliever. Redness and swelling are improving, but he still has pain one week after receiving vaccine. More
2828845 16 M ME 02/28/2025 UNK
 UNKNOWN MANUFACTURER
Unevaluable event Unevaluable event
None stated. None stated.
2828846 29 M OR 02/28/2025 HPV9
 MERCK & CO. INC.
 1965046
Pruritus, Rash, Urticaria Pruritus, Rash, Urticaria
Rash, hives, itching. Benadryl IM given. Pt had relief from the Benadryl. Rash, hives, itching. Benadryl IM given. Pt had relief from the Benadryl.
2828847 31 F OR 02/28/2025 UNK
 UNKNOWN MANUFACTURER
Unevaluable event Unevaluable event
Tdap, Polio, 2 step skin test for TB on 05/25/2025. These were given at the County Public Health De... Tdap, Polio, 2 step skin test for TB on 05/25/2025. These were given at the County Public Health Department. More
2828848 61 F IA 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 99Y4J
Hypoaesthesia oral, Swollen tongue, Throat irritation Hypoaesthesia oral, Swollen tongue, Throat irritation
ITCHY/SCRATCHY THROAT, TONGUE SWELLLING/NUMB ITCHY/SCRATCHY THROAT, TONGUE SWELLLING/NUMB
2828849 24 M OH 02/28/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 XN575
Extra dose administered Extra dose administered
THe patient received TDAP at another clinic earlier in the day. Then came to this clinic and receive... THe patient received TDAP at another clinic earlier in the day. Then came to this clinic and received another dose More
2828850 23 M MI 02/28/2025 HPV9
MENB
 MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
 x026926
dd72h
Rash, Rash erythematous; Rash, Rash erythematous Rash, Rash erythematous; Rash, Rash erythematous
bright red rash on both legs and feet bright red rash on both legs and feet
2828851 86 M MN 02/28/2025 COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EM9809
EN6202
FF8841
GJ3277
LN0589
Asthenia, Exposure to SARS-CoV-2, Fall, Laboratory test; Asthenia, Exposure to S... Asthenia, Exposure to SARS-CoV-2, Fall, Laboratory test; Asthenia, Exposure to SARS-CoV-2, Fall, Laboratory test; Asthenia, Exposure to SARS-CoV-2, Fall, Laboratory test; Asthenia, Exposure to SARS-CoV-2, Fall, Laboratory test; Asthenia, Exposure to SARS-CoV-2, Fall, Laboratory test More
Weakness, falls, exposure to COVID Weakness, falls, exposure to COVID
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2828852 81 F MN 02/28/2025 COVID19
COVID19
COVID19
COVID19
COVID19
UNK
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
UNKNOWN MANUFACTURER
 031L20A
031A21A
051F21A
056A22A
3030701
8080797
Cough, Nasal congestion, SARS-CoV-2 test; Cough, Nasal congestion, SARS-CoV-2 te... Cough, Nasal congestion, SARS-CoV-2 test; Cough, Nasal congestion, SARS-CoV-2 test; Cough, Nasal congestion, SARS-CoV-2 test; Cough, Nasal congestion, SARS-CoV-2 test; Cough, Nasal congestion, SARS-CoV-2 test; Cough, Nasal congestion, SARS-CoV-2 test More
Nasal congestion, cough Nasal congestion, cough
2828853 39 M MN 02/28/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 EW0162
EW0175
Cough, Nasopharyngitis, SARS-CoV-2 test; Cough, Nasopharyngitis, SARS-CoV-2 test Cough, Nasopharyngitis, SARS-CoV-2 test; Cough, Nasopharyngitis, SARS-CoV-2 test
Cough, cold symptoms Cough, cold symptoms
2828855 1.42 M CA 02/28/2025 IPV
 SANOFI PASTEUR
 W1C751M
Unevaluable event Unevaluable event
None reported. None reported.
2828856 89 F FL 02/28/2025 PNC20
 PFIZER\WYETH
 408730568976
Erythema, Pruritus Erythema, Pruritus
Patient had some itching and redness on the arm. Patient had some itching and redness on the arm.
2828857 74 F SD 02/28/2025 COVID19
COVID19
 MODERNA
MODERNA
 031L20A
031A21A
Chronic lymphocytic leukaemia, Lymphocyte count increased; Chronic lymphocytic l... Chronic lymphocytic leukaemia, Lymphocyte count increased; Chronic lymphocytic leukaemia, Lymphocyte count increased More
Routine labs showed elevated lymphocyte count in October 2021. Counts remained elevated and was diag... Routine labs showed elevated lymphocyte count in October 2021. Counts remained elevated and was diagnosed with chronic lymphocytic leukemia in April 2024, but has not required any treatment. Patient believes her CLL diagnosis may be related to Covid-19 vaccine. More
2828858 52 F OR 02/28/2025 FLU3
 SANOFI PASTEUR
 U8519EA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Administered high-dose flu vaccine to ineligible client. Administered high-dose flu vaccine to ineligible client.
2828859 37 M NY 02/28/2025 COVID19
 PFIZER\BIONTECH
 fj8757
Cardiac flutter, Impaired work ability Cardiac flutter, Impaired work ability
Patient reports "heart flutters" that caused him to "leave his job 6-7 months" a... Patient reports "heart flutters" that caused him to "leave his job 6-7 months" after getting the Pfizer COVID19 vaccine because he was not able to "carry copper and metal up the stairs anymore due there heart flutters" He says that these heart flutters were not evaluated by any medical professional More
2828860 0.75 F CO 02/28/2025 HEPA
 MERCK & CO. INC.
 Y008338
No adverse event, Wrong product administered No adverse event, Wrong product administered
Provider ordered Hepatitis B vaccine. Clinical staff administered Hepatitis A. No adverse effects r... Provider ordered Hepatitis B vaccine. Clinical staff administered Hepatitis A. No adverse effects reported. More
2828861 3 F CA 02/28/2025 HEPA
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 KH2BD
T5727
Y014182
Extra dose administered; Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered; Extra dose administered
Extra dose of MMR, Hep A and Vaircella given to patient Extra dose of MMR, Hep A and Vaircella given to patient
2828862 69 M NY 02/28/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 FH8022
FH8022
FH8022
Arthralgia, Hypoaesthesia, Immediate post-injection reaction, Magnetic resonance... Arthralgia, Hypoaesthesia, Immediate post-injection reaction, Magnetic resonance imaging, Muscle discomfort; Musculoskeletal discomfort, Myalgia, Nausea, Neck pain, Pain; Pain in extremity, Shoulder injury related to vaccine administration, Sleep disorder, Spinal X-ray, X-ray limb More
On 10/27/2021 i got a COVID booster at facility. The moment i was given the injection it felt very d... On 10/27/2021 i got a COVID booster at facility. The moment i was given the injection it felt very different from other vaccinations i had gotten in the past. On 11/1/2021 i contacted my PCP to inquire about the pain i was suffering in my right shoulder where i had gotten my last injection. Starting on the day after i got the booster i developed persistent excruciating joint pain in my right shoulder where i had the injection. I had CONSTANT pain and discomfort in the bicep, shoulder and neck. The pain became so severe i experienced trouble sleeping, and i got nauseous at times. I took Tylenol with no results. i tried medicated pads, but nothing relieved the incessant pain. On 11/03/2021 i messaged my PCP to let her know i was feeling a little better. That did not last too long. Eventually i was given meloxicam which helped a bit, but after a while i was taken off of it due to the dangers of side effects. I was referred to Dr (orthopedics). She determined that i suffer from SIRVA. Dr then prescribed a cortisone injection which gave me temporary relief. When i asked for another treatment i was told i had to be very careful not to have too many of them or i would suffer side effects. Dr then advised me to seek some Physical Therapy as an alternative to medications, so i went to PT for a complete regimen of PT for the shoulder. Again, the relief i got was temporary. I have periodically done the PT since, but it does not seem to do much, and at times it actually aggravates the problem. Dr left facility/practice and i began to see Dr. She agreed with Dr's assessment that i have SIRVA and she performed some tests to see if the previous cortisone injections had resulted in side effects, which they had not, and she allowed me to have another injection prior to going away on a vacation which allowed me to better enjoy my holiday. Dr prescribed diclofenac 75 mg EC tablets which at times work, but not always. When the cortisone wears off i am back to sleepless nights, chronic shoulder pain that radiates up my neck and down my arm, and into my right hand. i still have numbness in the hand when this occurs. Currently i am suffering more consistently. i have been taking the diclofenac 75 mg EC tablets once or twice a day, but they do not work well enough. At times when the pain becomes worse i will alternate between Tylenol and Advil as instructed by my doctor. More
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2828871 43 IL 02/28/2025 HPV9
 MERCK & CO. INC.
Intercepted product prescribing error, No adverse event Intercepted product prescribing error, No adverse event
no additional adverse event; looking for 2nd dose at 51 years of age. Patient is coming later today ... no additional adverse event; looking for 2nd dose at 51 years of age. Patient is coming later today with prescription from HCP; This spontaneous report was received from a pharmacist and refers to a an adult patient of unknown gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On an unknown date, at the age of 43, the patient was vaccinated with the first dose of Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASILοΏ½9) (strength,expiration date, lot #, route and site of administration were not reported) for prophylaxis. The patient was looking for the second dose at 51 years of age. The patient was about to come later on 25-FEB-2025 with a prescription (product prescribing issue). No additional adverse event was reported. Lot # is being requested and will be submitted if received. More
2828872 F 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Death, Guillain-Barre syndrome Death, Guillain-Barre syndrome
Guilluan barre syndrome; This serious case was reported by a consumer via interactive digital media ... Guilluan barre syndrome; This serious case was reported by a consumer via interactive digital media and described the occurrence of guillain barre syndrome in a female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received the 2nd dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced guillain barre syndrome (Verbatim: Guilluan barre syndrome) (serious criteria death and GSK medically significant). The patient died in 2024. The reported cause of death was guillain barre syndrome. It was unknown if the reporter considered the guillain barre syndrome to be related to Shingrix. The company considered the guillain barre syndrome to be unrelated to Shingrix. Additional Information: GSK Receipt Date: 25-FEB-2025 The case was received from the patient's husband via interactive digital media. The patient got 2 Shingrix shingles shots and died last summer from Guillain Barre syndrome. The reporter stated that it would of been better off with shingles.; Sender's Comments: Guillain-Barre syndrome is an unlisted event which is considered unrelated to GSK vaccine Shingrix.; Reported Cause(s) of Death: Guillain Barre syndrome More
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2828873 M OH 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incomplete course of vaccination Incomplete course of vaccination
states he did not have the second dose of SHINGRIX administered in the recommended time; This non-se... states he did not have the second dose of SHINGRIX administered in the recommended time; This non-serious case was reported by a consumer via call center representative and described the occurrence of incomplete course of vaccination in a 53-year-old male patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (first dose of Shingrix on 23-JUN-2021 four years ago). On an unknown date, the patient did not received the 2nd dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced incomplete course of vaccination (Verbatim: states he did not have the second dose of SHINGRIX administered in the recommended time). The outcome of the incomplete course of vaccination was not applicable. Additional Information: GSK Receipt Date: 17-FEB-2025 The patient was vaccinated with Shingrix first dose. The reporter stated he did not have the second dose of Shingrix administered in the recommended time specified in the package insert of two to six months for second dose. Till the time of reporting the patient had not received the second dose of Shingrix, which led to incomplete course of vaccination. More
2828874 M 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Pain Pain
aches and pains; This non-serious case was reported by a consumer via call center representative and... aches and pains; This non-serious case was reported by a consumer via call center representative and described the occurrence of pain in a male patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received the 1st dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced pain (Verbatim: aches and pains). The outcome of the pain was not reported. It was unknown if the reporter considered the pain to be related to Shingrix. It was unknown if the company considered the pain to be related to Shingrix. Additional Information: GSK Receipt Date: 13-FEB-2025 The patient's wife wanted to know if the patient can take Tylenol (acetaminophen) after the first dose of Shingrix. The patient had taken the first dose of Shingrix and had aches and pain. More
2828875 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Erythema, Pain in extremity Erythema, Pain in extremity
my arm is sore; Redness; This non-serious case was reported by a consumer via interactive digital me... my arm is sore; Redness; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of pain in arm in a patient who received Herpes zoster (Shingrix) for prophylaxis. On 12-FEB-2025, the patient received the 2nd dose of Shingrix. In FEB-2025, an unknown time after receiving Shingrix, the patient experienced pain in arm (Verbatim: my arm is sore) and erythema (Verbatim: Redness). The outcome of the pain in arm and erythema were not resolved. It was unknown if the reporter considered the pain in arm and erythema to be related to Shingrix. It was unknown if the company considered the pain in arm and erythema to be related to Shingrix. Additional Information: GSK receipt date: 15-FEB-2025 This case was reported by a patient via interactive digital media. The reporter reported that he/she had received second dose of Shingrix vaccine on Wednesday (12th February 2025) and experienced arm sore and redness was worse on the day of reporting than day before reporting. More
2828876 02/28/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Pain in extremity Pain in extremity
sore arm; This non-serious case was reported by a consumer and described the occurrence of pain in a... sore arm; This non-serious case was reported by a consumer and described the occurrence of pain in arm in a patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced pain in arm (Verbatim: sore arm). The outcome of the pain in arm was resolved (duration 1 month). It was unknown if the reporter considered the pain in arm to be related to Shingrix. It was unknown if the company considered the pain in arm to be related to Shingrix. Additional Information: GSK receipt Date: 19-FEB-2025 The case self reported by patient. The patient had the shingrix vaccine and sore arm was the only symptom got. More
2828877 02/28/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
Suspected vaccination failure; Shingles; This serious case was reported by a consumer via interactiv... Suspected vaccination failure; Shingles; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: Shingles). The outcome of the vaccination failure and shingles were not reported. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine. The company considered the vaccination failure to be unrelated to Shingles vaccine. It was unknown if the company considered the shingles to be related to Shingles vaccine. Additional Information: GSK Receipt Date: 23-FEB-2025 This case was reported by a patient's neighbour via interactive digital media. The patient still got it after shingles hot. This case was considered as suspected vaccination failure since the details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK Shingles vaccine. More
2828878 02/28/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Paraesthesia, Sensitive skin Paraesthesia, Sensitive skin
My legs were tingling; My legs were tingling and sensitive; This non-serious case was reported by a ... My legs were tingling; My legs were tingling and sensitive; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of tingling of extremity in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced tingling of extremity (Verbatim: My legs were tingling) and increased skin sensitivity (Verbatim: My legs were tingling and sensitive). The patient was treated with paracetamol (Tylenol). The outcome of the tingling of extremity and increased skin sensitivity were resolved (duration 48 hrs). It was unknown if the reporter considered the tingling of extremity and increased skin sensitivity to be related to Shingles vaccine. It was unknown if the company considered the tingling of extremity and increased skin sensitivity to be related to Shingles vaccine. Additional Information: GSK receipt date: 20-FEB-2025 This case was reported by a patient via interactive digital media. The reporter reported that the patient had recived Shigles vaccine and experienced his/her legs were tingling and sensitive and it was lasted for 48 hours. The reporter mentioned that his/her doctor told him/her to take Tylenol. More
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