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
2865176 58 F MO 10/12/2025 COVID19
NOVAVAX
6315MF002C
Chest pain Chest pain
Patient reported chest pain for several days after administration. Chest pain did not start until af... Patient reported chest pain for several days after administration. Chest pain did not start until after patient had got home. Patient came in to report event 10/12 after recieving vaccine on 10/6 More
2865177 63 M CO 10/12/2025 COVID19
FLU3
PFIZER\BIONTECH
SEQIRUS, INC.
na0739
409608
Rash; Rash Rash; Rash
Patient reported a rash present on insides of both arms, trunk and abodomen that began the morning o... Patient reported a rash present on insides of both arms, trunk and abodomen that began the morning of 10/8/25. Patient noticed rash when he woke in the morning. Patient states that rash did not itch. Rash was still present on trunk as of 10/12/25 as verified by pharmacist. Patient did not seek medical attention following a request from his provider to make an appointment after he advised PCP of rash development. Pharmacist will call provider on Monday, 10/13 to follow up. Patient states that he changed detergents recently, however, that was previous to vaccination. Also, patient states that he has had COVID and Flu shots previously with no reaction. More
2865178 73 F FL 10/12/2025 COVID19
PFIZER\BIONTECH
My9550
Eye pain, Retinal tear, Vitreous detachment, Vitreous floaters Eye pain, Retinal tear, Vitreous detachment, Vitreous floaters
Within hours of receiving vaccination patient had pain in right eye (similar to migraine pain, but p... Within hours of receiving vaccination patient had pain in right eye (similar to migraine pain, but patient only gets migraine pain in left eye) and then got floaters in eyes (they have not gone away). Patient went to a retinal specialist. Patient was diagnosed with acute posterior vitreous detachment and round retinal break without detachment. More
2865180 26 F NV 10/12/2025 COVID19
UNK
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER


Skin infection; Skin infection Skin infection; Skin infection
Skin infection in same arm as COVID vaccine, no reaction on other arm with Flu vaccine Skin infection in same arm as COVID vaccine, no reaction on other arm with Flu vaccine
2865181 32 F PA 10/12/2025 COVID19
COVID19
COVID19
COVID19
MODERNA
MODERNA
MODERNA
MODERNA
3052741
3052741
3043836
3043836
Alanine aminotransferase increased, Aspartate aminotransferase increased, Blood ... Alanine aminotransferase increased, Aspartate aminotransferase increased, Blood alkaline phosphatase increased, Blood bilirubin increased, Chest pain; Chromaturia, Immediate post-injection reaction, Liver disorder; Alanine aminotransferase increased, Aspartate aminotransferase increased, Blood alkaline phosphatase increased, Blood bilirubin increased, Chest pain; Chromaturia, Immediate post-injection reaction, Liver disorder More
Immediately upon receiving the vaccine at pharmacy, I started having really awful chest pain (though... Immediately upon receiving the vaccine at pharmacy, I started having really awful chest pain (though, that may be stress-related). I'm making this report because upon waking Saturday morning, my urine was a weird brown color -- like tea or cola. It was like that all day Saturday -- I had a ton of water and every time I used the restroom, my urine was an odd color. Finally, upon asking a nurse advice line about it, I went to the emergency room. There, my did a blood test and found that my liver seemed to be struggling. (See test results below.) I was ultimately discharged from the hospital today with instructions to follow up with a gastro doctor when they reach out and to get a repeat blood test to check my liver. I did not receive any clear information about what caused this, other than they thought I had a virus. I kept mentioning that I had just received the flu and COVID vaccines the day prior, and they said it would be highly unlikely that caused this, but that a virus would. I just think the whole thing is odd because I'm not sick -- I have no other viral symptoms -- and it seems to me that no matter how unlikely the doctors think it to be, this could very well have been caused by one or both of the vaccines I received. More
โœ“
2865183 69 F FL 10/12/2025 FLU3
SANOFI PASTEUR
UT8781AA
Injection site rash, Injection site swelling Injection site rash, Injection site swelling
Patient reported to have a rash and swelling where the vaccine was administered. She said the reacti... Patient reported to have a rash and swelling where the vaccine was administered. She said the reaction occurred 1-week after but healed and reported 1 month later. More
2865184 79 F PA 10/12/2025 COVID19
PNC21
PFIZER\BIONTECH
MERCK & CO. INC.
NA0587
Z009681
Injection site erythema, Injection site inflammation, Injection site pain, Injec... Injection site erythema, Injection site inflammation, Injection site pain, Injection site reaction; Injection site erythema, Injection site inflammation, Injection site pain, Injection site reaction More
Manifestation of local, injection site reaction after administration of both Capvaxive 21 and Comirn... Manifestation of local, injection site reaction after administration of both Capvaxive 21 and Comirnaty on anatomical site. Marked erythema, inflammation and pain for a period of 3 or more days since administration More
2865185 3 F MN 10/12/2025 FLU3
SANOFI PASTEUR
UT8817NA
Injection site bruising, Injection site erythema, Injection site pruritus, Injec... Injection site bruising, Injection site erythema, Injection site pruritus, Injection site swelling More
In the evening a few hours after getting the shot, there was a bruise at the injection site about th... In the evening a few hours after getting the shot, there was a bruise at the injection site about the size of a ping pong ball, as well as some reddness and swelling of the thigh. The next morning, her right thigh looked almost double the size of her left thigh and the reddness close to 3 inches each was around the injection site as well as bruising. The site was warm through her pants and hard. About 6pm on the 9th, her right thigh measured 14 inches around and her left thigh was 10 inches around. The reddness was 3 inches both ways. I called an on call nurse that morning and evening and was told this was an okay reaction to have since she had no other symptoms. The next morning (10th), the reddness was 4 inches both ways though the swelling seemed about the same. Her thigh was also itchy. A benadryl spray was used and this seemed to be helpful. Morning of the 11th, swelling was significantly decreased as was reddness. The bruise was more visible and the site remained warm and somewhat hard. The 12th, site still had some bruising and swelling, though not so much reddness. She has scratches from it being itchy. More
2865186 8 M WA 10/12/2025 FLUN3
FLUN3
FLUN3
FLUN3
FLUN3
FLUN3
MEDIMMUNE VACCINES, INC.
MEDIMMUNE VACCINES, INC.
MEDIMMUNE VACCINES, INC.
MEDIMMUNE VACCINES, INC.
MEDIMMUNE VACCINES, INC.
MEDIMMUNE VACCINES, INC.






COVID-19, Computerised tomogram head normal, Coordination abnormal, Cyanosis, Dr... COVID-19, Computerised tomogram head normal, Coordination abnormal, Cyanosis, Drooling; Electroencephalogram normal, Endotracheal intubation, Enterovirus test positive, Eye movement disorder, Headache; Human rhinovirus test positive, Hypercapnia, Hypopnoea, Hypoxia, Influenza A virus test positive; Influenza B virus test positive, Intensive care, Lumbar puncture normal, Postictal state, Pyrexia; SARS-CoV-2 test positive, Seizure, Somnolence, Status epilepticus, Tardive dyskinesia; Tongue movement disturbance, Tremor, Unresponsive to stimuli, Vomiting More
Presented with status epilepticus one day after receiving FluMist. As noted previously, had viral sy... Presented with status epilepticus one day after receiving FluMist. As noted previously, had viral symptoms about 10/4/25, including fever, headache, myalgias that had resolved. By 10/9 he had improved and received intranasal flu vaccine 10/10. That evening, he had one episode of emesis, and later that evening an episode of lip smacking, drooling, and purple lips, lasting about one minute. Unresponsive during the episode, but responsive afterward. He had 2 other similar episodes during the course of the night. (One of them had shaking of his arms.). No fevers during the time of the seizures. Family called EMS, and he had another seizure en route, for which they gave 4 mg IV versed. He has had associated headache for the last week, and the evening of 10/10 had some uncoordinated movements in which he dropped his books. No focal weakness, no slurred speech, no loss of consciousness, no history of brain injury, no previous history of seizures. In the ED he was febrile to 100.4, otherwise normal vitals. He had another seizure in the ED with R eye deviation and hypoxia. Neurology was consulted, and he was given 40 mg/kg of IV keppra and he was admitted to the acute care floor. On the floor, EEG was placed, which showed slowing but was generally unrevealing. He had 3 further seizures with tongue movements and head shaking over the course of 4 hours, and receive 3 doses of versed, as well as 10 mg/kg additional keppra in addition to his maintenance. Due to ongoing seizures with frequent AED dosing, he was transferred to the PICU. He was initially post ictal and sleepy, but maintaining his airway. After having further seizures, he received fosphenytoin, became hypopneic and hypercarbic, and was intubated. Head CT negative. LP was done, and CSF studies are reassuring against meningitis. MRI/MRV pending to rule out ADEM and thrombosis. Initial viral panel positive for flu A/B (thought to be false positive, given recent live flu vaccine). Follow up panel positive for COVID and rhino/enterovirus (and notably negative for flu). More
โœ“ โœ“
2865187 60 F FL 10/12/2025 PNC20
VARZOS
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
LP4947
7523j
Extra dose administered, Wrong product administered; Extra dose administered, Wr... Extra dose administered, Wrong product administered; Extra dose administered, Wrong product administered More
Patient reported that her paperwork stated she received Prevnar 20 twice from Pharmacy in September.... Patient reported that her paperwork stated she received Prevnar 20 twice from Pharmacy in September. After investigating, it was found she received a dose on 9-4-25 and on 9-24-25. On 9-24-25, the patient requested for the RSV vaccine but received Prevnar 20 in error. Patient reported this on 10/06/2025. More
2865188 75 F VT 10/12/2025 COVID19
MODERNA
8146545
Decreased appetite, Lethargy, Pain in extremity Decreased appetite, Lethargy, Pain in extremity
Patient states that her arm was still hurting days later but no redness or swelling. patient states... Patient states that her arm was still hurting days later but no redness or swelling. patient states that she is still very lethargic and has no appetite. More
2865189 77 M NC 10/12/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
NA4457
Extra dose administered Extra dose administered
PATIENT RECEIVED THE AREXVY VACCINE ON 12/12/2023 BUT IT WAS NOT RECORDED TO THE STATE REGISTERY. ON... PATIENT RECEIVED THE AREXVY VACCINE ON 12/12/2023 BUT IT WAS NOT RECORDED TO THE STATE REGISTERY. ON 10/11/2025, THE VACCINE WAS RECOMMENDED TO THE PATIENT SINCE IT SHOWED HE WAS OVERDUE FOR IT. THEREFORE, THE PATIENT RECEIVED A SECOND DOSE OF AREXVY. THE PATIENT NOR THE PHARMACIST GIVING IT KNEW THAT HE HAD RECEIVED IT IN 2023. More
2865190 68 M GA 10/12/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS

Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received the Arexvy on 9/14/2024. It was not registered with vaccine registry properly. Upon... Patient received the Arexvy on 9/14/2024. It was not registered with vaccine registry properly. Upon checking vaccine registry, patient's record did not show Arexvy was administered. We gave the patient another dose of Arexvy on 10/11/2025. No side effects were reported. More
2865191 80 F FL 10/12/2025 PNC20
PFIZER\WYETH
LN4927
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
Patient got Vaccine outside clinical guidelines and was not due for vaccine Patient got Vaccine outside clinical guidelines and was not due for vaccine
2865192 37 M MI 10/12/2025 COVID19
COVID19
MODERNA
MODERNA
3052553
8146545
Underdose; Underdose Underdose; Underdose
Patient received the child's dose of Moderna Spikevax (0.25ml). Pharmacist discovered error aft... Patient received the child's dose of Moderna Spikevax (0.25ml). Pharmacist discovered error after the family left the store. Called the patient and he returned to the pharmacy and received the adult dose of Moderna Spikevax More
2865193 63 M IN 10/12/2025 FLU3
SANOFI PASTEUR
U8874AA
Incorrect dose administered Incorrect dose administered
Patient was not eligible to receive Fluzone HD as he is only 63 years old. The vaccine is not recomm... Patient was not eligible to receive Fluzone HD as he is only 63 years old. The vaccine is not recommended in those younger than 65 years old. Fluzone HD was given to the patient at a vaccine clinic event happening at the (withheld location name) on October 12, 2025. Patient was contacted at provided phone number and a voice message was left. More
2865194 16 F WA 10/12/2025 COVID19
FLU3
PFIZER\BIONTECH
SEQIRUS, INC.
MY9548
409415
Dizziness, Incoherent, Seizure; Dizziness, Incoherent, Seizure Dizziness, Incoherent, Seizure; Dizziness, Incoherent, Seizure
Within 10 seconds after receiving second vaccine (Flucelvax), patient began to feel lightheaded whil... Within 10 seconds after receiving second vaccine (Flucelvax), patient began to feel lightheaded whilst in the chair and began grasping for something to hold onto. She had a brief seizure of roughly ~5 seconds and was responsive but overall incoherent. Patient's parents were in the room comforting her and making sure she felt alright, EpiPen was obtained but not administered. Patient was given some orange juice to restore fluid balance and provide glucose for energy, advised to seek medical attention once she felt better, and left in vaccine room with parents to recover. After roughly 5 minutes, the parents stated she was not "seeming to get much better", and was encouraged to seek medical attention right away. 911 was called, but parents emphasized they would bring her to emergency room for medical support. Hours later, patient's father returned to let us know that she was "doing much better". More
2865256 85 F SC 10/12/2025 COVID19
PNC20
PFIZER\BIONTECH
PFIZER\WYETH
NA4457
MG7421
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 . Patient received Prevnar 20 on 10/10/2022 and received another dose of Prevnar... No adverse reaction . Patient received Prevnar 20 on 10/10/2022 and received another dose of Prevnar 20 on 10/10/2025 More
2865257 87 M IA 10/12/2025 COVID19
FLU3
PFIZER\BIONTECH
SANOFI PASTEUR
NA0589
u8859BA
Joint swelling, Pyrexia, Skin warm, Tenderness; Joint swelling, Pyrexia, Skin wa... Joint swelling, Pyrexia, Skin warm, Tenderness; Joint swelling, Pyrexia, Skin warm, Tenderness More
Patient reported his right arm swelled up and was hot to the touch after about 24 hours. He reported... Patient reported his right arm swelled up and was hot to the touch after about 24 hours. He reported mild fever and pain associated with the reaction. After several days symptoms subsided but still slightly painful to the touch after 5 days More
2865258 33 F CT 10/12/2025 COVID19
COVID19
FLU3
FLU3
MODERNA
MODERNA
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
3052550
3052550
JE74J
JE74J
Differential white blood cell count normal, Electrocardiogram normal, Full blood... Differential white blood cell count normal, Electrocardiogram normal, Full blood count normal, Hyperhidrosis, Liver function test normal; Loss of consciousness, Metabolic function test normal, Nausea, Pyrexia, Syncope; Differential white blood cell count normal, Electrocardiogram normal, Full blood count normal, Hyperhidrosis, Liver function test normal; Loss of consciousness, Metabolic function test normal, Nausea, Pyrexia, Syncope More
Woke up the next morning after the injection feeling feverish. Extreme sweating. Felt very nauseous.... Woke up the next morning after the injection feeling feverish. Extreme sweating. Felt very nauseous. Fainted and lost consciousness for about 1-2 minutes at 8:15am. Went to urgent care then to emergency room for examination; was discharged after normal eval. More
2865260 53 M CA 10/12/2025 UNK
UNK
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER


Depressed mood, Injection site reaction, Neuralgia, Pain in extremity, Product a... Depressed mood, Injection site reaction, Neuralgia, Pain in extremity, Product administered at inappropriate site; Sleep disorder More
on the second day or 48 hours after my left arm had nerve pain, described as "zing'' ... on the second day or 48 hours after my left arm had nerve pain, described as "zing'' or ants inside of left arm that stopped at bottom Left forearm up to bicep and top of deltoid. I thought it would be ok and go away. My nights were difficult with zing pain. I took my prescribed Trazodone for sleep but would use the bathroom a few times at night and noticed zinging. I wrote on my calendar, "24 hour pain" because it was intermittent before that time. I wrote the 24 hour pain 11 days after the vaccine on September 28,2025. Now I lying around depressed and my girlfriend is angry with me. I wish the nurse would of given me the injection because the doc totally missed my deltoid, I knew this instantly. he even put a bandaid but it was behind my left deltoid and not IN MY DELTOID. I More
2865261 77 F KY 10/12/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
j9493
Arthralgia, Contusion, Myalgia, Pain, Pain in extremity Arthralgia, Contusion, Myalgia, Pain, Pain in extremity
Patient came into the pharmacy today to see if there was any OTC medicine that she could take to hel... Patient came into the pharmacy today to see if there was any OTC medicine that she could take to help with her sore arm. She mentioned that she received her vaccine almost 2 weeks ago and that she could not move her arm well due to muscle and joint pain in her right deltoid/shoulder. Upon looking at the arm there was bruising around the arm due to the fact that the patient received the arexvy and fluzone hd in the same arm and is also on blood thinners. She gets flu shot annually with no previous problems. She mentioned that the bruising is not sore and that any time she bruises it lasts a long time due to the blood thinners. However she cannot handle the joint/muscle pain when she raises her arm. She has been taking tylenol otc, and rotating heat and ice for over a week with little relief. She has AFIB and hypertension and does not take NSAIDS. I recommended a sling to help decrease movement, lidocaine to help with pain, to continue the use of heat and ice, and to follow up with pcp. Patient said she would follow up with provider if pain got worse or if there is no signs of improvement in the next few days. More
2865262 65 F AK 10/12/2025 COVID19
MODERNA
8146545
Chills, Injection site rash, Vomiting Chills, Injection site rash, Vomiting
PT CALLED PHARMACY TO INQUIRE WHAT MODERNA COVID VACCINE THEY RECEIVED. THEY WERE WONDERING IF THEY ... PT CALLED PHARMACY TO INQUIRE WHAT MODERNA COVID VACCINE THEY RECEIVED. THEY WERE WONDERING IF THEY RECEIVED A HIGHER DOSE SINCE THEY WERE HAVING MORE SEVERE REACTION THAN THEY HAD BEFORE WITH THE COVID VACCINE. IN THE PAST THEY WOULD HAVE A MILD RASH NEAR INJECTION SITE. THIS TIME, IT SEEMED TO BE MORE SEVERE, AS WELL AS PT WOKE UP AROUND 2 AM WITH MAJOR CHILLS, THEY ALSO WERE THROWING UP AS WELL. STATED IT SEEMED LIKE THEY HAD SYMPTOMS OF COVID. HAVE NOT TESTED YET. PT STATED IF THEY DON'T FEEL ANY BETTER, OR WORSE BY TOMORROW (MONDAY) THEY WILL GO TO THERE DOCTOR TO HAVE IT CHECKED OUT. ASKED PT IF SHE HAD ANY ISSUES WITH THE FLUZONE HD RECEIVED A FEW WEEKS PRIOR. PT STATED NO ISSUES. More
2865263 52 F CO 10/12/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS

Herpes zoster, Neuralgia, Rash, Rash vesicular Herpes zoster, Neuralgia, Rash, Rash vesicular
I have now been diagnosed with shingles, 4 days post shot. I have nerve pain all over my right arm ... I have now been diagnosed with shingles, 4 days post shot. I have nerve pain all over my right arm from finger tips to should blade. Yesterday I began developing the blistering rash in a line on my arm at the elbow. This is not the arm I had the shot in. More
2865264 52 M VA 10/12/2025 COVID19
FLU3
PFIZER\BIONTECH
SANOFI PASTEUR
MY9550
TFAA2501
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered More
Patient had requested the non mRNA covid vaccine when he scheduled his appointment on line but vacci... Patient had requested the non mRNA covid vaccine when he scheduled his appointment on line but vaccine was processed for the mRNA vaccine and the patient received the Pfizer mRNA vaccine instead. patient realized he received the mRNA vaccine after going home and reading through his paperwork. No adverse effects had been reported at this time. More
2865265 50 F GA 10/12/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS

Injection site discomfort, Injection site erythema, Injection site pruritus Injection site discomfort, Injection site erythema, Injection site pruritus
Circular area of local redness, discomfort, and pruritus where she had her Shingles vaccine 9/26/25,... Circular area of local redness, discomfort, and pruritus where she had her Shingles vaccine 9/26/25, starting 9/27/25 and lasting through 9/29/25. No other symptoms at the time of the vaccine, or after. More
2865065 7 OH 10/11/2025 HPV9
MERCK & CO. INC.

Product administered to patient of inappropriate age Product administered to patient of inappropriate age
GARDASIL 9 was administered to a patient who was 7 years old.; No symptoms reported.; This spontaneo... GARDASIL 9 was administered to a patient who was 7 years old.; No symptoms reported.; This spontaneous report was received from a nurse practitioner via company representative and refers to a 7-year-old patient of unknown 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 was vaccinated with Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL๏ฟฝ9), Suspension for injection (dose, route of administration, anatomical location, lot #, and expiration date were not reported) as prophylaxis (Product administered to patient of inappropriate age). No symptoms reported. Lot # is being requested and will be submitted if received More
2865066 F 10/11/2025 RVX
UNKNOWN MANUFACTURER
UNK
Death, Respiratory failure Death, Respiratory failure
This vaccine is a mistake and more for people who have conditions in the lungs , because of that vac... This vaccine is a mistake and more for people who have conditions in the lungs , because of that vaccine my sister's lungs ended and she died; This serious case was reported by a consumer via interactive digital media and described the occurrence of respiratory failure in a female patient who received RSVPreF3 adjuvanted (RSV vaccine) for prophylaxis. On an unknown date, the patient received RSV vaccine. On an unknown date, an unknown time after receiving RSV vaccine, the patient experienced respiratory failure (Verbatim: This vaccine is a mistake and more for people who have conditions in the lungs , because of that vaccine my sister's lungs ended and she died) (serious criteria death and GSK medically significant). The reported cause of death was respiratory failure. The reporter considered the respiratory failure to be related to RSV vaccine. The company considered the respiratory failure to be unrelated to RSV vaccine. Additional Information: GSK receipt date: 04-OCT-2025 This case was reported by a patient via interactive digital media. Reporter stated that this vaccine was a mistake and more for people who had conditions in the lungs, because of that vaccine reporter's sister's lungs ended and she died. The batch number was not provided, and we are unable to contact the reporter.; Sender's Comments: A case of respiratory failure, unknown time after receiving RSV vaccine, in a female patient. Based on the available information, a possible causality that the event was caused by the GSK product cannot be ascertained. Consent for further follow up has not been received.; Reported Cause(s) of Death: Respiratory failure More
โœ“
2865090 42 M NC 10/11/2025 COVID19
COVID19
MODERNA
MODERNA


Burning sensation, Electric shock sensation, Hypoaesthesia, Injection site rash,... Burning sensation, Electric shock sensation, Hypoaesthesia, Injection site rash, Muscular weakness; Pain in extremity, Rash macular More
red splotch surround the site of injection about the size of a post it note, numbness and pain in my... red splotch surround the site of injection about the size of a post it note, numbness and pain in my left middle finger that has subsided to now only being noticeable upon direct pressure it feel like someone is holding a lighter to it. I just began wearing a brace at night to sleep and after about two nights of wearing the brace is when it start to slowly become tolerable at it's worse depending on how I moved my wrist it felt like electricity and fire i also did not have any grip strength. More
2865091 53 F CO 10/11/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
?
Loss of personal independence in daily activities, Mobility decreased, Pain, Pai... Loss of personal independence in daily activities, Mobility decreased, Pain, Pain in extremity, Sleep disorder More
Extremely severe arm pain. Pain so intense it prevented sleep for >24 hours. Pain did not respond... Extremely severe arm pain. Pain so intense it prevented sleep for >24 hours. Pain did not respond to tylenol or ibuprofen. Any movement of arm was very difficult and painful. After 48 hours, pain began to subside, but pain with any movement of the arm has continued and remains. At 5 months post-injection, I still can not lift my arm, lie on this side or do any kind of lifting with this arm without debilitating pain. Pain is preventing activities of daily living. More
2865092 44 F TN 10/11/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH
FF2587
FF2587
Fear, Feeling hot, Headache, Hypoaesthesia, Laboratory test abnormal; Neck pain,... Fear, Feeling hot, Headache, Hypoaesthesia, Laboratory test abnormal; Neck pain, Palpitations, Sensory disturbance, Time perception altered More
I was employed by the hospital for only 2 months at the time, where I was given the shot in my arm ... I was employed by the hospital for only 2 months at the time, where I was given the shot in my arm (heart side).I left 20 min later.6 min into my drive home I felt a "POP" at tge top left side of my head then a warm feeling rushed over my body from head down to my toes.Immediately after that I got the worse pain in my neck up into my head.My entire left side went numb like it was asleep.I kept speaking out loud and checking in the mirror for signs of stroke but no symptoms like drooping of face, or speech issues.My heart raced and Time seemed to go in slow motion.A 9 mile ride felt like eternity to get home. More
โœ“ โœ“
2865093 65 F OR 10/11/2025 PNC20
PNC20
PFIZER\WYETH
PFIZER\WYETH


Back pain, Pain, Peripheral swelling, Pruritus, Rash; Skin warm, Sleep disorder Back pain, Pain, Peripheral swelling, Pruritus, Rash; Skin warm, Sleep disorder
Swelling, Warmth, itching, rash of upper deltoid area extending to elbow. I felt like it might be m... Swelling, Warmth, itching, rash of upper deltoid area extending to elbow. I felt like it might be my should also but it is hard to tell as I had a fusion from C2-C5 in the front of my neck (An ACDF) and fusion from C2 to T2 in the back which still has tightness. It was also sore. The symptoms kept me from sleeping. Ice pack helped. More
2865094 69 M FL 10/11/2025 FLU3
SANOFI PASTEUR
U8875AA
Contusion, Erythema Contusion, Erythema
Patient had redness and bruising running down arm after vaccine. Showed up 2 days after receiving ... Patient had redness and bruising running down arm after vaccine. Showed up 2 days after receiving injection. Patient experienced no pain, no heat or warmth of bruise, no signs of allergic reaction (no difficulty breathing). More
2865095 15 F TX 10/11/2025 HPV9
MNQ
TDAP
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
z010824
u8494aa
u8564aa
Mouth haemorrhage, Syncope, Tooth fracture; Mouth haemorrhage, Syncope, Tooth fr... Mouth haemorrhage, Syncope, Tooth fracture; Mouth haemorrhage, Syncope, Tooth fracture; Mouth haemorrhage, Syncope, Tooth fracture More
about 10 min after the vaccination of all three, patient fainted. she woke up 10 sec later without ... about 10 min after the vaccination of all three, patient fainted. she woke up 10 sec later without use of epipen. she hit her mouth while fainting and chipped her tooth. we stoped the bleeding , applied ice pack and advised father to seek dentist for her tooth More
2865096 4 F NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event No adverse event
no adverse events reported no adverse events reported
2865097 47 F VA 10/11/2025 COVID19
MODERNA

Brain fog, Injection site swelling, Myalgia, Pyrexia, Rash pruritic Brain fog, Injection site swelling, Myalgia, Pyrexia, Rash pruritic
1) Fever (1 day), Large itchy rash and swelling at injection site (1 week), Muscle aches (1 week), B... 1) Fever (1 day), Large itchy rash and swelling at injection site (1 week), Muscle aches (1 week), Brain fog (1.5 weeks) More
2865098 7 M NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865099 4 F NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865100 7 F NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865101 5 M NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865102 6 M NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865103 54 F IN 10/11/2025 PNC20
PFIZER\WYETH
MA2523
Injection site erythema, Injection site pain Injection site erythema, Injection site pain
redness, tenderness below site of injection. redness spreading for 2 days afterwards. redness, tenderness below site of injection. redness spreading for 2 days afterwards.
2865104 6 F NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865105 8 M NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event No adverse event
no adverse events reported no adverse events reported
2865106 5 F NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865107 7 F NH 10/11/2025 FLU3
SANOFI PASTEUR
u8823da
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
no adverse events reported no adverse events reported
2865108 68 M NC 10/11/2025 PNC20
PFIZER\WYETH
ma2523
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient received dose outside recommendations by package insert. Received dose of Prevnar 20 in 202... Patient received dose outside recommendations by package insert. Received dose of Prevnar 20 in 2022. No adverse effects reported by patient. More
2865109 68 F AL 10/11/2025 COVID19
FLU3
PNC21
VARZOS
MODERNA
SANOFI PASTEUR
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
3052036
U8764DB
Z009681
9C75Y
Hyperhidrosis, Palpitations, Syncope, Visual impairment; Hyperhidrosis, Palpitat... Hyperhidrosis, Palpitations, Syncope, Visual impairment; Hyperhidrosis, Palpitations, Syncope, Visual impairment; Hyperhidrosis, Palpitations, Syncope, Visual impairment; Hyperhidrosis, Palpitations, Syncope, Visual impairment More
syncope, sweating, vision changes, heart racing syncope, sweating, vision changes, heart racing
2865110 9 F VA 10/11/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH


Blood glucose, Confusional state, Dizziness, Electrocardiogram, Influenza virus ... Blood glucose, Confusional state, Dizziness, Electrocardiogram, Influenza virus test; Mental status changes, Streptococcus test, Syncope, Ultrasound abdomen, Urine analysis More
Altered mental status, syncope, dizziness, confusion Altered mental status, syncope, dizziness, confusion
2865111 3 F FL 10/11/2025 FLU3
GLAXOSMITHKLINE BIOLOGICALS

Abdominal pain upper, Injection site pain, Pain, Vomiting projectile Abdominal pain upper, Injection site pain, Pain, Vomiting projectile
3 years and 11 month old. Projectile vomiting about 8 hours after receiving vaccine, all through the... 3 years and 11 month old. Projectile vomiting about 8 hours after receiving vaccine, all through the night and morning. Still can?t keep even water down, now 19 hours after receiving shot. Ondasetron also thrown up 10 min after taking ondasetron. Belly aches. Also feeling pain in arm where she received shot and body aches. More