🏥 VAERS Vaccine Data Browser

🔒 Privacy & Data Disclaimer

About This Site

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

Data Source & Accuracy

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

Your Privacy

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

Medical Disclaimer

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

Data Interpretation

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

📖 Help & Search Guide

Column Icons Legend

💀 Death
🏥 Hospitalized
🚑 Emergency Room
♿ Disability
⚠️ Life Threatening

How to Search

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

Understanding the Data

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

Using the Table

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

💡 Frequently Asked Questions (FAQ)

What is this site?

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

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

What is VAERS?

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

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

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

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

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

Why does this site exist?

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

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

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

Where does the data come from?

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

The data is:

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

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

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

Important context:

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

What to do:

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

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

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

Limitations:

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

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

What are "adverse events"?

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

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

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

Why are some lot numbers listed multiple times?

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

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

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

How often is this data updated?

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

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

Where can I learn more?

⚠️ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
🔄 Reset 📥 Export CSV
ID Age Sex State Date ▼ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative 💀 🏥 🚑 ♿ ⚠️
2826579 59 F TX 02/17/2025 UNK
 UNKNOWN MANUFACTURER
 U7013DA
Cold sweat, Loss of consciousness, Pallor Cold sweat, Loss of consciousness, Pallor
On 02/14/2025 donor presented to clinic for donation. After she completed a donation she was schedu... On 02/14/2025 donor presented to clinic for donation. After she completed a donation she was scheduled to receive the Vaccinia Vaccination. Post Immunization the donor started to feel clammy, Pallor Skin or lips and also had LOC for less then 60 seconds. More
2826580 17 F IL 02/17/2025 COVID19
FLU3
MENB
 MODERNA
SANOFI PASTEUR
PFIZER\WYETH
 B0005
UT8415KA
HP9988
Syncope; Syncope; Syncope Syncope; Syncope; Syncope
Patient fainted after being given the vaccines while walking out of the room. Patient fainted after being given the vaccines while walking out of the room.
2826581 48 M MN 02/17/2025 COVID19
COVID19
 MODERNA
MODERNA
 034C21A
046C21A
Cough, Dyspnoea, Respiratory tract congestion, SARS-CoV-2 test; Cough, Dyspnoea,... Cough, Dyspnoea, Respiratory tract congestion, SARS-CoV-2 test; Cough, Dyspnoea, Respiratory tract congestion, SARS-CoV-2 test More
Chest congestion, cough, shortness of breath x5 days Chest congestion, cough, shortness of breath x5 days
✓
2826582 23 F PA 02/17/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 H2B22
Underdose Underdose
Patient was given Pediatric dose of 10 mcg/0.5 mL instead of adult dose 20 mcg/1 mL. Patient was given Pediatric dose of 10 mcg/0.5 mL instead of adult dose 20 mcg/1 mL.
2826583 43 F CA 02/17/2025 FLUC4
 SEQIRUS, INC.
 946619
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Error: Shoulder Joint Injury (prolon... Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: prevnar 20; Manufacturer: ; LotNumber: ; Route: same arm; BodySite: same arm; Dose: ; VaxDate: UNKNOWN More
2826584 21 F CA 02/17/2025 HPV9
HPV9
 MERCK & CO. INC.
MERCK & CO. INC.
 y018389
y018389
Dizziness, Flushing, Headache, Hyperhidrosis, Nausea; Paraesthesia, Visual impai... Dizziness, Flushing, Headache, Hyperhidrosis, Nausea; Paraesthesia, Visual impairment More
Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-... Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Nausea-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Systemic: Visual Changes/Disturbances-Medium, Other Vaccines: VaccineTypeBrand: boostrix tdap; Manufacturer: GSK; LotNumber: 9429j; Route: IM; BodySite: Left arm; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: menveo a-c-y-w; Manufacturer: GSK; LotNumber: xl223; Route: IM; BodySite: Left arm; Dose: ; VaxDate: UNKNOWN More
2826585 72 F TX 02/17/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EN6202
EN6202
EN6202
Anxiety, Arthralgia, Biopsy skin abnormal, Blood test abnormal, Fatigue; Inflamm... Anxiety, Arthralgia, Biopsy skin abnormal, Blood test abnormal, Fatigue; Inflammation, Lymphadenopathy, Mastication disorder, Pain, Polymyalgia rheumatica; Rash, Rash pruritic, Scar, Skin test, Tenderness More
Description of Symptoms (This description was given to Dr. rheumatologist on my 1st visit on Dec. 5,... Description of Symptoms (This description was given to Dr. rheumatologist on my 1st visit on Dec. 5, 2023) On March 9, 2021 I took my first dose of the Covid Vaccine and immediately had reactions to the shot. These reactions were within the first 24 hours after the shot. ( I took the second dose two weeks later and then the required booster shots.) My lymph nodes did swell and when I would sit down to eat I had difficulty chewing because it would seem to swell them further. It would cause anxiety every time I ate. Also, I developed at the same time an unexplained rash on my left leg and then later my right leg that would cause a lot of itching. I have continued to have these problems and my doctors and dermatologists could not seem to help. The inflammation comes and goes on my rash with each episode leaving permanent scarring on my skin. Every time it flares up it spreads wider and has even spread to my other leg. I just recently was seen by Dermatologists (Sept. 11, 2023) and they did a biopsy of which I have the report results. They gave me a cortisone shot and it seemed to help temporarily. I need to find what is causing this reaction. According to the biopsy report, I was advised to check further since it showed some kind of auto immune response. My next appointment was at Allergy where I was sent to lab for an intense blood work on all possible allergies and then later came back for a thorough airborne allergy skin testing. The blood work seemed to confirm an auto immune response. I have been experiencing unexplained fatigue whereby my whole body just aches and nothing seems to help except laying down and sleeping it off. I can experience aches concentrated on the certain areas marked on your questionnaire to all over achiness . I don?t know if all this is related to my rashes and lymph node swellings . Last week and through today it is concentrated on my right knee. 2 weeks ago was my right shoulder which felt like I was being stabbed sharply. The week before that (3 weeks ago) it was concentrated on my left shoulder and it felt very painful to touch right at the joint. Since my appoiintment with Dr. MD I have been referred to Dr. (Rhuematologist MD) . Dr. diagnosed me as having RA but referred me out for second opinion. Dr. diagnosed me with Polymyalgia Rheumatica. The medicines prescribed for my condition have been Hydroxychloroquine and Prednisone. More
2826586 69 F FL 02/17/2025 FLU3
 SANOFI PASTEUR
 u8944da
Injection site erythema, Injection site pain Injection site erythema, Injection site pain
redness and pain around injection site starting 2 days after injection. no longer red but still pain... redness and pain around injection site starting 2 days after injection. no longer red but still painful today 2/17/25 More
2826587 5 M PA 02/17/2025 COVID19
 MODERNA
 3044143
Product preparation error Product preparation error
Patient was given dose of vaccine before the vaccine was completely thawed. Given approximately 30 ... Patient was given dose of vaccine before the vaccine was completely thawed. Given approximately 30 minutes early, before correct thaw time. After consultation with Moderna and our senior staff as well as physician, patient was determined to not need revaccination More
2826588 71 F FL 02/17/2025 PNC21
 MERCK & CO. INC.
 Y013009
Injection site erythema, Injection site mass, Injection site pruritus Injection site erythema, Injection site mass, Injection site pruritus
Patient reported over phone: woke the next morning to a "knot" on her arm at the vaccine s... Patient reported over phone: woke the next morning to a "knot" on her arm at the vaccine site and well as some redness. The redness has since spread as far as her elbow. Patient states that is is itchy as well. More
2826589 40 F CA 02/17/2025 HPV9
 MERCK & CO. INC.
Arthralgia, Mobility decreased Arthralgia, Mobility decreased
Left should pain and loss of mobility Left should pain and loss of mobility
2826590 88 M RI 02/17/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 LN0588
LN0588
Blood glucose increased, Confusional state, Death, Dyspnoea, Fatigue; Headache, ... Blood glucose increased, Confusional state, Death, Dyspnoea, Fatigue; Headache, Loss of consciousness, Nausea, Peripheral coldness, Vomiting More
Upon awakening on October 25, 2024, which was the morning following the administration of the COVID ... Upon awakening on October 25, 2024, which was the morning following the administration of the COVID 19 vaccination given on October 24, 2024, his finger stick blood sugar was very high for him 177 (for the last 2 years his range has been 100-134, except on approximately 3 occasions after eating sweets the night prior), headache, intense fatigue, nausea, vomiting which continued through the night. The next morning on October 26, 2024, upon awakening his finger stick blood sugar was 174, again high for him especially with minimal intake, the symptoms from the day prior worsened during the day with additional new symptoms of shortness of breath, difficulty breathing, confusion and skin cool to the touch at which time EMS was called. Prior to their arrival, he became unconscious but breathing. He was transported to the nearest hospital and he was pronounced dead at 11:18pm (on October 26, 2024) which was shortly after arrival. More
✓
2826591 51 M CA 02/17/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 KB2YT
KB2YT
Arthralgia, Dysstasia, Gait disturbance, Influenza like illness, Injection site ... Arthralgia, Dysstasia, Gait disturbance, Influenza like illness, Injection site discomfort; Loss of personal independence in daily activities, Muscle spasms, Myalgia More
After approximately 36 hours post vaccination I began to experience mild flu-like symptoms ( low fev... After approximately 36 hours post vaccination I began to experience mild flu-like symptoms ( low fever, night sweating, upset stomach) in addition mild discomfort at injection site. On Monday 2/3/25 I woke up to intense and debilitating joint pain in my lower back which progressed the same day to both hips. Was in severe discomfort and was unable to stand up straight and could barely walk. The pain intensified over the next few days. On Wednesday 2/5/2205 the joint paint had not subsided and I began to experience muscle aches and spasms throughout both legs. It is now 2/17/25 and the pain is only beginning to subside with standing and walking becoming more comfortable. Prior to the shingles vaccination I had rarely if ever experience body aches and pains and had exercised daily for a minimum of 30 minutes. I am still unable to exercise. More
2826606 U 02/17/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 UNK
UNK
Herpes zoster, Vaccination failure; Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure; Herpes zoster, Vaccination failure
Suspected vaccination failure; to have shingles this month; This serious case was reported by a cons... Suspected vaccination failure; to have shingles this month; 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 (Shingrix) for prophylaxis. Co-suspect products included Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received the 2nd dose of Shingrix and the 1st dose of Shingrix. In JAN-2025, an unknown time after receiving Shingrix and Shingrix, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: to have shingles this month). The outcome of the vaccination failure was not reported and the outcome of the shingles was resolved. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingrix and Shingrix. The company considered the vaccination failure to be unrelated to Shingrix and Shingrix. It was unknown if the company considered the shingles to be related to Shingrix and Shingrix. Additional Information: GSK Receipt Date: 29-JAN-2025 This case was reported by a patient via (Shingles) interactive digital media. The patient received both doses of shingles vaccine in 2023 and 2024 and had shingles this month. The patient stated the good thing was did not had the blistering rash. The patient felt compel to let everyone know that they can have shingles without an outbreak. The patient stated please get vaccinated and maybe, should you come down with shingles, you will not have a rash. This case was considered as suspected vaccination failure as details regarding laboratory confirmation regarding shingles were unknown at the time of reporting The follow-up could not be possible as no contact details were available.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding time to onset and laboratory confirmation of disease) is considered unrelated to GSK vaccine Shingrix (Dose 1 and Dose 2). More
2826607 F TX 02/17/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 9R2D7
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
10 year old female patient received a dose of Infanrix; This non-serious case was reported by a othe... 10 year old female patient received a dose of Infanrix; This non-serious case was reported by a other health professional via call center representative and described the occurrence of inappropriate age at vaccine administration in a 10-year-old female patient who received DTPa (Infanrix) (batch number 9R2D7, expiry date 23-MAY-2025) for prophylaxis. On 31-OCT-2024, the patient received Infanrix. On 31-OCT-2024, an unknown time after receiving Infanrix, the patient experienced inappropriate age at vaccine administration (Verbatim: 10 year old female patient received a dose of Infanrix). The outcome of the inappropriate age at vaccine administration was unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 10-FEB-2025 The Vaccine Administration Facility was the same as Primary Reporter The Certified Medical Assistant called to report that a 10 year old patient received a dose of Infanrix vaccine, which led to inappropriate age at vaccine administration. They wanted to know if the patient needed to receive another dose. More
2826608 67 F 02/17/2025 COVID19
 MODERNA
COVID-19, Food poisoning, SARS-CoV-2 test COVID-19, Food poisoning, SARS-CoV-2 test
was ill with food poisoning; tested positive for COVID-19; This spontaneous case was reported by a p... was ill with food poisoning; tested positive for COVID-19; This spontaneous case was reported by a patient and describes the occurrence of FOOD POISONING (was ill with food poisoning) and COVID-19 (tested positive for COVID-19) in a 68-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Dec-2023, the patient received dose of mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use) .5 milliliter. On 13-Jan-2025, after starting mRNA-1273.815 (SPIKEVAX 2023-2024), the patient experienced COVID-19 (tested positive for COVID-19). On an unknown date, the patient experienced FOOD POISONING (was ill with food poisoning). At the time of the report, FOOD POISONING (was ill with food poisoning) outcome was unknown and COVID-19 (tested positive for COVID-19) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-Jan-2025, SARS-CoV-2 test: Positive. On 20-Jan-2025, SARS-CoV-2 test: Negative. The action taken with mRNA-1273.815 (SPIKEVAX 2023-2024) (Intramuscular use) was unknown. No concomitant medication was reported. She was originally set to receive the new COVID vaccine for the 2024-2025 season in Dec-2024, but due to food poisoning, her appointment was postponed to Jan-2025. On 13-Jan-2025, she tested positive for COVID-19 and missed the rescheduled vaccination. She had severe cold-like symptoms, including a runny nose and sneezing, but denied having a cough. Although she suspected it wasn't COVID, her daughter encouraged her to get tested. Ultimately, she tested negative on 20-Jan-2025, with no further information available. It was unknown if the patient experienced any additional symptoms or events. No treatment medication was reported. More
2826609 27 F NJ 02/17/2025 COVID19
 PFIZER\BIONTECH
 LN0591
Fatigue, Migraine, Nausea, Pain, Pyrexia Fatigue, Migraine, Nausea, Pain, Pyrexia
body aches; migraine; fever; nausea; exhaustion; This is a spontaneous report received from a Consum... body aches; migraine; fever; nausea; exhaustion; This is a spontaneous report received from a Consumer or other non HCP. A 27-year-old female patient (not pregnant) received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), on 09Feb2025 at 15:45 as dose 1, single (Lot number: LN0591) at the age of 27 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LO LOESTRIN FE, start date: Apr2015; SPIRONOLACTONE, start date: Jan2015. The following information was reported: PAIN (non-serious) with onset 09Feb2025 at 23:45, outcome "recovered" (12Feb2025), described as "body aches"; FATIGUE (non-serious) with onset 09Feb2025 at 23:45, outcome "recovered" (12Feb2025), described as "exhaustion"; PYREXIA (non-serious) with onset 09Feb2025 at 23:45, outcome "recovered" (12Feb2025), described as "fever"; MIGRAINE (non-serious) with onset 09Feb2025 at 23:45, outcome "recovered" (12Feb2025); NAUSEA (non-serious) with onset 09Feb2025 at 23:45, outcome "recovered" (12Feb2025). Therapeutic measures were not taken as a result of pain, migraine, pyrexia, nausea, fatigue. Additional information: The patient did not receive any other vaccines on the same date as the vaccine(s). The patient did not receive any other vaccines within 4 weeks PRIOR to the vaccine(s). More
2826610 M 02/17/2025 COVID19
 PFIZER\BIONTECH
Magnetic resonance imaging, Mobility decreased, Pain, Pain in extremity, X-ray Magnetic resonance imaging, Mobility decreased, Pain, Pain in extremity, X-ray
pain in his arm/hurting; barely can move my right arm/can barely move his arm; in pain; This is a sp... pain in his arm/hurting; barely can move my right arm/can barely move his arm; in pain; This is a spontaneous report received from a Consumer or other non HCP from medical information team, Program ID. A male patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "pain in his arm/hurting"; MOBILITY DECREASED (non-serious), outcome "unknown", described as "barely can move my right arm/can barely move his arm"; PAIN (non-serious), outcome "unknown", described as "in pain". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The caller said he took the Pfizer COVID vaccine and experienced pain in his arm and he would like to know how to remove the protein inside his body. per caller calling regarding Pfizer covid19 vaccine received vaccination per caller when you bombarded us with information you are going to die if you don't take a shot, 2-3 years ago No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2826611 F 02/17/2025 COVID19
FLUX
 PFIZER\BIONTECH
UNKNOWN MANUFACTURER

Vaccination site pain; Vaccination site pain Vaccination site pain; Vaccination site pain
arm was sore; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A... arm was sore; This is a spontaneous report received from a Consumer or other non HCP, Program ID. An adult (60-64 years old) female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), in 2025 as dose 1, single (Batch/Lot number: unknown), in arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), in 2025 as unk, single), in arm for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION SITE PAIN (hospitalization) with onset 2025, outcome "unknown", described as "arm was sore". Clinical course: This season; patient received the flu and Covid vaccines at the same time; in the same arm; so the scenarios were familiar. Arm was sore for a couple of days. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
✓
2826612 22 M OK 02/17/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 333SK
Blood pressure decreased, Feeling hot, Pallor Blood pressure decreased, Feeling hot, Pallor
patient blood pressure dropped, face pale and patient was feeling warm about 15 - minutes after get... patient blood pressure dropped, face pale and patient was feeling warm about 15 - minutes after getting immunization administered. patient said he gets very nervous about needles and it lasts around 20 minutes or so - happened during a blood draw about two months ago and when he watched his wife get an iv - after EMS came to evaluate patient and it was mentioned it may be vasovagal syncope patient said he remembered at his blood draw being told something about that (this information was not listed on his patient consent/questionnaire form - patient denied transport to the hospital via ambulance and was advised to go to a walk-in clinic or talk with his primary and given instructions of what to do if anything happens after leaving, wife was with him who verbalized understanding More
2826613 66 M VA 02/17/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FK9893
FK9893
Aldosterone/renin ratio, Blood chromogranin A, Blood magnesium normal, Blood thy... Aldosterone/renin ratio, Blood chromogranin A, Blood magnesium normal, Blood thyroid stimulating hormone normal, Coma; Electrocardiogram normal, Full blood count normal, Labile hypertension, Lipids normal More
Patient reports labile hypertension after COVID vaccination. Currently, he is not taking any medicat... Patient reports labile hypertension after COVID vaccination. Currently, he is not taking any medications. He is managed through lifestyle and monitoring at this time. More
2826614 69 F OH 02/17/2025 FLU3
FLU3
PNC20
PNC20
 SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH
 U8489AA
U8489AA
HE9173
HE9173
Computerised tomogram thorax, Deep vein thrombosis, Injected limb mobility decre... Computerised tomogram thorax, Deep vein thrombosis, Injected limb mobility decreased, Injection site erythema, Injection site pain; Injection site warmth, Ultrasound Doppler abnormal; Computerised tomogram thorax, Deep vein thrombosis, Injected limb mobility decreased, Injection site erythema, Injection site pain; Injection site warmth, Ultrasound Doppler abnormal More
Injection site hot, red, painful, decreased ROM at the shoulder. Sent to ER concern for cellulitis.... Injection site hot, red, painful, decreased ROM at the shoulder. Sent to ER concern for cellulitis. Dx'd DVT brachial vein. More
2826615 54 M WA 02/17/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EL3302
EL3302
EL9264
EL9264
Angiocardiogram, Angioplasty, Coronary angioplasty, Coronary arterial stent inse... Angiocardiogram, Angioplasty, Coronary angioplasty, Coronary arterial stent insertion, Myocardial infarction; Ultrasound Doppler; Angiocardiogram, Angioplasty, Coronary angioplasty, Coronary arterial stent insertion, Myocardial infarction; Ultrasound Doppler More
Adverse Event: 1.Massive Heart Attack in Proximal Circumflex Artery Segment -. Treatment: 1. Corona... Adverse Event: 1.Massive Heart Attack in Proximal Circumflex Artery Segment -. Treatment: 1. Coronary angiogram 2. Percutaneous transluminal angioplasty and primary intracoronary stent placement to the CxOM and balloon angioplasty of the Cx 3. Intravascular ultrasound of the Cx-OM More
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2826616 72 M CO 02/17/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Hypoaesthesia Hypoaesthesia
patient said his feet went numb. He said he went to his physicians office 3 times the first day. he ... patient said his feet went numb. He said he went to his physicians office 3 times the first day. he received the vaccine and within 6 hours of the vaccine he was having numbness in his feet. More
2826617 17 F MP 02/17/2025 MNQ
 SANOFI PASTEUR
 U8351CA
Dry skin, Erythema, Urticaria Dry skin, Erythema, Urticaria
Reported that after eating lunch, about an hour after vaccine, developed HA, facial urticaria. No SO... Reported that after eating lunch, about an hour after vaccine, developed HA, facial urticaria. No SOB, no fever, no swelling noted; Drank Tylenol & HA resolved. Washed face with soap & water but itchiness persisted; client observed actively scratching face, slight redness in left cheek, forehead, side of nose, dry skin but no hives; no hives observed elsewhere in body; Reported not eating anything or applying anything on skin that is "new"; CNP on site suggested 25mg diphenhydranine PO then & another 25mg after if itchiness persisted. Contacted mother who game permission to treat; instructed to bring to ED if symptoms do not resolve or worsens. Reported to school counselor a day later stating HA gone but took dipenhydramine as itchiness persists. Reported to school counselor a day later stating HA gone but took dipenhydramine once more and itchiness resolved. More
2826618 34 F NJ 02/17/2025 RSV
RSV
RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 ae435
ae435
AE435
AE435
Exposure during pregnancy, No adverse event, Product use issue; Exposure during ... Exposure during pregnancy, No adverse event, Product use issue; Exposure during pregnancy, Product use issue; Exposure during pregnancy, No adverse event, Product use issue; Exposure during pregnancy, Product use issue More
patient got arexvy at 36 weeks which its not indicated for. patient does not have any side effects b... patient got arexvy at 36 weeks which its not indicated for. patient does not have any side effects but since it does not have and indication for it we need to report it. More
2826619 33 F SC 02/17/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 026L20A
026L20A
026L20A
026L20A
026L20A
026L20A
026L20A
026L20A
Antinuclear antibody positive, Autoimmune disorder, Blood test, Condition aggrav... Antinuclear antibody positive, Autoimmune disorder, Blood test, Condition aggravated, Decreased appetite; Hyperhidrosis, Hypoaesthesia, Insomnia, Magnetic resonance imaging, Major depression; Nightmare, Nodule, Paraesthesia, Peripheral swelling, Sleep study normal; Somnambulism, Somnolence, Weight decreased, X-ray; Antinuclear antibody positive, Autoimmune disorder, Blood test, Condition aggravated, Decreased appetite; Hyperhidrosis, Hypoaesthesia, Insomnia, Magnetic resonance imaging, Major depression; Nightmare, Nodule, Paraesthesia, Peripheral swelling, Sleep study normal; Somnambulism, Somnolence, Weight decreased, X-ray More
Increased swelling in my right forearm and right hand, which resulted in blood tests, specifically a... Increased swelling in my right forearm and right hand, which resulted in blood tests, specifically a RA panel that was initially reported a positive ANA factor and had to seek out Rheumatology. I waited 16 months to be treated for the inflammatory auto immune disorder that was shown in my blood work. By this point my right forearm and right hand were so swollen, numbness and tingling. I began forming large dense nodules on the palms of both hands. Was then directed to a hand surgeon. Insomnia, excess sweating, nightmares and extreme daytime sleepiness, which resulted in getting a sleep study done that showed no pertinent results. Extreme weight loss, decrease appetite, which resulted in seeing my primary care doctor. I went from 114lbs to 91lbs in a short 8 months. Ended up under the treatment of neurology due to major depression, insomnia, and sleep walking. Neurology provided me a referral for counseling. More
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2826620 44 F IA 02/17/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 4ds4n
Malaise, Swelling Malaise, Swelling
Swelling, overall unwell feeling Swelling, overall unwell feeling
2826621 66 M CO 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93KK4
Extra dose administered, No adverse event, Wrong product administered Extra dose administered, No adverse event, Wrong product administered
PATIENT RECEIVED SHINGRIX (3RD DOSE) INSTEAD OF PNEUMONIA-- NO REACTIONS/ADVERSE EVENTS PATIENT RECEIVED SHINGRIX (3RD DOSE) INSTEAD OF PNEUMONIA-- NO REACTIONS/ADVERSE EVENTS
2826622 67 M CA 02/17/2025 COVID19
 PFIZER\BIONTECH
Eye pain, Facial pain, Nasopharyngitis, Pain in jaw, Pain of skin Eye pain, Facial pain, Nasopharyngitis, Pain in jaw, Pain of skin
A few hours after the vaccine was administered my left jaw became very painful spreading to my left ... A few hours after the vaccine was administered my left jaw became very painful spreading to my left eye, forehead and scalp. After another few hours I took an Ibuprofen tab 200mg and these symptom gradually subsided. It is now several days later and I'm having mild cold symptoms I expect will dissipate soon. More
2826623 59 F TX 02/17/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 LP2G2
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826624 75 M NJ 02/17/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 M4E4E
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826625 55 F FL 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 429mk
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826626 49 M MO 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7ye7t
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826627 72 F MA 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 2r375
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826629 86 F VA 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 9s252
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826630 75 F TX 02/17/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 H3SG9
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826631 81 F MO 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 5777f
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826632 66 M CA 02/17/2025 FLU4
 SANOFI PASTEUR
 U8044BA
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: M... Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: Moderna Bivalent; Manufacturer: Moderna; LotNumber: AS7643e; Route: IM; BodySite: Left Arm; Dose: 5; VaxDate: 08/01/2023 More
2826634 65 F TX 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 9hm59
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826635 69 M KY 02/17/2025 FLUA4
 SEQIRUS, INC.
 370267
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826636 72 F MI 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 274yd
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826637 77 F MO 02/17/2025 FLU4
 SANOFI PASTEUR
 u8044aa
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: p... Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: pfizer bivalent covid; Manufacturer: pfizer; LotNumber: gk0923; Route: intramuscular; BodySite: left deltoid; Dose: booster; VaxDate: 08/09/2023 More
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2826638 70 M CA 02/17/2025 FLUA4
 SEQIRUS, INC.
 371604
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826640 59 F PA 02/17/2025 FLU4
 GLAXOSMITHKLINE BIOLOGICALS
 944445
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: P... Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: Prevnar; Manufacturer: Wyeth/Pfizer; LotNumber: GW7964; Route: IM; BodySite: left arm/pt states it was given in right arm; Dose: ; VaxDate: UNKNOWN More
2826641 63 F NC 02/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 zsed7
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826642 66 M OK 02/17/2025 FLUA4
 SEQIRUS, INC.
 371603
Limb injury Limb injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826644 69 F TN 02/17/2025 FLUA4
 SEQIRUS, INC.
 371203
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: F... Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Other Vaccines: VaccineTypeBrand: FLUAD; Manufacturer: seqirus; LotNumber: 371203; Route: IM; BodySite: arm; Dose: ; VaxDate: UNKNOWN More
2826645 47 M CA 02/17/2025 FLUC4
 SEQIRUS, INC.
 944456
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2826646 82 F CA 02/17/2025 FLUA4
 SEQIRUS, INC.
 370267
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
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