🏥 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 💀 🏥 🚑 ♿ ⚠️
2840726 11 M SD 05/13/2025 UNK
UNK
UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER



Asthenia, Dizziness, Fall, Head injury, Pain in extremity; Syncope; Asthenia, Di... Asthenia, Dizziness, Fall, Head injury, Pain in extremity; Syncope; Asthenia, Dizziness, Fall, Head injury, Pain in extremity; Syncope More
pts father says he complained about having a sore arm after the vaccine. The next morning he woke up... pts father says he complained about having a sore arm after the vaccine. The next morning he woke up dizzy, weak, and fainted. He fell and hit his head. He feels extremely weak and was not able to attend class. The doctors office has been contacted and will get a call back from the nurse. More
2840727 43 F PA 05/13/2025 COVID19
 PFIZER\BIONTECH
Intensive care, Ischaemic stroke, Myocardial infarction, Thrombosis, Transient i... Intensive care, Ischaemic stroke, Myocardial infarction, Thrombosis, Transient ischaemic attack More
A week after the initial Pfizer shot, I suffered an acute left ischemic stroke, a TIA 3 months late... A week after the initial Pfizer shot, I suffered an acute left ischemic stroke, a TIA 3 months later on 09/26/2022, a heart attack 13 months later and an additional heart attack 10 months after this. My body has now been forming blood clots, despite not having high blood pressure, no diabetes, and no other contributing factors More
✓ ✓ ✓
2840728 92 F TX 05/13/2025 COVID19
 MODERNA
 3042645
Expired product administered, No adverse event Expired product administered, No adverse event
Vaccine expired on 5-9, administered on 5-13, patient not reporting any side effects since administr... Vaccine expired on 5-9, administered on 5-13, patient not reporting any side effects since administration, More
2840729 12 F 05/13/2025 COVID19
 MODERNA
 B0001
No adverse event No adverse event
no adverse reaction no adverse reaction
2840730 13 F 05/13/2025 COVID19
 MODERNA
 B0001
No adverse event No adverse event
no adverse reaction no adverse reaction
2840731 58 F CO 05/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Headache, Myalgia, Pain, Pyrexia Headache, Myalgia, Pain, Pyrexia
This was #2 dose of the Shingrix vaccine. The next morning prepared myself for work. Normal hygiene ... This was #2 dose of the Shingrix vaccine. The next morning prepared myself for work. Normal hygiene felt I was older than I am. Body/muscles aches I complained of body aches similar to labor pains but all over. At work walking slower and temperature was measured, Fever was 101.0 and was sent home. Headaches were managed alternating with Tylenol 1000mg every 6 hrs and Ibuprofen 800mg. Relief of Headache finally after 8 p.m. Drank plenty of fluids, Gatorade and rested and sleep. The next day symptoms resolved except for headache lingered. More
2840732 4 F RI 05/13/2025 MMRV
MMRV
 MERCK & CO. INC.
MERCK & CO. INC.
 X027624
X027624
Antibody test, Injection site reaction, Measles antibody, Mumps antibody test, P... Antibody test, Injection site reaction, Measles antibody, Mumps antibody test, Pruritus; Rubella antibody test, Skin lesion, Wrong technique in product usage process More
Immunization was not given correctly and has had a small pruritic lesion at injection site for 1 y... Immunization was not given correctly and has had a small pruritic lesion at injection site for 1 year More
2840733 73 M MS 05/13/2025 COVID19
 PFIZER\BIONTECH
 MD3414
Injection site bruising, Injection site swelling, Pyrexia Injection site bruising, Injection site swelling, Pyrexia
Patient says he has had a fever, a bruise at the site of injection, and swelling at the site since t... Patient says he has had a fever, a bruise at the site of injection, and swelling at the site since the day he received the vaccine. More
2840734 61 F GA 05/13/2025 COVID19
VARZOS
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
 PFIMD3414
A2F3R
Chills, Fatigue, Injection site nodule, Oral mucosal blistering; Chills, Fatigue... Chills, Fatigue, Injection site nodule, Oral mucosal blistering; Chills, Fatigue, Injection site nodule, Oral mucosal blistering More
First 24 hours felt tired, knot at site injection given (LD), chills and blisters all inside mouth a... First 24 hours felt tired, knot at site injection given (LD), chills and blisters all inside mouth and around mouth. More
2840735 AZ 05/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Skin lesion Skin lesion
open sores on 90 percent of my body; This non-serious case was reported by a consumer via call cente... open sores on 90 percent of my body; This non-serious case was reported by a consumer via call center representative and described the occurrence of skin lesion in a patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received Shingrix. On an unknown date, 3 months after receiving Shingrix, the patient experienced skin lesion (Verbatim: open sores on 90 percent of my body). The outcome of the skin lesion was not reported. It was unknown if the reporter considered the skin lesion to be related to Shingrix. It was unknown if the company considered the skin lesion to be related to Shingrix. Additional Information: GSK Receipt Date: 03-MAY-2025 and 05-MAY-2025 The patient had developed open sores on 90 percent of body. These started 3 months after Shingrix vaccines. More
2840736 F IN 05/13/2025 MMR
MMR
MMR
MMR
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 X013192
X013192
X013192
X013192
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event More
No symptoms, vaccine was past expiration date. RN spoke with MERCK and the vaccine counts as a valid... No symptoms, vaccine was past expiration date. RN spoke with MERCK and the vaccine counts as a valid dose and no revaccination is needed. More
2840737 14 F PA 05/13/2025 ADEN_4_7
HEP
IPV
MNQ
TDAP
VARCEL
 TEVA PHARMACEUTICALS
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
 Y008591
K4JH7
X1D141M
U8369BA
U8122AA
Y015559
Exposure during pregnancy, Ultrasound antenatal screen; Exposure during pregnanc... Exposure during pregnancy, Ultrasound antenatal screen; Exposure during pregnancy, Ultrasound antenatal screen; Exposure during pregnancy, Ultrasound antenatal screen; Exposure during pregnancy, Ultrasound antenatal screen; Exposure during pregnancy, Ultrasound antenatal screen; Exposure during pregnancy, Ultrasound antenatal screen More
Patient received vaccinations listed above at public health clinic on 4/1/2025. At the time of recei... Patient received vaccinations listed above at public health clinic on 4/1/2025. At the time of receiving vaccinations, it was unknown to patient and provider that she was pregnant, approximately 16 weeks gestational age. Patient later discovered pregnancy on 5/5/2025 during emergency room visit. More
2840738 74 M AZ 05/13/2025 COVID19
 PFIZER\BIONTECH
Eyelid ptosis, Muscular weakness, Myasthenia gravis, Nerve conduction studies ab... Eyelid ptosis, Muscular weakness, Myasthenia gravis, Nerve conduction studies abnormal, Speech disorder More
Approximately 30 days after receiving the second COVID19 booster I began showing symptoms of weaknes... Approximately 30 days after receiving the second COVID19 booster I began showing symptoms of weakness in the legs, ptosis and speech difficulties. Initially, my PC diagnosed the condition as Bells Palsy but subsequently referred me to a neurologist who diagnosed me with Generalized Myasthenia Gravis. Subsequent testing conformed the diagnosis. More
✓
2840739 65 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840740 45 F ME 05/13/2025 COVID19
COVID19
FLU3
FLU3
 PFIZER\BIONTECH
PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
 LP1776
LP1776
UT8485MA
UT8485MA
Asthenia, Blood test, Computerised tomogram head normal, Fatigue, Headache; SARS... Asthenia, Blood test, Computerised tomogram head normal, Fatigue, Headache; SARS-CoV-2 test negative, Sleep disorder; Asthenia, Blood test, Computerised tomogram head normal, Fatigue, Headache; SARS-CoV-2 test negative, Sleep disorder More
Severe debilitating headaches for about 5 weeks, woke at 2:30am and 2:30pm with extreme headaches, e... Severe debilitating headaches for about 5 weeks, woke at 2:30am and 2:30pm with extreme headaches, extreme fatigue (slept 16-18 hours a day) lasting 10 days. Antihistamines. Migraine medication. CT scan to rule out brain bleed. Benadryl, Reglan. Allegra and Ibuprofen. More
2840741 16 F NC 05/13/2025 MNP
MNP
MNP
MNP
MNP
MNP
MNP
MNP
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 LJ0077
LJ0077
LJ0077
LJ0077
LJ0077
LJ0077
LJ0077
LJ0077
Computerised tomogram abnormal, Computerised tomogram pelvis abnormal, Fatigue, ... Computerised tomogram abnormal, Computerised tomogram pelvis abnormal, Fatigue, Hypokalaemia, Hypomagnesaemia; Laboratory test abnormal, Leukocytosis, Oedema, Pain, Pain in extremity; Pyrexia; Arthralgia, Fatigue, Pain, Pyrexia; Computerised tomogram abnormal, Computerised tomogram pelvis abnormal, Fatigue, Hypokalaemia, Hypomagnesaemia; Laboratory test abnormal, Leukocytosis, Oedema, Pain, Pain in extremity; Pyrexia; Arthralgia, Fatigue, Pain, Pyrexia More
Patient had fever and severe body aches/leg pain and fatigue causing her parents to take her to the ... Patient had fever and severe body aches/leg pain and fatigue causing her parents to take her to the ER where she received IV fluids, CT scan and was admitted for observation More
✓
2840742 20 F WA 05/13/2025 HPV9
 MERCK & CO. INC.
Syncope Syncope
Patient fainted a few minutes after getting the vaccine Patient fainted a few minutes after getting the vaccine
2840743 44 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment is the first of a two-series vaccination; the outcome was uneventful, with no symptoms... The treatment is the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840744 62 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840745 16 F ID 05/13/2025 UNK
 UNKNOWN MANUFACTURER
 U7947AA
No adverse event, Wrong product administered No adverse event, Wrong product administered
No adverse event, patient was given incorrect vaccine, Vaxellis, instead of Meningitis. Spoke to Doc... No adverse event, patient was given incorrect vaccine, Vaxellis, instead of Meningitis. Spoke to Doctors about if any risks. Patients parent was contacted and informed. Asked to watch out if patient was having any reaction. Patients parent said no, and they are coming in to get the correct shot More
2840746 87 F NY 05/13/2025 COVID19
 MODERNA
 8080469
Arthralgia, Blindness, Headache, Inflammation, Nausea Arthralgia, Blindness, Headache, Inflammation, Nausea
Headache, joint pain, nausea within 20 hours of administration. Acute loss of vision, inflammation a... Headache, joint pain, nausea within 20 hours of administration. Acute loss of vision, inflammation after 1 day More
2840747 51 M TX 05/13/2025 COVID19
 MODERNA
Hypogeusia, Hyposmia, Palpitations, Tinnitus Hypogeusia, Hyposmia, Palpitations, Tinnitus
Tinnitus severe, diminished smell and taste, heart palpitations Tinnitus severe, diminished smell and taste, heart palpitations
2840748 35 M MA 05/13/2025 COVID19
 PFIZER\BIONTECH
 LR6262
Expired product administered Expired product administered
Expired dose of Covid vaccine administered. Dose expired on 4/30/25, administered on 5/13/25.I viewe... Expired dose of Covid vaccine administered. Dose expired on 4/30/25, administered on 5/13/25.I viewed the vaccine and expiration date and told the employee what I was giving him and that it was not an expired vaccine. I administered a Covid 19 Vaccine Comirnaty Pfizer 2024-2025 formulation to an employee. The employee is a physician, and he is aware of the incident. Lot # LR6262, Expiration 2025/04/30. This information is on clear glass prefilled syringe. I realized that I misread the expiration date, after administration, when the gray plunger was pulled nearly out of the syringe revealing the full date clearly. I misinterpreted the month as 06, not 04. This was obscured by the gray plunger making it difficult to read. More
2840749 83 F 05/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered Extra dose administered
patient received a third shingrix dose 12/12/2024. first 2 doses received in 2022, 2 months apart patient received a third shingrix dose 12/12/2024. first 2 doses received in 2022, 2 months apart
2840750 05/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Malaise Malaise
me too I received the shindrix however u spell it I got sick; This non-serious case was reported by ... me too I received the shindrix however u spell it I got sick; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of sickness 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 sickness (Verbatim: me too I received the shindrix however u spell it I got sick). The outcome of the sickness was not reported. It was unknown if the reporter considered the sickness to be related to Shingrix. It was unknown if the company considered the sickness to be related to Shingrix. Additional Information: GSK Receipt Date: 03-MAY-2025 This case was reported by a patient via interactive digital media. The patient received the Shingrix however spell it he/she got sick. More
2840751 86 M 05/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered Extra dose administered
patient received third shingrix dose in 2024. first 2 doses were in 2022, 2 months apart patient received third shingrix dose in 2024. first 2 doses were in 2022, 2 months apart
2840752 44 M MA 05/13/2025 COVID19
 MODERNA
 066H21A
No adverse event No adverse event
Pt was given 0.25ml twice to make 0.5ml (1 dose). Patient did not call us to report any adverse eve... Pt was given 0.25ml twice to make 0.5ml (1 dose). Patient did not call us to report any adverse events following administration. We only knew about this event after we received the email from DPH on 12/312024. More
2840754 12 M 05/13/2025 MNQ
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8361AA
U7983AA
Cold sweat, Feeling abnormal, Pallor; Cold sweat, Feeling abnormal, Pallor Cold sweat, Feeling abnormal, Pallor; Cold sweat, Feeling abnormal, Pallor
Pt was given Tdap and MCV4, in this order, in Left deltoid, greater than 1" apart. After MCV4 w... Pt was given Tdap and MCV4, in this order, in Left deltoid, greater than 1" apart. After MCV4 was given pt leaned forward and was asked if he felt ok, he voiced "no, I feel funny". Had pt lay down on exam table. Did not feel clammy at this time and his skin tone was still normal appearance. Call bell placed next to pt/father and advised to ring if needing assistance while this nurse went to get a cup of water. Water was given to pt, when entering room father voiced he did feel clammy at that time, and pt was pale skin tone. Ice pack was then placed on back of pt neck, and he was sitting up. Noted to have felt better. Had pt wait in exam room for 15mins post adminstration, consulted a provider in the office, it was agreed upon to not give the HPV9 d/t the rxn from other vaccines. Pt left office stating he felt fine, color was back to his normal and not feeling clammy any longer. More
2840755 37 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840756 39 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840757 23 M ND 05/13/2025 IPV
 SANOFI PASTEUR
 w1c831m
Blood pressure decreased, Heart rate decreased, Nausea, Presyncope Blood pressure decreased, Heart rate decreased, Nausea, Presyncope
Patient vasovagal upon receiving inactivated polio.. Symptoms included decrease in heart rate and bl... Patient vasovagal upon receiving inactivated polio.. Symptoms included decrease in heart rate and blood pressure as well as feeling the need to vomit. Pt was given ice pack to place on back of neck and laid supine to be given ammonia to smell. Vitals were taken and doctor observed and made to wait 15 minutes before rechecking for vitals again. More
2840758 30 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or sign of reaction reported. More
2840759 33 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840760 26 F CA 05/13/2025 COVID19
 PFIZER\BIONTECH
 LM2210
No adverse event No adverse event
Patient had no symptoms Patient had no symptoms
2840761 31 F 05/13/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
Wrong product administered Wrong product administered
My provider asked I could give the patient a vaccine around 10:40 a.m. I grabbed the vaccine from th... My provider asked I could give the patient a vaccine around 10:40 a.m. I grabbed the vaccine from the Hep B box and gave the patient the vaccine. When I realized I inject the patient with the wrong vaccine, I informed her right away and put her back in the room. I told the nurse about what happened, and she immediately told the provider. After the nurse told the provider what happened, she told me it was okay to give the correct vaccine. More
2840762 0.92 F CO 05/13/2025 MMR
 MERCK & CO. INC.
 X026327
Inappropriate schedule of product administration Inappropriate schedule of product administration
Given too soon at incorrect recommendation by medical assistant in triage position Given too soon at incorrect recommendation by medical assistant in triage position
2840763 29 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840764 23 F NY 05/13/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH


Arthralgia, Blood test, Erythema, Gait disturbance, Joint swelling; Musculoskele... Arthralgia, Blood test, Erythema, Gait disturbance, Joint swelling; Musculoskeletal discomfort, Pain in extremity, Peripheral swelling, Ultrasound Doppler, Venogram; X-ray More
Just a couple of days after I got the Pfizer covid booster vaccine, I noticed a lot of swelling and ... Just a couple of days after I got the Pfizer covid booster vaccine, I noticed a lot of swelling and redness in my left ankle. I had no prior injury or anything that stands out that would cause this issue. It has now been over 4 years and the pain in my left ankle is unbearable. It is majorly swollen on most days and I am in pain / discomfort every day. My foot does not fit in shoes normally and it hurts all the time. There is significant swelling around my ankle, foot, and toes. I can barely walk. More
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2840765 60 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840766 38 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00015
No adverse event No adverse event
The treatment was the firs of a two-series vaccination; the outcome was uneventful, with no symptoms... The treatment was the firs of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840767 05/13/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Pain, Pain in extremity Pain, Pain in extremity
arm was really sore; whole body hurts; This non-serious case was reported by a consumer via interact... arm was really sore; whole body hurts; 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 (Shingles vaccine) for prophylaxis. On 02-MAY-2025, the patient received the 1st dose of Shingles vaccine. In MAY-2025, less than a week after receiving Shingles vaccine, the patient experienced pain in arm (Verbatim: arm was really sore) and general body pain (Verbatim: whole body hurts). The outcome of the pain in arm and general body pain were not reported. It was unknown if the reporter considered the pain in arm and general body pain to be related to Shingles vaccine. It was unknown if the company considered the pain in arm and general body pain to be related to Shingles vaccine. Additional Information: GSK receipt date: 03-MAY-2025 This case was reported by a patient via interactive digital media The reporter guessed that everybody reacts differently, the patient got first shot yesterday and arm was really sore and whole body was hurting. More
2840768 22 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840769 16 F TX 05/13/2025 MENB
MENB
MENB
MENB
MNQ
MNQ
MNQ
MNQ
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 LP6524
LP6524
LP6524
LP6524
U8494AA
U8494AA
U8494AA
U8494AA
Abdominal discomfort, Chest discomfort, Dyspnoea, Enterovirus test negative, Fac... Abdominal discomfort, Chest discomfort, Dyspnoea, Enterovirus test negative, Facial discomfort; Frequent bowel movements, Headache, Human rhinovirus test, Influenza A virus test negative, Influenza B virus test negative; Injected limb mobility decreased, Pain in extremity, Pulse abnormal, Respiratory syncytial virus test negative, Retching; Streptococcus test negative; Abdominal discomfort, Chest discomfort, Dyspnoea, Enterovirus test negative, Facial discomfort; Frequent bowel movements, Headache, Human rhinovirus test, Influenza A virus test negative, Influenza B virus test negative; Injected limb mobility decreased, Pain in extremity, Pulse abnormal, Respiratory syncytial virus test negative, Retching; Streptococcus test negative More
Around 50 minutes after getting vaccines stomach started feeling uncomfortable, continued through t... Around 50 minutes after getting vaccines stomach started feeling uncomfortable, continued through the night with feeling of "brick in stomach" increased bowel movements and attempts of emesis with dry heaving, dyspnea with "chest having heavy feeling and gasping for breaths", "Headache with facial pressure" "Felt heart beating in throat". Difficulty moving left arm d/t pain. Feeling felt a little better this morning, then at school had similar feelings of difficulty taking deep breath, dyspnea. More
2840770 29 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840771 30 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the second of a two-series vaccination; the outcome was uneventful, with no sympto... The treatment was the second of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840772 M TX 05/13/2025 DTPPVHBHPB
PNC20
RV5
 MSP VACCINE COMPANY
PFIZER\WYETH
MERCK & CO. INC.
 U7907AA
LN4928
2096656
Erythema, Infant irritability, Swelling; Erythema, Infant irritability, Swelling... Erythema, Infant irritability, Swelling; Erythema, Infant irritability, Swelling; Erythema, Infant irritability, Swelling More
Redness, swelling, fussiness. Provider reccommended cold compresses, mark the area to see if redness... Redness, swelling, fussiness. Provider reccommended cold compresses, mark the area to see if redness or swelling spreads in the next hours, take appropriate dose of Tylenol and rtc if symptoms dont improve or new symptoms arise More
2840773 13 M TX 05/13/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 79s54
Incorrect dose administered Incorrect dose administered
Dr. sent in Engerix B pediatric dose, pharmacy entered adult dose and administered adult dose to ped... Dr. sent in Engerix B pediatric dose, pharmacy entered adult dose and administered adult dose to pediatric pt More
2840774 28 M AZ 05/13/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840775 76 M FL 05/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93KK4
Arthralgia, Back pain, Injected limb mobility decreased, Pain in extremity Arthralgia, Back pain, Injected limb mobility decreased, Pain in extremity
Patient reported having limitation in range of movement in his left arm and shoulder. He said that t... Patient reported having limitation in range of movement in his left arm and shoulder. He said that the pain moves periodically from his arm to shoulder and back but it is mostly in his shoulder. He said the the severity of the pain remains the same as when he started to experience it 30 minutes after the vaccine was administered. He said all these symptoms are still experienced today. More
2840776 05/13/2025 VARZOS
VARZOS
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 UNK
UNK
Feeling abnormal, Incomplete course of vaccination; Feeling abnormal, Incomplete... Feeling abnormal, Incomplete course of vaccination; Feeling abnormal, Incomplete course of vaccination More
That dang 1st shot was awful; never got a second shot of shingles vaccine; This non-serious case was... That dang 1st shot was awful; never got a second shot of shingles vaccine; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of feels awful in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. Co-suspect products included Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient did not receive the 2nd dose of Shingles vaccine and the 1st dose of Shingles vaccine. On an unknown date, not applicable after receiving Shingles vaccine and an unknown time after receiving Shingles vaccine, the patient experienced feels awful (Verbatim: That dang 1st shot was awful) and incomplete course of vaccination (Verbatim: never got a second shot of shingles vaccine). The outcome of the feels awful was not reported and the outcome of the incomplete course of vaccination was not applicable. It was unknown if the reporter considered the feels awful to be related to Shingles vaccine. It was unknown if the company considered the feels awful to be related to Shingles vaccine. Additional Information: GSK receipt date: 03-MAY-2025 This case was reported by a patient via interactive digital media The patient reported that dang 1st shot was awful, and the patient never got a second one which led to incomplete course of vaccination. But the patient also had the original one and he/ she was done. More
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