🏥 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 💀 🏥 🚑 ♿ ⚠️
2856370 62 F CT 09/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 99d52
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Mild, Site: Swelling at Injecti... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: Patient was given Shingrix on 8/4/25. She came back to the pharmacy one week later showing us that her arm is still sore, warm to the touch, and swollen. Based off of where the swollen area was, I can determine that it was in the middle of the deltoid (the intended injection site). I told her to continue to take NSAIDs, ice it and do proper stretches to help it feel better. I advised her to go to her PCP if any effects worsen. I continue to call her every Monday to check up on her. More
2856371 90 F FL 09/01/2025 FLU4
 SANOFI PASTEUR
 u880aa
Injection site bruising, Injection site pain, Injection site swelling Injection site bruising, Injection site pain, Injection site swelling
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Inje... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2856372 50 F TX 09/01/2025 FLU4
FLU4
FLU4
FLU4
FLU4
FLU4
FLU4
FLU4
FLU4
FLU4
FLU4
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 73bn2
73bn2
73bn2
73bn2
73bn2
73bn2
73bn2
73bn2
73bn2
73bn2
73bn2
Abdominal pain, Anaphylactic reaction, Arthralgia, Asthenia, Autoimmune disorder... Abdominal pain, Anaphylactic reaction, Arthralgia, Asthenia, Autoimmune disorder; Bell's palsy, Blood disorder, Cardiac disorder, Cerebrovascular accident, Chest discomfort; Chest pain, Chills, Confusional state, Diarrhoea, Dizziness; Dysphagia, Dyspnoea, Eye swelling, Fatigue, Flushing; Headache, Hyperhidrosis, Hypertension, Hyperventilation, Hypoaesthesia; Hypotension, Injection site bruising, Injection site erythema, Injection site pain, Injection site pruritus; Injection site swelling, Lethargy, Lymphadenopathy, Mouth swelling, Multisystem inflammatory syndrome; Myocardial infarction, Nausea, Nervous system disorder, Pain, Paraesthesia; Pruritus, Pyrexia, Rash, Seizure, Swelling face; Swollen tongue, Syncope, Tachycardia, Throat tightness, Tinnitus; Tremor, Unresponsive to stimuli, Visual impairment, Vomiting More
Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injec... Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Anaphylaxis-Mild, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Abdominal Pain-Mild, Systemic: Autoimmune Disease (diagnosed by MD)-Mild, Systemic: Bell's Palsy-Mild, Systemic: Blood Disorder (diagnosed by MD)-Mild, Systemic: Body Aches Generalized-Mild, Systemic: Cardiac Disorder (diagnosed by MD)-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Chills-Mild, Systemic: Confusion-Mild, Systemic: Diarrhea-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Fever-Mild, Systemic: Pt got allergic reaction-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Mild, Systemic: Heart Attack-Mild, Systemic: Hypertension-Mild, Systemic: Hyperventilation-Mild, Systemic: Hypotension-Mild, Systemic: Joint Pain-Mild, Systemic: Lymph Node Swelling-Mild, Systemic: MIS (Multisystem Inflammatory Syndrome)(diagnosed by MD)-Mild, Systemic: Nausea-Mild, Systemic: Neurological Disorder (diagnosed by MD)-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Seizure-Mild, Systemic: Shakiness-Mild, Systemic: Stroke-Mild, Systemic: Tachycardia-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Systemic: Tinnitus-Mild, Systemic: Unable to Sleep-Mild, Systemic: Visual Changes/Disturbances-Mild, Systemic: Vomiting-Mild, Systemic: Weakness-Mild More
2856373 72 M FL 09/01/2025 FLU4
 SANOFI PASTEUR
 ut8763ga
Injection site pain Injection site pain
Site: Pain at Injection Site-Severe Site: Pain at Injection Site-Severe
2856374 64 F PA 09/01/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 99d52
99d52
Injection site pain, Injection site swelling, Lymphadenopathy, Peripheral swelli... Injection site pain, Injection site swelling, Lymphadenopathy, Peripheral swelling, Rash; Rash erythematous More
Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Systemic: Swollen arm ... Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Systemic: Swollen arm and lymphs. red painful bumps on arm and back near her ribs (right side)-Severe, Additional Details: Patient mentioned they experience an adverse reaction from second dose of shingle vaccine. Mentioned she experienced red bumps on her arm and around her back near her ribs and that they felt painful. She also mentioned her arm was swollen and thay her lymphs also swell up. She said that she is much better now and the adverse event started hours after the vaccine. Symptom lasted approximately a week More
2856375 73 F CA 09/01/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 452R4
Injection site pain Injection site pain
Site: Pain at Injection Site-Mild, Additional Details: The patient has complianed about pain at the ... Site: Pain at Injection Site-Mild, Additional Details: The patient has complianed about pain at the injection site after receiving the Arexvy vaccine, I told her that it was a normal reaction after receiving the shot. I called and talked to her doctor today and the doctor also reassured the patient that it was a normal vigorous reaction and gave her a Toradol injection., Other Vaccines: VaccineTypeBrand: FLUZONE HIGH DOSE; Manufacturer: SANOFI; LotNumber: UT8779KA; Route: IM; BodySite: LEFT ARM; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: BOOSTRIX; Manufacturer: GSK; LotNumber: 37F34; Route: IM; BodySite: LEFT ARM; Dose: ; VaxDate: UNKNOWN More
2856376 68 M CA 09/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93kk4
Abdominal discomfort, Abdominal pain, Asthenia, Feeling hot, Tachycardia Abdominal discomfort, Abdominal pain, Asthenia, Feeling hot, Tachycardia
Systemic: Abdominal Pain-Medium, Systemic: Tachycardia-Severe, Systemic: Weakness-Medium, Additional... Systemic: Abdominal Pain-Medium, Systemic: Tachycardia-Severe, Systemic: Weakness-Medium, Additional Details: Patient had vaccine given at 10:40 am on on 8/26/25. got heart rate go up to 131 bpm aroun 5pm, morning of 8/27/25, heart rate went up to 180 bpm. need to be administered to the hospital. Pt reqort weakness, feel hot, stomach upset, and hight heart rate., Other Vaccines: VaccineTypeBrand: Abrysvo ACT-O-VIAL; Manufacturer: Pfizer; LotNumber: MD5462; Route: IM; BodySite: L; Dose: 1; VaxDate: 08/26/2025, VaccineTypeBrand: Fluzone High-dose 25-26; Manufacturer: Sanofi; LotNumber: UT8763FA; Route: IM; BodySite: L; Dose: 1; VaxDate: 08/26/2025 More
2856377 70 M HI 09/01/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 344J3
Dizziness, Syncope Dizziness, Syncope
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Other Vaccines... Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Other Vaccines: VaccineTypeBrand: Typhim VI; Manufacturer: ; LotNumber: 344J3; Route: IM; BodySite: ; Dose: ; VaxDate: 08/27/2025, VaccineTypeBrand: Tdap; Manufacturer: ; LotNumber: 37R35; Route: IM; BodySite: ; Dose: ; VaxDate: 08/18/2025 More
2856380 28 F MN 09/01/2025 TD
 SANOFI PASTEUR
 U803AA
No adverse event, Product identification number issue No adverse event, Product identification number issue
Systemic: No adverse events-Mild, Additional Details: Barcode from bottle was scanned instead of the... Systemic: No adverse events-Mild, Additional Details: Barcode from bottle was scanned instead of the QR code from box. More
2856381 40 M MN 09/01/2025 IPV
 SANOFI PASTEUR
 y1a201m
No adverse event, Product identification number issue No adverse event, Product identification number issue
Systemic: No adverse effects-Mild, Additional Details: Barcode from bottle was scanned instead of th... Systemic: No adverse effects-Mild, Additional Details: Barcode from bottle was scanned instead of the QR code from box. More
2856382 28 F PA 09/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 97YM7
Injection site pain, Product preparation issue Injection site pain, Product preparation issue
Site: Pain at Injection Site-Mild, Additional Details: VACCINE WAS NOT RECONSTITUTED/ ONLY THE LIQUI... Site: Pain at Injection Site-Mild, Additional Details: VACCINE WAS NOT RECONSTITUTED/ ONLY THE LIQUID WAS GIVEN More
2856383 76 F NJ 09/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 342XP
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection... Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild More
2856384 62 M NY 09/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 97YM7
Injection site pain, Product preparation issue Injection site pain, Product preparation issue
Site: Pain at Injection Site-Mild, Additional Details: VACCINE WAS NOT RECONSTITUTED/ONLY THE LIQUID... Site: Pain at Injection Site-Mild, Additional Details: VACCINE WAS NOT RECONSTITUTED/ONLY THE LIQUID WAS GIVEN More
2856385 20 M IN 09/01/2025 FLUC4
 SEQIRUS, INC.
 407799
Dizziness Dizziness
Systemic: Dizziness / Lightheadness-Mild, Additional Details: After Patient received his influenza v... Systemic: Dizziness / Lightheadness-Mild, Additional Details: After Patient received his influenza vaccine, he felt lightheadeness. He stayed seated for few minutes but we felt it might be better to lie down. He laid down for few more minutes until he felt better. He fully recovered before he left the pharmacy. We called him for follow up to see if there is any changes. He was feeling better and there was no issues. He did add he does get lightheadedness when he gets his blood drawn. No follow up is needed. , Other Vaccines: VaccineTypeBrand: flucelvax; Manufacturer: seqirus; LotNumber: 407799; Route: intramuscular; BodySite: arm; Dose: ; VaxDate: UNKNOWN More
2856386 73 M SC 09/01/2025 FLU4
 SANOFI PASTEUR
 ut8781ba
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injecti... Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Pt wife called to report reaction and get lot and mfgr info for urgent care visit More
2856387 52 F CA 09/01/2025 PNC21
 MERCK & CO. INC.
 z004302
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2856388 26 F NJ 09/01/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 4k5x2
Injection site pain Injection site pain
Site: Pain at Injection Site-Severe Site: Pain at Injection Site-Severe
2856389 61 M NY 09/01/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 ny2at
Incorrect route of product administration, Injection site pain Incorrect route of product administration, Injection site pain
Site: Pain at Injection Site-Mild, Additional Details: Patient was given shingrix on the left forear... Site: Pain at Injection Site-Mild, Additional Details: Patient was given shingrix on the left forearm by nurse as a subcutaneous injection. RPh contacted patient and there are no adverse side effects occuring, patient was appreciative of call. Glaxosmith was contacted on the error and patient does not require another vaccination at this time. Counseled patient on likelihood of increased side effects. Spoke with primary care doctor. More
2856390 52 F MI 09/01/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 2293b
Dizziness, Hypoaesthesia, Injection site swelling, Paraesthesia, Rash Dizziness, Hypoaesthesia, Injection site swelling, Paraesthesia, Rash
Site: Swelling at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Dizz... Site: Swelling at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium More
2856392 60 F NH 09/01/2025 HEPA
 MERCK & CO. INC.
 y009094
Injection site bruising, Injection site pain Injection site bruising, Injection site pain
Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Medium, Additional Details: We... Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Medium, Additional Details: Went to hospital after arm bruised all the way to the wrist. Doctor suspected blood clot, ran tests to rule out blood clot. More
2856393 40 F GA 09/01/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 947932
Arthritis, Injection site pain Arthritis, Injection site pain
Site: Pain at Injection Site-Severe, Site: Shoulder Joint Injury (prolonged pain, tingling, etc.)-Se... Site: Pain at Injection Site-Severe, Site: Shoulder Joint Injury (prolonged pain, tingling, etc.)-Severe, Systemic: Joint Pain-Severe, Additional Details: pain in right arm, shoulder neck. (withheld) rph reported at (withheld store) and forwarded info to (pharmacy and number withheld) where vaccine was given distress/concern, Other Vaccines: VaccineTypeBrand: Gardasil 9; Manufacturer: merck; LotNumber: z007847; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 08/18/2025, VaccineTypeBrand: flucelvax 25-26; Manufacturer: sequirus; LotNumber: 406981; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 08/18/2025, VaccineTypeBrand: moderna 24-25; Manufacturer: moderna; LotNumber: 3046734; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 08/18/2025 More
2856394 55 F FL 09/01/2025 RSV
RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 255t2
255t2
255t2
Chest discomfort, Chest pain, Chills, Dizziness, Fatigue; Injection site bruisin... Chest discomfort, Chest pain, Chills, Dizziness, Fatigue; Injection site bruising, Injection site erythema, Injection site pain, Injection site swelling, Lethargy; Pain, Pyrexia More
Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injec... Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Body Aches Generalized-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Other Vaccines: VaccineTypeBrand: Flucelvax; Manufacturer: seqirus; LotNumber: 407000; Route: injection; BodySite: right arm; Dose: 1; VaxDate: 08/01/2025 More
2856395 29 F CA 09/01/2025 FLUC4
 SEQIRUS, INC.
 406982
Injection site pruritus, Nausea, Pruritus, Wrong product administered Injection site pruritus, Nausea, Pruritus, Wrong product administered
Site: Itching at Injection Site-Mild, Systemic: Allergic: Itch Generalized-Mild, Systemic: Nausea-Mi... Site: Itching at Injection Site-Mild, Systemic: Allergic: Itch Generalized-Mild, Systemic: Nausea-Mild, Additional Details: patient was accidentally given flucelvax vaccine and was not aware she was receiving this vaccine. She thought she was getting the second dose of her varivax vaccine. It seems like there was a miscommunication and pharmacy personnel thought she said yes when asked if she wanted to get her flu shot. Pt was upset that she paid out of pocket for it $63.76 and is looking to get reimbursed which pharmacy will do. She left the pharmacy ok when apologized and told her we can reimburse her. , Other Vaccines: VaccineTypeBrand: varivax; Manufacturer: merck; LotNumber: z003883; Route: subcutaneous; BodySite: right upper arm; Dose: 1; VaxDate: 07/30/2025, VaccineTypeBrand: boostrix tdap; Manufacturer: gsk; LotNumber: 37R35; Route: intramuscular; BodySite: right deltoid; Dose: 1; VaxDate: 07/30/2025 More
2856396 5 F VA 09/01/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 a2b72
No adverse event, Product preparation issue No adverse event, Product preparation issue
Systemic: No adverse event. Vaccine was administered prior to being reconsititued, so patient only r... Systemic: No adverse event. Vaccine was administered prior to being reconsititued, so patient only received the diluent.-Mild, Additional Details: The patient received just the diluent as the vaccine was not reconstituted prior to administration., Other Vaccines: VaccineTypeBrand: Vaqta 25 units/0.5 ml Ped; Manufacturer: Merck; LotNumber: y014446; Route: IM; BodySite: Right deltoid; Dose: ; VaxDate: 08/20/2025 More
2856397 61 F IL 09/01/2025 PNC21
PNC21
PNC21
PNC21
PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 Z006076
Z006076
Z006076
z006076
z006076
z006076
Injection site erythema, Injection site pain, Injection site swelling; Celluliti... Injection site erythema, Injection site pain, Injection site swelling; Cellulitis, Chills, Injection site erythema, Injection site pain, Injection site swelling; Tremor; Injection site erythema, Injection site pain, Injection site swelling; Cellulitis, Chills, Injection site erythema, Injection site pain, Injection site swelling; Tremor More
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Was brought to (withheld name) attention on 8/28. Patient went into store (number withheld) and wanted to talk to pharmacy manager (name withheld) but she is on vacation this week. Went up front to talk to store manager who then called me and explained her symptoms and concern. I called patient back this morning and left a voicemail. More
2856398 75 F CT 09/01/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 h4k3s
Dizziness, Head injury, Loss of consciousness, Syncope Dizziness, Head injury, Loss of consciousness, Syncope
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Additional Det... Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Additional Details: patient recevied vaccine and experienced a syncopal event/passing out event in which she hit her head. the event happened inside of the pharmacy location where the vaccine was administered More
2856399 68 M NV 09/01/2025 PNC20
PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 LX2498
LX2498
LX2498
Asthenia, Chills, Flushing, Hyperhidrosis, Injection site bruising; Injection si... Asthenia, Chills, Flushing, Hyperhidrosis, Injection site bruising; Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling, Pain; Pyrexia More
Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injec... Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Fever-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Weakness-Severe, Additional Details: pt called us complaining about these side effects day after he got the vaccine , Other Vaccines: VaccineTypeBrand: FLUZONE HIGH DOSE; Manufacturer: SANOFI-PASTEUR; LotNumber: UT8763FA; Route: IM; BodySite: LEFT ARM; Dose: ; VaxDate: 08/28/2025 More
2856400 21 F NY 09/01/2025 HEP
HEP
 DYNAVAX TECHNOLOGIES CORPORATION
DYNAVAX TECHNOLOGIES CORPORATION
 946060
946060
Brain fog, Flushing, Hyperhidrosis, Lip discolouration, Loss of consciousness; S... Brain fog, Flushing, Hyperhidrosis, Lip discolouration, Loss of consciousness; Syncope, Unresponsive to stimuli More
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: p... Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: patient passed out for 10 seconds in chair-- was responsive and broke out in sweat with haziness, and discoloration of lips-- ems called checked patient over with vitals, blood sugars, etc. More
2856401 81 M NC 09/01/2025 FLU4
FLU4
 SANOFI PASTEUR
SANOFI PASTEUR
 ut8794ba
ut8794ba
Abdominal pain, Chills, Flushing, Headache, Hyperhidrosis; Nausea, Pain, Pyrexia Abdominal pain, Chills, Flushing, Headache, Hyperhidrosis; Nausea, Pain, Pyrexia
Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, S... Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Fever-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Nausea-Medium, Additional Details: intake form not filled out at pharmacy More
2856402 49 F NV 09/01/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 h4k3s
Injection site pain, Injection site swelling Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Po... Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Possible Arthus reaction. Swelling and pain in arm that presented about a week after receiving boostrix injection in right deltoid. , Other Vaccines: VaccineTypeBrand: ipol; Manufacturer: ; LotNumber: ; Route: ; BodySite: ; Dose: ; VaxDate: UNKNOWN More
2856403 29 F VA 09/01/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 4T93R
Dizziness, Syncope, Unresponsive to stimuli Dizziness, Syncope, Unresponsive to stimuli
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Severe, Additional Det... Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient fainted a few minutes after immunization. After waking up, she reported remaining feeling dizzy/lightheaded. More
2856404 49 F CA 09/01/2025 FLU4
 GLAXOSMITHKLINE BIOLOGICALS
 2ng23
Headache, Pain Headache, Pain
Systemic: Headache-Medium, Additional Details: pt stated radiating pain going down left arm followin... Systemic: Headache-Medium, Additional Details: pt stated radiating pain going down left arm following injection. severe headache followed. pt rested in pharmacy for about 20 minutes and then picked up her prescriptions and left. I offered visist to urgent care (2 doos down) but she said they do not take her insurance. More
2856405 57 F TX 09/01/2025 PNC21
 MERCK & CO. INC.
 z006889
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2856406 60 F PA 09/01/2025 FLUC4
 SEQIRUS, INC.
 406982
Injection site pruritus, Injection site swelling Injection site pruritus, Injection site swelling
Site: Itching at Injection Site-Mild, Site: Swelling at Injection Site-Mild Site: Itching at Injection Site-Mild, Site: Swelling at Injection Site-Mild
2856407 80 F CA 09/01/2025 RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 B5NJ9
B5NJ9
Arthralgia, Injected limb mobility decreased, Injection site pain, Injection sit... Arthralgia, Injected limb mobility decreased, Injection site pain, Injection site swelling, Pain; Pain in extremity More
Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Body Aches G... Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Joint Pain-Severe, Additional Details: PT C/O OF SWOLLEN, STABBING PAIN IN THE RIGHT ARM. CANNOT LIFT ARM. iNSTRUCTED PT TO TAKE APAP AND COLD PACK. IF PAIN PERSISTS, GO TO URGENT CARE OR SEE PRIMARY DOCTOR. PT IS SATISIFED. WILL SEE DOCTOR, Other Vaccines: VaccineTypeBrand: CAPVAXIVE; Manufacturer: MERCK; LotNumber: Z006889; Route: IM; BodySite: ARM; Dose: 1; VaxDate: UNKNOWN, VaccineTypeBrand: SHINGRIX; Manufacturer: GLAXOSMITHKLINE; LotNumber: 5Y9CA; Route: IM; BodySite: ARM; Dose: 1; VaxDate: UNKNOWN More
2856408 68 F CA 09/01/2025 PNC20
 PFIZER\WYETH
 LP4948
Decreased appetite, Injection site bruising, Injection site erythema, Injection ... Decreased appetite, Injection site bruising, Injection site erythema, Injection site pain, Injection site swelling More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injec... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: NO APPETITE-Medium, Additional Details: Shot was given on 8/25/25, patient came back on 8/29 and her left arm appeared to be red, swollen, warm to touch, and pt said she has no appetite for the last few days. Counseled pt to take an over the counter tylenol and benadryl and also cold pack to ease the pain. , Other Vaccines: VaccineTypeBrand: FLUZONE HD 2025-2026; Manufacturer: SANOFI; LotNumber: U8764CB; Route: IM; BodySite: LEFT ARM; Dose: 1; VaxDate: 08/25/2025 More
2856409 44 F TX 09/01/2025 COVID19
 PFIZER\BIONTECH
 ME6072
Injection site erythema, Injection site pain, Injection site swelling, Paraesthe... Injection site erythema, Injection site pain, Injection site swelling, Paraesthesia More
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: tingling in left arm, Other Vaccines: VaccineTypeBrand: fluarix 2025-2026-flu; Manufacturer: glaxosmithkline; LotNumber: 2NG23; Route: im; BodySite: left deltoid; Dose: 1; VaxDate: 08/24/2025, VaccineTypeBrand: capvaxive-pneumonia; Manufacturer: merck sharp & d; LotNumber: Z004302; Route: im; BodySite: right deltoid; Dose: 1; VaxDate: 08/24/2025, VaccineTypeBrand: boostrxi-TDAP; Manufacturer: glaxosmithkline; LotNumber: GH4279; Route: im; BodySite: right deltoid; Dose: 1; VaxDate: 08/24/2025 More
2856410 60 M TX 09/01/2025 FLU4
 SANOFI PASTEUR
 u8764cb
Injection site pruritus, Product administered to patient of inappropriate age Injection site pruritus, Product administered to patient of inappropriate age
Site: Itching at Injection Site-Mild, Additional Details: no adverse reaction has been reported. the... Site: Itching at Injection Site-Mild, Additional Details: no adverse reaction has been reported. the fluzone 65+ is given to a patient who was 60 years old More
2856411 63 F CA 09/01/2025 PNC20
 PFIZER\WYETH
 ma2523
Injection site erythema, Injection site induration, Injection site swelling, Ras... Injection site erythema, Injection site induration, Injection site swelling, Rash More
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic:... Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Additional Details: pt claims redness around injection site and induration. went to urgent care, and given antibiotics but she never took them and by 8/29 when she came into pharmacy, arm looks free of rash or rednees, complete resolution More
2856412 12 M FL 09/01/2025 FLUC4
FLUC4
 SEQIRUS, INC.
SEQIRUS, INC.
 406982
406982
Injected limb mobility decreased, Injection site bruising, Injection site pain, ... Injected limb mobility decreased, Injection site bruising, Injection site pain, Injection site swelling, Paraesthesia; Shoulder injury related to vaccine administration More
Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Swelling at Inje... Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Site: Shoulder Joint Injury (prolonged pain, tingling, etc.)-Severe, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: The patient is 12 years old and who came into pharmacy tonight with his mother. He received the vaccine on August 26,2025 which is Tuesday of this week. The 12 year old patient is experiencing SIRVA shoulder injury related to vaccine adiminstration. He cannot lift his left arm barely at all, his movement is restricted and limited, he is experiencing pain at the injection site, there is some mild to moderate swelling present. Pain and restricted movement left arm. More
2856413 48 F NC 09/01/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 Y013009
Y013009
Alanine aminotransferase increased, Chest X-ray, Chest X-ray normal, Metabolic f... Alanine aminotransferase increased, Chest X-ray, Chest X-ray normal, Metabolic function test normal, Neutrophil count increased; Pain, Troponin normal, Ventilation/perfusion scan normal, White blood cell count increased More
Severe pain all over her body started day of vaccine, required trip to ER the following day and trea... Severe pain all over her body started day of vaccine, required trip to ER the following day and treatment with a liter of normal saline, Benadryl, fentanyl, Toradol, Solu-Medrol, Compazine, and a liter of lactated Ringer's. Her symptoms did completely resolve More
2856181 80 M CA 08/31/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Pain in extremity, Rash Pain in extremity, Rash
Rash on chest, armpits and back. Upper arms painful Rash on chest, armpits and back. Upper arms painful
2856182 75 F CA 08/31/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 U8764DB
U8764DB
Decreased appetite, Dizziness, Heart rate increased, Nausea, Oral pain; Orophary... Decreased appetite, Dizziness, Heart rate increased, Nausea, Oral pain; Oropharyngeal pain, Swollen tongue More
Patient reported the following symptoms the day after vaccination: rapid heart rate, mouth pain, swo... Patient reported the following symptoms the day after vaccination: rapid heart rate, mouth pain, swollen tongue, sore throat, loss of appetite, dizziness and nausea. She reported her symptoms have improved significantly by day 8/30/25 and expects to be fully recovered by 9/1/2025 More
2856183 2 M WV 08/31/2025 DTAPHEPBIP
 GLAXOSMITHKLINE BIOLOGICALS
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Severe Left leg swelling with redness. Sent to emergency room that evening for IM steroids and antib... Severe Left leg swelling with redness. Sent to emergency room that evening for IM steroids and antibiotic. More
2856184 78 M VA 08/31/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 MD4414
MD4414
MD4414
MD4414
Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain ... Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain fog; Confusional state, Disorientation, Electrocardiogram, Electroencephalogram, Loss of consciousness; Magnetic resonance imaging, Muscle spasms, Neurological symptom, Oxygen saturation decreased, Seizure; Tachycardia, X-ray More
I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, corresponding to a d... I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, corresponding to a different vaccination date that led to a serious harmful event. Between February 3, 2021, and April 14, 2025, I received a total of nine COVID-19 vaccine injections, including boosters. Four of these injections resulted in adverse events requiring emergency transport to a hospital�each incident involved a different hospital, where I received emergency care. Three of these hospital admissions required an overnight stay. Each of the four harmful events presented with similar symptoms: unexpected loss of consciousness, seizure or stroke-like symptoms, elevated lactic acid levels, low oxygen saturation, muscle spasms, confusion, disorientation, brain fog, slight combativeness, and tachycardia. At every hospital, a comprehensive range of medical tests was performed, including extensive blood work, electrocardiograms (EKG), electroencephalograms (EEG), MRIs, CT angiograms of the neck, and various X-rays. Despite these efforts, no conclusive medical explanation was found for the adverse effects that prompted emergency care. None of the tests confirmed seizures or strokes. I have consulted at least four neurologists, both during my hospital stays and in follow-up clinical appointments. To date, there remains no definitive medical reason for these four harmful events. Given ongoing concerns, I have scheduled an appointment with a new neurologist on October 8, 2025. I believe these four adverse events were caused by the COVID-19 vaccine injections or associated booster shots, as I had never experienced such events prior to vaccination. The timing of each harmful event relative to vaccine administration supports this suspicion: o First vaccine on February 3, 2021, second vaccine on February 24, 2021, then first harmful event six months later on August 27, 2021 o Fourth vaccine on April 5, 2022, then second harmful event eleven days later on April 16, 2022 o Ninth vaccine on April 14, 2025, then third harmful event nineteen days later on May 3, 2025 o Fourth harmful event ninety days after the previous event, on August 7, 2025 If further information or assistance is needed, please feel free to contact me. More
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2856185 78 M VA 08/31/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 MD3414
MD3414
MD3414
MD3414
Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain ... Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain fog; Confusional state, Disorientation, Electrocardiogram, Electroencephalogram, Loss of consciousness; Magnetic resonance imaging, Muscle spasms, Neurological symptom, Oxygen saturation decreased, Seizure; Tachycardia, X-ray More
I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, each corresponding t... I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, each corresponding to different vaccination dates that led to a serious harmful event. Between February 3, 2021, and April 14, 2025, I received a total of nine COVID-19 vaccine injections, including boosters. Four of these injections resulted in adverse events requiring emergency transport to a hospital�each incident involved a different hospital, where I received emergency care. Three of these hospital admissions required an overnight stay. Each of the four harmful events presented with similar symptoms: unexpected loss of consciousness, seizure or stroke-like symptoms, elevated lactic acid levels, low oxygen saturation, muscle spasm confusion, disorientation, brain fog, slight combativeness, and tachycardia. At every hospital, a comprehensive range of medical tests was performed, including extensive blood work, electrocardiograms (EKG), electroencephalograms (EEG), MRIs, CT angiograms of the neck, and various X-rays. Despite these efforts, no conclusive medical explanation was found for the adverse effects that prompted emergency care. None of the tests confirmed seizures or strokes. I have consulted at least four neurologists, both during my hospital stays and in follow-up clinical appointments. To date, there remains no definitive medical reason for these four harmful events. Given ongoing concerns, I have scheduled an appointment with a new neurologist on October 8, 2025. I believe these four adverse events were caused by the COVID-19 vaccine injections or associated booster shots, as I had never experienced such events prior to vaccination. The timing of each harmful event relative to vaccine administration supports this suspicion: o First vaccine on February 3, 2021, second vaccine on February 24, 2021, then first harmful event six months later on August 27, 2021 o Fourth vaccine on April 5, 2022, then second harmful event eleven days later on April 16, 2022 o Ninth vaccine on April 14, 2025, then third harmful event nineteen days later on May 3, 2025 o Fourth harmful event ninety days after the previous event, on August 7, 2025 If further information or assistance is needed, please feel free to contact me. More
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2856187 75 M VA 08/31/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 FM0698
FM0698
FM0698
FM0698
Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain ... Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain fog; Confusional state, Disorientation, Electrocardiogram, Electroencephalogram, Loss of consciousness; Magnetic resonance imaging, Muscle spasms, Neurological symptom, Oxygen saturation decreased, Seizure; Tachycardia, X-ray More
I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, each corresponding t... I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, each corresponding to a different vaccination date that led to a serious harmful event. Between February 3, 2021, and April 14, 2025, I received a total of nine COVID-19 vaccine injections, including boosters. Four of these injections resulted in adverse events requiring emergency transport to a hospital�each incident involved a different hospital, where I received emergency care. Three of these hospital admissions required an overnight stay. Each of the four harmful events presented with similar symptoms: unexpected loss of consciousness, seizure or stroke-like symptoms, elevated lactic acid levels, low oxygen saturation, muscle spasms, confusion, disorientation, brain fog, slight combativeness, and tachycardia. At every hospital, a comprehensive range of medical tests was performed, including extensive blood work, electrocardiograms (EKG), electroencephalograms (EEG), MRIs, CT angiograms of the neck, and various X-rays. Despite these efforts, no conclusive medical explanation was found for the adverse effects that prompted emergency care. None of the tests confirmed seizures or strokes. I have consulted at least four neurologists, both during my hospital stays and in follow-up clinical appointments. To date, there remains no definitive medical reason for these four harmful events. Given ongoing concerns, I have scheduled an appointment with a new neurologist on October 8, 2025. I believe these four adverse events were caused by the COVID-19 vaccine injections or associated booster shots, as I had never experienced such events prior to vaccination. The timing of each harmful event relative to vaccine administration supports this suspicion: o First vaccine on February 3, 2021, second vaccine on February 24, 2021, then first harmful event six months later on August 27, 2021 o Fourth vaccine on April 5, 2022, then second harmful event eleven days later on April 16, 2022 o Ninth vaccine on April 14, 2025, then third harmful event nineteen days later on May 3, 2025 o Fourth harmful event ninety days after the previous event, on August 7, 2025 If further information or assistance is needed, please feel free to contact me. More
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2856188 73 M VA 08/31/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EL9261
EL9261
EL9261
EL9261
Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain ... Aggression, Arteriogram carotid, Blood lactic acid increased, Blood test, Brain fog; Confusional state, Disorientation, Electrocardiogram, Electroencephalogram, Loss of consciousness; Magnetic resonance imaging, Muscle spasms, Neurological symptom, Oxygen saturation decreased, Seizure; Tachycardia, X-ray More
I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, each corresponding t... I am a 78-year-old male submitting four separate Vaccine Adverse Event Reports, each corresponding to a different vaccination date that led to a serious harmful event. Between February 3, 2021, and April 14, 2025, I received a total of nine COVID-19 vaccine injections, including boosters. Four of these injections resulted in adverse events requiring emergency transport to a hospital�each incident involved a different hospital, where I received emergency care. Three of these hospital admissions required an overnight stay. Each of the four harmful events presented similar symptoms: unexpected loss of consciousness, seizure or stroke-like symptoms, elevated lactic acid levels, low oxygen saturation, muscle spasms, confusion, disorientation, brain fog, slight combativeness, and tachycardia. At every hospital, a comprehensive range of medical tests was performed, including extensive blood work, electrocardiograms (EKG), electroencephalograms (EEG), MRIs, CT angiograms of the neck, and various X-rays. Despite these efforts, no conclusive medical explanation was found for the adverse effects that prompted emergency care. None of the tests confirmed seizures or strokes. I have consulted at least four neurologists, both during my hospital stays and in follow-up clinical appointments. To date, there remains no definitive medical reason for these four harmful events. Given ongoing concerns, I have scheduled an appointment with a new neurologist on October 8, 2025. I believe these four adverse events were caused by the COVID-19 vaccine injections or associated booster shots, as I had never experienced such events prior to vaccination. The timing of each harmful event relative to vaccine administration supports this suspicion: o First vaccine on February 3, 2021, second vaccine on February 24, 2021, then first harmful event six months later on August 27, 2021 o Fourth vaccine on April 5, 2022, then second harmful event eleven days later on April 16, 2022 o Ninth vaccine on April 14, 2025, then third harmful event nineteen days later on May 3, 2025 o Fourth harmful event ninety days after the previous event, on August 7, 2025 If further information or assistance is needed, please feel free to contact me. More
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2856189 70 M CO 08/31/2025 FLU3
VARZOS
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS

Balance disorder, Dysstasia, Fall, Fatigue, Gait disturbance; Balance disorder, ... Balance disorder, Dysstasia, Fall, Fatigue, Gait disturbance; Balance disorder, Dysstasia, Fall, Fatigue, Gait disturbance More
I received the dose around noon on Saturday, Aug 30. Around 3PM I experienced extreme tiredness. T... I received the dose around noon on Saturday, Aug 30. Around 3PM I experienced extreme tiredness. Then, around 4:30PM i found myself unable to balance, fell down, extreme difficulty standing up and walking. This persisted and became worse. I found it difficult to control my body, stand or move. Around 6PM I put myself to bed. I slept for nearly 12 hours. When I woke up this morning I no longer had the vertigo. More
2856190 52 F 08/31/2025 FLU3
 SEQIRUS, INC.
 406984
Pollakiuria, Urinary incontinence Pollakiuria, Urinary incontinence
Pt called pharmacy on 8/31 to report side effect that she thought may have been related to the flu s... Pt called pharmacy on 8/31 to report side effect that she thought may have been related to the flu shot she was given on 8/28. She claims she has increased urinary leakage and frequency of urination. She says there are no new meds during this time. She is waiting on her md's response to this matter as well. More
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