🏥 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 💀 🏥 🚑 ♿ ⚠️
2847308 PA 06/26/2025 HEPA
 MERCK & CO. INC.
 X025342
Expired product administered, No adverse event Expired product administered, No adverse event
No additional AE.; HCP calling to report patient inadvertently received expired dose of VAQTA; This ... No additional AE.; HCP calling to report patient inadvertently received expired dose of VAQTA; This spontaneous report was received from a health care professional and refers to a patient of unknown age and gender. The patient's pertinent medical history, drug allergies or reactions, and concomitant medications were unknown by the reporter. On 24-JUN-2025, the patient was vaccinated with an expired dose of Hepatitis A Vaccine, Inactivated Suspension for injection, as a dose of 0.5 ml (route of administration, vaccination scheme frequency, and anatomical location were not provided; valid lot number X025342, with an expiration date of 12-MAY-2025) administered for prophylaxis (Expired product administered). No additional adverse event was reported. More
2847312 21 F VA 06/26/2025 COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
 Unknown
Unknown
Unknown
Cardiac flutter, Cardiac monitoring abnormal, Carditis, Chest pain, Confusional ... Cardiac flutter, Cardiac monitoring abnormal, Carditis, Chest pain, Confusional state; Dizziness, Dyspnoea, Fatigue, Laboratory test normal, Supraventricular tachycardia; Tachycardia More
Exhaustion, feeling like I was going to collapse, chest pain, feeling faint, confusion, fluttering i... Exhaustion, feeling like I was going to collapse, chest pain, feeling faint, confusion, fluttering in chest, shortness of breath More
✓
2847322 37 F MI 06/26/2025 HPV9
 MERCK & CO. INC.
 Y012865
No adverse event, Product storage error No adverse event, Product storage error
Confirmed no symptomatic adverse events reported; Caller states that a vaccine was activated by att... Confirmed no symptomatic adverse events reported; Caller states that a vaccine was activated by attaching a syringe on 6-JUN-2025 but ended up not being used and was immediately placed back in the fridge. The dose was then administered to a patient on 9-JUN-2025.; This spontaneous report was received from a medical assistant on 13-Jun-2025, referring to a 37-year-old female patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 09-Jun-2025, the patient was vaccinated with human papillomavirus 9-valent vaccine, recombinant (GARDASIL 9), lot #Y012865, expiration date: 10-Oct-2026, 0.5 mL / once, for prophylaxis (dose form, route of administration and anatomical site were not provided). The reporter stated that a vaccine was activated by attaching a syringe on 6-JUN-2025 but ended up not being used and was immediately placed back in the fridge. The dose was then administered to the patient on 09-JUN-2025 (Product storage error). No symptomatic adverse events reported. More
2847323 60 F NJ 06/26/2025 PNC21
 MERCK & CO. INC.
Back pain, Breast pain, Vertigo Back pain, Breast pain, Vertigo
She also reported having mild vertigo starting 6/21/2025.; started experiencing moderate breast and ... She also reported having mild vertigo starting 6/21/2025.; started experiencing moderate breast and back pain on 6/15/2025 on the same side that she received the vaccine.; started experiencing moderate breast and back pain on 6/15/2025 on the same side that she received the vaccine.; This spontaneous report was received from physician and refers to a 60-year-old female patient. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 13-Jun-2025, the patient was vaccinated with Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE) administered by intramuscular route for immunization (dose, lot #, expiration date and anatomical site of injection were not reported). On 15-Jun-2025, the patient experienced moderate breast and back pain on the same side where the vaccine was administered. On 21-Jun-2025, she experienced mild vertigo. At the reporting time, the patient was recovering from the events of breast pain, back pain and vertigo. The patient was treated with Celebrex. The causal relationship between the events and Pneumococcal 21-valent Conjugate Vaccine was not provided. No additional information was provided. More
2847324 06/26/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
Suspected vaccination failure; I've got the vaccine and still got Shingles; This serious case w... Suspected vaccination failure; I've got the vaccine and still got Shingles; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a 70-year-old patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, 3 weeks after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: I've got the vaccine and still got Shingles). The outcome of the vaccination failure was not reported and the outcome of the shingles was not resolved. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine. The company considered the vaccination failure to be unrelated to Shingles vaccine. It was unknown if the company considered the shingles to be related to Shingles vaccine. Additional Information: GSK receipt date: 19-JUN-2025 This case was reported by a patient via interactive digital media. Patient got the vaccine and still got Shingles. Patient was 70 years old and this was so painful. This Sunday was going to be 3 weeks. This case was considered as suspected vaccination failure as details regarding completion of primary vaccination schedule, time to onset for shingles and laboratory confirmation regarding shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK Shingles vaccine. More
2847325 64 F MI 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Herpes zoster, Pain Herpes zoster, Pain
I had a very severe case of Shingles requiring 5 days of hospitalization and treatment over many mon... I had a very severe case of Shingles requiring 5 days of hospitalization and treatment over many months affecting left back, buttock, and left lower front of torso with severe pain requiring Morphine and Oxycodone this first case was in 2016 post cancer tx to for NHL. I had the Shingrix Vaccine both doses in 2017. Since the vaccine I?ve had 2 Breakthrough reoccurrences of Shingles after having the Shingrix vaccine. First breakthrough shingles case was in 2021, moderate on my right shoulder, treated with valacyclovir 1 gram 3x day for. Week. Second shingles case was on 6/22/25 affected area was left hip annd buttock and crease where thigh meets torso. Treatment is the same and ongoing. Pain has been moderate with both cases. More
2847326 4 F 06/26/2025 VARCEL
 MERCK & CO. INC.
Rash pruritic, Rash vesicular, Scab Rash pruritic, Rash vesicular, Scab
Vesicular, pruritic rash 2 wks following varicella vaccination. Lesions have since crusted over. Vesicular, pruritic rash 2 wks following varicella vaccination. Lesions have since crusted over.
2847328 27 F VA 06/26/2025 COVID19
COVID19
HPV9
HPV9
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
MERCK & CO. INC.
MERCK & CO. INC.



Angioedema, Corneal cyst, Impaired work ability, Peripheral swelling, Pruritus; ... Angioedema, Corneal cyst, Impaired work ability, Peripheral swelling, Pruritus; Swelling, Urticaria; Angioedema, Corneal cyst, Impaired work ability, Peripheral swelling, Pruritus; Swelling, Urticaria More
After stopping zyrtec abruptly in summer of 2020, I developed intense itching as well as idopathic h... After stopping zyrtec abruptly in summer of 2020, I developed intense itching as well as idopathic hives and angioedema. This caused me to restart the medication with each episode. The itching occurred every day that I did not take zyrtec. The hive and angioedema occurred weekly to biweekly unless taking 10 mg of zyrtec twice daily along with pepcid. I had to see an allergist later that year. Allergy testing was negative for any allergens for my symptoms. I also had several vaccinations prior to the start of the hives, including covid initial vaccine and booster, and the first two vaccines for gardasil. I did not have any know infections with Covid-19 that year or any other noteworthy illness. The swelling and itching impacted my ability to perform my job as a surgical physician assistant due to episodic swelling of my hands. I continue to have episodes of itching, hives and angioedema if I do not take zyrtec daily. While taking zyrtec twice daily to treat my hives, I developed a corneal inclusion cyst in my right eye. I eventually started treatment for the hives with xolair which improved the symptoms. I became pregnant in 2024 and stopped the xolair. During my pregnancy I tried to stop zyrtec again, with recurrence of my symptoms (itching, hives, angioedema). I ultimately had to restart zyrtec during my pregnancy and continue it daily to prevent my symptoms. The only time I have been able to stop zyrtec without significant symptoms is while on xolair. More
2847329 42 F 06/26/2025 HEP
HEP
HEP
PNC21
PNC21
PNC21
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.





Arthralgia, Computerised tomogram normal, Fatigue, Joint swelling, Lethargy; Lym... Arthralgia, Computerised tomogram normal, Fatigue, Joint swelling, Lethargy; Lymphadenopathy, Mobility decreased, Neck pain, Odynophagia, Oropharyngeal pain; Pain, Swelling; Arthralgia, Computerised tomogram normal, Fatigue, Joint swelling, Lethargy; Lymphadenopathy, Mobility decreased, Neck pain, Odynophagia, Oropharyngeal pain; Pain, Swelling More
I received the capvaxive pneumonia vaccine on Monday 6/16 at about 11am. Tuesday 6/17 felt fatigued,... I received the capvaxive pneumonia vaccine on Monday 6/16 at about 11am. Tuesday 6/17 felt fatigued, at 10:30PM my supraclavicular lymph node was the size of a large grape and visible. Messaged the Dr saw Dr 9:30 6/18 and said yes it's probably from the vaccine and should go away, call if symptoms worsen. Injection was in text book location and no signs of infection. 6/19 woke up with my entire Right shoulder and neck in pain and swelling. Messaged Dr office. As the day went on my throat started to hurt and swallowing became painful. Called Dr office and they advised urgent care. I went to Urgent care and they were concerned about how enlarged my lymph's were and my throat being sore so they sent me to the emergency room. ER did blood work and CT found no underlying reason for the enlarged lymph nodes. Sent me home and said call us if you are struggling to breathe. 6/10 throat still hurts, very lethargic, lymph nodes still enlarged to the point it hurts to move my neck and I can not raise my hand above my clavical. Injection was given with Hep B in right deltoid. More
2847330 SC 06/26/2025 RAB
 NOVARTIS VACCINES AND DIAGNOSTICS
 FDP00527
Product contamination physical Product contamination physical
patient needed a Rabavert injection in the ER. Med was sent to the ER and when the nurse opened the ... patient needed a Rabavert injection in the ER. Med was sent to the ER and when the nurse opened the package, she noticed that there was a partical in the syringe. The drug and original package was sent back to pharmacy to inspect. Upon inspection, there was a piece of rubber in the syringe. More
2847331 17 M VA 06/26/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
Ear discomfort, Hyperacusis Ear discomfort, Hyperacusis
Had meningitis B vaccine on 5/22/25. Experiencing some related side effects including heightened hea... Had meningitis B vaccine on 5/22/25. Experiencing some related side effects including heightened hearing , ears clogging, right ears sensitive . More
2847332 51 F 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Axillary pain, Pain in extremity Axillary pain, Pain in extremity
Shingrix vaccine dose 1 received on Monday June 9th 2025 shot received on left arm Patient age 51. F... Shingrix vaccine dose 1 received on Monday June 9th 2025 shot received on left arm Patient age 51. Female. BMI 23.5 By Wednesday pain in arm moved to pain in left airmmpit. Pain in left arm Pit continues. More
2847333 48 F CO 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Heavy menstrual bleeding Heavy menstrual bleeding
48 yo woman on birth control. Immune compromised with persistent hypogammaglobulinemia following Rit... 48 yo woman on birth control. Immune compromised with persistent hypogammaglobulinemia following Rituxan exposure allowed me to get shingles vaxx. Received my second Shingrix vaccine on 5/17/25. 3 days later experienced unexpected off-cycle abrupt loss of uterine lining over course of 6 hours (heaviest chunkiest period of my life). Continued "normal" period-type bleeding for 1 week. Have had intermittent bleeding for 4 total weeks to date. My birth control is continuous monophasic, so I normally don't have a period at all. I did have some mild spotting after initial COVID vaccine boosters. I know Shingrix only recently cleared for those under 55, figure its impact on menstruation may not be well studied and my data point may help. More
2847334 69 M 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Gastrointestinal pain, Headache Gastrointestinal pain, Headache
Pharmacy administered Shingrix vaccine first dose May 27. I am 69 year old male in good health, no d... Pharmacy administered Shingrix vaccine first dose May 27. I am 69 year old male in good health, no diseases or treated conditions. No maintenance drugs. I am 10 days since shot and still gastrointestinal ache (3) level and daily light headache. More
✓
2847379 1 M OH 06/26/2025 VARCEL
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
 X011424
X011424
Body temperature increased, Rash papular, Scab, Skin lesion, Varicella virus tes... Body temperature increased, Rash papular, Scab, Skin lesion, Varicella virus test negative; Varicella zoster virus infection More
immunocompromised patient developed VZV after being vaccinated with VARIVAX/type of AE: rash papulov... immunocompromised patient developed VZV after being vaccinated with VARIVAX/type of AE: rash papulovesiculat/Herpes zoster; immunocompromised patient developed VZV after being vaccinated with VARIVAX.; This spontaneous report was received from a microbiologist and refers to a patient of unknown age and gender. The patient's concurrent conditions included immunocompromised. The patient's medical history and concomitant therapies were not reported. On an unknown date, the patient was vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), (dose, route of administration, lot # and expiration date were not reported) as prophylaxis (contraindicated product administered) which was reconstituted with sterile diluent (lot # and expiration date were not reported). On an unknown date, patient developed varicella-zoster virus (VZV) (Varicella zoster virus infection) after being vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX). The causal relationship between the event and the suspect vaccine/therapy was not provided. Follow-up information was received from Varicella Zoster Virus Identification Program (VZVIP) on 09-Jun-2025 and on 11-Jun-2025 from the physician. Patent's demographics were reported and referred to a 13-month-old male patient. The patient was enrolled in the Varicella Zoster Virus Identification Program to identify if VZV is present and if it is present, to identify if it is associated with the wild-type (WT) VZV strain or with the Oka/Merck vaccine strain. Specimen collection date o Source of specimen: blood o Was the patient on an oral antiviral (e.g., acyclovir, famciclovir or valacylovir) prior to specimen collections? No. o Final PCR Results: NEGATIVE (adequate sample, no VZV identified) The patient had no recent VZV exposure to chickenpox or shingles and had never had chickenpox and did not have a prior history of herpes zoster or herpes zoster ophthalmic. He had recurrent liver failure (moreover it was reported the following information difficult to read "new diagnosis ILF2 syndrome"). He did not have any allergies or concurrent medications. On 06-Feb-2024, the patient was vaccinated with the first dose of Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), (lot #X011424, expiration date not provided but upon internal validation established as: 19-Apr-2025), (dose and route of administration were not reported) reconstituted with sterile diluent (expiration date, and lot # were not reported) (contraindicated product administered, as previously reported). Rash did not occur at the site of injection following the vaccination. On 21-May-2025, the patient experienced a rash papulovesicular (description reported as "crusting by presentation", number of lesions were reported as "innumerable" [information difficult to read]), distribution of lesions: T1 (right side) and developed herpes zoster (dermatome T1)). On May-2025, body temperature showed maximum temperature: less than or equal to 100.4 F. On 26-May-2025, VZV Strain Identification PCR in blood was negative (adequate sample, no VZV identified) (as previously reported). The patient recovered from the event of herpes zoster on an unspecified day in 2025. The causal relationship between the event and suspect vaccine/therapy was not provided. More
2847380 M 06/26/2025 MMRV
MMRV
MMRV
MMRV
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.



Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event More
No symptoms reported at the time of the call; extradose adminsitered; This spontaneous report was re... No symptoms reported at the time of the call; extradose adminsitered; This spontaneous report was received from a health care professional on 23-Jun-2025 and refers to a 5-year-old male patient. The patient's medical history, and concurrent conditions were not reported. Historical vaccines included Measles, mumps, and rubella virus vaccine live (M-M-R II), and (Varicella zoster vaccine live (Oka/Merck)) (VARIVAX), administered on 15-Jun-2021. Concomitant therapies were not reported. On 02-Oct-2024, the patient was vaccinated with a second dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD)injection, dose: 0.5 mL (route of administration, anatomical location, lot # and expiration date were not reported) with sterile diluent, dose: 0.5 mL (route of administration, anatomical location, lot # and expiration date were not reported), on the same date for prophylaxis. On 29-May-2025, the patient was vaccinated with a third dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) injection,dose: 0.5 mL (route of administration, anatomical location, lot # and expiration date were not reported) with sterile diluent, dose: 0.5 mL (route of administration, anatomical location, lot # and expiration date were not reported), on the same date for prophylaxis (Extra dose administered). No symptoms reported at the time of the call. More
2847381 ND 06/26/2025 PNC21
 MERCK & CO. INC.
 Z002626
No adverse event, Product storage error No adverse event, Product storage error
no patient symptoms have been reported; 1 dose of CAPVAXIVE involved in a temperature excursion was ... no patient symptoms have been reported; 1 dose of CAPVAXIVE involved in a temperature excursion was administered to a patient; This spontaneous report was received from a pharmacy intern (also reported as medical student) and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 23-Jun-2025, the patient was vaccinated with Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE) (lot #Z002626, expiration date: 04-Sep-2026, strength and route were unknown), 1 dosage form for prophylaxis (Product storage error). No patient symptoms have been reported (No adverse event). Administered dose of Pneumococcal 21-valent Conjugate Vaccine (CAPVAXIVE) experienced the temperature excursion below 15.8degree Celsius [C] for 8 Hours 0 Minutes 0 Seconds. No previous temperature excursions reported. More
2847382 F CO 06/26/2025 MMR
 MERCK & CO. INC.
Antibody test negative Antibody test negative
Pharmacist called and reported that a consumer with Rheumatoid Arthritis had titers drawn for MMR-II... Pharmacist called and reported that a consumer with Rheumatoid Arthritis had titers drawn for MMR-II and had no levels.; Information has been received from a pharmacist and referred to a female patient of unknown age. The patient's concurrent condition included rheumatoid arthritis. Concomitant medication included tofacitinib citrate (XELJANZ). The patient's medical history was not reported. On an unknown date, the patient vaccinated with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) (strength, dose, frequency, route, lot # and expiration date were not reported) for prophylaxis, the vaccine was reconstituted with sterile diluent (MERCK STERILE DILUENT). On an unknown date, the patient had titers drawn for Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) and had no levels (Antibody test negative). The concomitant medication tofacitinib citrate (XELJANZ) was withheld by the physician so the patient could receive a booster dose of Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II). The patient had sought medical attention. At the reporting time, the patient had not recovered from the event. The causal relationship between the event and Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II), sterile diluent (MERCK STERILE DILUENT) was not provided. Lot# is being requested and will be submitted if received. More
2847383 F CA 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Neoplasm malignant Neoplasm malignant
she was diagnosed with cancer after receiving the first Shingrix vaccine; This serious case was repo... she was diagnosed with cancer after receiving the first Shingrix vaccine; This serious case was reported by a consumer via call center representative and described the occurrence of cancer in a female patient who received Herpes zoster (Shingrix) for prophylaxis. Concurrent medical conditions included hypertension. Concomitant products included lisinopril and amlodipine. In FEB-2025, the patient received the 1st dose of Shingrix. In FEB-2025, less than a month after receiving Shingrix, the patient experienced cancer (Verbatim: she was diagnosed with cancer after receiving the first Shingrix vaccine) (serious criteria GSK medically significant). The outcome of the cancer was unknown. It was unknown if the reporter considered the cancer to be related to Shingrix. The company considered the cancer to be unrelated to Shingrix. Additional Information: GSK Receipt Date: 18-JUN-2025 Customer reported that she was diagnosed with cancer after receiving first dose of Shingrix vaccine.; Sender's Comments: Neoplasm malignant is an unlisted event which is considered unrelated to GSK vaccine Shingrix. More
2847384 06/26/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Erectile dysfunction Erectile dysfunction
Penis won't get hard now; This serious case was reported by a consumer via interactive digital ... Penis won't get hard now; This serious case was reported by a consumer via interactive digital media and described the occurrence of erectile dysfunction in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On 19-JUN-2025, the patient received the 1st dose of Shingles vaccine. On 19-JUN-2025, less than a day after receiving Shingles vaccine, the patient experienced erectile dysfunction (Verbatim: Penis won't get hard now) (serious criteria GSK medically significant). The outcome of the erectile dysfunction was not resolved. It was unknown if the reporter considered the erectile dysfunction to be related to Shingles vaccine. The company considered the erectile dysfunction to be unrelated to Shingles vaccine. Additional Information: GSK Receipt Date: 19-JUN-2025 This case was reported by a patient via (Chatbot) interactive digital media. The patient got the first shot today now tonight the patient's penis will not get hard. The patient wanted to know when it would work again.; Sender's Comments: Erectile dysfunction is an unlisted event which is considered unrelated to GSK vaccine Shingles vaccine More
2847385 F 06/26/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Impaired work ability, Loss of personal independence in daily activities, Pain i... Impaired work ability, Loss of personal independence in daily activities, Pain in extremity More
Sore arm could not put shirt on missed day of work; Sore arm could not put shirt on missed day of wo... Sore arm could not put shirt on missed day of work; Sore arm could not put shirt on missed day of work; This non-serious case was reported by a nurse via sales rep and described the occurrence of pain in arm in a female patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received the 1st dose of Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced pain in arm (Verbatim: Sore arm could not put shirt on missed day of work) and activities of daily living impaired (Verbatim: Sore arm could not put shirt on missed day of work). The outcome of the pain in arm and activities of daily living impaired were resolved. The reporter considered the pain in arm and activities of daily living impaired to be related to Shingles vaccine. The company considered the pain in arm and activities of daily living impaired to be related to Shingles vaccine. Additional Information: GSK Receipt Date: 16-JUN-2025 The patient had Shingles vaccine first dose. The patient had sore arm, could not put shirt on missed day of work. The reporter would like to provide additional information about this report as said it had some years ago. More
2847386 F NJ 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incomplete course of vaccination Incomplete course of vaccination
she never received her second dose; This non-serious case was reported by a consumer via call center... she never received her second dose; This non-serious case was reported by a consumer via call center representative and described the occurrence of incomplete course of vaccination in a female patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (received 1st dose on 06-JAN-2024). On an unknown date, the patient did not receive the 2nd dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced incomplete course of vaccination (Verbatim: she never received her second dose). The outcome of the incomplete course of vaccination was not applicable. Additional Information: GSK receipt date: 16-JUN-2025 The patient reported that she received her first dose of Shingrix on 6th January 2024. Till the time of reporting, the patient did not receive 2nd dose of Shingrix, which led to incomplete course of vaccination. More
2847387 F MT 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Occupational exposure to product Occupational exposure to product
nurses at the healthcare facility was drawing up a shingrix vaccine (after the antigen and adjuvant ... nurses at the healthcare facility was drawing up a shingrix vaccine (after the antigen and adjuvant were mixed); Accidental exposure to product; drop sprayed in her eye; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of occupational exposure while preparing product for administration in a female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received Shingrix. On 16-JUN-2025, an unknown time after receiving Shingrix, the patient experienced occupational exposure while preparing product for administration (Verbatim: nurses at the healthcare facility was drawing up a shingrix vaccine (after the antigen and adjuvant were mixed)), inadvertent exposure to vaccine (Verbatim: Accidental exposure to product) and exposure via eye contact (Verbatim: drop sprayed in her eye). The outcome of the occupational exposure while preparing product for administration, inadvertent exposure to vaccine and exposure via eye contact were not applicable. Additional Information: GSK Receipt Date: 16-JUN-2025 Pharmacist reported that one of the nurses at the healthcare facility was drawing up a Shingrix vaccine (after the antigen and adjuvant were mixed) and a drop sprayed in her eye which led to inadvertent exposure to vaccine (Adverse event -Accidental Exposure). More
2847388 IL 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 594G2
Device connection issue, Syringe issue Device connection issue, Syringe issue
Vaccine preparation error; This non-serious case was reported by a nurse via call center representat... Vaccine preparation error; This non-serious case was reported by a nurse via call center representative and described the occurrence of wrong technique in product usage process in a patient who received Herpes zoster (Shingrix) (batch number 594G2) for prophylaxis. On 23-JUN-2025, the patient received Shingrix. On 23-JUN-2025, an unknown time after receiving Shingrix, the patient experienced wrong technique in product usage process (Verbatim: Vaccine preparation error). The action taken with Shingrix was unknown. The outcome of the wrong technique in product usage process was not applicable. Additional Information: GSK receipt date: 23-JUN-2025 HCP was the reporter. States when drawing up the final reconstituted solution of Shingrix the needle was not securely tightened to the syringe and medication leaked out of the syringe (preparation error.), which led to Wrong technique in product usage process. The patient received a dose of Shingrix using a different antigen/adjuvant of Shingrix. No further information was obtained/provided. More
2847389 06/26/2025 VARZOS
VARZOS
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 UNK
UNK
Herpes zoster, Pain, Vaccination failure; Herpes zoster, Pain, Vaccination failu... Herpes zoster, Pain, Vaccination failure; Herpes zoster, Pain, Vaccination failure More
suspected vaccination failure; shingles/pain; This serious case was reported by a consumer via inter... suspected vaccination failure; shingles/pain; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. Co-suspect products included Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received the 2nd dose of Shingles vaccine and the 1st dose of Shingles vaccine. On an unknown date, 6 years after receiving Shingles vaccine and Shingles vaccine, the patient experienced vaccination failure (Verbatim: suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: shingles/pain). The outcome of the vaccination failure and shingles were not reported. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine and Shingles vaccine. The company considered the vaccination failure to be unrelated to Shingles vaccine and Shingles vaccine. It was unknown if the company considered the shingles to be related to Shingles vaccine and Shingles vaccine. Additional Information: GSK Receipt Date: 17-JUN-2025 This case was reported by a patient via interactive digital media. Patient got both of those shots and still got shingles 6 years later. Also stated that their pain at the time reporting was a nine at best, and patient was on three different medications. This case was considered as suspected vaccination failure as details regarding laboratory confirmation regarding shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description and laboratory confirmation of disease) is considered unrelated to GSK vaccine Shingles vaccine (dose 1 and 2) More
2847390 06/26/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incorrect dose administered Incorrect dose administered
some patients who did not receive a full dose of Priorix; This non-serious case was reported by a co... some patients who did not receive a full dose of Priorix; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of incomplete dose administered in a patient who received MMR (Priorix) for prophylaxis. On an unknown date, the patient received Priorix. On an unknown date, an unknown time after receiving Priorix, the patient experienced incomplete dose administered (Verbatim: some patients who did not receive a full dose of Priorix). The outcome of the incomplete dose administered was not applicable. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 16-JUN-2025 This case was reported by a patient via interactive digital media. The reporter had some patients who did not receive a full dose of Priorix vaccine which led to Incomplete dose administered. More
2847391 7 M TN 06/26/2025 DTAP
 SANOFI PASTEUR
 3CA55C1
No adverse event, Wrong product administered No adverse event, Wrong product administered
Patient was inadvertently given DTaP when he was due for Td due to age of 7 years old. He was given ... Patient was inadvertently given DTaP when he was due for Td due to age of 7 years old. He was given TDaP last on 12/18/24. He displayed no adverse reaction to the DTaP vaccine. More
2847392 9 F AR 06/26/2025 IPV
IPV
TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 X1C891M
X1C891M
3CA33C1
3CA33C21
Headache, Loss of consciousness, Seizure like phenomena; Headache, Loss of consc... Headache, Loss of consciousness, Seizure like phenomena; Headache, Loss of consciousness, Seizure like phenomena; Headache, Loss of consciousness, Seizure like phenomena; Headache, Loss of consciousness, Seizure like phenomena More
Child received Tdap and polio and approximately 5 minutes after vaccination mother and child walked ... Child received Tdap and polio and approximately 5 minutes after vaccination mother and child walked to checkout, and child passed out briefly but also noticed seizure like activity. Sister was also present at time of event and also verified patient did not hit head. Patient fell on chair and slid down wall to floor. Also, patient stated when aroused she had a headache prior to passing out. Parent was encouraged to take child to PCP after appointment for follow up. Patient was stable leaving with mother and no longer had a headache. More
2847393 85 M IA 06/26/2025 COVID19
 MODERNA
 8057413
Death Death
Resident passed away Resident passed away
✓
2847394 14 M 06/26/2025 COVID19
 MODERNA
Unevaluable event Unevaluable event
NA NA
2847395 06/26/2025 COVID19
FLUX
RVX
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 UNK
UNK
UNK
Influenza, Respiratory syncytial virus infection, Vaccination failure; Influenza... Influenza, Respiratory syncytial virus infection, Vaccination failure; Influenza, Respiratory syncytial virus infection, Vaccination failure; Influenza, Respiratory syncytial virus infection, Vaccination failure More
Suspected vaccination failure; RSV; Flu; This serious case was reported by a consumer via interactiv... Suspected vaccination failure; RSV; Flu; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received RSVPreF3 adjuvanted (RSV vaccine) for prophylaxis. Co-suspect products included Influenza vaccine for prophylaxis and COVID-19 vaccine for prophylaxis. Previously administered products included Covid-19 vaccine (received 8 doses on an unknown date). On an unknown date, the patient received RSV vaccine, Influenza vaccine and the 9th dose of COVID-19 vaccine. On an unknown date, an unknown time after receiving RSV vaccine, Influenza vaccine and COVID-19 vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant), respiratory syncytial virus infection (Verbatim: RSV) and influenza (Verbatim: Flu). The outcome of the vaccination failure, respiratory syncytial virus infection and influenza were not reported. It was unknown if the reporter considered the vaccination failure, respiratory syncytial virus infection and influenza to be related to RSV vaccine, Influenza vaccine and COVID-19 vaccine. The company considered the vaccination failure to be unrelated to RSV vaccine. It was unknown if the company considered the respiratory syncytial virus infection and influenza to be related to RSV vaccine, Influenza vaccine and COVID-19 vaccine. It was unknown if the company considered the vaccination failure to be related to Influenza vaccine and COVID-19 vaccine. Additional Information: GSK Receipt Date: 19-JUN-2025 This case was reported by a patient via interactive digital media. The patient had a flu shot, an RSV shot, and 9th Covid shot in last fall but still got the Flu and respiratory syncytial virus before February. The patient spent some time in the hospital and then they brought nurses to saws the patient in the house for another few days four times a day. If patient not had insurance he/she would have been billed for over 16,000 dollars. This case was considered as suspected vaccination failure as details regarding completion of primary vaccination schedule, time to onset and laboratory test confirming shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK RSV vaccine. More
2847397 50 M TN 06/26/2025 HEP
TDAP
 DYNAVAX TECHNOLOGIES CORPORATION
GLAXOSMITHKLINE BIOLOGICALS
l5229
Inappropriate schedule of product administration, No adverse event; Inappropriat... Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event More
Boostrix vaccine was administered outside of CDC guidelines. No adverse event was reported. Boostrix vaccine was administered outside of CDC guidelines. No adverse event was reported.
2847398 70 M OR 06/26/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 xx9n4
Incorrect route of product administration, No adverse event Incorrect route of product administration, No adverse event
gave im instead of sq no reaction gave im instead of sq no reaction
2847399 52 M TX 06/26/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Decreased appetite, Dizziness, Dyspnoea, Feeling cold, Hallucination; Memory imp... Decreased appetite, Dizziness, Dyspnoea, Feeling cold, Hallucination; Memory impairment More
I woke up the next morning and i was light headed and tired i was having hallucination. I was having... I woke up the next morning and i was light headed and tired i was having hallucination. I was having trouble breathing like i was having an asthma attack. I was really cold i had to keep the heat up in the house. I had a lack of appetite and my memory is bad. More
2847400 51 F IL 06/26/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 em16200
em16200
em16200
em16200
em16200
en6206
en6206
en6206
en6206
en6206
fj1620
fj1620
fj1620
fj1620
fj1620
Amnesia, Anxiety, Arthralgia, Balance disorder, Blood test; Brain fog, Cognitive... Amnesia, Anxiety, Arthralgia, Balance disorder, Blood test; Brain fog, Cognitive disorder, Computerised tomogram, Dizziness, Electric shock sensation; Hyperacusis, Insomnia, Loss of personal independence in daily activities, Magnetic resonance imaging, Muscle atrophy; Myalgia, Paraesthesia, Photophobia, Temporomandibular pain and dysfunction syndrome, Tinnitus; Vertigo, Weight decreased; Amnesia, Anxiety, Arthralgia, Balance disorder, Blood test; Brain fog, Cognitive disorder, Computerised tomogram, Dizziness, Electric shock sensation; Hyperacusis, Insomnia, Loss of personal independence in daily activities, Magnetic resonance imaging, Muscle atrophy; Myalgia, Paraesthesia, Photophobia, Temporomandibular pain and dysfunction syndrome, Tinnitus; Vertigo, Weight decreased; Amnesia, Anxiety, Arthralgia, Balance disorder, Blood test; Brain fog, Cognitive disorder, Computerised tomogram, Dizziness, Electric shock sensation; Hyperacusis, Insomnia, Loss of personal independence in daily activities, Magnetic resonance imaging, Muscle atrophy; Myalgia, Paraesthesia, Photophobia, Temporomandibular pain and dysfunction syndrome, Tinnitus; Vertigo, Weight decreased More
I woke up at 230 am on Dec 15 with ringing in my ears. As the weeks went on I developed muscle and j... I woke up at 230 am on Dec 15 with ringing in my ears. As the weeks went on I developed muscle and joint pain, pins and needles, hearing sensitivity, light sensitivity, electrical currents going through my body, Insomnia, Brain fog, Anxiety, TMJ, Vertigo, Dizziness, off balance, weight and muscle loss. I could no longer function. Having conversations with people was hard. Memory loss and the list goes on, I saw at least 12 Western Medicine specialist and none of them would say it was from the Vaccine except one. So no one treated me for a Vaccine injury. I saw two Long Haul Covid Clinics. The outcome is I am still fighting to get my life back. I still have symptoms. More
✓
2847401 37 M MA 06/26/2025 HEP
MNQ
 DYNAVAX TECHNOLOGIES CORPORATION
NOVARTIS VACCINES AND DIAGNOSTICS
 945665
AMXB056A
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
Hep B given instead of Hep A. Hep B given instead of Hep A.
2847402 48 F AR 06/26/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH





Atrial fibrillation, Cardiac ablation, Cardiac monitoring, Cardiac stress test, ... Atrial fibrillation, Cardiac ablation, Cardiac monitoring, Cardiac stress test, Catheterisation cardiac; Computerised tomogram, Echocardiogram, Electrocardiogram, Impaired work ability, Implantable cardiac monitor insertion; Left atrial appendage closure implant, Loss of personal independence in daily activities, Thrombosis; Atrial fibrillation, Cardiac ablation, Cardiac monitoring, Cardiac stress test, Catheterisation cardiac; Computerised tomogram, Echocardiogram, Electrocardiogram, Impaired work ability, Implantable cardiac monitor insertion; Left atrial appendage closure implant, Loss of personal independence in daily activities, Thrombosis More
Got a blood clot in my left hand, ring finger and this required a couple of days in the hospital and... Got a blood clot in my left hand, ring finger and this required a couple of days in the hospital and missing lots of work. Was put on Eliquis 2 x a day and aspirin daily. On Dec 2021 I had to have a Heart Ablation done because I was also AFIB. I wear a couple of different heart monitors that then required me to get a Loop Monitor put into my chest in Oct 2022. In around Oct 2023 I had a Watchman Device put into my heart. I have several health issues these last 4 years and its been tough. I have so many follow up visits and scans, missing lots of work unpaid. Not being able to do the things I use to do before all this happened. Nothing good came out of getting this Vaccine. More
✓
2847403 51 F IL 06/26/2025 VARZOS
VARZOS
VARZOS
VARZOS
VARZOS
VARZOS
VARZOS
VARZOS
VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS




UNK
UNK
UNK
UNK
UNK
Asthma, Chills, Fatigue, Feeling abnormal, Headache; Hyperacusis, Influenza like... Asthma, Chills, Fatigue, Feeling abnormal, Headache; Hyperacusis, Influenza like illness, Nausea, Photophobia; Chills, Dysphonia, Fatigue, Feeling abnormal, Feeling hot; Headache, Hyperacusis, Impaired work ability, Influenza, Mental disorder; Nausea, Photophobia, Pyrexia; Asthma, Chills, Fatigue, Feeling abnormal, Headache; Hyperacusis, Influenza like illness, Nausea, Photophobia; Chills, Dysphonia, Fatigue, Feeling abnormal, Feeling hot; Headache, Hyperacusis, Impaired work ability, Influenza, Mental disorder; Nausea, Photophobia, Pyrexia More
Extreme exhaustion feeling like is have the flu, headaches, nausea, cognitive looseness-spacey, temp... Extreme exhaustion feeling like is have the flu, headaches, nausea, cognitive looseness-spacey, temperature steady at 99.1, chills, sensitive to sounds and light, nauseated. These all started on Sunday June 21st and still are all present to date . More
2847404 46 F 06/26/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 945657
Limb mass, Pain in extremity Limb mass, Pain in extremity
pt reported sore arm with knot. pt states she took tylenol, pharmacist recommended ibuprofen and see... pt reported sore arm with knot. pt states she took tylenol, pharmacist recommended ibuprofen and see primary or urgent care provider More
2847405 1.5 F UT 06/26/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 22349
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
erythema and swelling of the leg that worsened significantly 2 days later. Started to improve on Day... erythema and swelling of the leg that worsened significantly 2 days later. Started to improve on Day 3 and is now doing well. More
2847406 0.75 M MI 06/26/2025 FLU3
FLU3
FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 UT8496JA
UT8496JA
UT8496JA
UT8496JA
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event; Extra dose administered, No adverse event More
Gave extra dose of flu. No adverse symptoms as of now Gave extra dose of flu. No adverse symptoms as of now
2847407 0.5 F GA 06/26/2025 DTAPHEPBIP
HEP
PNC20
RV5
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.



Malaise, Pyrexia; Malaise, Pyrexia; Malaise, Pyrexia; Malaise, Pyrexia Malaise, Pyrexia; Malaise, Pyrexia; Malaise, Pyrexia; Malaise, Pyrexia
FEVER, GENERAL MALAISE FEVER, GENERAL MALAISE
2847408 50 F UT 06/26/2025 PNC20
TDAP
VARZOS
 PFIZER\WYETH
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 lx4482
u8389aa
pj353
Erythema, Peripheral swelling, Pruritus; Erythema, Peripheral swelling, Pruritus... Erythema, Peripheral swelling, Pruritus; Erythema, Peripheral swelling, Pruritus; Erythema, Peripheral swelling, Pruritus More
Patient said her arm was red and swollen and it was itchy Patient said her arm was red and swollen and it was itchy
2847409 CA 06/26/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Incomplete course of vaccination Incomplete course of vaccination
had their 1st dose a year a ago or two years ago; This non-serious case was reported by a pharmacist... had their 1st dose a year a ago or two years ago; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of incomplete course of vaccination in an unspecified number of patients who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (received first and a year ago or two years ago.). On an unknown date, the patients did not receive the 2nd dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced incomplete course of vaccination (Verbatim: had their 1st dose a year a ago or two years ago). The outcome of the incomplete course of vaccination was not applicable. Additional Information: GSK Receipt Date: 16-JUN-2025 The pharmacist reported some patients come in and had their 1st dose a year a ago or two years ago, what are the guidelines. The pharmacist reported they come and ask. When pharmacist was asked to clarify scenario and confirm if this occurred, pharmacist said, possibly but the number of patients is unknown. She states this is just a general question. Till the time of reporting, the patients did not receive 2nd dose of Shingrix, which led to incomplete course of vaccination. More
2847410 87 M FL 06/26/2025 HEPAB
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 P2443
LN4927
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Patient received a 2nd dose of Prevnar 20 on 6/24/2025 despite receiving a dose of the same on 2/3/2... Patient received a 2nd dose of Prevnar 20 on 6/24/2025 despite receiving a dose of the same on 2/3/2023. This 2nd dose was determined to be clinically inappropriate as current guidelines indicate patient should receive only one dose of Prevnar 20. More
2847411 0.17 M VA 06/26/2025 DTPPVHBHPB
PNC20
RV1
 MSP VACCINE COMPANY
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 U7921AA
LG5578
GG2YS
Hypotonia; Hypotonia; Hypotonia Hypotonia; Hypotonia; Hypotonia
NOT SURE MOM AND GRANDMA had different version, mom said it was normal, Grandma said baby was limp f... NOT SURE MOM AND GRANDMA had different version, mom said it was normal, Grandma said baby was limp for few seconds, did not turn blue or stopped breathing More
2847412 11 F TX 06/26/2025 MNQ
MNQ
MNQ
TDAP
TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 U8494AA (VFC -
U8494AA (VFC -
U8494AA (VFC -
4CA04C1 (TROPHY
4CA04C1 (TROPHY
4CA04C1 (TROPHY
Amnesia, Dyspnoea, Gaze palsy, Headache, Immediate post-injection reaction; Mala... Amnesia, Dyspnoea, Gaze palsy, Headache, Immediate post-injection reaction; Malaise, Musculoskeletal stiffness, Seizure like phenomena, Urinary incontinence, Visual impairment; Vomiting; Amnesia, Dyspnoea, Gaze palsy, Headache, Immediate post-injection reaction; Malaise, Musculoskeletal stiffness, Seizure like phenomena, Urinary incontinence, Visual impairment; Vomiting More
The patient is here with a seziure-like episode that occurred in the car about 15 minutes after she ... The patient is here with a seziure-like episode that occurred in the car about 15 minutes after she received her 11 year vaccines at Dr's office. After receiving the TdaP and Menquadfi vaccines, she immediately did not feel well and had to lay down. She had not had anything to eat or drink that morning. She felt beter after 10 minutes and they then left the office. In the car she reported to mom she did not feel well. She reports today seeing spots in her vision and then remembers nothing. Her mom reports she looked back and her head was turned to the left with her eyes rolled back, her right arm was stiff and flexed and her left arm was fully extended and stiff. There were no convulsions. Mom pulled over and the episode lated about 30 seconds. Mom then saw her breathing really heavily for about 30 seconds. She vomited foam and lost bladder control. She went home and slept for 2 hours after taking tylenol. She has since had pain at the top of her head and some neck tightness. More
2847413 1.25 M GA 06/26/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK225AB
No adverse event, Product preparation error No adverse event, Product preparation error
Patient was given Pentacel mixed with the wrong diluent. Used sterile diluent instead of the diluent... Patient was given Pentacel mixed with the wrong diluent. Used sterile diluent instead of the diluent included in the box with Pentacel. Therefore not considered active. There is no symptom/signs at this time. More
2847414 11 M MN 06/26/2025 HPV9
TDAP
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 Y013565
Syncope; Syncope Syncope; Syncope
Vasovagal syncope within 15 minutes of vaccines while walking out of clinic. No treatment needed. Vasovagal syncope within 15 minutes of vaccines while walking out of clinic. No treatment needed.
2847415 0.5 M GA 06/26/2025 DTPPVHBHPB
PNC20
 MSP VACCINE COMPANY
PFIZER\WYETH
 U8335AA
MF0416
Muscle twitching, Screaming, Staring, Tremor; Muscle twitching, Screaming, Stari... Muscle twitching, Screaming, Staring, Tremor; Muscle twitching, Screaming, Staring, Tremor More
Around 11pm 6/25/25 he screamed out like he was in pain and mom picked him up and noticed he was sha... Around 11pm 6/25/25 he screamed out like he was in pain and mom picked him up and noticed he was shaking/twitching all over and had a blank stare but he was not crying. This continued for about 5 minutes after which he seemed to be acting normally. He went to the ER and was examined and had a normal exam. He had no fever around that time. More
📋 Privacy Policy & Data Disclaimer