๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ Privacy & Data Disclaimer

About This Site

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

Data Source & Accuracy

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

Your Privacy

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

Medical Disclaimer

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

Data Interpretation

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

๐Ÿ“– Help & Search Guide

Column Icons Legend

๐Ÿ’€ Death
๐Ÿฅ Hospitalized
๐Ÿš‘ Emergency Room
โ™ฟ Disability
โš ๏ธ Life Threatening

How to Search

๐Ÿ’ก Search Tips:
  • Select Year: Choose a specific year OR "All Years" to search across all data
  • All Years requires filters: When searching all years, you must select at least one filter (lot number, vaccine type, outcome, etc.) for performance
  • Lot number tracking: Use "All Years" + Lot Number to track lots across multiple years
  • Combine filters: Use multiple filters together to narrow results (e.g., Age + Vaccine Type + Death)
  • VAERS ID: Search for specific report by ID number
  • Age: Enter exact age (e.g., 25) or decimal (e.g., 0.5 for 6 months)
  • State: Enter 2-letter state code (e.g., CA, NY, TX)
  • Vaccine Type: Search partial names (e.g., "COVID19", "FLU", "HPV")
  • Manufacturer: Search by company (e.g., "PFIZER", "MODERNA")
  • Lot Number: Search specific vaccine lot (works great with "All Years")
  • Symptoms: Search for any symptom keyword (e.g., "fever", "rash")
  • Death/Hospitalized: Filter to only show cases with these outcomes

Understanding the Data

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

Using the Table

  • Sort columns: Click column headers (ID, Age, Sex, Date, Died) to sort
  • Expand text: Click "More" to see full narrative or symptom text
  • Navigate pages: Use pagination controls at top and bottom of table
  • Export results: Click "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ VAERS Vaccine Data Browser is an independent, third-party data browser for publicly available VAERS (Vaccine Adverse Event Reporting System) data.

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

What is VAERS?

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

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

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

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

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

Why does this site exist?

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

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

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

Where does the data come from?

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

The data is:

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

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

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

Important context:

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

What to do:

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

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

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

Limitations:

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

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

What are "adverse events"?

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

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

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

Why are some lot numbers listed multiple times?

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

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

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

How often is this data updated?

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

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

Where can I learn more?

โš ๏ธ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2831562 65 M UT 03/14/2025 PNC20
 PFIZER\WYETH
 LP8151
Cough, Throat irritation Cough, Throat irritation
Tickle in throat and slight cough. Tickle in throat and slight cough.
2831563 16 M GA 03/14/2025 COVID19
 PFIZER\BIONTECH
 LM2212
Rash, Rash erythematous, Skin exfoliation, Streptococcus test negative, Tenderne... Rash, Rash erythematous, Skin exfoliation, Streptococcus test negative, Tenderness More
WITHIN A DAY AND A HALF OF RECEIVING COVID VACCINE, PATIENT'S PALMS HAD RED BUMPS APPEAR. PALMS... WITHIN A DAY AND A HALF OF RECEIVING COVID VACCINE, PATIENT'S PALMS HAD RED BUMPS APPEAR. PALMS CONTINUED TO GET RED AND THEN STARTED TO HURT. WITHIN A COUPLE MORE DAYS THE PALMS BEGAN TO PEEL AND BECOME TENDER. PATIENT WENT TO PROVIDER AND WAS TESTED FOR STREP BUT WAS NEGATIVE. THE PHYSICIAN AND PATIENT ARE THINKING IT IS IN RESPONSE TO THE COVID VACCINE. More
2831564 62 F KS 03/14/2025 PNC21
VARZOS
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 Y013009
N77J2
Headache, Pruritus, Pyrexia; Headache, Pruritus, Pyrexia Headache, Pruritus, Pyrexia; Headache, Pruritus, Pyrexia
Patient experienced headache, itching, and mild fever. Recommended Ibuprofen or Aleve OTC. Patient t... Patient experienced headache, itching, and mild fever. Recommended Ibuprofen or Aleve OTC. Patient to report to doctor if symptoms persist after two days. More
2831565 77 F FL 03/14/2025 PNC21
 MERCK & CO. INC.
 Y019158
Injection site erythema Injection site erythema
Patient came to pharmacy 3/14 and reported after getting her vaccine she developed a red spot on the... Patient came to pharmacy 3/14 and reported after getting her vaccine she developed a red spot on the injection site and another about 2 inches below the injection site. More
2831573 2 M CA 03/14/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 Y97N7
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Vaccine is considered not 'NOT VALID" next dose due until age 4 years. No symptoms relat... Vaccine is considered not 'NOT VALID" next dose due until age 4 years. No symptoms related to Vaccine. More
2831574 68 F 03/14/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Arthralgia, Eye swelling, Injection site erythema, Injection site pain, Malaise;... Arthralgia, Eye swelling, Injection site erythema, Injection site pain, Malaise; Myalgia More
Day after vaccine: malaise, joint and muscle pain, redness and soreness at injection site. 2nd day p... Day after vaccine: malaise, joint and muscle pain, redness and soreness at injection site. 2nd day post injection: both eyes swollen, continued redness and soreness at injection site. More
2831575 39 F CA 03/14/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 39LB7
Extra dose administered, No adverse event Extra dose administered, No adverse event
Double vaccine dose was given to patient. Patient report no symptoms. Double vaccine dose was given to patient. Patient report no symptoms.
2831576 50 F TN 03/14/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 29Z52
Rash, Rash pruritic Rash, Rash pruritic
The patient stopped by clinic on 03/14/2025 inquiring if she should get dose 2, reports that days af... The patient stopped by clinic on 03/14/2025 inquiring if she should get dose 2, reports that days after getting dose 1 developed a very itchy rash to both arms and chest and had to take benadryl as well as seek care at an outside facility and was prescribed steroids. More
2831577 53 M OR 03/14/2025 UNK
 UNKNOWN MANUFACTURER
 Y018157
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
none none
2831578 45 F AZ 03/14/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 AZ453
Fatigue, Hypoaesthesia, Injection site pain, Paraesthesia Fatigue, Hypoaesthesia, Injection site pain, Paraesthesia
Pt presented to clinic to report since she received the hep b and flu shot on 3/12/25 at clinic, she... Pt presented to clinic to report since she received the hep b and flu shot on 3/12/25 at clinic, she states yesterday 3/13/25 and today 3/14/25 she experienced numbness and " pins and needles sensation" tingling on left leg back hamstring/ left hip and top of left foot. She stated the vaccines were given in her left arm deltoid muscle. She has experienced fatigue and soreness at injection site. I re-assured her that fatigue and soreness are to be expected after vaccines and it would be ok to take OTC tylenol or ibuprofen for soreness at injection site if needed. She was able to ambulate from waiting room and getting up from a sitting position to a standing postion with no assistance or visible deficit. Spoke to our provider, he advised for pt to watch for any worsening symptoms and to go to ER or urgent care if symptoms persist or worsen. Also instructed pt to notify her PCP today of her symptoms of numbness/tingling, fatigue. Pt verbalized understanding. Vaers report completed. Notified Dr. at County Health Dept of situation, he advised for pt to follow up with PCP and if symptoms worsen or persist to go to urgent care/ ER to be evaluated. More
2831579 26 F TX 03/14/2025 HPV9
TDAP
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 Y010466
7KD5B
Syncope; Syncope Syncope; Syncope
Vasovagal syncope Vasovagal syncope
2831040 03/13/2025 COVID19
 JANSSEN
Adverse event, Injury Adverse event, Injury
side effects for 4 years; injury; This spontaneous report received from a patient concerned a patien... side effects for 4 years; injury; This spontaneous report received from a patient concerned a patient of unspecified age and sex. The patient's height and weight were not reported. Age at time of vaccination was unknown. No past medical history, concurrent conditions or pre-existing medical conditions were reported. The patient received janssen covid-19 vaccine (suspension for injection, intramuscular, batch number not reported) dose, frequency and therapy dates not reported, additional dosage information included: dose series 1, for covid-19 prophylaxis. The batch number was not reported. Company was unable to perform follow up to request batch/lot number. No concomitant medications were reported. On an unspecified date, the patient experienced side effects for 4 years and injury. (dose series 1) The patient took C19 Vaccine and have had all sorts of side effects for 4 years and was looking for help. The action taken with janssen covid-19 vaccine was not applicable. The outcome of side effects for 4 years and injury was not reported. This report was serious (disability/permanent damage).; Sender's Comments: V0-Adverse event, Injury. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event. Therefore, the WHO Causality is considered indeterminate. The company causality is considered unassessable. More
โœ“
2831054 03/13/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 43G92
Febrile convulsion Febrile convulsion
Febrile seizures; This serious case was reported by a pharmacist via sales rep and described the occ... Febrile seizures; This serious case was reported by a pharmacist via sales rep and described the occurrence of febrile seizure in a 1-year-old patient who received MMR (Priorix) (batch number 43G92) for prophylaxis. On 06-MAR-2025, the patient received the 1st dose of Priorix. In MAR-2025, an unknown time after receiving Priorix, the patient experienced febrile seizure (Verbatim: Febrile seizures) (serious criteria hospitalization and GSK medically significant). The outcome of the febrile seizure was resolving. The reporter considered the febrile seizure to be related to Priorix and Priorix Pre-Filled Syringe Device. The company considered the febrile seizure to be unrelated to Priorix and Priorix Pre-Filled Syringe Device. 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: 07-MAR-2025 The patient received a first dose of Priorix and experienced febrile seizure after vaccination. The patient required hospitalization and rapid response.; Sender's Comments: Febrile convulsion is a listed event which, due to the following criteria (insufficient information regarding medical history, concurrent conditions, concomitant medications, time to onset, confirmation of disease) is considered unrelated to GSK vaccine Priorix and Priorix PRE-FILLED SYRINGE DEVICE. More
โœ“
2831055 F 03/13/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Irritability, Pain, Pruritus, Vaccination failure Herpes zoster, Irritability, Pain, Pruritus, Vaccination failure
Suspected Vaccination failure; shingles; This serious case was reported by a consumer via interactiv... Suspected Vaccination failure; shingles; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a elderly female patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. In JUL-2024, an unknown time after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected Vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: shingles). The outcome of the vaccination failure and shingles were not reported. The reporter considered the vaccination failure and shingles to be related to Shingles vaccine. The company considered the vaccination failure and shingles to be unrelated to Shingles vaccine. Additional Information: GSK Receipt Date: 01-MAR-2025 This case was reported by a patient via interactive digital media. They had the shingle vaccination 2 years ago, just got shingles 80 in July 2024 hurt, itch and irritable. 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: Herpes zoster is an unlisted event which is considered unrelated to GSK Shingles vaccine. 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
2831056 F 03/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Herpes zoster, Pain, Vaccination failure Herpes zoster, Pain, Vaccination failure
Suspected vaccination failure; had shingles 3 times; This serious case was reported by a consumer vi... Suspected vaccination failure; had shingles 3 times; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a adult female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: had shingles 3 times). The outcome of the vaccination failure and shingles were not reported. The reporter considered the vaccination failure and shingles to be related to Shingrix. The company considered the vaccination failure and shingles to be unrelated to Shingrix. Additional Information: GSK Receipt Date: 08-MAR-2025 The case was received from the patient via (Instagram) interactive digital media. The reporter reported that you were the best person to encourage anyone, he/she had shingles 3 times unfortunately the vaccine did not work but he/she would not want anyone to suffer it's undescribable pain. This case was considered as suspected vaccination failure as details regarding completion of primary schedule, time to onset for shingles and laboratory confirmation regarding shingles were unknown at the time of reporting.; Sender's Comments: Herpes zoster is an unlisted event which is considered unrelated to GSK vaccine Shingrix. 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 vaccine Shingrix. More
2831057 F 03/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Herpes zoster, Pain, Vaccination failure Herpes zoster, Pain, Vaccination failure
suspected vaccination failure; had the shot and still got them they were on back and under skin very... suspected vaccination failure; had the shot and still got them they were on back and under skin very painful; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a adult female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced vaccination failure (Verbatim: suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: had the shot and still got them they were on back and under skin very painful). 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 Shingrix. The company considered the vaccination failure and shingles to be unrelated to Shingrix. Additional Information: GSK Receipt Date: 08-MAR-2025 This case was reported by a patient via interactive digital media. The patient had Shingrix shot and still got shingles on back and under skin, it was very painful. This case was considered as suspected vaccination failure as details regarding completion of primary schedule, time to onset for shingles and laboratory confirmation regarding shingles were unknown at the time of reporting.; Sender's Comments: Herpes zoster is an unlisted event which is considered unrelated to GSK vaccine Shingrix. 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 vaccine Shingrix. More
2831058 03/13/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
suspected vaccination failure; shingles; This serious case was reported by a consumer via interactiv... suspected vaccination failure; shingles; 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. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: suspected vaccination failure) (serious criteria GSK medically significant) and shingles (Verbatim: 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: 07-MAR-2025 This case was reported by a patient via interactive digital media. Patient had the vaccine and got shingles and stated that they were excruciating. The patient stated that one in three would get shingles. Also stated that it was day 10 they were long way from recovery. 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
2831059 03/13/2025 VARZOS
 UNKNOWN MANUFACTURER
 UNK
Herpes zoster, Vaccination failure Herpes zoster, Vaccination failure
Suspected vaccination failure; Ending Up Getting It; This serious case was reported by a consumer vi... Suspected vaccination failure; Ending Up Getting It; 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. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria hospitalization and GSK medically significant) and shingles (Verbatim: Ending Up Getting It) (serious criteria hospitalization). 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. The company considered the vaccination failure and shingles to be unrelated to Shingles vaccine. Additional Information: GSK Receipt Date: 09-MAR-2025 The case was received from the patient via interactive digital media. The patient got the shingle shot and ending up getting it. The patient was in the hospital. This case was considered as suspected vaccination failure as details regarding completion of primary 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 the completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK Shingles vaccine. Herpes zoster is an unlisted event which is considered unrelated to GSK Shingles vaccine. More
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2831060 F MO 03/13/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 3RT93
Product administered to patient of inappropriate age, Wrong product administered Product administered to patient of inappropriate age, Wrong product administered
maladministration of Kinrix instead of Pediarix dose; Maladministration of Kinrix on a pediatric pat... maladministration of Kinrix instead of Pediarix dose; Maladministration of Kinrix on a pediatric patient-underage; This non-serious case was reported by a other health professional via call center representative and described the occurrence of wrong vaccine administered in a 4-month-old female patient who received DTPa-IPV (Kinrix) (batch number 3RT93, expiry date 03-APR-2026) for prophylaxis. Co-suspect products included DTPa-HBV-IPV (Pediarix) for prophylaxis. On an unknown date, the patient received Kinrix and Pediarix. On an unknown date, an unknown time after receiving Kinrix and not applicable after receiving Pediarix, the patient experienced wrong vaccine administered (Verbatim: maladministration of Kinrix instead of Pediarix dose) and inappropriate age at vaccine administration (Verbatim: Maladministration of Kinrix on a pediatric patient-underage). The outcome of the wrong vaccine administered and inappropriate age at vaccine administration were 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 : 03-MAR-2025 Medical Assistant called to reported that the maladministration of Kinrix instead of Pediarix (pediatric patient, underage), which led to wrong vaccine administered and inappropriate age at vaccine administration. Vaccine detail and patient demographics were obtained from the reporter๏ฟฝs end. The vaccine administration facility was the same as primary reporter. No further information was obtained in this call. More
2831061 0.17 M CA 03/13/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK110AA
No adverse event, Product preparation issue No adverse event, Product preparation issue
hib component was not reconstituted with the Dtap-IPV component of PENTACEL, with no reported advers... hib component was not reconstituted with the Dtap-IPV component of PENTACEL, with no reported adverse event; Initial information received on 10-Mar-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 2 months old male patient and reporter reported that the HIB component was not reconstituted with the DTAP-IVP component of Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(Vero)/HIB(PRP/T) Vaccine [Pentacel] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Rotavirus Vaccine; Pneumococcal Vaccine Conj 15v (Crm197) And Hepatitis B vaccine for Immunisation. On 07-Mar-2025, the patient received a HIB component was not reconstituted with the DTAP-IVP component of Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(Vero)/HIB(PRP/T) Vaccine Powder and suspension for suspension for injection (lot UK110AA) (expiry date-31-Aug-2025) via intramuscular route in the left thigh as prophylactic vaccination (immunization) (latency-same day) and the HIB component was not reconstituted with the DTAP-IVP component with no reported adverse event (single component of a two-component product administered) Action taken: not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2831062 0.17 F PA 03/13/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK149AB
No adverse event, Product preparation issue No adverse event, Product preparation issue
inappropriate use due to the administration of the dtap-ipv liquid portion of pentacel with sterile ... inappropriate use due to the administration of the dtap-ipv liquid portion of pentacel with sterile water. acthib was not administered to the patient with no reported ae; Initial information received on 11-Mar-2025 regarding an unsolicited valid non-serious case received from a other healthcare professional. This case involves a 2 months old female patient who had inappropriate use due to the administration of the DTAP-IPV liquid portion of diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (vero)] with sterile water and ACTHIB was not administered to the patient with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included rotavirus vaccine, pneumococcal vaccine CONJ 20V (CRM197) (PREVNAR 20) and hepatitis B vaccine, all for Immunisation. On 14-Feb-2025 the patient developed a non-serious inappropriate use due to the administration of the DTAP-IPV liquid portion of standard dose of 0.5 ml of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine Suspension for injection once (Unknown strength) with lot UK149AB and expiry date 31-Aug-205 via intramuscular route in the right thigh for Immunization with sterile water. ACTHIB was not administered to the patient with no reported adverse event (single component of a two-component product administered) (Latency same day). Reportedly, This situation is pre-assessed as a medication error/an inappropriate use due to the administration of the DTAP-IPV liquid portion of pentacel with sterile water. ACTHIB was not administered to the patient. Medical Assistant reported that pentacel was diluted incorrectly and administered to a patient. The liquid portion (DTAP-IPV component) was mixed with another diluent (sterile water) and administered to a patient. The powder (ACTHIB) portion was not administered. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2831063 NY 03/13/2025 HIBV
 SANOFI PASTEUR
 UJ995AA
Expired product administered, No adverse event Expired product administered, No adverse event
expired dose of ACT-HIB was given to a patient with no reported adverse event; Initial information r... expired dose of ACT-HIB was given to a patient with no reported adverse event; Initial information received on 11-Mar-2025 regarding an unsolicited valid non-serious case received from a nurse. This case involves a patient of unknown gender and age who was inappropriately administered with an expired dose of HIB (PRP/T) Vaccine [ACT-HIB] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 01-Mar-2025, the patient received an expired unknown dose of suspect HIB (PRP/T) Vaccine, Powder and solvent for solution for injection (lot UJ995AA, expiry date 28-Feb-2025; strength standard, Frequency = Once) via unknown route in unknown administration site for immunization, with no reported adverse event (expired product administered) (latency same day). Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2831089 36 F AK 03/13/2025 FLU3
 SEQIRUS, INC.
 P100710103
Lymph node pain, Lymphadenopathy Lymph node pain, Lymphadenopathy
According to the patient she has been experiencing swollen lymph nodes in neck, behind the ear and u... According to the patient she has been experiencing swollen lymph nodes in neck, behind the ear and under arm on the left side. All tender to touch. Swelling lasting up to one week. More
2831090 50 F MO 03/13/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Immediate post-injection reaction, Myalgia, Pain in extremity, Peripheral swelli... Immediate post-injection reaction, Myalgia, Pain in extremity, Peripheral swelling, Pyrexia; Sleep disorder More
Was given a shingles shot, Shingrix This med hurt immediately while giving My left arm hurt so bad I... Was given a shingles shot, Shingrix This med hurt immediately while giving My left arm hurt so bad I couldn't sleep it hurt down to the muscle.. it was swollen about a quarter inch high and it was the size of a baseball around. This is March 6 and my muscle is still sore. I applied cold compresses and heat, the cold worked better. I was feverish and felt like someone had branded me More
2831091 68 F IA 03/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Injection site pain, Injection site rash, Pruritus Injection site pain, Injection site rash, Pruritus
Rash at site of Shingrex vaccination (first shot). Started day after shot, slightly larger the follo... Rash at site of Shingrex vaccination (first shot). Started day after shot, slightly larger the following day and slightly itchy, mild pain at injection site. Using ice and 1% hydrocortisone. More
2831092 F NY 03/13/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH

Headache, Injected limb mobility decreased, Malaise, Pain, Pain in extremity; Te... Headache, Injected limb mobility decreased, Malaise, Pain, Pain in extremity; Tenderness More
Received Prevnar21 on 3/06/2025. That night my arm where I received the injection really started to ... Received Prevnar21 on 3/06/2025. That night my arm where I received the injection really started to hurt. To the point that I could not move arm without significant pain. The next morning I started with body aches, headache and chills and over all not feeling well. Work up 3/8/3025 feeling a little better. Don't feel as chilled or feverish but still have headache and arm remains very tender, difficult to use arm where I received the injection. More
2831093 30 M MI 03/13/2025 FLUX
FLUX
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Asthenia, Chills, Gastrooesophageal reflux disease, Influenza like illness, Mala... Asthenia, Chills, Gastrooesophageal reflux disease, Influenza like illness, Malaise; Nausea, Rash pruritic, Vomiting More
Patient to ED by ambulance x 2 sick days with N/V, diarrhea, H/O diabetic gastroparesis(on Reglan), ... Patient to ED by ambulance x 2 sick days with N/V, diarrhea, H/O diabetic gastroparesis(on Reglan), GERD, weakness, chills, thought it was a gallbladder attack. Spouse sick. Allergy to Flu Vaccine: rash. For flu like symptoms initiated Tamiflu 75mg however shortly afterwards the patient did break out in a pruritic rash, no throat closing sensation or angioedema. Administered Benadryl IV which resolved the rash. Product: Tamiflu 75mg capsule Event: Rash Patient also has allergy to flu vaccine. More
2831094 65 M MA 03/13/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 er8737
er8737
ew0164
ew0164
Amnesia, Brain fog, Disturbance in attention, Fatigue, Gait disturbance; Hypoaes... Amnesia, Brain fog, Disturbance in attention, Fatigue, Gait disturbance; Hypoaesthesia, Muscular weakness, Myalgia, Nervous system disorder, Paraesthesia; Amnesia, Brain fog, Disturbance in attention, Fatigue, Gait disturbance; Hypoaesthesia, Muscular weakness, Myalgia, Nervous system disorder, Paraesthesia More
EXCESSIVE FATIQUE,WEAKNESS IN LEGS.COULD BARELY WALK .NEUROLOGICAL DISORDER.MUSCLE ACHES,TINGLING AN... EXCESSIVE FATIQUE,WEAKNESS IN LEGS.COULD BARELY WALK .NEUROLOGICAL DISORDER.MUSCLE ACHES,TINGLING AND NUMBNESS,,,BRAIN FOG,, LOSS OF MEMORY ,DIFFICULTY CONCENTRATING AND FOCUSING, I COULD BARELY WALK FOR 3 YEARS,UNTIL I STARTED TAKING SPIKE PROTEIN DETOXIFICATION MED. DAILY SAUNAS , DOING A 3 DAY FAST ONCE A MONTH TO GET RID OF IGG4 ANTIBODIES I HAD TO INVESTIGATE WHAT DOCTORS IN (REDACTED) WERE DOING FOR THEIR PATIENTS.TO DETOXIFY SPIKE PROTEIN AND IGG4 ANTIBODIES More
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2831095 57 M CA 03/13/2025 RSV
 PFIZER\WYETH
 LG9829
Device connection issue, Product preparation issue, Syringe issue Device connection issue, Product preparation issue, Syringe issue
5-6 faulty RSV vaccines since we started administering them in the clinic. The lurelock on the kit f... 5-6 faulty RSV vaccines since we started administering them in the clinic. The lurelock on the kit falls off when attempting to attach to the vial adapter and does not attach to the syringe/diluent porting of the vaccine in order to mix the solution resulting in inadequate mixing of the RSV vaccine and leaking More
2831096 16 M NM 03/13/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 99G34
Syringe issue Syringe issue
While I was trying to remove air from syringe of Men B vaccine Bexsero, the liquid kept seeping out ... While I was trying to remove air from syringe of Men B vaccine Bexsero, the liquid kept seeping out of the syringe. It was not able to remove the air and was left with only half a dose of the vaccine. This vaccine was not given to this pt. and was report as wasted. More
2831097 MI 03/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 KB2YT
Liquid product physical issue Liquid product physical issue
When Shingrix Lyophilized component was being reconstituted, a black particulate was noticed in the ... When Shingrix Lyophilized component was being reconstituted, a black particulate was noticed in the vial. Vial was not used or administered on a patient, but segregated from inventory and a new vial was used. More
2831131 58 M TX 03/13/2025 COVID19
FLU3
 MODERNA
GLAXOSMITHKLINE BIOLOGICALS

Atrial fibrillation, Deep vein thrombosis, Pulmonary embolism; Atrial fibrillati... Atrial fibrillation, Deep vein thrombosis, Pulmonary embolism; Atrial fibrillation, Deep vein thrombosis, Pulmonary embolism More
the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/b... the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmo; the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmon; I developed what turned out to be a DVT blood clot in my left calf/deep vein thrombosis (DVT) in the left calf/one week later, they developed a deep vein thrombosis (DVT) in the left calf; This spontaneous case was reported by a patient and describes the occurrence of PULMONARY EMBOLISM (the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmo), DEEP VEIN THROMBOSIS (I developed what turned out to be a DVT blood clot in my left calf/deep vein thrombosis (DVT) in the left calf/one week later, they developed a deep vein thrombosis (DVT) in the left calf) and ATRIAL FIBRILLATION (the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmon) in a 58-year-old male patient who received mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) for COVID-19 prophylaxis. Co-suspect product included non-company product Influenza vaccine inact split 3v (Fluarix) for an unknown indication. Previously administered products included for Product used for unknown indication: Pfizer BioNTech COVID-19 vaccine (Patient previously always had Pfizer). Past adverse reactions to the above products included No adverse effect with Pfizer BioNTech COVID-19 vaccine. Concomitant products included Docosahexaenoic acid, Eicosapentaenoic acid (Omega-3) for an unknown indication. On 15-Nov-2024, the patient received dose of mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) (Intramuscular use) 1 dosage form and dose of Influenza vaccine inact split 3v (Fluarix) (unknown route) 1 dosage form. In November 2024, the patient experienced DEEP VEIN THROMBOSIS (I developed what turned out to be a DVT blood clot in my left calf/deep vein thrombosis (DVT) in the left calf/one week later, they developed a deep vein thrombosis (DVT) in the left calf) (seriousness criteria hospitalization and medically significant). In January 2025, the patient experienced ATRIAL FIBRILLATION (the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmon) (seriousness criteria hospitalization and medically significant). On 17-Jan-2025, after starting mRNA-1273.712 (SPIKEVAX 2024-2025 PFS), the patient experienced PULMONARY EMBOLISM (the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmo) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from 22-Jan-2025 to 27-Jan-2025 due to ATRIAL FIBRILLATION, DEEP VEIN THROMBOSIS and PULMONARY EMBOLISM. At the time of the report, PULMONARY EMBOLISM (the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmo), DEEP VEIN THROMBOSIS (I developed what turned out to be a DVT blood clot in my left calf/deep vein thrombosis (DVT) in the left calf/one week later, they developed a deep vein thrombosis (DVT) in the left calf) and ATRIAL FIBRILLATION (the blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/blood clot moved to my lungs becoming a pulmonary embolism (my heart also then went into Afib)/the blood clot moved to the lungs, resulting in a pulmon) had not resolved. Patient was not allergic to any medications, food or other products. Patient treatment medication included M.E.E.S 50 plus once a day for product used for unknown indication. Patient was first time received Moderna Covid-19 vaccination as booter dose. Approximately one-week later post vaccination patient was developed a deep vein thrombosis (DVT) in the left calf. In January, the blood clot was moved to the lungs for patient, which caused a pulmonary embolism and atrial fibrillation for patient. Patient was developed a pulmonary embolism on 17-Jan-2025 in AM. Patient was hospitalized for five days from 22-Jan-2025 to 27-Jan-2025 and he went through a catheter-based clot removal, and since then patient was on unspecified blood thinners and beta blocker as a treatment medication. Due to symptom patient wear compression socks. Reporter was stated that blood clot and Covid booster felt like the only possibility as a cause. A hematology consultation was scheduled for further evaluation for patient. Most recent FOLLOW-UP information incorporated above includes: On 18-Feb-2025: Live Significant follow up added in which country of incident, Country in which Event Occurred, suspect drug coding, co-suspect drug coding, reported reaction, Reporter causality was updated. New reference number was added. On 18-Feb-2025: Live non-significant follow up was received and new reference number was added. On 27-Feb-2025: Significant follow-up received in which primary reporter detail was updated, and secondary reporter detail was added, patient demography was updated (Patient initial, age, height, weight, race, ethnic group, Suspect and co-suspect product vaccination site of administration was added, new concomitant medication was added nature made omega 3 and M.E.E.S 50 plus. Event outcome for the event of Deep vein thrombosis Atrial fibrillation and Pulmonary embolism was updated. For all the reported event seriousness was updated as Hospitalized and Medically Significant. Event onset date for the event Pulmonary embolism and Atrial fibrillation was updated. Case narrative was updated. On 28-Feb-2025: Live non-significant follow-up received in which other manufacturer Reference number was added.; Reporter's Comments: Concomitant Fluarix remains as a confounder. The benefit-risk relationship of mRNA-1273 (Spikevax) vaccine is not affected by this report. More
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2831173 52 F MI 03/13/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Injected limb mobility decreased, Nerve conduction studies, Pain, Pain in extrem... Injected limb mobility decreased, Nerve conduction studies, Pain, Pain in extremity, Ultrasound scan; X-ray More
pain in left arm , sharp shooting pain down arm. unable to use arm like before. being continually ... pain in left arm , sharp shooting pain down arm. unable to use arm like before. being continually getting worse. More
2831174 0.17 M AR 03/13/2025 DTPPVHBHPB
PNC15
RV1
 MSP VACCINE COMPANY
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 U7921AA
Y005351
HP495
Extra dose administered; Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered; Extra dose administered
Patient had 2 vaccine records in our IIS, they each had different last names and different spelling ... Patient had 2 vaccine records in our IIS, they each had different last names and different spelling of first name. Patient then received a second dose of RSV Beyfortus in error. First dose given on 01/31/2025 and second dose given on 03/11/2025. More
2831175 0.5 F MI 03/13/2025 DTAPIPVHIB
HEP
PNC20
RV5
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.
 UK149AB
LG749
LX2497
Y014317
Contraindication to vaccination, No adverse event; Contraindication to vaccinati... Contraindication to vaccination, No adverse event; Contraindication to vaccination, No adverse event; Contraindication to vaccination, No adverse event; Contraindication to vaccination, No adverse event More
NO ADVERSE EVENT OCCURRED. DUE TO THE PATIENT'S HEALTH HISTORY, IT WAS MEDICALLY CONTRAINDICATE... NO ADVERSE EVENT OCCURRED. DUE TO THE PATIENT'S HEALTH HISTORY, IT WAS MEDICALLY CONTRAINDICATED THAT THE PATIENT RECEIVE THE ROTAVIRUS VACCINE. More
2831176 4 F LA 03/13/2025 MMRV
 MERCK & CO. INC.
 Y018154
Injection site erythema Injection site erythema
patient developed redness around the injection site one day after the injection was given. MD exami... patient developed redness around the injection site one day after the injection was given. MD examined the patient and prescribed Prednisolone. More
2831177 0.25 M TN 03/13/2025 DTAPHEPBIP
HIBV
PNC20
RV1
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 D252F
Y00000000000000
LJ5282
5N2AN
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 noted or reported adverse events thus far No noted or reported adverse events thus far
2831178 69 F MI 03/13/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 LP1776
LP1776
Arthralgia, Chills, Condition aggravated, Fibromyalgia, Joint swelling; Migraine... Arthralgia, Chills, Condition aggravated, Fibromyalgia, Joint swelling; Migraine, Nausea, Pain, Pyrexia More
Side effects: Fever lasting 5 days, peaking at 101.3, chills, very bad body aches, joint pain/swelli... Side effects: Fever lasting 5 days, peaking at 101.3, chills, very bad body aches, joint pain/swelling(Fingers so swollen I could not make a fist.) Nausea, Headache causing a series of migraines. All triggering a new fibromyalgia flare. More
2831179 3 F MI 03/13/2025 FLU3
 SANOFI PASTEUR
 U8465CA
Extra dose administered Extra dose administered
Extra dose given. Patient get Influenza vaccine on 10-16-2024, did not need second dose for this se... Extra dose given. Patient get Influenza vaccine on 10-16-2024, did not need second dose for this season. More
2831180 33 F FL 03/13/2025 COVID19
 PFIZER\BIONTECH
 EW0161
Anti-thyroid antibody increased, Blood thyroid stimulating hormone increased Anti-thyroid antibody increased, Blood thyroid stimulating hormone increased
Lab results of TSH 8.4c and Thyroid Peroxidase Antibodies 462. Lab results of TSH 8.4c and Thyroid Peroxidase Antibodies 462.
2831181 80 F TN 03/13/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 unknown
Condition aggravated, Cough, Dyspnoea Condition aggravated, Cough, Dyspnoea
Re-exacerbation of her chronic cough and shortness of breath Re-exacerbation of her chronic cough and shortness of breath
2831182 61 F AL 03/13/2025 COVID19
COVID19
 MODERNA
MODERNA
 023M20A
003B21A
Chemotherapy, Endometrial cancer, Hysterectomy; Chemotherapy, Endometrial cancer... Chemotherapy, Endometrial cancer, Hysterectomy; Chemotherapy, Endometrial cancer, Hysterectomy More
Patient was diagnosed with endometrial cancer on 8/11/21. She had a complete hysterectomy and 6 rou... Patient was diagnosed with endometrial cancer on 8/11/21. She had a complete hysterectomy and 6 rounds of chemotherapy. She is currently cancer free. More
2831183 64 F IN 03/13/2025 COVID19
FLU3
 UNKNOWN MANUFACTURER
SEQIRUS, INC.

Chest pain, Dyspnoea, Palpitations; Chest pain, Dyspnoea, Palpitations Chest pain, Dyspnoea, Palpitations; Chest pain, Dyspnoea, Palpitations
pt says after getting the vaccines she came home and within an hour her heart started thumping and s... pt says after getting the vaccines she came home and within an hour her heart started thumping and she began having chest pains. She felt as if she couldn't breath. She thought she was having a heart attack so she used her inhaler. This helped her breath and calmed her down. She was scared and thought she was going to die. She went to bed and stayed there that night and the next day. She feels as is if it is an allergic reaction from the vaccine so will not be taking any more. She contacted her pharmacy and was told it maybe the norovirus that caused her to feel this way. She went to her physicians office and was told it was from the covid vaccine. She was given steroids and refilled albuterol. She continues to have breathing issues. More
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2831184 54 M CA 03/13/2025 TDAP
 SANOFI PASTEUR
 U8352AA
Arthralgia, Joint range of motion decreased, Mobility decreased, Muscle spasms Arthralgia, Joint range of motion decreased, Mobility decreased, Muscle spasms
Member reports pain in shoulder since last vaccine. Member reports pain has been constant since that... Member reports pain in shoulder since last vaccine. Member reports pain has been constant since that appt. ROM is limited at times. And at random times he has spasms and pain. Some times he cannot lift his groceries or rise his hand above his head More
2831186 11 F FL 03/13/2025 DTAP
 SANOFI PASTEUR
Erythema, Pain in extremity, Peripheral swelling, Pruritus Erythema, Pain in extremity, Peripheral swelling, Pruritus
Left arm sore, red, swollen, painful, itchy Left arm sore, red, swollen, painful, itchy
2831187 67 F IA 03/13/2025 RSV
RSV
RSV
RSV
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 LG9829
LG9829
LG9829
LG9829
Abdominal pain upper, Diarrhoea, Dizziness, Dysstasia, Nausea; Diarrhoea, Dizzin... Abdominal pain upper, Diarrhoea, Dizziness, Dysstasia, Nausea; Diarrhoea, Dizziness, Muscle spasms, Nausea; Abdominal pain upper, Diarrhoea, Dizziness, Dysstasia, Nausea; Diarrhoea, Dizziness, Muscle spasms, Nausea More
Extreme dizziness - couldn't stand up w/o feeling like I was going to pass out. Nausea, diarrh... Extreme dizziness - couldn't stand up w/o feeling like I was going to pass out. Nausea, diarrhea, stomach cramps. Dizziness and diarrhea continued the next day. Shot was on Tuesday and symptoms continued thru Wednesday. More
2831189 78 F RI 03/13/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3X97J
Dyspnoea, Vision blurred Dyspnoea, Vision blurred
PATIENT CLAIMS SHE HAD BLURRED VISION AND CONSTRICTED BREATHING FOR 36 HOURS AFTER VACCINE. SHE DID ... PATIENT CLAIMS SHE HAD BLURRED VISION AND CONSTRICTED BREATHING FOR 36 HOURS AFTER VACCINE. SHE DID NOT REPORT TO ANY MEDICAL PROFESSIONAL More
2831190 3 F MD 03/13/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Wrong product administered Wrong product administered
Patient mistakenly received the Tdap vaccine instead of the ordered Dtap. Patient mistakenly received the Tdap vaccine instead of the ordered Dtap.
2831191 56 M NY 03/13/2025 HPV9
HPV9
HPV9
HPV9
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 Y013469
Y013469
Y013469
Y013469
Arthralgia, Balance disorder, Body temperature decreased, Dizziness, Eye irritat... Arthralgia, Balance disorder, Body temperature decreased, Dizziness, Eye irritation; Eye pruritus, Headache, Inflammation, Loss of control of legs, Muscular weakness; Ocular discomfort, Oropharyngeal pain, Pharyngeal swelling, Pyrexia, Tenderness; Vision blurred More
I noticed first i was a little dizzy and i had some balance issues, I would be walking and this was ... I noticed first i was a little dizzy and i had some balance issues, I would be walking and this was around 10 and i was walking back from the store. And it was bad enough that for a couple mins i had to rest against the wall. The dizziness was in my head but the balance issues was like i wasn't able to control my legs very well. In additional i started having a itchy and burning issues in my eyes and my vision got blurry, and there is a lot of pressure, and they have kept going off and on since then. After 1 am i started having a really bad headache and its not responding to meds, I also have had a swollen and sore throat. The balance issues they have manifested i could be standing somewhere and then my body doesn't wanna continue standing. and my legs just weak, My body temp is low and i am now running a low grade fever. and nothing has been helping bring that down. Inflammation and pain for joint pain. Tenderness on whole body. More
2831192 57 F PA 03/13/2025 UNK
UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER


Arthralgia, Back pain, Blister, Burning sensation, Cerebrovascular accident; Lab... Arthralgia, Back pain, Blister, Burning sensation, Cerebrovascular accident; Laboratory test, Nausea, Oesophagogastroduodenoscopy, Pain in extremity, Rash; Rash pruritic More
pt says she became nauseated and her arm and shoulder area hurt really bad. About a month after tha... pt says she became nauseated and her arm and shoulder area hurt really bad. About a month after that she was hospitalized for a stroke. She was in Hospital (10 days) and then transferred to another hospital (10 days) and then to rehab (1 month) rehab center . She then moved and after a couple of months. She noticed that her body was changing. She then developed blisters and rash on her buttocks and between her legs. She was itching and scratching it. It cleared up eventually. She has pain and burning within the body in her hand, shoulder, back, arm and legs that will not go away. She was given cream meds and pain medication for it but it doesn't help much. She was told to follow up with her doctor and she is going to ask for a specialist. More
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