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
2818768 66 F NY 12/31/2024 COVID19
COVID19
FLU3
FLU3
COVID19
FLU3
 PFIZER\BIONTECH
PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\BIONTECH
SANOFI PASTEUR
 00069-2432-10
00069-2432-10
49281-0124-65
49281-0124-65
LN0591
UT8409DA
Full blood count, Injected limb mobility decreased, Metabolic function test, Pai... Full blood count, Injected limb mobility decreased, Metabolic function test, Pain in extremity, Peripheral swelling; Ultrasound scan; Full blood count, Injected limb mobility decreased, Metabolic function test, Pain in extremity, Peripheral swelling; Ultrasound scan; Injection site pain, Injection site swelling; Injection site pain, Injection site swelling More
Pain and swelling of the right arm progressed and intensified after the first five day of receiving ... Pain and swelling of the right arm progressed and intensified after the first five day of receiving the Influenza vaccine. On 12/18 /24 the pain and swelling intensified more than previous days with limited range of motion. Daily cold compression was started. On 12/ 23/ 24 I was seen by the PCP, an anti-inflammatory medication and an antibiotic was prescribed. On 12/24 24 pain was severe. On 12/25/24 went to ER for relief of pain. Toradol IV given, Lidocaine patch and antibiotic. Pain and swelling has decreased but still continues to be a problem. More
2820755 65 F TN 01/13/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 946626
Extra dose administered Extra dose administered
Patient had previously received Arexvy vaccine on January 6, 2024. Patient had previously received Arexvy vaccine on January 6, 2024.
2820756 70 M TN 01/13/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient previously received Arexvy vaccine on 1/6/2024. Second dose not needed. No side effects re... Patient previously received Arexvy vaccine on 1/6/2024. Second dose not needed. No side effects reported. More
2820757 73 M NM 01/13/2025 COVID19
FLU3
TDAP
 PFIZER\BIONTECH
SEQIRUS, INC.
SANOFI PASTEUR


Dyspnoea, Pain, Pyrexia; Dyspnoea, Pain, Pyrexia; Dyspnoea, Pain, Pyrexia Dyspnoea, Pain, Pyrexia; Dyspnoea, Pain, Pyrexia; Dyspnoea, Pain, Pyrexia
Difficulty breathing, hard time exhaling, felt I couldn't get enough air, 100 degrees fever, a... Difficulty breathing, hard time exhaling, felt I couldn't get enough air, 100 degrees fever, and the usual aches More
2820758 4 M IL 01/13/2025 PNC20
 PFIZER\WYETH
 hr3650
Erythema, Pyrexia, Skin warm, Swelling Erythema, Pyrexia, Skin warm, Swelling
1/7/25 received vaccine, 1/8/25 mom noticed warmth, redness and swelling, took to the ER. 1/9/25 mo... 1/7/25 received vaccine, 1/8/25 mom noticed warmth, redness and swelling, took to the ER. 1/9/25 mom called for a follow up due to no improvement and low grade fever. 1/10/25 mom called said swelling and fever gone and feeling better canelled appt. More
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2820459 36 F PA 01/12/2025 FLU3
 SEQIRUS, INC.
 aw1620a
Diarrhoea, Nausea Diarrhoea, Nausea
Patient returned to the clinic 2 hours after receiving the vaccine claiming she had diarrhea and nau... Patient returned to the clinic 2 hours after receiving the vaccine claiming she had diarrhea and nausea. No other complaints. More
2820460 68 F FL 01/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52Z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received original/first dose of Arexvy on 9/27/23 and received another dose of Arexvy on 11/... Patient received original/first dose of Arexvy on 9/27/23 and received another dose of Arexvy on 11/20/24. Patient reports not experiencing any adverse reaction but is not sure if or what she would have experienced as to what could constitute an adverse reaction. More
2820461 75 M AZ 01/12/2025 UNK
 UNKNOWN MANUFACTURER
 Unknown
Confusional state, Fatigue, Gait disturbance Confusional state, Fatigue, Gait disturbance
1st event (11/24/2024)--Extreme fatigue, greatly reduced gait, mental confusion, inability to compr... 1st event (11/24/2024)--Extreme fatigue, greatly reduced gait, mental confusion, inability to comprehend or remember things, lack of appetite, refusal to drink. 2nd event (01/06/2025)- Increased fatigue, reduced gait, mental confusion. Improved rapidly over 1 week. No dehydration. (He refused to drink during the first event) More
2820462 51 F FL 01/12/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Erythema, Induration, Pain, Skin warm Erythema, Induration, Pain, Skin warm
Very sore starting 2 hrs after vaccine. Developed large 7mm x 7 mm red area, hot and hard on 01/12/... Very sore starting 2 hrs after vaccine. Developed large 7mm x 7 mm red area, hot and hard on 01/12/2025. Spoke with pharmacist and he suggested going to a doctor. More
2820463 76 M TX 01/12/2025 COVID19
COVID19
 MODERNA
MODERNA

Cardiac arrest, Chills, Death, Discomfort, Headache; Syncope Cardiac arrest, Chills, Death, Discomfort, Headache; Syncope
? Severe headache occurred 24?48 hours after receiving the Moderna COVID-19 vaccine, described by... ? Severe headache occurred 24?48 hours after receiving the Moderna COVID-19 vaccine, described by the patient as ?the worst headache since 2015.? ? He experienced chills and severe discomfort the day after the vaccination. ? The headache persisted despite resting, leading the family to contact his doctor. The doctor prescribed Butalbital/Acetaminophen/Caffeine (for headaches) but did not advise him to go to the emergency room and did not see him in person. The medication was prescribed via phone. ? Despite taking the prescribed medication, his headache slightly improved but never fully subsided, and his overall discomfort continued. ? On the morning of September 14, 2024, he collapsed in the garage and passed away due to sudden cardiac arrest. ? Medical History: ? Prior to the vaccination, the patient was healthy and physically active, managing hypertension with medication. ? Regular cardiology visits confirmed no history of heart disease or cardiovascular complications. ? The coroner indicated hypertension as a contributing factor, but this was well-managed, and the patient had no clinical signs of heart disease prior to vaccination. ? Outcome: Death. More
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2820464 40 F TN 01/12/2025 COVID19
 MODERNA
Anaphylactic reaction, Food allergy Anaphylactic reaction, Food allergy
Developed a fish and shellfish allergy that is anaphylactic. Developed a fish and shellfish allergy that is anaphylactic.
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2820465 63 F FL 01/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
Patient received second dose of Arexvy on 12/30/2024. Previous dose was administered on 01/31/2024. ... Patient received second dose of Arexvy on 12/30/2024. Previous dose was administered on 01/31/2024. Unable to reach patient to gather adverse reactions. More
2820467 80 F OH 01/12/2025 FLU3
 SANOFI PASTEUR
Headache, Rash, Rash macular, Skin warm, Swelling face Headache, Rash, Rash macular, Skin warm, Swelling face
Headache. Temperature 100๏ฟฝ Cheeks swollen and red hot blotches also on forehead and temples. Calle... Headache. Temperature 100๏ฟฝ Cheeks swollen and red hot blotches also on forehead and temples. Called pharmacy told to use Benadryl. Did so. 2 doses in 24 hours. Less red and swollen today. Head feels better as well More
2820468 77 M ME 01/12/2025 COVID19
COVID19
 MODERNA
MODERNA

Computerised tomogram abdomen abnormal, Computerised tomogram head abnormal, Com... Computerised tomogram abdomen abnormal, Computerised tomogram head abnormal, Computerised tomogram thorax, Iliac artery occlusion, Intraventricular haemorrhage; Leg amputation, Peripheral ischaemia, Pulmonary embolism, Scan with contrast abnormal, Subarachnoid haemorrhage More
ADMTITED TO HOSPITAL 1/2/25 WITH ACUTE LEFT LEG ISCHEMIA NECESSITATING LEFT ABOVE KNEE AMPUTATION DE... ADMTITED TO HOSPITAL 1/2/25 WITH ACUTE LEFT LEG ISCHEMIA NECESSITATING LEFT ABOVE KNEE AMPUTATION DESPITE HAVING BEEN ON SYSTEMIC ANTICOAGULATION FOR ATRIAL FIBRILLATION. SUFFERED BRAIN HEMORRHAGE 1/10/25 WITH INTRAVENTICULAR HEMORRHAGE, UNCLEAR ETIOLOGY. WAS NOT TAKING HIS ANTICOAGULATION AT THE TIME. COURSE COMPLICATED BY LEFT UPPER AND LOWER LOBE PULMONARY EMBOLI. More
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2820469 65 F AZ 01/12/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH

Abdominal pain upper, Ageusia, Chest X-ray, Cough, Decreased appetite; Feeling c... Abdominal pain upper, Ageusia, Chest X-ray, Cough, Decreased appetite; Feeling cold, Haematochezia, Pain More
Emergency room 1-1-2025. Blood in stools. Pain in stomach. Coughing. Aches. Chills. Loss of appeti... Emergency room 1-1-2025. Blood in stools. Pain in stomach. Coughing. Aches. Chills. Loss of appetite. Can taste. More
2820470 62 M WA 01/12/2025 COVID19
 PFIZER\BIONTECH
Arthralgia, Depression, Muscle atrophy Arthralgia, Depression, Muscle atrophy
Severe depression, in April 17 2021, chronic joint pain and mussel degeneration 07/24 Severe depression, in April 17 2021, chronic joint pain and mussel degeneration 07/24
2820471 80 M FL 01/12/2025 PNC20
 PFIZER\WYETH
 LC5482
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received Prevnar 20 on 12/26/23 and again on 1/8/25. Patient did not need the second dose bu... Patient received Prevnar 20 on 12/26/23 and again on 1/8/25. Patient did not need the second dose but was given because patient requested it. He experienced no adverse effects per his report. More
2820472 67 M NM 01/12/2025 COVID19
 PFIZER\BIONTECH
 LM7786
Injection site erythema Injection site erythema
patient reported redness around the area of injection patient reported redness around the area of injection
2820473 69 F FL 01/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Erythema, Pain, Wound necrosis Erythema, Pain, Wound necrosis
PATIENT HAS A WOUND APPROXIMATELY AN INCH AND A HALF WIDE THAT APPEARS NECROTIC IN THE MIDDLE AND IS... PATIENT HAS A WOUND APPROXIMATELY AN INCH AND A HALF WIDE THAT APPEARS NECROTIC IN THE MIDDLE AND IS RED AND IRRITATED ON THE EXTERIOR BORDER. Patient REPORTS SEVERE PAIN IN AREA SINCE INJECTION. More
2820474 75 M FL 01/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255t2
Extra dose administered, Pain in extremity Extra dose administered, Pain in extremity
Patient received a second dose of RSV outside of current CDC guidelines. His first dose was 9/11/23... Patient received a second dose of RSV outside of current CDC guidelines. His first dose was 9/11/23, second dose was 1/7/25. Patient reports no adverse effects outside of arm soreness. Pharmacist went over signs and symptoms of Guillain-Barre syndrome due to new labeling. Patient denied any symptoms, stating he "feels fine." Reporting due to pharmacy policy to report such an event. More
2820475 39 F FL 01/12/2025 COVID19
COVID19
 MODERNA
MODERNA

Amnesia, Autoimmune disorder, Blood test abnormal, Fatigue, Impaired work abilit... Amnesia, Autoimmune disorder, Blood test abnormal, Fatigue, Impaired work ability; Migraine, Vomiting More
Started vomiting in September up to 17 x a day developed multiple autoimmune diseases have no memory... Started vomiting in September up to 17 x a day developed multiple autoimmune diseases have no memory of two years of my life have chronic migraines chronic fatigue can not work More
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2820476 75 F FL 01/12/2025 COVID19
 PFIZER\BIONTECH
 LT5636
Haemorrhage Haemorrhage
PATIENT HAD MORE BLEEDING THAN TYPICAL PATIENT HAD MORE BLEEDING THAN TYPICAL
2820498 66 F 01/12/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Erythema, Nodule, Pain in extremity, Skin warm Erythema, Nodule, Pain in extremity, Skin warm
Arm redness and warmth with pain, palpable nodule below skin, did not resolve after supportive measu... Arm redness and warmth with pain, palpable nodule below skin, did not resolve after supportive measures, required antibiotics for improvement More
2820499 29 M NY 01/12/2025 COVID19
 PFIZER\BIONTECH
 LP1780
Oral mucosal erythema, Oral pain, Palatal swelling Oral mucosal erythema, Oral pain, Palatal swelling
Swelling and pain in the right posterior palate area, accompanied by erythema Swelling and pain in the right posterior palate area, accompanied by erythema
2820500 79 F WA 01/12/2025 FLU3
 SANOFI PASTEUR
 tfaa2437
Dizziness, Gait disturbance Dizziness, Gait disturbance
Patient called 01/12/25 at 2:38pm stating that she is feeling dizzy and trouble walking. She thinks... Patient called 01/12/25 at 2:38pm stating that she is feeling dizzy and trouble walking. She thinks it is from the flu shot. She thinks its from mercury in the shot. I explained that we used a preservative free vaccine. She asked how often she gets the flus shot and her history shows she has gotten one every year for the at least the past four years. I told her to get checked out at the urgent care or emergency department. More
2820501 73 F AL 01/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 j9493
Fatigue, Loss of personal independence in daily activities, Pyrexia Fatigue, Loss of personal independence in daily activities, Pyrexia
patient said she started running a fever the next day and was very tired for 3 to 4 days after recei... patient said she started running a fever the next day and was very tired for 3 to 4 days after receiving vaccine. She stated she would have to rest and take breaks while doing normal daily tasks. More
2820502 36 M CO 01/12/2025 COVID19
FLU3
TDAP
 MODERNA
SANOFI PASTEUR
SANOFI PASTEUR
 8080799
TFAA2437
U8231AA
Dizziness, Pallor, Presyncope; Dizziness, Pallor, Presyncope; Dizziness, Pallor,... Dizziness, Pallor, Presyncope; Dizziness, Pallor, Presyncope; Dizziness, Pallor, Presyncope More
Patient had a vasovagal reaction following the administration of 3 vaccines (Moderna Covid, Flublok ... Patient had a vasovagal reaction following the administration of 3 vaccines (Moderna Covid, Flublok & Adacel). He did not completely pass out, but did feel faint, dizzy, pale. Provided the patient with cold water, a cool cloth and some sugar and he recovered within about 10 minutes. Patient didn't report a history of vasovagal reaction in the past, but said that he hadn't eaten anything that morning. More
2820503 76 M CA 01/12/2025 COVID19
TDAP
 MODERNA
SANOFI PASTEUR

Arthritis, Neck pain, Paraesthesia; Arthritis, Neck pain, Paraesthesia Arthritis, Neck pain, Paraesthesia; Arthritis, Neck pain, Paraesthesia
pain and tingling from front of right shoulder to right rear of head. Over a period of several weeks... pain and tingling from front of right shoulder to right rear of head. Over a period of several weeks, the pain decreased, and the tingling in the head stopped. More than two months later, the tingling continues sporadically from the front of right shoulder to back of neck. Doctor felt it was unrelated to the injection, but recommended heat, which occasionally provided temporary relief. More
2820509 53 F FL 01/12/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 E3XT9
Extra dose administered Extra dose administered
Third dose of vaccine administered; recommended vaccine schedule is only for 2 doses Third dose of vaccine administered; recommended vaccine schedule is only for 2 doses
2820410 F 01/11/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
Exposure during pregnancy, Product use issue Exposure during pregnancy, Product use issue
Received HEPLISAV-B while pregnant; Initial report received on 27-Nov-2024. The report was initia... Received HEPLISAV-B while pregnant; Initial report received on 27-Nov-2024. The report was initially received from the HEPLISAV-B Pregnancy Registry. A pharmacist reported that a female (age, race, and ethnicity not provided) received HEPLISAV-B (hepatitis B vaccine) for hepatitis B immunization while pregnant. Medical history, allergies, and concomitant medications were not reported. The last menstrual period date, pregnancy history, and pregnancy risk factors were not reported. On an unknown date, the patient received an unknown dose of HEPLISAV-B (lot #, expiration date, NDC #, site and route not reported) while pregnant. No other details were specified. The outcome of the event was unknown. The pregnancy registry was closed to new patients at the time of reporting. Company Comment: The company assessed the event as non-serious.; Sender's Comments: The company assessed the event as non-serious. More
2820411 F TN 01/11/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 943008
Discomfort Discomfort
Gave a Dose of HEPLISAV-B Which was Diluted with a Dose of MMR2; Injection "Felt Heavy"; I... Gave a Dose of HEPLISAV-B Which was Diluted with a Dose of MMR2; Injection "Felt Heavy"; Initial report received on 09-Dec-2024. A pharmacist reported that a 22-year-old female received HEPLISAV-B (hepatitis B vaccine) for hepatitis B immunization that had been diluted with a dose of measles, mumps, and rubella vaccine (MMR2) and then said the injection "felt heavy." No medical history or concomitant medications were reported. On 08-Dec-2024, the patient received a dose of a hepatitis B vaccine [HEPLISAV-B (lot number 943008, expiration date 20-Sep-2025, and NDC number 43528-0003-05)] intramuscularly in the left deltoid. The dose of HEPLISAV-B that had been diluted with a dose of MMR2. The patient stated that the injection "felt heavy" after injection. No other information was available. Company Comment: The company assessed the events as non-serious.; Sender's Comments: The company assessed the events as non-serious. More
2820419 71 F OR 01/11/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 4BN95
Discomfort, Erythema, Mass, Pruritus, Skin warm Discomfort, Erythema, Mass, Pruritus, Skin warm
3-4" round skin discoloration (red), a bit "hot" to touch; the red area is itchy and ... 3-4" round skin discoloration (red), a bit "hot" to touch; the red area is itchy and a little bit uncomfortable; there is a lump under the skin where the skin is red. This redness and lump have not resolved as of today (1/10/2025) -- 11 days and counting. More
2820420 25 F TX 01/11/2025 COVID19
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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
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
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6199
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
EN6207
Activated partial thromboplastin time shortened, Alanine aminotransferase normal... Activated partial thromboplastin time shortened, Alanine aminotransferase normal, Albumin globulin ratio decreased, Antiphospholipid antibodies negative, Antithrombin III; Aspartate aminotransferase normal, Basophil count decreased, Basophil percentage decreased, Beta-2 glycoprotein antibody negative, Blood albumin normal; Blood alkaline phosphatase normal, Blood bilirubin normal, Blood calcium decreased, Blood chloride normal, Blood creatinine normal; Blood glucose normal, Blood potassium normal, Blood sodium normal, Blood urea decreased, Blood urea nitrogen/creatinine ratio; Bronchoscopy abnormal, Carbon dioxide normal, Cardiolipin antibody negative, Coagulation factor V level normal, Computerised tomogram; Computerised tomogram abnormal, Computerised tomogram thorax, Deep vein thrombosis, Delivery, Eosinophil count decreased; Eosinophil percentage decreased, Full blood count, Globulins increased, Glomerular filtration rate normal, Haematocrit normal; Haemoglobin normal, Immature granulocyte count, Inflammation, Laboratory test, Lung opacity; Lymphocyte count normal, Maternal exposure before pregnancy, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal; Mean platelet volume normal, Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage decreased; Peripheral swelling, Platelet count normal, Pneumonia, Protein C, Protein S normal; Protein total normal, Prothrombin level, Prothrombin level normal, Red blood cell count normal, Red blood cell nucleated morphology; Red cell distribution width normal, Russell's viper venom time abnormal, Scan with contrast, Skin discolouration, Superficial vein thrombosis; Ultrasound Doppler abnormal, White blood cell count normal; Activated partial thromboplastin time shortened, Alanine aminotransferase normal, Albumin globulin ratio decreased, Antiphospholipid antibodies negative, Antithrombin III; Aspartate aminotransferase normal, Basophil count decreased, Basophil percentage decreased, Beta-2 glycoprotein antibody negative, Blood albumin normal; Blood alkaline phosphatase normal, Blood bilirubin normal, Blood calcium decreased, Blood chloride normal, Blood creatinine normal; Blood glucose normal, Blood potassium normal, Blood sodium normal, Blood urea decreased, Blood urea nitrogen/creatinine ratio; Bronchoscopy abnormal, Carbon dioxide normal, Cardiolipin antibody negative, Coagulation factor V level normal, Computerised tomogram; Computerised tomogram abnormal, Computerised tomogram thorax, Deep vein thrombosis, Delivery, Eosinophil count decreased; Eosinophil percentage decreased, Full blood count, Globulins increased, Glomerular filtration rate normal, Haematocrit normal; Haemoglobin normal, Immature granulocyte count, Inflammation, Laboratory test, Lung opacity; Lymphocyte count normal, Maternal exposure before pregnancy, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal; Mean platelet volume normal, Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage decreased; Peripheral swelling, Platelet count normal, Pneumonia, Protein C, Protein S normal; Protein total normal, Prothrombin level, Prothrombin level normal, Red blood cell count normal, Red blood cell nucleated morphology; Red cell distribution width normal, Russell's viper venom time abnormal, Scan with contrast, Skin discolouration, Superficial vein thrombosis; Ultrasound Doppler abnormal, White blood cell count normal; Activated partial thromboplastin time shortened, Alanine aminotransferase normal, Albumin globulin ratio decreased, Antiphospholipid antibodies negative, Antithrombin III; Aspartate aminotransferase normal, Basophil count decreased, Basophil percentage decreased, Beta-2 glycoprotein antibody negative, Blood albumin normal; Blood alkaline phosphatase normal, Blood bilirubin normal, Blood calcium decreased, Blood chloride normal, Blood creatinine normal; Blood glucose normal, Blood potassium normal, Blood sodium normal, Blood urea decreased, Blood urea nitrogen/creatinine ratio; Bronchoscopy abnormal, Carbon dioxide normal, Cardiolipin antibody negative, Coagulation factor V level normal, Computerised tomogram; Computerised tomogram abnormal, Computerised tomogram thorax, Deep vein thrombosis, Delivery, Eosinophil count decreased; Eosinophil percentage decreased, Full blood count, Globulins increased, Glomerular filtration rate normal, Haematocrit normal; Haemoglobin normal, Immature granulocyte count, Inflammation, Laboratory test, Lung opacity; Lymphocyte count normal, Maternal exposure before pregnancy, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal; Mean platelet volume normal, Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage decreased; Peripheral swelling, Platelet count normal, Pneumonia, Protein C, Protein S normal; Protein total normal, Prothrombin level, Prothrombin level normal, Red blood cell count normal, Red blood cell nucleated morphology; Red cell distribution width normal, Russell's viper venom time abnormal, Scan with contrast, Skin discolouration, Superficial vein thrombosis; Ultrasound Doppler abnormal, White blood cell count normal; Activated partial thromboplastin time shortened, Alanine aminotransferase normal, Albumin globulin ratio decreased, Antiphospholipid antibodies negative, Antithrombin III; Aspartate aminotransferase normal, Basophil count decreased, Basophil percentage decreased, Beta-2 glycoprotein antibody negative, Blood albumin normal; Blood alkaline phosphatase normal, Blood bilirubin normal, Blood calcium decreased, Blood chloride normal, Blood creatinine normal; Blood glucose normal, Blood potassium normal, Blood sodium normal, Blood urea decreased, Blood urea nitrogen/creatinine ratio; Bronchoscopy abnormal, Carbon dioxide normal, Cardiolipin antibody negative, Coagulation factor V level normal, Computerised tomogram; Computerised tomogram abnormal, Computerised tomogram thorax, Deep vein thrombosis, Delivery, Eosinophil count decreased; Eosinophil percentage decreased, Full blood count, Globulins increased, Glomerular filtration rate normal, Haematocrit normal; Haemoglobin normal, Immature granulocyte count, Inflammation, Laboratory test, Lung opacity; Lymphocyte count normal, Maternal exposure before pregnancy, Mean cell haemoglobin concentration normal, Mean cell haemoglobin normal, Mean cell volume normal; Mean platelet volume normal, Monocyte count normal, Monocyte percentage, Neutrophil count normal, Neutrophil percentage decreased; Peripheral swelling, Platelet count normal, Pneumonia, Protein C, Protein S normal; Protein total normal, Prothrombin level, Prothrombin level normal, Red blood cell count normal, Red blood cell nucleated morphology; Red cell distribution width normal, Russell's viper venom time abnormal, Scan with contrast, Skin discolouration, Superficial vein thrombosis; Ultrasound Doppler abnormal, White blood cell count normal More
A month after taking my second dose of Pfizer Covid-19 Vaccine I noticed a brown spot on the right l... A month after taking my second dose of Pfizer Covid-19 Vaccine I noticed a brown spot on the right lower leg. I thought that this was just a discoloration, or possibly a skin issue. These brown spots kept growing over time and they started apearing on the left leg too. I got pregnant with my second baby in august and I discussed my concern of the legs with my OBG/YN but he said they are not very noticeable and it could be nothing. However, these brown spots kept growing and I started having inflammation on my lower legs, therefore after the delivery in June 2022, I talked again to my OBGYN that I need to see some doctor regarding at this time swollen, inflamed spots and brown patches all over my lower legs. My OBGYN referred me to see Dr. (a vein specialist) and I was able to see him in December 2022. His assessment said that I had Superficial Vein Thrombosis and he suggested that I get an assessment from a hematologist since the SVT were very large for a young patient like me, and that he suspected occult malignancy. I was seen by Hematology in June 2023, they have done a series or Labs and a Doppler bilateral which revealed left peroneal vein thrombosis. I was put on Eliquis 5MG twice a day for 3 months and repeated the left leg doppler in 3 months. After three months there were no improvements, therefore I was recommended to stop Eliquis and get seen by my vein specialist. After going back to the vein doctor, I was suggested to get another assessment by hematology as well as take Xarelto 20mg, and I was referred to M.D. I saw Dr in December 2023. He suggested that I do some more labs and get a CAT Scan, also treat my DVT with XARELTO 20mg for 1 year. I got my CAT Scan done in December 26, 2023 3hich showed no obvious evidence of any malignancy. There was a small groundglass opacity in the right upper lobe. The hematologist recommended that I repeat my CAT Scan in 2024, which i did. The second CAT Scan done in October 2024 showed a growing groundglass opacity in the right upper lobe. At this time the hematologist suggested that I get seen by a Pulmonology immediately, and that I stop Xarelto in a month. I saw a pulmonary specialist the after three days, and he advised me to have a ION lung bronchoscopy done as soon as possible, and find out what is on my lung. I had my lung bronchoscopy done in 11/20/24 at clinic which revealed a lung infection due to unknown reason. The pulmonary specialist said that this infection could have been caused by a virus, but the biopsy cannot defy if a virus is the underlying reason. However, I have always suspected that my blood clots on my superficial veins and later deep vein thrombosis was a result of the COVID-19 Vaccine as I noticed the brown spots which turned to be clots right after i took the Covid-19 vaccine. I have expressed this concern with my OBG/YN doctor, with the vein specialist and later with my hematologist. More
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2820421 89 F FL 01/11/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255t2
Extra dose administered, No adverse event Extra dose administered, No adverse event
patient received rsv vaccine (arexvy) twice. Outside of CDC guidelines. No adverse events patient received rsv vaccine (arexvy) twice. Outside of CDC guidelines. No adverse events
2820423 68 F AL 01/11/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 255T2
Extra dose administered Extra dose administered
Originally Vaccine given 12/23. According to CDC, Pt should not of received another dose at this tim... Originally Vaccine given 12/23. According to CDC, Pt should not of received another dose at this time More
2820424 61 M FL 01/11/2025 PNC20
 PFIZER\WYETH
 LJ5281
Extra dose administered Extra dose administered
PATIENT RECEIVED A SECOND DOSE OF PREVNAR 20... FIRST DOSE WAS IN ANOTHER STATE ON 12/12/2023 AND RE... PATIENT RECEIVED A SECOND DOSE OF PREVNAR 20... FIRST DOSE WAS IN ANOTHER STATE ON 12/12/2023 AND RECIEVED A DUPLICATE/SECOND DOSE ON 01/10/2025. More
2820425 33 M AZ 01/11/2025 COVID19
 MODERNA
 N/A
Blister, Erythema, Herpes zoster, Rash, Scab Blister, Erythema, Herpes zoster, Rash, Scab
Got a herpes zoster outbreak on the first of the new year of 2025 after receiving vaccine on Friday ... Got a herpes zoster outbreak on the first of the new year of 2025 after receiving vaccine on Friday the 27th of December 2024. Went to see primary doctor on 3rd of January 2025 and was quickly diagnosed shingles. Was given Valacyclovir 1 gram tablets 3 times a day for 10 days. Infection is slowly clearing up, spots are still there but the rash, redness and fluid filled blisters are currently gone and is scabbed up. More
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2820426 33 F IL 01/11/2025 HEP
HEP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 95BJ9
95BJ9
No adverse event, Underdose; No adverse event, Underdose No adverse event, Underdose; No adverse event, Underdose
Event: The 33 year-old female patient was inadvertently vaccinated with a pediatric dose of Engerix-... Event: The 33 year-old female patient was inadvertently vaccinated with a pediatric dose of Engerix-B (Hepatitis B Vaccine injectable pre-filled syringe, for intramuscular use) 10mcg 0.5-mL instead of the adult dose which should have been 20 mcg 1 mL. Treatment: When the nurse who administered the vaccine recognized the error, we immediately called up our supervisor to seek guidance and consult of the proper procedure. The CDC immunization resource was reviewed, which indicated that when such an error occurs and is detected while the patient is still present, the remaining dose should be administered or a repeat dose scheduled. The exact wording from the CDC website is as follows: "What you do depends on when the error is identified. If the error is discovered while the person is still in the office, you can administer the other "half" of the Engerix-B dose. If the error is discovered later, the dose should not be counted. The person should be recalled to the office and given a full age-appropriate 1.0 mL repeat dose. The same recommendation would apply if the error was with Recombivax HB." Source: With the approval of our supervisor, a second pediatric dose was administered, as the patient was still in the clinic and remained in stable condition. The patient was informed of the situation, apologized for the error made, and consented to receive the additional dose. The patient and her husband were very understanding and willing to be given another pediatric dose. A second dose of Engerix-B 10mcg, 0.5mL was administered approximately 30 minutes after the first to rectify the mistake. The patient was given a Vaccine Information Sheet (VIS), and assured that the clinic is available to address any follow-up questions or concerns they may have. Outcome: Patient was asymptomatic, and no adverse reactions were noted during the observation period. Patient and husband left the clinic in stable condition. More
2820427 53 M NH 01/11/2025 FLU3
FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
 K72s4
K72s4
K72s4
Anti-ganglioside antibody positive, Asthenia, Dependence on respirator, Dysstasi... Anti-ganglioside antibody positive, Asthenia, Dependence on respirator, Dysstasia, Electromyogram abnormal; Guillain-Barre syndrome, Hypoaesthesia, Impaired work ability, Mobility decreased, Paraesthesia; Quadriplegia, Respiratory failure, Tracheostomy More
developed confirmed guillain-barre syndrome with symptom onset on 12/9/24. He noticed weakness begi... developed confirmed guillain-barre syndrome with symptom onset on 12/9/24. He noticed weakness beginning on 12/9 but was able to go to work. On 12/10 he felt weaker, noticed numbness/tingling, and stayed home from work. When he woke on 12/11 and tried to get out of bed, he slid to the floor and couldn't get up. EMS activated and brought to Hospital, where he had minimal distal movement (could grasp hands and wiggle toes) but otherwise fully plegic. rapidly progressive weakness thereafter that left him quadriplegic with neuromuscular respiratory failure. Today, 1/11/25 he remains a quadriplegic, ventilator dependent with tracheostomy More
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2820428 34 M KY 01/11/2025 COVID19
COVID19
 MODERNA
MODERNA

Biopsy kidney abnormal, Blood albumin decreased, Blood cholesterol increased, Bl... Biopsy kidney abnormal, Blood albumin decreased, Blood cholesterol increased, Blood urine present, Focal segmental glomerulosclerosis; Protein urine present More
Non-genetic primary focal segment glomerulosclerosis (FSGS). Blood i in urine, low albumin, protein ... Non-genetic primary focal segment glomerulosclerosis (FSGS). Blood i in urine, low albumin, protein in urine and new elevated levels of cholesterol. Treatment as consisted of a standard approach with the administration of amino, suppressant such as corticosteroids and cyclosporine treatment.. More
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2820429 43 F MD 01/11/2025 COVID19
 MODERNA
 3044202
Injection site induration, Injection site pain, Injection site rash, Injection s... Injection site induration, Injection site pain, Injection site rash, Injection site swelling, Rash erythematous More
Large very red rash at injection site that appeared about a day later and has gotten redder 2 days l... Large very red rash at injection site that appeared about a day later and has gotten redder 2 days later, significant swelling that is very hard. Pain has receded in second day though still sore. Worst of rash is about 3 inches in diameter. More
2820430 16 F FL 01/11/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.
 lt5636
946614
Loss of consciousness; Loss of consciousness Loss of consciousness; Loss of consciousness
After the patient was given both vaccines, we informed her to stay seated as she seemed concerned, a... After the patient was given both vaccines, we informed her to stay seated as she seemed concerned, after 5-10 minutes of remaining seated she began getting up. I then asked are you feeling okay to go ahead and get up and she responded with a verbal yes. We let them know to tell us if there was anything they needed. About 5 minutes later we were informed that the patient had passed out. More
2820431 4 F TX 01/11/2025 DTAPIPV
DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Eye swelling, Injection site erythema, Injection site reaction, Injection site s... Eye swelling, Injection site erythema, Injection site reaction, Injection site swelling, Ocular hyperaemia; Rash, Ultrasound Doppler normal, Urticaria More
Dtap+IPV (Kinrix/Quadracel) and MMR given in opposite thighs. Patient presented with Left leg swel... Dtap+IPV (Kinrix/Quadracel) and MMR given in opposite thighs. Patient presented with Left leg swelling 2 days after vaccination. Then over the next day had increased swelling and erythema to Left leg. Urticarial rash over left leg down to calf, right leg, and torso. R eye with erythema and swelling. S/p surgery on her eye 3 weeks prior, hard to know if to relate the eye symptoms to this presentation. More
2820432 76 M FL 01/11/2025 FLU3
RSV
 SEQIRUS, INC.
GLAXOSMITHKLINE BIOLOGICALS
 388490
255T2
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
PATIENT RECEIVED TWO SHOTS OF RSV VACCINE MORE THAN TWO YEARS APART. PATIENT GOT FIRST RSV VACCINE M... PATIENT RECEIVED TWO SHOTS OF RSV VACCINE MORE THAN TWO YEARS APART. PATIENT GOT FIRST RSV VACCINE MORE THAN TWO YEAR AGO ON 10/08/2023, PATIENT GOT ANOTHER SHOT ON 1/10/2025...PATIENT DID NOT REPORT ANY ADVERSE EVENT More
2820433 83 F NC 01/11/2025 COVID19
 PFIZER\BIONTECH
 EL9264
Dementia with Lewy bodies, Loss of personal independence in daily activities, Ne... Dementia with Lewy bodies, Loss of personal independence in daily activities, Neurological symptom More
Guillain Barre Syndrome symptoms began first, in May. She all of a sudden could no longer do yard an... Guillain Barre Syndrome symptoms began first, in May. She all of a sudden could no longer do yard and house work. Then neurological symptoms followed and she was diagnosed with Lewy Body Dementia. More
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2820434 70 M 01/11/2025 PNC20
 PFIZER\WYETH
 LC5482
Extra dose administered Extra dose administered
Patient received duplicate vaccine. Original vaccine administered 11/17/23. Re-administered 1/10/25. Patient received duplicate vaccine. Original vaccine administered 11/17/23. Re-administered 1/10/25.
2820435 84 F NC 01/11/2025 COVID19
 PFIZER\BIONTECH
 FJ8757
Condition aggravated, Dementia with Lewy bodies, Fall, Neurological symptom Condition aggravated, Dementia with Lewy bodies, Fall, Neurological symptom
Patient had already been diagnosed with Lewy Body Dementia and she already had Guillain Barre sympto... Patient had already been diagnosed with Lewy Body Dementia and she already had Guillain Barre symptoms. However, her condition worsened after each vaccine. Parkinsons/Lewy Body symptoms led to a fall, which led to hospitalization and move to a care facility. More
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2820436 54 F OH 01/11/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 58160084252
Neuralgia Neuralgia
I had intense nerve pain in the right side of my torso. I had the shingles vaccine in February and ... I had intense nerve pain in the right side of my torso. I had the shingles vaccine in February and May of 2020, but had shingles without the rash in April 2022 and the pain lasted daily until September 2022 and then fully stopped by December 2022. This caused pain in the same area of my right torso. My torso was swollen on that side. I had nerve pain which was intensified by touch. I had some muscle pain, but that was bearable. The pain is still there, but less intense. At its worst, it was an 8 on the pain scale. Currently, it's about a 3. Pain meds helped a very little bit and icing and heat made it worse. I just have to not wear any tighter bands--bras, etc,--in that area and no touch. Exercise does not seem to impact it at all, including shoveling, Jazzercise, or aerial, except yoga made it worse and when the silks hit it in aerial, that's bad. More
2820437 59 M CA 01/11/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3042648
U8440AA
Dermatitis contact, Hypoaesthesia, Injection site bruising, Muscular weakness, P... Dermatitis contact, Hypoaesthesia, Injection site bruising, Muscular weakness, Pain in extremity; Dermatitis contact, Hypoaesthesia, Injection site bruising, Muscular weakness, Pain in extremity More
Patient complaints that he bleed after injection. And after 2-3 days, his right arm is swollen and... Patient complaints that he bleed after injection. And after 2-3 days, his right arm is swollen and pain, numbs and weak. More
2820438 58 F IL 01/11/2025 FLU3
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 JT322
LJ5283
Anaphylactoid reaction, Pruritus, Urticaria, Wheezing; Anaphylactoid reaction, P... Anaphylactoid reaction, Pruritus, Urticaria, Wheezing; Anaphylactoid reaction, Pruritus, Urticaria, Wheezing More
Patient stated she received vaccinations on Monday, 1/6/25 around 5:30pm. Flu was given on top and P... Patient stated she received vaccinations on Monday, 1/6/25 around 5:30pm. Flu was given on top and Prevnar on bottom, both in right deltoid. She stated on Tuesday she woke up with a dime sized welt and itching. On Wednesday morning she claimed welt was bigger and itching was worse. She took a benadryl and about an hour later she felt she was having "anaphylactic" type symptoms and took her epipen. She went to the ER and spent 4 hours there where they treated her with 60mg of prednisone, 50mg of benadryl, and a "breathing treatment." She improved and they discharged her with minor wheezing. More
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