πŸ₯ VAERS Vaccine Data Browser

πŸ”’ 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.

πŸ“– Help & Search Guide

Column Icons Legend

πŸ’€ Death
πŸ₯ Hospitalized
πŸš‘ Emergency Room
β™Ώ Disability
⚠️ Life Threatening

How to Search

πŸ’‘ 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 "πŸ“₯ Export CSV" to download filtered data (max 10,000 records)

πŸ’‘ Frequently Asked Questions (FAQ)

What is this site?

πŸ₯ 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:

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

Limitations:

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

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

What are "adverse events"?

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

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

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

Why are some lot numbers listed multiple times?

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

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

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

How often is this data updated?

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

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

Where can I learn more?

⚠️ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
πŸ”„ Reset πŸ“₯ Export CSV
ID Age Sex State Date β–Ό Onset Days Vaccine Manufacturer Lot # Symptoms Narrative πŸ’€ πŸ₯ πŸš‘ β™Ώ ⚠️
2842702 72 F PA 05/26/2025 UNK
 UNKNOWN MANUFACTURER
 33FD3
Erythema, Fatigue, Injection site erythema, Injection site warmth, Lymphadenopat... Erythema, Fatigue, Injection site erythema, Injection site warmth, Lymphadenopathy More
Huge red mark on left shoulder, Swollen lymph node right side breast area, Fatigue, Site was red and... Huge red mark on left shoulder, Swollen lymph node right side breast area, Fatigue, Site was red and hot to the touch More
2842703 65 M TX 05/26/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 027B21A
027B21A
027B21A
027B21A
027A21A
027A21A
027A21A
027A21A
Atrial fibrillation, Atrial flutter, Cardiac failure, Cardiomegaly, Catheterisat... Atrial fibrillation, Atrial flutter, Cardiac failure, Cardiomegaly, Catheterisation cardiac normal; Chest pain, Chronic kidney disease, Dyspnoea, Echocardiogram abnormal, Ejection fraction decreased; Electrocardiogram, Electrocardiogram ambulatory abnormal, Full blood count, Heart rate increased, Heart rate irregular; Laboratory test abnormal, Urine analysis, Ventricular extrasystoles, Ventricular tachycardia; Atrial fibrillation, Atrial flutter, Cardiac failure, Cardiomegaly, Catheterisation cardiac normal; Chest pain, Chronic kidney disease, Dyspnoea, Echocardiogram abnormal, Ejection fraction decreased; Electrocardiogram, Electrocardiogram ambulatory abnormal, Full blood count, Heart rate increased, Heart rate irregular; Laboratory test abnormal, Urine analysis, Ventricular extrasystoles, Ventricular tachycardia More
Developed chest pain 7 days after 2nd shot followed by shortness of breath. Dentist visit determined... Developed chest pain 7 days after 2nd shot followed by shortness of breath. Dentist visit determined that I had irregular and rapid heartbeat during visit. Followed up with family MD who recommended Cardiology and Nephrology follow up. Was determined to have enlarged heart with Heart Failure. Also determined that I had Kidney damage with Stage 3 failure. More
βœ“
2842704 17 F LA 05/26/2025 MENB
MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
 3L339
3L339
Chills, Fatigue, Headache, Influenza virus test negative, Nausea; Pyrexia, SARS-... Chills, Fatigue, Headache, Influenza virus test negative, Nausea; Pyrexia, SARS-CoV-2 test negative More
FEVER, HEADACHE, NAUSEA, CHILLS, FATIGUE FEVER, HEADACHE, NAUSEA, CHILLS, FATIGUE
2842705 68 M MN 05/26/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 P2443
Rash Rash
Patient reported to the pharmacy with a mild rash on right lower arm 2 hours after receiving vaccine... Patient reported to the pharmacy with a mild rash on right lower arm 2 hours after receiving vaccine. He had no other symptoms. More
2842706 50 F CO 05/26/2025 PNC20
 PFIZER\WYETH
 00005-2000-10
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site reaction, Urticaria More
Pain at time of injection; soreness and itching for 7 days at injection site; redness and raised wel... Pain at time of injection; soreness and itching for 7 days at injection site; redness and raised welts at injection site started 5 days after injection and lasted 2 additional days More
2842709 CA 05/26/2025 HPV9
 MERCK & CO. INC.
 Y012508
No adverse event, Product storage error No adverse event, Product storage error
No additional AE/no PQC.; HCP reported that improperly stored GARDASIL 9 was administered. No sympto... No additional AE/no PQC.; HCP reported that improperly stored GARDASIL 9 was administered. No symptoms. Precautionary AE as temperature excursion was within the temperature excursion guidelines in the prescribing information for GARDASIL 9.; This spontaneous report has been received from a physician assistant (reported as medical assistant) (R.T), regarding a patient of unknown age and gender. The patient's medical history, concurrent conditions, concomitant therapies, previous drugs reactions and allergies were not reported. On 23-May-2025, the patient was vaccinated with an improperly stored dose of Human Papillomavirus 9-valent Vaccine, Recombinant Injection (GARDASIL 9) injection, 0.5 mL, administered as prophylaxis (Lot No. Y012508 has been verified to be a valid lot number for [human papillomavirus 9-valent vaccine, recombinant injection], expiration date reported and upon internal validation established as 01-Jan-2027) (strength, dose number, route and anatomical location of administration and vaccination scheme frequency was not provided) (product storage error), after a temperature excursion of 35.04 degree Fahrenheit (F) during a time frame of 2 hours and 14 minutes. No previous temperature excursion was reported. No additional information or adverse events or PQC were provided (no adverse event). More
2842710 05/26/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 77KA5
Incomplete course of vaccination Incomplete course of vaccination
possible incomplete dose administration; This non-serious case was reported by a nurse via call cent... possible incomplete dose administration; This non-serious case was reported by a nurse via call center representative and described the occurrence of incomplete dose administered in unspecified number of patients who received Men B NVS (Bexsero) (batch number 77KA5, expiry date 30-NOV-2027) for prophylaxis. This case was associated with a product complaint. On an unknown date, the patient received Bexsero. On an unknown date, an unknown time after receiving Bexsero, the patient experienced incomplete dose administered (Verbatim: possible incomplete dose administration). The outcome of the incomplete dose administered was not applicable. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 22-MAY-2025 The Vaccine Administration Facility is the same as Primary Reporter A registered nurse asked if she could give a lot number of Bexsero to avoid receiving it in a future order given that she had issues trying to expel the air bubble, like losing a significant amount of the vaccine fluid. The reporter mentioned that, approximately 10 patients receive it after trying to expel the bubble between April and May 2025 which led to incomplete dose administered. The adverse event details were taken but she had no data of exactly which patients received it. More
2842711 HI 05/26/2025 MEN
 UNKNOWN MANUFACTURER
 U8124AA
No adverse event, Product storage error No adverse event, Product storage error
patient received vaccine that was stored at -0, with no reported adverse event; Initial information ... patient received vaccine that was stored at -0, with no reported adverse event; Initial information received on 23-May-2025 regarding an unsolicited valid non-serious case received from a physician. This case involves an unknown age and gender patient who was administered with meningococcal a-c-y-w135 (t conj) vaccine [Menquadfi] that was stored at -0 temperature with no reported adverse event. On an unknown date, the patient received an unknown dose of suspect meningococcal a-c-y-w135 (t conj) vaccine, Solution for injection, lot U8124AA,expiry date:30-Sep-2027, strength not reported via unknown route in unknown administration site for immunization post excursion with temperature -0, with no reported adverse event (poor quality product administered). Reportedly, product was administered post-excursion. 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
2842717 11 F 05/26/2025 MNQ
TDAP
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 U8369BA
M77CC
Amnesia, Fall, Tearfulness; Amnesia, Fall, Tearfulness Amnesia, Fall, Tearfulness; Amnesia, Fall, Tearfulness
After 2nd vaccine, patient was falling down from standing position. Patient was place on the chair.... After 2nd vaccine, patient was falling down from standing position. Patient was place on the chair. Patient is alert, doesn't remember what happened with tears. Provided tissue and water. Vital sign is with in normal limit. Instructed patient to remain in waiting are for 15 minutes. More
2842595 23 F WI 05/25/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
Hypoaesthesia, Injection site pain, Injection site rash, Rash erythematous, Rash... Hypoaesthesia, Injection site pain, Injection site rash, Rash erythematous, Rash pruritic More
They day after I got my vaccine, I?ve experienced a bright red itchy rash at the injection site and ... They day after I got my vaccine, I?ve experienced a bright red itchy rash at the injection site and pain and extreme numbness in my left arm. More
2842596 77 F NH 05/25/2025 COVID19
 PFIZER\BIONTECH
Culture urine negative, Genitourinary symptom, Haematuria, Haemorrhage urinary t... Culture urine negative, Genitourinary symptom, Haematuria, Haemorrhage urinary tract, Micturition urgency More
UTI symptoms including significant hematuria including blood clots over a period of 5-6 hours that... UTI symptoms including significant hematuria including blood clots over a period of 5-6 hours that resolved with no treatment. Note that initial feeling of discomfort started ~9pm the night before with urgency and heaturia stargin ~4am the next morning. No fever or other indications of illness. More
2842598 55 F MA 05/25/2025 PNC21
 MERCK & CO. INC.
 Z002626
Lymphadenopathy, Rash, Rash erythematous Lymphadenopathy, Rash, Rash erythematous
Swelling of lymph nodes in underarm area 1 day after injection that is still present, especially on ... Swelling of lymph nodes in underarm area 1 day after injection that is still present, especially on the left side. Red Rash on left arm that began as one large red spot 3-4 days after receiving the vaccine and spread within 24 hours. More
2842599 61 F IA 05/25/2025 PNC21
PNC21
VARZOS
VARZOS
 MERCK & CO. INC.
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS



Burning sensation, Cough, Eye pain, Neck pain, Rash; Rash erythematous, Respirat... Burning sensation, Cough, Eye pain, Neck pain, Rash; Rash erythematous, Respiratory tract irritation; Burning sensation, Cough, Eye pain, Neck pain, Rash; Rash erythematous, Respiratory tract irritation More
During sleep, I experienced significant neck pain/ache starting at base of skull, also strange eyeba... During sleep, I experienced significant neck pain/ache starting at base of skull, also strange eyeball pain/ache. I also experienced lung "irritation" causing me to cough a bit. At 7:30 next morning, I noted a very bright red rash on the underside of my left breast. No itching and it doesn't appear similar to any other rash or hives I have experienced. It does have a burning sensation, similar to a heat type burn, which is sensitive when bathing. Currently, there is no blisteting. More
2842600 87 M NE 05/25/2025 COVID19
 MODERNA
 3032794
Gait inability, Paralysis, Walking aid user Gait inability, Paralysis, Walking aid user
Patient could not walk 11 weeks later. 7.5 months after paralysis, patient can walk with a walker. ... Patient could not walk 11 weeks later. 7.5 months after paralysis, patient can walk with a walker. Patient was treated with parkinson's medications (carbidopa/levadopa). More
βœ“ βœ“
2842601 32 F WI 05/25/2025 VARCEL
VARCEL
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.


Activated partial thromboplastin time, C-reactive protein, Computerised tomogram... Activated partial thromboplastin time, C-reactive protein, Computerised tomogram head, Full blood count, Headache; International normalised ratio, Macular oedema, Metabolic function test, Pharyngeal swelling, Prothrombin time; Rash, Red blood cell sedimentation rate, Streptococcus test negative, Urine analysis, Urticaria More
Full body hives/rash starting one day after administered vaccine. Hives lasting on and off for two w... Full body hives/rash starting one day after administered vaccine. Hives lasting on and off for two weeks. Throat swelling about a week after administered vaccine. Macular edema confirmed by optometrist with headaches 2 weeks after administered vaccine. More
2842602 23 F TN 05/25/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
 065K21A
065K21A
065K21A
065K21A
065K21A
057M21A
057M21A
057M21A
057M21A
057M21A
Biopsy skin, Blood test, Burning sensation, Chronic inflammatory demyelinating p... Biopsy skin, Blood test, Burning sensation, Chronic inflammatory demyelinating polyradiculoneuropathy, Electromyogram normal; Fatigue, Feeling abnormal, Gastrooesophageal reflux disease, Headache, Hypoaesthesia; Immunoglobulin therapy, Impaired gastric emptying, Joint noise, Meningitis aseptic, Muscle fatigue; Muscular weakness, Pain in extremity, Paraesthesia, Paralysis, Photophobia; Somnolence, Subacute inflammatory demyelinating polyneuropathy, Tilt table test, Wheelchair user; Biopsy skin, Blood test, Burning sensation, Chronic inflammatory demyelinating polyradiculoneuropathy, Electromyogram normal; Fatigue, Feeling abnormal, Gastrooesophageal reflux disease, Headache, Hypoaesthesia; Immunoglobulin therapy, Impaired gastric emptying, Joint noise, Meningitis aseptic, Muscle fatigue; Muscular weakness, Pain in extremity, Paraesthesia, Paralysis, Photophobia; Somnolence, Subacute inflammatory demyelinating polyneuropathy, Tilt table test, Wheelchair user More
I was considered healthy before 2022. I did have underlying health issues via Ulcerative colitis whe... I was considered healthy before 2022. I did have underlying health issues via Ulcerative colitis when I turned 7, histoplasmosis and asthma at 21 but all was well maintained and hadn?t flared in a few years. After receiving the first part of the Moderna vaccination I did notice that first month my legs were extremely sore and tired almost like growing pains with a burning/ achy feeling and I was taking a lot more naps than I usually do but didn?t think much of it considering I just started my new job at the hospital but thought it was a little strange due to all of my past jobs being physically demanding too so I wasn?t sure why my legs were so sore. After I received the second vaccine, 2 weeks later my feet started tingling. The tingling feeling is best described as pins and needles almost like your feet are asleep but it wouldn?t go away. I had went to urgent care and had mentioned it in my appointment to where they sent me to the er because they were concerned that they haven?t stopped tingling. The hospital had recommended for me to get an EMG test done and which I did and the results were normal but possible early stages of Guillian Barre Syndrome. I was considered a new patient so I couldn?t get into see that neurologist until that October. About another week went by and at this point my feet were completely numb but I was still able to walk and fully function at work It just felt extremely weird. I was still very exhausted and was crashing out every time I got home from work. The next week I was heading into work that morning and all of a sudden I almost felt a pop sensation in my back and immediately felt the pins and needles run down both of my arms my legs and even the tip of my tongue. My boss took me down to the er and that?s when I was admitted into the hospital. The neurologist diagnosed me with SIDP caused by a reaction to the Moderna vaccines I had just gotten weeks prior. His plan of treatment was to start IVIG. On day 2 of receiving the IVIG I felt the tingling starting to come back in my feet from them being completely numb. Unfortunately I was also developing an extreme headache to the point to where I couldn?t open my eyes and the light hurt. Come to find out the treatment was ran too fast they had pushed the IVIG within an hour which resulted in me developing aseptic meningitis. That neurologist stopped the IVIG treatment immediately and his next plan was to start plasmapheresis treatment. Due to it then being a holiday weekend the line team never came in and by that Monday a new doctor was on rotation and stated that she believed they had given me aseptic meningitis from administering the treatment too quickly and they needed to back off. I was told time and physical therapy would help and was then discharged without the SIDP diagnosis and no treatment plan. I then was begging for help for about 1 year later which physically resulted me to now be paralyzed from the sternum down along with extreme arm weakness I was wheelchair bound. I was then referred to Dr. who is an autoimmune expert in Neurology. He did a plethora of testing which includes EMG, skin biopsy?s, tilt table test, full panel blood tests which all confirmed I did indeed have SIDP but now called CIDP (Chronic Inflammatory Demyelinating Polyneuropathy) from being delayed from proper help. He has started me back on IVIG but ran at a much slower rate and done every 3 weeks. In hope to regain nerve regrowth and hope of building the correct nerve structure to get me to be able to walk again. Unfortunately due to having CIDP I now have to deal with a plethora of other health issues like gastroparesis (stomach paralysis), GERD (reflux from gut not working properly due to immobility). More
βœ“
2842603 68 M VA 05/25/2025 TDAP
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 793PT
X5T42
Immediate post-injection reaction, Injection site pain, Injection site reaction,... Immediate post-injection reaction, Injection site pain, Injection site reaction, Rash erythematous; Immediate post-injection reaction, Injection site pain, Injection site reaction, Rash erythematous More
Shingrix arm (left)- Pain in left arm from shoulder to elbow right after vaccination and beginning t... Shingrix arm (left)- Pain in left arm from shoulder to elbow right after vaccination and beginning to feel better 5/25/25. Also a red rashy patch below and laterally to injection site of shingrix of about 2in by 3in...said it showed up the following day More
2842604 19 F TX 05/25/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 75d3a
No adverse event, Wrong product administered No adverse event, Wrong product administered
No adverse reaction at this time. Patient was to receive a flu vaccine, but inadvertently received ... No adverse reaction at this time. Patient was to receive a flu vaccine, but inadvertently received Shingrix. More
2842605 79 M SC 05/25/2025 COVID19
 PFIZER\BIONTECH
 md3414
Arterial occlusive disease, Catheterisation cardiac abnormal Arterial occlusive disease, Catheterisation cardiac abnormal
Patient's wife stated that the patient was hospitalized on May 19th and had to go to the cath l... Patient's wife stated that the patient was hospitalized on May 19th and had to go to the cath lab. The cardiologist was unable to complete the procedure as the one artery was so occluded. He told the patient and his wife that he had not seen anything like it and it may be a result of a recent vaccine administration. More
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2842606 65 F TN 05/25/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 9L944
Influenza, Injected limb mobility decreased, Pain in extremity, Peripheral swell... Influenza, Injected limb mobility decreased, Pain in extremity, Peripheral swelling More
Pt stated she had all the symptoms of flu that lasted a few days and also pain and swelling in right... Pt stated she had all the symptoms of flu that lasted a few days and also pain and swelling in right arm that continues to this day. She states the pain is similar to the pain she had when her rotator cuff was torn, lack of motion. More
2842607 1.58 M ND 05/25/2025 MMR
 MERCK & CO. INC.
Diarrhoea, Laboratory test, Lethargy, Pyrexia, Vomiting Diarrhoea, Laboratory test, Lethargy, Pyrexia, Vomiting
Fever started the night of the vaccination. Fever for a total of 7 days at the time of reporting. De... Fever started the night of the vaccination. Fever for a total of 7 days at the time of reporting. Developed vomiting, diarrhea, lethargy. Admitted to the hospital on 5/23/25 for IV fluid. Continued with fevers. Possible incomplete Kawasaki disease. More
βœ“ βœ“ βœ“
2842608 47 F FL 05/25/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 P2443
Blood glucose decreased, Computerised tomogram normal, Mydriasis, Scan with cont... Blood glucose decreased, Computerised tomogram normal, Mydriasis, Scan with contrast normal, Vision blurred More
Blurred vision in left eye, left pupil dilated, low blood sugar Blurred vision in left eye, left pupil dilated, low blood sugar
βœ“
2842609 53 F MD 05/25/2025 PNC20
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 MF0416
93N4J
Abdominal distension, Injection site erythema, Pain, Pyrexia; Abdominal distensi... Abdominal distension, Injection site erythema, Pain, Pyrexia; Abdominal distension, Injection site erythema, Pain, Pyrexia More
Patient still has swelling, redness, soreness, and slight fever on 05/25/25, five days after the vac... Patient still has swelling, redness, soreness, and slight fever on 05/25/25, five days after the vaccines were given. The redness and swelling are limited to the upper left arm region above the elbow. Patient also states the presence of a slight fever. Patient is taking acetaminophen for the fever and soreness, and cold compresses for the swelling, and will wait to see the response. More
2842610 54 M OR 05/25/2025 HEP
PNC20
 DYNAVAX TECHNOLOGIES CORPORATION
PFIZER\WYETH
 945656
LG5575
Incomplete course of vaccination, Wrong product administered; Incomplete course ... Incomplete course of vaccination, Wrong product administered; Incomplete course of vaccination, Wrong product administered More
Pharmacist did not review records before administering vaccine to patient despite printing the form(... Pharmacist did not review records before administering vaccine to patient despite printing the form(s) out. HEPLISAV-B was administered on 01/07/2025 instead of the TWINRIX that he was originally receiving. This incident was repeated again on 2/11/2025 by pharmacist. As a result, the patient did not complete his original TWINRIX vaccination schedule and had to be scheduled to complete 2 doses of HAVRIX in order to have immunity for both hepatitis A and B. More
2842611 51 F NC 05/25/2025 PNC20
 PFIZER\WYETH
 LK6655
Chills, Injection site erythema, Injection site pain, Injection site pruritus Chills, Injection site erythema, Injection site pain, Injection site pruritus
PATIENT COMPLAINED ABOUT HAVING CHILLS THE NEXT DAY FOLLOWED BY REDNESS AROUND THE INJECTION SITE WI... PATIENT COMPLAINED ABOUT HAVING CHILLS THE NEXT DAY FOLLOWED BY REDNESS AROUND THE INJECTION SITE WITH ITCHING AND BEING SORE More
2842612 1.25 M IL 05/25/2025 MMRV
 MERCK & CO. INC.
Rash Rash
facial rash facial rash
2842649 40 F DC 05/25/2025 HPV9
 MERCK & CO. INC.
 Y012508
Immediate post-injection reaction, Injection site bruising, Injection site haemo... Immediate post-injection reaction, Injection site bruising, Injection site haemorrhage, Injection site pain, Paraesthesia More
There was immediate bruising and bleeding at the injection site on the upper left arm. A dark bruise... There was immediate bruising and bleeding at the injection site on the upper left arm. A dark bruise also appeared about an inch and a half down from the injection site on the upper left arm. The bruising lasted for two weeks. The arm was immediately sore at the injection site and continues to be sore nearly two months later. Tingling in the arm, which runs down to my left pinky and ring fingers, started after the injection, and continues today. More
2842551 F MI 05/24/2025 MMR
MMR
UNK
UNK
UNK
UNK
VARZOS
VARZOS
 MERCK & CO. INC.
MERCK & CO. INC.
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER







Arthralgia, Bone pain, Groin pain, Pain in extremity, Sleep disorder; Spinal X-r... Arthralgia, Bone pain, Groin pain, Pain in extremity, Sleep disorder; Spinal X-ray; Arthralgia, Bone pain, Groin pain, Pain in extremity, Sleep disorder; Spinal X-ray; Arthralgia, Bone pain, Groin pain, Pain in extremity, Sleep disorder; Spinal X-ray; Arthralgia, Bone pain, Groin pain, Pain in extremity, Sleep disorder; Spinal X-ray More
she began to experience pain in the side of her right thigh/ described this pain as feeling "li... she began to experience pain in the side of her right thigh/ described this pain as feeling "like someone punched her/ then spread to the front of her right thigh, then to her groin muscle/ then spread to her right knee and her right shin; unable to sleep; arthritis; sciatica; This spontaneous report was received from a 63-year-old female patient reporting on herself. The patient's concurrent conditions included arthtritis. Her medical history and concomitant therapies were not reported. On an unknown date in 2025 (reported as "before Easter"), the patient was vaccinated with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II), solution for injection administered as prophylaxis in the Right Arm and with Zoster Vaccine Live (reported as "shingles vaccine") booster, also administered as prophylaxis in the Left Arm, both vaccines were reconstituted with sterile diluent (dose, route of administration, lot # and expiration date were not reported). These vaccines were reconstituted with sterile diluent (lot # and expiration date were not provided). At the time of the vaccination, she did not have any side effects. On an unspecified date in 2025 (reported as "about a week later"), she began to experience pain in the side of her right thigh. She described this pain as feeling "like someone punched her". This pain then spread to the front of her right thigh, then to her groin muscle, she stated that the more she tried to stretch, the worse the pain was. In addition, she reported that the pain then spread to her right knee and her right shin. She said that "her knee felt like she knelt on a rock and her shin felt like she had shin splints". The patient did not have any tingling, numbness, or inflammation, just pain, she had tried taking muscle relaxers and icing the area but this had not helped. Furthermore, she was unable to sleep at night because of the pain (insomnia). Therefore, she went to urgent care as she did not have a primary care doctor, at urgent care, they took an x-ray of her "right butt cheek" (results not provided) and referred her to an osteopath. Afterwards, the osteopath then took x-rays of her back and spine (results not provided). The doctor thought that it was arthritis or sciatica, the patient stated that she had arthritis and she knew what that felt like and this felt different. On 29-Apr-2025 (reported as "today") she was going for an magnetic resonance imaging (MRI) of her back. At the reporting time, the outcome of insomnia was unknown and had not recovered from the remaining events. The causal relationship between the events and the suspect vaccines/therapy was not provided. It was reported that the patient did not know if this had anything to do with the Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II) vaccine that she received. Lot # is being requested and will be submitted if received More
2842552 1 F HI 05/24/2025 HEPA
MMRV
MMRV
 UNKNOWN MANUFACTURER
MERCK & CO. INC.
MERCK & CO. INC.
 Y007585
Y017511
No adverse event, Product storage error; No adverse event, Product storage error... No adverse event, Product storage error; No adverse event, Product storage error; No adverse event, Product storage error More
No additional AEs; reported vaccines administered after temperature excursions.; This spontaneous re... No additional AEs; reported vaccines administered after temperature excursions.; This spontaneous report was received from a Physician and refers to a 12-month-old female patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 07-MAR-2025, the patient was vaccinated with an improperly stored Hepatitis A Vaccine, Inactivated (VAQTA)(lot #Y007585, expiration date: 31-OCT-2025) administered by Intramuscular route in Right Thigh, and with Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) (lot #Y017511, expiration date: 15-APR-2026) administered by Subcutaneous route in Left Thigh, reconstituted with sterile diluent (BAXTER STERILE DILUENT) (left thigh), administered by Subcutaneous route (lot # and expiration date were not reported) for prophylaxis, administered after temperature excursion. No additional AEs. More
2842553 CA 05/24/2025 VARCEL
 MERCK & CO. INC.
 T004577
Circumstance or information capable of leading to medication error, No adverse e... Circumstance or information capable of leading to medication error, No adverse event, Product lot number issue More
Precautionary AE: HCP called to request Lot verifications for two products on a patient's vacci... Precautionary AE: HCP called to request Lot verifications for two products on a patient's vaccination record as they could not determine expiration dates but on the vaccination record it stated the products were MMR II and VARIVAX. Upon verification; no adverse event; Product lot number issue; This spontaneous report was received from a/an Nurse and refers to a(n) patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. According to vaccination records, the patient received with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), (lot #T004577, expiration date not reported) administered by for Prophylaxis. It was confirmed that the lot was not a company product, the nurse believed that the vaccination ecords were forged or incorrectly completed (Circumstance or information capable of leading to medication error, Product lot number issue). No adverse event was reported. This report was considered invalid due to lack of patient identifiers. More
2842554 F NY 05/24/2025 MMRV
 MERCK & CO. INC.
 Z003308
Circumstance or information capable of leading to medication error, Exposure via... Circumstance or information capable of leading to medication error, Exposure via eye contact, No adverse event, Underdose More
No additional AE/PQC.; HCP called and reported that during administration of PROQUAD to a child, the... No additional AE/PQC.; HCP called and reported that during administration of PROQUAD to a child, the child moved their arm near the end of the dose which caused some of the residual liquid from the syringe to splash into the mother's eyes.; This spontaneous report was received from a Licensed Practical Nurse and refers to a female patient of unknown age. The patient's concurrent conditions, medical history, concomitant therapies, drug reactions or allergies were not reported. On 05-May-2025, the patient's child was receiving a dose of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) (lot #Z003308, expiration date: 21-Jul-2026) as Prophylaxis; but during administration, the child moved the arm near the end of the dose (child case # 2282979), which caused some of the residual liquid from the syringe to splash into the patient's eye (accidental exposure to product); therefore, she was treated with eye flush rinse in the office, as treatment for the event. No additional adverse event (AE) was reported. At the reporting time, the outcome of the event was unknown. This is one of two cases reported by the same reporter. More
2842555 0.33 M VA 05/24/2025 VARCEL
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.

No adverse event, Product administered to patient of inappropriate age; No adver... No adverse event, Product administered to patient of inappropriate age; No adverse event, Product administered to patient of inappropriate age More
No symptoms of issues have been reported.; HCP reported administering VARIVAX to a 4 month old male ... No symptoms of issues have been reported.; HCP reported administering VARIVAX to a 4 month old male patient by mistake; This spontaneous report was received from a Physician and refers to a 4-month-old male patient with no reactions or allergies reported. The patient's medical history, concurrent conditions and concomitant therapies were not reported. 19-MAY-2025, the patient was vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), (expiration date: 19-MAY-2025), dose: 0.5 mL, (lot #,route of administration was reported as injectable, frequency, anatomical location, expiration date and indication were not reported) with sterile diluent (MERCK STERILE DILUENT), dose: 0.5 mL (lot #,route of administration was reported as injectable, frequency, anatomical location, expiration date and indication were not reported) by mistake for prophylaxis. No symptoms of issues had been reported More
2842556 PA 05/24/2025 DTPPVHBHPB
DTPPVHBHPB
HEP
HEP
DTPPVHBHPB
DTPPVHBHPB
HEP
HEP
 MSP VACCINE COMPANY
MSP VACCINE COMPANY
MERCK & CO. INC.
MERCK & CO. INC.
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MERCK & CO. INC.
MERCK & CO. INC.



U8335AA
U8335AA
Y007989
Y007989
Extra dose administered; Extra dose administered, No adverse event; Extra dose a... Extra dose administered; Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event More
the patient inadvertently received RECOMBIVAX HB and VAXELIS on the same day.; No symptomatic advers... the patient inadvertently received RECOMBIVAX HB and VAXELIS on the same day.; No symptomatic adverse events were reported.; This spontaneous report was received from a nurse and refers to a(n) patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 20-May-2025, the patient was inadvertently vaccinated with Hepatitis B Vaccine (Recombinant) (RECOMBIVAX HB) and diphtheria and tetanus toxoids and acellular pertussis vaccine adsorbed, inactivated poliovirus (VAXELIS) for the treatment of Prophylaxis (strength, specific dosage, dose number, route of administration, anatomical site of application, lot number and expiration date were not provided). No symptomatic adverse events were reported. This is one of two reports received from the same reporter.; Reporter's Comments: More
2842557 M 05/24/2025 COVID19
MENB
 UNKNOWN MANUFACTURER
NOVARTIS VACCINES AND DIAGNOSTICS
 UNK
UNK
Abnormal dreams, Cold sweat, Fatigue, Hyperaesthesia, Injection site pain; Abnor... Abnormal dreams, Cold sweat, Fatigue, Hyperaesthesia, Injection site pain; Abnormal dreams, Cold sweat, Fatigue, Hyperaesthesia, Injection site pain More
pain at injection site; Fatigue; Skin sensitivity/hyperesthesia; Alternating sweating and being real... pain at injection site; Fatigue; Skin sensitivity/hyperesthesia; Alternating sweating and being really cold; Weird dreams; This non-serious case was reported by a other health professional via sales rep and described the occurrence of injection site pain in a 17-year-old male patient who received Men B NVS (Bexsero) for prophylaxis. Co-suspect products included COVID-19 vaccine for prophylaxis. On 19-MAY-2025, the patient received the 1st dose of Bexsero (left arm) and COVID-19 vaccine. On 19-MAY-2025, less than a day after receiving Bexsero, the patient experienced abnormal dreams (Verbatim: Weird dreams). On 20-MAY-2025, the patient experienced injection site pain (Verbatim: pain at injection site), fatigue (Verbatim: Fatigue), hyperesthesia skin (Verbatim: Skin sensitivity/hyperesthesia) and cold sweat (Verbatim: Alternating sweating and being really cold). On 20-MAY-2025, the outcome of the abnormal dreams was resolved (duration 1 day). The outcome of the injection site pain, fatigue, hyperesthesia skin and cold sweat were not resolved. The reporter considered the injection site pain, fatigue, hyperesthesia skin, abnormal dreams and cold sweat to be related to Bexsero and Bexsero Pre-Filled Syringe Device. The company considered the injection site pain, fatigue, hyperesthesia skin, abnormal dreams and cold sweat to be related to Bexsero and Bexsero 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: 20-MAY-2025 The reporter reported that a male patient had received first dose of Bexsero vaccine at the same time as the Covid booster vaccine and experienced fatigue, pain at injection site, skin sensitivity or hyperesthesia, weird dreams and alternating sweating and being really cold (never in the middle). It was reported that fatigue, pain at injection site, skin sensitivity or hyperesthesia and alternating sweating and being cold had worsened. The weird dreams occurred the night that he received the vaccines. More
2842565 22 F GA 05/24/2025 COVID19
 PFIZER\BIONTECH
Vulvovaginal swelling Vulvovaginal swelling
One of my labia minora heavily swelled for 3-5 days after getting vaccinated. I am abstinent so it w... One of my labia minora heavily swelled for 3-5 days after getting vaccinated. I am abstinent so it wasn't an STD. I also had no other symptoms so I doubt it was an infection. It went away on its own after some days, so all that leaves is the vaccine since it only started the day after with no other symptoms. More
2842566 74 F 05/24/2025 COVID19
 MODERNA
 8080748
Injection site erythema, Injection site reaction Injection site erythema, Injection site reaction
"COVID arm": big, red spot where vaccine was administered, started the day vaccine was rec... "COVID arm": big, red spot where vaccine was administered, started the day vaccine was received on 5/20 and has stayed the same until 5/23 More
2842567 0.58 M IL 05/24/2025 DTPPVHBHPB
DTPPVHBHPB
 MSP VACCINE COMPANY
MSP VACCINE COMPANY

Cold sweat, Inflammation, Influenza virus test negative, Irritability, Lethargy;... Cold sweat, Inflammation, Influenza virus test negative, Irritability, Lethargy; Night sweats, Poor quality sleep, Pyrexia, Urine output decreased More
Each time my son has had this vaccine he experienced high fevers of 102F for a week after the vaccin... Each time my son has had this vaccine he experienced high fevers of 102F for a week after the vaccine along with lethargy, irritability, poor sleep, poor feeding and decreased wet diapers. This is not considered a normal vaccine response. There are likely too many vaccines in this vaccine causing a massive inflammatory response. despite round the clock Tylenol + Motrin at appropriate dosing as instructed by the pediatrician, our 7 month old continued to sweat through his pajamas three times each night. He is clammy. The pediatricians have said he has no infection and ruled out infection. More
2842569 78 F TX 05/24/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 58160082311
58160082311
Back pain, Chest X-ray, Chest pain, Cough, Headache; Muscle spasms, Sneezing Back pain, Chest X-ray, Chest pain, Cough, Headache; Muscle spasms, Sneezing
Muscle cramps, sneezing, severe coughing, headaches, chest and back pain Muscle cramps, sneezing, severe coughing, headaches, chest and back pain
2842570 66 F MD 05/24/2025 FLU3
 SANOFI PASTEUR
 u8515ba
Wheezing Wheezing
Patient reports having wheezing in the afternoon Patient reports having wheezing in the afternoon
2842571 82 F PA 05/24/2025 DT
 SANOFI PASTEUR
Inflammation, Pruritus Inflammation, Pruritus
Received pneumonia vaccine in Left upper arm. 5 days later it started to itch Today 5-24-25 it is s... Received pneumonia vaccine in Left upper arm. 5 days later it started to itch Today 5-24-25 it is still itchy and the shoulder is inflamed. There is no pain, no swelling and no signs of an infection. I do not have a fever. More
2842572 14 F NY 05/24/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EWO196
EWO196
EWO196
EWO196
EWO196
EWO196
EWO196
EWO196
EWO196
Alopecia, Anxiety, Autonomic nervous system imbalance, Biopsy skin, Chest pain; ... Alopecia, Anxiety, Autonomic nervous system imbalance, Biopsy skin, Chest pain; Chronic inflammatory demyelinating polyradiculoneuropathy, Cognitive disorder, Depression, Dissociation, Dizziness; Dyspnoea, Dysstasia, Eating disorder, Educational problem, Electrocardiogram normal; Electromyogram abnormal, Exercise tolerance decreased, Fatigue, Gastrooesophageal reflux disease, Hallucination, auditory; Hypoaesthesia, Hypometabolism, Insomnia, Intentional self-injury, Laryngoscopy normal; Magnetic resonance imaging head abnormal, Mental impairment, Nausea, Nerve conduction studies abnormal, Obsessive-compulsive disorder; Orthostatic intolerance, Palpitations, Paraesthesia, Peripheral vascular disorder, Positron emission tomogram; Postural orthostatic tachycardia syndrome, Small fibre neuropathy, Social anxiety disorder, Suicidal ideation, Syncope; Temperature intolerance, Temperature regulation disorder, Tilt table test positive More
I entered the second vaccine of the series in the report because my daughter's reaction took pl... I entered the second vaccine of the series in the report because my daughter's reaction took place after that specific vaccine, but I believe it to be a cumulative effect of the two initial vaccines and the booster which was given on January 11, 2022. Symptoms appeared to be a cumulative effect of three covid vaccines, with her symptoms emerging after the second vaccine and intensifying significantly after the third covid booster vaccine. Vaccine #1 was Pfizer EW0191 on 6/6/21 administered at Pharmacy and the third Covid Booster Vaccine was Pfizer FJ5682 administered on 1/11/22 by the State County Department of Health. Prior to my daughter's symptoms developing, she was an honor student on a full academic scholarship to a private high school. She was an accomplished athlete in many sports, but soccer was her favorite. She was the starting goalie for the varsity soccer team as a freshman and had been a competitive alpine ski racer, figure skater, Gaelic football player and track sprinter. She was a child genius, with an IQ of 141 who was accepted into (redacted) as a ten year old girl. She loved foreign languages, having studied (redacted). She was a viola player at the school orchestra. She was a member of her school's robotics team. She had a giant personality, full of laughter and confidence. She has a zest for life that quite frankly, we found it hard to keep up with! She was unstoppable, energetic and loved life. Late August 2021 she began to experience increased shortness of breath that we initially attributed to asthma. Fall (September) 2021 into Winter 2022 her athleticism diminished after the beginnings of orthostatic intolerance, occasional blood pooling when standing or walking, dizziness, nausea, fatigue, paresthesias, frequent fainting (several times a week) especially with position change, palpitations, shortness of breath (we initially thought it was exacerbated asthma, but it kept intensifying) insomnia and anxiety began to creep in. She was eventually diagnosed with POTS in 2024 by a cardiologist, after being dismissed as anxious for two years. We did not understand that her symptoms could be related to the vaccine because we were being reassured by providers that this was just anxiety. My daughter subsequently got the Covid booster on 1/11/22 and after that her symptoms got much more severe. By late January-February 2022 she was in full crisis, self harming regularly and crushed by social anxiety. As the winter went on her symptoms worsened, dissociation, auditory hallucinations, significant hair loss, depression, suicidal ideation, increased germ OCD, disordered eating, heat intolerance, trouble regulating hot and cold, tingling and numbness in her legs and feet, chest pains, and inability to stand for periods of time. She became unable to think clearly and perform academically as she used to, eventually having to leave her private school honors program and enter the public high school so that she could have academic accommodations for support. Ultimately those accommodations weren't enough and she was placed into a day school for students with disabilities that provides extra support in addition to the accommodations. My daughter is on many medications now to keep her functioning in the world, but her life is drastically different now than it was before the vaccines. As her anxiety and depression worsened between Winter 2022 into Fall of 2023 She found it increasingly difficult to function and has endured many inpatient hospitalizations for psychiatric symptoms, which have been very traumatic for her. She has had 8 psychiatric hospitalizations between September 2023 and present day (May 24, 2025). We have tried many things to bring her relief from depression, including many different medication trials, therapies, ketamine infusions, and ECT. She is scheduled to graduate high school this June, but has just deferred college for a year hoping to work on her recovery. She is hoping to be well enough to begin college in Fall of 2026. Here is a list of the diagnoses that she has had since vaccination that were not present before vaccination: Depression Anxiety Parasthesias CIDP POTS / Dysautonomia Autonomic dysfunction Gastro reflux Functional bloating Cognitive change Here is a list of her hospitalizations : Hospitalizations: entered here because the VAERS system times out after 20 minutes and won't allow time to enter all of the admissions At ER Admitted Discharged Hospital 9/28/23 9/29/23 10/17/23 (redacted) Behavioral Health N/A 11/3/23 11/10/23 Direct admission to (Redacted) 11/24/23 11/25/23 12/21/23 (redacted) Behavioral Health N/A 12/21/23 2/18/24 (redacted) horse farm residential therapeutic center in (redacted) 4/8/24 4/10/24 4/16/24 (redacted) Behavioral Health 5/23/24 5/24/24 5/31/24 (redacted) Behavioral Health 7/6/24 7/7/24 8/2/24 (redacted) Behavioral Health 10/5/24 10/7/24 11/20/24 (redacted) Behavioral Health 2/15/25 2/18/25 4/4/25 (redacted) Behavioral Health More
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2842573 63 F NJ 05/24/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 7R245
Hypoaesthesia, Injection site hypoaesthesia, Nerve injury, Pain, Paraesthesia Hypoaesthesia, Injection site hypoaesthesia, Nerve injury, Pain, Paraesthesia
Tingling pain, numbness radiating around shoulder and neck and down left arm from injection site to ... Tingling pain, numbness radiating around shoulder and neck and down left arm from injection site to finger tips. More
2842574 4 M MD 05/24/2025 DTAPIPV
MMRV
 SANOFI PASTEUR
MERCK & CO. INC.
 U7838AA
Y013573
Blood pressure decreased, Cough, Pruritus, Urticaria; Blood pressure decreased, ... Blood pressure decreased, Cough, Pruritus, Urticaria; Blood pressure decreased, Cough, Pruritus, Urticaria More
Patient returned to clinic for symptoms of hives and cough within 30 minutes of receiving MMRV and D... Patient returned to clinic for symptoms of hives and cough within 30 minutes of receiving MMRV and DTaP/IPV vaccines. - Was at the store when reaction was noted. Mom unaware of him eating anything. Breathing comfortably, minor cough, SpO2 was 97%. Hives noted on face, torso and extremities. Patient was itching. BP was 88/58 which is slightly decreased from BP prior to vaccine 90/64. He was given 5 mL of Benadryl. Unable to locate EpiPen in clinic. Mom advised on need to present to the ER for further monitoring and treatment. - Declined calling ambulance to clinic and preferred going by car. - Advised on importance to present as soon as possible as he needs continuous monitoring for symptoms and possible treatment with EpiPen. - Mom felt comfortable going to ED. - ED was called afterwards and patient was present in the ED and receiving treatment. More
2842575 84 M MA 05/24/2025 COVID19
 PFIZER\BIONTECH
 LM2221
Amnesia, Psychotic disorder, Swallow study, Vocal cord disorder Amnesia, Psychotic disorder, Swallow study, Vocal cord disorder
Altered reality. Acting as another person. Vocal cords affected. Complete loss of memory. Has had ... Altered reality. Acting as another person. Vocal cords affected. Complete loss of memory. Has had 20 weeks of speech therspy to improve memory. Has improved but not completely. After a hospital atay of 10 dayd waz in a rehab facility for 52 days More
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2842576 76 F OR 05/24/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 00069-2432-10
00069-2432-10
Arthralgia, Back pain, Feeling cold, Hyperhidrosis, Induration; Pain, Pain in ex... Arthralgia, Back pain, Feeling cold, Hyperhidrosis, Induration; Pain, Pain in extremity, Peripheral swelling More
Within approximately 24 hours my left arm was sore. Also, any location I've had surgeries (bac... Within approximately 24 hours my left arm was sore. Also, any location I've had surgeries (back, hip knee, shoulder all on right side) I became extremely achy. My right shin was injured by a vehicle airbag in September of 2024. Swelling was gone at time of vaccination. After the vaccination my shin swelled again and skin was shiny and tight. Also, had sweats and chills. More
2842577 36 F AZ 05/24/2025 COVID19
 MODERNA
 8081596
Dizziness, Erythema, Skin discolouration Dizziness, Erythema, Skin discolouration
Patient received covid vaccine around 10:00 am. After vaccination patient left upper arm became disc... Patient received covid vaccine around 10:00 am. After vaccination patient left upper arm became discolored, redness appeared, skin slightly risen. Few moments later patient felt faint and had to sit down, patient did not faint. EMS was called and arrived, vital signs were all stable. patient left on her own with family, did not get transferred via ems. More
2842578 65 F CA 05/24/2025 HPV9
 MERCK & CO. INC.
 EB499
No adverse event, Wrong product administered No adverse event, Wrong product administered
No adverse events after administration of the incorrect vaccine (HPV). Patient was monitored post-va... No adverse events after administration of the incorrect vaccine (HPV). Patient was monitored post-vaccination, and no immediate symptoms or reactions were observed. Provider was notified, and the incident was documented for follow-up. More
2842579 77 F OH 05/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 75D3A
Erythema, Oedema peripheral, Skin warm, Swelling Erythema, Oedema peripheral, Skin warm, Swelling
red hot swelling skin on back of neck and under left arm red hot swelling skin on back of neck and under left arm
2842580 50 F MN 05/24/2025 COVID19
COVID19
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 032H20A
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Abdominal pain lower, Affect lability, Anal fistula repair, Anovulvar fistula, A... Abdominal pain lower, Affect lability, Anal fistula repair, Anovulvar fistula, Anxiety; Atrophic vulvovaginitis, Axillary lymphadenectomy, Axillary pain, Back pain, Biopsy breast abnormal; Biopsy lung normal, Biopsy lymph gland, Biopsy vulva abnormal, Bone density decreased, Breast conserving surgery; Breast mass, COVID-19, Cervical spinal stenosis, Chemotherapy, Cholecystectomy; Computerised tomogram abdomen normal, Computerised tomogram thorax abnormal, Depressed mood, Distractibility, Eczema; Electrocardiogram normal, Epstein-Barr virus test positive, Fatigue, Full blood count normal, Gait disturbance; HER2 negative breast cancer, Herpes simplex, Hypothyroidism, Impaired work ability, Intervertebral disc degeneration; Intervertebral disc protrusion, Invasive ductal breast carcinoma, Joint range of motion decreased, Laboratory test normal, Lichen sclerosus; Lymphoedema, Magnetic resonance imaging abnormal, Magnetic resonance imaging breast abnormal, Magnetic resonance imaging pelvic, Mammogram abnormal; Metabolic function test normal, Metastases to lymph nodes, Mobility decreased, Neck pain, Oncotype test; Osteopenia, Pain, Pain in extremity, Palpitations, Peripheral swelling; Positron emission tomogram abnormal, Post procedural complication, Proctalgia, Pulmonary granuloma, Pulmonary mass; Radiotherapy, Rash, Renal cyst, SARS-CoV-2 antibody test positive, Scan with contrast normal; Secretion discharge, Seroma, Tearfulness, Tobacco abuse, Ultrasound breast abnormal; Vaginal lesion, Vertebral foraminal stenosis, Vulval ulceration, Vulvovaginal pain, Vulvovaginal swelling; X-ray limb normal; Abdominal pain lower, Affect lability, Anal fistula repair, Anovulvar fistula, Anxiety; Atrophic vulvovaginitis, Axillary lymphadenectomy, Axillary pain, Back pain, Biopsy breast abnormal; Biopsy lung normal, Biopsy lymph gland, Biopsy vulva abnormal, Bone density decreased, Breast conserving surgery; Breast mass, COVID-19, Cervical spinal stenosis, Chemotherapy, Cholecystectomy; Computerised tomogram abdomen normal, Computerised tomogram thorax abnormal, Depressed mood, Distractibility, Eczema; Electrocardiogram normal, Epstein-Barr virus test positive, Fatigue, Full blood count normal, Gait disturbance; HER2 negative breast cancer, Herpes simplex, Hypothyroidism, Impaired work ability, Intervertebral disc degeneration; Intervertebral disc protrusion, Invasive ductal breast carcinoma, Joint range of motion decreased, Laboratory test normal, Lichen sclerosus; Lymphoedema, Magnetic resonance imaging abnormal, Magnetic resonance imaging breast abnormal, Magnetic resonance imaging pelvic, Mammogram abnormal; Metabolic function test normal, Metastases to lymph nodes, Mobility decreased, Neck pain, Oncotype test; Osteopenia, Pain, Pain in extremity, Palpitations, Peripheral swelling; Positron emission tomogram abnormal, Post procedural complication, Proctalgia, Pulmonary granuloma, Pulmonary mass; Radiotherapy, Rash, Renal cyst, SARS-CoV-2 antibody test positive, Scan with contrast normal; Secretion discharge, Seroma, Tearfulness, Tobacco abuse, Ultrasound breast abnormal; Vaginal lesion, Vertebral foraminal stenosis, Vulval ulceration, Vulvovaginal pain, Vulvovaginal swelling; X-ray limb normal; Abdominal pain lower, Affect lability, Anal fistula repair, Anovulvar fistula, Anxiety; Atrophic vulvovaginitis, Axillary lymphadenectomy, Axillary pain, Back pain, Biopsy breast abnormal; Biopsy lung normal, Biopsy lymph gland, Biopsy vulva abnormal, Bone density decreased, Breast conserving surgery; Breast mass, COVID-19, Cervical spinal stenosis, Chemotherapy, Cholecystectomy; Computerised tomogram abdomen normal, Computerised tomogram thorax abnormal, Depressed mood, Distractibility, Eczema; Electrocardiogram normal, Epstein-Barr virus test positive, Fatigue, Full blood count normal, Gait disturbance; HER2 negative breast cancer, Herpes simplex, Hypothyroidism, Impaired work ability, Intervertebral disc degeneration; Intervertebral disc protrusion, Invasive ductal breast carcinoma, Joint range of motion decreased, Laboratory test normal, Lichen sclerosus; Lymphoedema, Magnetic resonance imaging abnormal, Magnetic resonance imaging breast abnormal, Magnetic resonance imaging pelvic, Mammogram abnormal; Metabolic function test normal, Metastases to lymph nodes, Mobility decreased, Neck pain, Oncotype test; Osteopenia, Pain, Pain in extremity, Palpitations, Peripheral swelling; Positron emission tomogram abnormal, Post procedural complication, Proctalgia, Pulmonary granuloma, Pulmonary mass; Radiotherapy, Rash, Renal cyst, SARS-CoV-2 antibody test positive, Scan with contrast normal; Secretion discharge, Seroma, Tearfulness, Tobacco abuse, Ultrasound breast abnormal; Vaginal lesion, Vertebral foraminal stenosis, Vulval ulceration, Vulvovaginal pain, Vulvovaginal swelling; X-ray limb normal; Abdominal pain lower, Affect lability, Anal fistula repair, Anovulvar fistula, Anxiety; Atrophic vulvovaginitis, Axillary lymphadenectomy, Axillary pain, Back pain, Biopsy breast abnormal; Biopsy lung normal, Biopsy lymph gland, Biopsy vulva abnormal, Bone density decreased, Breast conserving surgery; Breast mass, COVID-19, Cervical spinal stenosis, Chemotherapy, Cholecystectomy; Computerised tomogram abdomen normal, Computerised tomogram thorax abnormal, Depressed mood, Distractibility, Eczema; Electrocardiogram normal, Epstein-Barr virus test positive, Fatigue, Full blood count normal, Gait disturbance; HER2 negative breast cancer, Herpes simplex, Hypothyroidism, Impaired work ability, Intervertebral disc degeneration; Intervertebral disc protrusion, Invasive ductal breast carcinoma, Joint range of motion decreased, Laboratory test normal, Lichen sclerosus; Lymphoedema, Magnetic resonance imaging abnormal, Magnetic resonance imaging breast abnormal, Magnetic resonance imaging pelvic, Mammogram abnormal; Metabolic function test normal, Metastases to lymph nodes, Mobility decreased, Neck pain, Oncotype test; Osteopenia, Pain, Pain in extremity, Palpitations, Peripheral swelling; Positron emission tomogram abnormal, Post procedural complication, Proctalgia, Pulmonary granuloma, Pulmonary mass; Radiotherapy, Rash, Renal cyst, SARS-CoV-2 antibody test positive, Scan with contrast normal; Secretion discharge, Seroma, Tearfulness, Tobacco abuse, Ultrasound breast abnormal; Vaginal lesion, Vertebral foraminal stenosis, Vulval ulceration, Vulvovaginal pain, Vulvovaginal swelling; X-ray limb normal More
Laboratories: CT ABDOMEN PELVIS W IV CONTRAST This document is currently in Final Status CT ABDO... Laboratories: CT ABDOMEN PELVIS W IV CONTRAST This document is currently in Final Status CT ABDOMEN PELVIS W IV CONTRAST INDICATION: RLQ pain evaluation; COMPARISON: Ultrasound 4/2/2025, CT chest 1/6/2025 and MRI pelvis 6/30/2020 FINDINGS: Similar mild nodularity in the right middle lobe. Cholecystectomy. Tiny renal hypodensities, likely benign cysts. Liver, adrenal glands and pancreas are negative. Normal caliber small bowel. No free fluid. IMPRESSION: 1. No acute findings in the abdomen or pelvis. 2. Similar mild nodularity in the right middle lobe, presumably treatment related. Electronically Signed: physician 5/8/2025 10:46 AM I am in month 50. MY VACCINE ADVERSE REACTION HORROR STORY: as a healthcare worker I was in the first group of vaccinations January 2021. My last vaccination was May 2022. I had 4 Moderna shots total. Shortly after being vaccinated I developed an anal fissure that spread to my vulva, and I suffered vaginal lesions until a biopsy was performed and determined that I have an autoimmune disease with no cure, called Vulvar Lichen Sclerosis. I have over 440 photographs of my vulva since 2021 and all the medical records including testing positive for Epstein Barr virus when my clitoris hood swelled up and split open oozing for 5 weeks until that one healed. I have been documenting it all and have high resolution horrifying images of other oozing ulcers on my clitoris, vaginal lesions and atrophy of my vagina and labia that has completely decimated and severely disfigured me. The pain is unbearable, then in 2022 I developed a painful anal fistula. One doctor cut it out right there in the office but that procedure failed and on February 17, 2023 I went under full anesthesia for an Anal Fistulatomy. It would take more than 8 weeks of suffering for me to heal from that HORRIFIC procedure. Then in April, 2023 my annual mammogram came back abnormal, a biopsy was performed on my right breast and right axillary lymph node and determined I have invasive Ductal Carcinoma Cancer in my right breast and Metastatic Cancer to 3 of 9 (all removed) lymph nodes. I am devastated and can?t stop crying. Surgery for a double lumpectomy and complete lymph node removal was May 17, 2023 ? followed by 12 weeks of chemo (final chemo 8/22/23) and mapping for radiation starting the first week of September and I just finished 33 rounds of radiation. Next up is a treatment of gene therapy pills for 10 years to remove any remaining estrogen. Two spots in the breast were biopsied and about 20 days later in surgery there were four spots removed, making it a very aggressive ?Turbo Cancer?. I also experienced ?died suddenly clots? in my surgery drain lines - look for those photos on my social media account too. All nine lymph nodes were removed from my right armpit and three nodes had metastatic cancer. I have filed adverse reactions with V-SAFE, agency, and health department (Health Department where I received my first 2 doses of Moderna). They tricked me. It wasn?t a vaccine, it was an experimental gene therapy and now my immune system is scrambled - and there is nothing anyone can do. MY ILLNESSES: CANCER: Breast Cancer (Invasive Ductal Carcinoma + Metastatic Carcinoma to Lymph Nodes). VULVAR: Vulvar Lichen Sclerosus, Vulvar Aphthous Ulcers, Vaginal LipschοΏ½tz Ulcers, Anal Fissures + Fistulas, Right Arm Lymphedema, Two Lung granulomas (recently biopsied no carcinogens detected). A couple of months ago my claim required me to get an attorney to represent me and I am near maxed out on credit cards. Minimal balances are giving me anxiety and I?m terrified I won?t make it to disability approval. Please, God help me. I am praying for us all. My vaccines and vaccination dates are as follows, January 7, 2021 ? Moderna lot 032H20A, February 3, 2021 Moderna lot 010M20A, November 11, 2021 Moderna lot 091D21A, May 19, 2022 Moderna lot 056A22A. I?m now permanently disabled and these injuries have no doubt taken years off my lifespan. It?s never to late to file a VAERS report so here is mine. You better Welcome and stop the shots! God Bless Assessment: 54-year-old female with: 1. Right breast invasive ductal carcinoma, T1 (m) N1 M0, stage II. Grade 1. ER/PR 99% positive, HER2 negative. Ki-67 2%. Multifocal tumor with 4 lesions measuring less than 1 cm. Right axillary lymph node biopsy showed metastatic carcinoma suspicious for focal extracapsular extension. Reviewed MRI breast results and images from 4/20/2023 which showed abnormal masslike and non-mass-like enhancement in the right breast with a 1 cm mass in the anterior right breast and a cluster of small masses in the right breast at the middle approximately 8 to 9 cm from the nipple. Mildly prominent lymph nodes noted in the right axilla. Discussed diagnosis of stage II ER positive HER2 negative breast cancer and management with surgery followed by possible adjuvant chemotherapy, adjuvant radiation therapy and endocrine therapy. Her case was discussed with the tumor conference earlier today. Lumpectomy of both breast lesions is feasible. Given focal extracapsular extension noted in the axillary biopsy, she would be a candidate for axillary lymph node dissection. Discussed this with patient. She currently has other issues going on such as her lichen sclerosus and worsening of chronic pain issues. She has an appointment with Dermatology at Clinic in the works. She prefers to have surgery first which is reasonable. We will make referral. Underwent right lumpectomy and right axillary node dissection on 5/17/2023. Reviewed surgical pathology results which showed multifocal tumor with 4 separate masses measuring 14 mm, 10 mm, 4 mm and 2.5 mm, all grade 1 with accompanying DCIS and foci of ALH. Margins clear. 3 of 9 sentinel lymph nodes were involved with metastatic adenocarcinoma, the largest focus measuring 8 mm with extranodal extension. Recovering well from her surgery. Discussed adjuvant treatment with radiation therapy and endocrine therapy for 10 years. Given her node positive disease, I am leaning towards systemic chemotherapy. Discussed utilization of Oncotype DX test to define benefit from systemic chemotherapy. Patient is willing to proceed with the above tests. Discussed obtaining a PET CT scan to complete staging work-up. Reviewed PET CT scan images and results from 6/2/2023 which showed posttreatment changes in the right breast and no evidence of metastatic malignancy in the neck chest abdomen or pelvis. Oncotype DX test returned with recurrence score of 14. However given her node positive disease with extracapsular extension, I recommend 4 cycles of adjuvant Taxotere Cytoxan chemotherapy with Neulasta support. Reviewed schedule potential side effects. She is agreeable. Cycle 1 TC chemotherapy administered on 6/20/2023 with Neulasta support. Had bone pains with Neulasta. Also developed a groin rash which improved with creams. Currently on antibiotics for bacterial infection of skin. Completed 4 cycles of TC chemotherapy with fairly good tolerance. Completed adjuvant radiation treatments on 10/23/2023. Patient recently had COVID infection, recovering from it. She has intermittent flareups of her autoimmune conditions causing significant discomfort. Recovering from skin toxicity from radiation. Reviewed CT scan images and results from 12/8/2023 which showed decrease in the nodule of the right lower lobe consistent with granulomatous change. Lung findings noted consistent with recent inflammation/infection. Discussed adjuvant endocrine therapy for breast cancer with aromatase inhibitors. Reviewed schedule. The side effects including joint aches and pains, hot flashes, decrease in bone density etc. Started letrozole in December 2023. Follow-up CT scan in April 2024 showed minimal change in the postoperative seroma in the right breast and right axilla and stable lung findings. No evidence of recurrent disease. Seroma in the right breast appears larger than the right axilla. CT chest in January 2025 showed no etiology for the right axillary pain. Reviewed CT scan images and results from earlier today which showed no evidence of malignancy or any acute findings. Patient is doing fairly well clinically. Tolerating letrozole well. 2. Lichen sclerosis- improved. 3. Hypothyroidism-on Synthroid. TSH normal. 4. Labs in epic reviewed. CBC CMP normal. 5. Right upper extremity and breast lymphedema-seeing occupational therapy. Using sleeve. Using compression pump intermittently. 6. Groin rash-improved. Follows with Dermatology. Improved. 7. Right upper lobe lung nodule-measuring 1.9 cm. Reviewed CT images from outside facility. PET CT scan shows uptake with right hilar uptake as well. Recent scan shows improvement in lung nodule. 8. Tobacco abuse. 9. Bone health-reviewed bone density scan results from November 2024 which showed osteopenia. 10. COVID-vaccine injury-recent spike protein antibody test returned positive. 11. Complaints of frequent palpitations. No abnormalities on labs or EKG. 12. Left heel pain-ongoing for several months. X-ray did not show any acute issues. Plan: 1. Continue letrozole. 2. Return to office with me in 3 months with labs for follow-up. 3. Ortho referral for heel pain evaluation. Patient understands and agrees with the plan. Her questions were answered satisfactorily. She knows to call with any issues in the interim. Cancer Center, Hematology/Oncology Site: Cancer Center Reason for Visit: Right breast cancer Referred by: Physician (redacted) History of Present Illness: Patient is a 54 year old pleasant female with a diagnosis of thyroid disease, eczema etc. who underwent screening mammogram in March 2023 and was found to have a 6 mm lateral right breast abnormality. Further evaluation with ultrasound showed 2 suspicious masses in the right breast and associated abnormal axillary lymph node. Ultrasound biopsy of the 2 breast lesions and the lymph node were performed on 4/12/2023 and returned positive for invasive ductal carcinoma ER/PR strongly positive and HER2 negative, Ki-67 2%. Referred here for further evaluation and management. Patient also gives a history of significant side effects after receiving a COVID 19 vaccination. She was diagnosed with vaginal lichen sclerosis for which she has been referred to Dermatology at Clinic. Developed a perianal fistula for which she had examination under anesthesia with fistulotomy by Doc in February 2023. 4/19/2023-MRI breast showed abnormal mass like and non mass enhancement in the right breast with a 1 cm mass in the anterior right breast at 3 o'clock position and a cluster of small masses in the right breast at middle depth approximately 8 to 9 cm from the nipple. Right axillary biopsy clip noted, no suspicious lymph nodes noted. Left breast examination showed a few small sub-5 mm foci of enhancement. 5/17/2023-underwent right lumpectomy and right axillary lymph node dissection by Dr. Specimen sent for Oncotype DX testing. 6/2/2023-PET CT scan showed posttreatment changes in the right breast with fluid collection and no evidence of distant metastatic disease or other malignancy. 6/20/2023-started Taxotere Cytoxan chemotherapy with Neulasta support. 9/20/2023-low-dose lung cancer screening performed at facility showed a new spiculated lung nodule in the right upper lobe medially measuring 1.9 cm in maximum dimension, concerning for lung primary. 8/22/2023-completed cycle 4 chemotherapy. 10/19/2023-PET CT scan showed prior granulomatous disease process. 10/31/2023-right lung lesion biopsy was negative for malignancy, showed granulomatous inflammation. Completed adjuvant radiation treatments on 10/23/2023. Started letrozole. Patient presents today for their follow-up visit. She had a follow-up CT scan of the abdomen pelvis earlier today for evaluation of lower abdominal pain. Disability DETERMINATION This case is before the undersigned on a request for hearing dated January 3, 2024. On October 22, 2024, the undersigned held a telephone hearing. All participants attended the hearing by telephone. The claimant agreed to appear by telephone before the hearing and confirmed such agreement at the start of the hearing. The claimant is represented by, an attorney. an impartial vocational expert, also appeared at the healing. The claimant is alleging disability since September 18, 2021. FINDINGS OF FACT AND CONCLUSIONS OF LAW After careful consideration of the entire record, the undersigned makes the following findings: 1. The claimant's date last insured is December 31, 2028. 2. The claimant has not engaged in substantial gainful activity since September 18, 2021, the alleged onset date. The claimant has worked after the alleged onset date; however, the amounts earned fall below the requisite threshold for classification as substantial gainful activity. 3. The claimant has the following severe impairments: degenerative disc disease of the cervical lumbar and thoracic spine; lymphedema status-post breast carcinoma; anal fissures / fistula; Lichen Sclerosis; genital ulcers; and herpes simplex virus (HSV). The claimant has the following degree of limitation in the four broad areas of mental functioning set out in the disability regulations tor evaluating mental disorders and the mental disorder. Next Page remembering, or applying information; no limitation in interacting with others; no limitation in concentrating, persisting, or maintaining pace; and no limitation in adapting or managing oneself. 4. The claimant does not have an impairment or combination of impairments that meets or medically equals the severity of one of the listed impairments. 5. The claimant has the residual functional capacity to perform sedentary work as defined in article with the following additional limitations: occasional climbing ramps and stairs; never climbing ladders, ropes, or scaffolds; occasional stooping, kneeling, and crouching; no crawling; the avoidance of unprotected heights and workplace hazards; occasional oreaching to shoulder height with the right upper extremities and never reaching above shoulder height ,with the right upper extremity; frequent handling and fingering with the right hand; occasional pushing and pulling with the upper and longer extremities; the avoidance of beat and humidity; and the claimant must alternate between sitting and standing every 30 minutes while claimant on task. In making this finding, the undersigned has considered all symptoms and the extent to which these symptoms can reasonably be accepted as consistent with the objective medical evidence and other evidence, based on the requirements. The undersigned also considered the medical opinion(s) and prior administrative medical] finding(s) in accordance with the requirements. After careful consideration of the evidence, the undersigned finds that the claimant's medically determinable impairments could reasonably be expected to cause the alleged symptoms. The claimants statements concerning the intensity, persistence and limiting effects of these symptoms are generally consistent with the objective medical evidence and other evidence in the record. The description of the symptoms and limitations that the claimant has provided throughout the record generally has been consistent and persuasive. The claimant persuasively testified that her limitations hinder her ability to maintain functionality for extended periods of time. Her allegations are supported by doctor staten1ents, and the record contains no inconsistencies that bring her allegations into serious question. Examination of the record reveals ample evidence of the claimant severe impairments to merit the restrictions adopted above. J'he medical evidence of record shows that the claimant has a history of degenerative disc disease of the cervical, lumbar, and thoracic spine; lymphedema status-pos~ breast carcinoma; anal fissures/fistula; Lichen Sclerosis; genital ulcers; and herpes simplex virus (I-ISV). She has complained of physical symptoms including painful vaginal and anal lesions/growths, swelling/pain in the upper extremities, back pain, neck pain, and fatigue. (See generally treatment records) The extent of the claimant's physical allegations is supported by the findings on physical examination, imaging/testing, and the nature of the claimant's treatment. See Next Page :he_ claimant's allegations are supported by physical examination. Physical examination reveals a mildly antalgic gait, decreased range of motion in the lumbar and cervical spine:, straight leg raising, and positive facet compression maneuvers. The claimants?s allegations are supported by radiographic and other objective evidence. In 2021 imaging of the cervical spine revealed degenerative change most mar e a k d t C4 is where there is moderate spinal canal narrowing with cord contact and mild to moderate neural foraminal narrowing. In 2023, a thoracic MRI showed mild scattered degenerative changes, and a lumbar MRI showed multilevel degenerative disc disease and disc protrusion. The claimant's treatment for her physical conditions has been extensive and exhaustive in nature. The claimant was diagnosed with right breast invasive ductal carcinoma in April 2023. On May 17, 2023, the claimant underwent right lumpectomy and right axillary lymph node dissection with pathology showing a multifocal tumor with 4 separate masses. 3 out of 9 sentinel axillary lymph nodes were involved with metastatic adenocarcinoma. On June 2, 2023, a PET CT scan showed post treatment changes in the right breast and no evidence of metastatic malignancy in the neck chest abdomen or pelvis. On June 20, 2023, the claimant started Taxotere Cytoxan chemotherapy with Neulasta support. In August 2023, the claimant completed chemotherapy, and in November 2023, the claimant completed radiation. While malignancy has not recurred, the claimant is in occupational therapy for resultant lymphedema affecting the upper extremities. The claimant has a history of genital HSV infection, lichen sclerosis on the anus and vulva, and anal fissures. She has been treated with antiviral medication and high potency topical steroids and calcineurin inhibitors. She required anal fistula surgery in February 2023. Concerning the claimant' s musculoskeletal impairments, treatment has included opioid pain medication,. chiropractic, physical therapy, activity modifications, NSAID p medications, epidural steroid injections, and radio-frequency neurotonty. As for medical opinion(s) and prior administrative medical finding(s) we will not defer or give any specific evidentiary weight, including controlling weight, t any prior administrative medical finding(s) or medical opinion(s), including those from your, medical sources. We fully considered the medical opinions and prior administrative medical findings in your case as follows: Specifically, the undersigned considered the prior administration consultants. These doctors found to have findings of the state agency work with postural and environmental limitations. These doctors have a high level evidence in the record when generating their findings. However, the undersigned does not find the conclusions persuasive. The conclusions are partially supported by the examiners' detailed summary and analysis of records reviewed citing intact strength and range of motion in spite of multi-level degenerative disc disease throughout the spine. However, they are not consistent with records submitted after they reviewed the file. Later submitted records are consistent with greater exertion limitation. While malignancy has not reoccurred, the claimant is in occupational therapy for resultant lymphedema affecting the upper extremities. This in combination with her severe spinal impairments is consistent with sedentary work. The undersigned considered the opinion of M.D. The undersigned finds the opinion persuasive. Dr. supports his opinion citing aggressive non-surgical treatment in the form of physical therapy, medications, activity modification, epidural steroid injections, and radiofrequency neurotomy. Likewise, the opinion is consistent with the claimant's aggressive treatment for breast cancer resulting in upper extremity lymphedema. The undersigned considered the opinion of PT, DPT. The undersigned finds the opinion persuasive. Mr. supports his opinion citing ongoing chronic pain despite aggressive intervention. Likewise, the opinion is consistent with physical examination findings. Physical examination reveals a mildly antalgic gait, decreased range of ,notion in the lumbar and cervical spine, positive straight leg raising, and positive facet compression maneuvers. The undersigned considered the opinion of M.D. The undersigned finds the opinion persuasive. Dr. suppose her opinion citing painful lichen sclerosus and complex anal fissure impacting the claimant's ability to sit. Likewise, the opinion is consistent with physical examination findings. Physical examination reveals a mildly antalgic gait, decreased range of motion in the lumbar and cervical spine, positive straight leg raising, and positive facet compression maneuvers. Additionally, the undersigned considered the prior administrative findings of the state agency psychological consultants. These consultants found that the claimant?s mental impairments were non-severe. As with the medical consultants, the psychological consultants' findings deserve consideration as these doctors have a high level of understanding of the disability program and enjoy a review of all the available evidence in the record when finding their conclusions. The undersigned finds the conclusions persuasive. The conclusions are supported by the examiner' summary and analysis of records reviewed citing the claimant's conservative mental health treatment. Likewise, the conclusions are consistent with the largely intact mental status examination findings provided by the claimant's therapist. The undersigned considered the opinion of the psychological consultative examiner. The undersigned does not find the opinion persuasive. The opinion is partially supported by the claimant's performance at the psychological consultative explanation. At this exam, mental status examination revealed distractibility, tearfulness, labile affect, and depressed mood. However, the degree of limitation opined is not consistent with the claimant's Sec Nexl Page conservative mental health treatment. The claimant did not begin psychotherapy until 1 March 2024 ,. and mental status examination from these notes reveals largely intact mental status. examination findings. The claimant has not required psychiatric inpatient admission. In view of all the factors discussed above, the evidence supports the limitations on the claimant's capacities described earlier in this decision. 6. The claimant has no past relevant work. 7. The claimant was an individual closely approaching advanced age on the established disability onset date. 8. The claimant has at least a high school education. 9. Transferability of job skills is not an issue in this case because the claimant does not have past relevant work. 10. Considering the claimant's age, education, work experience, and residual functional capacity, there are no jobs that exist in significant numbers in the national economy that the claimant can perform. Even if the claimant had the residual functional capacity for the full range of sedentary work, a finding of '"disabled .. ' would be directed. by Rule. 11. The claimant has been under a disability as defined in the Act since September 18, 2021, the alleged onset date of disability. 12. The claimant's substance use disorder(s) is not a contributing factor material to the determination of disability. Applying the sequential evaluation process a second time, the claimant's other impairments would not improve to the point of non disability in the absence of the substance use disorder(s). In making this determination, the Administrative Law Judge noted that the claimant's records contained references to a history of stimulant use disorder. However, pursuant, the undersigned determined that this was not material to the outcome of this decision as the impact of her prior stimulant use was fully considered in developing the residual functional capacity statement. In particular, records revealed that the claimant's impairments exist independently of: her prior use, and there was no evidence that her impairments would improve in the absence of stimulant abuse. Furthermore, records indicate that the claimant's stimulant use disorder has been in sustained remission. According)y, the claimant would still be disabled in the absence of the substance use disorder(s). See Next Page Based on the application for disability and disability insurance benefits protectively filed on October 24 2024 the claimant has been disabled under sections of the Act since September 18, 2021 DECISION . . Page More
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2842581 76 F OR 05/24/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Blister, Herpes zoster, Rash macular Blister, Herpes zoster, Rash macular
Full blown case of shingles from left side of back of neck to around under chin. Started noticing on... Full blown case of shingles from left side of back of neck to around under chin. Started noticing on Monday, May 19th and then worse and more lesions and continues today, May 24th, 2025. Red blotches with liquid filled blisters. More
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