🏥 VAERS Vaccine Data Browser

🔒 Privacy & Data Disclaimer

About This Site

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

Data Source & Accuracy

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

Your Privacy

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

Medical Disclaimer

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

Data Interpretation

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

📖 Help & Search Guide

Column Icons Legend

💀 Death
🏥 Hospitalized
🚑 Emergency Room
♿ Disability
⚠️ Life Threatening

How to Search

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

Understanding the Data

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

Using the Table

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

💡 Frequently Asked Questions (FAQ)

What is this site?

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

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

What is VAERS?

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

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

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

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

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

Why does this site exist?

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

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

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

Where does the data come from?

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

The data is:

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

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

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

Important context:

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

What to do:

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

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

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

Limitations:

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

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

What are "adverse events"?

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

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

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

Why are some lot numbers listed multiple times?

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

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

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

How often is this data updated?

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

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

Where can I learn more?

⚠️ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
🔄 Reset 📥 Export CSV
ID Age Sex State Date ▼ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative 💀 🏥 🚑 ♿ ⚠️
2841058 67 M IA 05/15/2025 FLUX
VARZOS
 UNKNOWN MANUFACTURER
GLAXOSMITHKLINE BIOLOGICALS

Body temperature increased, Internal haemorrhage, Musculoskeletal stiffness, Pai... Body temperature increased, Internal haemorrhage, Musculoskeletal stiffness, Pain in extremity, Swelling; Body temperature increased, Internal haemorrhage, Musculoskeletal stiffness, Pain in extremity, Swelling More
Swelling in the left shoulder, Temp - 103 internal bleeding of my arm (shoulder to wrist) intense pa... Swelling in the left shoulder, Temp - 103 internal bleeding of my arm (shoulder to wrist) intense pain & stiffness. Emergency room visit 2xs. More
2841059 79 F IN 05/15/2025 RSV
RSV
RSV
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH


Arthralgia, Choking, Cough, Dyspnoea, Fatigue; Feeling hot, Injection site eryth... Arthralgia, Choking, Cough, Dyspnoea, Fatigue; Feeling hot, Injection site erythema, Injection site induration, Injection site pain, Injection site swelling; Myalgia, Pain in extremity, Peripheral swelling, Secretion discharge More
Left arm pain, redness and swelling at site and pain to elbow. I had fatigue. Pain in arm lasted 3 t... Left arm pain, redness and swelling at site and pain to elbow. I had fatigue. Pain in arm lasted 3 to 3 1/2. I had muscle pain and more joint pain at 6 am 3-8 I woke up coughing and coking had so much mucus thought I would choke and couldn't get breath, lasted 2 hours then went back to bed. Monday at 4AM on 10th woke up choking with mucus again couldn't get breath and coughing. I had the RSV shot 3-6-25. My left arm hurt, got swollen and felt warm. Continued til Tuesday 3-11. It still feels like my upper left arm is swollen or has a knot. I felt fatigued for a long time and muscle and joint pain. I woke up coughing and choking Saturday 3-8. I had so much mucus I thought I would choke to death - I couldn't breath for choking. That lasted 2 hours then I went back to bed after coughing up the mucus. Then Monday 3-10 at 4AM I woke up choking with mucus again and couldn't get breath - coughing so hard, spitting up mucus. I've had lots of mucus since shot. My left arm hurt clear to elbow. I did not go to hospital or doctor - I just got up and coughed it out. I should have never let my doctor talk us in to this RSV shot. It compromises your immune system for 3 weeks and is not very effective. It's useless! You are supposed to only get one shot ever but then I read only good for 18 months or 2 years. I received no written information from my doctor so went in next day 3-7 and asked for some printed information on this shot and found out it was Pfizer. More
2841061 84 F TX 05/15/2025 COVID19
PNC20
VARZOS
 MODERNA
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS


Feeding disorder, Pain in extremity, Skin warm; Feeding disorder, Pain in extrem... Feeding disorder, Pain in extremity, Skin warm; Feeding disorder, Pain in extremity, Skin warm; Feeding disorder, Pain in extremity, Skin warm More
Patient is hot Patient can not eat Arm is sore Patient is hot Patient can not eat Arm is sore
2841111 16 F IN 05/15/2025 MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
 52N4S
Syncope Syncope
patient fainted 5 mins after vaccine was given patient fainted 5 mins after vaccine was given
2841112 0.17 M MI 05/15/2025 DTAPIPVHIB
RV5
 SANOFI PASTEUR
MERCK & CO. INC.
 UK110AA
2096661
Haematochezia; Haematochezia Haematochezia; Haematochezia
After first dose of Rotateq, mom states that child had blood in his stool After first dose of Rotateq, mom states that child had blood in his stool
2841113 0.33 M MI 05/15/2025 RV5
 MERCK & CO. INC.
 2052023
Haematemesis Haematemesis
After second dose of Rotateq, child had blood in vomit. Second time having rotateq but had a similar... After second dose of Rotateq, child had blood in vomit. Second time having rotateq but had a similar reaction with first dose and have blood in his stool More
2841114 78 M 05/15/2025 RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 F4AC3
unknown
Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
Patient got Arexvy in October of 2023 but this was unknown to pharmacy and patient had forgotten. Pr... Patient got Arexvy in October of 2023 but this was unknown to pharmacy and patient had forgotten. Presented at pharmacy on 5/14/25 wanting Arexvy vaccine and it was administered after patient verbally stated they had never received one. Discovered after the fact that dose in May was a duplication of the single-dose series. Patient does not report any unexpected side effects at this time. More
2841115 36 F MT 05/15/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
 344J3
Rash, Rash erythematous, Rash papular Rash, Rash erythematous, Rash papular
Rash with raised red bumps on both arms. Patient called the pharmacy and explained her reaction to ... Rash with raised red bumps on both arms. Patient called the pharmacy and explained her reaction to me. I advised she take Diphenhydramine orally and apply Hydrocortisone 1% cream topically. I called her the next morning and she said her rash was just about completely resolved. More
2841116 77 F MD 05/15/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
Neck pain, Pain, Pain in extremity, Product administered at inappropriate site, ... Neck pain, Pain, Pain in extremity, Product administered at inappropriate site, Weight bearing difficulty More
Vaccine given in shoulder. Several hours later began experiencing pain in right arm up to neck. Co... Vaccine given in shoulder. Several hours later began experiencing pain in right arm up to neck. Could not raise arm without extreme pain. Cannot lift anything. More
✓
2841117 50 F AR 05/15/2025 PNC21
PNC21
TDAP
TDAP
VARZOS
VARZOS
 MERCK & CO. INC.
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 Y019158
Y019158
3CA17C1
3CA17C1
MG5S9
MG5S9
Abdominal pain upper, Asthenia, Decreased appetite, Drug withdrawal syndrome, Fa... Abdominal pain upper, Asthenia, Decreased appetite, Drug withdrawal syndrome, Fatigue; Headache, Pain, Vomiting; Abdominal pain upper, Asthenia, Decreased appetite, Drug withdrawal syndrome, Fatigue; Headache, Pain, Vomiting; Abdominal pain upper, Asthenia, Decreased appetite, Drug withdrawal syndrome, Fatigue; Headache, Pain, Vomiting More
Patient reports that when she woke up on 5/7/2025 (day following her injections) she was weak, had b... Patient reports that when she woke up on 5/7/2025 (day following her injections) she was weak, had body aches, throwing up with stomach cramps, did not eat for 2 days, fatigue, with a headache. Patient also reports that she was unable to get up to take her medication and had a gabapentin withdrawal. More
2841118 74 M MN 05/15/2025 COVID19
 MODERNA
COVID-19, SARS-CoV-2 test positive COVID-19, SARS-CoV-2 test positive
Hospitalization related to COVID 19 following completion of primary vaccine series Hospitalization related to COVID 19 following completion of primary vaccine series
✓
2841120 50 F CA 05/15/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 E754F
Arthralgia, Headache, Injection site pain, Injection site swelling, Myalgia Arthralgia, Headache, Injection site pain, Injection site swelling, Myalgia
Serious body pain (joints & muscles), moderate headache, mild pain/swelling at injection site. Serious body pain (joints & muscles), moderate headache, mild pain/swelling at injection site.
2841121 1.25 F NY 05/15/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
 LX4483
LX4483
Agitation, Erythema, Injection site cellulitis, Pyrexia, Swelling; Ultrasound sc... Agitation, Erythema, Injection site cellulitis, Pyrexia, Swelling; Ultrasound scan More
5/12/25 -Received Shot - Had Normal redness and swelling. 5/13/25 woke up with a different redness/ ... 5/12/25 -Received Shot - Had Normal redness and swelling. 5/13/25 woke up with a different redness/ swelling pattern in the same area I, the parent, Circled said "swollen area" for observation. Child was not bothered. Same day after dinner, baby spiked a fever of 101.6 and was agitated as expected- Administered Tylenol for fever. 5/14- I noticed at her first diaper change upon waking up- the swollen area doubled in size, and was now spreading toward her groin. More
2841122 65 F NY 05/15/2025 MENB
MNQ
 PFIZER\WYETH
SANOFI PASTEUR
 HP9987
U8361AA
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Patient received MenQuadfi/Bexsero on 03/13/25 while inpatient hospital. HCP referred patient to ano... Patient received MenQuadfi/Bexsero on 03/13/25 while inpatient hospital. HCP referred patient to another facility on 04/23/25 for completion doses of MenQuadfi/Trumenba and they were administered on 05/13/25 at home with nursing. More
2841123 1 M MI 05/15/2025 PNC15
TDAP
VARCEL
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 x01997
m77cc
y006524
Product administered to patient of inappropriate age; Product administered to pa... Product administered to patient of inappropriate age; Product administered to patient of inappropriate age; Product administered to patient of inappropriate age More
TDAP was given in lieu of the needed DTAP. TDAP was given in lieu of the needed DTAP.
2841124 56 F VA 05/15/2025 HEPA
 MERCK & CO. INC.
 X026485
Expired product administered, No adverse event Expired product administered, No adverse event
Patient received Vaqta Hepatitis A vaccine (5/14/25) that expired on 5/11/25, 3 days out of date. No... Patient received Vaqta Hepatitis A vaccine (5/14/25) that expired on 5/11/25, 3 days out of date. No reactions noted at this time, no plans to have pt return for redose at this time. More
2841125 26 F AK 05/15/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 CX4HL
Incorrect route of product administration, No adverse event Incorrect route of product administration, No adverse event
No adverse event, no treatment needed, outcome good. No adverse event, no treatment needed, outcome good.
2841126 67 F IL 05/15/2025 COVID19
COVID19
 MODERNA
MODERNA
 038K20A
038K20A
Cranial nerve paralysis, Dysarthria, Magnetic resonance imaging head normal, Pul... Cranial nerve paralysis, Dysarthria, Magnetic resonance imaging head normal, Pulmonary function test, Scan with contrast normal; Swallow study More
She had the 2nd vaccine a month later. 3 months after the 1st vaccine (reported info above) and 2 ... She had the 2nd vaccine a month later. 3 months after the 1st vaccine (reported info above) and 2 months after the 2nd vaccine booster (info available in her medical record), she had sudden onset of dysarthria. Has had full neurological work up and no progression or improvement. Idiopathic cranial nerve palsy is diagnosis at this time, but due to proximity of the vaccines to this neurological condition, M.D. felt obligated to report. More
✓
2841127 1 F IL 05/15/2025 HEPA
MMR
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 J4K4X
Y007613
Y011020
Measles antibody, Rash, Urticaria; Measles antibody, Rash, Urticaria; Measles an... Measles antibody, Rash, Urticaria; Measles antibody, Rash, Urticaria; Measles antibody, Rash, Urticaria More
Developed extensive urticarial rash on trunk, face, extremities on 4/17/25. Seen at ED on 4/18/25. S... Developed extensive urticarial rash on trunk, face, extremities on 4/17/25. Seen at ED on 4/18/25. Seen for follow-up in office on 4/25/25. More
2841128 32 M GA 05/15/2025 TYP
 BERNA BIOTECH, LTD.
 3004171
Dyspnoea, Nausea Dyspnoea, Nausea
Client reports that 4 hours after taking dose 1 he experienced SOB that felt like "my lungs wer... Client reports that 4 hours after taking dose 1 he experienced SOB that felt like "my lungs were being folded" and some nausea. Client called requesting for advice on the following day. At time of call, symptoms had resolved and client was instructed to discontinue this medication. Client was instructed to seek emergency medical care if he experienced further symptoms of allergic reaction. More
2841129 38 F TX 05/15/2025 MMR
MMR
 MERCK & CO. INC.
MERCK & CO. INC.
 Y014095
Y014095
Feeling abnormal, Hot flush, Injection site pain, Injection site reaction, Injec... Feeling abnormal, Hot flush, Injection site pain, Injection site reaction, Injection site swelling; Nausea, Urticaria More
1 inch raised welp located at the site of administration Tender to touch Slight swelling Hot flashes... 1 inch raised welp located at the site of administration Tender to touch Slight swelling Hot flashes Feels bad in general nausea More
2841130 1.25 F MI 05/15/2025 DTAP
DTAP
HIBV
HIBV
PNC20
PNC20
HIBV
HIBV
 SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
PFIZER\WYETH
MERCK & CO. INC.
MERCK & CO. INC.





W028534
W028534
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event; Expired product administered, No adverse event More
office called to state they gave the patient an expired dose of Pedvaxhib vaccine -expired on 5/10/2... office called to state they gave the patient an expired dose of Pedvaxhib vaccine -expired on 5/10/25. No AE at this time. More
2841131 67 M FL 05/15/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 XK5HC
Rash Rash
extreme rash on left arm extreme rash on left arm
2841132 0.5 F NC 05/15/2025 DTAPHEPBIP
PNC20
RV5
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
MERCK & CO. INC.
 9359N
MF0415
Y018147
Injection site reaction, Rash papular; Injection site reaction, Rash papular; In... Injection site reaction, Rash papular; Injection site reaction, Rash papular; Injection site reaction, Rash papular More
Rash on right leg about 1-1.5 hours following immunizations. Video provided by mother shows 3-4 sma... Rash on right leg about 1-1.5 hours following immunizations. Video provided by mother shows 3-4 small erythematous papules to right lower leg. More
2841133 60 F WA 05/15/2025 PNC20
PNC20
PNC20
RSV
RSV
RSV
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH
 MF0416
MF0416
MF0416
KD0161
KD0161
KD0161
Arthralgia, Cellulitis, Chills, Erythema, Injection site erythema; Injection sit... Arthralgia, Cellulitis, Chills, Erythema, Injection site erythema; Injection site pain, Injection site swelling, Joint swelling, Pruritus, Skin warm; Type IV hypersensitivity reaction; Arthralgia, Cellulitis, Chills, Erythema, Injection site erythema; Injection site pain, Injection site swelling, Joint swelling, Pruritus, Skin warm; Type IV hypersensitivity reaction More
Patient reported on 5/13/25 that her left shoulder was swollen, painful, red and itchy. Triage nurse... Patient reported on 5/13/25 that her left shoulder was swollen, painful, red and itchy. Triage nurse spoke with the patient and the patient explained the area was warm to the touch, even more swollen and painful and had chills the previous day. The nurse recommended the patient to visit out urgent care clinic. Patient visited the urgent care clinic and was evaluated. The findings was a 7X8 cm area of slightly raised, erythematous ovular shaped nonindurated skin at the left deltoid, minimally tender. DDX: delayed hypersensitivity reaction, cellulitis. Antihistamine was recommended over the next few days and if it did not resolve the patient was instructed to return for reconsideration of antibiotics. More
2841134 7 M IL 05/15/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 22349
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient was 7 years old at the time of receiving Infanrix. Patient should have received first dose o... Patient was 7 years old at the time of receiving Infanrix. Patient should have received first dose of Tdap instead. No adverse event. More
2841135 75 F CO 05/15/2025 COVID19
 PFIZER\BIONTECH
 30145BA
Hip arthroplasty, Loss of consciousness Hip arthroplasty, Loss of consciousness
PASS OUT / LOSE CONSCIOUSNESS TWICE THE DAY OF THE VACCINE, AND THE NEXT DAY, AND THEN ONCE AGAIN AF... PASS OUT / LOSE CONSCIOUSNESS TWICE THE DAY OF THE VACCINE, AND THE NEXT DAY, AND THEN ONCE AGAIN AFTER A SURGERY More
2841136 26 F CT 05/15/2025 VARCEL
 MERCK & CO. INC.
 Y014939
No adverse event No adverse event
Colleague was administered varicella vaccine despite having a previous immune titer on record. Call ... Colleague was administered varicella vaccine despite having a previous immune titer on record. Call placed to candidate the following day confirming she had no reaction to recieving vaccine. More
2841138 2 F VA 05/15/2025 HPV9
MMR
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 X024251
X026219
Y010373
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; No adverse event, Product administered to patient of inappropriate age More
Gave HPV9 to a child younger than 9years old which is outside the recommended age range. Mother inf... Gave HPV9 to a child younger than 9years old which is outside the recommended age range. Mother informed of error and Vaccine Information Sheet (VIS) on HPV9 given to mother. Informed mother that IAP was calling CDC for information now and that HD would let her know what they said. No adverse reaction noted during 45 min wait period after vaccine given. More
2841140 4 F MD 05/15/2025 DTAPIPV
DTAPIPV
MMRV
MMRV
 SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.



Injection site erythema, Injection site induration, Injection site pruritus, Inj... Injection site erythema, Injection site induration, Injection site pruritus, Injection site reaction, Injection site swelling; Injection site warmth; Injection site erythema, Injection site induration, Injection site pruritus, Injection site reaction, Injection site swelling; Injection site warmth More
Injection site reaction on right thigh. Entirely thigh is swollen from hip to knee, especially outer... Injection site reaction on right thigh. Entirely thigh is swollen from hip to knee, especially outer thigh. Area is red, hard, and warm to touch and she reports it is itchy and doesn?t feel good. More
2841141 23 F NC 05/15/2025 COVID19
 PFIZER\BIONTECH
Dysmenorrhoea, Heavy menstrual bleeding, Injection site pain Dysmenorrhoea, Heavy menstrual bleeding, Injection site pain
Terrible pain at injection site. Approx. one year of extremely heavy bleeding during menstrual cycle... Terrible pain at injection site. Approx. one year of extremely heavy bleeding during menstrual cycle. Went from having cramps maybe once a year during my period to having them every single month. 4 years later, the heavy bleeding has stopped, but my pain persists. I once had a healthy period, and I have not had the same periods ever since vaccination. More
2841142 82 F MT 05/15/2025 COVID19
 MODERNA
 8081260
Erythema, Pruritus, Skin warm, Swelling, Tenderness Erythema, Pruritus, Skin warm, Swelling, Tenderness
Received vaccine 05/13/2025 in the AM. 05/14/2025 AM staff notified us she had area of redness, swel... Received vaccine 05/13/2025 in the AM. 05/14/2025 AM staff notified us she had area of redness, swelling, warmth, itching, and tenderness. Picture sent to primary care provider who ordered Augmentin 875/125 BID X 7 days. More
2841143 31 F RI 05/15/2025 COVID19
 PFIZER\BIONTECH
Seizure Seizure
Started getting seizures 3 months after receiving the vaccine Started getting seizures 3 months after receiving the vaccine
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2841144 11 M MI 05/15/2025 MNQ
 SANOFI PASTEUR
 U8493AA
Extra dose administered Extra dose administered
patient was inadvertently given 2 menquadfi 1 in left arm other in right arm patient was inadvertently given 2 menquadfi 1 in left arm other in right arm
2841145 36 F CA 05/15/2025 COVID19
 MODERNA
 3043030
Chest pain, Limb discomfort Chest pain, Limb discomfort
On 05/09/2025 - Participant was vaccinated on the left arm at 1534. 10 minutes into the 15-minute ob... On 05/09/2025 - Participant was vaccinated on the left arm at 1534. 10 minutes into the 15-minute observation period, at approximately 1544, participant reported a "heavy feeling" in their left arm as well as a "mild, sharp chest pain" that lasted 5-10 seconds and immediately disappeared after. Participant vitals were assessed by nurses and vitals were documented as followed: 99.1 F; 98% Oxygen Saturation; 110/75 Blood Pressure. Participant was monitored for additional 25 minutes and during the additional observation, the participant did not report any additional symptoms. Towards the end of the additional observation period, participant stated: "I am feeling fine, this is probably just my anxiety." More
2841146 34 F MN 05/15/2025 HEPA
YF
 MERCK & CO. INC.
SANOFI PASTEUR
 Y017625
UK134AA
Abdominal pain upper, Nausea, Pruritus, Sensation of foreign body, Urticaria; Ab... Abdominal pain upper, Nausea, Pruritus, Sensation of foreign body, Urticaria; Abdominal pain upper, Nausea, Pruritus, Sensation of foreign body, Urticaria More
Patient was advised to remain in clinic 15-20 minutes post immunization. Patient presented to front ... Patient was advised to remain in clinic 15-20 minutes post immunization. Patient presented to front desk at 4:11 PM stating she was feeling nauseous. RN brought patient back to room and patient verbalized nauseous and epigastric pain. Vaccine ordering provider notified by RN and provider assessed patient. VS taken - WNL. Patient seen by another provider for treatment. Patient's symptoms progressed to itchiness and hives on bilateral arms, bilateral hands, and chest around 4:35-4:40PM. Ice packs given for comfort. Oral Benadryl administered at 4:43 PM per provider's orders. Patient verbalized "feeling lump in throat". Patient alert and oriented x4 and ambulating independently. Oxygen saturation monitored continuously - between 95-100%. EMS/911 called and arrived at clinic around 4:55PM. Patient taken to hospital for further treatment and per chart review discharged to home. More
2841147 12 M NC 05/15/2025 HPV9
 MERCK & CO. INC.
 Z005055
Erythema multiforme Erythema multiforme
Pt was diagnosed with erythema multiforme on 5/13. Unknown if related to HPV vaccine on 5/2. Provi... Pt was diagnosed with erythema multiforme on 5/13. Unknown if related to HPV vaccine on 5/2. Provider and Parent wanted to report potential reaction More
2841148 20 M PA 05/15/2025 FLU3
HEPA
TDAP
 SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
 TFAA2439
Y015027
3CA22C1
Underdose; Underdose; Underdose Underdose; Underdose; Underdose
Patient came into the office to discuss vaccines needed for his trip to (redacted). Dr. ordered him ... Patient came into the office to discuss vaccines needed for his trip to (redacted). Dr. ordered him to have Vaqta (ped/adolescent), Adacel, & Flubok. It was later discovered that patient received Vaqta pediatric/adolescent 0.5mL instead of the Adult version which would be 1mL. We contacted the manufacturer who said this is an error and that dose not count for the patient and he would need to be revaccinated unless we wanted to do serology studies on the patient. I presented this to our vaccine director who instructed us to make the patient aware of what happen and revaccinate him with the correct dose. Patient has been contacted to received the correct dose of Vaqta. More
2841149 79 M NJ 05/15/2025 COVID19
 PFIZER\BIONTECH
 md3414
Injection site erythema, Injection site irritation Injection site erythema, Injection site irritation
Patient has red irritated mark on arm where vaccine was administered. He stated that it has been ov... Patient has red irritated mark on arm where vaccine was administered. He stated that it has been over 3 weeks since vaccination and it is still irritated. More
2841150 0.17 F NH 05/15/2025 DTPPVHBHPB
PNC20
RV5
 MSP VACCINE COMPANY
PFIZER\WYETH
MERCK & CO. INC.
 U8265AA
LJ5282
2052021
Urticaria; Urticaria; Urticaria Urticaria; Urticaria; Urticaria
Intermittent, diffuse hives all over body and face for 1 month Intermittent, diffuse hives all over body and face for 1 month
2841151 10 M AL 05/15/2025 TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U815AA
U815AA
Gait disturbance, Headache, Influenza virus test negative, Pain, Pain in extremi... Gait disturbance, Headache, Influenza virus test negative, Pain, Pain in extremity; Pyrexia, SARS-CoV-2 test negative, Urine analysis normal More
2-3 hours after the TDaP vaccine was given, patient started having a severe headache, body ache, bil... 2-3 hours after the TDaP vaccine was given, patient started having a severe headache, body ache, bilateral thigh pain, which make it difficult for him to walk, and fever that rose as high as 105.1. He experienced no local reaction in his Left deltoid region. His parent took him to ED for evaluation on 5/14/25. After tests were negative for Flu, Covid and UTI, the ED staff diagnosed patient with a post-vaccine fever. on 5/15/25 , I talked with his mother, who reported that fever had stopped after ER visit and that he was feeling better More
2841152 59 F OR 05/15/2025 UNK
 UNKNOWN MANUFACTURER
Headache, Injection site erythema, Injection site pruritus, Injection site urtic... Headache, Injection site erythema, Injection site pruritus, Injection site urticaria, Pain More
severe body ackes for two full days and nights, headache for one week, redness at injection site the... severe body ackes for two full days and nights, headache for one week, redness at injection site the turned to a large hive encompassing my left bicept for seven days, itching off and on for several days. More
2841153 36 F GA 05/15/2025 TDAP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS

Inflammation, Injected limb mobility decreased, Joint range of motion decreased,... Inflammation, Injected limb mobility decreased, Joint range of motion decreased, Limb discomfort, Loss of personal independence in daily activities; Muscular weakness, Pain in extremity, Shoulder injury related to vaccine administration, X-ray More
Dead arm/weakness, immobile arm of injection, persistent pain, reduced range of motion, inflammation... Dead arm/weakness, immobile arm of injection, persistent pain, reduced range of motion, inflammation, impairment to quality of life. I went back to the doctor's office who gave the injection a month later (11/14/2022), they referred me to Physical Therapy. I did physical therapy on my arm/ shoulder from 11/17/2022-1/23/2023. I felt some relief after physical therapy with the occasional discomfort, pain and immobility. over the last two months 3/2025-5/2025 I have had severe immobility, and reduced range of motion effecting my daily activities and causing severe pain. On 5/15/2025 I went to an orthopedic doctor and they diagnosed me with SIRVA and suggested a cortisone shot. They administered the shot on 5/15/2025. More
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2841154 53 M OH 05/15/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93n4j
Nodule, Pain Nodule, Pain
patient stated that he's had a painful knott, he came to the pharmacy today 5/15/25 while he re... patient stated that he's had a painful knott, he came to the pharmacy today 5/15/25 while he received his vaccine on 5/6/25. he was wondering if this should last this long, i told him no it should last no longer than 2-3 days. he said he will check with his dr More
2841155 F AZ 05/15/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
Injection site reaction, Rash Injection site reaction, Rash
Hep B injection given in right leg at time of birth. Parents reported in a recent office visit for ... Hep B injection given in right leg at time of birth. Parents reported in a recent office visit for the patient, that vaccine has caused painful, persistent subcutaneous bumps. More
2841156 29 F MI 05/15/2025 TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 U8264AA
U8264AA
Exposure during pregnancy, Foetal death, Foetal heart rate abnormal, Haemorrhage... Exposure during pregnancy, Foetal death, Foetal heart rate abnormal, Haemorrhage, Muscle spasms; Pathology test, Stillbirth More
Healthy first pregnancy until fetus died. Went to hospital at 35 weeks and 2 days pregnant because a... Healthy first pregnancy until fetus died. Went to hospital at 35 weeks and 2 days pregnant because abnormal bleeding and cramps. Tdap vaccine recieved at 32 weeks pregnant. At hospital found no heart beat. Expected delivery was January 23, 2025. Stillborn birth weight was 1701 grams. More
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2841157 4 M CA 05/15/2025 DTAPIPV
DTAPIPV
DTAPIPV
MMRV
MMRV
MMRV
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 U8009AB
U8009AB
U8009AB
Y015257
Y015257
Y015257
Abdominal pain upper, Asthenia, Blood glucose decreased, Blood urine present, Ey... Abdominal pain upper, Asthenia, Blood glucose decreased, Blood urine present, Eye movement disorder; Fatigue, Foaming at mouth, Full blood count normal, Malaise, Metabolic function test normal; Tremor; Abdominal pain upper, Asthenia, Blood glucose decreased, Blood urine present, Eye movement disorder; Fatigue, Foaming at mouth, Full blood count normal, Malaise, Metabolic function test normal; Tremor More
The morning following his immunizations he began experiencing a stomach ache. He ate a normal breakf... The morning following his immunizations he began experiencing a stomach ache. He ate a normal breakfast. He had no fever and no vomiting. He was laying down on the couch because he felt ill. Mother runs a daycare and when a daycare aide was asked to check on him she immediately notified mother something was wrong. Mother found him frothing at the mouth and without strength when trying to stand him up. His eyes rolled back into his head and he was shaking rhythmically. No bladder or bowel incontinence. Felt very tired afterwards. Felt fine when in the Emergency Department and has been at baseline since then. More
2841158 38 F CA 05/15/2025 HEP
 VBI VACCINES
Pain, Skin warm Pain, Skin warm
Sore. And warm Sore. And warm
2841159 75 M CO 05/15/2025 PNC20
 PFIZER\WYETH
 hg7740
Expired product administered Expired product administered
pt was given an expired vaccine. provider was then notified. then I notified the patient. pt was given an expired vaccine. provider was then notified. then I notified the patient.
2841166 14 F OH 05/15/2025 HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
HPV4
 MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.





















Abdominal pain, Abdominal pain upper, Antinuclear antibody increased, Appendicec... Abdominal pain, Abdominal pain upper, Antinuclear antibody increased, Appendicectomy, Appendicitis; Areflexia, Asthenia, Back pain, Brain fog, Bronchitis; Chest pain, Chills, Colonoscopy, Cough, Diarrhoea; Disturbance in attention, Dyspnoea, Educational problem, Endometriosis, Endoscopy upper gastrointestinal tract; Fatigue, Gait disturbance, Gastrooesophageal reflux disease, General physical health deterioration, Guillain-Barre syndrome; Haematochezia, Headache, Heart rate decreased, Heart rate increased, Hyperhidrosis; Hypoaesthesia, Immunoglobulin therapy, Increased need for sleep, Irritable bowel syndrome, Lacrimation increased; Lethargy, Loss of personal independence in daily activities, Nausea, Neck pain, Oropharyngeal pain; Oxygen saturation decreased, Paraesthesia, Pelvic pain, Peripheral coldness, Pneumonia; Pupillary disorder, Reading disorder, Reflex test abnormal, Small fibre neuropathy, Vomiting; Walking aid user, Weight decreased, Wheelchair user, Wheezing; Abdominal pain, Abdominal pain upper, Antinuclear antibody increased, Appendicectomy, Appendicitis; Areflexia, Asthenia, Back pain, Brain fog, Bronchitis; Chest pain, Chills, Colonoscopy, Cough, Diarrhoea; Disturbance in attention, Dyspnoea, Educational problem, Endometriosis, Endoscopy upper gastrointestinal tract; Fatigue, Gait disturbance, Gastrooesophageal reflux disease, General physical health deterioration, Guillain-Barre syndrome; Haematochezia, Headache, Heart rate decreased, Heart rate increased, Hyperhidrosis; Hypoaesthesia, Immunoglobulin therapy, Increased need for sleep, Irritable bowel syndrome, Lacrimation increased; Lethargy, Loss of personal independence in daily activities, Nausea, Neck pain, Oropharyngeal pain; Oxygen saturation decreased, Paraesthesia, Pelvic pain, Peripheral coldness, Pneumonia; Pupillary disorder, Reading disorder, Reflex test abnormal, Small fibre neuropathy, Vomiting; Walking aid user, Weight decreased, Wheelchair user, Wheezing More
Numbness, pain and needles in both feet which quickly moved to her entire legs and arms, by the even... Numbness, pain and needles in both feet which quickly moved to her entire legs and arms, by the evening, her entire body was numb/ patient was no longer able to walk on her own/ She could not read/Guillain-Bane syndrome; her oxygen were low; her pulse was from 150 beats per minute to 120 per minute; Brian fog; Bloody stools; Autoimmune injuries/autoimmune dsorder; ice cold legs, feet, and hands; Her pupils were not changind size/her puplis wer not responding; Her reflex were not responding to any of the tests; paresthesia; pelvic pain/endometriosis; cough and pain in her chest/persistant cough, chest pain, shortness of breath and wheezing /Acute bronchitis; Lethargic, chills, swats, and chest hurt/pneumonia; small fiber neuropathy; she was having constant diarrhea, nausea and could not keep any food down/Irritable bowe syndrome*irritable bowel syndrome (IBS); Pleurisy; gastroesophageal reflux disease (GERD),; Elevated ANA; Chronic headache; Sleeping even more; severe abdominal pain/appendicitis; She had lost 20 pounds/weight loss; Being extremely tired after the vaccination; Information has been received from a lawyer regarding a case in litigation and refers to a 14-year-old female patient (pt). The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 12-Aug-2019, the patient was vaccinated with the first dose of Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL), (strength, dose, frequency, lot #, and expiration date were not reported). Healthcare provider recommended pt receive the vaccine, which was touted as a safe and effective vaccine for preventing cercal cancer. Following her Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL) injections, pt went to urgent care due to a cough and pain in her chest. She was diagnosed with bronchitis and prescribed medicine but after finishing the medicine, she did not improve and returned to urgent care. She had a persistent cough, chest pain, shortness of breath and wheezing. She was again treated for bronchitis with antibiotics and steroids, but her condition continued to worsen, and she returned to urgent care. She was treated for acute bronchitis and pneumonia with antibiotics and steroids. Thereafter, she went to her family doctor as she was lethargic, had chills, sweats, and her chest hurt so badly that it brought her to tears. She was given different antibiotics, and the steroids were increased. Pt remained in pain, and it was later thought that she had pleurisy. With the approval of her doctor, she went on a family trip, but she was physically unable to do any of the planned outings. Thereafter, she saw a pulmonary specialist, but he could not determine what was causing her chest pain. Elevated ANA levels were noted. Pt continued experiencing chronic chest pain, chronic headaches, and sore throats. She started sleeping even more and her grades started to drop. Not aware that Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL), could be the cause of her condition, on 09-Mar-2020, she was vaccinated with the second dose of Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL), (strength, dose, frequency, lot #, and expiration date were not reported). Following her second dose of vaccine, pt's condition worsened. She complained of being extremely tired after the vaccination. Her chest continued to hurt but her stomach started hurting as well. On an unspecified date, pt again went to the emergency room (ER) with severe abdominal pain, and it was thought that she had appendicitis, and she had her appendix removed. She had lost 20 pounds because she was having constant diarrhea, nausea and could not keep any food down. Thereafter, she had upper and lower scopes, and the doctors thought she had irritable bowel syndrome, but the medicines she took for this condition did not help. Even though her classes were virtual, she missed school because she was unable to concentrate. Next, pt began having numbness, pins and needles in both feet which quickly moved to her entire legs and arms. By the evening, her entire body was numb. On an unspecified date (also reported as the following month), pt was no longer able to walk on her own. She could not read. Her pupils were not changing size. She had a neurological workup in the hospital and her reflexes were not responding to any of the tests. She was admitted to the hospital with a diagnosis of Guillain-Barre syndrome and started on IVIG treatments. She was discharged but her condition deteriorated. She went back to the hospital, and it was determined that she also had small fiber neuropathy. Next, pt had pins and needles pain in her arms and legs, and it was so severe that once again she could not walk. She was sent to the hospital again and had chest pain, and her pupils were not responding. Her oxygen levels were low, and her pulse was from 50 beats per minute to 120 per minute all while lying in the hospital bed. She was cared for by rheumatology, internal medicine and neurology specialists and eventually released from the hospital. Shortly after returning home from the hospital, she had to return to the ER and was admitted again. Pt ultimately ended up having to use a walker and a wheelchair. She required help going to the toilet and dressing herself. Pt continued to have episodes every few weeks and continues to have severe abdominal pain. She continued to be seen by doctors for the various symptoms that started after the Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL) vaccination. As the months progressed, so did pt's symptoms. She was seen by multiple physicians and specialists for her complaints of fatigue, headaches, brain fog, chest pain, back and neck pain, severe abdominal pain, weight loss, numbness, pins and needles pain to both arms and legs, difficulty walking, weakness, pelvic pain, diarrhea and bloody stool, ice cold legs, feet, and hands. As a result of her post- Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL) symptoms, patient has been unable to engage in activities that a normal young person would enjoy. Prior to receiving the Gardasil vaccinations, she was active, energetic, she played on the girl's lacrosse and golf team, she often rode a bike 25 miles round trip three to seven days a week. She excelled in junior high and her first year of high school as she was in advanced classes, she was an honor roll student. It was her intent to enlist in the National Guard, and to attain a BSN to become a travel nurse. Based upon her chronic and severe post- Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL) symptoms, pt had been diagnosed with various medical conditions, including but not limited to, Guillain-Barre syndrome, small fiber neuropathy, irritable bowel syndrome (IBS), gastroesophageal reflux disease (GERD), endometriosis, and paresthesia. Pt contended that her Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (GARDASIL) injections caused her to develop serious and debilitating autoimmune injuries, including but not limited to Guillain-Barre syndrome, small fiber neuropathy, irritable bowel syndrome (IBS), gastroesophageal reflux disease (GERD), endometriosis, paresthesia, fatigue, headaches, brain fog, chest pain, severe abdominal pain, weight loss, numbness, pins and needles pain to both arms and legs, difficulty walking, weakness, pelvic pain, diarrhea and bloody stool, ice cold legs, feet, and hands, as well as a constellation of adverse symptoms, complications, injuries, and other adverse events, many of which are alleged herein and all of which were caused by Gardasil or otherwise linked to her Gardasil-induced autoimmune disorder. At the time of reporting the outcome of the events was not provided. Causal assessment with all the events was related. Upon internal review, the events pneumonia, appendicitis, and haematochezia was considered as medically significant. The events Guillain-Barre syndrome, small fibre neuropathy, irritable bowel syndrome, paresthesia, asthenia, pleurisy, and autoimmune disorder were considered as disabling events. This is one of several reports from the same reporter. More
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