๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ Privacy & Data Disclaimer

About This Site

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

Data Source & Accuracy

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

Your Privacy

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

Medical Disclaimer

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

Data Interpretation

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

๐Ÿ“– Help & Search Guide

Column Icons Legend

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

How to Search

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

Understanding the Data

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

Using the Table

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

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

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

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

What is VAERS?

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

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

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

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

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

Why does this site exist?

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

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

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

Where does the data come from?

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

The data is:

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

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

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

Important context:

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

What to do:

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

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

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

Limitations:

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

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

What are "adverse events"?

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

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

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

Why are some lot numbers listed multiple times?

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

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

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

How often is this data updated?

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

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

Where can I learn more?

โš ๏ธ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
1413779 63 F NY 06/21/2021 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
0171321A
0171321A
0171321A
0171321A
0171321A
0171321A
010A21A
Anion gap, Anti-GAD antibody, Anti-islet cell antibody, Blood glucose increased,... Anion gap, Anti-GAD antibody, Anti-islet cell antibody, Blood glucose increased, Blood insulin; Blood pH decreased, Blood phosphorus, Carbon dioxide, Diabetic ketoacidosis, Differential white blood cell count normal; Feeling abnormal, Full blood count normal, Hyperphagia, Infusion, Intensive care; Laboratory test, Oral candidiasis, Polydipsia, Polyuria, SARS-CoV-2 test negative; Scab, Skin lesion, Type 1 diabetes mellitus, Urine analysis, Urine ketone body present; Weight decreased; Type 1 diabetes mellitus More
pt was admitted on 6/19 with DKA, metabolic acidosis, severe oral thrush and non healing ear lesions... pt was admitted on 6/19 with DKA, metabolic acidosis, severe oral thrush and non healing ear lesions secondary to new onset type 1 diabetes. she has had no recent illnesses or infections. she takes no medications and has no known medical problems. she sees her primary care regularly and never had problems with her blood sugars before. she is very active and eats well. she has never smoked. she noticed about 2 months ago not feeling herself. she noticed 2 scabs and sores on the outside of her ears that would not heal and sudden weight loss. she then noticed polydipsia, polyuria and polyphagia and thrush in her mouth. she went to urgent care on 6/19 and her blood sugar was 474 and she was directed to the ER for evaluation where she was found to be in DKA with new type 1 diabetes and admitted to the icu on an insulin drip. She had her covid 19 vaccines on 3/3 and 3/31. No hx illnesses or infections. she takes no medications. she has never had covid 19 to her knowledge. with iv fluids, insulin and treatment for her thrush her blood sugars were better controlled and she was transferred out of the icu to the medical floor for further education on management of new diabetes and placed on lantus, humalog with meals and sliding scale. she was seen by the diabetes educator and will be following up with endocrinology after discharge. autoimmune antibody panel for LADA pending. More
โœ“ โœ“
2821386 61 M NY 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
N77J2
Atrial fibrillation, Condition aggravated Atrial fibrillation, Condition aggravated
Developed afib 2 days after receiving the 2nd dose of Shingrix Developed afib 2 days after receiving the 2nd dose of Shingrix
2821387 77 M NY 01/16/2025 COVID19-2
PFIZER\BIONTECH
lm2223
Injection site pain Injection site pain
Site: Pain at Injection Site-Medium Site: Pain at Injection Site-Medium
2821388 62 F TX 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
B4942
Fatigue, Lethargy Fatigue, Lethargy
Systemic: Exhaustion / Lethargy-Medium, Additional Details: Patient reported feeling extremely tired... Systemic: Exhaustion / Lethargy-Medium, Additional Details: Patient reported feeling extremely tired for a day after getting the shot More
2821389 62 M TX 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
B4942
Fatigue, Lethargy Fatigue, Lethargy
Systemic: Exhaustion / Lethargy-Medium, Additional Details: Patient reported feeling extremely tired Systemic: Exhaustion / Lethargy-Medium, Additional Details: Patient reported feeling extremely tired
2821390 71 F IL 01/16/2025 PNC20
PFIZER\WYETH
LG5577
Dermatitis allergic, Injection site erythema, Injection site pain, Rash Dermatitis allergic, Injection site erythema, Injection site pain, Rash
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Ras... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium More
2821391 78 F AZ 01/16/2025 COVID19
MODERNA
208H23A
Abdominal discomfort, Dizziness Abdominal discomfort, Dizziness
Systemic: Dizziness / Lightheadness-Medium, Systemic: Upset stomach-Medium, Additional Details: Pati... Systemic: Dizziness / Lightheadness-Medium, Systemic: Upset stomach-Medium, Additional Details: Patient reported that she feels upset stomach and light headed after receiving all vaccines, Other Vaccines: VaccineTypeBrand: PREVNAR 20; Manufacturer: PFIZER; LotNumber: ; Route: ; BodySite: ; Dose: 1; VaxDate: 04/04/2024 More
2821392 74 M MA 01/16/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
a9kr2
Fatigue, Injection site erythema, Injection site pruritus, Lethargy, Nausea Fatigue, Injection site erythema, Injection site pruritus, Lethargy, Nausea
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Exhaustion... Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Nausea-Medium, Additional Details: got on the same day as boostrix but that was given in the right deltoid muscle More
2821393 58 F FL 01/16/2025 FLUC4
SEQIRUS, INC.
391416
Injection site erythema, Pruritus, Pruritus allergic Injection site erythema, Pruritus, Pruritus allergic
Site: Redness at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)... Site: Redness at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium More
2821396 18 M MO 01/16/2025 COVID19
PFIZER\BIONTECH
LM2212
Dizziness, Fall, Pallor, Syncope, Unresponsive to stimuli Dizziness, Fall, Pallor, Syncope, Unresponsive to stimuli
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Det... Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: Just a few minutes following vaccine administration, patient began to stand up from chair and fainted (fell backwards into privacy wall, knocking it over). Pt quickly regained consciousness and face/lips looked pale. Pt was helped back into seated position where he remained for approximately 15-20 minutes. EMS was not needed and pt walked out of pharmacy recovered. Pt did indicate on questionaire/consent form that he has gotten dizzy or fainted before, during or after immunization., Other Vaccines: VaccineTypeBrand: Influenza seasonal Flucelvax Trivalent; Manufacturer: Seqirus, INC.; LotNumber: 946606; Route: intramuscular; BodySite: left deltoid; Dose: ; VaxDate: UNKNOWN More
2821397 65 M RI 01/16/2025 COVID19
MODERNA
3043822
Burning sensation, Injection site erythema, Injection site pruritus, Injection s... Burning sensation, Injection site erythema, Injection site pruritus, Injection site swelling More
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at In... Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient stated burning, itchiness, redness and swelling started about 5 to 6 hours after injection. Patient went to urgent care and was given prednisone and cephalexin. More
2821398 61 M MA 01/16/2025 RSV
RSV
PFIZER\WYETH
PFIZER\WYETH
kd0161
kd0161
Confusional state, Dizziness, Flushing, Hyperhidrosis, Pallor; Presyncope, Synco... Confusional state, Dizziness, Flushing, Hyperhidrosis, Pallor; Presyncope, Syncope, Unresponsive to stimuli More
Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating... Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Medium, Additional Details: wife noticed patient's face went pale after the second shot was given (Abrysvo in right arm), and recognized signs of syncope and vasovagal response which patient has a hx of in response to pain. Pt became confused, & non responsive verbally. Rx tech and wife assisted patient to the floor for safety. A instant cold pack was given to put on back of his neck (trick that worked for family during previous episodes). After about 15 min patient pt became verbal, but still confused, called EMS., Other Vaccines: VaccineTypeBrand: Prevnar; Manufacturer: Pfizer; LotNumber: LG5579; Route: IM; BodySite: Left Arm; Dose: 0; VaxDate: UNKNOWN More
2821399 61 F PA 01/16/2025 COVID19
MODERNA
8058877
Malaise, Pyrexia Malaise, Pyrexia
Systemic: Fever-Mild, Additional Details: patient stated she always gets sick for a few days after t... Systemic: Fever-Mild, Additional Details: patient stated she always gets sick for a few days after taking the vaccine. More
2821400 34 M CT 01/16/2025 FLUR4
PROTEIN SCIENCES CORPORATION
tfaa2420
Injection site pain Injection site pain
Site: Pain at Injection Site-Mild, Additional Details: Pharm. D gave Patient pfizer comirnaty and fl... Site: Pain at Injection Site-Mild, Additional Details: Pharm. D gave Patient pfizer comirnaty and flublock influenza vaccine. When patient recieved vaccinations, the rph hand shook while administering the vaccine. Patient still recieved both vaccinations in the correct location of the left deltioid. , Other Vaccines: VaccineTypeBrand: comirnaty; Manufacturer: pfizer; LotNumber: ln0589; Route: im; BodySite: left; Dose: ; VaxDate: UNKNOWN More
2821401 35 M CA 01/16/2025 HEP
DYNAVAX TECHNOLOGIES CORPORATION
945658
Hypoaesthesia, Rash Hypoaesthesia, Rash
Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Numbness (specify: fa... Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Additional Details: Received a call from the mother (2:06pm) several hrs after pt received the vaccine, stating that his son's elbow has a rash and pt's arm and hands are numb. Informed the mother to take pt to the ER or urgent care. I called at 4:55pm to see the condition of the pt, but mother states that they just arrived to ER and pt's symptoms are still the same. Informed mother to keep us informed or I will call back the following day. More
2821402 50 F CA 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
4KG45
Chills, Fatigue, Lethargy, Pain Chills, Fatigue, Lethargy, Pain
Systemic: Body Aches Generalized-Mild, Systemic: Chills-Mild, Systemic: Exhaustion / Lethargy-Mild Systemic: Body Aches Generalized-Mild, Systemic: Chills-Mild, Systemic: Exhaustion / Lethargy-Mild
2821403 61 M PA 01/16/2025 COVID19
MODERNA
au3832b
Butterfly rash, Injection site pruritus, Lyme disease, Rash pruritic, Systemic l... Butterfly rash, Injection site pruritus, Lyme disease, Rash pruritic, Systemic lupus erythematosus More
Site: Itching at Injection Site-Medium, Systemic: Butterfly rash, itchy - was told lyme then lupus-M... Site: Itching at Injection Site-Medium, Systemic: Butterfly rash, itchy - was told lyme then lupus-Medium More
2821404 36 F AZ 01/16/2025 VARCEL
MERCK & CO. INC.
y005922
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
2821405 71 F FL 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
9L5P2
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection... Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild More
2821406 46 M FL 01/16/2025 PPV
MERCK & CO. INC.
Y009239
Deafness unilateral Deafness unilateral
Systemic: Hearing loss in right ear (about 10% hearing)-Medium Systemic: Hearing loss in right ear (about 10% hearing)-Medium
2821407 68 F AL 01/16/2025 FLU4
FLU4
SANOFI PASTEUR
SANOFI PASTEUR
ut8470ca
ut8470ca
Injection site bruising, Injection site erythema, Injection site necrosis, Injec... Injection site bruising, Injection site erythema, Injection site necrosis, Injection site nodule, Injection site pain; Injection site swelling More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injec... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: local swelling, knot, necrosis - likely to leave a scar More
2821408 87 F IN 01/16/2025 COVID19
PFIZER\BIONTECH
Unknown
Chills, Malaise, Pyrexia Chills, Malaise, Pyrexia
Systemic: Chills-Severe, Systemic: Fever-Severe, Additional Details: Date is approximate because pat... Systemic: Chills-Severe, Systemic: Fever-Severe, Additional Details: Date is approximate because patient stated it was the 4th or 5th dose of the Covid vaccine that caused her symptoms. Patient reports also not feeling well after her recent (8/26/24) Fluzone High Dose Triv but could not provide any details other than she felt "sick" More
2821409 55 F AZ 01/16/2025 COVID19
MODERNA
AU3920B
Chills, Fatigue, Lethargy, Pain Chills, Fatigue, Lethargy, Pain
Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Me... Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium, Additional Details: Patient states similar effects for the last 3 Covid vaccinations received More
2821410 65 F FL 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
74NC9
Injection site erythema Injection site erythema
Site: Redness at Injection Site-Mild Site: Redness at Injection Site-Mild
2821411 71 F CA 01/16/2025 VARZOS
VARZOS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
9r397
9r397
Erythema, Eye swelling, Mouth swelling, Rash, Rash pruritic; Swelling face, Swol... Erythema, Eye swelling, Mouth swelling, Rash, Rash pruritic; Swelling face, Swollen tongue More
Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash (speci... Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Additional Details: Patient stated start having swelling of eyes and rash on face. She came in the pharmacy today and said gotten better but wanted cream to relieve the itching and benadryl since doctor told patient to go to the pharmacy to get OTC meds. No more swelling but redness on face is still present. More
2821412 14 F MA 01/16/2025 COVID19
PFIZER\BIONTECH
LM2216
Dizziness, Syncope, Unresponsive to stimuli Dizziness, Syncope, Unresponsive to stimuli
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild
2821413 56 F FL 01/16/2025 COVID19
MODERNA
Unknown
Chills, Influenza like illness, Pyrexia Chills, Influenza like illness, Pyrexia
Systemic: Chills-Medium, Systemic: Fever-Medium, Additional Details: Flu-like symptoms Systemic: Chills-Medium, Systemic: Fever-Medium, Additional Details: Flu-like symptoms
2821414 8 M AL 01/16/2025 FLUC4
SEQIRUS, INC.
388522
Chills, Dizziness, Flushing, Hyperhidrosis Chills, Dizziness, Flushing, Hyperhidrosis
Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild
2821415 60 M CA 01/16/2025 COVID19
MODERNA
3030371
Chills, Nasopharyngitis, Pyrexia Chills, Nasopharyngitis, Pyrexia
Systemic: Chills-Mild, Systemic: Fever-Mild, Systemic: Cold-Mild, Additional Details: Patient report... Systemic: Chills-Mild, Systemic: Fever-Mild, Systemic: Cold-Mild, Additional Details: Patient reported having bad reaction such as a cold, fever, chills and it last for a couple of days. More
2821416 37 F CA 01/16/2025 COVID19
MODERNA
3043823
Muscle spasms Muscle spasms
Systemic: pt complained about severe muscle spasm and pharmacy called EMS-Severe, Additional Details... Systemic: pt complained about severe muscle spasm and pharmacy called EMS-Severe, Additional Details: pt complained about severe muscle spasm throughout her body and she complained about feeling it the most in her throat and chest. Pharmacy called EMS with pt consent., Other Vaccines: VaccineTypeBrand: influenza vaccine; Manufacturer: seqirus; LotNumber: 946619; Route: im; BodySite: right arm; Dose: 1; VaxDate: 01/10/2025 More
2821418 23 F OH 01/16/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
3d72s
Injection site erythema, Injection site pruritus, Injection site swelling Injection site erythema, Injection site pruritus, Injection site swelling
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Inject... Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Other Vaccines: VaccineTypeBrand: varvivax with diluent; Manufacturer: merck; LotNumber: Y011020; Route: subcutaneous; BodySite: right arm; Dose: ; VaxDate: UNKNOWN More
2821419 4 M IL 01/16/2025 FLUC4
SEQIRUS, INC.
388533
Vomiting Vomiting
Systemic: Vomiting-Mild, Additional Details: This was for the flucelevax trivalent-quadravalent was ... Systemic: Vomiting-Mild, Additional Details: This was for the flucelevax trivalent-quadravalent was only formulation listed More
2821420 68 M FL 01/16/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
4y2p4
Chills, Pyrexia Chills, Pyrexia
Systemic: Chills-Mild, Systemic: Fever-Mild, Additional Details: Patient stated that symptoms just l... Systemic: Chills-Mild, Systemic: Fever-Mild, Additional Details: Patient stated that symptoms just lasted a few hours More
2821421 36 M NY 01/16/2025 FLUC4
SEQIRUS, INC.
946635
Dermatitis contact, Injection site vesicles, Wound Dermatitis contact, Injection site vesicles, Wound
Systemic: PATIENT REPORTED OPEN WOUND BLISTER FROM ADHESIVE FROM BANDAID USED-Medium, Additional Det... Systemic: PATIENT REPORTED OPEN WOUND BLISTER FROM ADHESIVE FROM BANDAID USED-Medium, Additional Details: PATIENT REPORTED RX COMPLAINT IN MY CUSTOMER CONNECTION 01/10/2025 THAT HE EXPERIENCED AN OPEN WOUND BLISTER FROM ADHESIVE. I CALLED HIM AS A FOLLOW UP 01/13/2025 TO GET MORE DETAIL AND FIND OUT IF THERE WAS ANYTHING ELSE HE WOULD LIKE ME TO ADD TO ADVERSE EVENT REPORT. HE DID NOT SEEK ANY ADDITIONAL MEDICAL CARE OR REQUIRED ANY URGENT CARE VISIT. IN SPEAKING HE SAID IT WAS BETTER TODAY. I ASKED HIM IF IN THE FUTURE HE USES PHARMACY FOR ANY ADDITIONAL VACCINES TO PLEASE MAKE SURE WE ARE AWARE., Other Vaccines: VaccineTypeBrand: COVID; Manufacturer: PFIZER; LotNumber: LN0588; Route: IM; BodySite: LEFT ARM; Dose: 1; VaxDate: 01/06/2025 More
2821422 50 M PA 01/16/2025 PNC21
MERCK & CO. INC.
Y011819
Dizziness, Malaise, Syncope Dizziness, Malaise, Syncope
Patient received 2 vaccines Capvaxive and Flublok. Patient fainted and was not feeling well for abou... Patient received 2 vaccines Capvaxive and Flublok. Patient fainted and was not feeling well for about 15 minutes post vaccines. We gave patient a cold pack to put on his neck and gave him a soda to drink to increase blood sugar. We also had patient sit on floor after he started feeling dizzy and faint. More
2821423 17 F ID 01/16/2025 MNQ
SANOFI PASTEUR
U8361AA
Dyspnoea, Pallor, Tremor Dyspnoea, Pallor, Tremor
Pt was sitting in the upright position, prepared left deltoid, IM injection given, spot band-aid app... Pt was sitting in the upright position, prepared left deltoid, IM injection given, spot band-aid applied. pt was sitting calmly. I proceeded to prepare right deltoid area and pt stated she needed to lay back. Pt was directed to lay down, I proceeded to elevate her feet. I noticed pt became very pale, started to shake, gasping for breaths were noted. Mother was immediately by her side as I continued to talk to the patient. approximately 10 seconds passed and pt awoke startled, she tried to jump up to her feet, her mother and myself calmly held her and stopped her from standing. pt was able to understand us at that time and we were able to get her to lay down, provider was called immediately, mother remained next to her. provider came to the room, an ice pack was placed to the back of pt neck, cold wet towels placed to her forehead and abdomen area. pt slowly became aware of what had happened. pt remained laying as provider talked to her and mother. 2 4 ounce containers of juice were given to the pt. pt tolerated and was able to regain color back in her face. Pt mother, at that time declined/refused that she receive the Meningococcal B vaccine, which would have been #1 in the series. pt recovered approximately 15 min after vaccine administration, she ambulated on her own, with her mother nearby with no further concerns noted. More
2821424 7 F UT 01/16/2025 COVID19
PFIZER\BIONTECH
LM2045
Expired product administered, No adverse event Expired product administered, No adverse event
Vaccine expired, no none adverse reactions Vaccine expired, no none adverse reactions
2821425 81 F CA 01/16/2025 UNK
UNKNOWN MANUFACTURER
LN0589
Musculoskeletal pain Musculoskeletal pain
persistent musculoskeletal pain persistent musculoskeletal pain
2821426 79 M CA 01/16/2025 COVID19
PFIZER\BIONTECH
LM2210
Ageusia, Lethargy, Myalgia Ageusia, Lethargy, Myalgia
The patient's symptoms included myalgia, lethargy, and a loss of taste, which has persisted for... The patient's symptoms included myalgia, lethargy, and a loss of taste, which has persisted for seven weeks. More
2821427 33 F TX 01/16/2025 COVID19
COVID19
FLU3
FLU3
PFIZER\BIONTECH
PFIZER\BIONTECH
SEQIRUS, INC.
SEQIRUS, INC.
LN0589
LN0589
388532
388532
Butterfly rash, Chills, Diarrhoea, Fatigue, Headache; Injection site pain, Pain ... Butterfly rash, Chills, Diarrhoea, Fatigue, Headache; Injection site pain, Pain in extremity; Butterfly rash, Chills, Diarrhoea, Fatigue, Headache; Injection site pain, Pain in extremity More
Chills, headache, fatigue, diarrhea, soreness of butt and thighs, soreness at injection site Chills, headache, fatigue, diarrhea, soreness of butt and thighs, soreness at injection site
2821428 44 F OR 01/16/2025 COVID19
PFIZER\BIONTECH
LN0589
Joint range of motion decreased, Magnetic resonance imaging abnormal, Pain in ex... Joint range of motion decreased, Magnetic resonance imaging abnormal, Pain in extremity, Periarthritis, X-ray More
left arm pain, reduced range of motion. MRI in December revealed Adhesive Capsulitis. left arm pain, reduced range of motion. MRI in December revealed Adhesive Capsulitis.
2821435 43 F TX 01/16/2025 FLU3
SEQIRUS, INC.

Injection site pain, Product administered at inappropriate site Injection site pain, Product administered at inappropriate site
Patient states her Left arm still hurts/aches from time to time in the area where she received her ... Patient states her Left arm still hurts/aches from time to time in the area where she received her Flu vaccine. She was given vaccine on October 23rd, 2024. She is able to move and use her Left arm. She has not had another vaccine since in that arm. She has not contacted her doctor as of yet. She states vaccine was giving lower than she is used to. More
2821436 37 F LA 01/16/2025 TDAP
GLAXOSMITHKLINE BIOLOGICALS
333SK
Headache, Pain, Pain in jaw Headache, Pain, Pain in jaw
Patient reported Headaches, Jaw pain, and pains throughout body. Patient took Fioricet, Ibuprofe... Patient reported Headaches, Jaw pain, and pains throughout body. Patient took Fioricet, Ibuprofen, and Ajovy Injection to get pain to subside but will only last for a couple of hours before reoccurring. More
2821437 33 F ND 01/16/2025 FLU3
FLU3
FLU3
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR



Arthralgia, Bursitis, Hypoaesthesia, Immediate post-injection reaction, Joint ra... Arthralgia, Bursitis, Hypoaesthesia, Immediate post-injection reaction, Joint range of motion decreased; Ligament pain, Mobility decreased, Pain, Paraesthesia, Product administered at inappropriate site; Shoulder injury related to vaccine administration, Sleep disorder, Tendonitis, X-ray limb normal More
Nurse administered the vaccine into subacromial space rather than the deltoid muscle. This caused im... Nurse administered the vaccine into subacromial space rather than the deltoid muscle. This caused immediate pain on administration and inability to move. Left shoulder within 20 minutes following the injection. Have experienced ongoing left shoulder pain, left arm numbness and tingling, and restricted range of motion due to pain since that time. Three weeks after initial injection, range of motion significantly worsened as well as the pain, which also affected ability to sleep. Was evaluated on 11/15/24, diagnosed with SIRVA, tendonitis, and bursitis. X-ray completed 11/15/24 was normal. Took Medrol dosepak at that time. Continued use of Aleve twice daily. Multiple visits with occupational medicine since then and physical therapy, and this has continued since that time. Dry needling has been helpful in reducing the numbness and tingling in the arm. Continued pain deep in the shoulder joint and ligaments. Pain persists with flexion, extension, and external rotation of the shoulder. Evaluated by orthopedics 1/15/25, received Kenalog 80mg injection into shoulder joint. MRI to follow in a couple weeks. The influenza vaccine is not to blame for the injury, incorrect administration of the vaccine into the subacromial space is what caused the injury. More
2821438 4 F CA 01/16/2025 DTAPIPV
GLAXOSMITHKLINE BIOLOGICALS
42Y93
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Mom stated swelling and warmth noted on left arm almost down to the elbow the next day after receivi... Mom stated swelling and warmth noted on left arm almost down to the elbow the next day after receiving vaccine. Mom stated there was a circle of redness like an raised doughnut that spread down towards the elbow. Mom stated this redness and swelling was painful for the child and the child was given Motrin then in a few hours Tylenol. Mom stated today the area is slightly fading and there is less of a complaint from the child. Mom denies child having a bug or insect bite. Mom stated definitely from the shot. More
2821439 74 F GA 01/16/2025 RSV
GLAXOSMITHKLINE BIOLOGICALS
52z52
Extra dose administered Extra dose administered
Patient was accidentally given a second dose of Arexvy, First dose was administered 4/25/2024 Patient was accidentally given a second dose of Arexvy, First dose was administered 4/25/2024
2821440 10 F CA 01/16/2025 IPV
SANOFI PASTEUR
X1D141M
Cough, Hypersensitivity, Swelling face, Urticaria Cough, Hypersensitivity, Swelling face, Urticaria
Within hours of receiving polio vaccine patient "start cough, swelling face, hives generalized.... Within hours of receiving polio vaccine patient "start cough, swelling face, hives generalized." Patient was seen at Urgent Care facility and urticarial rash was noted. Patient was treated for allergic reaction with signs concerning for evolving anaphylaxis per review of Urgent Care note. Patient was treated with prednisone, diphenhydramine, albuterol treatment. Symptoms resolved. More
2821441 0.17 F NV 01/16/2025 DTPPVHBHPB
HPV9
RV5
MSP VACCINE COMPANY
MERCK & CO. INC.
MERCK & CO. INC.



Infant irritability, Product administered to patient of inappropriate age, Pyrex... Infant irritability, Product administered to patient of inappropriate age, Pyrexia, Vomiting, Wrong product administered; Infant irritability, Product administered to patient of inappropriate age, Pyrexia, Vomiting, Wrong product administered; Infant irritability, Product administered to patient of inappropriate age, Pyrexia, Vomiting, Wrong product administered More
was suppose to receive PCV20, instead received HPV9. had fever on vomiting the night of. was irritab... was suppose to receive PCV20, instead received HPV9. had fever on vomiting the night of. was irritable for 2 days after. on 01/16/2025 was stable and better More
2821442 77 F AK 01/16/2025 FLU3
SANOFI PASTEUR
UT8425DA
Anaphylactic reaction, Dyspnoea, Rash, Rash macular, Urticaria Anaphylactic reaction, Dyspnoea, Rash, Rash macular, Urticaria
PATIENT EXPERIENCED NEAR ANAPHYLAXIS, HAD BLOTCHY NECK WITH RASH AND HIVES, BEGAN TO HAVE TROUBLE BR... PATIENT EXPERIENCED NEAR ANAPHYLAXIS, HAD BLOTCHY NECK WITH RASH AND HIVES, BEGAN TO HAVE TROUBLE BREATHING AND TOOK BENADRYL IMMEDIATELY. REACTION OCCURED 3HRS POST IMMUNIZATION More
2820931 4 U MD 01/15/2025 MMRV
MERCK & CO. INC.
X018580
Expired product administered, No adverse event Expired product administered, No adverse event
the patient involved has not experienced any medical concerns or symptoms as of the time of this int... the patient involved has not experienced any medical concerns or symptoms as of the time of this interaction; A dose of PROQUAD had a labeled expiration date of 1/5/2025 and was inadvertently administered to a patient today, 1/10/2025; This spontaneous report was received from a medical assistance and refers to a 4-year-old patient of unknown gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 10-JAN-2025, the patient was inadvertently vaccinated with a dose of two-dose series of measles, mumps, rubella and varicella (oka-merck) virus vaccine live (PROQUAD), 0.5 milliliter, lot #X018580, (labeled expiration date: 05-JAN-2025), administered for prophylaxis (strength, and route of administration were not provided) (Expired product administered). The patient involved had not experienced any medical concerns or symptoms as of the time of this report. No additional information provided. No additional adverse event (AE) reported. More