🏥 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 💀 🏥 🚑 ♿ ⚠️
2814034 81 F MD 12/05/2024 COVID19
FLU3
COVID19
 PFIZER\BIONTECH
SANOFI PASTEUR
PFIZER\BIONTECH


Erythema, Laboratory test normal, Pruritus, Skin test negative, Urticaria; Eryth... Erythema, Laboratory test normal, Pruritus, Skin test negative, Urticaria; Erythema, Laboratory test normal, Pruritus, Skin test negative, Urticaria; Urticaria More
Developed red, itchy bumps known as hives and still have. Show up anywhere: stomach, mostly arms, ne... Developed red, itchy bumps known as hives and still have. Show up anywhere: stomach, mostly arms, neck and face! More
2819404 69 F GA 01/04/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52Z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
A second dose of Arexvy was given upon patient request. First dose was unknown to vaccinating pharma... A second dose of Arexvy was given upon patient request. First dose was unknown to vaccinating pharmacist and was not documented in the registry. Patient experienced no ill effects from second vaccination. More
2819451 53 F WA 01/04/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 MD9SL
Gout, Pain in extremity Gout, Pain in extremity
Pt claims pain in left foot later that evening - Resulted in Gout Pt claims pain in left foot later that evening - Resulted in Gout
2819452 67 F MA 01/04/2025 SMALLMNK
 BAVARIAN NORDIC
 968G7
Incorrect route of product administration, No adverse event Incorrect route of product administration, No adverse event
No adverse events Administration was IM not sub Q No adverse events Administration was IM not sub Q
2819177 0.17 U LA 01/03/2025 HIBV
 MERCK & CO. INC.
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
booster, dose at 7-months old, which is earlier than the recommended age for the booster; no adverse... booster, dose at 7-months old, which is earlier than the recommended age for the booster; no adverse event; This spontaneous report was received from a consumer and refers to a 15-month-old patient of unknown gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On an unknown date at 2 months old, the patient received the first dose of haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) intramuscular injection (dose, strength, lot #, expiry date, and route of administration were not provided). On an unspecified date at 4 months old received the second dose of haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) intramuscular injection (dose, strength, lot #, expiry date, and route of administration were not provided). On an unspecified date at 7 months old, the patient received the booster and third haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) intramuscular injection, 0.5 milliliter, administered for prophylaxis (strength, lot #, expiry date, and route of administration were not provided), this was earlier than the recommended age for booster dose (inappropriate schedule of product administration). No additional adverse event was reported. More
2819178 59 F 01/03/2025 COVID19
PNC21
UNK
 UNKNOWN MANUFACTURER
MERCK & CO. INC.
UNKNOWN MANUFACTURER
 6024MF016A
Y011819
TFAA2437
Injection site cellulitis, Injection site inflammation; Injection site celluliti... Injection site cellulitis, Injection site inflammation; Injection site cellulitis, Injection site inflammation; Injection site cellulitis, Injection site inflammation More
Injection site cellulitis; Injection site inflammation; Initial information received on 26-Dec-2024 ... Injection site cellulitis; Injection site inflammation; Initial information received on 26-Dec-2024 regarding an unsolicited valid non-serious courtesy case received from a consumer/non-hcp (non-healthcare professional). This case involves 59 years old female patient who experienced injection site cellulitis and injection site inflammation after receiving Pneumococcal vaccine conj 21v (CRM197) (Capvaxive) and Covid-19 Vaccine Prot. Subunit (Nvx Cov 2373) (Novavax Covid-19 Vaccine) and Influenza Trivalent Recombinant Vaccine [Flublok TIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. No concomitants used/reported. On 06-Nov-2024, the patient received a dose 1 of suspect novavax covid-19 vaccine not produced by Sanofi Pasteur Injection with strength 0.5 ml (lot 6024MF016A) for COVID-19 immunization; received a dose 1 of suspect Capvaxive not produced by Sanofi Pasteur injection (lot Y011819) for prophylactic vaccination (Immunisation) and received a dose 1 of suspect influenza trivalent recombinant vaccine Solution for injection(lot TFAA2437) for prophylactic vaccination (Immunisation), all via intramuscular route in unknown administration site. On 07-NOV-2024 the patient developed injection site cellulitis and injection site inflammation (latency- 1 day) following the administration of influenza trivalent recombinant vaccine, novavax covid-19 vaccine and Capvaxive. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Not Recovered / Not Resolved for both the events. The CDC's (Centers for Disease Control and Prevention) adverse event description (narrative) was provided as follows: lnflamation/cellulitus below injection site approximately 6 inches wide and 8 inches long More
2819196 64 F MN 01/03/2025 COVID19
 MODERNA
 016B21A
Laboratory test, Stress fracture Laboratory test, Stress fracture
I am not aware of worsening bone mineral density or an increase in fracture risk as a result of the ... I am not aware of worsening bone mineral density or an increase in fracture risk as a result of the covid vaccines, but there is a correlation in timing with her and She raises concerns regarding COVID-19 vaccine and stress fractures of her feet. First foot stress fracture was in July 2021 And now has had 5 foot/stress fractures in total,. Her Moderna COVID-19 vaccines were: 3/29/21 and 4/26/21 She wonders / thinks these vaccines might have caused some changes that led to her stress/foot fracture More details July 2021: Right foot fracture Oct 2021: Left foot fracture, fracture of fifth metatarsal Nov 2022: possible right foot stress fracture Jan 2023: fracture fifth metarsal bone on my left foot again July 2024: left foot fracture (4th metatarsal) Per patient Dec'24: That makes FIVE factures of my feet (two on the right and three on the left). More
2819197 4 F CA 01/03/2025 DTAP
DTAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 47y5m
47y5m
Diarrhoea, Dizziness, Fatigue, Injection site swelling, Rash; Urticaria Diarrhoea, Dizziness, Fatigue, Injection site swelling, Rash; Urticaria
Rash started within 12 hours. Extreme fatigue, dizziness, lightheadedness upon awaking the next day... Rash started within 12 hours. Extreme fatigue, dizziness, lightheadedness upon awaking the next day. Rash appeared to look like a chemical burn after 36hours and turned to hives after 48hours .which lasted a week. Diarrhea persisted throughout. There is still a bump at injection site. More
2819198 F TX 01/03/2025 FLU3
HEP
 SANOFI PASTEUR
MERCK & CO. INC.

No adverse event, Product administered to patient of inappropriate age, Wrong pr... No adverse event, Product administered to patient of inappropriate age, Wrong product administered; No adverse event, Product administered to patient of inappropriate age, Wrong product administered More
Accidently administered Fluzone instead of the intended vaccine hepatitis B with no reported adverse... Accidently administered Fluzone instead of the intended vaccine hepatitis B with no reported adverse event.; Accidently administered Fluzone instead of the intended vaccine hepatitis B with no reported adverse event.; This spontaneous report was received from a health care professional and refers to a 15-day-old female patient. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 14-NOV-2024, the patient was accidentally vaccinated with influenza vaccine (FLUZONE [INFLUENZA VACCINE]) suspension for injection, 0.5 milligram, administered for prophylactic vaccination (strength, lot #, expiry date, route and anatomical site of administration were not provided) instead of the intended hepatitis b vaccine (recombinant) (RECOMBIVAX HB) intramuscular injection (Wrong product administered) with no reported adverse event (No adverse event). The reported inquired about any potential concerns they should be aware of when the patient was transferred to them, including possible side effects or any they could do regarding this situation. She reiterated that this did not happen in their facility. More
2819199 56 F WV 01/03/2025 COVID19
 MODERNA
Headache, Injection site erythema, Injection site swelling Headache, Injection site erythema, Injection site swelling
Large red spot (about the size of a 50 cent coin) with some swelling below injection site. Headache. Large red spot (about the size of a 50 cent coin) with some swelling below injection site. Headache.
2819201 51 F 01/03/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Eye pain, Fatigue, Pain in extremity Eye pain, Fatigue, Pain in extremity
arm soreness; fatigue; pain in the ophthalmic; This non-serious case was reported by a consumer via ... arm soreness; fatigue; pain in the ophthalmic; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of pain in arm in a 51-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. The patient's past medical history included shingles (had in her 30s). On an unknown date, the patient received the 1st dose of Shingrix. On an unknown date, an unknown time after receiving Shingrix, the patient experienced pain in arm (Verbatim: arm soreness), fatigue (Verbatim: fatigue) and eye pain (Verbatim: pain in the ophthalmic). The outcome of the pain in arm, fatigue and eye pain were not resolved. It was unknown if the reporter considered the pain in arm, fatigue and eye pain to be related to Shingrix. It was unknown if the company considered the pain in arm, fatigue and eye pain to be related to Shingrix. Additional Information: GSK receipt date: 06-DEC-2024 This case was reported by a patient via interactive digital media. The patient reported that she had shingles in her 30s and got vaccinated at 51 and interestingly the first shot had a more robust reaction in terms of arm soreness and fatigue. The reporter reported that she even developed return of a bit of pain in the ophthalmic region where her earlier shingles attack happened. More
2819204 10 M IL 01/03/2025 DTAPIPV
 GLAXOSMITHKLINE BIOLOGICALS
 42Y93
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
The patient was too old to recveive the Kinrix Vaccine. The patient was too old to recveive the Kinrix Vaccine.
2819205 7 F IL 01/03/2025 DTAPIPV
HEP
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 42Y93
42b22
Y010292
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
The patient was too old to receive the Kinrix vaccine. The patient was too old to receive the Kinrix vaccine.
2819250 11 F TN 01/03/2025 IPV
MMR
TDAP
 SANOFI PASTEUR
MERCK & CO. INC.
SANOFI PASTEUR
 X1C891M
X026329
3CA22C1
Drooling, Ear discomfort, Posture abnormal; Drooling, Ear discomfort, Posture ab... Drooling, Ear discomfort, Posture abnormal; Drooling, Ear discomfort, Posture abnormal; Drooling, Ear discomfort, Posture abnormal More
Pt to clinic with mother for immunizations. Mother states NKA. Pt is needing Tdap, IPV, and MMR for ... Pt to clinic with mother for immunizations. Mother states NKA. Pt is needing Tdap, IPV, and MMR for school. Pt given vaccines around 1400 and as soon as last vaccine administered patient slumps forward on clinical bed. Pt leaned back and laid down on clinical bed where she is fully responsive with little drool on face and complaining of her "ears feel clogged." Pt was only out for about 5 seconds. Mother states pt has not eaten all day and stated last time she had her blood drawn she had done the same thing. Pt was given juice and a snack as she laid back. Pt then sat up for a few minutes before having pt stand. Pt states felt good before she left the clinic. More
2819251 1.75 M 01/03/2025 FLU3
 SEQIRUS, INC.
 AW1556A
Incorrect dose administered Incorrect dose administered
This pt received 0.5 mL Afluria 2024-2025 formula on 3 Jan 25. The on call provider was notified, PS... This pt received 0.5 mL Afluria 2024-2025 formula on 3 Jan 25. The on call provider was notified, PSR and VAERS form have been placed. The child received a higher dose than is recommended for his age group. Afluria is approved for his age group at a dose of 0.25ml. More
2819252 87 F PR 01/03/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 PH457
Pain in extremity, Peripheral swelling, X-ray normal Pain in extremity, Peripheral swelling, X-ray normal
The patient claims that 3 to 4 days after receiving the flu vaccine at our vaccination center, her a... The patient claims that 3 to 4 days after receiving the flu vaccine at our vaccination center, her arm began to swell and hurt. She states that she went to her primary care physician and was given pain medication, but saw no improvement. Her husband came to the pharmacy and was recommended to take (Aleve "Naproxen"). Naproxen provided a lot of relief, but time passed and the patient still has pain, inflammation, and feels that the pain is reaching her leg. The patient had to go to the emergency room yesterday, January 2, 2025. The patient has been in this situation for over a month now. She was prescribed Ultracet, Indometacin, and Medrol dose pack. At the pharmacy, she was recommended that if the treatment is not effective, she should visit a physiatrist. More
2819253 57 F MN 01/03/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 029L20A
024M20A
013F21A
023H22A
Cough, Oropharyngeal pain, SARS-CoV-2 test; Cough, Oropharyngeal pain, SARS-CoV-... Cough, Oropharyngeal pain, SARS-CoV-2 test; Cough, Oropharyngeal pain, SARS-CoV-2 test; Cough, Oropharyngeal pain, SARS-CoV-2 test; Cough, Oropharyngeal pain, SARS-CoV-2 test More
Cough, sore throat x3 weeks Cough, sore throat x3 weeks
2819254 90 F AR 01/03/2025 COVID19
 MODERNA
 3031897
COVID-19 COVID-19
covid infection after vaccination covid infection after vaccination
✓
2819255 83 F AR 01/03/2025 COVID19
 MODERNA
 AS7140C
COVID-19 COVID-19
covid infection after vaccination covid infection after vaccination
2819256 23 F MN 01/03/2025 COVID19
COVID19
COVID19
 MODERNA
MODERNA
PFIZER\BIONTECH
 023C21A
051C21A
HD9876
Chest pain, Cough, Nasal congestion, Pain, SARS-CoV-2 test; Chest pain, Cough, N... Chest pain, Cough, Nasal congestion, Pain, SARS-CoV-2 test; Chest pain, Cough, Nasal congestion, Pain, SARS-CoV-2 test; Chest pain, Cough, Nasal congestion, Pain, SARS-CoV-2 test More
Cough, chest aches, dry cough, nasal congestion, body aches Cough, chest aches, dry cough, nasal congestion, body aches
2819258 84 M AR 01/03/2025 COVID19
 MODERNA
 060F22A
COVID-19 COVID-19
covid infection after vaccination covid infection after vaccination
2819259 26 F DC 01/03/2025 RSV
 PFIZER\WYETH
 LG9829
Dyspnoea, Exposure during pregnancy, Heart rate irregular Dyspnoea, Exposure during pregnancy, Heart rate irregular
33 weeks pregnant at time of vaccine. Due date Feb 16 2025. Uncomplicated. Adverse event was irregul... 33 weeks pregnant at time of vaccine. Due date Feb 16 2025. Uncomplicated. Adverse event was irregular heart rhythm and breathlessness starting at 1130 PM Lasted for about 30-45 minutes. I verified irregular heart rhythm with my Omren blood pressure cuff and it picked it up as well. Heart rate was normal. Once my heart was back in rhythm nothing else happened. I had an OB appt the next day and brought it up. More
2819260 79 M FL 01/03/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 x357e
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Pt got Boostrix in 01/31/24 and received another vaccine on 01/03/25. Pt is fine, he is okay and has... Pt got Boostrix in 01/31/24 and received another vaccine on 01/03/25. Pt is fine, he is okay and has had no adverse reaction More
2819261 67 F OH 01/03/2025 COVID19
 PFIZER\BIONTECH
 EM9810
Aortic dilatation, Cardiomegaly, Computerised tomogram heart abnormal, Laborator... Aortic dilatation, Cardiomegaly, Computerised tomogram heart abnormal, Laboratory test More
Pt says on 8/1/24 she was getting her calcium scoring and there was an indidental finding that it wa... Pt says on 8/1/24 she was getting her calcium scoring and there was an indidental finding that it was low. She was asked if she had shortness of breath or trouble breathing. She had mulitple test and was dx with mild cardiomegaly aortic ectasia of the ascending aorta measuring up to 4.2 centameters. She was prescibed lisinapril. This is all new dx for her since being vaccinated. She will follow up after taking up medication after taking this mediciation after a month and will have more of these test in july or aug 2025. She is hoping that she has started treament early enough to have not caused permanent damage. More
✓
2819262 78 M CO 01/03/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 7l3st
Pain, Pain in extremity Pain, Pain in extremity
He started feeling pain in his arm that radiated to his wrist and hand, which continued for 30 hours... He started feeling pain in his arm that radiated to his wrist and hand, which continued for 30 hours. He took so Ibuprofen and it relieved the pain some what. He has no symptoms or anything now. More
2819263 79 M SC 01/03/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Extra dose administered Extra dose administered
Patient received second dose of RSV vaccine. First dose received in Oct 2023 Patient received second dose of RSV vaccine. First dose received in Oct 2023
2819264 48 F MI 01/03/2025 COVID19
 MODERNA
Underdose Underdose
Pediatric dose was administered to adult in error. Pediatric dose was administered to adult in error.
2819265 0.67 F WI 01/03/2025 DTPPVHBHPB
PNC20
 MSP VACCINE COMPANY
PFIZER\WYETH

Fatigue, Lethargy, Pallor; Fatigue, Lethargy, Pallor Fatigue, Lethargy, Pallor; Fatigue, Lethargy, Pallor
Fatigued in the afternoon. Episode of increased lethargy and pale skin around 7:30. Patients lips tu... Fatigued in the afternoon. Episode of increased lethargy and pale skin around 7:30. Patients lips turned white. More
2819266 64 F CO 01/03/2025 COVID19
 PFIZER\BIONTECH
 LP1780
Erythema, Pruritus, Urticaria Erythema, Pruritus, Urticaria
pt says about 10 days after getting vaccine she was itching and developed hives. She had already sta... pt says about 10 days after getting vaccine she was itching and developed hives. She had already started weining herself off the bromelain papain natural supplement and noticed she was starting to itch but then after the vaccine she now has the hives. She started using oatmeal wash in her bath to help ease the itch. She had red welps on her left side of her torso that she was treating with aloe and lotion. After going to bed it erupted on the right side of her torso. Her symptoms are worse at night. She went to see her doctor and was prescribed hydroxyzine. She will follow up after taking meds if needed. More
2819267 67 F VA 01/03/2025 IPV
TYP
 SANOFI PASTEUR
SANOFI PASTEUR
 X1D141M
W1A361M
Injected limb mobility decreased, Injection site bruising, Injection site erythe... Injected limb mobility decreased, Injection site bruising, Injection site erythema, Pain; Injected limb mobility decreased, Injection site bruising, Injection site erythema, Pain More
Patient noted a quarter sized bruise at injection side and red area approx. 3? in same location that... Patient noted a quarter sized bruise at injection side and red area approx. 3? in same location that continued to get worse causing limited mobility of arm. Client saw Urgent Care on 12/27/24 and began a 5 day course of Prednisone. Patient followed up with primary care physician on 01/03/2025 and reported to this provider that PCP determined there was not a frozen shoulder or infection noted at this time. The patient reports gradual improvement of pain, bruising and redness. More
2819268 29 M TN 01/03/2025 COVID19
 MODERNA
Hypoacusis, Tinnitus Hypoacusis, Tinnitus
Tinnitus, Constant Ringing and Muffled Sound in Right Ear, Varies in Volume Tinnitus, Constant Ringing and Muffled Sound in Right Ear, Varies in Volume
2819269 68 F 01/03/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
patient stated they had redness and swelling to the size of "a golf ball" at the site patient stated they had redness and swelling to the size of "a golf ball" at the site
2819270 73 F 01/03/2025 COVID19
 MODERNA
Pain in extremity Pain in extremity
stated arm is still sore since September stated arm is still sore since September
2819271 76 F TX 01/03/2025 FLU3
PNC20
RSV
 SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH


Arthralgia, Arthritis, Neck pain, Pain in extremity; Arthralgia, Arthritis, Neck... Arthralgia, Arthritis, Neck pain, Pain in extremity; Arthralgia, Arthritis, Neck pain, Pain in extremity; Arthralgia, Arthritis, Neck pain, Pain in extremity More
Patient has Arthritis. Patient took RSV ,Prevnar 20,and Flu vaccines at the same day , same arm. pat... Patient has Arthritis. Patient took RSV ,Prevnar 20,and Flu vaccines at the same day , same arm. patient suffered from arm , shoulder , and neck pain More
2819272 57 F UT 01/03/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3J994
Product preparation issue Product preparation issue
the pharmacist that administered the vaccine only gave the patient two vials of the adjuvant instead... the pharmacist that administered the vaccine only gave the patient two vials of the adjuvant instead of the active component of the vaccine. More
2819273 62 M IL 01/03/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FC3181
FC3181
Amyotrophic lateral sclerosis, Blood test, Electromyogram abnormal, Magnetic res... Amyotrophic lateral sclerosis, Blood test, Electromyogram abnormal, Magnetic resonance imaging head, Magnetic resonance imaging spinal; Muscle atrophy, Spinal operation More
Pt had a EMG where they found a blockage in his neck and then had surgery on Dec 5th 2021. After h... Pt had a EMG where they found a blockage in his neck and then had surgery on Dec 5th 2021. After his extensive rehab period his doctor referred him to other doctors for further treatment and testing. He started loosing the muscle between the index fingers and the thumbs on both hands. DX was muscle atrophy and is now on active treatment for ALS. (motor neuron disease) He continues to pursue doctors for treatment and to confirm other diagnosis. He will be going to clinic on Jan 22 for an further eval. More
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2819274 14 F OH 01/03/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 4799G
Head injury, Headache, Loss of consciousness Head injury, Headache, Loss of consciousness
Vaccination was given. Pt left the treatment area and went to nursing station to make a follow up ap... Vaccination was given. Pt left the treatment area and went to nursing station to make a follow up appointment. Per mom, she signaled to her that she was going to pass out, then she went down. She hit her head on the floor. She came around quickly with no need to use any inhalants. Cold pack was applied to head. No open wounds noted. CNP on staff notified and she examined pt. She was given juice and sat up on her own. She then stood up and said she was fine but her head hurt. Tylenol samples given to mom for future use. Instructed to go to ER if further complications, ie continued HA or vomiting. More
2819275 73 F SC 01/03/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52Z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient received Arexvy vaccine on 1/2/25. Patient had previously received vaccine on 12/29/2023. Pa... Patient received Arexvy vaccine on 1/2/25. Patient had previously received vaccine on 12/29/2023. Patient had no reaction or any complication. More
2819276 4 F CA 01/03/2025 DTAPIPV
DTAPIPV
MMRV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 5G23D
5G23D
Y010930
Y010930
Erythema, Injection site swelling, Injection site warmth, Ocular hyperaemia, Pru... Erythema, Injection site swelling, Injection site warmth, Ocular hyperaemia, Pruritus; Pyrexia, Urticaria; Erythema, Injection site swelling, Injection site warmth, Ocular hyperaemia, Pruritus; Pyrexia, Urticaria More
12-02-24, the evening of the immunization, the left deltoid swelled-up, warm to touch and low fever ... 12-02-24, the evening of the immunization, the left deltoid swelled-up, warm to touch and low fever for 1 day . There were some itchy splotches on the face . When examined 2 days later, 12-04-24, there was no shortness of breath and no edema. Treatment included discussing care at length, ordered Benadryl and Tylenol as needed for fever or pain. Ice to arm. Follow-up 2 days later, on 12-06-2024, there was redness of eyes, some hives on neck, decreased swelling and redness on arm. Patient was still taking Benadryl at this time. Patient had no previous adverse events with vaccinations. Referral made to allergy/immunology and has appointment scheduled for 02-19-2025. On 01-03-2025, parent reports that there is no longer any issues from this adverse event and patient is fin. More
2819277 1.08 F CA 01/03/2025 FLU3
 SEQIRUS, INC.
 946628
Cough, Dyspnoea, Pyrexia Cough, Dyspnoea, Pyrexia
Difficulty Breathing, Cough, & Low-Grade Fever about 10 Hours after the vaccine was administered... Difficulty Breathing, Cough, & Low-Grade Fever about 10 Hours after the vaccine was administered. Treated with humidifier, saline mist 3 days after the vaccine required a nebulizer treatment and oral prednisone. Symptoms significantly improved on day 4. By day 5 her cough, fever, & respiratory distress resolved. More
2819278 57 F CO 01/03/2025 COVID19
 MODERNA
Lymphadenopathy Lymphadenopathy
swollen lymph node swollen lymph node
2819279 78 F WY 01/03/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
UT8473BA
Abdominal discomfort, Headache; Abdominal discomfort, Headache Abdominal discomfort, Headache; Abdominal discomfort, Headache
Pt. reports a headache treated with Tylenol, upset stomach that was made better by eating something... Pt. reports a headache treated with Tylenol, upset stomach that was made better by eating something. More
2819281 63 F MD 01/03/2025 FLU3
 SANOFI PASTEUR
 UT8470AA
Product administered to patient of inappropriate age Product administered to patient of inappropriate age
patient is 63, received high dose flu shot patient is 63, received high dose flu shot
2819282 16 F WI 01/03/2025 MNQ
 SANOFI PASTEUR
 U8271AB
Injection site swelling Injection site swelling
LOCALIZED SWELLING OF INJECTION SITE LOCALIZED SWELLING OF INJECTION SITE
2819283 0.17 F MI 01/03/2025 RV5
 MERCK & CO. INC.
Extra dose administered, No adverse event Extra dose administered, No adverse event
There was no adverse affect. Patient received first dose on 12/24/24 in this office. Patient vomited... There was no adverse affect. Patient received first dose on 12/24/24 in this office. Patient vomited immediatly after getting the oral vaccine. Patient was brought back in today for another dose. After completing the dose, talked with employee at the health department and was educated that even with vomiting that another dose should not have been administered. More
2819284 84 F PA 01/03/2025 FLU3
 SANOFI PASTEUR
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient asked for a flu shot at the pharmacy on 1/2/25. On 1/3/25, it was discovered that the patien... Patient asked for a flu shot at the pharmacy on 1/2/25. On 1/3/25, it was discovered that the patient already received a dose this season on 9/20/24. Patient was not experiencing any adverse reactions for the additional vaccine per her phone call with the pharmacist today. More
2819285 74 F AL 01/03/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient had already received this vaccine in October 2023. Patient was unaware that only one vaccina... Patient had already received this vaccine in October 2023. Patient was unaware that only one vaccination for RSV is needed. Patient received an additional RSV vaccine on 12/30/24. Patient was notified on 01/02/25 and has not had any adverse reactions from receiving additional dose. More
2819286 50 M PA 01/03/2025 PNC20
 PFIZER\WYETH
 LP151
Erythema, Mobility decreased, Pain, Skin warm, Swelling Erythema, Mobility decreased, Pain, Skin warm, Swelling
Patient had vaccine Saturday, felt pain initially, and increased in swelling and soreness on Sunday.... Patient had vaccine Saturday, felt pain initially, and increased in swelling and soreness on Sunday. By Monday, he states he could not lift his arm without pain. Wednesday redness and swelling increasing. Friday at MD appt, MD said warm to touch and was concerned about infection, prescribed antibiotic. More
2819287 1.25 M TN 01/03/2025 DTAPIPVHIB
 SANOFI PASTEUR
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Pt came in for vaccines, nurse was in hurry and did not pay attention that 4th dose of polio was not... Pt came in for vaccines, nurse was in hurry and did not pay attention that 4th dose of polio was not due at time because child was only 1. Pt was given Pentacel, MMR, Varicella, and PCV. Pt had with no reaction, no issues, dose did not count, just given too soon. More
2819288 50 F MI 01/03/2025 PNC20
TDAP
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 LG5577
CX4HL
KB2YT
Arthralgia, Contusion, Pain in extremity, Peripheral swelling; Arthralgia, Contu... Arthralgia, Contusion, Pain in extremity, Peripheral swelling; Arthralgia, Contusion, Pain in extremity, Peripheral swelling; Arthralgia, Contusion, Pain in extremity, Peripheral swelling More
The patient called the pharmacy to report side effects. Patient describes dime size bruising on inje... The patient called the pharmacy to report side effects. Patient describes dime size bruising on injection arm, soreness, the area feeling swollen, and joint pain. The patient said the onset happened shortly after administration and is continuing. The patient was instructed to use an ice pack and to go into their provider or seek other medical attention if no relief, bothersome, or worsening symptoms. More
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