🏥 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 💀 🏥 🚑 ♿ ⚠️
2857316 8 M KY 09/08/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 19515-904-41
Injection site urticaria Injection site urticaria
Single localized hive over vaccine site (on R. deltoid) occurred the morning following injection. No... Single localized hive over vaccine site (on R. deltoid) occurred the morning following injection. No spreading. No history of past reactions to flu vaccine. Resolved with Benadryl cream on injection site. More
2857317 5 F TX 09/08/2025 DTAPIPV
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
 3RT93
Z009075
Extra dose administered; Extra dose administered Extra dose administered; Extra dose administered
Public Health was providing a mass vaccine clinic in conjunction with schools. School nurses have as... Public Health was providing a mass vaccine clinic in conjunction with schools. School nurses have assess to state vaccine registry. We were allowing those to proceed that had an official letter from the school nurse listing what vaccines they have and what they are delinquent and needing. This client showed she needed DTaP, Polio, MMR and Varicella. Client received Kinrix and Proquad. Vaccines were documented in EMR. Copy of school nurses letter was kept to make sure all vaccines are in state registry. While checking ImmTrac state registry at a later date it was found that client had already had these vaccines and these were not required. Vaccines received 02/01/2024. School nurse was contacted RN BSN. She claims she thought she checked all students. Does not know how she missed this. More
2857318 14 F AL 09/08/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 JF7DM
Wrong product administered Wrong product administered
Administration error, original intent was to give pt Tdap. Administration error, original intent was to give pt Tdap.
2857319 F WA 09/08/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 JB4K2
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
Patient given 2 Hep B vaccines outside of vaccination schedule. No apparent harm seen at 2 dose Patient given 2 Hep B vaccines outside of vaccination schedule. No apparent harm seen at 2 dose
2857320 3 M TN 09/08/2025 COVID19
 PFIZER\BIONTECH
 LN7305
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
No adverse event; vaccine was administered after update stating restrictions on EUA Covid vaccines f... No adverse event; vaccine was administered after update stating restrictions on EUA Covid vaccines from 2024-2025 More
2857321 67 M CA 09/08/2025 FLU3
 SEQIRUS, INC.
 407256
Dyspnoea, Malaise Dyspnoea, Malaise
Patient reports, the day after the vaccine, patient went for a walk with his dog. While walking, he... Patient reports, the day after the vaccine, patient went for a walk with his dog. While walking, he states he could not breath. Patient did not go to ER or see MD or contact pharmacy. He states he went home sat down and felt better, but every time he got up his HR was over 100 and he did not feel good, but did not seek medical attention. After that, each day he felt a little better and today, he is back to normal. He states it was not his asthma and that is was an allergic reaction to the vaccine. More
2857323 14 F MI 09/08/2025 HEP
HEPA
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 AZ4TN
Y018582
Y011214
Blood iron, Full blood count, No adverse event, Product administered to patient ... Blood iron, Full blood count, No adverse event, Product administered to patient of inappropriate age; Blood iron, Full blood count, No adverse event, Product administered to patient of inappropriate age; Blood iron, Full blood count, No adverse event, Product administered to patient of inappropriate age More
No adverse reactions at this time No adverse reactions at this time
2857324 70 M CO 09/08/2025 PNC20
TDAP
 PFIZER\WYETH
SANOFI PASTEUR
 MA2505
U8389AA
Death, Resuscitation, Unresponsive to stimuli; Death, Resuscitation, Unresponsiv... Death, Resuscitation, Unresponsive to stimuli; Death, Resuscitation, Unresponsive to stimuli More
Patient was found unresponsive and without vital signs at home at 10:45 AM on 9/6/25; approximately... Patient was found unresponsive and without vital signs at home at 10:45 AM on 9/6/25; approximately 72 hours after vaccine administration. Cardiopulmonary Resuscitation was initiated and emergency medical services were dispatch but patient was unable to be revived. Patient had multiple visits from licensed nurses and unlicensed caregivers between vaccination and event appearing well each time, the last being approximately 5:00 PM on 9/5/25. More
✓
2857325 59 F OH 09/08/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 NR4T5
Injected limb mobility decreased, Injection site inflammation, Injection site sw... Injected limb mobility decreased, Injection site inflammation, Injection site swelling, Pain in extremity More
patient has a large area of swelling and inflammation around injection site, says that it was very l... patient has a large area of swelling and inflammation around injection site, says that it was very large, she has limited mobility of arm and says that she is also experience pain in her hand. Says tylenol or advil is not touching the pain and she has been icing as well with no help More
2857326 11 F DE 09/08/2025 HPV9
MNQ
TDAP
 MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
 1967338
u8194aa
u7870aa
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 More
Adacel vaccine expired on 8/23/2025; administered on 8/28/25; no adverse symptoms reported Adacel vaccine expired on 8/23/2025; administered on 8/28/25; no adverse symptoms reported
2857327 1.58 F AL 09/08/2025 HEPA
HIBV
IPV
 MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
 Z005852
UK166AB
Y1A212M
Injection site erythema, Pyrexia; Injection site erythema, Pyrexia; Injection si... Injection site erythema, Pyrexia; Injection site erythema, Pyrexia; Injection site erythema, Pyrexia More
redness at injection site and fever redness at injection site and fever
2857328 0.42 F NY 09/08/2025 HEP
PNC15
 MERCK & CO. INC.
MERCK & CO. INC.
 Y014090
Z003633
Crying, Injection site reaction, Irritability, Rash, Rash erythematous; Crying, ... Crying, Injection site reaction, Irritability, Rash, Rash erythematous; Crying, Injection site reaction, Irritability, Rash, Rash erythematous More
patient developed an erythematous rash on bilateral lower extremities (mostly from knees down) and m... patient developed an erythematous rash on bilateral lower extremities (mostly from knees down) and minimal similar rash on the back, as well as crying and irritability within 5-10 minutes of receiving both vaccines. Pte was given Benadryl 12.5mg/5ml 2.5 ml orally, rash resolved withing 8 minutes after she took the Benadryl, patient was monitored for another 40 minutes and then discharged home after no more side effects or allergic reactions More
2857329 0.17 M AZ 09/08/2025 DTAPHEPBIP
HIBV
PNC20
RV1
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 9C295
Z003407
LX4486
7YS93
Injection site discolouration, Injection site erythema, Injection site infection... Injection site discolouration, Injection site erythema, Injection site infection, Injection site swelling; Injection site discolouration, Injection site erythema, Injection site infection, Injection site swelling; Injection site discolouration, Injection site erythema, Injection site infection, Injection site swelling; Injection site discolouration, Injection site erythema, Injection site infection, Injection site swelling More
Child got a vaccine last week and his injection site is red, swollen and now has what looks to be a ... Child got a vaccine last week and his injection site is red, swollen and now has what looks to be a white head acne spot. YOUR PLAN: SKIN INFECTION: Patient has a mild skin infection, likely from a vaccine site reaction. -Start taking Cephalexin (Keflex) as prescribed: Take 1.4 mL by mouth 3 (three) times every day in the morning, at noon, and in the evening for 7 days. -Apply warm compresses to the affected area. -Reassess if there is no improvement or if the condition worsens after three days. More
2857330 35 M NY 09/08/2025 SMALLMNK
 BAVARIAN NORDIC
Anaphylactic reaction, Anaphylaxis treatment, Dyspnoea, Pyrexia, Urticaria Anaphylactic reaction, Anaphylaxis treatment, Dyspnoea, Pyrexia, Urticaria
Patient experienced anaphylaxis accompanied by fevers, shortness of breath, urticaria, full body hiv... Patient experienced anaphylaxis accompanied by fevers, shortness of breath, urticaria, full body hives More
✓ ✓
2857331 30 F CA 09/08/2025 FLU3
 SEQIRUS, INC.
 407359
Exposure during pregnancy, Rash Exposure during pregnancy, Rash
The employee informed her supervisor that she had received her flu shot on 09/04/2025, during the Em... The employee informed her supervisor that she had received her flu shot on 09/04/2025, during the Employee Flu Clinic. Following the vaccination after she left, the employee noticed a rash developing on her thighs. She initially believed it to be a heat rash and did not raise concern at the time. However, on 09/08/2025, the employee reported the rash had worsened and was spreading. The employee is pregnant. The employee was sent to get evaluated at UC on 09/08. More
2857332 M DC 09/08/2025 DTPPVHBHPB
PNC15
 MSP VACCINE COMPANY
MERCK & CO. INC.
 U8265AA
Y019380
Wrong product administered; Wrong product administered Wrong product administered; Wrong product administered
wrong vaccine given to patient- Dr. spoke to mom and examine patient wrong vaccine given to patient- Dr. spoke to mom and examine patient
2857333 8 M MI 09/08/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 JF7DM
Wrong product administered Wrong product administered
Client was due for Tdap and was inadvertently given Dtap Client was due for Tdap and was inadvertently given Dtap
2857334 55 M CA 09/08/2025 PNC20
 PFIZER\WYETH
 LN4932
Injection site erythema, Injection site swelling, Injection site warmth, Pyrexia Injection site erythema, Injection site swelling, Injection site warmth, Pyrexia
Per patient he experienced a low grade fever and noticed that the area around the injection site wa... Per patient he experienced a low grade fever and noticed that the area around the injection site was swollen, redness and hot. The redness appeared below the injection site. These symptoms started the same night as the vaccination. As per NP's recommendation, to continue to monitor the symptoms and have been advised to go to the Emergency Department if they worsen: increased pain, swelling, spreading of the redness, chest pain, shortness of breath, palpitation, neck, face or airway swelling. More
2857335 38 M WA 09/08/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.

Blood test normal, Chest X-ray, Chest X-ray normal, Chest pain, Gastrointestinal... Blood test normal, Chest X-ray, Chest X-ray normal, Chest pain, Gastrointestinal disorder; Blood test normal, Chest X-ray, Chest X-ray normal, Chest pain, Gastrointestinal disorder More
Unknown chest pain that has lasted over 4 hours, in solar plexus area. Sought emergency room treatme... Unknown chest pain that has lasted over 4 hours, in solar plexus area. Sought emergency room treatment. Cause unknown. (I suspect it is intestinal/stomach distress and has nothing to do with the vaccines) More
2857336 18 M WI 09/08/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 47XP4
No adverse event, Wrong product administered No adverse event, Wrong product administered
No side effects. Wrong vaccine was given. Patient was supposed to get Men.B, however Hep B was ina... No side effects. Wrong vaccine was given. Patient was supposed to get Men.B, however Hep B was inadvertently administered. More
2857337 0.42 F MI 09/08/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK305AB
Wrong product administered Wrong product administered
Client was to receive Pentacel Vaccine, inadvertently given ActHib with sterile diluent not included... Client was to receive Pentacel Vaccine, inadvertently given ActHib with sterile diluent not included with Pentacel vaccine. Dose not countable, instructed parent that client needs to be revaccinated with all three antigens, More
2857338 70 M CA 09/08/2025 FLU3
FLU3
PNC21
PNC21
 SEQIRUS, INC.
SEQIRUS, INC.
MERCK & CO. INC.
MERCK & CO. INC.
 407249
407249
Z006889
Z006889
Arthralgia, Fatigue, Injection site bruising, Injection site erythema, Injection... Arthralgia, Fatigue, Injection site bruising, Injection site erythema, Injection site haemorrhage; Muscular weakness, Myalgia, Pain, Pain in extremity, Pyrexia; Arthralgia, Fatigue, Injection site bruising, Injection site erythema, Injection site haemorrhage; Muscular weakness, Myalgia, Pain, Pain in extremity, Pyrexia More
Patient received two vaccines on 9/3/25 afternoon, an influenza and pneumococcal vaccine in the delt... Patient received two vaccines on 9/3/25 afternoon, an influenza and pneumococcal vaccine in the deltoids. He reported when receiving the vaccine in the left arm (according to the paperwork it was the Fluad influenza vaccine) he has some bleeding from the vaccine and the vaccine administer cleaned up the blood and place a bandage on the vaccine. A few hours later he noticed redness at the site and extreme arm pain. Patient did mention he experienced fever, tiredness, muscle aches, join pain after his vaccines at night. His left arm has more pain and the pain still exists the next day until now. However, he noticed more bruising spreading from the site down towards his elbow and was black and blue starting the next day. Currently, we can see he still has some brusing around the arm towards the elbow and he noticed it got a little better. However, patient is concerned about the his arm being weak and painful when he tries to raise his arm and the left arm could not be raised pass the shoulder. I informed patient to monitor the site of bruising and to reach out to his doctor to have it checked out. In the mean time, if needed, I recommend if he can take an anti-inflammatory such as ibuprofen to help with the pain. More
2857339 0.33 F KS 09/08/2025 DTPPVHBHPB
FLU3
PNC15
RV5
 MSP VACCINE COMPANY
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.
 U8265AA
UT877ONA
Z003633
Y018515
Inappropriate schedule of product administration; Inappropriate schedule of prod... Inappropriate schedule of product administration; Inappropriate schedule of product administration; Inappropriate schedule of product administration; Inappropriate schedule of product administration More
Flu shot given too early Flu shot given too early
2857340 50 F MA 09/08/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93N4J
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Patient has redness and swelling at the vaccine site that she says is getting bigger as time passes Patient has redness and swelling at the vaccine site that she says is getting bigger as time passes
2857342 66 F NJ 09/08/2025 PNC21
 MERCK & CO. INC.
 Z003579
Chills, Injection site erythema, Injection site pain, Injection site pruritus, P... Chills, Injection site erythema, Injection site pain, Injection site pruritus, Pyrexia More
redness, itching, burning and injection site reaction along with chillls and fever. has appointment ... redness, itching, burning and injection site reaction along with chillls and fever. has appointment with Dr to see if it may be cellulitis. patient took motrin and tylenol alternating without any resolution with the red and pain, however fever and body chills has stopped More
2857343 45 F IA 09/08/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 FA6780
FA6780
Chest pain, Electrocardiogram, Electrocardiogram ambulatory, Heart rate increase... Chest pain, Electrocardiogram, Electrocardiogram ambulatory, Heart rate increased, Palpitations; Chest pain, Electrocardiogram, Electrocardiogram ambulatory, Heart rate increased, Palpitations More
Symptoms began approximately 4 weeks after the 2nd dose. Symptoms were elevated heart rate, palpit... Symptoms began approximately 4 weeks after the 2nd dose. Symptoms were elevated heart rate, palpitations, and chest pain while at rest. HR would fluctuate from 140-160 bpm when not physically active. More
✓
2857344 70 F TN 09/08/2025 UNK
 UNKNOWN MANUFACTURER
 NR4T5
Abdominal pain upper, Chills, Diarrhoea, Pyrexia, Vomiting Abdominal pain upper, Chills, Diarrhoea, Pyrexia, Vomiting
Patient said she got her first Shingles vaccination about 12 noon. At about 4pm she started having d... Patient said she got her first Shingles vaccination about 12 noon. At about 4pm she started having diarrhea, vomiting, fever, chills and stomach cramps. She was not able to attribute they symptoms to anything that she had eaten or anything else. After reviewing the VIS again she noticed that these effects had been reported as possible side effects. She said they lasted for about 3 days. She came back to the pharmacy and reported. Was advised to also let her md about the effects she experienced and was advised against the second shot. More
2857345 20 M NH 09/08/2025 PNC20
 PFIZER\WYETH
Blood test, Electrocardiogram, Pericarditis, Ultrasound scan Blood test, Electrocardiogram, Pericarditis, Ultrasound scan
Developed a heart condition. Pericarditis. Developed a heart condition. Pericarditis.
✓ ✓
2857346 1.25 F MT 09/08/2025 DTAPIPVHIB
 SANOFI PASTEUR
Food refusal, Immunisation reaction, Pyrexia Food refusal, Immunisation reaction, Pyrexia
Patient was given Dtap & HIB during her 15 month check up. After a few days, she started develop... Patient was given Dtap & HIB during her 15 month check up. After a few days, she started developing a 104 fever, would?ve eat or drink anything. Took her to the emergency room on the following Friday, without any answers. They tried telling us she was teething. Stated she would?ve had a fever within 24 hours, if it was from the shots. The following day, she was not doing any better and her fever lingered. Again was told to go back to the emergency room. Ended up taking her to a new pediatrician confirmed she had a reaction to the D tap shot. More
2857347 78 F SC 09/08/2025 COVID19
 MODERNA
Death, Neoplasm malignant Death, Neoplasm malignant
Death, Cancer, others Death, Cancer, others
✓ ✓ ✓
2857348 84 F CT 09/08/2025 FLU3
 SEQIRUS, INC.
 407244
Gait disturbance, Loss of personal independence in daily activities, Myalgia Gait disturbance, Loss of personal independence in daily activities, Myalgia
the patient reports extensive pain in muscle all over the body. She had trouble walking and dressing... the patient reports extensive pain in muscle all over the body. She had trouble walking and dressing herself for 48 hours post vaccination More
2857349 72 F AR 09/08/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 24M94
Rash, Urticaria Rash, Urticaria
Patient reported a rash/hives that started on the back of her right shoulder and moved across her ba... Patient reported a rash/hives that started on the back of her right shoulder and moved across her back and up her neck. More
2857350 73 F TX 09/08/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93KK4
Hypersomnia Hypersomnia
PATIENT CALLED TODAY AND SAID THAT SHE HAS BEEN SLEEPING ALOT SINCE THE DAY SHE GOT HER SHINGRIX VAC... PATIENT CALLED TODAY AND SAID THAT SHE HAS BEEN SLEEPING ALOT SINCE THE DAY SHE GOT HER SHINGRIX VACCINE SHOT AND SHE HAS SCHEDULED A N APPOINTMENT TO SEE HER PCP TOMORROW More
2857351 82 F MD 09/08/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 2293B
Product administered at inappropriate site, Rash, Rash erythematous Product administered at inappropriate site, Rash, Rash erythematous
Patient came to the pharmacy to get an antibiotic from her provider for the rash she got after getti... Patient came to the pharmacy to get an antibiotic from her provider for the rash she got after getting the RSV vaccine. She stated the shot was given low and had a red rash that hurt on her arm. More
2857352 79 F FL 09/08/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 342xp
Injection site pruritus, Injection site urticaria Injection site pruritus, Injection site urticaria
Itchining and hives near the site Itchining and hives near the site
2857353 13 F MA 09/08/2025 HEP
 GLAXOSMITHKLINE BIOLOGICALS
 EB9ZX
Incorrect dose administered Incorrect dose administered
Patient received adult dose of hep B. Pt denied dizziness, lightheadedness. Ambulatory out of clinic... Patient received adult dose of hep B. Pt denied dizziness, lightheadedness. Ambulatory out of clinic with strong steady gait. More
2857354 17 M IN 09/08/2025 MENB
MENB
 PFIZER\WYETH
PFIZER\WYETH
 HP9988
HP9988
Dysphemia, Gait disturbance, Laboratory test normal, Muscular weakness, Nausea; ... Dysphemia, Gait disturbance, Laboratory test normal, Muscular weakness, Nausea; Tremor, Vomiting More
HISTORY GIVEN PER MOM: ABOUT 3 HOURS AFTER VACCINATION, PT STARTED C/O LEG WEAKNESS, TROUBLE WALKING... HISTORY GIVEN PER MOM: ABOUT 3 HOURS AFTER VACCINATION, PT STARTED C/O LEG WEAKNESS, TROUBLE WALKING, SHAKINESS/TREMORS, TROUBLE WITH SPEAKING/STUDDERING, N/V. MOM TOOK PATIENT TO THE ER FOR EVALUATION. PER MOM, THE ER GAVE BENADRYL, IVF'S, COLLECTED LABS (WHICH WERE NORMAL). More
2857355 72 F AR 09/08/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 GJ952
Injection site erythema, Injection site pain, Local reaction, Pain in extremity Injection site erythema, Injection site pain, Local reaction, Pain in extremity
Patient originally called and described a local reaction. I told her to monitor it and call me back ... Patient originally called and described a local reaction. I told her to monitor it and call me back in a couple days. She said it was red and tender. Patient said it wasn't at the injection site but under/around it. She went to the doctor's office and the doctor office called me saying nearly a month later, her arm was still painful. More
2857356 57 M OH 09/08/2025 FLU3
HEP
PNC20
RSV
 SEQIRUS, INC.
DYNAVAX TECHNOLOGIES CORPORATION
PFIZER\WYETH
PFIZER\WYETH
 406986
946889
LJ5281
MM9159
Injection site bruising, Injection site haemorrhage, Injection site swelling; In... Injection site bruising, Injection site haemorrhage, Injection site swelling; Injection site bruising, Injection site haemorrhage, Injection site swelling; Injection site bruising, Injection site haemorrhage, Injection site swelling; Injection site bruising, Injection site haemorrhage, Injection site swelling More
Bleeding and bruising from the injection site with the flu shot. Local Swelling with RSV and Prevna... Bleeding and bruising from the injection site with the flu shot. Local Swelling with RSV and Prevnar. Recommended a cool compress. More
2857357 79 F 09/08/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 NR4T5
Erythema, Peripheral swelling, Pruritus Erythema, Peripheral swelling, Pruritus
redness, swelling in lower arm, itching on day 3 after vaccination redness, swelling in lower arm, itching on day 3 after vaccination
2857358 71 M IL 09/08/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 MY9547
U8837AA
Injection site pain, Injection site rash, Injection site swelling, Injection sit... Injection site pain, Injection site rash, Injection site swelling, Injection site warmth; Injection site pain, Injection site rash, Injection site swelling, Injection site warmth More
Patient came into the pharmacy and reported that his left upper arm was swollen, warm to touch, and ... Patient came into the pharmacy and reported that his left upper arm was swollen, warm to touch, and he had minor pain. He stated the rash/swelling developed within 24 hours. More
2857360 1.25 F MA 09/08/2025 HIBV
 SANOFI PASTEUR
 UK304AA
Product preparation issue Product preparation issue
Patient potentially only received the diluent as an extra vial of unconstituted vaccine was found on... Patient potentially only received the diluent as an extra vial of unconstituted vaccine was found on 9/8/2025 and only 2 patients received the Hib vaccine from this box More
2857361 0.42 M KY 09/08/2025 DTPPVHBHPB
PNC21
RV1
 MSP VACCINE COMPANY
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS


Electroencephalogram, Pyrexia, Scan brain, Seizure; Electroencephalogram, Pyrexi... Electroencephalogram, Pyrexia, Scan brain, Seizure; Electroencephalogram, Pyrexia, Scan brain, Seizure; Electroencephalogram, Pyrexia, Scan brain, Seizure More
Seizures. High fever that evening. Second seizure the next morning around 11am. Took him for the sca... Seizures. High fever that evening. Second seizure the next morning around 11am. Took him for the scan on his brain. No following seizures. None since his 2 month shots. Doctors said it wasn't the vaccines but that it definitely sounded like seizure. Worried me pretty bad. No fever present for the second seizure. More
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2857362 66 F TX 09/08/2025 COVID19
FLU3
PNC21
 PFIZER\BIONTECH
SEQIRUS, INC.
MERCK & CO. INC.


Cellulitis, Injection site erythema, Injection site swelling, Pruritus, Pyrexia;... Cellulitis, Injection site erythema, Injection site swelling, Pruritus, Pyrexia; Cellulitis, Injection site erythema, Injection site swelling, Pruritus, Pyrexia; Cellulitis, Injection site erythema, Injection site swelling, Pruritus, Pyrexia More
Cellulitis - Red swollen injection site, fever, itching. Cephalexin 500mg for 7 days Cellulitis - Red swollen injection site, fever, itching. Cephalexin 500mg for 7 days
2857363 30 F TX 09/08/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 946065
Erythema, Eye swelling, Lip swelling, Pruritus, Urticaria Erythema, Eye swelling, Lip swelling, Pruritus, Urticaria
Patient stated that next day, in the evening she experienced swelling to eyes an lips. Patient state... Patient stated that next day, in the evening she experienced swelling to eyes an lips. Patient stated that then she had a few red itchy hives on her hands. By that night (9/5/2025) the hives started to spread across her body. She stated that today (9/8/2025) she still has hives and is itchy. More
2857364 1.25 F MA 09/08/2025 DTAP
HIBV
PNC20
 SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
 3CA55C1
UK304AA
LX2496
Product preparation issue; Product preparation issue; Product preparation issue Product preparation issue; Product preparation issue; Product preparation issue
Patient may have received diluent only. Two patients received the Hib vaccine form the same box in t... Patient may have received diluent only. Two patients received the Hib vaccine form the same box in the same timeframe, and an extra vial of the powder vaccine was discovered More
2857365 9 M IL 09/08/2025 COVID19
 MODERNA
 3042647
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
NO ADVERSE EVENT. WRONG DOSE PROVIDED FOR 9 YO AT THE TIME FOR A BOOSTER. SPIKEVAX 24-25 50MCG 12YO+... NO ADVERSE EVENT. WRONG DOSE PROVIDED FOR 9 YO AT THE TIME FOR A BOOSTER. SPIKEVAX 24-25 50MCG 12YO+ WAS PROVIDED FOR BOOSTER DOSE. More
2857366 4 M FL 09/08/2025 FLU3
 SANOFI PASTEUR
Wrong product administered Wrong product administered
Wrong vaccine was given without any written, implied or verbal consent Wrong vaccine was given without any written, implied or verbal consent
2857367 74 F OH 09/08/2025 FLU3
PNC20
 SANOFI PASTEUR
PFIZER\WYETH
 u8830ca
ma2505
Mobility decreased, Pain in extremity; Mobility decreased, Pain in extremity Mobility decreased, Pain in extremity; Mobility decreased, Pain in extremity
Very sore arm, patient reports not being able to move arm after receiving vaccine on 9/2/25. As of 9... Very sore arm, patient reports not being able to move arm after receiving vaccine on 9/2/25. As of 9/8/25, patient is able to slightly move the arm more More
2857368 73 M AZ 09/08/2025 COVID19
 MODERNA
 3051995
Cough, Dyspnoea, Respiratory distress Cough, Dyspnoea, Respiratory distress
AFTER ADMINISTRATION PATIENT STOOD UP STARTED WITH RESPIRATORY DISTRESS. RR 88 THEN INCREASED TO 111... AFTER ADMINISTRATION PATIENT STOOD UP STARTED WITH RESPIRATORY DISTRESS. RR 88 THEN INCREASED TO 111 AFTER 15 MINS. PATIENT HAD DIFFICULTY BREATHING AND CONTINUOUSLY COUGHING. AIR WAY WAS SWOLLEN. EPIPEN 0.3 WAS ADMNISTERED THEN EMS ARRIVED 5 MINS LATER. PATIENT DID NOT IMPROVE UNTIL HOURS LATER AT THE HOSPITAL. PER PATIENT WAS GIVEN MORE EPINEPHRINE, STEROID, ANTIBIOTICS, AND NEBULIZING TREATMENT More
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