🏥 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 💀 🏥 🚑 ♿ ⚠️
2840467 1.5 F DE 05/12/2025 VARCEL
 MERCK & CO. INC.
 Z003767
Extra dose administered Extra dose administered
Patient was accidently MMR Combo along with a separate Varicella vaccine. Patient was accidently MMR Combo along with a separate Varicella vaccine.
2840468 64 F ME 05/12/2025 IPV
PNC21
 SANOFI PASTEUR
MERCK & CO. INC.
 8081260
Z002626
Burning sensation, Erythema, Skin warm; Burning sensation, Erythema, Skin warm Burning sensation, Erythema, Skin warm; Burning sensation, Erythema, Skin warm
redness, 4 inches long down her arm towards her elbow, burning sensation, hot to touch, ibuprofen an... redness, 4 inches long down her arm towards her elbow, burning sensation, hot to touch, ibuprofen and benadryl prn More
2840469 24 M TN 05/12/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 945660
Extra dose administered Extra dose administered
PT WAS GIVEN EXTRA DOSE OF HEP B PT WAS GIVEN EXTRA DOSE OF HEP B
2840470 39 F MA 05/12/2025 PNC20
 PFIZER\WYETH
 LX4484
Injection site erythema, Injection site swelling, Injection site warmth Injection site erythema, Injection site swelling, Injection site warmth
Erythema, warmth, swelling at injection site, 6 cm in diameter Erythema, warmth, swelling at injection site, 6 cm in diameter
2840471 31 F OH 05/12/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 EB499
Injection site discolouration, Injection site erythema, Injection site warmth Injection site discolouration, Injection site erythema, Injection site warmth
Pt has a large area of discoloration, redness and warmth at and below injection site. Onset of sx re... Pt has a large area of discoloration, redness and warmth at and below injection site. Onset of sx reported to have started the following day. More
2840472 38 M SC 05/12/2025 PNC21
 MERCK & CO. INC.
 Y019157
Injection site erythema Injection site erythema
Erythema to injection site noted two day after immunization Erythema to injection site noted two day after immunization
2840473 40 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00017
No adverse event No adverse event
The treatment was for the 2nd series of a 2-series vaccination; the outcome was uneventful, with no ... The treatment was for the 2nd series of a 2-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840474 18 M IN 05/12/2025 MENB
 PFIZER\WYETH
 LL0637
Headache, Injection site erythema, Injection site swelling Headache, Injection site erythema, Injection site swelling
Patient developed redness and swelling at injection site. He also developed a headache that worsene... Patient developed redness and swelling at injection site. He also developed a headache that worsened with sitting up. The headache lasted for about 3 days. A similar but more severe case of this reaction happened to his sister when she received the 2nd dose of the same vaccine. More
2840475 66 F FL 05/12/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 9L944
Mobility decreased, Pain in extremity Mobility decreased, Pain in extremity
PT SAYS SHE HAS HAD ARM PAIN SINCE A COUPLE OF DAYS AFTER RECEIVING IMZ AND IT IS STILL AFFECTING HE... PT SAYS SHE HAS HAD ARM PAIN SINCE A COUPLE OF DAYS AFTER RECEIVING IMZ AND IT IS STILL AFFECTING HER RANGE OF MOTION STILL TO THE PRESENT DAY . SHE HAS TAKE NO MEDS FOR IT ON ONLY USED "SPRAY ICE" More
2840476 35 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first two-series vaccination; the outcome was uneventful, with no symptoms or ... The treatment was the first two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840477 0.75 F MO 05/12/2025 DTAPIPVHIB
 SANOFI PASTEUR
 uk114aa
Wrong product administered Wrong product administered
Pt was administered pentacel when not needed. Pt was administered pentacel when not needed.
2840478 27 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840479 53 M 05/12/2025 PNC20
 PFIZER\WYETH
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Severe redness and swelling at injection site >3 days since injection Severe redness and swelling at injection site >3 days since injection
2840480 11 F OR 05/12/2025 COVID19
 PFIZER\BIONTECH
Incorrect dose administered Incorrect dose administered
pt was given covid vaccine from age group 12-18 instead of her age gap. pt was given covid vaccine from age group 12-18 instead of her age gap.
2840481 17 F PA 05/12/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 945656
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Administered to 17-year-old. No patient issues. Administered to 17-year-old. No patient issues.
2840483 10 F OR 05/12/2025 COVID19
 PFIZER\BIONTECH
Incorrect dose administered Incorrect dose administered
Patient was given wrong age group vaccine. Patient was given dose for 12 yrs - 18 yrs. Patient was given wrong age group vaccine. Patient was given dose for 12 yrs - 18 yrs.
2840484 16 F SC 05/12/2025 MNQ
 SANOFI PASTEUR
 U8256BA
Erythema multiforme, Urticaria Erythema multiforme, Urticaria
4 days after vaccine patient developed hives and suspected erythema multiforme. Hives have improved ... 4 days after vaccine patient developed hives and suspected erythema multiforme. Hives have improved but EM rash is still present. More
2840485 31 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00015
No adverse event No adverse event
The treatment was the second series of a two-series vaccination; the outcome was uneventful, with no... The treatment was the second series of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840486 73 M FL 05/12/2025 HEPA
IPV
TDAP
YF
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 SKBV27PD
PMCIA201M
SKBXN575
PMCUK133AB
Abdominal pain upper, Dehydration, Diarrhoea, Pyrexia; Abdominal pain upper, Deh... Abdominal pain upper, Dehydration, Diarrhoea, Pyrexia; Abdominal pain upper, Dehydration, Diarrhoea, Pyrexia; Abdominal pain upper, Dehydration, Diarrhoea, Pyrexia; Abdominal pain upper, Dehydration, Diarrhoea, Pyrexia More
Late friday night I got at stomach ache with bad runs and my wife called 911. I was dehydrated with ... Late friday night I got at stomach ache with bad runs and my wife called 911. I was dehydrated with a low grade fever and they admitted me for a couple of days. More
✓
2840487 65 F AZ 05/12/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EW0161
EW0161
EW0177
EW0177
Cognitive disorder, Computerised tomogram normal, Electroencephalogram normal, L... Cognitive disorder, Computerised tomogram normal, Electroencephalogram normal, Laboratory test normal, Magnetic resonance imaging head normal; Myocardial infarction, Sjogren's syndrome, Systemic lupus erythematosus, Tremor; Cognitive disorder, Computerised tomogram normal, Electroencephalogram normal, Laboratory test normal, Magnetic resonance imaging head normal; Myocardial infarction, Sjogren's syndrome, Systemic lupus erythematosus, Tremor More
2ND COVID BOOSTER PROVIDED ON JULY 1 2021, PATIENT HAD A HEART ATTACK IN AUGUST 2021 (HOSPITALIZED);... 2ND COVID BOOSTER PROVIDED ON JULY 1 2021, PATIENT HAD A HEART ATTACK IN AUGUST 2021 (HOSPITALIZED); ONSET OF TREMOR AND COGNITIVE DECLINE SEPTEMBER 2021; DX WITH LUPUS AND SJOGRENS SYNDROME 2025. More
2840488 60 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00015
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840489 31 M FL 05/12/2025 COVID19
 JANSSEN
 2024A21A
Alopecia, Lichen planus, Rash, Rash erythematous Alopecia, Lichen planus, Rash, Rash erythematous
Red bumps on arm and wrists consistent and hair loss consistent with Lichen Planus Red bumps on arm and wrists consistent and hair loss consistent with Lichen Planus
2840490 23 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first two-series vaccination; the outcome was uneventful. With no symptoms or ... The treatment was the first two-series vaccination; the outcome was uneventful. With no symptoms or signs of reactions reported. More
2840492 32 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 96867
No adverse event No adverse event
The treatment was the first two-series vaccination; the outcome was uneventful, with no symptoms or ... The treatment was the first two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840493 11 M NM 05/12/2025 HPV9
MNQ
TDAP
 MERCK & CO. INC.
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 Y010466
U7996BB
F4T5L
Injection site erythema, Injection site pruritus, Injection site swelling; Injec... Injection site erythema, Injection site pruritus, Injection site swelling; Injection site erythema, Injection site pruritus, Injection site swelling; Injection site erythema, Injection site pruritus, Injection site swelling More
ITCHING TO LEFT ARM, 2 INCH DIAMETER, REDNESS SWELLING NO PAIN FOR 2 DAYS AFTER INJECTION TO SITE. ... ITCHING TO LEFT ARM, 2 INCH DIAMETER, REDNESS SWELLING NO PAIN FOR 2 DAYS AFTER INJECTION TO SITE. FOLLOWED UP 5 DAYS LATER AND THE ISSUE WAS RESOLVED. More
2840494 45 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840495 13 F MI 05/12/2025 COVID19
FLU3
TYP
 MODERNA
SANOFI PASTEUR
SANOFI PASTEUR
 3043000
Ut8459JA
X1A271M
Incorrect dose administered, No adverse event; Incorrect dose administered, No a... Incorrect dose administered, No adverse event; Incorrect dose administered, No adverse event; Incorrect dose administered, No adverse event More
Incorrect dose of Moderna Covid vaccine given to patient. No adverse event noticed. Patient was cont... Incorrect dose of Moderna Covid vaccine given to patient. No adverse event noticed. Patient was contacted and told they should be revaccinated with the correct dose to ensure protection. More
2840496 26 M WY 05/12/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 4N222
Incorrect route of product administration Incorrect route of product administration
Not able to contact patient, left a message on phone for a return call. Priorix is to be given SQ a... Not able to contact patient, left a message on phone for a return call. Priorix is to be given SQ and we administered IM. More
2840497 0.75 M 05/12/2025 DTAPIPVHIB
 SANOFI PASTEUR
 UK024AA
Expired product administered Expired product administered
Patient was given an expired vaccination Patient was given an expired vaccination
2840498 5 M ID 05/12/2025 DTAPIPV
HPV9
MMRV
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
 3RT93
Y007322
Y019465
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
Patient was given the HPV shot that was meant for his 12 year old sister. Patient was given the HPV shot that was meant for his 12 year old sister.
2840499 66 M CA 05/12/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3334Y
Pruritus, Skin warm Pruritus, Skin warm
Patient started developing warm, itchy spots on random parts of the body (arms, legs) after shower. ... Patient started developing warm, itchy spots on random parts of the body (arms, legs) after shower. Lasts about an hour and then goes away. Has persisted since vaccination 3/23/25 to today, 5/12/25, though the severity of the itchiness has gradually decreased More
2840500 0.33 KS 05/12/2025 RV5
 MERCK & CO. INC.
 2003166
No adverse event, Product storage error No adverse event, Product storage error
No adverse event; HCP calling to report AE for a vaccine that was inadvertently administered after a... No adverse event; HCP calling to report AE for a vaccine that was inadvertently administered after a temperature excursion. ? Name of vaccines involved (including lot/exp): ROTATEQ 2003166 9/8/2025 ? Temperature: 1.5C ? Time frame; This spontaneous report was received from a registered nurse and refers to a) 4-month-old patient of unknown gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 14-APR-2025, the patient was inadvertently vaccinated with an improper stored dose of Rotavirus Vaccine, Live, Oral, Pentavalent (ROTATEQ), (valid lot #2003166, expiration date reported as 08-SEP-2025, but upon internal validation established as 06-SEP-2025) 2 ml, once, administered by oral route as prophylaxis. The temperature excursion was reported 1.5 degree Celsius with a time frame of 50 minutes. No previous temperature excursion reported. In addition, the reported stated that the patient did not have any reactions or symptoms (no adverse event). More
2840501 45 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 96868
No adverse event No adverse event
The treatment was the second dose of a two-series vaccination; the outcome was uneventful, with no s... The treatment was the second dose of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840502 16 F OH 05/12/2025 MENB
MNQ
 NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
 49M9N
U8493AA
Injection site erythema, Injection site oedema, Injection site pain, Injection s... Injection site erythema, Injection site oedema, Injection site pain, Injection site swelling, Paraesthesia; Injection site erythema, Injection site oedema, Injection site pain, Injection site swelling, Paraesthesia More
On the afternoon of 5/8/2025, patient developed soreness at site of injections. Took Ibuprofen. The ... On the afternoon of 5/8/2025, patient developed soreness at site of injections. Took Ibuprofen. The next morning she noticed tingling in RT hand and distal half of forearm when lifting hand toward face, noticed when applying make up. Still with pain at injection site and noticed mild redness and swelling. On exam she has 2cm x 2cm erythema and mild edema of RT deltoid area. RT hand and arm has good strength and tone and sensation intact. More
2840503 62 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00015
No adverse event No adverse event
The treatment was the second dose of a two-series vaccination; the outcome was uneventful, with no s... The treatment was the second dose of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840504 51 M CA 05/12/2025 FLU3
 SEQIRUS, INC.
 AW3225B
Arthralgia, Asthenia, Sleep disorder Arthralgia, Asthenia, Sleep disorder
Severe pain in shoulder causing lack of sleep and loss of strength in arm. Patient has not slept a ... Severe pain in shoulder causing lack of sleep and loss of strength in arm. Patient has not slept a full night's sleep since pain began in November 2024. More
✓
2840505 0.25 M NC 05/12/2025 RV1
 GLAXOSMITHKLINE BIOLOGICALS
 7E9X2
Vomiting projectile Vomiting projectile
Projectile Vomiting x3 Projectile Vomiting x3
2840506 65 F NJ 05/12/2025 PNC21
 MERCK & CO. INC.
 Y013009
Erythema, Pain Erythema, Pain
Redness and soreness around the area Redness and soreness around the area
2840507 65 F PA 05/12/2025 COVID19
COVID19
TDAP
TDAP
 MODERNA
MODERNA
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 3046731
3046731
DY3K7
DY3K7
Fatigue, Hypersensitivity, Inflammation, Injection site erythema, Injection site... Fatigue, Hypersensitivity, Inflammation, Injection site erythema, Injection site pain; Injection site pruritus, Malaise, Pyrexia; Fatigue, Hypersensitivity, Inflammation, Injection site erythema, Injection site pain; Injection site pruritus, Malaise, Pyrexia More
Documentation copied from provider's office visit note today (5/12/25): "Patient is a 65 ... Documentation copied from provider's office visit note today (5/12/25): "Patient is a 65 y.o. female who presents today to walk-in clinic regarding vaccine reaction. Had tetanus and COVID vaccines on Friday (5/9/25). Afterwards, was not feeling well. Was fatigued, had fever 100.8 over the weekend. Was taking Benadryl and Tylenol over the weekend. Has noticed redness at injection sites on both her arms. Describes the areas as intermittently painful and pruritic. Was advised not to get her routine allergy shot today due to the symptoms. Her next shot is tomorrow, and following one will be Friday. Suspect patient's symptoms are due to recent vaccination injections. Notably, injections were administered to the mid-upper arm bilaterally, rather than higher in the deltoid. Suspect inflammatory and/or allergic reaction. Advised to continue with Zyrtec or Benadryl, Tylenol as needed for pain control, local ice/cold compresses to reduce inflammation. Cannot take NSAIDs due to prior stroke. Follow up if symptoms worsen or persist. Skin Comments: Erythematous macular region present on bilateral upper arms, at sites of previous injections." More
2840508 16 M NE 05/12/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 945664
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
Patient is 16 years old. Was given Heplisav B which is indicated for patients 18 years and older. Di... Patient is 16 years old. Was given Heplisav B which is indicated for patients 18 years and older. Did not experience any adverse event or side effects per mother. More
2840509 12 M CA 05/12/2025 HPV9
HPV9
MNQ
MNQ
TDAP
TDAP
HPV9
HPV9
MNQ
MNQ
TDAP
TDAP
 MERCK & CO. INC.
MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 Y014510
Y014510
FX3ED
FX3ED
4RF9D
4RF9D
Y024510
Y024510
FX3ED
FX3ED
4RF9D
4RF9D
Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face; Eryth... Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face; Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face; Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face; Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face; Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face; Erythema, Eye pruritus, Rash; Erythema, Eye pruritus, Rash, Swelling face More
The patient presented to the clinic for routine vaccinations, including TDaP, meningococcal, and HPV... The patient presented to the clinic for routine vaccinations, including TDaP, meningococcal, and HPV immunizations. The vaccines were administered successfully, and the patient was monitored for 15 minutes with no adverse reactions observed. Approximately 80 minutes later, the mother returned with her son, who exhibited a mild rash on the jaw extending to the neck and partially to the cheeks bilaterally. After five minutes, the patient developed facial redness and reported itching of the eyes. The patient was evaluated promptly, and appropriate treatment was administered, including intramuscular epinephrine (0.3 mg/mL) and 25 mg of diphenhydramine (Benadryl) The patient presented to the clinic for routine vaccinations, including TDaP, meningococcal, and HPV immunizations. The vaccines were administered successfully, and the patient was monitored for 15 minutes with no adverse reactions observed. Approximately 80 minutes later, the mother returned with her son, who exhibited a mild rash on the jaw extending to the neck and partially to the cheeks bilaterally. After five minutes, the patient developed facial redness and reported itching of the eyes. The patient was evaluated promptly, and appropriate treatment was administered, including intramuscular epinephrine (0.3 mg/mL) and 25 mg of diphenhydramine (Benadryl)The patient presented to the clinic for routine vaccinations, including TDaP, meningococcal, and HPV immunizations. The vaccines were administered successfully, and the patient was monitored for 15 minutes with no adverse reactions observed. Approximately 80 minutes later, the mother returned with her son, who exhibited a mild rash on the jaw extending to the neck and partially to the cheeks bilaterally. After five minutes, the patient developed facial redness and reported itching of the eyes. The patient was evaluated promptly, and appropriate treatment was administered, including intramuscular epinephrine (0.3 mg/mL) and 25 mg of diphenhydramine (Benadryl)The patient presented to the clinic for routine vaccinations, including TDaP, meningococcal, and HPV immunizations. The vaccines were administered successfully, and the patient was monitored for 15 minutes with no adverse reactions observed. Approximately 80 minutes later, the mother returned with her son, who exhibited a mild rash on the jaw extending to the neck and partially to the cheeks bilaterally. After five minutes, the patient developed facial redness and reported itching of the eyes. The patient was evaluated promptly, and appropriate treatment was administered, including intramuscular epinephrine (0.3 mg/mL) and 25 mg of diphenhydramine (Benadryl) The rash and facial redness resolved shortly after treatment.. More
2840510 39 F NM 05/12/2025 HPV9
 MERCK & CO. INC.
 y010656
Rash, Rash erythematous Rash, Rash erythematous
red bumpy rash starting at inside of elbow and extending to top of hand, seems to be getting worse. ... red bumpy rash starting at inside of elbow and extending to top of hand, seems to be getting worse. has tried hydrocortisone cream with no relieve, has also tried eczema cream. More
2840511 35 M OR 05/12/2025 COVID19
 PFIZER\BIONTECH
 MD3414
Rash, Rash pruritic, Rash vesicular Rash, Rash pruritic, Rash vesicular
Patient reported having fluid filled bumps that are itchy, patient declined any shortness of breath,... Patient reported having fluid filled bumps that are itchy, patient declined any shortness of breath, tightness in the throat or difficulty breathing, stated that bumps are all over his body and that steroid cream is not helpful in getting rid of them but do help with the itching. Patient was advised to take Benadryl, and to follow up if symptoms did not resolve in a week, or if new symptoms arised. More
2840512 43 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00015
No adverse event No adverse event
The treatment was the second of a two-series vaccination. The outcome was uneventful, with no sympto... The treatment was the second of a two-series vaccination. The outcome was uneventful, with no symptoms or signs of reaction reported. More
2840513 45 M WA 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 96868
Incorrect route of product administration, No adverse event Incorrect route of product administration, No adverse event
Dose was accidentally administered IM versus subq. Patient stayed in clinic for 15 minutes following... Dose was accidentally administered IM versus subq. Patient stayed in clinic for 15 minutes following immunization reporting no adverse symptoms at this time. Encouraged patient to reach out with current questions or concerns. Charge notified. More
2840514 35 M AZ 05/12/2025 SMALLMNK
VARZOS
 BAVARIAN NORDIC
GLAXOSMITHKLINE BIOLOGICALS
 FDP00016
E7335
No adverse event; No adverse event No adverse event; No adverse event
Treatment was first of a two-series vaccination; the outcome was uneventful, with no symptoms or sig... Treatment was first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reaction reported. More
2840515 60 F VA 05/12/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 4B22T
No adverse event No adverse event
No Adverse even No Adverse even
2840516 44 F CA 05/12/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 PG3RP
Paraesthesia, Peripheral swelling Paraesthesia, Peripheral swelling
12-18 Hours following the vaccine, tingling and swelling in both hands and arms began. It has conti... 12-18 Hours following the vaccine, tingling and swelling in both hands and arms began. It has continued until this date (9 days post-vaccine) even with anti-inflammatories (Naproxen) and compression gloves. More
2840517 31 M AZ 05/12/2025 SMALLMNK
 BAVARIAN NORDIC
 FDP00016
No adverse event No adverse event
The treatment was the second of a two-series vaccination; the outcome was uneventful, with no sympto... The treatment was the second of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
2840518 54 M AZ 05/12/2025 PNC20
SMALLMNK
 PFIZER\WYETH
BAVARIAN NORDIC
 LK6650
96867
No adverse event; No adverse event No adverse event; No adverse event
The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptom... The treatment was the first of a two-series vaccination; the outcome was uneventful, with no symptoms or signs of reactions reported. More
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