🏥 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 💀 🏥 🚑 ♿ ⚠️
2824169 28 M CA 02/03/2025 COVID19
 MODERNA
 025B21A
Vertigo, Vomiting Vertigo, Vomiting
Reported Symptoms: 10047340:VERTIGO; 10047700:VOMITING; Narrative: Other Relevant: HX: VERTIGO Reported Symptoms: 10047340:VERTIGO; 10047700:VOMITING; Narrative: Other Relevant: HX: VERTIGO
2824170 64 M AZ 02/03/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 EN6205
EN6205
Breakthrough COVID-19, Chest X-ray, Computerised tomogram abdomen, Computerised ... Breakthrough COVID-19, Chest X-ray, Computerised tomogram abdomen, Computerised tomogram thorax, SARS-CoV-2 test positive; Sepsis, Systemic inflammatory response syndrome More
Reported Symptoms: 10054112:HOSPITALISATON; 10067923:VACCINE BREAKTHROUGH INFECTION; 10084401:COVID-... Reported Symptoms: 10054112:HOSPITALISATON; 10067923:VACCINE BREAKTHROUGH INFECTION; 10084401:COVID-19 RESPIRATORY INFECTION; Narrative: 68 year old male with PMH of ESRD s/p renal transplant in 2005 on MM, tacrolimus, and daily prednisone admitted for acute covid infection w/o hypoxia. Patient with sepsis by SIRS criteria, likely secondary to acute covid infection per 8/7/24 hospitalist note. Given the risk of progression/severe disease in chronically immunosuppressed patient, patient was started on empiric remdesivir. Patient discharged home after completing 5 days of IV antiviral. Other Relevant HX: PMH significant for Afib, DM2, HTN, hyperlipidemia, HFpEF, gout, BPH, IDA, and CKD s/p kidney transplant in 2008 on immunosuppression Other: Hospitalization for treatment of Covid infection s/p vaccination More
✓
2824171 69 M AZ 02/03/2025 COVID19-2
COVID19-2
FLUA4
FLUA4
 PFIZER\BIONTECH
PFIZER\BIONTECH
SEQIRUS, INC.
SEQIRUS, INC.
 GL0446
GL0446
346378
346378
Breakthrough COVID-19, Chest X-ray normal, Computerised tomogram thorax normal, ... Breakthrough COVID-19, Chest X-ray normal, Computerised tomogram thorax normal, Dyspnoea, Hypoxia; SARS-CoV-2 test positive, Scan with contrast normal, Wheezing; Breakthrough COVID-19, Chest X-ray normal, Computerised tomogram thorax normal, Dyspnoea, Hypoxia; SARS-CoV-2 test positive, Scan with contrast normal, Wheezing More
Reported Symptoms: 10054112:HOSPITALISATION; 10067923:VACCINE BREAKTHROUGH INFECTION; 10084401:COVID... Reported Symptoms: 10054112:HOSPITALISATION; 10067923:VACCINE BREAKTHROUGH INFECTION; 10084401:COVID-19 RESPIRATORY INFECTION; Narrative: Patient is a 71 year old MALE with PMH of recent CAP PNA treated with inpatient stay and antibiotics presented to ED from assisted care facility for 4-5 days of increasing work of breathing, SOB, and wheezing. Patient found to be Covid positive and hypoxic to the mid 80s. H&P from 8/9/24 expressed concern for potential undiagnosed COPD based on extensive tobacco use history. Patient treated with remdesivir and dexamethasone and discharged back to assisted living facility. Other Relevant HX: PMH of recent CAP PNA treated with inpatient stay and antibiotics, persistent leukocytosis, mechanical aortic valve, mitral valve stenosis, HTN, HLD, renal cysts, BPH, GERD, CKDstage 3, Ulcerative colitis, and paroxysmal a-fib with extensive tobacco use history, concern for COPD. Other: Hospitalization for treatment of Covid infection s/p vaccination More
✓
2824172 66 M AZ 02/03/2025 COVID19-2
COVID19-2
 PFIZER\BIONTECH
PFIZER\BIONTECH
 GJ6796
GJ6796
Blood gases abnormal, Breakthrough COVID-19, COVID-19 pneumonia, Computerised to... Blood gases abnormal, Breakthrough COVID-19, COVID-19 pneumonia, Computerised tomogram thorax, Dyspnoea; Headache, Malaise, SARS-CoV-2 test positive More
Reported Symptoms: 10054112:HOSPITALISATION; 10067923:VACCINE BREAKTHROUGH INFECTION; 10084401:COVID... Reported Symptoms: 10054112:HOSPITALISATION; 10067923:VACCINE BREAKTHROUGH INFECTION; 10084401:COVID-19 RESPIRATORY INFECTION; Narrative: 67 y/o male who presented to the ED on 8/17/24 w/ shortness of breath, malaise, and headache of one day's duration and was found to have COVID pneumonia. His ABG O2 on initial presentation was 58 and he was initially requiring O2 in order to maintain his oxygen saturations. He was admitted for management of his suspected COVID pneumonia. Patient discharged to home after completing treatment with remdesivir. Other Relevant HX: PMHx of T2DM w/ diabetic nephropathy, HTN, HLD, PTSD, GERD, OSA, and osteoarthritis of the knees s/p left TKA on 6/24/24 Other: Hospitalization for treatment of Covid infection s/p vaccination More
✓
2824173 72 M MT 02/03/2025 COVID19
 MODERNA
 029L20A
Breakthrough COVID-19, COVID-19 pneumonia, SARS-CoV-2 test positive, Treatment n... Breakthrough COVID-19, COVID-19 pneumonia, SARS-CoV-2 test positive, Treatment noncompliance More
Reported Symptoms: 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: Patient was living independen... Reported Symptoms: 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: Patient was living independently for approximately one month following being a resident at a long term facility. Patient received two doses of the Moderna Covid-19 vaccine (12/29/2020 & 01/26/2021). On 09/28/2021 patient presented to an emergency department at a different facility where he tested positive for the COVID-19 infection. Patient had stopped taking all his home medications (including but limited to carbidopa/levodopa, quetiapine and ropinirole) without tapering or under the advisement of a physician due to his caretaker also being sick with the infection. Patient was transferred to the local facility for quarantine and supportive care. All medications were re-initiated. The COVID-19 pneumonia infection did not require any treatment. Patient had no where to discharge to until 10/14/2021 when he returned back to the long term care facility he had lived at previously. Other Relevant HX: Past medical history relevant for: T2DM, deep brain stimulation, GERD, parkinsonism, anxiety disorder, hyperlipidemia Other: COVID-19 Breakthrough Infection More
✓
2824174 97 M MT 02/03/2025 COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
 031L20A
031L20A
031L20A
Acute myocardial infarction, Anuria, Blood glucose increased, Blood lactic acid ... Acute myocardial infarction, Anuria, Blood glucose increased, Blood lactic acid increased, Blood pressure decreased; Breakthrough COVID-19, Death, Decreased appetite, Dyspnoea, Heart rate increased; Hypoxia, Renal impairment, SARS-CoV-2 test positive, Troponin increased More
Reported Symptoms: 10011906:DEATH; 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: patient livin... Reported Symptoms: 10011906:DEATH; 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: patient living at home with wife and had four daughters as caretakers. Patient received two doses of Moderna COVID-19 vaccine (01/13/2021 & 02/10/2021). At presentation to emergency department (10/03/2021), patient had elevated heart rate, elevated blood sugars, appeared short of breath, not eating and requiring 6L of oxygen. COVID-19 test came back positive, along with elevated troponin, elevated lactate and worsening kidney function from baseline. Patient's kidney function did not support treatment with remdesivir, was was treated solely with dexamethasone. Patient's oxygen needs continued to escalate, blood pressure dropped, and was anuria throughout his stay in the hospital prior to expiring 10/05/2021. Other Relevant HX: Problem list significant for: CKD stage 4, T2DM, HTN, Troponin positive on admission for non-STMI Acute hypoxemia Other: COVID-19 Breakthrough Infection More
✓
2824175 83 M MT 02/03/2025 COVID19
COVID19
 MODERNA
MODERNA
 019B21A
019B21A
Asthenia, Breakthrough COVID-19, Condition aggravated, Cough, Death; Dyspnoea, H... Asthenia, Breakthrough COVID-19, Condition aggravated, Cough, Death; Dyspnoea, Hypoxia, Respiratory failure, SARS-CoV-2 test positive More
Reported Symptoms: 10011906:DEATH; 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: Patient who l... Reported Symptoms: 10011906:DEATH; 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: Patient who lives in an assisted living facility received two COVID-19 immunizations (05/06/2021 & 06/10/2021). Patient has a medical history significant for COPD, OSA, pulmonary hypertension, and hypoxia requiring 3-4L of oxygen at baseline. While at home, patient developed a cough and shortness of breath. Caregiver administered an at-home COVID test on 09/24/2021. His condition worsened, and was escorted the emergency department on 10/01/2021 where diagnosis of COVID was confirmed with a PCR test. Patient was admitted to floor with hypoxemic respiratory failure and started on IV dexamethasone and CA-pneumonia antibiotics. Remdesivir and baricitinib were added to his treatment regimen as well. Patient returned to baseline oxygen needs and was discharged back to the assisted living home. Primary care notes indicate continued worsening condition over the next weeks. Patient presented back to the ED 10/22/2021 for increasing hypoxia (oxygen requirements up to 6L/min), weakness and dyspnea. Patient was admitted to the floor, and expired a few hours after admission. Other Relevant HX: Lives in assisted living facility on 3-4L oxygen at baseline Problem list significant for: COPD, hypoxia, pulmonary hypertension, OSA Other: Breakthrough COVID-19 infection More
✓ ✓
2824176 70 M MT 02/03/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 en9581
en9581
Asthenia, Back pain, Breakthrough COVID-19, Fall, Respiratory depression; SARS-C... Asthenia, Back pain, Breakthrough COVID-19, Fall, Respiratory depression; SARS-CoV-2 test positive More
Reported Symptoms: 10038678:RESPIRATORY DEPRESSION; 10067923:VACCINE BREAKTHROUGH INFECTION; Narrati... Reported Symptoms: 10038678:RESPIRATORY DEPRESSION; 10067923:VACCINE BREAKTHROUGH INFECTION; Narrative: Patient received two doses of Pfizer COVID-19 vaccine (01/27/2021 & 02/19/2021). On 09/20/2021 patient presented to the ED for chief complain of back pain due to frequent falls. Patient was sent home with Tylenol and cyclobenzaprine. A COVID-19 sample was taken at this time. Patient presented to the ED again on 09/24/2021 with a chief complain of weakness. Labs were reviewed, patient was COVID positive. Patient was admitted, received a four day course of dexamethasone 6mg daily, 2L of oxygen and was empirically treated with ceftriaxone 2g. Patient returned to baseline and was discharged 10/01/2021. Other Relevant HX: Pfizer COVID-19 vaccine dose #1 (01/27/2021) Pfizer COVID-19 vaccine dose #2 (02/19/2021) Problem list significant for: CHF, COPD, CAD, OSA, HTN, obesity Other: Breakthrough COVID-19 infection More
✓
2824177 94 M MT 02/03/2025 COVID19
 PFIZER\BIONTECH
COVID-19, COVID-19 pneumonia, Computerised tomogram thorax abnormal, Cough, SARS... COVID-19, COVID-19 pneumonia, Computerised tomogram thorax abnormal, Cough, SARS-CoV-2 test positive More
Reported Symptoms: 10084401:COVID-19 RESPIRATORY INFECTION; Narrative: Vaccinated patient (received... Reported Symptoms: 10084401:COVID-19 RESPIRATORY INFECTION; Narrative: Vaccinated patient (received both doses of Pfizer COVID vaccine 1/2021) was a resident of an assisted living facility that experienced a COVID-19 outbreak. He tested positive for COVID on 9/15/21, and noted increased oxygen requirements (2L at baseline up to 5L), along with cough (no fever or other symptoms reported). Admitted to the medical facility and treated with dexamethasone 6mg daily. Repeated COVID testing on 9/21/21 also positive). Chest CT was consistent w/ COVID-19 pneumonia. He improved to baseline and was discharged back to the assisted living facility. Dates of admission 9/21-9/27/21. Other Relevant HX: Problem list includes hypertension, diabetes, dyspnea Other: COVID-19 infection More
✓
2824178 77 M MT 02/03/2025 COVID19
 MODERNA
 025B21A
Extra dose administered, Wrong product administered Extra dose administered, Wrong product administered
Reported Symptoms: 10063978: WRONG VACCINE ADMINISTERED; Narrative: On 04/10/2021 Patient was admin... Reported Symptoms: 10063978: WRONG VACCINE ADMINISTERED; Narrative: On 04/10/2021 Patient was administered one dose of the Janssen COVID-19 Vaccine. Patient returned on 05/08/2021 requesting his second dose. Moderna COVID-19 vaccine was then administered. The individual administering the vaccine did not review the chart prior to injection. The chart accurately showed the patient received Janssen the month prior, thus a second dose of any COVID-19 vaccine would have been inappropriate. Other Relevant HX: Other: Dose of Moderna COVID-19 vaccine given following a dose of Janssen COVID-19 vaccine More
2824179 M NV 02/03/2025 COVID19
 PFIZER\BIONTECH
Syncope Syncope
Reported Symptoms: 10042772:SYNCOPE; Narrative: Other Relevant HX: Reported Symptoms: 10042772:SYNCOPE; Narrative: Other Relevant HX:
2824180 M NV 02/03/2025 COVID19
 MODERNA
Cough Cough
Reported Symptoms: 10011232:COUGHING; Narrative: Other relevant H: COUGH Reported Symptoms: 10011232:COUGHING; Narrative: Other relevant H: COUGH
2824181 55 M NV 02/03/2025 COVID19
 MODERNA
 3031707
Expired product administered, No adverse event, Product storage error Expired product administered, No adverse event, Product storage error
Reported Symptoms: 10058327:EXPIRED DRUG USED; 10081576:PRODUCT ADMINISTRATION ERROR; Narrative: Vac... Reported Symptoms: 10058327:EXPIRED DRUG USED; 10081576:PRODUCT ADMINISTRATION ERROR; Narrative: Vaccine administration errors, not associated with an adverse event. On 4/26/2024, nurse administered covid-19 vaccine past the expiration/beyond use date. Covid-19 vaccine beyond use date was labeled as 4/24/2024, but was administered on 4/26/2024. No adverse effect to report. Other Relevant HX: Other: Dose administered past the expiration/beyond-use date More
2824182 65 M NV 02/03/2025 COVID19
COVID19
 MODERNA
MODERNA
 030h21b
030h21b
Acute myocardial infarction, Coronary artery bypass, Cough, Dyspnoea, Hyperhidro... Acute myocardial infarction, Coronary artery bypass, Cough, Dyspnoea, Hyperhidrosis; Syncope, Tachypnoea More
Reported Symptoms: 10011232:COUGHING; 10042772:SYNCOPE; 10043088:TACHYPNEA; Narrative: Patient recei... Reported Symptoms: 10011232:COUGHING; 10042772:SYNCOPE; 10043088:TACHYPNEA; Narrative: Patient received Moderna COVID booster (monovalent) as he was due at PCP office. Several hours later her reported to the ED. This was the providers report: "This 65 yr. old male presents with a history of shortness of breath, sudden onset 1 hours ago, associated with cough, and diaphoresis, patient thought it was pneumonia and came in. he had his Covid 19 booster earlier today. Otherwise well prior to onset, he relates simialr symptoms when 'I had my heart attack'. Was treated at Medical Center.' -Patient found to have STEMI and transferred to hospital where CABG x 3 was performed. Other Relevant HX: Other: More
✓
2824183 11 F ID 02/03/2025 COVID19
HPV9
MNQ
TDAP
 PFIZER\BIONTECH
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
 LM2221
Y012864
U8361AA
3CA22C1
Incorrect dose administered, Pain in extremity; Incorrect dose administered, Pai... Incorrect dose administered, Pain in extremity; Incorrect dose administered, Pain in extremity; Incorrect dose administered, Pain in extremity; Incorrect dose administered, Pain in extremity More
Patient left office with only sore arms which is typical for post injection administration. No other... Patient left office with only sore arms which is typical for post injection administration. No other adverse reactions were noted. Patient was administered COVID Pfizer for the age group of 12+ instead of 5-11 years. Grandmother accompanied patient to her wellness exam on 1/31/2025. Consent was obtained from mother via phone while in office. Dose does not need to be repeated. System accepted the dose for COVID for the season. More
2824184 60 F MT 02/03/2025 PNC20
 PFIZER\WYETH
 LK6650
Erythema, Fatigue, Headache, Tinnitus Erythema, Fatigue, Headache, Tinnitus
arm redness 2-3'', fatigue, headache, tinnitus for 6 days arm redness 2-3'', fatigue, headache, tinnitus for 6 days
2824185 73 M MD 02/03/2025 TDAP
 UNKNOWN MANUFACTURER
Bursitis, Injection site pain, Product administered at inappropriate site, Ultra... Bursitis, Injection site pain, Product administered at inappropriate site, Ultrasound joint More
On December 3, 2024 I received a tetanus vaccination where the needle was inserted too high on my sh... On December 3, 2024 I received a tetanus vaccination where the needle was inserted too high on my shoulder and was later diagnosed to have hit my bursa sac. I thought the technician was prepping an injection location too high on my shoulder but didn't say anything. The vaccination itself was uneventful but within 2 days. I had near constant pain in the L shoulder around the injection site. Icing and Advil/Alleve did not resolve the issue. I met with Nurse Practitioner on December 10, and she referred me to Dr. who I saw on December 17. He gave me ultrasound and suggested a cortisone shot but I declined on the grounds that I did not want anymore needles in my shoulder. He referred me to another Dr for further treatment. I saw Dr. on December 18. He used ultrasound to diagnos bursitis and suggested a cortisone shot. I declined the shot. He prescribed Meloxicam (Mobic) which I took for almost 3 weeks as the pain symptoms subsided. After about 6 weeks I felt my left shoulder had been relieved of pain and was back to normal. More
2824186 69 F WI 02/03/2025 TDAP
TDAP
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 3335K
3335K
Chills, Diarrhoea, Hyperhidrosis, Loss of consciousness, Pyrexia; Tinnitus, Vomi... Chills, Diarrhoea, Hyperhidrosis, Loss of consciousness, Pyrexia; Tinnitus, Vomiting More
1/13 chills in afternoon 1/14 Low grade fever all day 1/15 About 5 am - woke to soaking wet nightgow... 1/13 chills in afternoon 1/14 Low grade fever all day 1/15 About 5 am - woke to soaking wet nightgown, hair was wet, ringing in my ears - stood up to go to bathroom and ringing increased ten fold - passed out. Then throwing up + diarrhea. Finally stopped about 6:15 am More
2824187 0.17 M MI 02/03/2025 DTAPHEPBIP
HIBV
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
PFIZER\WYETH
 2G273
Y008355
LK6651
Infant irritability, Pyrexia, Somnolence; Infant irritability, Pyrexia, Somnolen... Infant irritability, Pyrexia, Somnolence; Infant irritability, Pyrexia, Somnolence; Infant irritability, Pyrexia, Somnolence More
Fever of 101, increased fussiness, sleepy Fever of 101, increased fussiness, sleepy
2824236 93 F IA 02/03/2025 COVID19
 MODERNA
 3043159
Death Death
Death Death
✓
2824237 4 F NY 02/03/2025 DTAPIPV
MMRV
 SANOFI PASTEUR
MERCK & CO. INC.
 U8209CB
Y014307
Injection site erythema, Injection site urticaria, Rash, Urticaria; Injection si... Injection site erythema, Injection site urticaria, Rash, Urticaria; Injection site erythema, Injection site urticaria, Rash, Urticaria More
Patient returned to clinic at 3 pm following DTaP/Polio and MMR/Varicella vaccinations reaction. Lef... Patient returned to clinic at 3 pm following DTaP/Polio and MMR/Varicella vaccinations reaction. Left arm site where DTaP/Polio was given was severely red and had hives present. Chest, behind ears and hands had some minor hives. benadryl (12.5/5) 7 ml given in office. Patient observed for 2 hours with minor improvement in rash. No difficulty breathing, O2 95%, no vomiting, no diarrhea. Patient's mother confirms epipen (up to date) in care. Informed of anaphlyaxis sx, if appears to give epipen and call 911. Mother understood and left office with child. More
2824238 10 M NY 02/03/2025 HEPA
 GLAXOSMITHKLINE BIOLOGICALS
 22GP3
Nausea, Pallor, Vomiting Nausea, Pallor, Vomiting
Patient became pale and nauseous, patient had 1 episode of emesis and had to sit down. Patient was g... Patient became pale and nauseous, patient had 1 episode of emesis and had to sit down. Patient was given apple juice and crackers, 0940 BP was taken with results being 80s over 40s. Pulse oximeter was placed for monitoring purposes. 0942 BP taken 100/62, patient stated they felt better. 0952 BP taken again 100/62 SPO2 98-100%, HR sustained in 90s-100s. Patient stated they felt much better. More
2824239 16 M NJ 02/03/2025 HPV9
 MERCK & CO. INC.
 Y007322
Extra dose administered Extra dose administered
Patient was given Gardasil vaccine on 1/29/25 by error .Patient had already received the Gardasil v... Patient was given Gardasil vaccine on 1/29/25 by error .Patient had already received the Gardasil vaccine series on 7/18/20 & 8/3/19 More
2824240 35 F IL 02/03/2025 PNC20
 PFIZER\WYETH
 Ig5579
No adverse event, Vaccination error No adverse event, Vaccination error
Pt inadvertently received Prevnar 20 vaccine. No adverse side effects noted. Pt inadvertently received Prevnar 20 vaccine. No adverse side effects noted.
2824241 81 F WV 02/03/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 D5AP5
Myalgia Myalgia
Patient reports muscle soreness that started 1 day post vaccine and has persisted for over 2 months.... Patient reports muscle soreness that started 1 day post vaccine and has persisted for over 2 months. Patient says that she still feels some muscle pain and that it "comes and goes", especially with movement. More
2824242 38 M 02/03/2025 FLU3
FLU3
MMR
MMR
TD
TD
VARCEL
VARCEL
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.







Abdominal distension, Asthenia, Blood test normal, Diarrhoea, Disturbance in att... Abdominal distension, Asthenia, Blood test normal, Diarrhoea, Disturbance in attention; Dizziness, Fatigue, Malaise; Abdominal distension, Asthenia, Blood test normal, Diarrhoea, Disturbance in attention; Dizziness, Fatigue, Malaise; Abdominal distension, Asthenia, Blood test normal, Diarrhoea, Disturbance in attention; Dizziness, Fatigue, Malaise; Abdominal distension, Asthenia, Blood test normal, Diarrhoea, Disturbance in attention; Dizziness, Fatigue, Malaise More
No immediate symptoms following immunization, it was weeks later he felt extremely sick. Couldn'... No immediate symptoms following immunization, it was weeks later he felt extremely sick. Couldn't wake up and had weakness, diarrhea, bloating, and dizziness. Unable to concentrate and fatigue followed. Gut issues persist to this day. More
2824243 10 F VA 02/03/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 ln7302
u8531ba
Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event More
None- covid vaccine expired 1/23/25 (10 weeks in refrigerator) and was administered 2/1/25 None- covid vaccine expired 1/23/25 (10 weeks in refrigerator) and was administered 2/1/25
2824244 67 M MD 02/03/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 paa226428
paa226428
Abdominal pain, Chills, Malaise, Myalgia, Nausea; Syncope Abdominal pain, Chills, Malaise, Myalgia, Nausea; Syncope
myalgias, chills, malaise. nausea (no vomiting), abdominal cramping and 1 large loose stool and subs... myalgias, chills, malaise. nausea (no vomiting), abdominal cramping and 1 large loose stool and subsequent syncopal episode felt to be a vagal reaction. symptomatic treatment, recovered in 2 days More
2824245 66 F AR 02/03/2025 COVID19
 PFIZER\BIONTECH
Death Death
Patient admitted 1/29. Expired 2/1 Patient admitted 1/29. Expired 2/1
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2824246 65 M FL 02/03/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH

Abdominal pain, Arthralgia, C-reactive protein, Pain in extremity, Polymyalgia r... Abdominal pain, Arthralgia, C-reactive protein, Pain in extremity, Polymyalgia rheumatica; Red blood cell sedimentation rate More
The vaccine that caused the autoimmune response was Capvaxive but that was not available as a choice... The vaccine that caused the autoimmune response was Capvaxive but that was not available as a choice above so I selected other vaccine. Within 24 hours I had severe pain in the shoulders/upper arms and waist. I initially went to a neurologist who diagnosed my problem as Polymyalgia Rhumatica (PMR). This was confirmed today 2/3/25 by a Rhumatologist. More
2824247 36 M FL 02/03/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
 AU1059A
AU1059A
Computerised tomogram thorax, Differential white blood cell count, Feeling hot, ... Computerised tomogram thorax, Differential white blood cell count, Feeling hot, Flushing, Full blood count; Headache, Liver function test, Paraesthesia, Scan with contrast More
3 days after vaccine developed severe and frequent headaches. Then on day 5 developed intermittent s... 3 days after vaccine developed severe and frequent headaches. Then on day 5 developed intermittent stinging sensation (pins and needles) on the entire left side of his body as well as warmth and flushing on the the left side of his face. These sensations lasted for a couple weeks. More
2824248 68 F PA 02/03/2025 FLU3
RSV
 SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 388490
255t2
Injection site reaction, Rash, Rash erythematous; Injection site reaction, Rash,... Injection site reaction, Rash, Rash erythematous; Injection site reaction, Rash, Rash erythematous More
Patient expresses that they noticed a large red rash at the site of injection the day following immu... Patient expresses that they noticed a large red rash at the site of injection the day following immunization. Over the course of the next few days, the rash spread from the injection site to a full body rash. The patient denies any other symptoms such as difficulty breathing or painful rash sites. The patient returned to the pharmacy on January 27th, 2025 to discuss this event and says the rash was gone when they returned. The patient claims they experience similar full body rashes when exposed to respiratory illnesses. The patient did not express that they treated the rash with any medication or seek medical treatment. More
2824249 0.5 F KS 02/03/2025 DTPPVHBHPB
PNC20
 MSP VACCINE COMPANY
PFIZER\WYETH
 U7829AA
LC5483
Infant irritability, Pyrexia, Swelling, Urticaria, Vomiting; Infant irritability... Infant irritability, Pyrexia, Swelling, Urticaria, Vomiting; Infant irritability, Pyrexia, Swelling, Urticaria, Vomiting More
Reported to me by mother that approx. 6 hours later, child developed high fever, hives, bumps that l... Reported to me by mother that approx. 6 hours later, child developed high fever, hives, bumps that looked similar to chicken pox, neck started to swell, fussy and vomiting. More
2824250 87 F NJ 02/03/2025 RSV
RSV
RSV
RSV
RSV
RSV
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS


UNK
UNK
UNK
Arthralgia, Immediate post-injection reaction, Nausea, Walking aid user; Arthral... Arthralgia, Immediate post-injection reaction, Nausea, Walking aid user; Arthralgia, Back pain, Full blood count normal, Gait inability, Mobility decreased; Myalgia, Nausea, Pain in extremity; Arthralgia, Immediate post-injection reaction, Nausea, Walking aid user; Arthralgia, Back pain, Full blood count normal, Gait inability, Mobility decreased; Myalgia, Nausea, Pain in extremity More
Nausea immediately following vaccine which lasted at least 20 minutes. Followed by immediate pain i... Nausea immediately following vaccine which lasted at least 20 minutes. Followed by immediate pain in right knee which accelerated during the day, requiring a cane and avoidance of walking. Pain was intense. Went to bed and approximately 7 hours later was able to walk normally with no pain. Anticipated reaction regarding joint pain needs to be emphasized under "possible side effects. It was very alarming! More
2824251 56 F NY 02/03/2025 FLU3
PNC20
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
 AW1696A
LJ5284
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling, Injection site warmth; Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling, Injection site warmth More
PATIENT REPORTS REDNESS, SWELLING, WARMTH, PAIN AND EXTREME ITCHING TO IMMUNIZATION SITE PATIENT REPORTS REDNESS, SWELLING, WARMTH, PAIN AND EXTREME ITCHING TO IMMUNIZATION SITE
2824252 12 M MI 02/03/2025 COVID19
 MODERNA
 3043409
Expired product administered, No adverse event Expired product administered, No adverse event
Client received Covid vaccine that was thawed over the allowable time frame. No adverse events repo... Client received Covid vaccine that was thawed over the allowable time frame. No adverse events reported. Phone call was made to parents to recommend a repeat vaccine per CDC guidelines. More
2824253 68 F ID 02/03/2025 FLU3
PNC20
 SEQIRUS, INC.
PFIZER\WYETH
 388488
LK6650
Unevaluable event; Unevaluable event Unevaluable event; Unevaluable event
Patient reports going to the hospital after receiving the two vaccines in the same arm. Patient reports going to the hospital after receiving the two vaccines in the same arm.
2824254 29 M TN 02/03/2025 COVID19
COVID19
 MODERNA
MODERNA
 062e21a
076c21a
Epilepsy, Focal dyscognitive seizures, Generalised tonic-clonic seizure, Pain, P... Epilepsy, Focal dyscognitive seizures, Generalised tonic-clonic seizure, Pain, Pyrexia; Epilepsy, Focal dyscognitive seizures, Generalised tonic-clonic seizure, Pain, Pyrexia More
I took my first dose on 09/11/2021 at a store while still on work travel. I took My second somewhere... I took my first dose on 09/11/2021 at a store while still on work travel. I took My second somewhere else. I took the vaccine and came home sick with a fever and body aches for multiple days. I began to having tonic clonic seizures on December 7 and was medicated then began having complex partial seizures until medicine was balanced. I am now diagnosed epileptic. I have seen multiple other individuals who are saying similar things. This was a life changing condition. More
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2824255 78 F AL 02/03/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 334T3
Erythema, Skin burning sensation, Swelling face Erythema, Skin burning sensation, Swelling face
Swelling, redness and burning to the face 2 days after vaccine. Continues through today. Improvement... Swelling, redness and burning to the face 2 days after vaccine. Continues through today. Improvement in swelling, but redness and minimal swelling continues. Denies any involvement of mouth or throat. More
2824256 68 F TX 02/03/2025 COVID19
 PFIZER\BIONTECH
 EWO185
Atrial fibrillation, Cardiac ablation, Cardiac monitoring Atrial fibrillation, Cardiac ablation, Cardiac monitoring
A few weeks after my second covid vaccine I began having Atrial Fibrillation episodes. ( I took the... A few weeks after my second covid vaccine I began having Atrial Fibrillation episodes. ( I took the first dose on May 13, 2021 at the same store; Pfizer EW0168) I saw a cardiologist who had me monitored for several weeks. He diagnosed me with Afib somewhere around September 2021. While I previously did have arrythmia (well-controlled through a small dosage of metoprolol) I had never had Afib before I took the Covid vaccine. I continued having Afib episodes approximately every 5-6 weeks, each lasting 24-36 hours, until June 2023, when I had an episode that lasted 5 days. I went to the ER after the first 2 days and they encouraged me to follow up with my cardiologist. He encouraged me to be cardioverted, but my Afib episode ended on its own. However, I did begin taking Multaq, an anti-arrythmic medicated to control the Afib, which it did quite well, but caused some unpleasant side effects. In April 2023 I received an ablation by a different cardiologist (by this time we had moved to Texas.) After the ablation, as of this date, I have had no more episodes of Afib. More
2824257 81 F MO 02/03/2025 FLU3
 SANOFI PASTEUR
 UT8409BA
Chills, Diplegia, Muscular weakness, Tremor Chills, Diplegia, Muscular weakness, Tremor
A few hours after injection, patient had severe shaking chills and reports BL leg paralysis. Symptom... A few hours after injection, patient had severe shaking chills and reports BL leg paralysis. Symptoms lasted until the next morning. Legs still had some weakness but she returned to her baseline the next day. More
2824258 75 F AL 02/03/2025 PNC20
 PFIZER\WYETH
 lc5482
Extra dose administered Extra dose administered
No verification prompted pharmacist to notify her that patient had received Prevnar 20 previously. F... No verification prompted pharmacist to notify her that patient had received Prevnar 20 previously. First dose was not listed in system. More
2824259 4 F MA 02/03/2025 TDAP
 SANOFI PASTEUR
 3CA22C1
Product administered to patient of inappropriate age, Wrong product administered Product administered to patient of inappropriate age, Wrong product administered
A Tdap was given to the patient when it should have been a Dtap A Tdap was given to the patient when it should have been a Dtap
2824261 78 F FL 02/03/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 52z52
Extra dose administered Extra dose administered
Patient got two vaccines one in 2023 one in 2025 this should be a one time only vaccine Patient got two vaccines one in 2023 one in 2025 this should be a one time only vaccine
2824262 0.58 F NY 02/03/2025 COVID19
 PFIZER\BIONTECH
 LN8272
Inappropriate schedule of product administration Inappropriate schedule of product administration
Of the Series, dose 2 of COVID vaccine given earlier than due at nursing visit. Of the Series, dose 2 of COVID vaccine given earlier than due at nursing visit.
2824263 52 F CA 02/03/2025 UNK
 UNKNOWN MANUFACTURER
Unevaluable event Unevaluable event
None stated. None stated.
2824264 1.67 M MO 02/03/2025 COVID19
 PFIZER\BIONTECH
 LN7305
Syringe issue Syringe issue
As vaccine was being administered some of the vaccine leaked out As vaccine was being administered some of the vaccine leaked out
2824265 58 M MN 02/03/2025 FLU3
PNC21
TDAP
VARZOS
 SANOFI PASTEUR
MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 UT8408JA
Y013009
XN575
7ZM55
Hypoaesthesia; Hypoaesthesia; Hypoaesthesia; Hypoaesthesia Hypoaesthesia; Hypoaesthesia; Hypoaesthesia; Hypoaesthesia
The patient came into the pharmacy and stated that in two outer fingers on his left hand have numbne... The patient came into the pharmacy and stated that in two outer fingers on his left hand have numbness since the date of the vaccine. He had not had it evaluated by a doctor and I recommended him to do that. More
2824266 42 M CA 02/03/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 79K45
Extra dose administered, No adverse event Extra dose administered, No adverse event
The patient received a second dose of flulaval (influenza vaccine) there was no observed immediate s... The patient received a second dose of flulaval (influenza vaccine) there was no observed immediate side effects. We contacted the patient again the next day on 1/31/2025 and RN assessment was done via telephone, the patient has no delayed reaction nor any side effects from the Flulaval that was given. More
2824267 0.17 M AZ 02/03/2025 DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
DTPPVHBHPB
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
UNK
 MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
MSP VACCINE COMPANY
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 U7295AA
U7295AA
U7295AA
U7295AA
U7295AA
U7295AA
U7295AA
U7295AA
U7295AA
U7295AA
1918226
1918226
1918226
1918226
1918226
1918226
1918226
1918226
1918226
1918226
W036242
W036242
W036242
W036242
W036242
W036242
W036242
W036242
W036242
W036242
Abdominal discomfort, Anaemia, Blood test normal, Body temperature decreased, Br... Abdominal discomfort, Anaemia, Blood test normal, Body temperature decreased, Bradycardia; Bronchiolitis, Cardiac murmur, Cerebral haemorrhage, Coagulation factor, Computerised tomogram head abnormal; Cough, Decorticate posture, Discoloured vomit, Dyspnoea, Food refusal; Gaze palsy, Generalised tonic-clonic seizure, Head injury, Imaging procedure, Infant irritability; Irregular breathing, Laboratory test normal, Lactic acidosis, Laryngomalacia, Lethargy; Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Malaise, Pain, Partial seizures; Peripheral coldness, Poor quality sleep, Respiratory acidosis, Respiratory tract congestion, Resuscitation; Retinal haemorrhage, Rhinorrhoea, Spinal epidural haematoma, Spinal subdural haematoma, Subdural haematoma; Tachycardia, Thrombocytosis, Toxicologic test normal, Unresponsive to stimuli, Urine analysis; Victim of child abuse, Vomiting; Abdominal discomfort, Anaemia, Blood test normal, Body temperature decreased, Bradycardia; Bronchiolitis, Cardiac murmur, Cerebral haemorrhage, Coagulation factor, Computerised tomogram head abnormal; Cough, Decorticate posture, Discoloured vomit, Dyspnoea, Food refusal; Gaze palsy, Generalised tonic-clonic seizure, Head injury, Imaging procedure, Infant irritability; Irregular breathing, Laboratory test normal, Lactic acidosis, Laryngomalacia, Lethargy; Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Malaise, Pain, Partial seizures; Peripheral coldness, Poor quality sleep, Respiratory acidosis, Respiratory tract congestion, Resuscitation; Retinal haemorrhage, Rhinorrhoea, Spinal epidural haematoma, Spinal subdural haematoma, Subdural haematoma; Tachycardia, Thrombocytosis, Toxicologic test normal, Unresponsive to stimuli, Urine analysis; Victim of child abuse, Vomiting; Abdominal discomfort, Anaemia, Blood test normal, Body temperature decreased, Bradycardia; Bronchiolitis, Cardiac murmur, Cerebral haemorrhage, Coagulation factor, Computerised tomogram head abnormal; Cough, Decorticate posture, Discoloured vomit, Dyspnoea, Food refusal; Gaze palsy, Generalised tonic-clonic seizure, Head injury, Imaging procedure, Infant irritability; Irregular breathing, Laboratory test normal, Lactic acidosis, Laryngomalacia, Lethargy; Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Malaise, Pain, Partial seizures; Peripheral coldness, Poor quality sleep, Respiratory acidosis, Respiratory tract congestion, Resuscitation; Retinal haemorrhage, Rhinorrhoea, Spinal epidural haematoma, Spinal subdural haematoma, Subdural haematoma; Tachycardia, Thrombocytosis, Toxicologic test normal, Unresponsive to stimuli, Urine analysis; Victim of child abuse, Vomiting More
Summary from Medical Records 1. On Tuesday, Jan. 23, 2024, patient was cleared for bronchiolitis by ... Summary from Medical Records 1. On Tuesday, Jan. 23, 2024, patient was cleared for bronchiolitis by his Primary Care Physician (PCP) but proceeded to vomit yellow fluid 3 times during the subsequent overnight period with vomiting NOT occurring with feeds. Mom reported that patient was fussier through that night. 2. On Wednesday, Jan. 24, 2024, patient was brought back to his PCP for vomiting at which time routine recommendations were made. Mom reported that patient was acting ?lethargic? and not wanting to take formula, but did take 4 oz of ?hydration drink.? As per medical records reported by Physician, ?Mom reported that patient was fussier throughout Wednesday night, he was hard to consoled (sic) but eventually consoled for dad. Mom reported that patient acted like he was in pain and did not sleep well. 3. Thursday morning, patient was smiling and appeared to be back to his normal self prior to being dropped off at daycare. 4. Thursday evening, around 7 pm, the caretaker called parents and informed them that ?the baby is not well, baby is not breathing well.? EMS was called and the adult son of the caretaker initiated CPR. 5. As per EMR and review of EMS documentation: ?they arrived at the house to find the baby being held by MPD; he was lethargic, unresponsive, had irregular respirations and was cool to touch. They lad the baby on the couch for assessment; the baby subsequently had ?decorticate posturing? with Left gaze deviation GCS =3. He had a total of 3 of these spells and was given midazolam. En route to the ED the baby had intermittent bradycardia, then tachycardia and irregular respirations. On arrival to ED the baby was being bagged BVM. He subsequently had bradycardia and a rapid response was called; he required full resuscitation. He had intermittent generalized tonic/clonic seizures and was given lorazepam followed by a bolus of levetiracetam 50 mg/kg x1. He then had Right focal seizures and was given bolus of fosphenytoin 20 mg/kg x1. He was able to maintain an airway with adequate saturation and did not require intubation. Initial temperature = 35.6 rectal Routine laboratory diagnostics revealed anemia, thrombocytosis, lactic/respiratory acidosis. Routine neuroimaging [head CT] revealed mixed density bilateral SDH R> L; there was acute bleed in the bilateral cerebral convexities L > R. ? 6. Patient arrived at the hospital unresponsive, receiving assisted breaths via BVM. Patient became bradycardic-chest compressions were started and epi x2 and bicarb given. The patient was not intubated and was put on high flow NC. Patient was taken to the CT scanner where he was noted to have acute intracranial bleeding. 7. MRIs revealed that patient had stable subacute bilateral subdural hematomas as well as a predominantly dorsal subdural hematoma extending from the level of the lower thoracic spine through the sacrum. A smaller ventral bleed was also present in the lumbar spine. Ophthalmology exam revealed bilateral retinal hemorrhages. All tests for underlying blood and clotting disorders were negative. 8. No signs of external trauma were found. No bone fractures were found. No accidents or intentional trauma were noticed by any caregivers of the child. 9. Due to the brain bleeding, spinal bleeding and retinal hemorrhages, physicians determined that patient?s presentation was consistent with abusive head trauma (sometimes referred to as ?Shaken Baby Syndrome?) and law enforcement was called to investigate. More
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