🏥 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 💀 🏥 🚑 ♿ ⚠️
2852689 08/04/2025 RVX
 UNKNOWN MANUFACTURER
 UNK
Cardiac ablation, Respiratory syncytial virus infection, Supraventricular tachyc... Cardiac ablation, Respiratory syncytial virus infection, Supraventricular tachycardia, Traumatic lung injury, Vaccination failure More
had it; Permanent lung damage; supraventricular tachycardia needing an ablation; Suspected vaccinati... had it; Permanent lung damage; supraventricular tachycardia needing an ablation; Suspected vaccination failure; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received RSVPreF3 adjuvanted (RSV vaccine) for prophylaxis. On an unknown date, the patient received RSV vaccine. On an unknown date, an unknown time after receiving RSV vaccine, the patient experienced vaccination failure (Verbatim: Suspected vaccination failure) (serious criteria GSK medically significant), respiratory syncytial virus infection (Verbatim: had it) (serious criteria hospitalization), lung injury (Verbatim: Permanent lung damage) (serious criteria hospitalization) and supraventricular tachycardia (Verbatim: supraventricular tachycardia needing an ablation) (serious criteria hospitalization). The outcome of the vaccination failure, respiratory syncytial virus infection, lung injury and supraventricular tachycardia were not reported. It was unknown if the reporter considered the vaccination failure, respiratory syncytial virus infection, lung injury and supraventricular tachycardia to be related to RSV vaccine. The company considered the vaccination failure, respiratory syncytial virus infection, lung injury and supraventricular tachycardia to be unrelated to RSV vaccine. Additional Information: GSK Receipt Date: 27-JUL-2025 This case was reported by a patient via interactive digital media. The patient had it and after that hospitalized for10 days. The patient had permanent lung damage and supraventricular tachycardia needing an ablation and now on permanent nocturnal oxygen. The patient had the vaccine too late. This case was considered as suspected vaccination failure as details regarding completion of primary vaccination schedule, time to onset and laboratory test confirming shingles were unknown at the time of reporting.; Sender's Comments: Vaccination failure is a listed event which, due to the following criteria (insufficient information provided about the clinical description, details regarding completion of primary vaccination schedule, time to onset and laboratory confirmation of disease) is considered unrelated to GSK RSV vaccine. A case of Respiratory syncytial virus infection, Traumatic lung injury and Supraventricular tachycardia, unknown time after receiving RSV vaccine, in a patient. Based on the available information a possible causality that the events were caused by the GSK product cannot be ascertained. Consent for further follow up has not been received. More
✓
2852690 3 M 08/04/2025 DTAP
 GLAXOSMITHKLINE BIOLOGICALS
 5H773
Expired product administered Expired product administered
a patient had been given an Infanrix dose that expired on 13th July 2025; This non-serious case was ... a patient had been given an Infanrix dose that expired on 13th July 2025; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 3-year-old male patient who received DTPa (Infanrix) (batch number 5H773, expiry date 13-JUL-2025) for prophylaxis. On 31-JUL-2025, the patient received Infanrix. On 31-JUL-2025, an unknown time after receiving Infanrix, the patient experienced expired vaccine used (Verbatim: a patient had been given an Infanrix dose that expired on 13th July 2025 ). The outcome of the expired vaccine used was not applicable. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 31-JUL-2025 Medical assistant called to request information about what to do after a patient had been given an Infanrix dose that expired on 13th July 2025 which led to expired vaccine used. The dose was given to patient on 31st July 2025. More
2852691 78 M IL 08/04/2025 DTAPIPVHIB
 SANOFI PASTEUR
No adverse event, Off label use No adverse event, Off label use
Intentional Off Label Prescription by HCP: Pentacel is prescribed with off label diagnosis: Cochlear... Intentional Off Label Prescription by HCP: Pentacel is prescribed with off label diagnosis: Cochlear implant status, with no reported adverse event; Initial information received on 30-Jul-2025 regarding an unsolicited valid non-serious case received from a physician. This case involves a 78 years old male patient who had an intentional off label prescription by HCP (healthcare professional): diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (VERO)] was prescribed with off label diagnosis: cochlear implant status, with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient had an intentional off label prescription by HCP: diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine Powder and suspension for suspension for injection at a dose of 0.5 ml with frequency- 4 times (strength, expiry date and lot not reported) via intramuscular route in unknown administration site was prescribed with off label diagnosis: cochlear implant (Cochlea implant) status, with no reported adverse event (off label use) (same day latency). Information on the batch number could not be requested corresponding to the one at time of event occurrence. Action taken was not applicable. More
2852692 53 F CT 08/04/2025 RAB
 SANOFI PASTEUR
 Y1A8CP1
Incomplete course of vaccination Incomplete course of vaccination
started a two-dose pre-exposure series but never received her second dose with no reported ae; Initi... started a two-dose pre-exposure series but never received her second dose with no reported ae; Initial information received on 01-Aug-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 53-year-old female patient who started a two-dose pre-exposure series of Rabies (HDC) vaccine [IMOVAX Rabies] but never received her second dose with no reported ae (adverse event). The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 25-Jun-2025, the patient received a first dose of 0.5ml of suspect Rabies (HDC) vaccine Powder and solvent for suspension for injection (lot Y1A8CP1, standard strength, frequency once, and expiry date-28-Feb-2025) via intramuscular route in unknown administration site for Immunization and was to receive two-doses of pre-exposure series but never received her second dose with no reported ae (routine immunisation schedule not administered). Reportedly-Patient missed the second dose they wanted to know if they can get the second dose or they need to restart. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2852693 8 M MD 08/04/2025 IPV
 SANOFI PASTEUR
 WIC831M
No adverse event, Product storage error No adverse event, Product storage error
temperature excursion reached 5 hours and 38 minutes at 33.6F + 48 minutes at 46.8F, they had admini... temperature excursion reached 5 hours and 38 minutes at 33.6F + 48 minutes at 46.8F, they had administered an opened IPOL to 2 patients with no reported adverse event; Initial information received on 01-Aug-2025 regarding an unsolicited valid non-serious case received from a physician. This case involves a 7 years old male patient who was administered with IPV (VERO) [IPOL] that had a temperature excursion at 33.6f for 5 hours and 38 minutes + at 46.8f for 48 minutes with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 26-May-2025, the patient received a dose of 0.5ml of suspect IPV (VERO) Suspension for injection (lot WIC831M, standard strength, frequency once and expiry date-30-Nov-2025) via intramuscular route in unknown administration site for Immunization that had a temperature excursion at 33.6f for 5 hours and 38 minutes + at 46.8f for 48 minutes with no reported adverse event (poor quality product administered) (latency-same day). Reportedly-The product was administered to two patients; They were not aware there was excursion prior administration; The door of refrigerator that may have been left open. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. More
2852694 TX 08/04/2025 FLU3
 SEQIRUS, INC.
 No batch number
Arthralgia, Mobility decreased, Product administered at inappropriate site Arthralgia, Mobility decreased, Product administered at inappropriate site
Mobility issues; Shoulder pain; Needle goes into the tendon instead of the muscle when administering... Mobility issues; Shoulder pain; Needle goes into the tendon instead of the muscle when administering Afluria PFS; This spontaneous case, initially received on 25-Jul-2025, was reported by a health professional and concerns a patient of unknown age/gender. Administration of company suspect drug: On an unknown date in 2025, the patient received Afluria (TIV) for Influenza prophylaxis, Dose regimen: Not reported, Route of administration: Not reported, Anatomical site: Not reported, Lot number: No batch number available would be requested upon follow-up. No additional suspect drugs. Adverse reactions/events and outcomes: On an unknown date in 2025, the patient experienced Mobility issues (outcome: Not Reported), Shoulder pain (outcome: Not Reported), Needle goes into the tendon instead of the muscle when administering Afluria PFS (outcome: Not Reported). Healthcare professional (HCP) inquired about any records of adverse events where needle went into the tendon instead of the muscle when administering Afluria Prefilled syringe (PFS). When asked if there was a patient involved in this question, Healthcare professional (HCP states that they are still investigating and event was not yet confirmed; therefore, they did not wish to report any details yet. She mentioned a situation involving a patient who received Afluria 6 months ago and has been experienced shoulder pain and mobility issues. Caller stated that patient was given the 2023-2024 season formula, but mentions that this occurred last winter, in Jan (Sic!). Healthcare professional (HCP stated not knowing the size of the needle and that they were trying to figure out if the needle was long enough to go that deep; also mentions not having that much of clinical knowledge about the situation to share any details Afluria (TIV) action taken: Not Applicable Reporter's assessment: The reporter did not provide the seriousness and causality assessment for the events Mobility issues, Shoulder pain and Needle goes into the tendon instead of the muscle when administering Afluria PFS.; Reporter's Comments: Causality: Due to the spontaneous nature of the case, events are considered related for reporting purposes. There is insufficient information regarding events for meaningful causal assessment (events onset dates, temporality, site of vaccination and shoulder pain, route of administration, etc.). Of note, wrong technique in product usage process might be considered as confounding factors for the events occurrence. More
2852695 30 F AZ 08/04/2025 COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
 015M20A
015M20A
032M20A
032M20A
Altered visual depth perception, Dizziness, Migraine, Photophobia, Pyrexia; SARS... Altered visual depth perception, Dizziness, Migraine, Photophobia, Pyrexia; SARS-CoV-2 RNA undetectable; Altered visual depth perception, Dizziness, Migraine, Photophobia, Pyrexia; SARS-CoV-2 RNA undetectable More
severe migraine >10, fever, dizziness, loss of depth perception for <10 hours, fever, light se... severe migraine >10, fever, dizziness, loss of depth perception for <10 hours, fever, light sensitivity. More
✓
2852696 75 M AL 08/04/2025 HEP
VARZOS
 DYNAVAX TECHNOLOGIES CORPORATION
GLAXOSMITHKLINE BIOLOGICALS
 945655
93N4J
Pain in extremity; Pain in extremity Pain in extremity; Pain in extremity
Pt recieved shingrix vaccination in right deltoid at 3pm then called pharmacy to report arm soreness... Pt recieved shingrix vaccination in right deltoid at 3pm then called pharmacy to report arm soreness/pain at 6pm. Pt informed that if otc pain medication such as tylenol or motrin may be used as pt did not report any hepatic or renal compromise. More
2852697 60 M CA 08/04/2025 PNC21
PNC21
 MERCK & CO. INC.
MERCK & CO. INC.
 Z003579
Z003579
Bell's palsy, Facial paralysis, Guillain-Barre syndrome, Muscle spasms, Res... Bell's palsy, Facial paralysis, Guillain-Barre syndrome, Muscle spasms, Respiratory disorder; Vomiting More
patient started having leg cramps, and vomiting about 1 week after vaccine pt went to emergency room... patient started having leg cramps, and vomiting about 1 week after vaccine pt went to emergency room first was diagnosed with bell's palsy with one side of his face dropping - patient was not getting better then went to primary care doctor that said go to University and they diagnosed him with Gillian barre syndrome (patient has issues with his face, legs, and breathing ) More
✓
2852698 66 F CA 08/04/2025 COVID19
 MODERNA
 3046732
Atrophy, Fatigue, Incorrect route of product administration Atrophy, Fatigue, Incorrect route of product administration
Patient think that administrator gave her with shorter needle with let to SQ. So she had atrophy on... Patient think that administrator gave her with shorter needle with let to SQ. So she had atrophy on her arm. More
2852704 50 F CA 08/04/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
 LN4930
LN4930
Chills, Erythema, Inflammation, Pain in extremity, Pruritus; Pyrexia, Skin tight... Chills, Erythema, Inflammation, Pain in extremity, Pruritus; Pyrexia, Skin tightness, Skin warm More
Symptoms: arm pain, extreme redness to upper arm - spreading to lower arm, warm to touch, itchy and... Symptoms: arm pain, extreme redness to upper arm - spreading to lower arm, warm to touch, itchy and feels tight. chills, fever, temperature of 101 (tympanic). Treatment: shut down inflammatory response with Prednisone, Zyrtec, Triamcinolone cream, and Doxycycline. More
2852705 12 F CA 08/04/2025 VARCEL
 MERCK & CO. INC.
 X020150
Expired product administered, No adverse event Expired product administered, No adverse event
Vaccine expired 8/1/2025, no symptoms at time of administration. Discussed with patient that she wi... Vaccine expired 8/1/2025, no symptoms at time of administration. Discussed with patient that she will need to repeat the vaccine and wrote a note so she would be allowed enter school. We would call to arrange repeat vaccine with non expired vaccine in four weeks given it is a live vaccine. More
2852706 82 F CA 08/04/2025 PNC20
 PFIZER\WYETH
 LN4930
Erythema, Pain in extremity, Pruritus, Skin warm, Tenderness Erythema, Pain in extremity, Pruritus, Skin warm, Tenderness
Symptoms: arm pain, redness spreading to lower arm, at times itchy, warm to touch, tender. Treatme... Symptoms: arm pain, redness spreading to lower arm, at times itchy, warm to touch, tender. Treatment: Zyrtec, Doxycycline, pepcid, prednisone, Triamcinolone cream More
2852707 1 F CA 08/04/2025 IPV
 SANOFI PASTEUR
 W1B511M
No adverse event, Wrong product administered No adverse event, Wrong product administered
patient was given wrong vaccine: polio @ 11:16am. Pt needed to have MMR administered instead. Pt lef... patient was given wrong vaccine: polio @ 11:16am. Pt needed to have MMR administered instead. Pt left with no symptoms. More
2852708 74 F WA 08/04/2025 COVID19
 PFIZER\BIONTECH
 ME6072
Contusion, Sensitive skin, Swelling face, Tenderness Contusion, Sensitive skin, Swelling face, Tenderness
Patient describes spontaneous facial bruising below the right eye with swelling and tenderness. Add... Patient describes spontaneous facial bruising below the right eye with swelling and tenderness. Additionally, she reports scalp sensitivity. More
2852709 17 M VA 08/04/2025 MENB
MENB
 NOVARTIS VACCINES AND DIAGNOSTICS
PFIZER\WYETH

Headache, Pain; Headache, Pain Headache, Pain; Headache, Pain
Not sure which meningococcal vaccine he received. Patient was fine from 2:46pm until he started gett... Not sure which meningococcal vaccine he received. Patient was fine from 2:46pm until he started getting a bad headache and chills and bodyaches around 8:45pm. Symptoms started and progressed rapidly after about 30 minutes of vigorous game play on his VR headset. More
2852710 52 F NV 08/04/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 3273H
Urticaria Urticaria
PT called and reported that she is having hives since she got shingrix vaccine on 08/02/2025. She... PT called and reported that she is having hives since she got shingrix vaccine on 08/02/2025. She is taking antihistamine cetirizine now to help with the symptoms More
2852432 77 M CA 08/03/2025 COVID19
COVID19
COVID19
COVID19
VARZOS
VARZOS
VARZOS
VARZOS
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 MD3414
MD3414
MD3414
MD3414
2HJ99
2HJ99
2HJ99
2HJ99
Angiogram cerebral abnormal, Brain oedema, Carotid artery stenosis, Cerebral art... Angiogram cerebral abnormal, Brain oedema, Carotid artery stenosis, Cerebral artery occlusion, Cerebral infarction; Computerised tomogram head abnormal, Dysarthria, Extensor plantar response, Eye movement disorder, Facial paresis; Hemianopia, Hemiparesis, Magnetic resonance imaging, Middle cerebral artery stroke, Neurologic neglect syndrome; Reflexes abnormal, Sensory loss, Vertebral artery stenosis; Angiogram cerebral abnormal, Brain oedema, Carotid artery stenosis, Cerebral artery occlusion, Cerebral infarction; Computerised tomogram head abnormal, Dysarthria, Extensor plantar response, Eye movement disorder, Facial paresis; Hemianopia, Hemiparesis, Magnetic resonance imaging, Middle cerebral artery stroke, Neurologic neglect syndrome; Reflexes abnormal, Sensory loss, Vertebral artery stenosis More
Dysarthria. Can answer simple questions. Left facial weakness, dense right gaze preference and left... Dysarthria. Can answer simple questions. Left facial weakness, dense right gaze preference and left field cut vs neglect. Right side 5/5, left with dense hemiparesis. Reflexes brisker on the left and left plantr response is extensor. Patient does not recognize his left hand and has absent sensation to temperature and vibration on the left. NIHSS 23 CT shows early infarct of most of right hemisphere sparing right aca territory CTA shows occlusion of right mca Also left vertebral artery and has intracranial stenosis of both ica's Impression: patient with large right mca stroke with dense left hemiparesis and early cerebral edema. More
✓ ✓ ✓
2852433 34 F TN 08/03/2025 COVID19
 MODERNA
Injection site pain, Injection site swelling, Pain in extremity Injection site pain, Injection site swelling, Pain in extremity
Pain into entire right arm. Localized swelling and pain at site of injection Pain into entire right arm. Localized swelling and pain at site of injection
2852434 64 F OK 08/03/2025 UNK
 UNKNOWN MANUFACTURER
Chronic inflammatory demyelinating polyradiculoneuropathy, Guillain-Barre syndro... Chronic inflammatory demyelinating polyradiculoneuropathy, Guillain-Barre syndrome, Lumbar puncture, Paralysis More
2017: GBS. Paralyzed R side . 2024: CIDP. Paralyzed L side 2017: GBS. Paralyzed R side . 2024: CIDP. Paralyzed L side
✓ ✓
2852435 63 M ID 08/03/2025 TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR

Cough, Injection site pain, Injection site pruritus, Muscle spasms, Productive c... Cough, Injection site pain, Injection site pruritus, Muscle spasms, Productive cough; Wheezing More
Severe muscle cramps, coughing wheezing, phlegm. Burning and itching at the site of injection that p... Severe muscle cramps, coughing wheezing, phlegm. Burning and itching at the site of injection that persists to date. More
2852436 12 M WV 08/03/2025 MNQ
MNQ
MNQ
TDAP
TDAP
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 3443E
3443E
3443E
U8339BA
U8339BA
U8339BA
Cyanosis, Dyskinesia, Echocardiogram, Electrocardiogram, Electrocardiogram ambul... Cyanosis, Dyskinesia, Echocardiogram, Electrocardiogram, Electrocardiogram ambulatory; Electrocardiogram normal, Electroencephalogram, Genetic testing, Imaging procedure, Laboratory test; Unresponsive to stimuli; Cyanosis, Dyskinesia, Echocardiogram, Electrocardiogram, Electrocardiogram ambulatory; Electrocardiogram normal, Electroencephalogram, Genetic testing, Imaging procedure, Laboratory test; Unresponsive to stimuli More
Event occurred on the evening of 11/30/2024 around 8:50pm. My son was sitting on the couch, almost a... Event occurred on the evening of 11/30/2024 around 8:50pm. My son was sitting on the couch, almost asleep when I looked at him and noticed his arms were moving away from his body in a slow motion and his lips began to turn blue. I immediately called 911 and after calling I noticed my son had stopped with the arms movements. But his entire body looked lifeless and he was unresponsive . He was not breathing and had turned completely blue. He was rushed to our local hospital. When we arrived at the hospital he was taken immediately back to the trauma area and was laid on the exam table. He finally became responsive again, this was shortly after 9pm. More
2852437 62 F KY 08/03/2025 PNC20
TDAP
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS

Erythema, Hyperhidrosis, Pain, Pyrexia, Swelling; Erythema, Hyperhidrosis, Pain,... Erythema, Hyperhidrosis, Pain, Pyrexia, Swelling; Erythema, Hyperhidrosis, Pain, Pyrexia, Swelling More
fever, sweating, pain with movement of the extremity, localized swelling and erythema fever, sweating, pain with movement of the extremity, localized swelling and erythema
2852438 71 F 08/03/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
Injection site erythema, Injection site oedema, Injection site pain, Local react... Injection site erythema, Injection site oedema, Injection site pain, Local reaction More
localized reactions. Erythema, edema, pain surrounding administration site localized reactions. Erythema, edema, pain surrounding administration site
2852439 72 F NC 08/03/2025 COVID19
 MODERNA
Arthralgia, Burning sensation, Hypoaesthesia, Myalgia, Paraesthesia Arthralgia, Burning sensation, Hypoaesthesia, Myalgia, Paraesthesia
Muscle aches and some joint pain. Most severe was waking up the morning following vaccination with m... Muscle aches and some joint pain. Most severe was waking up the morning following vaccination with my hands burning. This continued for 4-5 days. Currently I still have numbness in my right hand. And occasional tingling in my left hand. More
2852440 65 F FL 08/03/2025 PNC20
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 LN4927
7523J
Injection site erythema, Injection site pain, Injection site swelling; Injection... Injection site erythema, Injection site pain, Injection site swelling; Injection site erythema, Injection site pain, Injection site swelling More
PATIENT REPORTS PAIN AND SORENESS IN LEFT DELTOID. THE LEFT DELTOID IS SWOLLEN AND RED. PATIENT REPORTS PAIN AND SORENESS IN LEFT DELTOID. THE LEFT DELTOID IS SWOLLEN AND RED.
2852441 61 F NJ 08/03/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 ek225
Dry skin, Formication Dry skin, Formication
pt claims has feeling of something crawling on her right leg. Started night of the shot and did not ... pt claims has feeling of something crawling on her right leg. Started night of the shot and did not go away and now dry skin all from foot up to where the feeling of the crawling on leg More
2852442 36 M SC 08/03/2025 COVID19
 PFIZER\BIONTECH
 unknown
Amnesia, Cataract, Tooth disorder Amnesia, Cataract, Tooth disorder
Cataract in right eye, memory loss, teeth issues Cataract in right eye, memory loss, teeth issues
✓
2852443 74 F FL 08/03/2025 HEPAB
 GLAXOSMITHKLINE BIOLOGICALS
Blood alkaline phosphatase increased Blood alkaline phosphatase increased
I had the twinrix series in accelerated dose. 6/22, 6/28, 7/12. Because of my lung disease I have ... I had the twinrix series in accelerated dose. 6/22, 6/28, 7/12. Because of my lung disease I have my liver enzymes monitored periodically. They have always been normal. Very stable. On June 3rd my Alk Phospatase was 48, on July 14th it was 142. On July 22 it was 321. My AST on June 3rd was 22, on July 14th it was 56. On July 22 it was 163. On June 3rd ALT was 20, on July 14th it was 101, on July 22, it was 198. The only change was that my Doctor took me off of CellCept 1500mg BID after the July 14 blood test, which I had been on with stable liver enzymes of over 2 years. He did this in case Cell Cept may be the , when tested a week later (July 22) they increased further. I don't know if twinrix accelerated series is a reason, but it certainlly seems suspicious. More
2852444 M AR 08/03/2025 HEP
 MERCK & CO. INC.
Respiration abnormal, Urticaria Respiration abnormal, Urticaria
Hives and different breathing, hives lasted 48 hours. Mostly on back and chest/neck, no treatment &q... Hives and different breathing, hives lasted 48 hours. Mostly on back and chest/neck, no treatment "normal for babies to have skin breakouts" More
2852445 48 F FL 08/03/2025 COVID19
FLU3
TDAP
 PFIZER\BIONTECH
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 me6072
tfaa2502
y3z9p
Erythema; Erythema; Erythema Erythema; Erythema; Erythema
Developed redness on face similar looking to sunburn, but she did not get prolonged exposure to the ... Developed redness on face similar looking to sunburn, but she did not get prolonged exposure to the sun. This occurred the morning after receiving the vaccines. No itching, swelling, trouble breathing was reported. More
2852446 65 F NE 08/03/2025 PNC20
VARZOS
 PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS

Migraine; Migraine Migraine; Migraine
Patient called my store reporting she had gotten 2 vaccines at another location and stated she is ex... Patient called my store reporting she had gotten 2 vaccines at another location and stated she is experiencing a severe migraine lasting more than 24 hours after receiving the vaccines. She stated she took Excedrine migraine and ice but it did not help. More
2852396 TN 08/02/2025 HEP
 MERCK & CO. INC.
 X027728
No adverse event, Product storage error No adverse event, Product storage error
No additional AE; Customer called to report TE.; This spontaneous report was received from a pharmac... No additional AE; Customer called to report TE.; This spontaneous report was received from a pharmacist, concerning to a neonate patient of unknown gender. The patient's medical history, patient's concurrent conditions and concomitant therapies were not reported. On an unknown date, the vaccine Hepatitis B Vaccine (Recombinant) experienced a temperature (TE) excursion at 11.5 C for 2 hours. On 18-Jun-2025, the patient was vaccinated with the vaccine involved in the TE, Hepatitis B Vaccine (Recombinant) (lot #X027728 has been verified to be valid as a pre-filled syringe, expiration date reported and confirmed as 16-Oct-2026) (dose and route were not provided), as prophylaxis (Product storage error). No additional adverse event reported (No adverse event). More
2852397 CO 08/02/2025 MMRV
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.

Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
No additional AE; co-administration of PROQUAD and VARIVAX to a patient.; This spontaneous report wa... No additional AE; co-administration of PROQUAD and VARIVAX to a patient.; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. The patient's medical history, current conditions and concomitant therapies was not reported. On 10-APR-2025, the patient received inadvertent concomitant administration of Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), Injection (exact dose, strength, anatomical route of administration, lot # and expiration date were not reported) and Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), Injection (exact dose, strength, anatomical route of administration, lot # and expiration date were not reported) (Accidental overdose). There were no symptomatic events reported (no adverse event). This is an invalid case due to lack of patient's identifiers. Lot number is being requested and will be submitted if received. More
2852398 CA 08/02/2025 HPV9
 MERCK & CO. INC.
 W014513
Expired product administered, No adverse event Expired product administered, No adverse event
No additional AE/No PQC.; Pharmacist calling to inquire about revaccination. Pharmacist reports a pa... No additional AE/No PQC.; Pharmacist calling to inquire about revaccination. Pharmacist reports a patient received an expired dose of GARDASIL 9 on 28JUL2025. Pharmacist reports the GARDASIL 9 expired on 26JAN2025 and no temperature excursion ever occurred. Pharmacist did inf; This spontaneous report was received from a/an Pharmacist and refers to a(n) patient of unknown age and gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 28-Jul-2025, the patient started therapy with Human Papillomavirus 9-valent Vaccine, Recombinant (lot #W014513, expiration date: 26-Jan-2025), dose number 3, (3rd dose (last dose)),. On an unknown date, the patient started therapy with unknown dosage. The patient started therapy with for the treatment of prophylaxis. The patient started therapy with Human Papillomavirus 9-valent Vaccine, Recombinant for the treatment of prophylaxis. On 28-Jul-2025, the patient experienced Pharmacist calling to inquire about revaccination. Pharmacist reports a patient received an expired dose of GARDASIL 9 on 28JUL2025. Pharmacist reports the GARDASIL 9 expired on 26JAN2025 and no temperature excursion ever occurred. Pharmacist did inf. On an unknown date, the patient experienced No additional AE/No PQC. Lot # is being requested and will be submitted if received. More
2852399 F RI 08/02/2025 MMRV
MMRV
UNK
UNK
VARCEL
VARCEL
MMRV
MMRV
VARCEL
VARCEL
 MERCK & CO. INC.
MERCK & CO. INC.
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.
 Y014437
Y014437


Y011018
Y011018
Y014437
Y014437
Y011018
Y011018
Extra dose administered, No adverse event; Extra dose administered; Extra dose a... Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event; Extra dose administered; Extra dose administered, No adverse event; Extra dose administered More
No additional AE; patient was given VARIVAX vaccine in left thigh and inadvertently administered PRO... No additional AE; patient was given VARIVAX vaccine in left thigh and inadvertently administered PROQUAD vaccine in right thigh.; patient was given VARIVAX vaccine in left thigh and inadvertently administered PROQUAD vaccine in right thigh.; This spontaneous report was received from a nurse and refers to a 4-year-old female patient. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 31-Jul-2025, the patient was vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX) (strength, dose, frequency, and route of administration were not provided) in the left thigh; lot # Y011018 has been verified to be valid and expiration date was 18-Jun-2026; in addition, the patient was inadvertently vaccinated with Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) (strength, dose, frequency, and route of administration were not provided) in the right thigh; lot # Y014437 has been verified to be valid and expiration date was 22-Feb-2026; both vials were diluted in a sterile diluent (lot #, and expiration date were not provided), as prophylaxis (Inappropriate schedule of product administration and Accidental exposure to product). No additional adverse event (AE) was reported. More
2852400 F CA 08/02/2025 COVID19
 PFIZER\BIONTECH
COVID-19, Drug ineffective COVID-19, Drug ineffective
COVID; COVID; This is a spontaneous report received from a Consumer or other non HCP. A 72-year-old... COVID; COVID; This is a spontaneous report received from a Consumer or other non HCP. A 72-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1-DOSE 8, SINGLE (unspecified valent)), for Covid-19 Immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID". The patient reported that she was fully vaccinated and all of them was Pifizer shots, she thought she have had 9 over the last four years. Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient had taken Paxlovid. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202500091010 same reporter/patient, different vaccine and event; More
2852401 M OK 08/02/2025 MENB
 PFIZER\WYETH
 LX2636
Headache, Neck pain, Pallor, Vomiting Headache, Neck pain, Pallor, Vomiting
neck pain; done pale; vomiting 7 to 8 times/ Went home and then got vomited two hours later one time... neck pain; done pale; vomiting 7 to 8 times/ Went home and then got vomited two hours later one time and then in the evening one time; bad headache/ severe headache; This is a spontaneous report received from a Physician and a Consumer or other non HCP from medical information team. A 17-year-old male patient received meningococcal group b Rlp2086 (TRUMENBA), on 28Jul2025 as dose 2, 0.5 ml single (Lot number: LX2636, Expiration Date: 31Jan2027) intramuscular, in right deltoid for immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: Sulfur, reaction(s): "allergic to Sulfur". Vaccination history included: Trumenba (DOSE 1, SINGLE), administration date: 2024, for immunization. The following information was reported: HEADACHE (non-serious) with onset Jul2025, 1 hr after the suspect product(s) administration, outcome "recovered" (Jul2025), described as "bad headache/ severe headache"; PALLOR (non-serious) with onset Jul2025, 1 hr after the suspect product(s) administration, outcome "recovered" (Jul2025), described as "done pale"; NECK PAIN (non-serious) with onset Jul2025, 1 hr after the suspect product(s) administration, outcome "recovered" (Jul2025); VOMITING (non-serious) with onset Jul2025, 1 hr after the suspect product(s) administration, outcome "recovered" (Jul2025), described as "vomiting 7 to 8 times/ Went home and then got vomited two hours later one time and then in the evening one time". The events "neck pain", "done pale", "vomiting 7 to 8 times/ went home and then got vomited two hours later one time and then in the evening one time" and "bad headache/ severe headache" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of neck pain, pallor, vomiting, headache. Additional information: It was reported that the patient experienced severe headache, neck hurting and he started vomiting about seven-eight times, he vomited, he turned pale, and he came back to the office for 45 minutes and his vitals were and reporter made him lay down and observed him for a half hour, monitored his pulse oximeter and his oxygen, everything, he was back to normal, so reporter let him go home, reporter checked on him, two hours later, he vomited one time and then one time in the evening. He did not vomited, he slept pretty good quite a bit day before reporting day afternoon his mom says but he was back to normal and this was the second episode. He was not on any other medications. He had not been sick or had not any other vaccination in one month prior. His mom gave him Tylenol when he returned home after leaving their office. Reporter thought that it was due to Trumenba vaccine. After 1 year of first vaccination. Within first 10 minutes of medical observation, there was no reaction. One hour later, patient experienced severe headache, vomiting 8 times at mall; 2 times at home, was pale. So, this was his second dose, and he was, we watched him 10-15 minutes in the office to make sure that he was okay before they go and he left, after one hour, he called and start having a neck pain, headache, severe headache, vomited about 7 to 8 times, became pale. They came to the office, they observed him, made him lie down, monitor the blood pressure everything, got better, went home. He was back to normal. More
2852402 F 08/02/2025 COVID19
 PFIZER\BIONTECH
COVID-19, Disease recurrence, Drug ineffective, SARS-CoV-2 test COVID-19, Disease recurrence, Drug ineffective, SARS-CoV-2 test
has taken the Pfizer Covid-19 vaccines and has had covid 4 times; has taken the Pfizer Covid-19 vacc... has taken the Pfizer Covid-19 vaccines and has had covid 4 times; has taken the Pfizer Covid-19 vaccines and has had covid 4 times; has taken the Pfizer Covid-19 vaccines and has had covid 4 times; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A 76-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), DISEASE RECURRENCE (medically significant), outcome "unknown" and all described as "has taken the Pfizer Covid-19 vaccines and has had covid 4 times". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Clinical course: Patient reported that she contracted covid and because she is on (Withheld) for Life, she apparently doesn't get to take Paxlovid. She was told by the pharmacist that Paxlovid doesn't kill the virus and as you go forward, you may fall back into symptoms. Her symptoms were mild, she was in excellent health, and does not have any underlying diseases. She was within close proximity with since testing positive for covid and she has had to cancel plans. She stated the only medications that she takes does not interact with Paxlovid and is not a contraindication. She stated that she has taken the Pfizer Covid-19 vaccines and has had covid 4 times. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2852403 56 F SC 08/02/2025 PNC20
 PFIZER\WYETH
Nausea, Pruritus Nausea, Pruritus
Itching; nauseated; This is a spontaneous report received from a Physician from a sales representati... Itching; nauseated; This is a spontaneous report received from a Physician from a sales representative. A 56-year-old female patient (not pregnant) received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), on 28Jul2025 as dose number unknown, single (Batch/Lot number: unknown) at the age of 56 years for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Diphtheria, for immunization, reaction(s): "allergy"; Typhoid, for immunization, reaction(s): "allergy". The following information was reported: PRURITUS (non-serious) with onset 28Jul2025, outcome "recovered" (28Jul2025), described as "Itching"; NAUSEA (non-serious) with onset 28Jul2025, outcome "recovered" (28Jul2025), described as "nauseated". The events "itching" and "nauseated" required emergency room visit. Therapeutic measures were taken as a result of pruritus, nausea. Additional information: The patient did not receive any other vaccines on the same date as the vaccine(s) for which they were reporting. The patient did not receive any other vaccines within 4 weeks prior to the vaccine(s) for which they were reporting. It was unknown if the patient taking any other medications within 2 weeks of the event starting. Patient had an adverse event after she was given Prevnar 20. Itching, and then feeling nauseated. She was taken to the ER. Later found out she was allergic to diphtheria typhoid and also had this reaction to tdap. Physician didn't know that a patient shouldn't receive Prevnar 20 if they were allergic to diphtheria typhoid. The patient received Prednisone and Epipen as treatment for the adverse events. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2852413 75 F FL 08/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7523j
No adverse event, Product preparation issue No adverse event, Product preparation issue
Pt only got the liquid portion of the without the medication being mixed in. this had on 08/01/2025 ... Pt only got the liquid portion of the without the medication being mixed in. this had on 08/01/2025 no reaction as of today More
2852414 12 M MI 08/02/2025 HPV9
 MERCK & CO. INC.
 Y014510
Chest X-ray normal, Epstein-Barr virus test negative, Full blood count normal, I... Chest X-ray normal, Epstein-Barr virus test negative, Full blood count normal, Inflammatory marker test, Lymphadenopathy More
swelling of left supraclavicular lymph node (same side as injection site) swelling of left supraclavicular lymph node (same side as injection site)
2852415 40 F AR 08/02/2025 COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 EL1284
EL1284
El3247
El3247
Facial pain, Feeling cold, Feeling hot, Infectious mononucleosis, Muscle spasms;... Facial pain, Feeling cold, Feeling hot, Infectious mononucleosis, Muscle spasms; Neurological symptom, Trismus; Facial pain, Feeling cold, Feeling hot, Infectious mononucleosis, Muscle spasms; Neurological symptom, Trismus More
Initial symptoms were very nerve related. Had a spot on my face the size of a medium circle that fel... Initial symptoms were very nerve related. Had a spot on my face the size of a medium circle that felt hot and cold constantly for several days to a week. However, symptoms followed later in the form of mono (a disease that you?re usually immune to by 40) then it was muscle spasms, not able to open my mouth, multiple specialists and continued pain today on the same side (right) More
2852416 79 F OH 08/02/2025 PPV
 MERCK & CO. INC.
 Y009239
Confusional state, Memory impairment Confusional state, Memory impairment
Patient reports feeling confused and forgetful about 20-30 minutes after receiving the vaccine. Repo... Patient reports feeling confused and forgetful about 20-30 minutes after receiving the vaccine. Reports she waited in the store for about 20 minutes after receiving the vaccine and felt fine. When she went to drive herself home, she reports she didn't remember how to get home and drove around until she found her way. Patient reports she has forgotten how to use a knife and other various things around the house and this has continued daily since the vaccine. She reports she saw her PCP 5 days after she received her vaccine and her PCP told her she may have had a TIA related to the vaccine. More
2852417 16 M GA 08/02/2025 DTAP
DTAP
DTAP
DTAP
MENB
MENB
MENB
MENB
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS
NOVARTIS VACCINES AND DIAGNOSTICS







Acne, Amnesia, Confusional state, Dysarthria, Dyskinesia; Headache, Heart rate i... Acne, Amnesia, Confusional state, Dysarthria, Dyskinesia; Headache, Heart rate increased, Hyperhidrosis, Hypoacusis, Malaise; Ocular hyperaemia, Seizure like phenomena, Speech disorder, Syncope, Tremor; Vision blurred; Acne, Amnesia, Confusional state, Dysarthria, Dyskinesia; Headache, Heart rate increased, Hyperhidrosis, Hypoacusis, Malaise; Ocular hyperaemia, Seizure like phenomena, Speech disorder, Syncope, Tremor; Vision blurred More
After 8-10 minutes after receiving the injection, my son was laying down after shot, then he rested ... After 8-10 minutes after receiving the injection, my son was laying down after shot, then he rested for the amount of time listed above, and stood up to speak to doctor. Showed her his acne on body and face standing, and wasn?t feeling well. He sat down across the patient room in a chair and about one minute after sitting, he says ?not feeling right?.every thing is getting blurry? . After he proceeded to look like he was having a seizure, and this lasted approximately 1 to 2 minutes. His eyes were open, his mouth was open as well, and the doctor held his chin up, to keep him from either hurting himself in case he went into seizure but she was assured me this wasn?t the case and it was that vasoconstriction syncope. He also had jerking movements with his arms and hands, and was seeming to have a small seizure, once he woke up & could comprehend what we were saying to him, his eyes were blood shot, he could not hear and his speech was very muffled and slurred. His head was hurting very bad and he was profusely sweating and extremely shaken and upset. Not remembering anything that happened after telling us that he wasn?t feeling well. He proceeded to drink water and sit while doctor made sure he wss ok. He stated he felt the urge to use the bathroom, poop after and was scared he was going to poop himself but he was able to keep from doing so and went to the bathroom visibly shaking from nervous of passing out or having such an event occur again. Later thru day his speech returned to normal and his hearing remained a bit muffled and he exhibited signs of fever, sweating, and overall not feeling well and elevated heart rate. More
2852418 79 F OK 08/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 FT95N
Anaphylactic reaction, Lip swelling, Swollen tongue Anaphylactic reaction, Lip swelling, Swollen tongue
Pt daughter came in and reported next day. Said patient had anaphylaxis, swollen lips and swollen to... Pt daughter came in and reported next day. Said patient had anaphylaxis, swollen lips and swollen tongue and reported to hospital ER on evening of 8/1/25. More
2852419 16 M KY 08/02/2025 MENB
MNQ
TDAP
 PFIZER\WYETH
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 GL0426
u8169ab
793pt
Immediate post-injection reaction, Syncope; Immediate post-injection reaction, S... Immediate post-injection reaction, Syncope; Immediate post-injection reaction, Syncope; Immediate post-injection reaction, Syncope More
Syncope immediately following administration of Trumenba Syncope immediately following administration of Trumenba
2852420 4 M CA 08/02/2025 DTAPIPVHIB
MMR
MMRV
 SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.


Injection site movement impairment, Pyrexia, Urticaria; Injection site movement ... Injection site movement impairment, Pyrexia, Urticaria; Injection site movement impairment, Pyrexia, Urticaria; Injection site movement impairment, Pyrexia, Urticaria More
Fever, hives, immobilization in both arms Fever, hives, immobilization in both arms
2852421 55 M 08/02/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7523J
Erythema, Pain in extremity, Swelling Erythema, Pain in extremity, Swelling
Redness, swelling, pain in the upper arm, planned to take a Benadryl and possibly seek medical care.... Redness, swelling, pain in the upper arm, planned to take a Benadryl and possibly seek medical care. Started a few hours after the injection and continued into today 24 hour later More
2852422 56 F TX 08/02/2025 PNC21
VARZOS
 MERCK & CO. INC.
GLAXOSMITHKLINE BIOLOGICALS
 Y019158
47n3y
Rash; Rash Rash; Rash
Patient states she has been getting on and off rash since she got CAPVAXIVE 0.5ML INJ and SHINGRIX 5... Patient states she has been getting on and off rash since she got CAPVAXIVE 0.5ML INJ and SHINGRIX 50MCG INJ. . Patient says the rash goes away with a steroid prescription but has came back a couple times. More
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