๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ 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.

๐Ÿ“– Help & Search Guide

Column Icons Legend

๐Ÿ’€ Death
๐Ÿฅ Hospitalized
๐Ÿš‘ Emergency Room
โ™ฟ Disability
โš ๏ธ Life Threatening

How to Search

๐Ÿ’ก 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 "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ 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:

  • โœ… Early warning system for potential safety signals
  • โœ… Open and transparent - publicly accessible
  • โœ… Accepts all reports regardless of likelihood of causation
  • โœ… Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • โš ๏ธ Reports are unverified - not investigated before publication
  • โš ๏ธ Cannot determine if vaccine caused the event
  • โš ๏ธ Underreporting - not all adverse events are reported
  • โš ๏ธ Overreporting - coincidental events may be reported
  • โš ๏ธ 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?

โš ๏ธ 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
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2847827 F NY 06/30/2025 DTAPIPVHIB
 SANOFI PASTEUR
Inappropriate schedule of product administration, No adverse event Inappropriate schedule of product administration, No adverse event
received PENTACEL out of sequence, got it one-month early and now she is due for the 15-month dose w... received PENTACEL out of sequence, got it one-month early and now she is due for the 15-month dose with no reported AE; Initial information received on 26-Jun-2025 regarding an unsolicited valid non-serious case received from a physician. This case involves Infant female patient who had received Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine [Pentacel (Vero)] out of sequence, got it one-month early and now she is due for the 15-month dose 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 received 0.5 ml dose of suspect Diphtheria/Tetanus/5 Hybrid Ac Pertussis/Ipv(Vero)/Hib(Prp/T) Vaccine, Suspension for injection, (lot number, strength and expiry date not reported) frequency: once via unknown route in unknown administration site for immunisation, out of sequence, got it one-month early and now she is due for the 15-month dose with no reported ae (inappropriate schedule of product administration) (latency: same day). Information on the batch number was requested corresponding to the one at time of event occurrence. 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
2847828 1.5 M MI 06/30/2025 IPV
 SANOFI PASTEUR
 x1c891m
Extra dose administered, No adverse event Extra dose administered, No adverse event
It was a extra dose of Polio that was given to pt. He had no reaction to this. It was a extra dose of Polio that was given to pt. He had no reaction to this.
2847829 62 F MI 06/30/2025 MMRV
 MERCK & CO. INC.
 Y014307
Wrong product administered Wrong product administered
Administered an MMRV, was scheduled for MMR Administered an MMRV, was scheduled for MMR
2847830 67 F FL 06/30/2025 PNC20
 PFIZER\WYETH
 lk6655
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site warmth More
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Inject... Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Additional Details: Patient came back to pharmacy to report adverse reaction to vaccine. Starting the day after receiving vaccine, patient experienced general pain in the arm vaccine was administered in. She later noticed redness and warmth. When she came in on 6/17/25, arm was red in the area well below administration site and spread towards the front of the arm, almost reaching elbow. Patient later reported seeing provider on 6/17/25 and received prednisone 20 mg BID for 5 days, then QD for 5 days. More
2847831 62 M PA 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 55th4
Hypoaesthesia, Injection site erythema, Injection site pruritus, Injection site ... Hypoaesthesia, Injection site erythema, Injection site pruritus, Injection site swelling More
Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at In... Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Additional Details: numbness between right shoulder and spine area More
2847832 TN 06/30/2025 TD
 SANOFI PASTEUR
Product storage error Product storage error
unsuitable product administered with no reported adverse event; Initial information received on 26-J... unsuitable product administered with no reported adverse event; Initial information received on 26-Jun-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a patient with unknown age and gender who was administered to unsuitable Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult [Tenivac] 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 received an unknown dose of suspect Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult, Suspension for injection (lot number, expiry date and strength not reported) via unknown route in unknown administration site for Immunization and unsuitable product was administered with no reported adverse event (poor quality product administered) (latency same day). Information on the batch number was requested corresponding to the one at time of event occurrence. Reportedly, the duration of temperature excursion: 48 hours and maximum/minimum temperature reached: 5๏ฟฝC but the reported stated that she was not sure for the temperature. It was not related to human error. 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
2847833 19 F SC 06/30/2025 MENB
 PFIZER\WYETH
 HG6057
Dizziness, Syncope, Unresponsive to stimuli Dizziness, Syncope, Unresponsive to stimuli
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe
2847834 39 F FL 06/30/2025 MMR
 GLAXOSMITHKLINE BIOLOGICALS
 xx9n4
Dizziness, Dyspnoea, Hyporesponsive to stimuli, Loss of consciousness, Syncope Dizziness, Dyspnoea, Hyporesponsive to stimuli, Loss of consciousness, Syncope
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemi... Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient complained after shot of feeling light headed, went to go get water for her, by the time I got back with it my tech said she passed out in the chair. She was slightly resposive when I checked her, called 911 who sent paramedics and she was taken to the hospital from here. Bp was 80/60 when they checked. Patient's husband came later to report she recovered, relayed she had a semiglutide injection recently and was fasting for her blood draw that morning. , Other Vaccines: VaccineTypeBrand: heplisav-b; Manufacturer: dynavax; LotNumber: 946063; Route: IM; BodySite: left arm; Dose: 1; VaxDate: 06/20/2025, VaccineTypeBrand: Varivax; Manufacturer: merck; LotNumber: 2004455; Route: IM; BodySite: left arm; Dose: ; VaxDate: 06/20/2025 More
2847835 69 M IN 06/30/2025 COVID19
 PFIZER\BIONTECH
 ME6072
Pruritus, Rash, Rash pruritic Pruritus, Rash, Rash pruritic
Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash Generalized-Mild, Additional Det... Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash Generalized-Mild, Additional Details: RASHES APPEARED ON UPPER ARMS YESTERDAY WITH ITCHING More
2847836 19 M PA 06/30/2025 HPV9
 MERCK & CO. INC.
 x020725
Syncope, Unresponsive to stimuli Syncope, Unresponsive to stimuli
Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient somewhat fainted for about 5 sec... Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient somewhat fainted for about 5 seconds after receiving the injection of Gardasil 9. His father was there, so the patient did not fall off of the chair. 911 was called. Patient seemed to be ok. The medics checked him out and he seemed to be ok. His dad said this has happened in the past with other vaccines., Other Vaccines: VaccineTypeBrand: Gardasil 9; Manufacturer: Merck; LotNumber: x020725; Route: im; BodySite: arm; Dose: ; VaxDate: UNKNOWN More
2847837 29 F TX 06/30/2025 VARCEL
 MERCK & CO. INC.
 y015101
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
2847838 75 F IL 06/30/2025 COVID19-2
 PFIZER\BIONTECH
 ME6072
Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site swelling, Mobility decreased More
Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection ... Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Mild, Additional Details: Pt does take 2 benadryl at night as a routine medication and she took on wed,thr and fri but sysmtomps did not get better. Pt does have difficulty raising arm or no tingling running towards finger. Advised patient to seek medical attention either with PCP or urgent care or immediate care due to weekend. Per pt, if it continues she will contatct her PCP on monday or seek medical attention sooner. , Other Vaccines: VaccineTypeBrand: Boostrix TDAP; Manufacturer: GSK; LotNumber: 793PT; Route: IM; BodySite: Right Deltoid; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: Arexvy; Manufacturer: GSK; LotNumber: 4F45Z; Route: IM; BodySite: Right Deltoid; Dose: ; VaxDate: UNKNOWN More
2847839 72 F FL 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 39H2S
Injection site swelling, Rash Injection site swelling, Rash
Site: Swelling at Injection Site-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties... Site: Swelling at Injection Site-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Additional Details: Patient had a "hamburger sized" injection site swelling, that decreased day after. (06/21/25). Patient started developing rash starting 06/21/25 evening rash from her upper thigh towards the glute. Started spraeding with bumps not blistering. Patient woke up at 06/22/25 and devleoped another rash across abdomin with same features. Patinet has been taking tylenol 500mg by mouth once daily since day of injection 06/20/25. Patient has been counselled to seek further medical help and advise., Other Vaccines: VaccineTypeBrand: Shingrix (Shingles); Manufacturer: Glaxosmithkline; LotNumber: 39H2S; Route: IM; BodySite: Right Arm; Dose: ; VaxDate: UNKNOWN More
2847840 68 F CA 06/30/2025 RSV
 GLAXOSMITHKLINE BIOLOGICALS
 XA53Y
Injection site erythema, Injection site pain, Injection site swelling Injection site erythema, Injection site pain, Injection site swelling
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Pt received Arexvy vaccine on Thursday 6/19/25. Pt came to pharmacy on Sunday 6/22/25 and reported redness, swelling, and pain in arm below injection site that has lasted for 3 days. Recommended pt take ibuprofen and diphenhydramine to alleviate symptoms. Will follow up with pt the next day., Other Vaccines: VaccineTypeBrand: Arexvy; Manufacturer: GSK; LotNumber: XA53Y; Route: IM; BodySite: ; Dose: ; VaxDate: UNKNOWN More
2847841 50 M GA 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 93kk4
Injection site pain, Pain, Pain in extremity, Sleep disorder Injection site pain, Pain, Pain in extremity, Sleep disorder
Site: Pain at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Additional Details: Pt... Site: Pain at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Additional Details: Pt said that his all extremites are very painful and he is not able to sleep on left side at all., Other Vaccines: VaccineTypeBrand: Heplisav B; Manufacturer: dynavax; LotNumber: 947931; Route: intramusular; BodySite: right arm; Dose: 1; VaxDate: 06/16/2025 More
2847842 56 M FL 06/30/2025 PNC21
 MERCK & CO. INC.
 2002626
Injection site bruising Injection site bruising
Site: Bruising at Injection Site-Severe, Additional Details: patient reported to pharmacy to today w... Site: Bruising at Injection Site-Severe, Additional Details: patient reported to pharmacy to today with severe bruising of large area of right arm. patient was advised to see a doctor immediately by rph both in person when in the pharmacy and later on phone. patient has refused to see doctor or go to the emergency room , Other Vaccines: VaccineTypeBrand: boostrix; Manufacturer: ; LotNumber: pd324; Route: intramuscular; BodySite: left deltoid; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: pfizer comirnity; Manufacturer: ; LotNumber: md3414; Route: intramuscular; BodySite: left deltoid; Dose: ; VaxDate: UNKNOWN More
2847843 71 F CA 06/30/2025 PNC20
 PFIZER\WYETH
 ln4929
Injection site erythema, Injection site infection, Injection site swelling Injection site erythema, Injection site infection, Injection site swelling
Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: pat... Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: patient said the injection site turned red and swelling after a few days, patient went to the doctor to get it check out, and doctor said it was infected, and prescribed patient oral antibiotics, no other symtoms specified, patient called to let us know, no other complaints. More
2847844 31 F PA 06/30/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 me6072
me6072
Chest discomfort, Chest pain, Dizziness, Dyspnoea, Flushing; Hyperhidrosis, Naus... Chest discomfort, Chest pain, Dizziness, Dyspnoea, Flushing; Hyperhidrosis, Nausea More
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium... Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium More
2847845 18 M CA 06/30/2025 MNQ
MNQ
MNQ
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 u8194aa
u8194aa
u8194aa
Arthralgia, Dyskinesia, Facial pain, Fall, Headache; Hyperhidrosis, Lip injury, ... Arthralgia, Dyskinesia, Facial pain, Fall, Headache; Hyperhidrosis, Lip injury, Loss of consciousness, Syncope, Thirst; Unresponsive to stimuli More
Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient got MENACWY vaccine in his lef... Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient got MENACWY vaccine in his left arm. In 5 min patient got HPV vaccine in right arm, was doing well for 2 minutes, and was talking. Suddenly fell face forward and was unconscious. Had a couple second episode of jerking movements, SBP 150, patient was diaphoretic, in a couple of minutes started talking and was oriented to self, situation and place, was complaining of face pain due to trauma to the lip from falling and right knee pain, as well as headache. Was thirsty and was drinking, Other Vaccines: VaccineTypeBrand: HPV; Manufacturer: merck; LotNumber: z005469; Route: IM; BodySite: right deltoid; Dose: 1; VaxDate: 06/24/2025 More
2847846 66 F CT 06/30/2025 PNC21
 MERCK & CO. INC.
 z004302
Infection, Injection site abscess Infection, Injection site abscess
Site: Redness at Injection Site-Mild, Additional Details: Husband reports patient was seen for an in... Site: Redness at Injection Site-Mild, Additional Details: Husband reports patient was seen for an infection, treated with short term course of kefelx, dispensed from pharmacy More
2847847 51 M CA 06/30/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 5Y9CA
5Y9CA
Fatigue, Injection site bruising, Injection site pain, Lethargy, Pain; Rash, Sca... Fatigue, Injection site bruising, Injection site pain, Lethargy, Pain; Rash, Scan normal, X-ray normal More
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Mild, Systemic: Allergic: Rash... Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Body Aches Generalized-Mild, Systemic: Exhaustion / Lethargy-Mild, Additional Details: Patient received 2nd dose of Shingles vaccine on 6/6/2025. His first dose was in 2024. He does not recall if he had any reactions after the 1st dose. He complained for arm soreness, pain, and upper extremity rash. Those symptoms started 2 days after the vaccine. He visited the ER. The ER did X-rays and scans, which all came back normal. They prescriber stated patient may have possible reaction from vaccine. Pt will follow up with PCP. More
2847848 CA 06/30/2025 HIBV
 SANOFI PASTEUR
No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age
ACTHIB being given to children 6 to 7 weeks of age with no reported AE; Initial information received... ACTHIB being given to children 6 to 7 weeks of age with no reported AE; Initial information received on 27-Jun-2025 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves Infant and unknown gender patient for whom HIB (PRP/T) vaccine [ACT-HIB] being given to children 6 to 7 weeks of age with no reported ae (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 received an unknown dose of suspect HIB (PRP/T) vaccine; Powder and solvent for solution for injection (lot number, strength and expiry date not reported) via unknown route in unknown administration site for Immunization; being given to children 6 to 7 weeks of age with no reported ae (product administered to patient of inappropriate age) (latency: same day). Information on the batch number was requested corresponding to the one at time of event occurrence. 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
2847849 78 F FL 06/30/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 H4279
Dizziness, Syncope, Unresponsive to stimuli Dizziness, Syncope, Unresponsive to stimuli
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details... Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: Feeling faint, laid on the floor to recover More
2847850 67 F NC 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 4n9pf
Injection site pruritus, Rash, Rash pruritic Injection site pruritus, Rash, Rash pruritic
Site: Itching at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)... Site: Itching at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Additional Details: patient states approx 48 hrs after vaccination she experienced an "intensely itchy rash" on upper right arm and right ankle More
2847851 69 F FL 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 99d52
Injection site bruising, Injection site erythema, Injection site pruritus, Injec... Injection site bruising, Injection site erythema, Injection site pruritus, Injection site swelling More
Site: Bruising at Injection Site-Mild, Site: Itching at Injection Site-Mild, Site: Redness at Inject... Site: Bruising at Injection Site-Mild, Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: Patient stated she feels itchy at the site of injection and swelling was there but does not bother her. She wants some itching symptom relief. Advice her to get benadryl tablet to take, also she can use benadryl cream for itching. Recommended ice pack or warm compression on arm. Patient stated she will monitor and seek for medical help if needed. More
2847852 73 F FL 06/30/2025 PNC21
 MERCK & CO. INC.
 y013009
Blood disorder, Deep vein thrombosis Blood disorder, Deep vein thrombosis
Systemic: Blood Disorder (diagnosed by MD)-Medium, Additional Details: Patient developed a DVT in h... Systemic: Blood Disorder (diagnosed by MD)-Medium, Additional Details: Patient developed a DVT in her right leg, has had a history of 3 previous DVTs in the right leg More
2847853 36 F CA 06/30/2025 TDAP
 GLAXOSMITHKLINE BIOLOGICALS
 793pt
Erythema, Skin warm Erythema, Skin warm
Systemic: felt hot and redness on neck and arms-Mild, Additional Details: patient feels hot and redn... Systemic: felt hot and redness on neck and arms-Mild, Additional Details: patient feels hot and redness on arms and neck More
2847854 45 M AL 06/30/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
 946904
Injection site pain, Lymphadenopathy, Pruritus Injection site pain, Lymphadenopathy, Pruritus
Site: Pain at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild... Site: Pain at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: had some itching on wrist and says lympth node on that side swollen-Mild, Other Vaccines: VaccineTypeBrand: boostrix; Manufacturer: glaxosmith; LotNumber: hr4279; Route: im; BodySite: left arm; Dose: ; VaxDate: UNKNOWN, VaccineTypeBrand: gardasil; Manufacturer: merck; LotNumber: 2005055; Route: im; BodySite: left arm; Dose: ; VaxDate: UNKNOWN More
2847855 87 M NC 06/30/2025 PNC21
 MERCK & CO. INC.
 Z005765
Dizziness, Injection site pain Dizziness, Injection site pain
Site: Pain at Injection Site-Medium, Systemic: Dizziness / Lightheadness-Mild Site: Pain at Injection Site-Medium, Systemic: Dizziness / Lightheadness-Mild
2847856 66 F NC 06/30/2025 PNC21
 MERCK & CO. INC.
 Z005765
Chills, Injection site erythema, Injection site pain, Injection site swelling, P... Chills, Injection site erythema, Injection site pain, Injection site swelling, Pyrexia More
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injec... Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Chills-Medium, Systemic: Fever-Medium More
2847857 72 F FL 06/30/2025 PPV
 MERCK & CO. INC.
 Y016291
Joint injury Joint injury
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)- Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
2847858 0.25 F AL 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 not known
Injection site pruritus Injection site pruritus
Site: Itching at Injection Site-Mild, Additional Details: pt said they had itching reaction when ask... Site: Itching at Injection Site-Mild, Additional Details: pt said they had itching reaction when asked if they wanted to finish the series. i asked patient if she wanted me to report she said yes. i can't view any of the other info in rx system More
2847860 60 M FL 06/30/2025 VARZOS
VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 74NC9
74NC9
Autoimmune disorder, Blister, Erythema, Injection site erythema, Pruritus; Rash Autoimmune disorder, Blister, Erythema, Injection site erythema, Pruritus; Rash
Site: Redness at Injection Site-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)... Site: Redness at Injection Site-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Autoimmune Disease (diagnosed by MD)-Medium, Additional Details: patient states that he gets several blisters, patches of red spots with fluids all over the body including back of hair and butt. symptoms goes away after 7-8 days and comes back. this is 3rd time having these symptoms after second dose of shingrix... 1st dose was fine..., Other Vaccines: VaccineTypeBrand: prevnar 20; Manufacturer: wyeth Pharmaceuticals LLC; LotNumber: LJ5281; Route: IM; BodySite: right arm; Dose: 00; VaxDate: 02/28/2025 More
2847861 80 F TX 06/30/2025 COVID19
 MODERNA
 3044069
Injection site bruising, Injection site erythema, Injection site pain, Injection... Injection site bruising, Injection site erythema, Injection site pain, Injection site swelling, Pruritus More
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injec... Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium More
2847863 0.33 F SC 06/30/2025 RV5
 MERCK & CO. INC.
 2117044
Crying, Diarrhoea haemorrhagic, Food refusal Crying, Diarrhoea haemorrhagic, Food refusal
Inconsolable crying, decreased PO intake, developed bloody diarrhea on day 3 after vaccine Inconsolable crying, decreased PO intake, developed bloody diarrhea on day 3 after vaccine
2847865 19 M GA 06/30/2025 COVID19
 MODERNA
 8080803
Expired product administered, Injection site pain Expired product administered, Injection site pain
The patient received an expired vaccine at his appointment. On 06/12/2025 he received a COVID 19 vac... The patient received an expired vaccine at his appointment. On 06/12/2025 he received a COVID 19 vaccine that expired 06/11/1025. He had soreness at injection site for 3 days. Has not had any new symtoms since. More
2847866 18 F GA 06/30/2025 COVID19
 MODERNA
 8080803
Expired product administered, No adverse event Expired product administered, No adverse event
Patient received a COVID vaccine on 06/13/2025, this vaccine expired on 06/11/3025. Patient did not ... Patient received a COVID vaccine on 06/13/2025, this vaccine expired on 06/11/3025. Patient did not experience any adverse reactions from this injection. More
2847867 15 M 06/30/2025 COVID19
 MODERNA
 8080803
Expired product administered, No adverse event Expired product administered, No adverse event
Patient was given a COVID 19 vaccine on 6/17/2025 that expired on 6/11/2025. I spoke to parents and ... Patient was given a COVID 19 vaccine on 6/17/2025 that expired on 6/11/2025. I spoke to parents and patient did not experience any adverse resctions to this vaccine. More
2847868 0.17 M CO 06/30/2025 RV5
 MERCK & CO. INC.
Diarrhoea, Vomiting Diarrhoea, Vomiting
Diarrhea and spit up for 7 days Diarrhea and spit up for 7 days
2847869 39 F AL 06/30/2025 HPV9
 MERCK & CO. INC.
 X022735
Rash Rash
PATIENT STATES THAT A DAY OR TWO AFTER RECEIVING HPV VACCINE SHE BROKE OUT IN A SEVERE RASH TO THE A... PATIENT STATES THAT A DAY OR TWO AFTER RECEIVING HPV VACCINE SHE BROKE OUT IN A SEVERE RASH TO THE ARM SHE RECEIVED THE VACCINE IN (RIGHT) AND TO THE TRUNK OF HER BODY. SHE WAS SEEN BY PMD AND WAS TOLD THAT SHE HAD A SEVERE REACTION TO THE VACCINE AND SHE IS STILL BEING TREATED FOR THE REACTION AT THIS TIME. More
2847870 11 M GA 06/30/2025 MNQ
TDAP
 SANOFI PASTEUR
SANOFI PASTEUR
 pmcu8256ba-cp
pmcu8115aa-cp
Injection site swelling; Injection site swelling Injection site swelling; Injection site swelling
Patient had swelling at lower injection site (meq site). Swelling got bigger throughout the day. Ibu... Patient had swelling at lower injection site (meq site). Swelling got bigger throughout the day. Ibuprofen was administered. Swelling still present 2 days after noticing. More
2847871 40 M VA 06/30/2025 TD
 SANOFI PASTEUR
 u8492BA
Muscular weakness, Pain Muscular weakness, Pain
States soreness, limited ROM, muscles weakness at times x 10 days States soreness, limited ROM, muscles weakness at times x 10 days
2847872 0.33 M 06/30/2025 DTAPHEPBIP
 GLAXOSMITHKLINE BIOLOGICALS
 9P329
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
Patient recieved dtap-hep b-ipv vaccine instead of recommended dose of dtap-hib-ipv (pentacel), afte... Patient recieved dtap-hep b-ipv vaccine instead of recommended dose of dtap-hib-ipv (pentacel), after patient received incorrect dose patient was acting his normal self. RN placed call to parent to inform of incorrect vaccine no answer, RN left message to have parent call clinic back. More
2847873 50 F TX 06/30/2025 PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
 LN4930
LN4930
Chills, Headache, Injected limb mobility decreased, Pain, Pyrexia; Tremor Chills, Headache, Injected limb mobility decreased, Pain, Pyrexia; Tremor
Beginning around four hours after the injection I had limited to no mobility in my arm. A couple mor... Beginning around four hours after the injection I had limited to no mobility in my arm. A couple more hours into the evening, I developed a really bad fever, had an immense headache, and severe chills. My teeth were chattering, and I could not stop shaking. It was about 10:30pm when I had to take some Aleve, as the pain was so intense. I was finally able to go to sleep, as the fever broke and stopped shaking. It has taken about three days for my arm to be at 90% of full range of motion. I have never experienced that fever or shaking before, as I don't ever get sick. More
2847874 77 M 06/30/2025 COVID19
 PFIZER\BIONTECH
 ME6072
Flushing, Lacrimation increased, Pain, Pyrexia, Rhinorrhoea Flushing, Lacrimation increased, Pain, Pyrexia, Rhinorrhoea
At 0730 resident BP was 167/81 T 100.3 vital placed in vitals section in PCC, face was flushed has r... At 0730 resident BP was 167/81 T 100.3 vital placed in vitals section in PCC, face was flushed has running nose and watery eyes, lip was red and slightly swollen. Resident stated it possibly could be related having the covid vaccine yesterday. Writer updated NP on call had given one time order Benadryl 25 mg and Tylenol 650 mg q 4 hours prn for fever/pain. Resident said he does not want to go to the hospital. Nursing staff will continue to monitor resident. More
2847875 52 F AL 06/30/2025 PNC21
 MERCK & CO. INC.
 Y019158
Injection site reaction, Urticaria Injection site reaction, Urticaria
Welts near site of injection Welts near site of injection
2847876 61 F LA 06/30/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 PJ353
Diarrhoea, Rash, Rash pruritic Diarrhoea, Rash, Rash pruritic
PATIENT IS EXPERIENCING A ITCHY AND PAINFUL RASH. SHE IS ALSO HAVING DIARRHEA PATIENT IS EXPERIENCING A ITCHY AND PAINFUL RASH. SHE IS ALSO HAVING DIARRHEA
2847877 55 F CA 06/30/2025 PNC20
 PFIZER\WYETH
 LP4947
Injection site erythema, Injection site pain, Injection site rash, Injection sit... Injection site erythema, Injection site pain, Injection site rash, Injection site swelling More
Pt has injection site rash with erythema, swelling and pain Pt has injection site rash with erythema, swelling and pain
2847878 17 F NM 06/30/2025 HPV9
MENB
MNQ
TDAP
 MERCK & CO. INC.
PFIZER\WYETH
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 Z002903
HP9988
U8438AA
PG3RP
Inappropriate schedule of product administration, No adverse event; Inappropriat... Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event More
Tdap inadvertently given too soon. Patient did not suffer any adverse effects after inadvertent admi... Tdap inadvertently given too soon. Patient did not suffer any adverse effects after inadvertent administration of Tdap. More
2847879 22 F IL 06/30/2025 IPV
 SANOFI PASTEUR
 W1C7851M
Incorrect route of product administration Incorrect route of product administration
Patient was given Poliovirus intradermally instead of TB. No symptoms at time of injection Patient was given Poliovirus intradermally instead of TB. No symptoms at time of injection
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