🏥 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 💀 🏥 🚑 ♿ ⚠️
2873442 55 M CO 11/18/2025 UNK
UNK
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 407245
407245
Bone pain, Dizziness, Headache, Muscle spasms, Nausea; Product administered to p... Bone pain, Dizziness, Headache, Muscle spasms, Nausea; Product administered to patient of inappropriate age More
Light headed; Nausea; Muscle spasms; Headache; Bone pain; Vaccine was administered to 55 year old pa... Light headed; Nausea; Muscle spasms; Headache; Bone pain; Vaccine was administered to 55 year old patient; This spontaneous case, initially received on 06-Nov-2025, was reported by a health professional and concerns n adult male patient. Concomitant Medications: Unknown Medical History: Unknown Administration of company suspect drug: On 04-Nov-2025, the patient received Fluad (TIV) for Indication not reported, Dose regimen: 0.5 ml, route of administration: not reported, anatomical location: not reported, Lot number: 407245. No additional suspect drugs. Adverse reactions/events and outcomes: On 04-Nov-2025, the patient experienced Vaccine was administered to 55 year old patient (outcome: Unknown). On an unknown date, the patient experienced Light headed (outcome: Unknown), Nausea (outcome: Unknown), Muscle spasms (outcome: Unknown), Headache (outcome: Unknown), Bone pain (outcome: Unknown). Nurse called and informed that Fluad vaccine for 65 and older was administered to a patient aged adult patient. The nurse described that the patient had some adverse events: light-headedness, nausea, muscle spasms, headache, and bone pain. The nurse informed that the doctor was in contact with the patient and suggested that the patient take plenty of water, and the symptoms were expected to improve with time. Fluad (TIV) action taken: Not Applicable Reporter's assessment: The reporter did not provide the seriousness and causality assessment of the events.; Reporter's Comments: Due to the spontaneous nature of the case, the all events are considered related for reporting purposes except Vaccine was administered to 55 year old patient is not related due to nature of event (special situation). More
2873444 68 F KS 11/18/2025 COVID19
 PFIZER\BIONTECH
 MY9547
Unevaluable event Unevaluable event
Unknown Unknown
2873445 92 F FL 11/18/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 NA0589
u8859ba
Lip swelling, Mouth swelling, Oral pain; Lip swelling, Mouth swelling, Oral pain Lip swelling, Mouth swelling, Oral pain; Lip swelling, Mouth swelling, Oral pain
customer said she had swelling in her mouth and lips. It also made her mouth sore. It lasted about 3... customer said she had swelling in her mouth and lips. It also made her mouth sore. It lasted about 30 days. More
2873446 81 M CA 11/18/2025 COVID19
 PFIZER\BIONTECH
 NA0739
Injection site rash, Rash Injection site rash, Rash
Patient reported a small rash that he noticed when removing the band aid on 11/4/25. Since then, it ... Patient reported a small rash that he noticed when removing the band aid on 11/4/25. Since then, it has traveled from his shoulder down his back. Patient did seek medical attention, and the provider gave him a steroid cream as well as the patient used some over the counter allergy cream. Patient is still having symptoms ?bumps? are still present as of today?s date 11/18/25. More
2873447 54 F PA 11/18/2025 COVID19
COVID19
PNC21
PNC21
 MODERNA
MODERNA
MERCK & CO. INC.
MERCK & CO. INC.
 3052864
3052864
Z010457
Z010457
Chills, Cough, Ear pain, Feeling cold, Headache; Palpitations; Chills, Cough, Ea... Chills, Cough, Ear pain, Feeling cold, Headache; Palpitations; Chills, Cough, Ear pain, Feeling cold, Headache; Palpitations More
Chills started about 10 hours after administration of the vaccines. I could not stop shivering, and ... Chills started about 10 hours after administration of the vaccines. I could not stop shivering, and could not get warm. Not long after that , the back of my head started hurting , and the headache was awful. I took 1g acetaminophen at 1:00 am, and another 1g at 8 am. This kept the headache around 5/10. Randomly, throughout the day and continuing into the evening of 11/18/25, I'm experiencing sharp, stabbing pains behind my right ear. They are fast, and 10/10. At 6:00 pm I am having palpitations that are strong enough to make me cough. This has lasted 10 minutes so far. More
2873448 14 F IL 11/18/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 ES4H5
Blood glucose decreased, Dyskinesia, Loss of consciousness, Syncope Blood glucose decreased, Dyskinesia, Loss of consciousness, Syncope
Patient fainted and lost conscienousness for ~20 seconds, momentarily had jerky movements. Glucose w... Patient fainted and lost conscienousness for ~20 seconds, momentarily had jerky movements. Glucose was low, 67 when tested by local paramedics More
2873464 68 F VA 11/18/2025 FLU3
 SANOFI PASTEUR
 ut8794aa
Chills, Diarrhoea, Myalgia Chills, Diarrhoea, Myalgia
The patient reported muscle aches, chills and diarrhea that she treated with an antihistamine and a ... The patient reported muscle aches, chills and diarrhea that she treated with an antihistamine and a otc pain medication. Her symptoms resolved. More
2873466 27 F TX 11/18/2025 FLU3
HEP
MMR
TDAP
VARCEL
 SANOFI PASTEUR
DYNAVAX TECHNOLOGIES CORPORATION
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
MERCK & CO. INC.
 u8832da
946913
fa4c9
u8669aa
z010438
Laboratory test normal, Syncope; Laboratory test normal, Syncope; Laboratory tes... Laboratory test normal, Syncope; Laboratory test normal, Syncope; Laboratory test normal, Syncope; Laboratory test normal, Syncope; Laboratory test normal, Syncope More
patient fainted patient fainted
2873468 57 M MN 11/18/2025 COVID19
FLU3
PNC20
VARZOS
 MODERNA
SEQIRUS, INC.
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS



Injection site erythema, Injection site pain, Injection site pruritus, Injection... Injection site erythema, Injection site pain, Injection site pruritus, Injection site warmth; Injection site erythema, Injection site pain, Injection site pruritus, Injection site warmth; Injection site erythema, Injection site pain, Injection site pruritus, Injection site warmth; Injection site erythema, Injection site pain, Injection site pruritus, Injection site warmth More
RED BLOTCHY SPOT AT SITE OF INJECTION. SPOT WAS WARM, ITCHY. PAINFUL TO MOVE ARM AND TOUCH SITE. HAP... RED BLOTCHY SPOT AT SITE OF INJECTION. SPOT WAS WARM, ITCHY. PAINFUL TO MOVE ARM AND TOUCH SITE. HAPPENED DAY(S) AFTER VACCINATIONS More
2873472 84 F 11/18/2025 FLU3
 SANOFI PASTEUR
Injection site swelling, Oedema peripheral, Skin warm Injection site swelling, Oedema peripheral, Skin warm
Arm became swollen in the dorsolateral area roughly 1 inch below the injection site. Patient has ve... Arm became swollen in the dorsolateral area roughly 1 inch below the injection site. Patient has very thin papery skin and fluid collected underneath the skin down to an inch above the elbow. The area aformentioned became swollen with fluid and was warm to touch the initial day and the day after. The patient did not report overall fever. The swollen area was soft to touch and is slowly reducing in size as of 11/18/2025. More
2873492 5 F OR 11/18/2025 COVID19
FLUN3
 PFIZER\BIONTECH
MEDIMMUNE VACCINES, INC.
 NA0846
YS2587B
Swelling face; Swelling face Swelling face; Swelling face
Face swollen am of 10/22/25. No breathing difficulties treated with Benadryl at 3AM & Claritin a... Face swollen am of 10/22/25. No breathing difficulties treated with Benadryl at 3AM & Claritin at 0745 symptoms resolved in a couple days. Hx of food allergies. Had not had any foods she was allergic to. Usually reacts with stomach pain and vomiting. More
2873004 F NJ 11/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 UNK
Herpes zoster, Ophthalmic herpes zoster, Pain Herpes zoster, Ophthalmic herpes zoster, Pain
she was diagnosed with ocular shingles in her right eye; This serious case was reported by a consume... she was diagnosed with ocular shingles in her right eye; This serious case was reported by a consumer and described the occurrence of ophthalmic herpes zoster in a 71-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. The patient's past medical history included shingles (Consumer does have a positive past history of shingles outbreaks). Previously administered products included Zostavax (Consumer states she was vaccinated with Zostavax years ago). On an unknown date, the patient received the 1st dose of Shingrix (right arm). On an unknown date, 1 week after receiving Shingrix, the patient experienced ophthalmic herpes zoster (Verbatim: she was diagnosed with ocular shingles in her right eye) (serious criteria GSK medically significant). The patient was treated with Antivirals. The outcome of the ophthalmic herpes zoster was not reported. It was unknown if the reporter considered the ophthalmic herpes zoster to be related to Shingrix. The company considered the ophthalmic herpes zoster to be unrelated to Shingrix. Additional Information: GSK Receipt Date: 05-NOV-2025 Consumer was the reporter. Consumer stated she received her first dose of Shingrix and one week later she was diagnosed with ocular shingles in her right eye. Consumer did not have a positive past history of shingles outbreaks. Consumer stated she was vaccinated with Zostavax years ago. Consumer reported the past June she had a mild outbreak on her trunk. Consumer stated she knows what to do when she has an outbreak and will use lidocaine patches and takes an antiviral medication. The consumer stated she is using an eye drop for her ocular shingles. Consumer stated she was in pain and did not want to lose vision in her eye.; Sender's Comments: A case of Ophthalmic herpes zoster,1 week after receiving 1st dose of Shingrix, in a 71-year-old female patient. Based on the available information a?possible causality that the event was caused by the GSK product cannot be ascertained. Further follow up information has been sought. More
2873005 11/17/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
Expired product administered Expired product administered
Flulaval expired dose administered; This non-serious case was reported by a other health professiona... Flulaval expired dose administered; 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 patient who received Flu Seasonal TIV Quebec (FluLaval 2024-2025 season) for prophylaxis. On an unknown date, the patient received FluLaval 2024-2025 season. On an unknown date, an unknown time after receiving FluLaval 2024-2025 season, the patient experienced expired vaccine used (Verbatim: Flulaval expired dose administered). 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: 13-NOV-2025 The patient received an expired 2024-2025 Flulaval was given to a patient. The batch number was not provided, and we are unable to contact the reporter. More
2873011 F 11/17/2025 COVID19
 MODERNA
Aura Aura
More frequent macular aura; This spontaneous case was reported by a consumer and describes the occur... More frequent macular aura; This spontaneous case was reported by a consumer and describes the occurrence of AURA (More frequent macular aura) in a female patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (Pfizer had horrid reaction chills, flu, and feverish for at least two days.), PFIZER BIONTECH COVID-19 VACCINE (Pfizer had horrid reaction chills, flu, and feverish for at least two days.), PFIZER BIONTECH COVID-19 VACCINE (Pfizer had horrid reaction chills, flu and and feverish for at least two days.). Past adverse reactions to the above products included Chills with PFIZER BIONTECH COVID-19 VACCINE; Feverish with PFIZER BIONTECH COVID-19 VACCINE; and Flu with PFIZER BIONTECH COVID-19 VACCINE. Concurrent medical conditions included Macular degeneration. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced AURA (More frequent macular aura). At the time of the report, AURA (More frequent macular aura) had resolved. First problem with the Pfizer vaccine reported and then mentioned the Moderna vaccine. Pfizer had horrid reaction chills, flu, and feverish for at least two days. No concomitant medication was reported. From moderna vaccine, patient had more frequent macular aura after the first two or three vaccines. It was unknown if the patient experienced any additional symptoms/events. No treatment medication was reported. Reporter causality was not reported. More
2873012 39 F MD 11/17/2025 COVID19
COVID19
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER

Feeling abnormal, Headache, Heavy menstrual bleeding, Influenza like illness, Me... Feeling abnormal, Headache, Heavy menstrual bleeding, Influenza like illness, Menstruation irregular; Pain in extremity More
flu-like symptoms; feeling icky; sore arm; bad headaches; period was horribly heavy; period was &quo... flu-like symptoms; feeling icky; sore arm; bad headaches; period was horribly heavy; period was "horribly heavy" and arrived about 2 weeks earlier than normal after receiving the dose of NUVAXOVID; Initial information received on 10-Nov-2025 regarding an unsolicited valid non-serious case received from a Patient. This case involves a 39 years old female patient who had flu-like symptoms, feeling icky, sore arm, bad headaches and period was "horribly heavy" and arrived about 2 weeks earlier than normal after receiving the dose of NVX-COV2373 (original) adjuvanted vaccine [Nuvaxovid]. The patient's past vaccination(s) included MRNA COVID vaccine (her periods were heavier for a while). The patient's past medical history, medical treatment(s) and family history were not provided. At the time of the event, the patient had ongoing Crohn's disease. On 02-Nov-2025, the patient received unknown dose of suspect NVX-COV2373 (original) adjuvanted vaccine, Injection (strength, lot number and expiry date not reported) via intramuscular route in the left deltoid for COVID vaccine (COVID-19 immunization). Information on batch number and expiry date corresponding to the one at time of event occurrence was requested. On 02-Nov-2025 on same day the patient developed flu-like symptoms (influenza like illness), feeling icky (feeling abnormal) , sore arm (pain in extremity) and bad headaches (headache). On unknown date in Nov-2025 the patient reported period was horribly heavy and arrived about 2 weeks earlier than normal after receiving the dose of nuvaxovid (heavy menstrual bleeding) (menstruation irregular) (unknown latency). Action taken: Not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Recovered / Resolved on 06-Nov-2025 for the event (flu-like symptoms, feeling icky, bad headaches and sore arm) and was Unknown for the event (heavy menstrual bleeding, menstruation irregular) . More
2873013 48 F MA 11/17/2025 UNK
 UNKNOWN MANUFACTURER
 No batch number
Rash, Urticaria Rash, Urticaria
Hives returned much, much worse; Rash that got progressively worse; This spontaneous case, initially... Hives returned much, much worse; Rash that got progressively worse; This spontaneous case, initially received on 04-Nov-2025, was reported by a non health professional and concerns an adult female patient. Medical history was reported as unknown and no concomitant medications were taken. Administration of company suspect drug: On 13-Oct-2025, the patient received Flucelvax (TIV) for active immunization for the prevention of influenza disease, Dose regimen: 0.5 ml, Route of administration: not reported, Anatomical location: Not reported Lot number: No batch number available and will be requested upon follow up. No additional suspect drugs. Adverse reactions/events and outcomes: On 13-Oct-2025, the patient experienced Rash that got progressively worse (outcome: Not reported). On an unknown date, the patient experienced Hives returned much, much worse. (outcome: Not reported). On 13-Oct-2025, the individual received a flu vaccination at her local pharmacy. Approximately five days later, she began to notice a rash that progressively worsened over the course of the week. On 24-Oct-2025, she visited her doctor, who prescribed a course of corticosteroids. After completing the five-day course, the medication appeared to keep the hives under control for about another week. However, the hives returned the following night with significantly increased severity. She remained under the care of a physician and expressed concern about continuing corticosteroid treatment. She had no underlying health conditions and described herself as a healthy adult woman who took no medications, exercised regularly, practiced yoga, and taught meditation. She noted that this was the most serious health issue she had ever experienced, for which she was otherwise grateful. She offered to share a photo of the rash if needed and sought further insight, mentioning that her doctor had indicated similar reactions had been reported in post-marketing. She described the reaction as a severe allergic. Flucelvax (TIV) action taken: Not Applicable Treatment medication: Corticosteroids Reporter's assessment: The reporter assessed the events non-serious and did not provide causality assessment.; Reporter's Comments: Due to the spontaneous nature of the case, events considered related for reporting purposes More
2873014 78 F 11/17/2025 UNK
 UNKNOWN MANUFACTURER
 No batch number
Urticaria Urticaria
Hives at arm and waist; Hives at arm and waist; This spontaneous case, initially received on 03-Nov-... Hives at arm and waist; Hives at arm and waist; This spontaneous case, initially received on 03-Nov-2025, was reported by a non health professional (patient) and concerns an elderly female patient. Drug history included Penicillin (Reaction: Hives). Administration of company suspect drug: On 28-Oct-2025, the patient received Fluad (TIV) for Indication not reported, Dose regimen: not reported, route of administration: not reported, Anatomical Location: Arm, Lot number: No batch number available and would be requested upon follow up. No additional suspect drugs. Adverse reactions/events and outcomes: On 30-Oct-2025, the patient experienced Hives at arm and waist (outcome: Recovered / Resolved, stop date: 31-Oct-2025). On 01-Nov-2025, the patient experienced Hives at arm and waist (outcome: Recovering / Resolving). Consumer reported: She had been having the flu vaccines for over 20 years and never had any reaction before. Last Tuesday 28-Oct-2025 she had got the flu vaccine and two days later she developed hives on her arm and around her waist. She thought they were insect bites but it was hives and she used an anti-itch medication and the next day it seemed it disappeared. However, the next day it came back again so she used the anti-itch medication again and then she also took an antihistamine Claritin so that cleared it up. She just wanted to know if there was something different about the flu vaccine this year some ingredient that was different because she needed to also make a decision next year whether she should get the flu vaccine again. It was recommended to discuss with her HCP whether or not she should receive the vaccine next time. Again, she had always been getting the flu vaccine and she knew that they changed the ingredients and they were not always the same, but she was just wondering what it was in that flu vaccine this year that caused she such a reaction. She knew that came from the vaccine because she was not exposed to anything else that could have created that. The anti-itch Sarna really helped but she needed to take the antihistamine really to get rid of it. When asked if the consumer had seen a Health Care Professional, she mentioned she would have if it had not gone away it just came and when it showed up it was in the evening kind of late at night so she did not want to go to an emergency room, she used the anti-itch medication and the next day it disappeared then she knew for sure that was hives because mosquito bites do not disappear like that and she thought she was good so the next evening she had it again around the waist and then on the arm and then she did a research and read that the first line of treatment for hives was an antihistamine. So, she had Claritin at home and tried the antihistamine and saw if it helped and it did but if that had not helped she would have gone to an urgent care but she was able to take care of it on her own. She had hives once before years ago to penicillin and the case was so bad that it took three weeks to get rid of the hives it was all over her body. Fluad (TIV) action taken: Not Applicable Treatment medication: Claritin, Sarna Reporter's assessment: The reporter assessed the events Hives at arm and waist and Hives at arm and waist related to the administration of Fluad (TIV) and did not provide the seriousness.; Reporter's Comments: Due to the spontaneous nature of the case, the events Hives at arm and waist and Hives at arm and waist are considered related for reporting purposes. More
2873024 M IL 11/17/2025 COVID19
 MODERNA
Myalgia Myalgia
Reported Symptoms: 10028322:MUSCLE PAIN; Narrative: Per chart notes, patient declined the 2025 COVID... Reported Symptoms: 10028322:MUSCLE PAIN; Narrative: Per chart notes, patient declined the 2025 COVID vaccine and reported since his last COVID vaccine (2024) he had experienced chronic right shoulder pain, in the same place that he had last received the vaccine. Per records, the vaccine had been administered outside of the facility. Records had been uploaded into the system through the database. Patient had received vaccine prior to this without documented complaints. Immunization Series Date Facility Reaction Info COVID-19 (PFIZER), MRNA, LNP-S, * 5 11/14/2022 DATABASE:STATE IIS COVID-19 (PFIZER), MRNA, LNP-S, * 3 04/21/2022 Pharmacy* COVID-19 (PFIZER), MRNA, LNP-S, * 3 10/12/2021 DATABASE:STATE IIS COVID-19 (PFIZER), MRNA, LNP-S, * 2 04/07/2021 Pharmacy* COVID-19 (PFIZER), MRNA, LNP-S, * 1 03/10/2021 Pharmacy* COVID-19 (PFIZER), MRNA, LNP-S, * 4 04/21/2022 DATABASE:STATE IIS COVID-19 (PFIZER), MRNA, LNP-S, * 4 10/12/2021 Pharmacy* COVID-19 (PFIZER), MRNA, LNP-S, * 6 03/23/2024 DATABASE:STATE IIS Other Relevant HX: Other: MUSCLE PAIN More
2873026 75 F OH 11/17/2025 FLU3
 SANOFI PASTEUR
 U8875BA
Syncope Syncope
Syncope that lead to ER visit. Syncope that lead to ER visit.
2873081 60 F ME 11/17/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
PFIZER\BIONTECH
PFIZER\BIONTECH
 0255209
0255209
0132209
0132209
067F21A
067F21A
GH9703
GH9703
COVID-19, Computerised tomogram, Dural arteriovenous fistula, Intracranial hypot... COVID-19, Computerised tomogram, Dural arteriovenous fistula, Intracranial hypotension, Magnetic resonance imaging; Spinal myelogram, Therapeutic embolisation; COVID-19, Computerised tomogram, Dural arteriovenous fistula, Intracranial hypotension, Magnetic resonance imaging; Spinal myelogram, Therapeutic embolisation; COVID-19, Computerised tomogram, Dural arteriovenous fistula, Intracranial hypotension, Magnetic resonance imaging; Spinal myelogram, Therapeutic embolisation; COVID-19, Computerised tomogram, Dural arteriovenous fistula, Intracranial hypotension, Magnetic resonance imaging; Spinal myelogram, Therapeutic embolisation More
After vaccinations and subsequent Covid infection which was treated with Paxlovid. I got rebound sym... After vaccinations and subsequent Covid infection which was treated with Paxlovid. I got rebound symptoms. Subsequent intracranial hypotension was diagnosed in 2023. Symptoms began in November. I was diagnosed with Inctracranial Hypotension with multiple dural venous fistulas. Over the past 3 years, I have been to [withheld] for treatment/embolization of 11 of these recurring rare dural venous fistulas. They speculated that I have some collagen issue or some type of auto immune issue which causes my dura/ vasculature to be weakened. More
✓ ✓
2873082 77 M NY 11/17/2025 COVID19
 MODERNA
Platelet count increased, Thrombocytosis Platelet count increased, Thrombocytosis
Thrombocytosis - Platelets went up to 753 Thrombocytosis - Platelets went up to 753
2873083 62 F 11/17/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.

Injection site reaction, Rash erythematous, Rash macular, Rash pruritic; Injecti... Injection site reaction, Rash erythematous, Rash macular, Rash pruritic; Injection site reaction, Rash erythematous, Rash macular, Rash pruritic More
Thu-11/13/25 (~9pm): small, pink, and itchy rash; approximately 2 inches below injection site; 2 d... Thu-11/13/25 (~9pm): small, pink, and itchy rash; approximately 2 inches below injection site; 2 days post inoculation Fri-11/14/25: rash brighter pink, still itchy; took Benadryl (1 capsule) at bedtime Sun-11/16/25: rash now red, splotchy, and has spread; still itchy; took Benadryl (2 capsules) at bedtime Mon-11/17/25: same as yesterday, but has spread alittle more More
2873084 34 F VT 11/17/2025 FLU3
 SEQIRUS, INC.
 ax4606a
Diarrhoea, Limb discomfort, Pain, Pain in extremity, Paraesthesia Diarrhoea, Limb discomfort, Pain, Pain in extremity, Paraesthesia
On Monday 11/10/2025, patient received the flu shot. She reported that a few hours later she felt he... On Monday 11/10/2025, patient received the flu shot. She reported that a few hours later she felt heaviness in her legs, slight pain/ache that didn't go away until she took tylenol the next day. Then she noticed the arm she received the flu shot still is sore, slightly tingly from the elbow down and painful when she bends it. She notes not having a reaction to previous flu shots. No fever but diarrhea for the past two days. Patient reported this information on 11/14/2025. Advised her to seek ED attention if symptoms worsen over weekend. Checked in this morning, patient reports feeling better, but not completely resolved and symptoms did not worsen. More
2873085 73 M FL 11/17/2025 COVID19
 PFIZER\BIONTECH
Abdominal pain upper, Myalgia, Pyrexia, Tremor Abdominal pain upper, Myalgia, Pyrexia, Tremor
Fever. Shakes. Muscle Aches. Stomach Ache. Lasted 18 hours. Fever. Shakes. Muscle Aches. Stomach Ache. Lasted 18 hours.
2873086 60 F MD 11/17/2025 FLU3
 SEQIRUS, INC.
 406996
Muscular weakness, Myalgia Muscular weakness, Myalgia
muscle weakness in upper arm and soreness continuing for 1 month muscle weakness in upper arm and soreness continuing for 1 month
2873087 52 F 11/17/2025 FLU3
FLU3
PNC20
PNC20
 SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH
 UT8873KA
UT8873KA
mg7416
mg7416
Chills, Contusion, Erythema, Pain, Peripheral swelling; Pyrexia, Skin warm; Chil... Chills, Contusion, Erythema, Pain, Peripheral swelling; Pyrexia, Skin warm; Chills, Contusion, Erythema, Pain, Peripheral swelling; Pyrexia, Skin warm More
subjective fever, chills, body pain, swelling to left arm and bruising noted. warmth to L arm and re... subjective fever, chills, body pain, swelling to left arm and bruising noted. warmth to L arm and redness- pt scheduled for an appt with PCP and advised of urgent care clinics she could go to. More
2873094 72 F KS 11/17/2025 COVID19
FLU3
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
 na0739
UT8869BA
UT8869BA
Extra dose administered, Wrong product administered; Extra dose administered, Wr... Extra dose administered, Wrong product administered; Extra dose administered, Wrong product administered; Extra dose administered, Wrong product administered More
MA accidentally administered 2 flu vaccines instead of a covid and flu. Covid was also given once m... MA accidentally administered 2 flu vaccines instead of a covid and flu. Covid was also given once mistake was realized. More
2873095 48 F NY 11/17/2025 COVID19
 PFIZER\BIONTECH
Cognitive disorder, Fatigue, Gastrointestinal disorder, Headache, Poor quality s... Cognitive disorder, Fatigue, Gastrointestinal disorder, Headache, Poor quality sleep More
since then, and worsening after second vaccine i have had headaches, overwhelming fatigue, GI issues... since then, and worsening after second vaccine i have had headaches, overwhelming fatigue, GI issues. I do not get effective sleep, and am always fatigued. needing to see specialists. this starting with vaccination and is getting progressively worse-- with other changes noted possibly due to the fatigue or juat cognitive issues. More
✓
2873096 58 F WA 11/17/2025 COVID19
 PFIZER\BIONTECH
Haematuria Haematuria
Hematuria x 24 hours Hematuria x 24 hours
2873097 80 F TX 11/17/2025 COVID19
 PFIZER\BIONTECH
 NA0589
Injected limb mobility decreased, Injection site pain Injected limb mobility decreased, Injection site pain
Severe pain at injection site. Patient reportedly unable to lift arm on the day after administration... Severe pain at injection site. Patient reportedly unable to lift arm on the day after administration. More
2873098 82 F TX 11/17/2025 FLU3
 SANOFI PASTEUR
 U8859DA
Rash Rash
PATIENT RECEIVED HER FLU SHOT ON THURSDAY 11/13/2025 AND DEVELOPED A RASH ON HER ENTIRE TORSO (FROM ... PATIENT RECEIVED HER FLU SHOT ON THURSDAY 11/13/2025 AND DEVELOPED A RASH ON HER ENTIRE TORSO (FROM WAIST TO NECK) ON FRIDAY 11/14/2025. More
2873099 28 M ND 11/17/2025 COVID19
 MODERNA
 3052859
No adverse event, Underdose No adverse event, Underdose
Pediatric dose given to adult. No adverse reaction noted during appointment. Pediatric dose given to adult. No adverse reaction noted during appointment.
2873100 66 M IN 11/17/2025 COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 RX# 6112129N, N
RX# 6112129N, N
RX# 6112129N, N
Back pain, Chest X-ray normal, Computerised tomogram head normal, Computerised t... Back pain, Chest X-ray normal, Computerised tomogram head normal, Computerised tomogram spine normal, Differential white blood cell count normal; Electrocardiogram normal, Full blood count normal, Head injury, Hyperhidrosis, Loss of consciousness; Metabolic function test normal, Photophobia, Polyuria, Vision blurred More
Severe lower back pain experienced beginning at 2 AM and woke every 30-60 minutes during the night. ... Severe lower back pain experienced beginning at 2 AM and woke every 30-60 minutes during the night. Proceeded to urinate 4 times (very unusual). Upon arising at 7 AM, proceeded to kitchen, sat down to consume coffee. After 5 minutes, the kitchen lighting became overwhelming and vision was blurred. Proceeded to move back to bed, passed out in great room, making contact with curio table injuring two locations on head. Was only out for a few seconds and then crawled to the bed, where profuse sweating started while under the covers. After laying in bed for 15 minutes, relaxed on the couch, and returned to the kitchen for breakfast. More
2873102 49 F UT 11/17/2025 COVID19
COVID19
 MODERNA
MODERNA
 3052864
3052864
Asthenia, Diplegia, Fatigue, Hypoaesthesia, Paraesthesia; Somnolence Asthenia, Diplegia, Fatigue, Hypoaesthesia, Paraesthesia; Somnolence
TINGLING THROUGHOUT MY ENTIRE BODY, LEADING TO NUMBNESS AND EVENTUAL PARALYSIS OF MY ARMS AND HANDS.... TINGLING THROUGHOUT MY ENTIRE BODY, LEADING TO NUMBNESS AND EVENTUAL PARALYSIS OF MY ARMS AND HANDS. MY HANDS LOCKED INTO A "DOLL HANDS" POSITION FOR SEVERAL HOURS. EXTREME WEAKNESS AND FULL-BODY FATIGUE. EXTREME SLEEPINESS More
2873103 77 F WA 11/17/2025 COVID19
 MODERNA
 3052996
Extra dose administered Extra dose administered
I was given two Covid-19 shots at the same pharmacy three months apart. I received the first Covid-1... I was given two Covid-19 shots at the same pharmacy three months apart. I received the first Covid-19 shot on Sep 7. The information for that shot is: Name: COVID-19 12Y+ SEASONAL (Pfizer) Manufacturer: Pfizer, INC Lot #: MY9547 Location: Pharmacy On Nov 14, 2025 I received a text message from pharmacy that new Covid shots are now available. I had forgotten that I already received a Covid shot at that same pharmacy earlier this year on Sep 7. When I arrived at the pharmacy I don't recall them asking if I already had a shot and they did not look in their records to see if I already had one for this year. Because of this, I was administered a second Covid-19 shot again. I called the nurse hotline and they asked that I report this incident. I did not experience any adverse symptoms from the early second dosage. More
2873107 20 M 11/17/2025 COVID19
FLU3
 PFIZER\BIONTECH
GLAXOSMITHKLINE BIOLOGICALS
 NA0738
34N52
Hyperhidrosis, Immediate post-injection reaction, Pallor, Syncope; Hyperhidrosis... Hyperhidrosis, Immediate post-injection reaction, Pallor, Syncope; Hyperhidrosis, Immediate post-injection reaction, Pallor, Syncope More
Patient arrives at clinic and states he is nervous and has fainted previously with a blood draw. St... Patient arrives at clinic and states he is nervous and has fainted previously with a blood draw. States he has never had difficulty with injections. States he has eaten 2 meals today and is well hydrated. Tolerated first injection well. Syncopal episode immediately following second injection. Patient fainted briefly - 2 to 3 seconds. Responded quickly to name being called and with positioning of elevated legs. Was diaphoretic and pale. Pulse was 72 and strong. Applied cold compress to forehead and given time to recover. After about 7 minutes, Sat patient up and gave water, candy bar, and encouragement. Continued to recover well. Observed for approximately 20 more minutes before being allowed to leave clinic. Advised to go home and to make sure a friend/roommate was present. Advised to receive future injections at PCP clinic rather than at a community site. More
2873108 16 M FL 11/17/2025 FLU3
FLU3
HPV9
HPV9
MENB
MENB
MNQ
MNQ
 SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.
PFIZER\WYETH
PFIZER\WYETH
SANOFI PASTEUR
SANOFI PASTEUR
 UY8861JA
UY8861JA
Y020531
Y020531
LK2636
LK2636
U8562AA
U8562AA
Brain fog, Confusional state, Dizziness, Fatigue, Injection site erythema; Injec... Brain fog, Confusional state, Dizziness, Fatigue, Injection site erythema; Injection site warmth, Pain; Brain fog, Confusional state, Dizziness, Fatigue, Injection site erythema; Injection site warmth, Pain; Brain fog, Confusional state, Dizziness, Fatigue, Injection site erythema; Injection site warmth, Pain; Brain fog, Confusional state, Dizziness, Fatigue, Injection site erythema; Injection site warmth, Pain More
Pt started the next day with tiredness & body aches. This was accompanied by redness & warmt... Pt started the next day with tiredness & body aches. This was accompanied by redness & warmth on his right upper arm. The 2nd day post vaccines he developed brain fog, confusion, exhaustion, dizziness & body aches. More
2873109 66 M TX 11/17/2025 COVID19
 PFIZER\BIONTECH
 LM2211
Exercise tolerance decreased, Gait disturbance, Tremor Exercise tolerance decreased, Gait disturbance, Tremor
shuffling gait, exercise intolerance, shaking/tremors shuffling gait, exercise intolerance, shaking/tremors
2873110 67 F MI 11/17/2025 FLU3
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 LT9HP
LT9HP
Chest discomfort, Dizziness, Dyspnoea, Headache, Musculoskeletal stiffness; Rash... Chest discomfort, Dizziness, Dyspnoea, Headache, Musculoskeletal stiffness; Rash, Rash macular, Tremor More
Patient came into the office today for Flu vaccine. Patient received a regular Flu vaccine. Patient ... Patient came into the office today for Flu vaccine. Patient received a regular Flu vaccine. Patient then stood up to walk to her car but turned around because she began to feel dizziness, chest tightness, and short of breath. These symptoms started about 5-10 minutes after receiving the Flu vaccine. Patient sat back down in the chair and nursing staff called a MERT for more assistance. Patient has not had a reaction to the Flu vaccine in the past. Nursing arrived and completed an evaluation of patient. The chest tightness was located at her breasts and moved up into her neck/jaw, described as a pressure. She denies chest pain. Patient is on oxygen baseline due to pulmonary fibrosis, asthma history. She is on 2-4L's depending on activity. At time of evaluation, patient was on 4L of oxygen. Patient was also having symptoms of leg stiffness, headache, red blotchy rash on face, and arm shakiness. Given persistent symptoms, 911/EMS was called Vitals: 98% sp02, 87-94 HR, 140/84 BP Patient states she received a Nucala injection about a month ago. After this medication was administered, patient states she felt similar symptoms but worse. Patient is due to received another Nucala injection in two days. Nursing recommended patient speak with MD to see if this injection is still recommended given recent reactions. Patient's daughter was called and informed of the above information. Patient is being taken to hospital for further work-up. More
2873112 78 M TX 11/17/2025 FLU3
 SANOFI PASTEUR
 UT8804AA
Pain, Pain in extremity, Product administered at inappropriate site Pain, Pain in extremity, Product administered at inappropriate site
injection sit was too high, just below shoulder bone, not in muscle. high soreness, unable to lift ... injection sit was too high, just below shoulder bone, not in muscle. high soreness, unable to lift arm above shoulder height without a great deal of pain. pain continues for a month and a half. More
2873114 56 F SC 11/17/2025 FLU3
 SEQIRUS, INC.
 407244
No adverse event, Product administered to patient of inappropriate age, Wrong pr... No adverse event, Product administered to patient of inappropriate age, Wrong product administered More
Patient came into the office on this day, and she requested and Flu vaccine. This MA gave the wrong ... Patient came into the office on this day, and she requested and Flu vaccine. This MA gave the wrong vaccine (Fluad High dose) No reverse action was view while in the clinic. More
2873115 22 M NE 11/17/2025 COVID19
 PFIZER\BIONTECH
Cardiac monitoring, Myocarditis Cardiac monitoring, Myocarditis
I developed Myocarditis after the vaccine I developed Myocarditis after the vaccine
✓
2873116 89 M MI 11/17/2025 COVID19
 MODERNA
 3053777
Pruritus, Rash Pruritus, Rash
Patient reported wide spread itching feeling throughout body and some rash on body Patient reported wide spread itching feeling throughout body and some rash on body
2873117 5 F CA 11/17/2025 FLU3
 SEQIRUS, INC.
 409415
Circumstance or information capable of leading to medication error, Injection si... Circumstance or information capable of leading to medication error, Injection site haemorrhage, Scratch More
Patient's mom was holding her in a hug position as immunization was being administered and chil... Patient's mom was holding her in a hug position as immunization was being administered and child abruptly pulled away causing immunizer to move with the child and slightly scratching the arm after removal of the needle syringe. No major injuries except a scratch on the child arm with minor bleeding from injection site. More
2873119 73 F WA 11/17/2025 FLU3
FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR


Back pain, Cough, Diarrhoea, Dyspepsia, Ear pain; Headache, Nausea, Paranasal si... Back pain, Cough, Diarrhoea, Dyspepsia, Ear pain; Headache, Nausea, Paranasal sinus discomfort, Productive cough, Respiratory tract congestion; Vomiting More
about an hour and half I became extremely congested in my chest. I threw up a lot of phlegm about 3 ... about an hour and half I became extremely congested in my chest. I threw up a lot of phlegm about 3 times. I had diarrhea, developed a back ache, headache, earache, indigestion, coughing, back pain, sinus pressure and I was nauseated with no temperature. These symptoms last several days. Contacted doctors office the next day and was told to drink a lot of fluids. Put hot compress on ear and back. Stay away from foods that will cause indigestion and follow back up with them in a few days. I have been sleeping a lot and today I feel some better but still feel nauseated with indigestion and have headache with the sinus pressure and earache. More
2873121 51 F GA 11/17/2025 FLU3
 SANOFI PASTEUR
 U8832CA
Arthralgia, Hypoaesthesia, Product administered at inappropriate site Arthralgia, Hypoaesthesia, Product administered at inappropriate site
patient is complaining of shoulder pain and numbness in her left arm. Complaining that immunization... patient is complaining of shoulder pain and numbness in her left arm. Complaining that immunization was given higher than she normally receives them. More
2873122 23 M 11/17/2025 FLU3
 SANOFI PASTEUR
 UT8836KA
Extra dose administered Extra dose administered
Patient says that he already got the influenza vaccine two weeks ago and shows documentation on syst... Patient says that he already got the influenza vaccine two weeks ago and shows documentation on system, upon looking at the date of 07/11/2025 there is an encounter in system but no update to his record was made until today 17/11/2025 where there was an update. More
2873125 71 F AZ 11/17/2025 COVID19
COVID19
COVID19
 NOVAVAX
NOVAVAX
NOVAVAX
 6315MF002C
6315MF002C
6315MF002C
Asthenia, Blood test, Diarrhoea, Dizziness, Fall; Fatigue, Headache, Incontinenc... Asthenia, Blood test, Diarrhoea, Dizziness, Fall; Fatigue, Headache, Incontinence, Influenza like illness, Muscular weakness; Pain in extremity, Pyrexia, Respiratory disorder More
the bottom of my feet started hurting. My arm was sore and I was achy. The next morning I woke with ... the bottom of my feet started hurting. My arm was sore and I was achy. The next morning I woke with flu like symptoms with 101.6 fever. I was incontinent and had diarrhea. Felt so very weak and dizzy then I fell. I have a headache and have some respiratory changes. I am some better today but I am still tired feeling and my legs are still very weak. I was in bed for 6 days. Felt like I was going to faint upon standing. I went to my doctor and was told I would have to ride out my symptoms. They did blood work since I am having leg aches and pain. More
2873129 82 M PA 11/17/2025 COVID19
 MODERNA
 3051995
Pericarditis Pericarditis
pt was diagnosed with pericarditis approx on 10/24/25 which was 3 weeks after the covid vaccine , pt... pt was diagnosed with pericarditis approx on 10/24/25 which was 3 weeks after the covid vaccine , pt was discharged 10/31/25 and is currently ambulatory and on ibuprofen and colchicine More
✓
2873131 53 M NC 11/17/2025 FLU3
 SANOFI PASTEUR
Hypoaesthesia, Pain, Sleep disorder Hypoaesthesia, Pain, Sleep disorder
Initial pain following dose. Assumed it was just from getting a flu shot. Pain steadily has gotten w... Initial pain following dose. Assumed it was just from getting a flu shot. Pain steadily has gotten worse. Numbness in thumb and had appeared around Nov. 5. Pain steadily increased until urgent care visit on 11/11 (and continues). Pain bad enough that Tylenol does not correct and I am awakened overnight. More
📋 Privacy Policy & Data Disclaimer