🏥 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 💀 🏥 🚑 ♿ ⚠️
2868042 77 M WV 10/23/2025 FLU3
 SANOFI PASTEUR
 U8764BB
Balance disorder, Extra dose administered, Influenza like illness, Pain Balance disorder, Extra dose administered, Influenza like illness, Pain
The patient received Fluzone HD 10/17/25. Two days after being vaccinated (10/19/25), the patient e... The patient received Fluzone HD 10/17/25. Two days after being vaccinated (10/19/25), the patient experienced aches, pains, flu-like symptoms, and felt his balance was off. By 10/22/25, the aches, pains, and flu-like symptoms had abated, but his balance is still currently bothering him. More
2868043 60 F MO 10/23/2025 FLU3
 SANOFI PASTEUR
 U8864AA
Injection site erythema, Injection site warmth Injection site erythema, Injection site warmth
Patient called to inform that she is having a reaction to the flu shot that she received in her left... Patient called to inform that she is having a reaction to the flu shot that she received in her left arm. She has redness that she described as being about 4 finger-widths wide running from the injection site down her bicep. She said it feels warm, but not worsening with minor pain. I offered for her to seek medical attention ASAP if she thinks it is needed. She said she is not going to ER immediately and would monitor the redness throughout the evening and tomorrow. I told her if she seeks medical attention to please let us know. More
2868044 79 F TX 10/23/2025 FLU3
 SEQIRUS, INC.
Injection site erythema Injection site erythema
Redness where injection was given; Redness where injection was given;
2868045 67 F VA 10/23/2025 FLU3
 SANOFI PASTEUR
 u8862AA
Syncope Syncope
Fainted after vaccine Fainted after vaccine
2868047 38 F AL 10/23/2025 FLU3
 SANOFI PASTEUR
 U8864BA
Extra dose administered Extra dose administered
Patient was accidentally given another flushot after receiving one at doctor's office on 10/8 Patient was accidentally given another flushot after receiving one at doctor's office on 10/8
2868048 65 F UT 10/23/2025 FLU3
FLU3
PNC21
PNC21
 SANOFI PASTEUR
SANOFI PASTEUR
MERCK & CO. INC.
MERCK & CO. INC.
 U8847BA
U8847BA
Z003579
Z003579
Ataxia, Decreased appetite, Headache, Malaise, Nasal congestion; Nausea, Pain, P... Ataxia, Decreased appetite, Headache, Malaise, Nasal congestion; Nausea, Pain, Pyrexia, Respiratory tract congestion; Ataxia, Decreased appetite, Headache, Malaise, Nasal congestion; Nausea, Pain, Pyrexia, Respiratory tract congestion More
Headache, body aches, ataxia, nasal congestion, chest congestion, fever (101.2), malaise. Symptoms ... Headache, body aches, ataxia, nasal congestion, chest congestion, fever (101.2), malaise. Symptoms resolving within 24 hours but followed by anorexia and nausea continuing to date (8 days so far) More
2868049 45 F VA 10/23/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 P327D
Erythema, Feeling hot, Swelling face Erythema, Feeling hot, Swelling face
Patient received the Influenza vaccine on 10/21/25 and 10:06 am from a nurse at a staff flu vaccine ... Patient received the Influenza vaccine on 10/21/25 and 10:06 am from a nurse at a staff flu vaccine clinic in the lobby. Patient reports she experienced facial swelling, facial warmth and redness approximately 2 hours after the injection and last most of the day. Denies any airway issues. Vaccine supervisor recommended patient follow up with Team Member Health for reporting and testing. More
2868056 62 M TN 10/23/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 cy53g
Blood test, Cellulitis, Influenza, Pain in extremity, Rash Blood test, Cellulitis, Influenza, Pain in extremity, Rash
Patient received fluarix vaccine on 10/19 at 10am. Had onset of severe flu symptoms 10/19 at 11:30p... Patient received fluarix vaccine on 10/19 at 10am. Had onset of severe flu symptoms 10/19 at 11:30pm. Evening of 10/20 his rt leg hurt and developed a rash from ankle up towards knee. He went to the ER to rule out blood clot or shingles. ER Dr treated him for Cellulitis at rt leg with antibiotics. More
2868057 21 M AK 10/23/2025 FLU3
 SANOFI PASTEUR
 U8983AA
Cardiac monitoring, Dyspnoea, Feeling hot, Throat tightness Cardiac monitoring, Dyspnoea, Feeling hot, Throat tightness
throat tightening (mild) associated with hot feeling, but no difficulty swallowing or angioedema on ... throat tightening (mild) associated with hot feeling, but no difficulty swallowing or angioedema on exam. Sensation of a little short of breath on time of arrival but this did not advance to visible of objective signs or symptoms. All vitals normal the entire 60+ minutes of observation and all symptoms resolved at time of discharge. More
2868058 72 M CA 10/23/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.
 HD9876
370274
Insomnia, Malaise, Restlessness; Insomnia, Malaise, Restlessness Insomnia, Malaise, Restlessness; Insomnia, Malaise, Restlessness
Felt ill and restless. Could not sleep. Would toss and turn all night. The worst phase lasted one we... Felt ill and restless. Could not sleep. Would toss and turn all night. The worst phase lasted one week. Took a second week to fully recover. More
2868059 72 M 10/23/2025 COVID19
COVID19
FLU3
FLU3
 MODERNA
MODERNA
SANOFI PASTEUR
SANOFI PASTEUR



Atrial fibrillation, Atrial flutter, Blood test, Echocardiogram, Electrocardiogr... Atrial fibrillation, Atrial flutter, Blood test, Echocardiogram, Electrocardiogram; Tachycardia; Atrial fibrillation, Atrial flutter, Blood test, Echocardiogram, Electrocardiogram; Tachycardia More
Tachycardia with aFib and aFlutter starting signs the eve of Sep 15/16 and clear tachycardia ongoing... Tachycardia with aFib and aFlutter starting signs the eve of Sep 15/16 and clear tachycardia ongoing for 4 days (Sep 20, 21, 22, 23) - ER on 23 but unaware of tachycardia prior. Due to timing post vaccination, cannot rule out antiidiotypic antibody response leading to aFib. More
✓
2868065 1.25 M AZ 10/23/2025 FLU3
 SEQIRUS, INC.
 407001
Extra dose administered Extra dose administered
Patient was given a second dose of flu vaccine this year when he had already received one for this f... Patient was given a second dose of flu vaccine this year when he had already received one for this flu season on 10/7. He had already received the recommended 2 dose series for 1st time administration last year More
2868066 22 F IN 10/23/2025 FLU3
TDAP
 SEQIRUS, INC.
GLAXOSMITHKLINE BIOLOGICALS

Flushing, Pruritus; Flushing, Pruritus Flushing, Pruritus; Flushing, Pruritus
Light reaction: all over itching full body itching arms, back, scalp, minimal face flushing, feels l... Light reaction: all over itching full body itching arms, back, scalp, minimal face flushing, feels like onset of hives but have had worse hive outbreaks, not that bad. (likely Related to Tdap Boostrix, patient receives seasonal influenza shots with no reactions.) (Received shots little over 24 hours after a whole blood donation.) More
2868078 1.25 F VA 10/23/2025 FLU3
 SANOFI PASTEUR
Extra dose administered Extra dose administered
She had Fluzone on 10/13/25 & was given another Fluzone on 10/22/25 by error. She had Fluzone on 10/13/25 & was given another Fluzone on 10/22/25 by error.
2868448 26 F WA 10/23/2025 FLU3
 SANOFI PASTEUR
 U8764DB-PVT
Exposure during pregnancy, Product administered to patient of inappropriate age Exposure during pregnancy, Product administered to patient of inappropriate age
Pt was notified. EDD 2/24/26 G: 5 P: 4 No Sx from Pt Pt was notified. EDD 2/24/26 G: 5 P: 4 No Sx from Pt
2867507 IL 10/22/2025 HPV9
 MERCK & CO. INC.
 W026152
Expired product administered, No adverse event Expired product administered, No adverse event
No additional AE; Nurse reported that an expired dose of GARDASIL 9 was administered to a patient.; ... No additional AE; Nurse reported that an expired dose of GARDASIL 9 was administered to a patient.; This spontaneous report has been received from an other health professional, regarding to a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, concomitant medications, and previous drug reactions or allergies were not reported. On 14-Oct-2025, the patient was vaccinated with a expired dose of Human Papillomavirus 9-valent Vaccine, Recombinant (GARDASIL 9) at a dose of 0.5 milliliter (ml), as prophylaxis (lot #W026152, expiration date: 29-JAN-2025) (dose, route of administration, anatomical site of injection)( Expired product administered). More
2867508 IL 10/22/2025 HEP
 DYNAVAX TECHNOLOGIES CORPORATION
Inappropriate schedule of product administration Inappropriate schedule of product administration
Patient Late Getting the Second Dose; Initial report received on 02-Oct-2025. A pharmacist reported... Patient Late Getting the Second Dose; Initial report received on 02-Oct-2025. A pharmacist reported that a patient received HEPLISAV-B (hepatitis B vaccine) for hepatitis B immunization and has not received the second dose yet. No medical history or concomitant medications were reported. In Dec-2024, the patient received dose 1 of a hepatitis B vaccine [HEPLISAV-B (lot number, expiration date, NDC number, route, and site not available)]. On 02-Oct-2025, approximately 305 days after receiving the first dose of HEPLISAV-B, the patient attempted to receive the second dose of HEPLISAV-B. The outcome was not reported. Reporter declined to provide further information. Company Comment: The company assessed the event as non-serious.; Sender's Comments: The company assessed the event as non-serious. More
2867509 66 M FL 10/22/2025 PNC20
PNC20
PNC20
 PFIZER\WYETH
PFIZER\WYETH
PFIZER\WYETH


Arthralgia, Back pain, Fatigue, Free prostate-specific antigen positive, Headach... Arthralgia, Back pain, Fatigue, Free prostate-specific antigen positive, Headache; Influenza A virus test negative, Influenza B virus test negative, Malaise, Myalgia, Pain in extremity; Pyrexia, SARS-CoV-2 test negative, Sleep disorder More
headache; muscle ache; joint pain; fever; was in such pain I couldn't sleep; fatigue; upper/low... headache; muscle ache; joint pain; fever; was in such pain I couldn't sleep; fatigue; upper/lower legs, my knees, my back, and my muscles were aching; upper/lower legs, my knees, my back, and my muscles were aching; sounds like a virus; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A 66-year-old male patient received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), on 06Oct2025 as dose number unknown, single (Batch/Lot number: unknown) at the age of 66 years, in right arm for immunisation. The patient's relevant medical history included: "High cholesterol" (ongoing); "Hypertension" (ongoing); "low testosterone" (unspecified if ongoing); "thyroid cancer" (unspecified if ongoing); "thyroid was removed" (unspecified if ongoing). Concomitant medication(s) included: TESTOPEL taken for blood testosterone decreased; METOPROLOL oral taken for hypertension; AMLODIPINE/BENAZEPRIL oral taken for hypertension; ROSUVASTATIN oral; LEVOTHYROXINE oral taken for thyroid cancer. Vaccination history included: Covid-19 vaccine (DOSE 1, SINGLE, UNKNOWN MANUFACTURER), for Covid-19 Immunization; Covid-19 vaccine (DOSE 2, SINGLE, UNKNOWN MANUFACTURER), for Covid-19 Immunization. The following information was reported: FATIGUE (non-serious) with onset 12Oct2025, outcome "unknown"; PYREXIA (non-serious) with onset 12Oct2025, outcome "unknown", described as "fever"; HEADACHE (non-serious) with onset 12Oct2025, outcome "unknown"; ARTHRALGIA (non-serious) with onset 12Oct2025, outcome "recovering", described as "joint pain"; MYALGIA (non-serious) with onset 12Oct2025, outcome "recovering", described as "muscle ache"; VIRAL INFECTION (non-serious) with onset 12Oct2025, outcome "unknown", described as "sounds like a virus"; PAIN IN EXTREMITY (non-serious), BACK PAIN (non-serious) all with onset 12Oct2025, outcome "unknown" and all described as "upper/lower legs, my knees, my back, and my muscles were aching"; SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE (non-serious) with onset 12Oct2025, outcome "unknown", described as "was in such pain I couldn't sleep". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache, myalgia, arthralgia, pyrexia, sleep disorder due to general medical condition, insomnia type, fatigue, pain in extremity, back pain, viral infection. Additional information: The patient got every adverse reactions possible and they were still lingering on 4 days after they've started. The patient's doctor had really no recommendation in terms of how to treat medically to either reduce the severity or to eliminate the side effects which the patient got, headache, muscle ache, joint pain, fever, everyone that's listed except for pain at the injection site. Most of the muscle pain and joint pain had subsided, but the patient had waves of fever, the patient got a low-grade fever and then it went away, it came back. The patient did not take any previous pneumonia vaccines, like Prevnar 13 and primary doctor said the patient had got this new Prevnar 20 and it only takes one shot, so, the patient agreed give it to him, but he didn't discuss any of the potential side effects, the patient felt like he had pneumonia. The patient was in such pain he couldn't sleep the other night, his muscles... legs, upper/lower legs, knees, back, and muscles were aching and so were his joints. The patient didn't' get any side effects until 7 days later. He felt perfectly fine for the first week. It was Sunday night into Monday morning that the patient started feeling poorly, started feeling it the patient thought it was on 12Oct2025, 4 days ago. The patient even tested under his doctor's recommendation; the patient went out and took the covid and flu A and B test and they were all negative. That's why the patient started to search the side effects of the vaccine and low and behold, the patient had virtually every one of them. The doctor told patient to take Mucinex cold and flu and Nyquil at night, the patient was actually been doing that and that's minimized most of the symptoms but the patient certainly didn't expect that after he had a low grade fever and then it went away that it would come back and it's done that 2 or 3 times. The patient had never had this type of reaction to any vaccines. None. In addition to the Mucinex and Nyquil, caller added, and lots of water. The patient also had the headache came and went and been taking Ibuprofen for that because the other medications didn't seem to touch the headache. But they addressed muscle pains and aches and not sure they were doing anything for the fever either. When the patient spoke to doctors, they didn't have a lot of answers, they didn't even suggest, when the patient mentioned it could be side effects from the vaccination, they said it sounds like a virus and recommended the guidance the patient said. The patient doubted it, he took off sick days maybe once every 5 years, the patient didn't get sick very often, the patient never had covid and the patient only took the first two doses of the vaccine. The patient felt better off and on, it just kept coming back, which was the part that was more frustrating then anything, it just kept coming back. 7 days after vaccination, the patient felt like he was "dying". The patient had muscle ache, joint hurt. The patient had headache. The patient had a fever. He couldn't sleep. The patient was not made aware of the side effects. The side effects that came on basically Sunday (12Oct2025) evening of this week, which was 6 and a half days after the took the shot, Monday the 6th of Oct (06Oct2025). Muscle pain and the couldn't sleep, fatigue, headache, joint pain. All of the side effects could have listed on website, except for pain at the injection site. The patient didn't have any pain or swelling. The patient had taken Tylenol. He had taken Mucinex. He had taken ZzzQuil. He had taken all kinds of things, Mucinex, Ibuprofen. Batch/lot number is not provided, and it cannot be obtained. More
2867510 F FL 10/22/2025 COVID19
 PFIZER\BIONTECH
Vasculitis Vasculitis
neuropathy vasculitis; This is a spontaneous report and received from Consumer or other non HCPs fro... neuropathy vasculitis; This is a spontaneous report and received from Consumer or other non HCPs from medical information team, Program ID. A female patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications and included unspecified blood thinners. On an unspecified date, the patient experienced from neuropathy vasculitis and began shortly after she received the Pfizer Comirnaty vaccines. The reporter strongly believes there is a connection between the vaccine and the diagnosis. He expressed a desire to know whether Pfizer is aware of this as a side effect and how many patients have been affected by this. And, if so, what can be done to treat or possibly reverse it. He acknowledged that no one has a clear finger to point with 100% confidence in the connection, but there is a strong likelihood of a suspected connection. Other professionals have also correlated the COVID vaccine with his mother's condition, especially considering her current and previous medical history of being on blood thinners, which may have contributed to the condition in combination with the vaccine. He suggested that this could be an uncharted area or something not publicized. He shared that his mother is in daily, constant pain due to nerve conditions and can barely walk. The condition has had a negative impact and affects the entire family. Since the onset, they have been consulting various medical professionals, who remain puzzled. She has been referred to every department and even undergone cancer treatment reviews to explore possible solutions. Outcome of the event was not recovered. The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received. More
2867511 F 10/22/2025 COVID19
 PFIZER\BIONTECH
Exposure via partner, Vaginal discharge Exposure via partner, Vaginal discharge
vaginal discharge following vaccination of husband; vaginal discharge following vaccination of husba... vaginal discharge following vaccination of husband; vaginal discharge following vaccination of husband; This is a spontaneous report received from a Consumer or other non HCP. A female patient in her 40's was exposed to BNT162b2 (BNT162B2 NOS), as dose number unknown, single (Batch/Lot number: unknown) other for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: EXPOSURE VIA PARTNER (non-serious), VAGINAL DISCHARGE (non-serious), outcome "recovered" and all described as "vaginal discharge following vaccination of husband". Additional information: The patient experienced vaginal discharge for one week following her husband's vaccination with the Pfizer COVID-19 Vaccine. The patient believed this to be the result of "shedding" from the vaccine. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. Amendment: This follow-up report is being submitted to amend previous information: case validity (reassessed as valid due to exposure via partner). More
2867533 1.33 F 10/22/2025 DTAP
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
 9PT2F
U8767BA
Erythema, Swelling; Erythema, Swelling Erythema, Swelling; Erythema, Swelling
Mother of patient presented to clinic 22Oct25, 2 days after the vaccines were administered. She stat... Mother of patient presented to clinic 22Oct25, 2 days after the vaccines were administered. She stated patient had a swollen red area larger than the patients palm, approximately 4-5 inches in diameter. Mother was informed of creation of the VAERS report and recommended the patient to be seen by a pediatrician or ER. Mother stated no other symptoms. More
2867535 26 F MD 10/22/2025 FLU3
 SEQIRUS, INC.
Diarrhoea, Fatigue Diarrhoea, Fatigue
Diarrhea followed by increasing fatigue Diarrhea followed by increasing fatigue
2867536 0.33 M KY 10/22/2025 DTAPIPV
HIBV
PNC20
RV5
 SANOFI PASTEUR
MERCK & CO. INC.
PFIZER\WYETH
MERCK & CO. INC.
 u8623aa
Wrong product administered; Wrong product administered; Wrong product administer... Wrong product administered; Wrong product administered; Wrong product administered; Wrong product administered More
Wrong Vaccine given (Quadacel) Wrong Vaccine given (Quadacel)
2867537 10 M WI 10/22/2025 COVID19
 MODERNA
 5PP37
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
No adverse reaction at the time, just wrong dose given to patient No adverse reaction at the time, just wrong dose given to patient
2867538 6 F WI 10/22/2025 COVID19
 MODERNA
 5PP37
Incorrect dose administered, No adverse event Incorrect dose administered, No adverse event
No adverse reaction, wrong dose given No adverse reaction, wrong dose given
2867540 73 F VA 10/22/2025 FLU3
 SANOFI PASTEUR
 u8862ca
Bladder disorder, Blood urine present, Diarrhoea Bladder disorder, Blood urine present, Diarrhoea
Patient reported diarrhea, bladder issues and blood in urine. Per patient went to the ER. Was unable... Patient reported diarrhea, bladder issues and blood in urine. Per patient went to the ER. Was unable to gather what treatment besides epipen was given. More
2867542 63 F MD 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 7FY52
Pruritus, Urticaria Pruritus, Urticaria
Employee reported hives to the inner thighs, lower abdomen, back and along the bra line the day afte... Employee reported hives to the inner thighs, lower abdomen, back and along the bra line the day after receiving vaccine. Reported Mild itching from hives. No redness or swelling to the site of injection. Denies SOB or trouble breathing. Took Xyzal and sx resolved. More
2867543 37 F MI 10/22/2025 COVID19
COVID19
FLU3
FLU3
 PFIZER\BIONTECH
PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
 NA0738
NA0738
UT8852JA
UT8852JA
Appendicectomy, Diarrhoea, Gastrointestinal disorder, Imaging procedure, Laborat... Appendicectomy, Diarrhoea, Gastrointestinal disorder, Imaging procedure, Laboratory test; Malaise; Appendicectomy, Diarrhoea, Gastrointestinal disorder, Imaging procedure, Laboratory test; Malaise More
Patient came into the Wellness Center for influenza and COVID 19 vaccinations on 10/10/2025 at 0916A... Patient came into the Wellness Center for influenza and COVID 19 vaccinations on 10/10/2025 at 0916AM. She reports " I felt yucky Friday evening, Saturday morning I had diarrhea, and slowly my stomach got worse and worse! I went to ER at 1030 and had an emergency appendectomy at 2 in the morning! They said it was 18cm or mm? I?m not sure supposed to be 1-4 and it was 18 and ready to burst!" More
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2867545 76 F OH 10/22/2025 COVID19
COVID19
COVID19
FLU3
FLU3
FLU3
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR
 LN0588
LN0588
LN0588
Arterial catheterisation, Cardiac pacemaker insertion, Central venous catheteris... Arterial catheterisation, Cardiac pacemaker insertion, Central venous catheterisation, Computerised tomogram, Dysphagia; Endotracheal intubation, Laboratory test, Magnetic resonance imaging, Middle cerebral artery stroke, Myocarditis bacterial; Septic cerebral embolism, Streptococcal endocarditis, Subacute endocarditis, X-ray; Arterial catheterisation, Cardiac pacemaker insertion, Central venous catheterisation, Computerised tomogram, Dysphagia; Endotracheal intubation, Laboratory test, Magnetic resonance imaging, Middle cerebral artery stroke, Myocarditis bacterial; Septic cerebral embolism, Streptococcal endocarditis, Subacute endocarditis, X-ray More
Endocarditis Myocarditis Infection by Streptococcus Acute and subacute bacterial endocarditis Arteri... Endocarditis Myocarditis Infection by Streptococcus Acute and subacute bacterial endocarditis Arterial ischemic stroke, MCA, left acute(HCC) Septic Embolism Streptococcal endocarditis (HCC) Dysphagia More
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2867546 82 M IA 10/22/2025 COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
RSV
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
MODERNA
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
PFIZER\BIONTECH
 NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
3041770
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
NA0589
Acute myocardial infarction, Alanine aminotransferase normal, Albumin globulin r... Acute myocardial infarction, Alanine aminotransferase normal, Albumin globulin ratio normal, Anion gap, Aspartate aminotransferase increased; Base excess decreased, Basophil count normal, Basophil percentage decreased, Blood albumin normal, Blood alkaline phosphatase normal; Blood bicarbonate decreased, Blood bilirubin increased, Blood calcium normal, Blood chloride normal, Blood creatinine increased; Blood glucose normal, Blood lactic acid increased, Blood pH increased, Blood potassium normal, Blood sodium decreased; Blood urea nitrogen/creatinine ratio, Blood urea normal, Brain natriuretic peptide increased, C-reactive protein normal, Carbon dioxide abnormal; Carbon dioxide normal, Chest X-ray, Computerised tomogram thorax, Electrocardiogram, Eosinophil count normal; Eosinophil percentage, Fibrin D dimer increased, Globulins increased, Glomerular filtration rate decreased, Haematocrit decreased; Haemoglobin decreased, Immature granulocyte count, Lymphocyte count normal, Lymphocyte percentage decreased, Mean cell haemoglobin concentration normal; Mean cell haemoglobin increased, Mean cell volume increased, Mean platelet volume increased, Monocyte count increased, Monocyte percentage increased; Neutrophil count increased, Neutrophil percentage increased, PCO2 decreased, PO2 decreased, Platelet count normal; Procalcitonin normal, Protein total normal, Red blood cell count decreased, Red cell distribution width normal, Troponin I increased; Venous oxygen saturation normal, White blood cell count increased; Asthenia, Burning sensation, Chest discomfort, Disorientation, Fatigue; Hypoaesthesia, Myocardial infarction, Pallor; Acute myocardial infarction, Alanine aminotransferase normal, Albumin globulin ratio normal, Anion gap, Aspartate aminotransferase increased; Base excess decreased, Basophil count normal, Basophil percentage decreased, Blood albumin normal, Blood alkaline phosphatase normal; Blood bicarbonate decreased, Blood bilirubin increased, Blood calcium normal, Blood chloride normal, Blood creatinine increased; Blood glucose normal, Blood lactic acid increased, Blood pH increased, Blood potassium normal, Blood sodium decreased; Blood urea nitrogen/creatinine ratio, Blood urea normal, Brain natriuretic peptide increased, C-reactive protein normal, Carbon dioxide abnormal; Carbon dioxide normal, Chest X-ray, Computerised tomogram thorax, Electrocardiogram, Eosinophil count normal; Eosinophil percentage, Fibrin D dimer increased, Globulins increased, Glomerular filtration rate decreased, Haematocrit decreased; Haemoglobin decreased, Immature granulocyte count, Lymphocyte count normal, Lymphocyte percentage decreased, Mean cell haemoglobin concentration normal; Mean cell haemoglobin increased, Mean cell volume increased, Mean platelet volume increased, Monocyte count increased, Monocyte percentage increased; Neutrophil count increased, Neutrophil percentage increased, PCO2 decreased, PO2 decreased, Platelet count normal; Procalcitonin normal, Protein total normal, Red blood cell count decreased, Red cell distribution width normal, Troponin I increased; Venous oxygen saturation normal, White blood cell count increased; Asthenia, Burning sensation, Chest discomfort, Disorientation, Fatigue; Hypoaesthesia, Myocardial infarction, Pallor; Acute myocardial infarction, Alanine aminotransferase normal, Albumin globulin ratio normal, Anion gap, Aspartate aminotransferase increased; Base excess decreased, Basophil count normal, Basophil percentage decreased, Blood albumin normal, Blood alkaline phosphatase normal; Blood bicarbonate decreased, Blood bilirubin increased, Blood calcium normal, Blood chloride normal, Blood creatinine increased; Blood glucose normal, Blood lactic acid increased, Blood pH increased, Blood potassium normal, Blood sodium decreased; Blood urea nitrogen/creatinine ratio, Blood urea normal, Brain natriuretic peptide increased, C-reactive protein normal, Carbon dioxide abnormal; Carbon dioxide normal, Chest X-ray, Computerised tomogram thorax, Electrocardiogram, Eosinophil count normal; Eosinophil percentage, Fibrin D dimer increased, Globulins increased, Glomerular filtration rate decreased, Haematocrit decreased; Haemoglobin decreased, Immature granulocyte count, Lymphocyte count normal, Lymphocyte percentage decreased, Mean cell haemoglobin concentration normal; Mean cell haemoglobin increased, Mean cell volume increased, Mean platelet volume increased, Monocyte count increased, Monocyte percentage increased; Neutrophil count increased, Neutrophil percentage increased, PCO2 decreased, PO2 decreased, Platelet count normal; Procalcitonin normal, Protein total normal, Red blood cell count decreased, Red cell distribution width normal, Troponin I increased; Venous oxygen saturation normal, White blood cell count increased; Asthenia, Burning sensation, Chest discomfort, Disorientation, Fatigue; Hypoaesthesia, Myocardial infarction, Pallor More
NSTEMI, given albuterol/ipratropium 3ml inhalation; aspirin chewable 324m; nitroglycerin continuous... NSTEMI, given albuterol/ipratropium 3ml inhalation; aspirin chewable 324m; nitroglycerin continuous infusion; furosemide 20mg IV push; heparin infusion. More
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2867547 46 F NE 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 LD9Y5
Injection site abscess, Injection site inflammation, Injection site pain, Inject... Injection site abscess, Injection site inflammation, Injection site pain, Injection site vesicles, Nausea More
Presented to clinic post treatment for abscess to left deltoid post influenza vaccine on 9/19/25. St... Presented to clinic post treatment for abscess to left deltoid post influenza vaccine on 9/19/25. States area was inflamed, painful to the touch, fluid filled and causing nausea 10 days post injection. More
2867548 33 F GA 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 D5h44
Musculoskeletal chest pain, Mycobacterium tuberculosis complex test negative, Pa... Musculoskeletal chest pain, Mycobacterium tuberculosis complex test negative, Pain More
15 minutes after flu shot , started having sharp chest pain left side 3rd ICS and Left side 5th mid ... 15 minutes after flu shot , started having sharp chest pain left side 3rd ICS and Left side 5th mid clavicular ICS. Sharp pain intermittent for the next 16 hours . Some sharp pains throughout body but mostly chest pain . I do not typically have chest pains More
2867549 19 F OH 10/22/2025 FLU3
 SEQIRUS, INC.
 406995
Arthralgia, Pain in extremity Arthralgia, Pain in extremity
influenza vaccine 9/17/25 persistent, intermittent (2-3 days per weak) right arm/shoulder pain sinc... influenza vaccine 9/17/25 persistent, intermittent (2-3 days per weak) right arm/shoulder pain since receiving vaccine More
2867551 40 F CO 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
Eye swelling, Urticaria Eye swelling, Urticaria
hives and swollen eye hives and swollen eye
2867552 66 F NY 10/22/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 UA47CA
UA47CA
Abdominal pain upper, Dizziness, Headache, Hypoaesthesia, Nausea; Trismus Abdominal pain upper, Dizziness, Headache, Hypoaesthesia, Nausea; Trismus
Lock Jaw, face numb, Nausea Dizzy Headache Stomach ache Lock Jaw, face numb, Nausea Dizzy Headache Stomach ache
2867553 81 F PA 10/22/2025 COVID19
FLU3
 MODERNA
SANOFI PASTEUR
 3052671
U8764BB
Abdominal pain upper, Diarrhoea, Rash, Rash erythematous, Rash pruritic; Abdomin... Abdominal pain upper, Diarrhoea, Rash, Rash erythematous, Rash pruritic; Abdominal pain upper, Diarrhoea, Rash, Rash erythematous, Rash pruritic More
The patient reports that a couple of days of after vaccination she developed a slight rash on her st... The patient reports that a couple of days of after vaccination she developed a slight rash on her stomach that was red and a little itchy but not bumpy. She also reports stomach pain and diarrhea. After 2 days she called her primary care provider. She was told to wait one more day and then call back if it had not resolved. However, by the next day her symptoms had improved and her rash was gone so she did not call back. She states that this is the first time she has had a reaction after receiving these vaccines. More
2867554 57 M MO 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 9CC9K
Arthralgia, Shoulder injury related to vaccine administration Arthralgia, Shoulder injury related to vaccine administration
Employee reported ongoing pain in right shoulder/deltoid after receiving required seasonal influenza... Employee reported ongoing pain in right shoulder/deltoid after receiving required seasonal influenza vaccine. More
2867556 1.25 M MN 10/22/2025 COVID19
COVID19
COVID19
 MODERNA
MODERNA
MODERNA
 3052579
3052579
3052579
C-reactive protein normal, Haematocrit normal, Haemoglobin normal, Lymphocyte pe... C-reactive protein normal, Haematocrit normal, Haemoglobin normal, Lymphocyte percentage increased, Neutrophil percentage; Platelet count normal, Red blood cell sedimentation rate normal, Streptococcus test negative, Synovitis, White blood cell count normal; X-ray limb normal More
synovitis of L leg synovitis of L leg
2867557 43 F TN 10/22/2025 FLU3
 SANOFI PASTEUR
 tfaa2542
Arthralgia, Pain in extremity Arthralgia, Pain in extremity
Pt has shoulder and arm pain 6 days post vaccine- advised pt to take ibuprofen see MD if it doesn�... Pt has shoulder and arm pain 6 days post vaccine- advised pt to take ibuprofen see MD if it doesn't resolve More
2867560 63 M CA 10/22/2025 COVID19
 PFIZER\BIONTECH
 NA4457
Fatigue, Myalgia, Pyrexia, Rhinorrhoea Fatigue, Myalgia, Pyrexia, Rhinorrhoea
Runny nose, fever, muscle aches, fatigue for 9 days Runny nose, fever, muscle aches, fatigue for 9 days
2867561 82 F WA 10/22/2025 COVID19
 PFIZER\BIONTECH
 NA4457
Asthenia, Chills, Headache, Pain, Pyrexia Asthenia, Chills, Headache, Pain, Pyrexia
chills, fever, headache, all over achy, no energy chills, fever, headache, all over achy, no energy
2867562 29 F ME 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 5EF45
Arthralgia Arthralgia
left shoulder pain left shoulder pain
2867563 23 F MO 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 33CM4
Nausea, Rash, Urticaria Nausea, Rash, Urticaria
Hives, rash from scalp to feet, nausea. Self administration of p.o. Benadryl, Zyrtec, Tylenol. IM st... Hives, rash from scalp to feet, nausea. Self administration of p.o. Benadryl, Zyrtec, Tylenol. IM steroid. More
2867564 79 F PA 10/22/2025 COVID19
COVID19
 MODERNA
MODERNA
 3052087
3052087
Dry eye, Dysgeusia, Eye irritation, Eye pain, Eye pruritus; Heart rate increased... Dry eye, Dysgeusia, Eye irritation, Eye pain, Eye pruritus; Heart rate increased, Nasal congestion, Pruritus, Upper-airway cough syndrome, Urticaria More
pt says about 10 minutes after the vaccine she developed a burning feeling in both eyes. She had fas... pt says about 10 minutes after the vaccine she developed a burning feeling in both eyes. She had fast heart rate some metalic taste, nasal congestion, nasal drip that went away. Her face and body was itching. Had a few hives on her chin. Both eyes started itching, burning and had sharp pains in them. The eye pain was so bad it caused her to see her eye Dr. She was told to try using vevye drops, blink vitamin, refresh releva. She is still having eye pain and dry eyes so will also use Restasis and bion drops. She will follow up with her eye Dr. in 2 weeks. More
2867566 54 F GA 10/22/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 NA05687
NA05687
Fatigue, Injection site erythema, Injection site pain, Injection site reaction, ... Fatigue, Injection site erythema, Injection site pain, Injection site reaction, Injection site swelling; Malaise, Urticaria More
Beginning the day after the vaccine (10/15/2025), patient experienced pain, swelling, and a welt at ... Beginning the day after the vaccine (10/15/2025), patient experienced pain, swelling, and a welt at the injection site. The area of swelling and redness expanded down to the patient's elbow. Today (10/22/2025), the swelling is going down, but the patient continues to feel malaise and fatigue that she associates with the adverse reaction. More
2867567 6 F GA 10/22/2025 FLU3
 GLAXOSMITHKLINE BIOLOGICALS
 D5H4Y
Injection site discolouration, Injection site erythema Injection site discolouration, Injection site erythema
Large erythematous patch coving majority of deltoid and bicep. Injection site noted with white ring ... Large erythematous patch coving majority of deltoid and bicep. Injection site noted with white ring surrounding site. Treated with oral Benadryl and Topical Triamcinolone on 10/21/25 and 10/22/25. Symptoms started on 10/21/2025. More
2867569 54 M GA 10/22/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 3052296
406986
Fatigue, Malaise, Rash, Rash macular; Fatigue, Malaise, Rash, Rash macular Fatigue, Malaise, Rash, Rash macular; Fatigue, Malaise, Rash, Rash macular
The day after the vaccines (10/07/2025), the patient developed painless, flat, red spots in a cluste... The day after the vaccines (10/07/2025), the patient developed painless, flat, red spots in a cluster on his right leg. The patient also reported experiencing malaise and fatigue. Symptoms had resolved by 10/10/2025 More
2867570 57 M 10/22/2025 COVID19
FLU3
VARZOS
 MODERNA
SANOFI PASTEUR
GLAXOSMITHKLINE BIOLOGICALS
 3052087
UT8770KA
9C75Y
Ear swelling, Skin warm; Ear swelling, Skin warm; Ear swelling, Skin warm Ear swelling, Skin warm; Ear swelling, Skin warm; Ear swelling, Skin warm
Patient came to the pharmacy to report swelling and heat in his right ar. He states he called his pr... Patient came to the pharmacy to report swelling and heat in his right ar. He states he called his provider and was advised to go to the Urgent Care for follow-up. Patient was given 7 days worth of Cephalexin 500mg BID. He was told to return in 7 days if symptoms have not improved and to use moist heat over the area. More
2867572 78 F MN 10/22/2025 COVID19
 PFIZER\BIONTECH
Extra dose administered, No adverse event Extra dose administered, No adverse event
Patient did not report receiving covid immunization the previous month. No adverse events noted aft... Patient did not report receiving covid immunization the previous month. No adverse events noted after monitoring patient. Patient educations on sign/symptoms to monitor for by provider More
2867573 72 F MN 10/22/2025 COVID19
 PFIZER\BIONTECH
 NA4452
Arthralgia, Chills, Myalgia, Pain in extremity Arthralgia, Chills, Myalgia, Pain in extremity
Patient had a dose of the covid vaccine in the morning and that evening she had a sore arm that even... Patient had a dose of the covid vaccine in the morning and that evening she had a sore arm that evening. Later in the evening and on the following day she had chills, more muscle aches, and achy joints. She started to take tylenol 1000mg every 6 hours on Monday night through Wednesday morning. She stated the pains and chills had subsided by Wednesday and that she was then feeling much better. More
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