๐Ÿฅ VAERS Vaccine Data Browser

๐Ÿ”’ Privacy & Data Disclaimer

About This Site

This is a public data browser for the Vaccine Adverse Event Reporting System (VAERS). By using this site, you acknowledge and agree to the following:

Data Source & Accuracy

  • Public Data: All data displayed comes from the publicly available VAERS database maintained by the CDC and FDA.
  • No Verification: VAERS accepts all reports without verifying medical accuracy. Reports do not prove causation between vaccines and adverse events.
  • Anyone Can Report: Healthcare providers, patients, family members, and anyone else can submit reports to VAERS.
  • Research Purpose: This data is for transparency, research, and monitoring vaccine safety signals only.

Your Privacy

  • No Personal Data Collection: This site does not collect, store, or track any personal information about visitors.
  • No Cookies: We do not use cookies except for remembering that you've seen this disclaimer (stored locally in your browser).
  • No Analytics: We do not use Google Analytics or any other tracking services.
  • Search Privacy: Your searches and filters are not logged or stored on our servers.
  • Public Data Only: The VAERS data shown here is already public and contains no personally identifiable information.

Medical Disclaimer

  • Not Medical Advice: This tool is for informational purposes only and does not provide medical advice.
  • Consult Healthcare Providers: Always consult qualified healthcare professionals for medical decisions.
  • No Liability: We are not responsible for decisions made based on this data.

Data Interpretation

  • The presence of a report does not mean the vaccine caused the adverse event.
  • Coincidental events are often reported (e.g., a heart attack that happened to occur after vaccination).
  • Serious adverse events must be reported by law, even if unrelated to the vaccine.
  • The database is useful for detecting safety signals that require further investigation.

๐Ÿ“– Help & Search Guide

Column Icons Legend

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

How to Search

๐Ÿ’ก Search Tips:
  • Select Year: Choose a specific year OR "All Years" to search across all data
  • All Years requires filters: When searching all years, you must select at least one filter (lot number, vaccine type, outcome, etc.) for performance
  • Lot number tracking: Use "All Years" + Lot Number to track lots across multiple years
  • Combine filters: Use multiple filters together to narrow results (e.g., Age + Vaccine Type + Death)
  • VAERS ID: Search for specific report by ID number
  • Age: Enter exact age (e.g., 25) or decimal (e.g., 0.5 for 6 months)
  • State: Enter 2-letter state code (e.g., CA, NY, TX)
  • Vaccine Type: Search partial names (e.g., "COVID19", "FLU", "HPV")
  • Manufacturer: Search by company (e.g., "PFIZER", "MODERNA")
  • Lot Number: Search specific vaccine lot (works great with "All Years")
  • Symptoms: Search for any symptom keyword (e.g., "fever", "rash")
  • Death/Hospitalized: Filter to only show cases with these outcomes

Understanding the Data

  • Reports are unverified: VAERS accepts all reports without medical verification
  • Not proof of causation: A report does not mean the vaccine caused the event
  • Anyone can report: Healthcare providers, patients, and family members can submit reports
  • Multiple vaccines: One report may list multiple vaccines given at the same time
  • Blank fields: Not all fields are required, so some data may be missing

Using the Table

  • Sort columns: Click column headers (ID, Age, Sex, Date, Died) to sort
  • Expand text: Click "More" to see full narrative or symptom text
  • Navigate pages: Use pagination controls at top and bottom of table
  • Export results: Click "๐Ÿ“ฅ Export CSV" to download filtered data (max 10,000 records)

๐Ÿ’ก Frequently Asked Questions (FAQ)

What is this site?

๐Ÿฅ VAERS Vaccine Data Browser is an independent, third-party data browser for publicly available VAERS (Vaccine Adverse Event Reporting System) data.

Important: This site is NOT affiliated with, endorsed by, or operated by the CDC, FDA, or any government agency. We are an independent service that makes public VAERS data easier to search and analyze.

What is VAERS?

VAERS (Vaccine Adverse Event Reporting System) is a national early warning system established in 1990 to detect possible safety problems with vaccines. It's co-managed by the CDC (Centers for Disease Control and Prevention) and FDA (Food and Drug Administration).

VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination.

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

  • Publicly available - Published by the CDC/FDA on their official website
  • De-identified - Contains no personally identifiable information (names, addresses, contact info removed)
  • Legally accessible - Available to researchers, media, and the general public under FOIA (Freedom of Information Act)
  • Not protected health information - Once de-identified and published by the government, it's no longer covered by HIPAA restrictions

This site displays the same public data available at vaers.hhs.gov/data.

Why does this site exist?

We believe in transparency and public access to health data. While the CDC/FDA provide VAERS data, their official site:

  • Is difficult to search and filter
  • Requires downloading large CSV files and technical knowledge
  • Is not user-friendly for the average person

This independent site makes the same publicly available data easier to search, filter, and understand for researchers, journalists, healthcare workers, and concerned citizens.

Where does the data come from?

All data is downloaded directly from the official CDC/FDA VAERS website at vaers.hhs.gov/data.

The data is:

  • Publicly released by the CDC/FDA every week
  • Available as downloadable CSV files
  • Imported into this site's database for easier searching
  • Displayed exactly as provided (no modifications or filtering)

This site does not collect, modify, or add to the official VAERS data.

My vaccine lot number matches one with deaths/serious events - should I be worried?

Important context:

  • VAERS reports do NOT prove causation - A report means an event occurred after vaccination, but doesn't mean the vaccine caused it
  • Anyone can report - Reports are not verified for medical accuracy before being published
  • Coincidences happen - When millions of people get vaccinated, some will experience unrelated medical events afterward
  • Large lot numbers - Popular vaccines may have hundreds of thousands of doses from one lot number
  • More vaccinations = more reports - Lots used widely will naturally have more reports

What to do:

  • Don't panic - VAERS data requires expert analysis to interpret
  • Talk to your doctor if you have concerns
  • Check official CDC/FDA safety communications for genuine safety signals
  • Remember: billions of vaccine doses have been safely administered

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

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

Limitations:

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

Bottom line: VAERS is an important tool for safety monitoring, but individual reports should not be used as proof that a vaccine caused harm.

What are "adverse events"?

An adverse event is any undesirable health occurrence that happens after vaccination, including:

  • Common reactions: Sore arm, mild fever, fatigue (usually expected)
  • Serious events: Hospitalization, disability, life-threatening illness, death
  • Coincidental events: Medical conditions that would have occurred anyway

Important: An adverse event doesn't mean the vaccine caused it - only that it occurred after vaccination. Many reported events are coincidental or unrelated.

Why are some lot numbers listed multiple times?

This is normal and expected! A person may receive multiple doses of the same vaccine from the same lot number:

  • COVID vaccines require 2-3 doses
  • HPV, Hepatitis B, and other vaccines have multi-dose schedules
  • Each dose is recorded as a separate entry

Example: Person receives Pfizer COVID dose 1 (lot ABC123) and dose 2 (lot ABC123) - lot ABC123 appears twice in their report.

How often is this data updated?

The CDC/FDA releases new VAERS data every Friday. This site is typically updated:

  • Weekly or bi-weekly for recent data
  • Check the available years to see what data is currently loaded
  • During updates, the site may be in maintenance mode temporarily

Where can I learn more?

โš ๏ธ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
๐Ÿ”„ Reset ๐Ÿ“ฅ Export CSV
ID Age Sex State Date โ–ผ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative ๐Ÿ’€ ๐Ÿฅ ๐Ÿš‘ โ™ฟ โš ๏ธ
2833283 F 03/26/2025 COVID19
COVID19
PFIZER\BIONTECH
PFIZER\BIONTECH


Allergic reaction to excipient, Arthralgia, Erythema, Pain in extremity, Swellin... Allergic reaction to excipient, Arthralgia, Erythema, Pain in extremity, Swelling; Thyroid mass More
thyroid nodules; an allergic reaction (swelling, redness) / allergy to ingredient in COVID-19 vaccin... thyroid nodules; an allergic reaction (swelling, redness) / allergy to ingredient in COVID-19 vaccine; an allergic reaction (swelling, redness); an allergic reaction (swelling, redness); pain in both arms and legs/ pain from left arm to leg, right arm to leg; pain in shoulder; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Miralax, reaction(s): "drug allergy". Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for Covid-19 immunization, reaction(s): "allergic reaction (swelling, redness)", "pain in shoulder", "allergic reaction (swelling, redness)", "pain in both arms and legs", "allergic reaction (swelling, redness)". The following information was reported: THYROID MASS (non-serious), outcome "unknown", described as "thyroid nodules"; ALLERGIC REACTION TO EXCIPIENT (non-serious), outcome "unknown", described as "an allergic reaction (swelling, redness) / allergy to ingredient in COVID-19 vaccine"; SWELLING (non-serious), ERYTHEMA (non-serious), outcome "unknown" and all described as "an allergic reaction (swelling, redness)"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "pain in both arms and legs/ pain from left arm to leg, right arm to leg"; ARTHRALGIA (non-serious), outcome "unknown", described as "pain in shoulder". The event "thyroid nodules" required physician office visit. Therapeutic measures were not taken as a result of thyroid mass. Additional information: Caller (patient) received 2 doses of the COVID-19 vaccine and her son received 3 doses. She developed thyroid nodules, and her son developed Grave's disease. After administering the dose of the vaccine, they noticed symptoms she identifies as an allergic reaction (swelling, redness) as well as pain in both arms and legs. No family history of thyroid problems. It was further reported that both caller (patient) and caller's son have an allergy to ingredient in COVID-19 vaccine, clarified a PEG, 3350 or something, allergy, an allergy to Miralax. Said the ingredient in Miralax is also in the vaccine. Caller has something that feels like pain from left arm to leg, right arm to leg, shoulder, sometimes swollen and red like an allergic reaction. Caller and caller's son both have allergy to Miralax. Caller has thyroid nodule. Wants to report this kind of problem, checked website, said 25.1 people have Grave's disease, and the size of the thyroid. This occurred after vaccine. Did not have thyroid problem before. Was after caller's 2nd dose that caller had thyroid nodule. Wants to ask how do people treat this from the vaccine since caused the problem? Caller saw endocrinologist, did not do anything, told caller to observe. Family does not have any thyroid problems. Occurred after got the vaccine, thinks not the only one case, other people have. Wants to check therapies, wants suggestion from doctor, wants to know how to treat, what do people do since was because of vaccine? Wants to know what treatment can be given.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202500063398 same reporter/patient, different vaccine dose/event (DOSE 1); More
2833284 M 03/26/2025 COVID19
PFIZER\BIONTECH

Allergy to vaccine Allergy to vaccine
they noticed symptoms/have an allergy to ingredient in COVID-19 vaccine; This is a spontaneous repor... they noticed symptoms/have an allergy to ingredient in COVID-19 vaccine; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A male patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Peg 3350, reaction(s): "Allergy: PEG 3350", notes: PEG, 3350 or something; Miralax, reaction(s): "allergy to Miralax". The following information was reported: ALLERGY TO VACCINE (non-serious), outcome "unknown", described as "they noticed symptoms/have an allergy to ingredient in COVID-19 vaccine". Additional information: The patient received 3 doses. The patient had an allergy to ingredient in COVID-19 vaccine, clarified a PEG 3350 or something allergy, an allergy to MiraLAX (said the ingredient in Miralax was also in the vaccine). No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202500063102 Same patient, product, different dose number and event;US-PFIZER INC-202500063399 Same patient, product, different dose number and event; More
2833285 83 F FL 03/26/2025 PNC20
PFIZER\WYETH

Arthralgia, Gait inability Arthralgia, Gait inability
she had severe joint pain in her back/pain; I cannot walk; This is a spontaneous report received fro... she had severe joint pain in her back/pain; I cannot walk; This is a spontaneous report received from a Consumer or other non HCP from medical information team. An 83-year-old female patient received pneumococcal 20-valent conjugate vaccine (diphtheria crm197 protein) (PREVNAR 20), on 18Mar2025 as dose number unknown, single (Batch/Lot number: unknown) at the age of 83 years, in right arm for immunisation. The patient's relevant medical history included: "very long time diabetic" (unspecified if ongoing), notes: well controlled; "sciatic" (unspecified if ongoing). Concomitant medication(s) included: ELIQUIS. The patient also took other concomitant therapy. The following information was reported: GAIT INABILITY (non-serious) with onset Mar2025, outcome "unknown", described as "I cannot walk"; ARTHRALGIA (non-serious) with onset 18Mar2025, outcome "unknown", described as "she had severe joint pain in her back/pain". Therapeutic measures were taken as a result of arthralgia. Additional information: The patient stated she was a very long time diabetic and on a few medications, but generally in pretty good health and her diabetes was well controlled. She had the pneumococcal 20 vaccine in the afternoon on Tuesday 18Mar2025. When she got home, she was fine and then in the evening, she had pain/severe joint pain in her back and the bottom of her back on the right side. She stated she thought it was possibly a sciatic which she had before and she just kind of ignored it. The next day, she was in extreme pain and she had never had the pain like that. She took a couple of TYLENOL which started to ease it. Caller states by Thursday the pain started on the left side which she had never had before and it has continually gotten worse. She took quite a few TYLENOL in the beginning which she shouldn't because she was on ELIQUIS (so she was very concerned about taking the Tylenol), but she took it anyway because the pain was so severe and now she was taking them sporadically and she was in terrific pain and it was not helping. She took from Wednesday to Thursday (19Mar2025 to 20Mar2025) about five TYLENOL. On Thursday afternoon, Thursday night it went to the other side from the right side to the left side which she never had before and now, she took some more TYLENOL, and she stopped taking them on Friday (21Mar2025), because she did not want to take anymore. On Sunday 23Mar2025, it was so bad that she had to start taking another TYLENOL at 6pm and she had to have another one in the morning (24Mar2025). The pain was so terrible that she cannot walk, and was in severe pain. She stated this all went on over the weekend. Other than the injection she had no idea why she was in such pain, but she looked at the website and saw that the side effect was joint pain. She was perfectly fine before the vaccination. The information on the batch/lot number for pneumococcal 20-valent conjugate vaccine (diphtheria crm197 protein) will be requested and submitted if and when received. More
2833286 F 03/26/2025 PNC20
PFIZER\WYETH

Extra dose administered, Feeling abnormal, Pain in extremity Extra dose administered, Feeling abnormal, Pain in extremity
Sore arm/achy the next day or two/sore arm, feeling kind of spacey and a little funny the first day ... Sore arm/achy the next day or two/sore arm, feeling kind of spacey and a little funny the first day or two, like achy; accidentally got Prevnar 20 shot twice in a year; This is a spontaneous report received from a Consumer or other non HCP from medical information team. A 69-year-old female patient received pneumococcal 20-val conj vac (dipht CRM197 protein) (PREVNAR 20), in Mar2025 as dose 2, single (Batch/Lot number: unknown). The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Prevnar 20 (dose 1), administration date: 2024, for immunisation. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Mar2025, outcome "unknown", described as "Sore arm/achy the next day or two/sore arm, feeling kind of spacey and a little funny the first day or two, like achy "; INCORRECT DOSE ADMINISTERED (non-serious) with onset Mar2025, outcome "unknown", described as "accidentally got Prevnar 20 shot twice in a year". Additional information: The patient got Prevnar 20 last summer and then got the same one in Mar2025 (a week before 24Mar2025). Forgot already got it. The patient had normal reaction that she had with all the vaccine she got in. Sore arm and kind of achy the next day or two and the patient was feeling normal no other concerning side effects. And also reported as the patient was just fine, had normal side effects, sore arm, feeling kind of spacey and a little funny the first day or two, like achy and just nothing serious at all. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2833287 M AZ 03/26/2025 COVID19
PFIZER\BIONTECH

COVID-19, Drug ineffective COVID-19, Drug ineffective
Covid after Vaccine; Covid after Vaccine; This is a spontaneous report received from a Consumer or o... Covid after Vaccine; Covid after Vaccine; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 69-year-old male patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Covid after Vaccine". Additional information: The caller stated "I'm speaking with my local doctor here, in the next little while, possibly by tomorrow morning, you know, so I'll have the full written prescription from him". When discussing the process of online enrollment, the caller stated "I feel like I have a really bad cold. I've never had Covid before, this is the first time. I dodged all of this and then I go see my grandson and they both have snotty noses and sure enough. He's 6 months old. He got Covid. We all got Covid God, I never get sick, it's so weird" After the manual FPL check was done, the caller mentioned they were going to enroll their wife and stated "I think she is speaking with her endocrinologist, cause she wanted to verify kidney function or something". After obtaining the voucher processing details, the caller stated "It's crazy, like I said when you don't get sick, you just go what the heck is going on It's been such a weird thing that you know, how are we supposed to feel or not feel. I've had all my vaccinations, so" While the caller was enrolling their spouse online, they stated " I'm half delirious as it is". The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received. More
2833288 F FL 03/26/2025 COVID19
PFIZER\BIONTECH

Therapeutic response unexpected Therapeutic response unexpected
for 24 hours after the shot I had no pain and the following week I had very little pain, that's... for 24 hours after the shot I had no pain and the following week I had very little pain, that's happened every time I've taken the Pfizer vaccine or the boosters; This is a spontaneous report received from a Consumer or other non HCP, Program ID. An 80-year-old female patient received BNT162b2 (BNT162B2 NOS), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "horribly allergic to a lot of things" (unspecified if ongoing); "Constant pain" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "for 24 hours after the shot I had no pain and the following week I had very little pain, that's happened every time I've taken the Pfizer vaccine or the boosters". Additional information: She had a mild case of Covid at the time and so she didn't take the medicine because of the listed side effects. She was horribly allergic to a lot of things and so she wasn't going to chance it, and it was a very mild case because she had had all the boosters and the vaccines. She was the only person that she knows that the next 24 hours after the Pfizer vaccine, she had absolutely no pain in her body. She was 80 years old now and she lived with constant pain, so for 24 hours after the shot she had no pain. The following week, she had very little pain and that's happened every time she had taken the Pfizer vaccine or the boosters. She didn't know what's in the Pfizer thing, but it worked for her. On 10Jan2024, she was diagnosed as positive with the Covid. She went to the ER on 08Jan with COVID but was negative on the Tuesday (09Jan2024). On Wednesday, the 10Jan2024, she was already positive, but it was a very mild case just like a little cold. She got the Paxlovid, but she ended up not using it because of side effects. She decided she was not doing any kind of drugs except for her normal regimen just because she doesn't want to end up in the ER. She had a list of 20 do not give her medicines including Benadryl. She stays away as much as possible from drugs of any kind. She was on 3 blood thinners at this point so there were two of them that were blood thinners still. Many of these drugs come with a fear of that. Batch/lot number is not provided, and it cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202500035385 same patient/drug, different event/dose; More
2833289 4 M VI 03/26/2025 UNK
UNKNOWN MANUFACTURER
LG5574
Cellulitis, Erythema, Peripheral swelling Cellulitis, Erythema, Peripheral swelling
On 3/11, arm became red. On 3/12, arm became swollen. Pt seen in ED on 3/14 and given benadryl. P... On 3/11, arm became red. On 3/12, arm became swollen. Pt seen in ED on 3/14 and given benadryl. Pt seen again 3/17 in clinic, diagnosed with cellulitis and started on Augmentin. Also had vaccines on 3/3/2025: dtap/IPV-Sanofi-2CA54C3 right arm MMRV-Merck-Y018163- left arm Hep A-Merck-Y013274-left arm More
2833290 39 F PR 03/26/2025 ANTH
ANTH
ANTH
ANTH
EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
300215A
300215A
300215A
300215A
Blood glucose normal, Burning sensation, Chest X-ray, Dizziness, Heart sounds ab... Blood glucose normal, Burning sensation, Chest X-ray, Dizziness, Heart sounds abnormal; Hypertension, Hypoaesthesia, Hypoaesthesia oral, Laboratory test, Muscular weakness; Musculoskeletal pain, Nausea, Pallor, Paraesthesia, Peripheral coldness; Speech disorder, Tachycardia, Tremor More
after member received the vaccine the following started: nausea, dizziness, pain in the shoulder bla... after member received the vaccine the following started: nausea, dizziness, pain in the shoulder blade, tingle in the fingers, cold extremities, paleness, tachycardia, high blood pressure, extremities weakness, body tremors, numb tongue, speech difficulty. at first doctors taught it was a diabetic emergency but blood sugars were normal range, Emergency Doctor auscultate mu heart and found the S2 delayed. After the event patient still has the following symptoms. Numbness of the arms and neck, tingle of the fingers, burning sensation on the shoulder blade. More
โœ“
2833291 1.25 F MA 03/26/2025 DTAP
DTAP
HIBV
HIBV
PNC20
PNC20
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH
Y97N7
Y97N7
UK201AC
UK201AC
L65574
L65574
Abdominal wall mass, Computerised tomogram abnormal, Culture negative, Drain pla... Abdominal wall mass, Computerised tomogram abnormal, Culture negative, Drain placement, Leukocytosis; Psoas abscess, Shift to the left, Swelling, Ultrasound scan abnormal, White blood cell count increased; Abdominal wall mass, Computerised tomogram abnormal, Culture negative, Drain placement, Leukocytosis; Psoas abscess, Shift to the left, Swelling, Ultrasound scan abnormal, White blood cell count increased; Abdominal wall mass, Computerised tomogram abnormal, Culture negative, Drain placement, Leukocytosis; Psoas abscess, Shift to the left, Swelling, Ultrasound scan abnormal, White blood cell count increased More
is a 15 m.o. female who presents to the office with her parents. A couple of hours ago parents noti... is a 15 m.o. female who presents to the office with her parents. A couple of hours ago parents noticed a lump on LL abdomen and walking and fine and some times standing with left knee bent. Had her 15 month WCC yesterday and had vaccines in both legs and 2 vaccines in the left thigh and one in the right thigh. Had Dtap Hib and Prevnar. The lump is on the left side in the diaper area Parent concern since pt on January 19, 2025 admitted for Bilateral inguinal node abscesses and admitted for 3 days. I and D IV clindamycin MSSA. On 01/20/25. D/C to home for 14 day course of Keflex. On 01/28/25 need I and D on the right side. Consulted with Dr and then called ER as call to expect the pt. Parents drove directly to pediatric ER. More
โœ“
2833292 52 M TX 03/26/2025 RAB
NOVARTIS VACCINES AND DIAGNOSTICS
FDP00613
Rash erythematous, Scab Rash erythematous, Scab
DONOR PRESENTS WITH RED BUMPS WITH SCABS TO THE LEFT FOREARM AND BICEP. DENIES ANY ITHCINESS AT THIS... DONOR PRESENTS WITH RED BUMPS WITH SCABS TO THE LEFT FOREARM AND BICEP. DENIES ANY ITHCINESS AT THIS TIME. More
2833293 0.17 M 03/26/2025 PNC15
MERCK & CO. INC.

Tremor Tremor
one week after receiving vaccine infant began having tremor like hand movements that have continued ... one week after receiving vaccine infant began having tremor like hand movements that have continued for two months More
2833294 70 F NY 03/26/2025 MMR
GLAXOSMITHKLINE BIOLOGICALS
2JX7Y
Incorrect route of product administration, No adverse event Incorrect route of product administration, No adverse event
Patient inadvertently given PRIORIX IM. No adverse event noted or reported Patient inadvertently given PRIORIX IM. No adverse event noted or reported
2833295 42 F GA 03/26/2025 IPV
SANOFI PASTEUR
X1D141M
Dysgeusia, Paraesthesia, Sensory disturbance Dysgeusia, Paraesthesia, Sensory disturbance
Immediately after Polio vaccine, patient reported feeling a "weird" feeling in her arm, st... Immediately after Polio vaccine, patient reported feeling a "weird" feeling in her arm, stomach then a "weird" taste in mouth. Then a tingly feeling in arm. No respiratory issues reported by patient. Patient was observed for 15-20 mins, she said the "weird" feeling and taste was gone. More
2833296 28 M CO 03/26/2025 FLU3
FLU3
FLU3
SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.
944467
944467
944467
Alcohol use, Arthralgia, Dizziness, Fatigue, Lymph node pain; Myalgia, Odynophag... Alcohol use, Arthralgia, Dizziness, Fatigue, Lymph node pain; Myalgia, Odynophagia, Oropharyngeal pain, Pyrexia, SARS-CoV-2 test negative; Sleep disorder, Streptococcus test negative More
I worked here and this was my former employer. 24 hours later I began to feel really faint and tire... I worked here and this was my former employer. 24 hours later I began to feel really faint and tired. I believe that I asked to go home. That evening, I developed a severe throat and swallowing pain around my neck lymph nodes that persisted for the next five days. I also had general internal infection-like reactions of a mild fever and aching joints and muscles that could be somewhat alleviated by alternating 800 mg doses of ibuprofen and 1000 mg doses of Tylenol every four hours. I got a test done at the doctor's office, and I had neither strep nor Covid-19, yet was not tested for the flu. I was woken every night for those five nights in immense pain as the either previous dose of ibuprofen or Tylenol wore off. After being wretchedly sick for five days, I decided that I was not going to miss a planned weekend trip in the golden leaf-changing trees, and so I went and took even more ibuprofen and Tylenol and still drank plenty of whiskey talking with friends old and new around the fire before passing out in the trunk of my friend's car camper for the night. I believe I shocked my system back to normalcy, because the next morning I awoke feeling wonderful and had no further problems. More
2833297 71 F FL 03/26/2025 COVID19
MODERNA

Arthralgia, Inflammation Arthralgia, Inflammation
Inflammation and pain on inside of left wrist. Same arm as injection Inflammation and pain on inside of left wrist. Same arm as injection
2833298 52 F IL 03/26/2025 VARZOS
VARZOS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS


Dyspnoea, Feeling jittery, Gait inability, Influenza like illness, Loss of consc... Dyspnoea, Feeling jittery, Gait inability, Influenza like illness, Loss of consciousness; Musculoskeletal stiffness, Nausea, Respiratory arrest, Sleep disorder More
During the night following the vaccine, I started feeling flu like symptoms and was unable to sleep.... During the night following the vaccine, I started feeling flu like symptoms and was unable to sleep. I was also very jittery. When I started to feel as if I was going to vomit or pass out, I tried to get to the bathroom but was unable to walk once I got from the bedroom to the hallway. I fell to the floor and called to my husband. He rushed to my side, and I blacked out, went stiff, started breathing very heavily, then was not breathing. This lasted approximately 10 seconds. More
2833299 45 F WA 03/26/2025 HEPA
MERCK & CO. INC.
Y017625
Disturbance in attention, Dizziness, Tremor Disturbance in attention, Dizziness, Tremor
Body trimmers, 100 degree fever, dizzy, unable to focus Body trimmers, 100 degree fever, dizzy, unable to focus
2833300 2 F OR 03/26/2025 DTAPIPV
GLAXOSMITHKLINE BIOLOGICALS

Product administered to patient of inappropriate age Product administered to patient of inappropriate age
patient did not report a vaccine reaction. the age of the patient was the concern as the age requir... patient did not report a vaccine reaction. the age of the patient was the concern as the age requirement was not met. More
2833301 48 F VA 03/26/2025 COVID19
COVID19
MODERNA
MODERNA


Alopecia, Blood test, Burning sensation, Computerised tomogram, Crying; Hypoaest... Alopecia, Blood test, Burning sensation, Computerised tomogram, Crying; Hypoaesthesia, Muscle atrophy, Pain More
Body aches, burning sensations, numbness in face and back of neck, hair is GONE from all her skin, m... Body aches, burning sensations, numbness in face and back of neck, hair is GONE from all her skin, muscle loss, looks like she is a skeleton, pain all the time. Dr does nothing for her , we are trying a new DR More
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2833302 27 M MO 03/26/2025 MNQ
TYP
NOVARTIS VACCINES AND DIAGNOSTICS
SANOFI PASTEUR
AMVB030A
W1A361M
Arthralgia, Hypoaesthesia, Muscular weakness, Pain, Paraesthesia; Arthralgia, Hy... Arthralgia, Hypoaesthesia, Muscular weakness, Pain, Paraesthesia; Arthralgia, Hypoaesthesia, Muscular weakness, Pain, Paraesthesia More
The member stated he first observed the symptoms on the same day the vaccination was given. At first... The member stated he first observed the symptoms on the same day the vaccination was given. At first the symptom was tingling, especially down his right arm, from the tricep down to fingertips. The week of March 17 he started feeling pain in his elbow and wrist, infrequent and mostly not bad, I'd rate it a 4 out of 10 , but could be a 8/10 in rare occasions. The pain happens when his arm or wrist is at a different angle than normal and when it happens the pain is very fast and doesn't normally linger. That same week the feeling of being numb, especially in his ring and pinky fingers up to the right side of his upper forearm was and is happening more consistently. His grip strength and arm strength feels weaker than normal. The treatment plan is for the member to receive bilateral upper extremity nerve conduction and an electromyography study done ASAP as of 3/25/2025. More
2833303 36 F FL 03/26/2025 MMR
MMR
MMR
MERCK & CO. INC.
MERCK & CO. INC.
MERCK & CO. INC.



Blood ethanol, Brain natriuretic peptide, Creatinine renal clearance, Fibrin D d... Blood ethanol, Brain natriuretic peptide, Creatinine renal clearance, Fibrin D dimer, Full blood count; International normalised ratio, Loss of consciousness, Malaise, Metabolic function test, Prothrombin time; Toxicologic test, Troponin, Urine analysis More
MMR was given and approximately 30 minutes after receiving the vaccine, employee felt 'sick... MMR was given and approximately 30 minutes after receiving the vaccine, employee felt 'sick'. Sat on toilet to move bowels and passed out. Brough to ER where she was treated with IVF's and monitored for other symptoms. More
2833304 78 F GA 03/26/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
47N3Y
Injection site erythema Injection site erythema
PT CAME IN FOLLOWING DAY (3/26/25) COMPLAINING OF REDNESS AT THE INJECTION SITE. I ENCOURAGED HER T... PT CAME IN FOLLOWING DAY (3/26/25) COMPLAINING OF REDNESS AT THE INJECTION SITE. I ENCOURAGED HER TO KEEP A COOL COMPRESS AND APPLY TOPICAL TO TREAT ITCHING More
2833305 69 M ID 03/26/2025 COVID19
PFIZER\BIONTECH
33130134
Blood test, Computerised tomogram, Death, Haematological malignancy Blood test, Computerised tomogram, Death, Haematological malignancy
no immediate reaction. 3 years later rare aggressive blood cancer fatal in one week. no immediate reaction. 3 years later rare aggressive blood cancer fatal in one week.
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2833306 10 F MA 03/26/2025 HPV9
MERCK & CO. INC.
Y012865
Syncope Syncope
The patient arrived to the clinic this morning for their well child check. The patient's PCP or... The patient arrived to the clinic this morning for their well child check. The patient's PCP ordered a Gardasil (HPV) vaccine at the visit and this nurse went to administer at the end of the appointment. Mom chose to not wait the recommended 15 minute observation time. The patient was walking out of the clinic and experienced a syncopal event. This nurse caught her by placing this nurse hands/arms under the patient's armpits. and was lowered in to a chair to prevent a fall to the floor. The patient was still not responsive but slowly came to a few seconds later. The patient vomited x 2 and was pale and sweaty. This nurse assessed patient's blood pressure and it was a low result. The patient rested for about 5-10 minutes and then was able to have some crackers and water. The patient's blood pressure was checked again about 15 minutes later and was then stable. The pcp came in and assessed the patient and it was determined that the patient was safe to leave the clinic. More
2833307 67 F ID 03/26/2025 COVID19
PFIZER\BIONTECH
33130134
Blood test, Polymyalgia rheumatica Blood test, Polymyalgia rheumatica
4 years later diagnosed with Polymyalgia Rheumatica 4 years later diagnosed with Polymyalgia Rheumatica
2833308 83 F NC 03/26/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
9L944
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
THE EVENING AFTER RECEIVING THE VACCINE, THE PATIENT EXPERIENCED SIGNIFICANT SWELLING AND REDNESS AT... THE EVENING AFTER RECEIVING THE VACCINE, THE PATIENT EXPERIENCED SIGNIFICANT SWELLING AND REDNESS AT THE INJECTION SITE. SUGGESTED COOL COMPRESS OR ICE TO THE AREA AND SEE THE DOCTOR IF NO IMPROVEMENT IN 1 WEEK. SUGGESTED IBUPROFEN ALSO BUT PATIENT IS HIGHLY ALLERGIC TO NSAIDS SO WILL TAKE TYLENOL ARTHRITIS. More
2833309 49 M 03/26/2025 TDAP
GLAXOSMITHKLINE BIOLOGICALS
Y59D4
Injection site erythema, Injection site mass, Injection site pruritus, Injection... Injection site erythema, Injection site mass, Injection site pruritus, Injection site swelling More
Patient reports "a knot" under the skin at injection sit. Patient also reports redness, it... Patient reports "a knot" under the skin at injection sit. Patient also reports redness, itchiness and swelling to the injection site. Symptoms began approximately one day after administration and was ongoing for several days. More
2833310 32 F NY 03/26/2025 HPV9
MERCK & CO. INC.
Y010802
Extra dose administered Extra dose administered
Additional (extra) dose given. Pt verbalized that she had had 2 doses, 3 doses were documented. Additional (extra) dose given. Pt verbalized that she had had 2 doses, 3 doses were documented.
2833311 15 M OH 03/26/2025 IPV
SANOFI PASTEUR
W1C741M
Nausea, Pallor, Tachypnoea Nausea, Pallor, Tachypnoea
Shortly after second immunization (IPV) patient developed significant nausea, tachypnea, And pale di... Shortly after second immunization (IPV) patient developed significant nausea, tachypnea, And pale discoloration. - No rash, blood pressure remained stable, no vomiting - Prescribed dose of Zofran and provided patient with juice. Patient was monitored for approximately 20 minutes before third injection was given. Patient tolerated the next injection well and was monitored for approximately 20 minutes after. More
2833312 6 M WI 03/26/2025 DTAPIPV
HEP
MMR
VARCEL
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
5G23d
4D333
Y004114
Y011015
Malaise, Vomiting; Malaise, Vomiting; Malaise, Vomiting; Malaise, Vomiting Malaise, Vomiting; Malaise, Vomiting; Malaise, Vomiting; Malaise, Vomiting
RN gave patient vaccines. Patient went to waiting room while his sibling was vaccinated. Within 10 m... RN gave patient vaccines. Patient went to waiting room while his sibling was vaccinated. Within 10 minutes, patient started vomiting. Patient's mother then said patient was not feeling well and had not eaten anything all day. RN gave patient water and nutrigrain bar and continued to observe patient for several minutes. Patient then said he was feeling ok and wanted to leave. Patient's other sibling does have chicken pox and Patient was exposed to that child as well. More
2833313 71 M IN 03/26/2025 COVID19
MODERNA
EG6V4N1F621R
Mass, Pain, Skin discolouration Mass, Pain, Skin discolouration
So his wife came in today and stated that pt said he got a lump after his vaccine 4 weeks later, it ... So his wife came in today and stated that pt said he got a lump after his vaccine 4 weeks later, it started small and it is now the size of a golf ball has not gone down, it is painful and discolored. More
2833314 1 F MN 03/26/2025 HEPA
MMR
VARCEL
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
DN273
Y004116
Y011712
Body temperature increased, Cough, Drug hypersensitivity, Rash morbilliform; Bod... Body temperature increased, Cough, Drug hypersensitivity, Rash morbilliform; Body temperature increased, Cough, Drug hypersensitivity, Rash morbilliform; Body temperature increased, Cough, Drug hypersensitivity, Rash morbilliform More
Full body measles rash from head to toe for 7 days, 103 degree temperature for 4 days, cough for 7 d... Full body measles rash from head to toe for 7 days, 103 degree temperature for 4 days, cough for 7 days More
2833315 34 F VA 03/26/2025 UNK
UNK
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
FAV041
FAV041
Asthenia, Dizziness, Erythema, Face oedema, Rash; Rash pruritic, Urticaria Asthenia, Dizziness, Erythema, Face oedema, Rash; Rash pruritic, Urticaria
WEAKNESS, LIGHT HEADED, PRURITIS RASH (ENTIRE BODY), FACIAL EDEMA, MACULAR ERYTHEMA, URTICARIAL WHEA... WEAKNESS, LIGHT HEADED, PRURITIS RASH (ENTIRE BODY), FACIAL EDEMA, MACULAR ERYTHEMA, URTICARIAL WHEALS. GIVEN 40MG MEDROL, 50 MG BENADRYL. More
2833316 0.83 M AZ 03/26/2025 DTAPIPVHIB
SANOFI PASTEUR
UJ994AA
Expired product administered Expired product administered
Expired vaccine given - date of expiration date is 3/14/25 Expired vaccine given - date of expiration date is 3/14/25
2833317 71 F CT 03/26/2025 VARZOS
GLAXOSMITHKLINE BIOLOGICALS
fj9a7
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
per ma at office pt presented to office with redness and swelling around injection site 1 week after... per ma at office pt presented to office with redness and swelling around injection site 1 week after faccine More
2833318 40 M TX 03/26/2025 MMR
TDAP
GLAXOSMITHKLINE BIOLOGICALS
SANOFI PASTEUR


Extra dose administered, No adverse event; Extra dose administered, No adverse e... Extra dose administered, No adverse event; Extra dose administered, No adverse event More
On March 21, 2025, the patient visited the clinic for due vaccines and presented her shot record. MM... On March 21, 2025, the patient visited the clinic for due vaccines and presented her shot record. MMR , Hep B , Flu , Varicella and TD vaccines were administered and the patient was monitored for fifteen minutes without experiencing any side effects. It was brought to my attention by the provider of the week, who alerted me to the mistake that I had given the MMR vaccine too early. I did a review of this patient chart and found out that I administered another MMR vaccine, which the patient had already received 3 days prior due to an oversight. I noted the vaccine's received date as March 18, 2024, instead of the correct date, March 18, 2025, which was an oversight. i followed up with the patient on 3/24/2025 and patient denied any adverse effect and stated that he is okay. moving forward I will ensure that I am more meticulous when conducting review of patients records to prevent a reoccurrence of such. More
2833319 4 F WA 03/26/2025 MMRV
MERCK & CO. INC.
Y018157
Injection site erythema, Injection site rash, Injection site swelling, Rash, Ras... Injection site erythema, Injection site rash, Injection site swelling, Rash, Rash pruritic More
Rash starting on right thigh at injection site 3/24/25. Enlarging for the past few days. Now, erythe... Rash starting on right thigh at injection site 3/24/25. Enlarging for the past few days. Now, erythematous raised boarders with central clearning without crusting or scale. No warmth or tenderness. Describes rash as mildly painful and pruritic. No vesicles noted. More
2833320 68 M VA 03/26/2025 FLU3
FLU3
FLU3
SANOFI PASTEUR
SANOFI PASTEUR
SANOFI PASTEUR



Allergy test positive, Allergy to plants, Arthralgia, Bursitis, Exercise toleran... Allergy test positive, Allergy to plants, Arthralgia, Bursitis, Exercise tolerance decreased; Food allergy, Inflammation, Injection site pain, Milk allergy, Muscular weakness; Pain, Pain in extremity, Seasonal allergy More
After the shot, pain began developing close to my left humerus in the biceps brachii (long head) alo... After the shot, pain began developing close to my left humerus in the biceps brachii (long head) along a 3-4 zone. It has not abated over time, and my arm becomes quite weak and sore with various exercises (I can no long do any pushups, for example). Raising my arm upwards or exercising generates considerable pain, and the shoulder joint also seems sore. I decided to give my condition a full six months before filing this report, hoping it would subside, but it has not. I received the shot 10 days after receiving a yellow jacket sting in the same arm, but the injury had fully subsided before getting the Fluzone injection. More
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2833321 80 F IN 03/26/2025 COVID19
RSV
PFIZER\BIONTECH
PFIZER\WYETH
LP1776
LG9827
Dizziness, Nausea, Urticaria; Dizziness, Nausea, Urticaria Dizziness, Nausea, Urticaria; Dizziness, Nausea, Urticaria
Reports developed hives on entire body within 48 hours of receiving vaccines. Had nausea and lighthe... Reports developed hives on entire body within 48 hours of receiving vaccines. Had nausea and lightheadedness the first few days. Reporting symptoms on 3/26/25 and that still has hives on chest and back. Denied and difficulty breathing. More
2833322 2 M WI 03/26/2025 HEPA
MMRV
VARCEL
GLAXOSMITHKLINE BIOLOGICALS
MERCK & CO. INC.
MERCK & CO. INC.
DN273
Y014435
Y014868
No adverse event, Wrong patient; No adverse event, Wrong patient; No adverse eve... No adverse event, Wrong patient; No adverse event, Wrong patient; No adverse event, Wrong patient More
Patient presented to the clinic with his mother to get caught up on immunizations. Patient's si... Patient presented to the clinic with his mother to get caught up on immunizations. Patient's sister was also present to get caught up on her immunizations as well. Patient was due for a Hepatitis A, MMR and Varicella. Patient was given a Hepatitis A, Varicella and mistakenly given his sister's MMRV instead of plain MMR. Patient's mother was notified right away, the doctor who evaluated was also notified right away. She then contacted the pharmacy to ensure patient safety. No adverse reactions or symptoms occurred. More
2833323 4 F CA 03/26/2025 MMRV
MERCK & CO. INC.

No adverse event, Product storage error No adverse event, Product storage error
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per... Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event. More
2833324 4 M GA 03/26/2025 DTAPIPV
GLAXOSMITHKLINE BIOLOGICALS
U8209CB
Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling
Localized reaction to right thigh progressively enlarged to 5x5 inches of redness since approximatel... Localized reaction to right thigh progressively enlarged to 5x5 inches of redness since approximately 8:00am on 3/25/2025. He has associated swelling and tenderness to the thigh. No respiratory symptoms or fevers. Seen at provider on 3/26/2025 at 2:15 pm. Patient is clinically well appearing. Recommended Tylenol, Motrin, Benadryl for comfort. More
2833325 36 F TX 03/26/2025 HEP
DYNAVAX TECHNOLOGIES CORPORATION
945658
Injection site erythema, Injection site induration, Injection site warmth Injection site erythema, Injection site induration, Injection site warmth
RIGHT DELTOID, INJECTION SITE, HOT TO TOUCH, LARGE KNOT, PAINFUL ARM WITH MOVEMENT, REDNESS. TREATME... RIGHT DELTOID, INJECTION SITE, HOT TO TOUCH, LARGE KNOT, PAINFUL ARM WITH MOVEMENT, REDNESS. TREATMENT- ANTIHISTAMINE, ICE, ADVIL More
2833326 23 F NY 03/26/2025 COVID19
COVID19
MODERNA
MODERNA
007B21A
006C21A
Agoraphobia, Anxiety, Menstruation irregular, Panic attack; Agoraphobia, Anxiety... Agoraphobia, Anxiety, Menstruation irregular, Panic attack; Agoraphobia, Anxiety, Menstruation irregular, Panic attack More
I had been on Zoloft for 9 years and was told that I did not need to see a therapist or psychiatrist... I had been on Zoloft for 9 years and was told that I did not need to see a therapist or psychiatrist after college and could you receive Zoloft through my general practitioner; this is to provide context of how well mental health wise I was doing before this. Around 2 weeks after the first dose, I experienced intense anxiety seemingly randomly (still experiencing), anxiety and panic attacks (for a year after), agoraphobia (for 2-3 years after), and an irregular menstrual cycle with intense physical symptoms (for 3 years after). More
2833327 8 M 03/26/2025 COVID19
PFIZER\BIONTECH
LM2045
Expired product administered, No adverse event Expired product administered, No adverse event
PATIENT RECEIVED EXPIRED VACCINE, NO ADVERSE EVENT REPORTED BY FAMILY PATIENT RECEIVED EXPIRED VACCINE, NO ADVERSE EVENT REPORTED BY FAMILY
2833328 4 F CA 03/26/2025 MMRV
MERCK & CO. INC.
y019465
No adverse event, Product storage error No adverse event, Product storage error
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per... Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event. More
2833329 64 F NM 03/26/2025 TDAP
VARZOS
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
7kd5b
H97H2
Lip pruritus, Lip swelling, Pruritus, Swelling face; Lip pruritus, Lip swelling,... Lip pruritus, Lip swelling, Pruritus, Swelling face; Lip pruritus, Lip swelling, Pruritus, Swelling face More
approx 1-2 hours from inoculation: Swelling of lips, jaw, itching at site of swelling, lasting at le... approx 1-2 hours from inoculation: Swelling of lips, jaw, itching at site of swelling, lasting at least until 2 days after. benadryl helping, told to seek medical attention if any difficulty breathing occurs or if symptoms dont improve with benadryl More
2833330 1.17 M CA 03/26/2025 MMRV
MERCK & CO. INC.
y019465
No adverse event, Product storage error No adverse event, Product storage error
Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per... Vaccine was shipped refrigerated and then subsequently placed in the freezer for clinic storage. Per manufacturer, patient needing to be revaccinated. No adverse symptoms or outcome related to the event. More
2833331 84 F FL 03/26/2025 RSV
PFIZER\WYETH

Fatigue, Lymphadenopathy, Myalgia, Pyrexia Fatigue, Lymphadenopathy, Myalgia, Pyrexia
Patient comes to the office 3/25/2025 accompanied by her husband. She had the RSV vaccine on Friday... Patient comes to the office 3/25/2025 accompanied by her husband. She had the RSV vaccine on Friday. Since then she has developed some swollen glands underneath her jaw, fever yesterday, fatigue and myalgias. Her chronic headache is no different. She was developing a canker sore on her right lip before she got the vaccine. No chills, night sweats, ear pain, sore throat, shortness of breath, cough, nausea or vomiting. No diarrhea. More
2833332 65 F NY 03/26/2025 RSV
PFIZER\WYETH

Rash pruritic Rash pruritic
Body itch rash starting from Ears, to neck, face, back, chest, arms. No treatment except for allergy... Body itch rash starting from Ears, to neck, face, back, chest, arms. No treatment except for allergy OTC stuff. More