🏥 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)

⚠️ 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

ER Visits

1,191

Disabilities

570

Life Threatening

Year: VAERS ID: Age: Sex: State: Vaccine Type: Manufacturer: Lot Number: Site: Symptom: Death: Hospitalized:

🔄 Reset 📥 Export CSV

Showing 14,701 to 14,750 of 34,052 reports (Page 295 of 682)

« First ‹ Prev 1 ... 292 293 294 295 296 297 298 ... 682 Next › Last »

ID	Age	Sex	State	Date ▼	Vaccine	Manufacturer	Lot #	Symptoms	Narrative	💀
2850539	19	F	NC	07/21/2025	HPV9	MERCK & CO. INC.	Y015180	Extra dose administered Extra dose administered	3rd Dose of HPV vaccine given after previously receiving completed series. 3rd Dose of HPV vaccine given after previously receiving completed series.
2850540	6	M	TN	07/21/2025	DTAPIPV HEPA MMRV	GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC.	42Y93 H3N97 Y009348	Inappropriate schedule of product administration, No adverse event; Inappropriat... Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event; Inappropriate schedule of product administration, No adverse event More	No adverse reaction was noted. All vaccines were given on day of visit but were not needed. No adverse reaction was noted. All vaccines were given on day of visit but were not needed.
2850541	19	F	IN	07/21/2025	MMR VARCEL	MERCK & CO. INC. MERCK & CO. INC.	X026222 Y005922	Oral mucosal blistering, Oropharyngeal pain; Oral mucosal blistering, Oropharyng... Oral mucosal blistering, Oropharyngeal pain; Oral mucosal blistering, Oropharyngeal pain More	About 6 hours after getting the vaccines, the patient c/o sore throat then started getting blisters ... About 6 hours after getting the vaccines, the patient c/o sore throat then started getting blisters inside her mouth. States symptoms got worse over the following next 2 days. More
2850543	58	F	IN	07/21/2025	VARZOS	GLAXOSMITHKLINE BIOLOGICALS	EK225	Arthralgia, Mobility decreased, Shoulder injury related to vaccine administratio... Arthralgia, Mobility decreased, Shoulder injury related to vaccine administration More	Patient received shingrix vaccination on 6/6/25. On 7/21/25, the husband reported to me that shortly... Patient received shingrix vaccination on 6/6/25. On 7/21/25, the husband reported to me that shortly after the vaccination she began to have shoulder pain and restricted mobility in that arm. She went to the doctor and they referred her to an orthopedic MD. The orthopedic MD diagnosed her with SIRVA and suspects that the cause was due to the vaccine potentially being given too high. More
2850544	18	F	TN	07/21/2025	MENB	NOVARTIS VACCINES AND DIAGNOSTICS	7mn4c	Discomfort, Pain, Pain in extremity, Sleep disorder Discomfort, Pain, Pain in extremity, Sleep disorder	Two weeks post injection (7/11/25) parent called office to report patient complaints of arm throbbin... Two weeks post injection (7/11/25) parent called office to report patient complaints of arm throbbing when she's trying to sleep, hurts during the day, and hurts when she lifts her arm. Patient seen 3 days later (7/14/2025) in office for examination as pain was still present. There was no point tenderness, swelling or redness in her deltoid muscle near site of injection. No pain with passive range of motion. Treatment with naproxen sodium 220mg AM and 440mg PM since pain was worse in the evening. Recommended gentle stretching exercises to prevent stiffness, heat and ice depending which makes it feel better. 7/18/2025 Mom called back stating patient was still in discomfort. Patient was taking naproxen sodium 440mg qhs which helped but not taking the 220mg qam regularly. Still complaints of "pinching/burning" pain intermittently. Recommended increasing naproxen sodium to 440 mg BID, starting Medrol dose pack and range of motion exercises 2x/day. Recommended ortho evaluation if not improving. More
2850545	11	M	LA	07/21/2025	MNQ	NOVARTIS VACCINES AND DIAGNOSTICS	76F79	Injection site erythema, Injection site swelling Injection site erythema, Injection site swelling	Around 48 hours after injection, the patient experienced swelling and redness over upper right arm t... Around 48 hours after injection, the patient experienced swelling and redness over upper right arm that continued to worsen for around 24 hours. Parent reports treating with topical betamethasone and oral loratadine. Now resolving. Patient's parent is a family medicine physician, so it did not require an office visit. More
2850546	19	F	NY	07/21/2025	TDAP	GLAXOSMITHKLINE BIOLOGICALS	H4279	Incorrect route of product administration, Product administered at inappropriate... Incorrect route of product administration, Product administered at inappropriate site More	On 07/15/2025, I was training my new vaccine on nurse visits we had this patient, in for a PPD place... On 07/15/2025, I was training my new vaccine on nurse visits we had this patient, in for a PPD placement and TDAP. picked both vaccines I checked them; in the pts chart it showed she received her last TDAP 2017. After we brought the pt back and confirmed DOB and name, we informed the patient that her last TDAP was 2017 and she would not be due till 2027, but if she had any recent injuries like a "dog bite or cut by a rusty nail" then she could receive it sooner. Patient verbalized that she wanted the PPD first and she would call to see if she needed a PPD for nursing school she expressed that she did have "some scratches recently". As the patient was thinking on the Administration we continued with the PPD. collected the syringe and needle while I spoke to the patient about nursing school. I looked down and noticed the syringe was the TDAP (Boostrix) and she administered this as a PPD in the right mid forearm totaling the amount to 0.5 ml . I advise the patient to wait in the room and we will be back i instructed to follow me. In the hallway i said "Do you notice what just happened?" responded "oh my gosh I'm so sorry". I advised her "It's okay, we are human we make mistakes, we are going to talk to a provider and figure out how to go about this". We went to the provider by the nurse's station which was NP and brought her to a room to discuss the situation. confirmed the patient received no harm, yes, a vaccine error but it will not provide immunity to the patient and to discuss with Dr on next steps for the next date for a TDAP. We then returned to the patient and informed her of the error. The patient gave me permission to administer her PPD in the left midforearm. I placed the PPD and documented in the chart. and I then discussed with the patient that the TDAP given will not be regiven today. Patient verbalized understanding and we instructed her this will not provide immunity for TDAP, the patient expressed no symptoms and encouraged to call us if she develops any pt verbalized understanding and agreed with the plan. documented the incident in her nurse's note. As well as was made aware. On 07/16/2025 I met with Dr informed him of the situation and he verbalized that the patient's father had texted him about the incident and wanted Dr to call her and discuss. Dr stated that he will contact the patient and discuss next steps with her. Dr stated "we don't offer Tdap sooner unless they are there for a new injury so she would not be due, that will not provide her immunity" I stated "Yes I understand, I should have not brought that in the room, definitely a learning moment for all". TDAP (Boostrix) NDC 58160-842-52 Lot H4279 Exp 08/30/2027 Manufacturer GSK More
2850547	84	M	IA	07/21/2025	COVID19	MODERNA		Death Death	Resident passed away Resident passed away	✓
2850548	17	F	PA	07/21/2025	MENB	NOVARTIS VACCINES AND DIAGNOSTICS	49M9N	Laboratory test normal, Mobility decreased, Pain in extremity, X-ray normal Laboratory test normal, Mobility decreased, Pain in extremity, X-ray normal	Patient experienced severe arm pain with inability to lift arm 1 day after receiving vaccine which c... Patient experienced severe arm pain with inability to lift arm 1 day after receiving vaccine which continued through 7/14/2025 when evaluated in office More
2850549	1.08	M	CO	07/21/2025	RV5	MERCK & CO. INC.	Z007575	Extra dose administered Extra dose administered	inadvertent administration inadvertent administration
2850550	1.08	M	AR	07/21/2025	VARCEL	MERCK & CO. INC.	X021280	Faeces discoloured, Pyrexia, Rash macular, Urine output decreased Faeces discoloured, Pyrexia, Rash macular, Urine output decreased	Red, spotty rash, decreased urine out put, white stool, fever Red, spotty rash, decreased urine out put, white stool, fever
2850551	54	F	TX	07/21/2025	PNC20 PNC20 VARZOS VARZOS	PFIZER\WYETH PFIZER\WYETH GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS	lx4482 lx4482 332l4 332l4	Burning sensation, Erythema, Limb discomfort, Peripheral swelling, Pruritus; Pyr... Burning sensation, Erythema, Limb discomfort, Peripheral swelling, Pruritus; Pyrexia, Rash; Burning sensation, Erythema, Limb discomfort, Peripheral swelling, Pruritus; Pyrexia, Rash More	1 week after vaccinations patient came to show us her arms. Left arm had a slight rash with no fever... 1 week after vaccinations patient came to show us her arms. Left arm had a slight rash with no fever or swelling. Right arm was red, slightly swollen, and feverish. Patient stated that her arms have felt heavy with burning and itching sensations in both. More
2850552	33	F	CO	07/21/2025	HEP	GLAXOSMITHKLINE BIOLOGICALS	AZ4TN	Underdose Underdose	Patient was given pediatric dose of 0.5 ML instead of adult dose of 1ML. Patient was given pediatric dose of 0.5 ML instead of adult dose of 1ML.
2850553	57	M	UT	07/21/2025	PNC20 PNC20	PFIZER\WYETH PFIZER\WYETH	LP4948 LP4948	Asthenia, Erythema, Fatigue, Headache, Pain; Peripheral swelling, Pyrexia, Tende... Asthenia, Erythema, Fatigue, Headache, Pain; Peripheral swelling, Pyrexia, Tenderness More	extreme low energy, fatigue, weakness, body ache, headache, fever, arm swelling, redness and tendern... extreme low energy, fatigue, weakness, body ache, headache, fever, arm swelling, redness and tenderness More
2850554	4	M	AR	07/21/2025	DTAPIPV MMRV	SANOFI PASTEUR MERCK & CO. INC.	U7908AB Y014438	Injection site erythema, Injection site swelling, Injection site warmth; Injecti... Injection site erythema, Injection site swelling, Injection site warmth; Injection site erythema, Injection site swelling, Injection site warmth More	Parent called agency on 04/30/25. Mom reports right arm is red, swollen and warm to touch.Patient re... Parent called agency on 04/30/25. Mom reports right arm is red, swollen and warm to touch.Patient received MMRV and Quadracel on 4/29/25. Nurse looked in database and patient received Quadracel in Right arm. Was advised by nurse to apply cold cloth to site. Advised motrin or tylenol for pain. Was advised by nurse that if it looks concerning to see PCP for evaulation. Mom stated that she wanted to try cool compress first and if not better she will go to PCP for evaulation. Mother later reported that she took child to facility on 04/30/25 due to redness and rash to right arm and he was dx with and allergic reaction and was given Benadryl. More
2850555	41	F	CA	07/21/2025	UNK	UNKNOWN MANUFACTURER		Immediate post-injection reaction, Injection site pain, Pain Immediate post-injection reaction, Injection site pain, Pain	Pain at injection instantly and continued for a month. I eventually started using my right arm as mu... Pain at injection instantly and continued for a month. I eventually started using my right arm as much as I could even though I m left handed because the pain was so intense when I left my left arm a certain way. Months later, now July, my pain is almost as severe as when I first received the flu vaccine last year in October. More
2850556	59	F	NJ	07/21/2025	PNC20	PFIZER\WYETH	P-LP4947	Injection site rash, Pyrexia Injection site rash, Pyrexia	Received 0.5 mL dose of Pfizer's Pneumoccal Vaccine (Prevnar-20) IM on 7/16/2025. Slight fever ... Received 0.5 mL dose of Pfizer's Pneumoccal Vaccine (Prevnar-20) IM on 7/16/2025. Slight fever and small rash appeared on 7/17/2025. Then 7/18/2025-7/21/2025, the rash expanded but still only at the area of the administered vaccine. Rash becomes itchy and red. Called primary care doctor about symptoms on 7/21/2025. Doctor office instructed to take Benadryl and ice the area and monitor additional symptoms (must see urgent care if shortness of breath symptoms appear). First dose of Benadryl taken on 7/21/2025 and to monitor symptoms. No evidence of shortness of breath. More
2850557	14	F	IN	07/21/2025	MNQ	SANOFI PASTEUR	U8574AA	Headache, Hemiparesis, Immediate post-injection reaction, Injection site irritat... Headache, Hemiparesis, Immediate post-injection reaction, Injection site irritation, Pyrexia More	Pt had immediate muscle weakness and site irritation. Next morning, pt had fever, headache and more ... Pt had immediate muscle weakness and site irritation. Next morning, pt had fever, headache and more significant muscle weakness on her right side. By 7/18/25, all symptoms had resolved. More
2850558	11	M	WI	07/21/2025	HEP HEPA HPV9 IPV PNC20 TDAP	GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC. SANOFI PASTEUR PFIZER\WYETH GLAXOSMITHKLINE BIOLOGICALS	47D3S DN273 1965035 W1C831M HM0312 CX4HL	No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered More	Client did not experience any adverse events or treatments. The Prevnar 20 Vaccine was inadvertently... Client did not experience any adverse events or treatments. The Prevnar 20 Vaccine was inadvertently given instead of the Meningococcal ACWY Vaccine. More
2850559	12	M	AZ	07/21/2025	TDAP	SANOFI PASTEUR	U8015AA	Injection site erythema, Injection site pruritus, Injection site swelling, Injec... Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth More	The entire top of the left arm was significantly swollen, hot, itchy and red. His mother gave him ib... The entire top of the left arm was significantly swollen, hot, itchy and red. His mother gave him ibuprofen and BENADRYL before calling the clinic. All symptoms were improved by 7/17/2025, and were completely resolved by 7/19/2025. More
2850560	63	F	VA	07/21/2025	PNC20	PFIZER\WYETH	LN4931	Erythema, Pain, Pruritus, Swelling Erythema, Pain, Pruritus, Swelling	Patient presented to the clinic 5 days after receiving PCV20 vaccine in the left upper arm. Noted ar... Patient presented to the clinic 5 days after receiving PCV20 vaccine in the left upper arm. Noted area had swelling, redness, painful, and itchy. Area measured 3x2 3/4 inches in diameter. No fever, no rash/hives, no SOB, and no N/V noted at the time of her assessment. Ice pack applied. Patient seen by Dr. for further evaluation. Per his orders, patient is to continue applying ice and follow up as needed. No further actions indicated at this time. BP 131/76, Pluse 89, Respirations 18, and Temp. 98.4 oral. O2 pulse Ox 96%. More
2850561	58	F	FL	07/21/2025	UNK	UNKNOWN MANUFACTURER	U7013DA	Erythema, Induration, Injection site ulcer, Swelling, Tenderness Erythema, Induration, Injection site ulcer, Swelling, Tenderness	On 07/21/2025 donor presented with extended redness, induration, swelling, tenderness, and possible ... On 07/21/2025 donor presented with extended redness, induration, swelling, tenderness, and possible infection. RP contact and says ulcers present at site. F4100 referenced and DAE 10.2 initiated. RP request donor goes to personal physician for evaluation. More
2850562	12	F	WI	07/21/2025	HEPA HPV9 PNC20 TDAP VARCEL	GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC. PFIZER\WYETH GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC.	DN273 1965035 Y009956 CX4HL Y009956	No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered More	Prevnar 20 was administered, when the client should have received Meningococcal ACWY vaccines. Clien... Prevnar 20 was administered, when the client should have received Meningococcal ACWY vaccines. Client has not experienced any adverse reactions, events, treatments or outcomes. More
2850563	59	F	CA	07/21/2025	HEP HEP IPV IPV MMR MMR TDAP TDAP VARCEL VARCEL	DYNAVAX TECHNOLOGIES CORPORATION DYNAVAX TECHNOLOGIES CORPORATION SANOFI PASTEUR SANOFI PASTEUR MERCK & CO. INC. MERCK & CO. INC. GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS MERCK & CO. INC. MERCK & CO. INC.	945659 945659 Y1A201M Y1A201M Y008592 Y008592 DY3K7 DY3K7 Y014181 Y014181	Myalgia, Neck pain, Pain, Pain in extremity, Paraesthesia; Sleep disorder; Myalg... Myalgia, Neck pain, Pain, Pain in extremity, Paraesthesia; Sleep disorder; Myalgia, Neck pain, Pain, Pain in extremity, Paraesthesia; Sleep disorder; Myalgia, Neck pain, Pain, Pain in extremity, Paraesthesia; Sleep disorder; Myalgia, Neck pain, Pain, Pain in extremity, Paraesthesia; Sleep disorder; Myalgia, Neck pain, Pain, Pain in extremity, Paraesthesia; Sleep disorder More	Patients states that 3 days after receiving the vaccinations, she started experiencing pain and ting... Patients states that 3 days after receiving the vaccinations, she started experiencing pain and tingling sensation in her Left Arm from her shoulder down to her wrist (no fingers). Patient also complains of neck pain and pain in the muscle between her shoulder and neck. Patient has difficulty raising her left arm up without pain. Patient states that it is very difficult for her to sleep because of the pain. She is still experiencing the pain now. More
2850564	12	M	AZ	07/21/2025	UNK	UNKNOWN MANUFACTURER		Fall, Loss of consciousness Fall, Loss of consciousness	Passed out and fell down in the health dept lobby (I caught him and kept him from hitting his head).... Passed out and fell down in the health dept lobby (I caught him and kept him from hitting his head). I had him sit & drink water once he could stand up again. More
2850565	36	M	GA	07/21/2025	HEP	GLAXOSMITHKLINE BIOLOGICALS	N733B	Pruritus Pruritus	excessive itching approximately 2 hours after vaccine was given. excessive itching approximately 2 hours after vaccine was given.
2850566	1.33	M	VA	07/21/2025	DTAPIPV	SANOFI PASTEUR	U8623AA	No adverse event, Product administered to patient of inappropriate age No adverse event, Product administered to patient of inappropriate age	Quadracel was given to the 16 month old patient on 7/21/25. This vaccine is only indicated for child... Quadracel was given to the 16 month old patient on 7/21/25. This vaccine is only indicated for children ages 4-6yrs. Not aware of any reactions. More
2850567	69	M	MI	07/21/2025	TDAP	GLAXOSMITHKLINE BIOLOGICALS	l5229	Inappropriate schedule of product administration Inappropriate schedule of product administration	Patient was not due for the vaccine. Last Tdap vaccine received was on 11/17/2023. Patient was not due for the vaccine. Last Tdap vaccine received was on 11/17/2023.
2850568	66	F	ID	07/21/2025	PNC20	PFIZER\WYETH	LN4929	Erythema Erythema	Pt reported to pharmacy that her arm has a 3 inch diameter red spot. Pt reported to pharmacy that her arm has a 3 inch diameter red spot.
2850569	14	F	NJ	07/21/2025	HPV9 HPV9	MERCK & CO. INC. MERCK & CO. INC.	Z002903 Z002903	Activated partial thromboplastin time normal, Blood glucose normal, Full blood c... Activated partial thromboplastin time normal, Blood glucose normal, Full blood count normal, Loss of consciousness, Oral mucosal discolouration; Petechiae, Prothrombin time normal, Rash, Syncope More	5 minutes after receiving vaccine patient had an episode of vasovagal syncope. Patient lost complete... 5 minutes after receiving vaccine patient had an episode of vasovagal syncope. Patient lost complete consciousness for 20-30 seconds. Vitals were reassessed. After third attempt was able to obtain BP reading 82/45, blood sugar 94. EMS was called but mom denied transport and stated she would monitor at home. 12 hours after vaccine patient developed a non blanching rash on the anterior rash, petechial in size, given the history of HPV vaccination yesterday, will workup for any reason for petechiae. CBC and PT and PTT ordered which came back normal. About 30 hours after vaccine patient was advised to go to ED due to rash spreading to whole face and black dislocation in the mouth. More
2850570	70	F	NC	07/21/2025	VARZOS	GLAXOSMITHKLINE BIOLOGICALS	35a77	Erythema Erythema	Local red reaction on skin. Not treated Local red reaction on skin. Not treated
2850571	67	F	OH	07/21/2025	RSV VARZOS	PFIZER\WYETH GLAXOSMITHKLINE BIOLOGICALS	LN5487 93N4J	Erythema, Pain in extremity, Peripheral swelling, Pruritus; Erythema, Pain in ex... Erythema, Pain in extremity, Peripheral swelling, Pruritus; Erythema, Pain in extremity, Peripheral swelling, Pruritus More	One day after receiving the vaccines the patient reported swelling, redness, and itching from her sh... One day after receiving the vaccines the patient reported swelling, redness, and itching from her shoulder to her elbow. She stated it was very painful. It was recommended that she use OTC Tylenol, Advil, and Benadryl to treat her condition. She has a follow up visit with her PCP on 7/24/25. More
2850572	5	F	PR	07/21/2025	DTAP IPV	GLAXOSMITHKLINE BIOLOGICALS SANOFI PASTEUR		Vomiting; Vomiting Vomiting; Vomiting	she had a Vomit. she had a Vomit.
2850573	12	F	TN	07/21/2025	TDAP	GLAXOSMITHKLINE BIOLOGICALS	EB499	Crying, Feeling abnormal, Injection site pain, Loss of consciousness, Musculoske... Crying, Feeling abnormal, Injection site pain, Loss of consciousness, Musculoskeletal stiffness More	Patient was sitting on exam table. Within 1 to 2 minutes of vaccine administration she mentioned &qu... Patient was sitting on exam table. Within 1 to 2 minutes of vaccine administration she mentioned "feeling weird". Immediately after that she lost consciousness for about 5 seconds, her arms and leg muscles were stiff on extended position. No skin pallor, no gurgling sounds with respiration. She was placed on supine position, elevating her legs. Immediate reading Pulse and O2 : SpO2 99%, HR 84. Patient started crying, she did not know how to explain how she was feeling. Admits to some pain on administration site. BP reading at 110/70. Patient had water and a dum dum Lolli pop. After complete recovering she was monitored for about more 15 minutes, no regression on symptoms and felt normal. More
2850574	58	M	CA	07/21/2025	COVID19 COVID19 COVID19	PFIZER\BIONTECH PFIZER\BIONTECH PFIZER\BIONTECH		Computerised tomogram normal, Dizziness, Magnetic resonance imaging normal, Naus... Computerised tomogram normal, Dizziness, Magnetic resonance imaging normal, Nausea; Computerised tomogram normal, Dizziness, Magnetic resonance imaging normal, Nausea; Computerised tomogram normal, Dizziness, Magnetic resonance imaging normal, Nausea More	Extreme dizziness and nausea. Dizziness was almost paralyzing. Any movement at all would make me wan... Extreme dizziness and nausea. Dizziness was almost paralyzing. Any movement at all would make me want to throw up. Symptoms occurred almost daily for a week or two. All test results (CT scans, MRIs, etc) were negative. Went to the ER one time. More
2850575	0.33	M	VA	07/21/2025	RV5	MERCK & CO. INC.		Circumstance or information capable of leading to medication error, Inappropriat... Circumstance or information capable of leading to medication error, Inappropriate schedule of product administration, Refusal of vaccination More	Around 9am on 7/21/25, the nurse gave my son the 2nd dose of the Rotavirus vaccine . I told her he n... Around 9am on 7/21/25, the nurse gave my son the 2nd dose of the Rotavirus vaccine . I told her he never had the first dose and that we didn't t want him to have it. She dismissed what I stated and said, ?that doesn?t make sense? and continued to administer the vaccine, ignoring what I said. More
2850576	14	F	PA	07/21/2025	HPV9	MERCK & CO. INC.	Y010656	Malaise, Unresponsive to stimuli Malaise, Unresponsive to stimuli	Patient presented to office for a well-child visit. Patient was finished with exam and visit. Pati... Patient presented to office for a well-child visit. Patient was finished with exam and visit. Patient was leaving to go to check out when she stated that she does not feel so good and the clinician that had given patient her vaccine had quickly ran over the patient and lowered her to the floor. Patient did not hit her head but was unresponsive for a period of time. 911 was called and presented to office to take patient to ED to be evaluated. Patient did start responding to the provider. More
2850577	17	F	GA	07/21/2025	MENB	NOVARTIS VACCINES AND DIAGNOSTICS	CD44A	Rash Rash	RASH STARTED 2 DAYS AFTER VACCINATION NO TREATMENT NECESSARY. RASH STARTED 2 DAYS AFTER VACCINATION NO TREATMENT NECESSARY.
2850578	44	F	IA	07/21/2025	HEP HEP	GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS	7NX57 7NX57	Underdose; Underdose Underdose; Underdose	Gave the patient the vaccine in her right arm. When I went to chart the information of the vaccine i... Gave the patient the vaccine in her right arm. When I went to chart the information of the vaccine is when I realized that I grabbed the wrong dose. I notified my boss, and she informed me that I can give the patient a second dose to make it a full adult dose. I notified the patient of what happened, and the patient was understanding about the situation. More
2850579	0.58	M	ND	07/21/2025	DTPPVHBHPB DTPPVHBHPB PNC20 PNC20 RV1 RV1	MSP VACCINE COMPANY MSP VACCINE COMPANY PFIZER\WYETH PFIZER\WYETH GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS	U8267AA U8267AA MF0415 MF0415 3Z34X 3Z34X	Abnormal behaviour, Dyspnoea, Moaning, Pyrexia, Seizure like phenomena; Staring,... Abnormal behaviour, Dyspnoea, Moaning, Pyrexia, Seizure like phenomena; Staring, Tremor; Abnormal behaviour, Dyspnoea, Moaning, Pyrexia, Seizure like phenomena; Staring, Tremor; Abnormal behaviour, Dyspnoea, Moaning, Pyrexia, Seizure like phenomena; Staring, Tremor More	Patient was seen today for catch up of 4 month shots. He received vaxelis, pcv 20, and rotovirus aro... Patient was seen today for catch up of 4 month shots. He received vaxelis, pcv 20, and rotovirus around 9:30 AM. Dad stated he woke up from nap at 1pm and was acting "strange", couldn't breath, groaning, fever, would only look one way, seemed like he as in another planet, shaking, acted like a seizure. ER doctor was thinking it was a febrile seizure due to vaccine that was given. Doctor stated to continue to monitor for the next 24 hours and to alternate between tylenol and motrin. Doctor also stated to give one vaccine at a time next visit to see if the reaction happened again and to what vaccine it would happen to. More
2850580	70	F	CA	07/21/2025	PNC20	PFIZER\WYETH	Y019157	Unevaluable event Unevaluable event	Patient received PCV 21 per report Patient received PCV 21 per report
2850581	15	F	AZ	07/21/2025	DTAP	SANOFI PASTEUR	3CA20C1	Erythema, Peripheral swelling Erythema, Peripheral swelling	PATIENT HAS RED AND SWOLLEN ARM PATIENT HAS RED AND SWOLLEN ARM
2850582	19	F	AR	07/21/2025	VARCEL	MERCK & CO. INC.	Y006524	Dry skin, Dyshidrotic eczema, Pustule, Skin fissures Dry skin, Dyshidrotic eczema, Pustule, Skin fissures	Severe, burn like dyshidrotic eczema on palms of hands, fingers, wrist, antecubital fossa. Presente... Severe, burn like dyshidrotic eczema on palms of hands, fingers, wrist, antecubital fossa. Presented as small, circular spot of dry skin on wrist, quickly spread across thenar eminence up into interdigital folds. Puss filled pockets and cracked dry skin resulted over the next 7 months with little relief, used a multitude of moisturizers, triamcinolone acetonide 0.1%, clobetasol propionate 0.05%, More
2850583	35	F	OR	07/21/2025	HPV9	MERCK & CO. INC.	Z007940 (OLD MI	Myalgia Myalgia	prolonged muscular soreness in arm without paresthesia, sensation changes, or neurovascular compromi... prolonged muscular soreness in arm without paresthesia, sensation changes, or neurovascular compromise More
2850584	52	F	CO	07/21/2025	RAB RAB	SANOFI PASTEUR SANOFI PASTEUR	Y1B401M Y1B401M	Chest discomfort, Dizziness, Nausea, Palpitations, Sensation of foreign body; Sw... Chest discomfort, Dizziness, Nausea, Palpitations, Sensation of foreign body; Swollen tongue More	On 7/21/25, when the client came to receive her 4th dose of rabies vaccine, client reported symptoms... On 7/21/25, when the client came to receive her 4th dose of rabies vaccine, client reported symptoms of chest tightness, palpitations, "feeling of something stuck in the throat", nausea, lightheadedness, and tongue swelling that occurred on 7/14/25, 15 minutes post-injection of 3rd dose of rabies vaccine during drive home from clinic. Client went to PCP and reported symptoms. PCP did not provide interventions for anaphylactic reaction. More
2850589	9	F	TX	07/21/2025	MMRV MMRV	MERCK & CO. INC. MERCK & CO. INC.	X027626	Expired product administered, No adverse event; Expired product administered, No... Expired product administered, No adverse event; Expired product administered, No adverse event More	no additional AE; expired dose of PROQUAD was administered to a 9 year old, female patient; This spo... no additional AE; expired dose of PROQUAD was administered to a 9 year old, female patient; This spontaneous report was received from the Office Manager and refers to a 9-year-old female patient. Her medical history, concurrent conditions and concomitant therapies were not reported. On 25-Jun-2025, the patient started therapy with Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), (lot #X027626, expiration date: 28-May-2025) 0.5 mL (reported as .5 ml), administered by unknown route as prophylaxis (Expired product administered). The vaccine was reconstituted with sterile diluent (MERCK STERILE DILUENT) (no details provided). No additional adverse events (AE). At the reporting time, the outcome of the events was unknown. The action taken with the suspect products was not applicable. More
2850591	73	F	OK	07/21/2025	VARZOS	GLAXOSMITHKLINE BIOLOGICALS	UNK	Inappropriate schedule of product administration Inappropriate schedule of product administration	the second today/ Wrong schedule; This non-serious case was reported by a nurse via call center repr... the second today/ Wrong schedule; This non-serious case was reported by a nurse via call center representative and described the occurrence of drug dose administration interval too long in a 73-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. Previously administered products included Shingrix (received first dose on 28-APR-2023). On 14-JUL-2025, the patient received the 2nd dose of Shingrix (right arm). On 14-JUL-2025, an unknown time after receiving Shingrix, the patient experienced drug dose administration interval too long (Verbatim: the second today/ Wrong schedule). The outcome of the drug dose administration interval too long was not applicable. Additional Information: GSK Receipt Date: 14-JUL-2025 The Registered Nurse reported on behalf of a patient who received her first Shingrix vaccine on April 28th of 2023 and the second dose today which led to drug dose administration interval too long More
2850592		M	VA	07/21/2025	VARZOS VARZOS	GLAXOSMITHKLINE BIOLOGICALS GLAXOSMITHKLINE BIOLOGICALS	UNK UNK	Herpes zoster, Incomplete course of vaccination; Herpes zoster, Incomplete cours... Herpes zoster, Incomplete course of vaccination; Herpes zoster, Incomplete course of vaccination More	The patient never went back for the second dose of the series; shingles on the back of his left leg ... The patient never went back for the second dose of the series; shingles on the back of his left leg hamstring area; This non-serious case was reported by a consumer via call center representative and described the occurrence of shingles in an elderly male patient who received Herpes zoster (Shingrix) for prophylaxis. Co-suspect products included Herpes zoster (Shingrix) for prophylaxis. In AUG-2024, the patient received the 1st dose of Shingrix (left arm). On an unknown date, the patient received the 2nd dose of Shingrix. In AUG-2024, not applicable after receiving Shingrix and an unknown time after receiving Shingrix, the patient experienced incomplete course of vaccination (Verbatim: The patient never went back for the second dose of the series). In SEP-2024, the patient experienced shingles (Verbatim: shingles on the back of his left leg hamstring area). In OCT-2024, the outcome of the shingles was resolved (duration 1 month). The outcome of the incomplete course of vaccination was not applicable. It was unknown if the reporter considered the shingles to be related to Shingrix. It was unknown if the company considered the shingles to be related to Shingrix. Additional Information: GSK Receipt Date: 15-JUL-2025 The patient received his first dose of Shingrix in August of 2024 left arm. One month later he developed shingles on the back of his left leg hamstring area. The shingles resolved one month after getting the rash. The patient never went back for the second dose of the series which led to incomplete course of vaccination. More
2850593				07/21/2025	VARZOS	UNKNOWN MANUFACTURER	UNK	Diarrhoea, Feeling cold, Vomiting Diarrhoea, Feeling cold, Vomiting	Gastrointestional symptoms; vomiting; diarrhea; felt very cold and could not seem to warm up; This n... Gastrointestional symptoms; vomiting; diarrhea; felt very cold and could not seem to warm up; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of gastrointestinal symptom nos in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received Shingles vaccine. On 09-JUL-2025, an unknown time after receiving Shingles vaccine, the patient experienced gastrointestinal symptom nos (Verbatim: Gastrointestional symptoms), vomiting (Verbatim: vomiting), diarrhea (Verbatim: diarrhea) and cold (Verbatim: felt very cold and could not seem to warm up). The outcome of the gastrointestinal symptom nos, vomiting, diarrhea and cold were not reported. It was unknown if the reporter considered the gastrointestinal symptom nos, vomiting, diarrhea and cold to be related to Shingles vaccine. It was unknown if the company considered the gastrointestinal symptom nos, vomiting, diarrhea and cold to be related to Shingles vaccine. Additional Information: GSK Receipt Date: 10-JUL-2025 This case was reported by a patient via (Shingrix Chatbot) interactive digital media. The patient had received the herpes (Shingles) vaccination on Monday and yesterday, they had severe gastrointestinal symptoms with vomiting and diarrhea. After that they felt very cold, and could not seem to warm up More
2850594				07/21/2025	VARZOS	GLAXOSMITHKLINE BIOLOGICALS	UNK	Herpes zoster Herpes zoster	shingles; This non-serious case was reported by a consumer via interactive digital media and describ... shingles; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of shingles in a patient who received Herpes zoster (Shingrix) for prophylaxis. On 07-JUL-2025, the patient received Shingrix. On 08-JUL-2025, 1 days after receiving Shingrix, the patient experienced shingles (Verbatim: shingles). The outcome of the shingles was not reported. It was unknown if the reporter considered the shingles to be related to Shingrix. It was unknown if the company considered the shingles to be related to Shingrix. Additional Information: GSK Receipt Date: 11-JUL-2025 Patient received the Shingrix vaccine on July 7th 2025 and instantly developed shingles within 24 hours. Patient wanted to know why did this happen as the vaccine is supposedly 100 percent not supposed to cause this. Patient visited their doctor and he was able to explain it. This case was reported by a patient via interactive digital media. More

‹ Previous Page 295 of 682 Next ›

🏥 VAERS Vaccine Data Browser

🔒 Privacy & Data Disclaimer

About This Site

Data Source & Accuracy

Your Privacy

Medical Disclaimer

Data Interpretation

📖 Help & Search Guide

Column Icons Legend

How to Search

Understanding the Data

Using the Table

💡 Frequently Asked Questions (FAQ)

What is this site?

What is VAERS?

Is this data HIPAA compliant?

Why does this site exist?

Where does the data come from?

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

Can I trust VAERS data?

What are "adverse events"?

Why are some lot numbers listed multiple times?

How often is this data updated?

Where can I learn more?