The OpenVAERS Project

VAERS is the Vaccine Adverse Event Reporting System put in place in 1990. It is a voluntary reporting system that has been estimated to account for only 1% ( see the Lazarus Report) of vaccine injuries. OpenVAERS is built from the HHS data available for download at vaers.hhs.gov.

The OpenVAERS Project allows browsing and searching of the reports without the need to compose an advanced search (more advanced searches can be done at medalerts.org or vaers.hhs.gov). To start searching OpenVAERS, please use the red button below.

Reports are current through June 17, 2022.

All fields can be combined as filters. Each search term will narrow the search. The text fields can accept only a single search term.

V-Safe Reports Only

Report Received
Deceased
State
Gender
Age Range
can also be used as a min or max age
VAERS ID:
Vax Type:
eg. "DTP" or "MMR"
Vax Name:
eg. "covid19" or "gardasil"
Symptom:
Description:

Page 5 of 24602 Results 41 - 50 of 246017

Deceased
Recovered
VAERS ID: 1000472
AGE: UNK SEX: F

ISCHEMIC STROKE; This is a spontaneous report from a contactable healthcare professional downloaded from the Regulatory Authority-WEB (NO-NOMAADVRE-FHI-2021-U3xw4 and NO-NOMAADVRE-E2B_00014128). An 88-year-old female patient received the first dose of BNT162B2 (COMIRNATY; Lot number: EM0477), intramuscularly in the left arm, on 13Jan2021 at 12:20 at a single dose for COVID-19 vaccination. Medical history included palliative care, stroke on 12Dec2019, living in nursing home, ongoing hypertension, …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Ischaemic stroke

VAERS ID: 1000658
AGE: 68 SEX: M

Stroke; leukemia; This is a spontaneous report from a contactable consumer. This consumer reported for a 68-year-old male (consumer's husband) received the first dose of BNT162B2 (PFIZER COVID-19 VACCINE, lot number: EL0140, Expiry Date: Mar2021), via an unspecified route of administration on 31Dec2020 13:30 at single dose on right upper shoulder for COVID-19 prophylaxis. Medical history included smoker for 50 years, and blockage in his carotid artery. His grandma died of a stroke and his folks, …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Arteriogram carotid abnormal, Dyskinesia, Leukaemia, Carotid artery stent insertion, Dysstasia, Magnetic resonance imaging abnormal, Cerebrovascular accident, Hemiplegia, Syncope, Choking sensation, Hypoaesthesia oral, Dysarthria, Intensive care

VAERS ID: 1000670
AGE: 87 SEX: F

she was hurting at her chest/ Chest pain; on her left arm hurt real bad that's what the clot on her left arm; on her left arm hurt real bad that's what the clot on her left arm; She passed away; heart attack; This is a spontaneous report from a contactable consumer. An 87-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Jan2021 at single dose for COVID-19 immunisation. Medical history included diabetes mellitus, for which …
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Chest pain, Stent placement, Death, Thrombosis, Myocardial infarction, Pain in extremity, SARS-CoV-2 test negative

VAERS ID: 1000727
AGE: 42 SEX: F

a week after vaccination, patient developed fatigue and weakness, SOB, eye ptosis similar to her myasthenia flares. she was admitted for IVIG and discharged 1/31
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA))


SYMPTOM(S): Asthenia, Immunoglobulin therapy, Condition aggravated, Myasthenia gravis, Dyspnoea, Eyelid ptosis, Fatigue

VAERS ID: 1000754
AGE: 89 SEX: F

on 2/1/2021 Resident Reported Back pain given Tylenol Medication orally For Relief. APPRoximately 30 Min Later. complaint of & Noted Diarrhea, Shivering, and vomiting SenT To ER 2/1 And Admitted Diagnosis: Sepsis
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Back pain, Vomiting, Chills, Condition aggravated, Diarrhoea, Sepsis

VAERS ID: 1000775
AGE: 99 SEX: F

on 1/26/21 Found laying on Bathroom Floor in Bedroom Apt. Complaint of Right Shoulder paiN bleeding (unknown origin) then discovered origin HANd/FiNgers. (Head on Floor towARds WALL) SeNT TO ER 1/26/21, Admitted 1/26/21 Diagnosis: AoRtic STENOSIS
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Aortic stenosis, Arthralgia, Haemorrhage

VAERS ID: 1000784
AGE: 75 SEX: F

T.C. from sister to communicate the hospitalization of her sister. She reported that on Friday patient collapsed and started foaming at the mouth and was rushed to hospital. She stated that patient is on a ventilator and at 5PM today they are going to take her off. Sister was very upset and I was uncomfortable asking more questions. She will call me with more information at a later time. She did say that the hospital staff was not sure of what caused her collapse.
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Foaming at mouth, Mechanical ventilation, Syncope

VAERS ID: 1000840
AGE: 70 SEX: F

Weakness, dizziness, nausea, vomiting, rash on (L) arm
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA))


SYMPTOM(S): Asthenia, Vomiting, Dizziness, Injection site rash, Nausea, Rash

VAERS ID: 1000849
AGE: 62 SEX: M

Narrative: Respiratory failure / respiratory depression went to ED / ICU 2/1/2021. Frail patient. 1st vaccine 12/23/2020 Moderna Lot 039K20A exp 6/20/2021, 2nd vaccine 1/20/2020 Moderna Lot 013L20A exp 7/8/2021
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA))


SYMPTOM(S): Asthenia, Intensive care, PO2 decreased, Respiratory depression, Respiratory failure

VAERS ID: 1000852
AGE: 41 SEX: F

Dizziness & NauseaVomiting Narrative: discharge diagnosis of acute labrinathis requiring walker to ambulate. Having falls
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VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA))


SYMPTOM(S): Dizziness, Walking aid user, Fall, Labyrinthitis, Nausea, Vomiting

Page 5 of 24602 Results 41 - 50 of 246017

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OpenVAERS is a private organization that posts publicly available CDC/FDA data of injuries reported post-vaccination. Reports are not proof of causality.