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 January 7, 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 6 of 189464 Results 51 - 60 of 1894633

Deceased
Recovered
VAERS ID: 2013621
AGE: 72 SEX: F

Headache sore arm
Read FULL REPORT >


VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (MODERNA))


SYMPTOM(S): Headache, Pain in extremity

VAERS ID: 2013616
AGE: UNK SEX: M

Drug Interaction; CARDIAC FIBRILLATION; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from the regulatory authority. Regulatory number: NO-NOMAADVRE-PASRAPP-2021-Umm4na. Other Case identifier(s): NO-NOMAADVRE-E2B_00064616. A 54 year-old male patient received bnt162b2 (COMIRNATY), intramuscular, administered in arm left, administration date Sep2021 (Lot number: Unknown) as dose 2, single for covid-19 immunisation. Relevant medical history included: …
Read FULL REPORT >


VACCINE TYPE(S): UNK
VACCINE NAME(S): VACCINE NOT SPECIFIED (NO BRAND NAME)


SYMPTOM(S): Cardiac fibrillation, Drug ineffective, Drug interaction

VAERS ID: 2013613
AGE: UNK SEX: F

This is a spontaneous report received from a non-contactable reporter(s) (consumer or other non-HCP) from Regulatory Authority. Regulatory number: NO-NOMAADVRE-PASRAPP-2021-UJ1A83 (RA). Other Case identifier(s): NO-NOMAADVRE-E2B_00061748 (RA). A 24-year-old female patient received bnt162b2 (COMIRNATY), intramuscular, administered in arm left, administration date 14Apr2021 at 10:35 (Lot number: Unknown) as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Contraception" …
Read FULL REPORT >


VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Fatigue

VAERS ID: 2013593
AGE: UNK SEX: F

death is thought to be due to acute heart failure due to acute cardiac arrhythmia.; CPR and eventually advanced CPR were implemented immediately; death is thought to be due to acute heart failure due to acute cardiac arrhythmia.; The patient complained some about HEARTBURN the first week after dose No. 2.; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP, Physician and Other HCP) from the Regulatory Authority. Regulatory number: NO-NOMAADVRE-PASRAPP-2021-U2zxm1 …
Read FULL REPORT >


VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Arrhythmia, Autopsy, Cardiac failure acute, Dyspepsia, Resuscitation

VAERS ID: 2013591
AGE: UNK SEX: F

DEATH; Booster; This is a spontaneous report received from a contactable reporter(s) (Physician) from the Regulatory Authority-WEB. Regulatory number: NO-NOMAADVRE-FHI-2021-Vqz8kb (RA). Other Case identifier(s): NO-NOMAADVRE-E2B_00067077 (RA). A 51 year-old female patient (unknown if pregnant) received BNT162b2 (COMIRNATY), intramuscular, administration date 13Dec2021 (Lot number: FK9706) as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "metastatic cancer" …
Read FULL REPORT >


VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Death, Immunisation

VAERS ID: 2013586
AGE: UNK SEX: M

Death due to hypersensitivity myocarditis; Increasingly worse with multi-organ failure, and eventually death.; This is a spontaneous report received from a contactable reporter(s) (Physician) from the Agency Agency-WEB. Regulatory number: NO-NOMAADVRE-FHI-2021-Vejqqb. Other Case identifier(s): NO-NOMAADVRE-E2B_00065918. A 76 year-old male patient received bnt162b2 (COMIRNATY), intramuscular, administration date 19May2021 (Lot number: EW8904) as dose 2, single for covid-19 immunisation. Relevant …
Read FULL REPORT >


VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Autopsy, Multiple organ dysfunction syndrome, Brain natriuretic peptide, Troponin, C-reactive protein, Electrocardiogram, Hypersensitivity myocarditis

VAERS ID: 2013577
AGE: UNK SEX: M

low blood glucose/ 3 mmol/L; Death NOS; Booster; Booster; This is a spontaneous report received from contactable reporter(s) (Physician and nurse) from the Regulatory Authority-WEB. Regulatory number: NO-NOMAADVRE-FHI-2021-V8g7wj (RA). Other Case identifier(s): NO-NOMAADVRE-E2B_00067078 (RA). A 86 year-old male patient received bnt162b2 (COMIRNATY), intramuscular, administration date 12Nov2021 (Lot number: FJ3438) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: …
Read FULL REPORT >


VACCINE TYPE(S): COVID19
VACCINE NAME(S): COVID19 (COVID19 (PFIZER-BIONTECH))


SYMPTOM(S): Blood glucose, Blood glucose decreased, Death, Immunisation, Off label use

VAERS ID: 2013576
AGE: UNK SEX: U

No adverse event; Sterile Injectable;Loose / Rotating Luer Lock;Syringe Hub Defect; Information has been received from a nurse on 28-DEC-2021. Syringe Hub Defect -- Loose / Rotating Luer Lock; Upon preparing, the luer lock adapter rotated and cannot attach the needle; Needle manufactuer: NIPRO; Needled Size; 24G; Needle Lot #; 21A271; Based on the Intake Report, this product is not us ed for the patient, so this case is NOT Biohazard. PQC sample WILL BE shipped.
Read FULL REPORT >


VACCINE TYPE(S): HPV4
VACCINE NAME(S): HPV (GARDASIL)


SYMPTOM(S): Device breakage

VAERS ID: 2013575
AGE: 1 SEX: M

FEVER > = 39.5; Information has been downloaded from regulatory authority (IT-MINISAL02-821286). This spontaneous report was received from a health care professional, concerning a 1-year-old male patient. No information was reported regarding the patient's relevant medical history, concurrent conditions, concomitant therapies and previous drug reactions or allergies. On 04-NOV-2021, the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live (therapy type: …
Read FULL REPORT >


VACCINE TYPE(S): MMRV
VACCINE NAME(S): MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD)


SYMPTOM(S): Pyrexia

VAERS ID: 2013554
AGE: 1 SEX: F

This literature marketed/study report has been received from the authors of a published literature article, titled as stated above and refers to a female infant, who was clinically well previously. Family history revealed a sister who had passed away after presenting with a severe vasculitic rash as a child. On an unknown date, at the age of 1 year old, the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live (manufacturer unknown) (strength, dose, frequency, …
Read FULL REPORT >


VACCINE TYPE(S): MMRV
VACCINE NAME(S): MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD)


SYMPTOM(S): Antibody test abnormal, CD4 lymphocytes decreased, Gene mutation, Immunoglobulins normal, Rash vesicular, Vasculitis, B-cell aplasia, CSF test abnormal, Gene mutation identification test positive, Immunosuppression, Skin lesion, Viral titre, Biopsy skin abnormal, Cutaneous vasculitis, Gene sequencing, Lymphocyte count normal, T-cell receptor gene rearrangement test, Biopsy thymus gland abnormal, Disseminated varicella, Illness, Purpura, Thymus disorder, Bone marrow transplant, Full blood count normal, Immunoglobulin therapy, Pyrexia, Varicella post vaccine

Page 6 of 189464 Results 51 - 60 of 1894633

Questions? Comments? Bugs?
[email protected]
Due to the high volume of inquiries, please be patient with response times.

AND PLEASE read the FAQ first.

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