Source: VAERS.HHS.GOV
VAERS accepts reports of adverse events and reactions that occur following vaccination. Healthcare providers, vaccine manufacturers, and the public can submit reports to the system. While very important in monitoring vaccine safety, VAERS reports alone cannot be used to determine if a vaccine caused or contributed to an adverse event or illness. The reports may contain information that is incomplete, inaccurate, coincidental, or unverifiable. In large part, reports to VAERS are voluntary, which means they are subject to biases. This creates specific limitations on how the data can be used scientifically. Data from VAERS reports should always be interpreted with these limitations in mind.
The strengths of VAERS are that it is national in scope and can quickly provide an early warning of a safety problem with a vaccine. As part of CDC and FDA’s multi-system approach to post-licensure vaccine safety monitoring, VAERS is designed to rapidly detect unusual or unexpected patterns of adverse events, also known as “safety signals.” If a safety signal is found in VAERS, further studies can be done in safety systems such as the CDC’s Vaccine Safety Datalink (VSD) or the Clinical Immunization Safety Assessment (CISA) project. These systems do not have the same scientific limitations as VAERS, and can better assess health risks and possible connections between adverse events and a vaccine.
Key considerations and limitations of VAERS data:
VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.
Thursday the 16th of September he was extra tired and a little bit of a headache on Friday he had a little bit of fever and on Saturday he told me he didn't feel good and I gave him some cough drops for the sore throat on Sunday he was sleepy and tired and complain of sore threat and saying he felt something in his chest like and at 3am he went to my room and he didn't feel well he said he was exhausted his jaw was hurting really bad, his chest was tight his felt was racing and he was holding his left arm and I called 911 and an ambulance took him to the ED and did and EKG and an Echo they diagnosed him for myocarditis after they ruled out heartburn and he was admitted. Infectious disease doctor was alerted.
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(If this is a foreign report without a description you will be able to read the description in the Wayback Machine on Medalerts if the report became public for the first time before November 18, 2022.)
| Name | Dose # | Type | Manufacturer | Lot | Route | Site |
|---|---|---|---|---|---|---|
| COVID19 (COVID19 (PFIZER-BIONTECH)) | 2 | COVID19 | PFIZER\BIONTECH | PF25088 | IM | RA |
| RECVDATE: | 10-04-2021 | RPT_DATE: |
| CAGE_YR: | 14 |
| CAGE_MO: | |
| DIED: | U |
| DATEDIED: | |
| L_THREAT: | U |
| ER_VISIT: | |
| HOSPITAL: | Y |
| HOSPDAYS: | 2 |
| X_STAY: | U |
| DISABLE: | U |
| RECOVD: | N |
| LAB_DATA: | EKG, Echocardiogram ,Lab work |
| V_ADMINBY: | PHM |
| OTHER_MEDS: | ADHD- Concerta Albuterol as need Melatonin as needed Tums as needed |
| CUR_ILL: | |
| HISTORY: | Asthma ADHD |
| PRIOR_VAX: | |
| SPLTTYPE: | vsafe |
| FORM_VERS: | |
| TODAYS_DATE: | 10-04-2021 |
| BIRTH_DEFECT: | U |
| OFC_VISIT: | Y |
| ER_ED_VISIT: | Y |
| ALLERGIES: | Penicillin |
| V_FUNDBY: |
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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.