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.
1627: informed patient was experiencing nausea 1630: BP:118/68; P:72; RR:18; patient sitting in waiting area after receiving COVID-19 vaccine; stated she was fine but had some nausea; had eaten at ~1100 today and feeling fine; stated hx of Lupus and gave names of meds she had taken earlier; stated she had been cleared to receive vaccine by PCP and Rheumatologist 1635: BP:140/88; P:68; RR:18; patient began to slump down on chair and left hand began to go limp - 911 activated. Patient did not have LOC and tears rolled down her eyes; began to lose color on face; patient placed on cot in supine position and removed jacket she was wearing. Skin was warm but not clammy/diaphoretic. 1640:BP: 122/82; P:68; RR:18; patient lucid but began to slur words - continued to monitor, airway in tact and no LOC 1642: EMS arrival, report given to EMS and care transferred Blood sugar p/EMS: 80 1707: EMS departed, patient remained supine in cot; this nurse assisted patient from cot to a chair and patient did great. ~1720: Patient and her mom were escorted to her vehicle by another nurse 2013: This nurse called patient and she sounded wonderful; stated she was about to get showered; patient appreciative for f/u call.
Open in Wayback Machine
(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 (MODERNA)) | 1 | COVID19 | MODERNA | 025L20A | IM | LA |
RECVDATE: | 12-30-2020 | RPT_DATE: |
CAGE_YR: | 52 |
CAGE_MO: | |
DIED: | U |
DATEDIED: | |
L_THREAT: | U |
ER_VISIT: | |
HOSPITAL: | U |
HOSPDAYS: | |
X_STAY: | U |
DISABLE: | U |
RECOVD: | Y |
LAB_DATA: | |
V_ADMINBY: | PUB |
OTHER_MEDS: | Hydroxychloroquine 400mg daily Dolamide 300mg daily Vitamin D daily |
CUR_ILL: | |
HISTORY: | Lupus |
PRIOR_VAX: | |
SPLTTYPE: | |
FORM_VERS: | |
TODAYS_DATE: | 12-30-2020 |
BIRTH_DEFECT: | U |
OFC_VISIT: | U |
ER_ED_VISIT: | U |
ALLERGIES: | NKA |
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.