Your Health. Your Family. Your Choice.
|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA||041C21A / 2||LA / IM|
Administered by: Pharmacy Purchased by: ??
Symptoms: No adverse event, Interchange of vaccine products
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Other Medications: none
Current Illness: unknown
Preexisting Conditions: unknown
Diagnostic Lab Data: none needed
CDC 'Split Type':
Write-up: Please note: this is not an adverse event rather an administration error The incident occurred in a Sunday afternoon at around 12:45 pm. This patient showed up in the drop-off window asking for getting her second dose of COVID-19 vaccine. The patient came with her husband/boyfriend (relationship unknown) and a translator. The technician asked whether she received her first dose from Moderna. She assured the technician positively and decided to take the shot. After administering the vaccine, I discovered in the vaccine card that the patient received her first dose from Pfizer. While the patient was waiting in the observational area, I called CDC hotline to ensure if she needs further follow-up. An on-call physician assured me that the patient should be fine and should not be re-dosed and also guided me to the CDC recommendation fact sheet. I printed the fact sheet for the patient and assured patient about the CDC recommendation. I observed the patient for 30 minutes and didn''t see any adverse events occurred. Patient left the store without any signs or symptoms of adverse effects.
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