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This is VAERS ID 1414857

History of Changes from the VAERS Wayback Machine

First Appeared on 7/23/2021

VAERS ID: 1414857
VAERS Form:2
Age:66.0
Sex:Female
Location:Foreign
Vaccinated:2021-06-02
Onset:2021-06-04
Submitted:0000-00-00
Entered:2021-06-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -

Administered by: Other      Purchased by: ??
Symptoms: Abscess oral, Hypersensitivity, Oropharyngeal pain

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CLONAZEPAM; SERTRALINE; ALPRAZOLAM; SEDATIF PC
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Allergy (To many things); COVID-19; Hysterectomy; Tonsillectomy
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': COPFIZER INC2021658701

Write-up: Left side pain in the throat; Abscess on the palate; Allergy in the skin, neck and face; This is a spontaneous report from a non-contactable consumer (patient) from the COVAES portal. A 66-year-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 vaccine), dose 1 administered in arm right on 02Jun2021 10:00 (Batch/Lot number was not reported) as 1st dose, single for covid-19 immunisation. Medical history included a hysterectomy and a tonsillectomy on an unknown date and known allergies (reported as "to many things"). The patient informed that she was diagnosed with COVID-19 Prior to vaccination. Concomitant medications received within 2 weeks of vaccination included clonazepam (unknown manufacturer), sertraline (unknown manufacturer), alprazolam (unknown manufacturer) and abrus precatorius, aconitum napellus, atropa belladonna, calendula officinalis, chelidonium majus, viburnum opulus (SEDA TIF PC); all of them taken for an unspecified indication, start and stop date were not reported. On 04Jun2021 18:30 the patient experienced left side pain in the throat, abscess on the palate, an allergy in the skin, neck and face; all this on 04Jun2021 and 06Jun2021 (reported as 2 and 4 days after the vaccination). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The patient indicated that therapeutic measures were taken in response to the events, she received an injected antiallergic (decadron duo). The outcome for the events was unknown. Information of the lot/batch number has been requested.

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