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This is VAERS ID 1725551

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First Appeared on 9/24/2021

VAERS ID: 1725551
VAERS Form:2
Age:
Sex:Female
Location:Unknown
Vaccinated:2021-01-20
Onset:0000-00-00
Submitted:0000-00-00
Entered:2021-09-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown      Purchased by: ??
Symptoms: Endocarditis, Cardiac disorder

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? Yes, days:     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Heavy smoker; Pericardial window (she had a pericardial window placed in her heart)
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USPFIZER INC202101213572

Write-up: infectious endocarditis; cardiac symptoms; This is a spontaneous report received from a contactable Pharmacist reported for a female patient. A female patient of late 50''s-early 60''s received bnt162b2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection; Batch no/Lot number: not reported) received via unspecified route of administration on 30Dec2020 as dose 1, single for covid-19 immunization and bnt162b2 (COMIRNATY, PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection; Batch no/Lot number: not reported) received via unspecified route of administration on 20Jan2021 as dose 2, single for covid-19 immunization. Patient medical history included heavy smoker and she had a pericardial window placed in her heart. It was reported that patient experienced cardiac symptoms approximately 2 months following the 2nd dose of the Pfizer-BioNTech COVID-19 vaccine. Patient was hospitalized due to events caused and she was admitted to the ICU and placed on a ventilator. Patient had a pericardial window placed in her heart and she received antibiotics at one point during her care and for what they thought could be an infectious Endocarditis, but no organism grew on culture. Treatment received for the events caused. Event took place after use of product. Outcome of the events was unknown. The lot number for the vaccine (BNT162B2), was not provided and will be requested during follow-up.; Sender''s Comments: Based on the reported information ,a causal relationship between the events and suspected drug cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

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