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This is VAERS ID 1415586

History of Changes from the VAERS Wayback Machine

First Appeared on 7/23/2021

VAERS ID: 1415586
VAERS Form:2
Age:
Sex:Male
Location:Foreign
Vaccinated:2021-06-03
Onset:2021-06-03
Submitted:0000-00-00
Entered:2021-06-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ET8885 / UNK - / -

Administered by: Other      Purchased by: ??
Symptoms: Chest discomfort, Chest pain, Dyspnoea, Heart rate, Heart rate increased, Hypertension, SARS-CoV-2 test

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:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Suspected COVID-19
Allergies:
Diagnostic Lab Data: Test Date: 20210603; Test Name: a small walk to bathroom takes its o 130+; Result Unstructured Data: Test Result:130+; Test Date: 20210603; Test Name: Resting heart rate; Result Unstructured Data: Test Result:105; Test Date: 20210603; Test Name: while doing something remotely more physiological such as wiping the dining table take it to 150+; Result Unstructured Data: Test Result:150+; Test Date: 20201116; Test Name: COVID-19 virus test; Test Result: Positive ; Comments: Yes - Positive COVID-19 test
CDC 'Split Type': GBPFIZER INC2021657207

Write-up: shortness of breath; Hypertension; resting heart rate and blood preachers started to increase; Severe chest discomfort/heart; Severe chest discomfort/heart/mall walk to bathroom takes it to 130+ while doing something remotely more physiological such as wiping the dining table take it to 150+; This is a spontaneous report from a contactable consumer received from the Agency Regulatory Authority. The regulatory authority report number is GB-MHRA-APPCOVID-20210605071402, Safety Report Unique Identifier GB-MHRA-ADR 25425069. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Et8885, expiry date not reported), via an unspecified route of administration on 03Jun2021 as unknown dose number, single for COVID-19 immunisation. Medical history included suspected COVID-19 from 14Nov2020 to 05Jan2021. Patient is not enrolled in clinical trial. The patient''s concomitant medications were not reported. The patient experienced shortness of breath and hypertension on 03Jun2021. It was reported that resting heart rate and blood preachers started to increase immediately after vaccine however on the reported data patient feel slight shortness of breath and discomfort in heart when doing the smallest of activities. Resting heart rate is 105 and a small walk to bathroom takes it to 130+ while doing something remotely more physiological such as wiping the dining table take it to 150+ with severe discomfort of the chest/heart. Watch taking constant heart rate readings and showing high heart rate warning. The events were reported as serious (Other medically important condition). The patient underwent lab tests and procedures which included COVID-19 virus test: positive (yes - positive COVID-19 test) on 16Nov2020. The patient had not recovered from hypertension, recovering from shortness of breath, while outcome of the remaining events was unknown. No follow-up attempts are Possible. No further information is expected.

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