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This is VAERS ID 1255323

History of Changes from the VAERS Wayback Machine

First Appeared on 4/30/2021

VAERS ID: 1255323
VAERS Form:2
Age:35.0
Sex:Female
Location:Virginia
Vaccinated:2021-04-10
Onset:2021-04-11
Submitted:0000-00-00
Entered:2021-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9810 / 2 LA / -

Administered by: Private      Purchased by: ??
Symptoms: Fall, Headache, Hyperhidrosis, Nausea, Syncope

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: LEXAPRO
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Fatty liver; Sulfonamide allergy
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USPFIZER INC2021396111

Write-up: went to go lay back down/fainted; went to go lay back down; felt nauseous; Went to lay in bed and was sweating a lot; Before I fainted I had taken some ibuprofen for the headache; This is a spontaneous report from a contactable consumer patient(herself) reported. A 35-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EM9810, Expiration date: unknown), via an unspecified route of administration in arm left on 10Apr2021 at 12:00 PM as single dose for covid-19 immunization. The patient historical vaccine included first dose BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, lot number: EM9810, Expiration date: unknown), via an unspecified route of administration in left arm on 20Mar2021 at12:00 PM as single dose Covid-19 immunization. Patient medical history included fatty liver disease. Patient had known to allergies sulfa medication. Patient concomitant medication in two weeks included escitalopram oxalate (LEXAPRO), allergy medicine, allergy nasal spray. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the post vaccination. Patient experienced about 16 hours after the vaccine went to go lay back down, felt nauseous and fainted, got back up and fainted again. Went to lay in bed and was sweating a lot 11Apr2021 at 05:15 AM. Before fainted, patient had taken some ibuprofen for the headache. Patient not received treatment for the events. The outcome of the event was unknown.


Changed on 5/7/2021

VAERS ID: 1255323 Before After
VAERS Form:2
Age:35.0
Sex:Female
Location:Virginia
Vaccinated:2021-04-10
Onset:2021-04-11
Submitted:0000-00-00
Entered:2021-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9810 / 2 LA / -

Administered by: Private      Purchased by: ??
Symptoms: Fall, Headache, Hyperhidrosis, Nausea, Syncope

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: LEXAPRO
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Fatty liver; Sulfonamide allergy
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USPFIZER INC2021396111

Write-up: went to go lay back down/fainted; went to go lay back down; felt nauseous; Went to lay in bed and was sweating a lot; Before I fainted I had taken some ibuprofen for the headache; This is a spontaneous report from a contactable consumer patient(herself) reported. A 35-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EM9810, Expiration date: unknown), via an unspecified route of administration in arm left on 10Apr2021 at 12:00 PM as single dose for covid-19 immunization. The patient historical vaccine included first dose BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, lot number: EM9810, Expiration date: unknown), via an unspecified route of administration in left arm on 20Mar2021 at12:00 PM as single dose Covid-19 immunization. Patient medical history included fatty liver disease. Patient had known to allergies sulfa medication. Patient concomitant medication in two weeks included escitalopram oxalate (LEXAPRO), allergy medicine, allergy nasal spray. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the post vaccination. Patient experienced about 16 hours after the vaccine went to go lay back down, felt nauseous and fainted, got back up and fainted again. Went to lay in bed and was sweating a lot 11Apr2021 at 05:15 AM. Before fainted, patient had taken some ibuprofen for the headache. Patient not received treatment for the events. The outcome of the event was unknown.


Changed on 5/14/2021

VAERS ID: 1255323 Before After
VAERS Form:2
Age:35.0
Sex:Female
Location:Virginia
Vaccinated:2021-04-10
Onset:2021-04-11
Submitted:0000-00-00
Entered:2021-04-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EM9810 / 2 LA / -

Administered by: Private      Purchased by: ??
Symptoms: Fall, Headache, Hyperhidrosis, Nausea, Syncope

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: LEXAPRO
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Fatty liver; Sulfonamide allergy
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USPFIZER INC2021396111

Write-up: went to go lay back down/fainted; went to go lay back down; felt nauseous; Went to lay in bed and was sweating a lot; Before I fainted I had taken some ibuprofen for the headache; This is a spontaneous report from a contactable consumer patient(herself) reported. A 35-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EM9810, Expiration date: unknown), via an unspecified route of administration in arm left on 10Apr2021 at 12:00 PM as single dose for covid-19 immunization. The patient historical vaccine included first dose BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, lot number: EM9810, Expiration date: unknown), via an unspecified route of administration in left arm on 20Mar2021 at12:00 PM as single dose Covid-19 immunization. Patient medical history included fatty liver disease. Patient had known to allergies sulfa medication. Patient concomitant medication in two weeks included escitalopram oxalate (LEXAPRO), allergy medicine, allergy nasal spray. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the post vaccination. Patient experienced about 16 hours after the vaccine went to go lay back down, felt nauseous and fainted, got back up and fainted again. Went to lay in bed and was sweating a lot 11Apr2021 at 05:15 AM. Before fainted, patient had taken some ibuprofen for the headache. Patient not received treatment for the events. The outcome of the event was unknown.

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