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From the 9/17/2021 release of VAERS data:

This is VAERS ID 1408577

Case Details

VAERS ID: 1408577 (history)  
Form: Version 2.0  
Sex: Female  
Location: Foreign  
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other       Purchased by: ?
Symptoms: Hyperhidrosis, Investigation, Loss of consciousness, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased
Diagnostic Lab Data: Test Date: 202106; Test Name: Observation; Result Unstructured Data: Test Result:within normal range
CDC Split Type: GBPFIZER INC2021649185

Write-up: sweaty; passed out; Syncope; This is a spontaneous report from a contactable physician received from the regulatory authority, report number is GB-MHRA-WEBCOVID-202106021153152400-Z5NHN. Safety Report Unique Identifier is GB-MHRA-ADR 25404472. A 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EY5456), via an unspecified route of administration on 01Jun2021 as first dose, single dose for COVID-19 immunization. Medical history included lactation decreased. Patient has not had symptoms associated with COVID-19, she has not had a COVID-19 test, and she was not enrolled in clinical trial. She was not pregnant and was not currently breastfeeding. The patient''s concomitant medications were not reported. The patient experienced sweaty and passed out on Jun2021; and syncope on 02Jun2021. The events were reported as non-serious. The clinical course was reported as follows: Had vaccine and felt sweaty. Stood up to have fresh air but passed out very briefly. Put in recovery position. Recovered ok and observed for 30minutes. All observation within normal range. Discharged home on Jun2021. Patient has not tested positive for COVID-19 since having the vaccine. This report does not relate to possible blood clots or low platelet counts. The events sweaty and passed out recovered on Jun2021. The outcome of syncope was recovering. No follow-up attempts are possible. No further information is expected.

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