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From the 9/10/2021 release of VAERS data:

This is VAERS ID 1412002

Case Details

VAERS ID: 1412002 (history)  
Form: Version 2.0  
Age: 28.0  
Sex: Female  
Location: Foreign  
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other       Purchased by: ?
Symptoms: Body temperature, Dyspnoea, Hypoaesthesia oral, Pruritus, Swelling
SMQs:, Anaphylactic reaction (narrow), Angioedema (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (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? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Atopy; Food allergy
Diagnostic Lab Data: Test Date: 20210603; Test Name: body temperature; Result Unstructured Data: Test Result:36.4 Centigrade; Comments: Before vaccination
CDC Split Type: JPPFIZER INC2021659067

Write-up: Dyspnoea; Numbness of lips; itching; swelling; This is a spontaneous report from the contactable physician received from the Regulatory Authority. The Regulatory authority report number is v21111760. The patient was 28-year-old female. Body temperature before the vaccinations was 36.4 degrees centigrade on 03Jun2021. The patient''s history according to the Vaccine Screening Questionnaire was atopy, allergy to shrimp, crab, squid. The patient''s concomitant drug was not provided. On 03Jun2021 at 14:00 (the day of vaccination, at the age of 28-year-old), the patient received the first dose of BNT162B2 (COMIRNATY, Intramuscular injection, Lot number: EY2173, expiration date: 31Aug2021), via an unspecified route of administration as a single dose for COVID-19 immunisation. On 03Jun2021 at 14:05 (the day of vaccination), the patient experienced dyspnoea, numbness of lips, itching. The outcome of the event was recovering on 03Jun2021 (The day of vaccination). Clinical course of the event was reported as follows: The patient experienced dyspnoea, numbness of lips, swelling a few minutes after vaccination. In addition, before vaccination, the patient did not eat meat that can cause allergy. So the relationship assessed as related. After administration of antihistamine, the symptoms was recovering. The reporter classified the event as non-serious and the causality between the event and the vaccines was Related. Other possible cause of the event such as any other diseases was no.

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