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

This is VAERS ID 1416053



Case Details

VAERS ID: 1416053 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-06-02
Onset:2021-06-03
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-06-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Cough, Lacrimation increased, Lymphadenopathy, Nasopharyngitis, Oropharyngeal pain, Rhinorrhoea
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Lacrimal disorders (narrow), 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: Lactation decreased
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021657224

Write-up: runny nose; watery eye; Common cold; chesty cough/Cough; Sore throat; raised glands; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106060516094650-EGX5M. Safety Report Unique Identifier GB-MHRA-ADR 25426696. A 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 02Jun2021 (Batch/Lot number was not reported) as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history included lactation decreased. It was reported that the patient is usually very fit and well. Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not pregnant, Patient is not currently breastfeeding. The patient''s concomitant medications were not reported. It was reported that the day after the jab (03Jun2021), the patient developed a sore throat with raised glands. The day after that (04Jun2021, also reported as "03Jun2021"), she had an all-out cold. The patient also experienced chesty cough on 04Jun2021, runny nose and watery eyes on an unspecified date. The events were assessed as serious (medically significant). Patient has not tested positive for COVID-19 since having the vaccine. The outcome of the events cold and sore throat was not recovered; while unknown for the rest of the events. No follow-up attempts are possible, information about the batch number cannot be obtained.


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