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

This is VAERS ID 1408575



Case Details

VAERS ID: 1408575 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-06-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: Pruritus, Rhinorrhoea, Seasonal allergy
SMQs:, Anaphylactic reaction (broad), Conjunctival disorders (narrow), 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: Lactation decreased
Allergies:
Diagnostic Lab Data:
CDC Split Type: GBPFIZER INC2021649055

Write-up: Itching; Runny nose; Hay fever; This is a spontaneous report from a contactable consumer received from the Regulatory Authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202106021139475190-ECHE9. Safety Report Unique Identifier: GB-MHRA-ADR 25404444. A 33-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 01Jun2021 (Batch/Lot number was not reported) at the age of 33 years old, single dose, for Covid-19 immunisation. Medical history included lactation decreased. Patient has not tested positive for COVID-19 since having the vaccine. Patient has not had symptoms associated with COVID-19; not had a COVID-19 test. Patient was not enrolled in clinical trial. Patient was not pregnant at the time of vaccination. Patient was not currently breastfeeding. The patient''s concomitant medications were not reported. The patient experienced runny nose, and hay fever on 01Jun2021; itching on 02Jun2021. The events were reported as medically significant. Outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


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