Adverse Event Reporting

VAERS ID	1150930
Gender	Female
Age
StateCode
Pharmaceutical Company	PFIZER\BIONTECH
Lot Number
Number of vaccinations	1
Vaccinated
Onset
Condition	Permanent Disability

Symptoms

• Anaphylactic reaction

Current Illness

Preexisting Conditions

Other Medications

Previous Vaccinations

Allergies

Laboratory Data

Write-up

serious reaction and is on disability.
She described it as continuous anaphylaxis; This is a spontaneous report received from a non-contactable consumer.
An unspecified aged female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Solution for injection, Lot Number: unknown) via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization.
The patient medical history was not provided.
Concomitant medications were reported as none.
On an unspecified date patient was reported as she received her first Pfizer COVID vaccine and had a serious reaction and is on disability.
She described it as continuous anaphylaxis.
It was unknown if the patient received any treatment.
The outcome of the event was unknown.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.