VAERS 1791876
PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ZN6205
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 25.02.2021
- Beginn
- 05.03.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- - / LA
Symptomtext
The day I was vaccinated I had the usual soreness at the injection site and for the next day; Headache; Lymph nodes at the back of my neck were swollen; This is a spontaneous report from a contactable consumer, the patient. A 65-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ZN6205) via an unspecified route of administration in the arm left on 25Feb2021 at 15:45 (at the age of 64-year-old) as a single dose for COVID-19 immunisation. The patient had no medical history. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had no known allergies to medications, food, or other products. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications taken within two weeks included fexofenadine hydrochloride (ALLEGRA) from an unknown date for an unknown indication. On 05Mar2021 at 03:30, on the day of vaccination, the patient experienced usual soreness at the injection site and for the next day. A week after she got the shot she got a headache so bad she had to take Tylenol for it but she also noticed her lymph nodes at the back of her neck were swollen, she called her daughter, she's working on her PHD in infectious diseases, and told her about her swollen lymph nodes and her daughter told her that she need to report it. The daughter told that means the vaccine was working and her body was doing what it's suppose to be doing. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of the events vaccination site pain, headache and swollen lymph nodes and included treatment with paracetmol (TYLENOL). Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events vaccination site pain, headache and swollen lymph nodes was resolved in Mar2021. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- ALLEGRA
- Allergien
- -
- Vorherige Impfungen
- -