VAERS Reports EU0168

VAERS 1463772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Eu0168

mild

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 12.07.2021
Impfdatum: 05.06.2021
Beginn: 01.06.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal distension Fatigue Menstruation delayed

Symptomtext

Late menstrual cycle not due to pregnancy. I experience extreme bloating and tiredness. My cycle averages 27 days and is never so late unless pregnant. Bloating started about 2 wks before cycle due date with extreme bloating a week before due date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1767601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EU0168

gering

Staat: VT
Alter: 36,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 10.08.2021
Beginn: 10.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Contusion

Symptomtext

Bruising; This is a spontaneous report from a contactable other health care professional (patient). A 36-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EU0168 and expiration date: not reported), via intramuscular, in Left Deltoid, on 10Aug2021 (at the age of 36-year-old) as DOSE 1, SINGLE for covid-19 immunization. Relevant medical history and concomitant medications were reported as none. The patient didn't receive any other vaccines within 4 weeks prior to the COVID -19 vaccine. The patient experienced bruising on 10Aug2021. No treatment was received for the adverse event. The outcome of event was not recovered at time of report.; Sender's Comments: The event of bruising is assessed as possibly related to the suspect vaccine Comirnaty based on strong temporal association "The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Contusion
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -