Page breadcrumb nav

VAERS Report 2156722

Case Report Section

Détails du rapport Vaer

Âge: 31 ans

Genre: Female

Région : Outside US

Patient décédé?
Non
Renseignements sur les vaccins

Nom: COVID19 (COVID19 (PFIZER-BIONTECH))

Type : Coronavirus 2019 vaccine

Fabricant: PFIZER

Lot: unknown


Date de réception du rapport
2022-03-04
Date à laquelle le formulaire est complèté
Date de vaccination
2022-02-12
Date d’apparition
0
Nombre de jours (date d’apparition – date de vaccination)
0
Description de l’événement indésirable

gastritis; diarrhea; stomach pain/ very sore stomach; severe trapped wind in upper back/chest; began to feel nauseous; lost appetite; bloated stomach; acid reflux; unable to eat; indigestion; this is a spontaneous report received from a contactable reporter (consumer or other non hcp) from the regulatory agency (ra). regulatory number: gb-mhra-webcovid-202202142245051970-fhate (ra). other case identifier: gb-mhra-adr 26604339 (ra). a 31-year-old female patient (not pregnant) received bnt162b2 (comirnaty), administration date 12feb2022 (batch/lot number: unknown) at the age of 31 years as dose 3 (booster), single for covid-19 immunisation. the patient's relevant medical history and concomitant medications were not reported. the patient's last menstrual date was on 30jan2022. the patient had no symptoms associated with covid-19 and not had a covid-19 test. the patient was not pregnant and was not breastfeeding at the time of this report. the patient was not enrolled in clinical trial. vaccination history included: bnt162b2 (dose 1, single; lot number: unknown; route of administration: unspecified), for covid-19 immunisation; bnt162b2 (dose 2, single; lot number: unknown; route of administration: unspecified), for covid-19 immunisation. the following information was reported: gastritis (disability) with onset 13feb2022, outcome "not recovered", described as "gastritis"; diarrhoea (disability) with onset 13feb2022, outcome "recovering", described as "diarrhea"; abdominal pain upper (disability) with onset 13feb2022, outcome "recovering", described as "stomach pain/ very sore stomach"; feeding disorder (disability) with onset feb2022, outcome "recovering", described as "unable to eat"; dyspepsia (disability) with onset feb2022, outcome "recovering", described as "indigestion"; nausea (disability) with onset 12feb2022, outcome "unknown", described as "began to feel nauseous"; decreased appetite (disability) with onset 12feb2022, outcome "unknown", described as "lost appetite"; flatulence (disability) with onset 13feb2022, outcome "unknown", described as "severe trapped wind in upper back/chest"; abdominal distension (disability) with onset feb2022, outcome "unknown", described as "bloated stomach"; gastrooesophageal reflux disease (disability) with onset feb2022, outcome "unknown", described as "acid reflux". the patient was not tested positive for covid-19 since having the vaccine. clinical course: approximately 12 hours after vaccine, the patient began to feel nauseous and lost appetite. began to experience stomach pain, diarrhoea and severe trapped wind in upper back/chest next day (which couldn't pass). the patient was unable to eat and had symptoms of indigestion, very sore and bloated stomach, acid reflux. the report of the patient was not related to possible inflammation of the heart (myocarditis or pericarditis). no follow-up attempts are possible; information about lot/batch number cannot be obtained. no further information is expected

Données de laboratoire
na
Liste des symptômes
diarrhoea nausea decreased appetite gastrooesophageal reflux disease flatulence dyspepsia gastritis abdominal pain upper abdominal distension feeding disorder
Patient décédé?
Non
Date de décès
N/A
Anomalie congénitale
false
Vaccin administré par :
Other
Vaccin acheté par :
Inconnu
Visite d’un patient à l’urgence?
Non
Patient hospitalisé?
Non
Séjour à l’hôpital
Non
Nombre de jours à l’hôpital
Non spécifié
Invalidité permanente?
Oui
Allergies:
na
Maladie actuelle
na