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VAERS Report 2156616

Case Report Section

Détails du rapport Vaer

Âge: N/A

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
2022-01-27
Date d’apparition
1
Nombre de jours (date d’apparition – date de vaccination)
1
Description de l’événement indésirable

shortness of breath; fever; chills; hot & cold; aching joints; dizzy & light headed, almost fainted; pounding headaches; no energy, weakness; sore throat; congestion/ congestion nasal; loss of smell; this is a spontaneous report received from a contactable reporter (consumer) from a regulatory authority. the reporter is the patient. other case identifiers: gb-mhra-vac-202202141650427980-x2vak and gb-mhra-adr 26602671. a 56-year-old female patient received bnt162b2 (comirnaty), administration date 27jan2022 (batch/lot number: unknown) as dose number unknown (booster), single for covid-19 immunisation. the patient's relevant medical history and concomitant medications were not reported. vaccination history included: covid-19 vaccine (primary immunization series complete; unknown manufacturer), for covid-19 immunisation. the following information was reported: dyspnoea (medically significant) with onset 28jan2022, outcome "not recovered", described as "shortness of breath"; pyrexia (medically significant) with onset 28jan2022, outcome "not recovered", described as "fever"; chills (medically significant) with onset 28jan2022, outcome "not recovered", described as "chills"; feeling of body temperature change (medically significant) with onset 28jan2022, outcome "not recovered", described as "hot & cold"; arthralgia (medically significant) with onset 28jan2022, outcome "not recovered", described as "aching joints"; dizziness (medically significant) with onset 28jan2022, outcome "not recovered", described as "dizzy & light headed, almost fainted"; headache (medically significant) with onset 28jan2022, outcome "not recovered", described as "pounding headaches"; asthenia (medically significant) with onset 28jan2022, outcome "not recovered", described as "no energy, weakness"; oropharyngeal pain (medically significant) with onset 28jan2022, outcome "not recovered", described as "sore throat"; nasal congestion (medically significant) with onset 28jan2022, outcome "not recovered", described as "congestion/ congestion nasal"; and anosmia (medically significant) with onset 28jan2022, outcome "not recovered", described as "loss of smell." clinical course: once the patient received the covid vaccine booster, the following day, the side-effects became full-blown and "lasted beyond 3 weeks" (as reported). she contacted her gp who advised her to remain at home and declared her unfit for work. blood test, blood pressure, and chest x-ray appointments were also organized for her. the medicine was obtained from a covid walk-in medical centre. 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
nasal congestion chills headache arthralgia asthenia dizziness dyspnoea pyrexia oropharyngeal pain feeling of body temperature change anosmia
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?
Non
Allergies:
na
Maladie actuelle
na