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VAERS Report 2156595

Case Report Section

Détails du rapport Vaer

Âge: N/A

Genre: Male

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
2021-12-15
Date d’apparition
1
Nombre de jours (date d’apparition – date de vaccination)
1
Description de l’événement indésirable

tinnitus aggravated; this is a spontaneous report received from a contactable reporter(s) (consumer or other non hcp) from the regulatory agency (ra). other case identifier(s): gb-mhra-vac-202202122142333260-otpob (mhra), gb-mhra-adr 26598161 (ra), gb-mhra-vac-202202122142333260-otpob (ra). a male patient of an unspecified age received bnt162b2 (comirnaty; batch number: unknown) via an unspecified route of administration on 15dec2021 as a single dose for covid-19 immunisation. medical history included tinnitus and it was ongoing. concomitant medications were not reported. on 16dec2021, 1 day after vaccination, the patient experienced tinnitus aggravated; reported as serious for being medically significant. this reaction did not occur as a result of a mistake made in the administration of the vaccine. the clinical outcome of the event tinnitus aggravated was not resolved at the time of this report. no follow-up attempts are possible; information about batch number cannot be obtained. no further information is expected

Données de laboratoire
na
Liste des symptômes
tinnitus
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
tinnitus