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VAERS Report 2157243

Case Report Section

Détails du rapport Vaer

Âge: 59 ans

Genre: Female

Région : Outside US

Patient décédé?
Non
Renseignements sur les vaccins

Nom: COVID19 (COVID19 (MODERNA))

Type : Coronavirus 2019 vaccine

Fabricant: MODERNA

Lot: 214023


Date de réception du rapport
2022-03-04
Date à laquelle le formulaire est complèté
Date de vaccination
2021-10-10
Date d’apparition
65
Nombre de jours (date d’apparition – date de vaccination)
65
Description de l’événement indésirable

tinnitus, never previously warned, as soon as i received the third dose of anticovid vaccine, which increased over the days and persists despite treatment.; this case was received (reference number: it-minisal02-841268) on 25-feb-2022 and was forwarded to moderna on 25-feb-2022. this regulatory authority case was reported by a consumer and describes the occurrence of tinnitus (tinnitus, never previously warned, as soon as i received the third dose of anticovid vaccine, which increased over the days and persists despite treatment.) in a 59-year-old female patient who received mrna-1273 (spikevax) (batch no. 214023) for covid-19 vaccination. no medical history information was reported. on 10-oct-2021, the patient received dose of mrna-1273 (spikevax) (intravenous) 50 microgram. on 14-dec-2021, after starting mrna-1273 (spikevax), the patient experienced tinnitus (tinnitus, never previously warned, as soon as i received the third dose of anticovid vaccine, which increased over the days and persists despite treatment.) (seriousness criterion disability). at the time of the report, tinnitus (tinnitus, never previously warned, as soon as i received the third dose of anticovid vaccine, which increased over the days and persists despite treatment.) had not resolved. no concomitant product was provided by the reporter. no treatment medication was provided. company comment: this literature case concerns a 59-year-old female with no medical who experienced the serious (disability), unexpected event of tinnitus 66 days after an unknown dose of mrna-1273. treatment and testing not reported. the outcome is not resolved. the risk-benefit relationship of mrna-1273 vaccine is not affected by this report.; reporter's comments: tinnitus when administering dose booster anticovid vaccine; sender's comments: this literature case concerns a 59-year-old female with no medical who experienced the serious (disability), unexpected event of tinnitus 66 days after an unknown dose of mrna-1273. treatment and testing not reported. the outcome is not resolved. the risk-benefit relationship of mrna-1273 vaccine is not affected by this report

Données de laboratoire
na
Liste des symptômes
tinnitus
Patient décédé?
Non
Date de décès
N/A
Anomalie congénitale
false
Vaccin administré par :
Unknown
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