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