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VAERS Report 2157243

Case Report Section

Vaer Report Details

Age: 59 years old

Gender: Female

State: Outside US

Patient Died?
No
Vaccine information

Name: COVID19 (COVID19 (MODERNA))

Type: Coronavirus 2019 vaccine

Manufacturer: MODERNA

Lot: 214023


Date report was received
2022-03-04
Date form completed
Date Vaccinated
2021-10-10
Date of Onset
65
Number of days (onset date – vaccination date)
65
Adverse Event Description

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

Lab Data
na
List of symptoms
tinnitus
Patient Died?
No
Date Died
NA
Birth defect
false
Vaccine Administered By:
Unknown
Vaccine Purchased By:
Unknown
Patient visit ER?
No
Patient Hospitalized?
No
Stay in hospital
No
Days in hospital
Unspecified
Permanent disability?
Yes
Allergies:
na
Current Illness
na