Adverse Event Reporting

VAERS ID 1589157
Gender Female
Age
StateCode FR
Pharmaceutical Company PFIZER\BIONTECH
Lot Number
Number of vaccinations 1
Vaccinated
Onset 2021-04-01
Condition
Symptoms
  • Asthenia
  • Vertigo
  • Tinnitus
  • Lethargy

Current Illness

Preexisting Conditions

Medical History/Concurrent Conditions: Lactation decreased; Tinnitus

Other Medications

Previous Vaccinations

Allergies

Laboratory Data

Write-up

vertigo; lethargic; low in energy; tinnitus; Lethargy; Worsening of tinnitus; This is a spontaneous report from a contactable consumer downloaded from a regulatory authority-WEB, regulatory authority number GB-MHRA-WEBCOVID-202107291453366110-ZZGN5, Safety Report Unique Identifier GB-MHRA-ADR 25727253.
A 41-year-old non-pregnant female patient received First dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on an unspecified date as dose 1, single and second dose via an unspecified route of administration on 10Jul2021 as dose 2, single for COVID-19 immunisation (at the age of 41-year-old).
Medical history included Lactation decreased and tinnitus with unknown ongoing.
Patient has not had symptoms associated with COVID-19, not had a COVID-19 test.
Patient was not currently breastfeeding.
The patient's concomitant medications were not reported.
Reporter stated that, she was experienced several bouts of Tinnitus (ringing in ears / deafness like ear popping in both ears randomly) after the 1st vaccine, about 1-2 weeks later.
Also experienced slight vertigo along with the tinnitus.
Reported it to the nurse delivered her 2nd dose.
She has been extremely lethargic weeks after her 2nd dose (3 weeks later and still very lethargic, low in energy).
No changed to diet or routine, finding myself falling asleep if I lie down at all.
On an unspecified date, the patient experienced vertigo, lethargic, low in energy and tinnitus; worsening of tinnitus on Apr2021, lethargy on 10Jul2021.
Patient has not tested positive for COVID-19 since having the vaccine.
Patient was not enrolled in clinical trial.
The outcome of the event Worsening of tinnitus and Lethargy was not recovered and other events was recovering.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.
No further information is expected.