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VAERS Report 2157040

Case Report Section

Vaer Report Details

Age: NA

Gender: Male

State: Outside US

Patient Died?
No
Vaccine information

Name: COVID19 (COVID19 (PFIZER-BIONTECH))

Type: Coronavirus 2019 vaccine

Manufacturer: PFIZER

Lot: unknown


Date report was received
2022-03-04
Date form completed
Date Vaccinated
Date of Onset
0
Number of days (onset date – vaccination date)
0
Adverse Event Description

fungal infection nos; smell change; taste changed; perspiration excessive; this is a spontaneous report received from a contactable reporter (consumer) from the regulatory authority web. regulatory number: gr-greof-20217502. a 66-year-old male patient received bnt162b2 (comirnaty) (lot number: unknown) as dose number unknown, single for covid-19 immunisation. the patient's relevant medical history was not reported. concomitant medications included: holisten; co-renitec; salospir; all received for 6 years. the following information was reported: fungal infection (hospitalization) with onset 01aug2021, outcome "not recovered", described as "fungal infection nos"; parosmia (disability) with onset 01jun2021, outcome "unknown", described as "smell change"; taste disorder (disability) with onset 01jun2021, outcome "unknown", described as "taste changed"; hyperhidrosis (non-serious) with onset 01jun2021, outcome "unknown", described as "perspiration excessive". no follow-up attempts are possible; information about lot/batch number cannot be obtained. no further information is expected

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