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