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Reporte zur Charge EN0172

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
1Bleibende Schaeden
IL 1 MA 1 CA 1 VA 1 OH 1

VAERS 1321160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN0172

schwer
Staat
IL
Alter
14,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
15.05.2021
Beginn
15.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Syncope Unresponsive to stimuli

Symptomtext

14 year old female fainted. alert and oriented X 0 not verbally responsive

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
female taken to the nearest hospital via ambulance
Aktuelle Erkrankungen
per mother no illnesses
Vorgeschichte
-
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2210931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN0172

mild
Staat
MA
Alter
43,0
Geschlecht
F
Eingang
01.04.2022
Impfdatum
20.04.2021
Beginn
04.05.2021
Tage bis Beginn
14,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pruritus SARS-CoV-2 test Vaccination site mass Vaccination site pain

Symptomtext

raised lump formed at the injection site/ is sore and slightly itchy; raised lump formed at the injection site/ is sore and slightly itchy; raised lump formed at the injection site/ is sore and slightly itchy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Apr2021 12:00 (Lot number: EN0172) at the age of 43 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing); "GERD" (unspecified if ongoing). Concomitant medication(s) included: ESCITALOPRAM. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8734, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 30Mar2021, when the patient was 43 years old, for Covid-19 Immunization.The following information was reported: VACCINATION SITE MASS (non-serious), VACCINATION SITE PAIN (non-serious), INJECTION SITE PRURITUS (non-serious) all with onset 04May2021 12:00, outcome "not recovered" and all described as "raised lump formed at the injection site/ is sore and slightly itchy". The event "raised lump formed at the injection site/ is sore and slightly itchy", "raised lump formed at the injection site/ is sore and slightly itchy" and "raised lump formed at the injection site/ is sore and slightly itchy" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site mass, vaccination site pain, injection site pruritus. Additional Information: It was reported that About 2 weeks after the 2nd vaccine, patient experienced a raised lump formed at the injection site. It's about 5mm and was sore and slightly itchy. Patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19, Since the vaccination, the patient has been tested for COVID-19, had no known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
Test Date: 20211118; Test Name: Icare; Test Result: Positive; Comments: Nasal Swab.
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anxiety; GERD.
Andere Medikamente
ESCITALOPRAM.
Allergien
-
Vorherige Impfungen
-

VAERS 1263084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN0172

mild
Staat
CA
Alter
37,0
Geschlecht
M
Eingang
27.04.2021
Impfdatum
24.04.2021
Beginn
24.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chills Headache Nausea

Symptomtext

10:58 am - chills 11:20am - headache 11:30 am patient took Tylenol 500mg 11:45am- Nausea advised to go to the ER for further evaluation Patient refused to go to the ER and said he will be fine. He don't want to go to the ER. BP: 122/90 Pulse: 76 o2- 99% Signed a letter stating patient refuses to go to the ER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2260087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN0172

gering
Staat
VA
Alter
-
Geschlecht
F
Eingang
06.05.2022
Impfdatum
-
Beginn
10.04.2022
Tage bis Beginn
-
Dosis
2
Route/Site
JET / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Deafness neurosensory Inner ear disorder

Symptomtext

A sensorineural hearing loss happens when there is damage in my inner ear; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: PH8078), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (ongoing); "BP" (ongoing). The patient did not have any known allergies. The patient took concomitant medications and other medications in two weeks which included BP and diabetes. Vaccination history included: BNT162b2 (Dose 1, Lot number: EP6955, Location of injection: Arm left, Vaccine administration time: 10:00 am), administration date: 28Mar2021, when the patient was 56-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, Lot number: EN0172, Location of injection: Arm left, Vaccine administration time: 11:00 am), administration date: 23Apr2021, when the patient was 56-year-old, for COVID-19 immunization. The following information was reported: DEAFNESS NEUROSENSORY (disability, medically significant) with onset 10Apr2022 at 07:00, outcome "not recovered", described as "A sensorineural hearing loss happens when there is damage in my inner ear". Therapeutic measures were taken as a result of deafness neurosensory which included storied shots in inner left ear. The facility where the most recent COVID-19 vaccine was administered was Hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Deafness neurosensory
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
BP
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: DIABETES, Continue: Yes
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1360444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En0172

gering
Staat
OH
Alter
26,0
Geschlecht
F
Eingang
29.05.2021
Impfdatum
22.04.2021
Beginn
08.05.2021
Tage bis Beginn
16,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaginal haemorrhage

Symptomtext

Spotting/bleeding two weeks into the first shot; This is a spontaneous report from a contactable consumer. A 26-year-old female patient received first dose of bnt162b2 (BNT162B2), via an unspecified route of administration, administered in Right Arm on 22Apr2021 17:00 (Lot Number: En0172) as 1ST DOSE, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Prior to vaccination, the patient has not been diagnosed with COVID-19 On 08May2021, patient experienced spotting/bleeding two weeks into the first shot. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the event was unknown. No treatment was received. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaginal haemorrhage
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-