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Reporte zur Charge EN1283

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
1Lebensbedrohlich
0Bleibende Schaeden
ID 1 TN 1 HI 1

VAERS 1507894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN1283

schwer
Staat
ID
Alter
58,0
Geschlecht
F
Eingang
28.07.2021
Impfdatum
08.05.2021
Beginn
08.07.2021
Tage bis Beginn
61,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
SARS-CoV-2 test Thrombosis

Symptomtext

Blood clots; This is a spontaneous report from a contactable consumer or other non hcp. A 58-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch Number/Lot Number: EN1283), via an unspecified route of administration on 08May2021 (at the age of 58-Years-old) as Dose number Unknown, Single for COVID-19 immunization. Given facility where the most recent COVD-19 vaccine was administered. The patient was not pregnant at the time of vaccination. The patient medical history was reported as many and concomitant medications were not reported. Allergies were reported as Yes. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine (prior vaccination was none). The patient received other unknown medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient experienced blood clots on 08Jul2021. AE resulted in doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care as the event was life threatening illness having immediate risk of death from the event. Since the vaccination, the patient has been tested for COVID-19. The patient underwent lab tests and procedures which included SARS-COV-2 test with result negative on 10May2021. The patient was treated with blood thinners for the reported event. The patient have known allergies and many other medical history. Device date reported as 20Jul2021. The outcome of the event was reported as not recovered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
Test Date: 20210510; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2168677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN1283

gering
Staat
TN
Alter
84,0
Geschlecht
F
Eingang
09.03.2022
Impfdatum
03.02.2021
Beginn
05.02.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
SYR / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Deafness Injection

Symptomtext

Loss of hearing in both ears. Reported to primary care physician first and was treated with an ear cleaning and an antibiotic. Did not improve, and was checked again with worsening hearing loss. Was referred immediately to ENT and was given a 10-day cortisone medication. This did not help, so was given three injections into the eardrum, once weekly for three weeks. The hearing improved slightly, but has never been the same as before the vaccination event. She has been to Hearing Center several times for hearing test, plus another hearing aide center, plus another ENT to see if she was a candidate for a cochlear implant. All, with no resolution of this problem so far. We are now in the process of purchasing a new hearing aide due to the drastic loss of hearing since the vaccination. The cost of the new hearing aide is $6000.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Deafness
Hospital-Tage
-
Labordaten
I do not have dates, but could obtain them if needed. She has had multiple hearing tests, all showing profound hearing loss compared to before the adverse event with the vaccine.
Aktuelle Erkrankungen
None.
Vorgeschichte
-
Andere Medikamente
Levothyroxine, Carvedilol, Viactiv, Vitamin D3, Preservision
Allergien
NKA
Vorherige Impfungen
-

VAERS 1375876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN1283

gering
Staat
HI
Alter
-
Geschlecht
F
Eingang
04.06.2021
Impfdatum
03.02.2021
Beginn
03.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration Lymphadenopathy

Symptomtext

Lymph nodes under both arms have been swollen for 4 weeks; The patient received first dose and second dose on same day; The patient received first dose and second dose on same day; This is a spontaneous report from a contactable consumer. A 76-years-old non pregnant female consumer (patient) reported for herself that she received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EN1283) via an unspecified route of administration on 03Feb2021 at 10:00 in left arm as a single dose and second dose (Batch/Lot Number: EN5318) via an unspecified route of administration on 03Feb2021 at 12:00 in right arm as a single dose for covid-19 immunization. Medical history included known allergies and concomitant medications were not reported. The patient did not received any other vaccine in four weeks or other medication in two weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had not been tested for COVID-19. On 10Feb2021 at 12:00, the patient reported he had lymph nodes under both arms and they were swollen for four weeks.The patient received first dose and second dose on same day. The patient did not received any treatment. The outcome of the event lymphadenopathy was not recovered and for other events was unknown. No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-