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Reporte zur Charge EN6119

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

7Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IN 1 CA 1 MN 1 WA 1 OR 1 OH 1 NJ 1

VAERS 1085369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6119

moderat
Staat
IN
Alter
66,0
Geschlecht
M
Eingang
09.03.2021
Impfdatum
01.03.2021
Beginn
08.03.2021
Tage bis Beginn
7,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Musculoskeletal chest pain

Symptomtext

Soreness in chest muscles, I can breathe fine, taking deep breaths no problem. When I cough or sneeze, my chest feels like I have been punched in chest..

Weitere VAERSDATA-Felder
Praegender Schweregrund
Musculoskeletal chest pain
Hospital-Tage
-
Labordaten
None yet
Aktuelle Erkrankungen
None
Vorgeschichte
Diabetic, type two
Andere Medikamente
Metformin, goli Apple cider vinegar, Keto supplement.
Allergien
Unable to use statin drugs for cholesterol, ( affects muscle movement.) No other known allergies
Vorherige Impfungen
-

VAERS 1653191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6119

mild
Staat
CA
Alter
71,0
Geschlecht
M
Eingang
29.08.2021
Impfdatum
03.03.2021
Beginn
04.03.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Headache Vaccination site pain Vertigo positional

Symptomtext

Pain at injection site for 2 weeks; Headache; positional Vertigo; This is a spontaneous report from a contactable consumer, the patient. A 71-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6119) via an unspecified route of administration in the left arm on 03Mar2021 (at the age of 71-years-old) as a single dose for COVID-19 immunisation. Medical history included coronary artery disease(CAD) and sulfonamide allergy. Concomitant medication included losartan (MANUFACTURER UNKNOWN); from an unknown date for an unknown indication and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EN6201) via an unspecified route of administration in the left arm on 10Feb2021 for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 04Mar2021 at 04:00 AM, the patient experienced pain at injection site for 2 weeks, headache the next day and was still having them and also had positional vertigo. The event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of the adverse events and included Duloxetine for headache. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events pain at injection site, headache and positional vertigo was not recovered at the time of this report.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Coronary artery disease; Sulfonamide allergy
Andere Medikamente
LOSARTAN
Allergien
-
Vorherige Impfungen
-

VAERS 1376059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6119

mild
Staat
MN
Alter
57,0
Geschlecht
F
Eingang
05.06.2021
Impfdatum
06.03.2021
Beginn
07.03.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia

Symptomtext

Sore shoulder woke up with pain; This is a spontaneous report from a contactable consumer (patient). A 57-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection, Batch/Lot Number: EN6119, expiration date unknown) 1st dose, via an unspecified route of administration administered in Arm Right on 06Mar2021 15:45 pm, (at the age of 57-years-old) as first dose single dose for covid-19 immunization. Medical history included hypothyroidism. Patient had no known allergies. patient had not Covid prior vaccination and not Covid tested post vaccination. patient did not received any other vaccine in four weeks. Concomitant medication included levothyroxine taken for an unspecified indication, start and stop date were not reported. On 07Mar2021 04:00 am patient experienced sore shoulder woke up with pain. The outcome of the event was recovering. No follow-up attempts are possible; no further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente
LEVOTHYROXINE
Allergien
-
Vorherige Impfungen
-

VAERS 1373552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6119

mild
Staat
WA
Alter
39,0
Geschlecht
F
Eingang
04.06.2021
Impfdatum
04.03.2021
Beginn
16.03.2021
Tage bis Beginn
12,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Fatigue Headache

Symptomtext

Headache; Chills; Exhaustion; This is a spontaneous report from a contactable consumer, the patient. A 39-year-old non-pregnant female patient received the first dose of BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: EN6119) via an unspecified route of administration in the left arm on 04Mar2021 at 17:30 (at the age of 39-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient did not have any allergies to medications, food or other products. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications include spironolactone (MANUFACTURER UNKNOWN), vitamin D (MANUFACTURER UNKNOWN), vitamin B-12 (MANUFACTURER UNKNOWN) for an unknown indication. The patient was not tested for COVID-19 since the vaccination. On 16Mar2021 at 16:00, the patient felt chills. The patient felt fine until about mid-day and she felt she needed to take a nap. On the same day, the patient also felt exhaustion. On 17Mar2021 (reported as this morning), the patient had a slight headache. No therapeutic measures were taken for the reported events. The clinical outcome of the events chills, exhaustion and headache were unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
VITAMIN B-12; SPIRONOLACTONE
Allergien
-
Vorherige Impfungen
-

VAERS 1454749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6119

gering
Staat
OR
Alter
59,0
Geschlecht
F
Eingang
07.07.2021
Impfdatum
06.07.2021
Beginn
06.07.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Expired dose give, no adverse events at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
-
Andere Medikamente
Meloxicam 7.5 mg, Diclofenac Sodium 3% Gel, Aripiprazole 15 mg, Diazepam 10 mg.
Allergien
Demerol, Klonopin, Oxycodone HCL, Seroquel, Tylenol
Vorherige Impfungen
-

VAERS 1364245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6119

gering
Staat
OH
Alter
63,0
Geschlecht
F
Eingang
01.06.2021
Impfdatum
11.03.2021
Beginn
11.03.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Pharyngeal swelling

Symptomtext

Throat started swelling on one side (side of injection); Face turned red; This is a spontaneous report received from a non-healthcare professional, contactable patient. A 63-year-old non-pregnant female patient received the single dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot/batch number: EN6119), via an unspecified route of administrated in the right arm on 11Mar2021 at 1:00 PM (at the age of 63- years old) for COVID-19 Immunisation. The patients medical history included breast cancer, asthma and past drug history included allergic to codeine and morphine. The concomitant medications included fenofibrate (MANUFACTURER UNKNOWN) dose of 145 mg, pravastatin (MANUFACTURER UNKNOWN) dose of 20 mg and vitamin-D (MANUFACTURER UNKNOWN) of an unspecified dose used within 2 weeks of vaccination for an unknown indication. The patient did not receive any other vaccine with in four weeks prior to the vaccine. Prior and since the vaccination the patient was not diagnosed with COVID-19. On 11Mar2021 the patient experienced throat started swelling on one side (side of injection as reported) and face turned red. The clinical outcome of throat swelling and face red was recovered at the time of this reporting (Mar2021). No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Breast cancer
Vorgeschichte
Medical History/Concurrent Conditions: Asthma
Andere Medikamente
PRAVASTATIN; Vitamin d; FENOFIBRATE
Allergien
-
Vorherige Impfungen
-

VAERS 1273181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6119

gering
Staat
NJ
Alter
56,0
Geschlecht
F
Eingang
30.04.2021
Impfdatum
05.03.2021
Beginn
01.03.2021
Tage bis Beginn
-
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Middle ear effusion Tinnitus

Symptomtext

I developed tinnitus. At first it was intermittent, but progressed into a very constant high pitched sound. It occurs in both ears and sometimes feels like buzzing at the back of my skull.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Middle ear effusion
Hospital-Tage
-
Labordaten
ENT visit found no fluid in my ears. Hearing test showed minimal loss, probably age related.
Aktuelle Erkrankungen
high bp, reflux
Vorgeschichte
-
Andere Medikamente
Amlodipine 10mg, Esomeprazole 40 mg
Allergien
clydamycin
Vorherige Impfungen
-