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Reporte zur Charge FN2903

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 1 NJ 1

VAERS 2642200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2903

mild
Staat
MI
Alter
73,0
Geschlecht
M
Eingang
07.06.2023
Impfdatum
06.06.2022
Beginn
30.09.2022
Tage bis Beginn
116,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Ageusia COVID-19 Hypoaesthesia Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 on 09/30/2022. I had a fever, aches and loss sense of taste. The bottom of my feet felt numb at times. I contacted my doctor and got a prescription for Paxlovid. I had no complications taking the medication. As of today, I have no lingering symptoms from COVID-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
30SEPT2022 COVID-19 Test - Positive
Aktuelle Erkrankungen
N/A
Vorgeschichte
Heart Disease; Kidney Disease
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2573860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2903

mild
Staat
NJ
Alter
85,0
Geschlecht
F
Eingang
03.02.2023
Impfdatum
14.07.2022
Beginn
14.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test Inappropriate schedule of product administration Urticaria

Symptomtext

Onset of severe hives rash occurred 4 days after shot on 18Jul2022. Medical treatments have been administered until the present time.; dose dose number=1, administration date=04Nov2021; dose dose number=2, administration date=14Jul2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 85-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Jul2022 at 14:00 as dose 2, single (Lot number: FN2903) at the age of 85 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "prediabetes" (unspecified if ongoing); "right bundle block of heart" (unspecified if ongoing), notes: right bundle block of heart; "mild hypertension" (unspecified if ongoing); "Latex" (unspecified if ongoing), notes: known allergies Latex; "known allergies Black Pepper" (unspecified if ongoing), notes: known allergies Black Pepper,; "known allergies shrimp" (unspecified if ongoing), notes: known allergies shrimp. Concomitant medication(s) included: SIMVASTATIN; ASPIRIN [ACETYLSALICYLIC ACID]; BISOPROLOL. Past drug history included: Cortisone, reaction(s): "known allergies Cortisone", notes: known allergies Cortisone. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: 330268D, Location of injection: Arm Left, Vaccine Administration Time: 12:30 PM), administration date: 04Nov2021, when the patient was 84-year-old, for Covid-19 immunization. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 14Jul2022, outcome "unknown", described as "dose dose number=1, administration date=04Nov2021; dose dose number=2, administration date=14Jul2022"; URTICARIA (non-serious) with onset 18Jul2022 at 12:30, outcome "recovering", described as "Onset of severe hives rash occurred 4 days after shot on 18Jul2022. Medical treatments have been administered until the present time.". The event "onset of severe hives rash occurred 4 days after shot on 18jul2022. medical treatments have been administered until the present time." required physician office visit and emergency room visit. Therapeutic measures were taken as a result of urticaria. Additional information: It was reported that no other vaccine in four weeks. other medications in two weeks as Simvastatin Aspirin 81mg Bisoprolol 10mg. Onset of severe hives rash occurred 4 days after shot on 18Jul2022. Medical treatments have been administered until the present time. AE treatment with Prednisone, Elavil, Claritin, Allegra, Montelukast. No covid prior vaccination. Covid tested post vaccination Nasal Swab. Sender's Comments: Linked Report(s) :PFIZER INC-202300044092 same patient/drug, different dose/event;

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Heart block bundle branch (right bundle block of heart); Hypertension; Latex allergy (known allergies Latex); Prediabetes; Shellfish allergy (known allergies shrimp); Spice allergy (known allergies Black Pepper,)
Andere Medikamente
SIMVASTATIN; ASPIRIN [ACETYLSALICYLIC ACID]; BISOPROLOL
Allergien
-
Vorherige Impfungen
-