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Reporte zur Charge UJ76AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NC 2 NJ 1

VAERS 2050788

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (FOREIGN) · Charge UJ76AA

kritisch
Staat
NC
Alter
-
Geschlecht
U
Eingang
05.02.2022
Impfdatum
25.10.2021
Beginn
25.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Cardiac arrest

Symptomtext

Sudden Cardiac Arrest/My heart stopped beating for 20 minutes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 25Oct2021 15:30 (Lot number: Fh8020) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series completed, dose number unknown, MANUFACTURER UNKNOWN), for COVID-19 immunization. The following information was reported: CARDIAC ARREST (hospitalization, medically significant) with onset 25Oct2021 17:00, outcome "unknown", described as "Sudden Cardiac Arrest/My heart stopped beating for 20 minutes". The patient was hospitalized for cardiac arrest (start date: 25Oct2021, discharge date: 05Nov2021, hospitalization duration: 11 day(s)). Therapeutic measures were taken as a result of cardiac arrest (an ICD (Implantable defibrillator) was implanted in my upper-left chest). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
11,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1794024

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ76AA

mild
Staat
NC
Alter
65,0
Geschlecht
F
Eingang
17.10.2021
Impfdatum
16.10.2021
Beginn
16.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Erythema Flushing Malaise Pain in extremity

Symptomtext

Approximately 3-4 mins after I left the room where I got the vaccine, I became very flushed/red in my face and felt very "uncomfortable" with heat throughout my body. I remained in the area for the full 15 mins and the redness slowly subsided during that time. The pharmacist was made aware of the my condition and observed the redness of my face. When I left the pharmacy I felt okay. I believe I had a histamine/allergic reaction to something in the vaccine. This has never happened to me before, but this was my first time getting the high dose vaccine. About 4 hours later I had "standard" side effects of malaise, chills and aches of my legs. This was my first high dose flu vaccine being that I turned 65 this year.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
no illnesses
Vorgeschichte
Osteoporosis
Andere Medikamente
Vit K2, Mag Glycinate, Vit D2
Allergien
NKDA
Vorherige Impfungen
Malaise, aches and chills after Moderna second dose, 4/2021. No previous reactions to influenza vaccines.

VAERS 2724184

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ76AA

gering
Staat
NJ
Alter
0,3
Geschlecht
M
Eingang
14.12.2023
Impfdatum
06.12.2023
Beginn
06.12.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product preparation issue

Symptomtext

PENTACEL was given on 06DEC2023 but only the liquid part was administered and not the lyophilized component with no reported adverse event; Initial information was received on 06-Dec-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 months old male patient who was given DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] on 06-dec-2023 but only the liquid part was administered and not the lyophilized component with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included ROTAVIRUS VACCINE (ROTAVIRUS VACCINE) and PREVNAR 15 for Immunisation. On 06-Dec-2023, the patient received 0.5 ml, 1x (total) of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE, Suspension for injection (lot UJ76AA) but only the liquid part was administered and not the lyophilized component with no reported adverse event (single component of a two-component product administered) (latency same day) via intramuscular route in the left thigh for immunization. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
ROTAVIRUS VACCINE
Allergien
-
Vorherige Impfungen
-