Zurueck zur Suche

Reporte zur Charge U8084AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

13Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MA 4 WI 2 VA 1 IL 1 VT 1 MD 1 NJ 1 DC 1

VAERS 2695831

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

schwer
Staat
WI
Alter
70,0
Geschlecht
F
Eingang
13.10.2023
Impfdatum
11.10.2023
Beginn
11.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Dizziness Fatigue Feeling cold Nausea Pain Palpitations Syncope Tremor

Symptomtext

Before 12 o'clock and within 30 minutes I started feeling achey, the aches intensified all afternoon, followed by the chills, and by 4 o'clock I was wrapped up in blankets on the couch. My hands were freezing cold and I was shaking uncontrollably. At 5 o'clock while walking upstairs to bed, I became nauseated and began to pass out. I fell to the ground and kept my head down until the feeling passed. My heart was racing and pounding. My husband helped to bed, my heart rate was 93 and it continued racing well into the evening. (my heart rate usually runs 60's) I continued feeling nauseated on/off during the evening. I was fine in the morning, just tired. Today, I am tired, however, I am fine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None I did not seek treatment
Aktuelle Erkrankungen
None
Vorgeschichte
Left Ventricular Cardiomyopathy with low ejection fraction, 49%.
Andere Medikamente
None
Allergien
Atropine-low blood pressure, fainting Demeral-vomiting
Vorherige Impfungen
-

VAERS 2705545

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

moderat
Staat
VA
Alter
-
Geschlecht
M
Eingang
30.10.2023
Impfdatum
21.10.2023
Beginn
22.10.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chest discomfort Discomfort Echocardiogram normal Electrocardiogram abnormal Hypotension Laboratory test normal Myocardial ischaemia Scan myocardial perfusion abnormal Sinus bradycardia Ventricular extrasystoles

Symptomtext

10/22/2023 new onset severe sinus bradycardia with PVCs and hypotension not related to MI, CAD or new heart block or conduction delay. History of RBBB only, mild HTN and HLD. Patient received Fluzone HD 23-24 PFS Sano, Lot U8984AB on 10/21/2023

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypotension
Hospital-Tage
-
Labordaten
EKG, 22-Oct-2023, Sinus bradycardia, unifocal PVCs and bigemeny, SECONDS, 42 bpm. All lab work WNL. Symptomatic hypotension, chest tightness, heavyness. Echocardiogram nl, Nuclear med stress test no arrthhmia precipitated, small area apical anterior lateral ischemia.
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma
Andere Medikamente
Simvastatin; Lisinopril; Tylenol; Aleve; Advair; Fluticasone propionate nasal spray
Allergien
-
Vorherige Impfungen
-

VAERS 2719673

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge U8084AB

mild
Staat
-
Alter
-
Geschlecht
F
Eingang
30.11.2023
Impfdatum
12.10.2023
Beginn
01.10.2023
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bowel movement irregularity Cognitive disorder Decreased appetite Diarrhoea Food intolerance Impaired work ability Mental impairment Morning sickness Nausea

Symptomtext

Nausea gravidarum; had trouble thinking and making decision; "could not tolerate any type of sauce with salt"; One week later I was nauseous/nauseousness lasted for 2 weeks; diarrhea; my cognitive abilities were affected/had trouble thinking and making decisions; bowel movements were not normal for 3 weeks; appetite for about 2 weeks after the onset of the nauseousness; This serious case was reported by a consumer and described the occurrence of difficulty thinking in a 72-year-old female patient who received Flu Seasonal QIV Dresden (Fluarix Tetra 2023-2024 season) (batch number U8084AB, expiry date 30-JUN-2024) for prophylaxis. On 12-OCT-2023, the patient received Fluarix Tetra 2023-2024 season. In OCT-2023, 1 week after receiving Fluarix Tetra 2023-2024 season, the patient experienced difficulty thinking (Verbatim: had trouble thinking and making decision) (serious criteria GSK medically significant), nausea (Verbatim: One week later I was nauseous/nauseousness lasted for 2 weeks), diarrhea (Verbatim: diarrhea), cognitive function abnormal (Verbatim: my cognitive abilities were affected/had trouble thinking and making decisions), bowel movement irregularity (Verbatim: bowel movements were not normal for 3 weeks) and food intolerance (Verbatim: "could not tolerate any type of sauce with salt"). On 19-OCT-2023, the patient experienced nausea gravidarum (Verbatim: Nausea gravidarum). On an unknown date, the patient experienced appetite lost (Verbatim: appetite for about 2 weeks after the onset of the nauseousness). In OCT-2023, the outcome of the nausea was resolved (duration 2 weeks). The outcome of the difficulty thinking and food intolerance were not reported and the outcome of the nausea gravidarum was resolving and the outcome of the diarrhea and bowel movement irregularity were resolved (duration 3 weeks) and the outcome of the cognitive function abnormal and appetite lost were resolved (duration 2 weeks). It was unknown if the reporter considered the difficulty thinking, nausea gravidarum, nausea, diarrhea, cognitive function abnormal, bowel movement irregularity, appetite lost and food intolerance to be related to Fluarix Tetra 2023-2024 season and Fluarix Tetra Pre-Filled Syringe Device. It was unknown if the company considered the difficulty thinking, nausea gravidarum, nausea, diarrhea, cognitive function abnormal, bowel movement irregularity, appetite lost and food intolerance to be related to Fluarix Tetra 2023-2024 season and Fluarix Tetra Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK receipt date: 20-NOV-2023 The reporter reported that the patient received Fluarix for flu vaccine shot. the patient was nauseousness lasted for 2 weeks with cognitive abilities and abnormal bowel movements for 3 weeks. The reporter stated that there must had been a sodium type preservative in the vaccine. One week later I was nauseous, could not tolerate any type of sauce with salt, cognitive abilities were affected, had trouble thinking and making decisions. The patient had diarrhea and my bowel movements were not normal for 3 weeks later. The patient did not had an appetite for about 2 weeks after the onset of the nauseousness. The patient's co-workers could told by the patient facial expression something was wrong with the patient. One of the patient's coworkers did not want to get a flu shot since the patient had such a bad reaction. The patient was making mistakes at work for about 2 weeks. The symptoms were not treated. The patient never had an allergic reaction to a flu shot and will never get another one manufactured by GlaxoSmithKline. The reporter consented to follow up.

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

VAERS 2709149

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

mild
Staat
IL
Alter
74,0
Geschlecht
F
Eingang
02.11.2023
Impfdatum
01.11.2023
Beginn
01.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site reaction Injection site swelling Injection site warmth

Symptomtext

PT CALLED AND STATED SHE HAS REDNESS/SWELLING/WARMTH AT INJECTION SITE- SOUNDS LIKE INJECTION SITE REACTION, PT TOLD TO MONITOR AND LET PHARMACY KNOW IF IT DOESNT GET BETTER/IF SYMPTOMS WORSEN

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

VAERS 2703742

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

mild
Staat
VT
Alter
75,0
Geschlecht
F
Eingang
27.10.2023
Impfdatum
26.10.2023
Beginn
27.10.2023
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site induration Injection site swelling Injection site warmth

Symptomtext

PATIENT REPORTED BACK TO PHARMACY THE DAY AFTER VACCINATION AT ~11AM. PATIENTS LEFT UPPER ARM WAS VERY SWOLLEN AND RED FROM THE DELTOID TO THE ELBOW. DOES NOT REPORT PAIN. PATIENT STATES HARDNESS AND WARMNESS IN THE AREA. RECOMMENDED THE PATIENT REPORT TO URGENT CARE OR EMERGENCY ROOM FOR EVALUATION. RECOMMENDED ICING THE AREA IN THE MEANTIME TO REDUCE SWELLING. PATIENT STATES SHE MAY NOT BE ABLE TO SEEK MEDICAL EVALUATION DUE TO TAKING CARE OF A FAMILY MEMBER AT HOME.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NONE STATED
Vorgeschichte
NONE STATED
Andere Medikamente
UNKNOWN. CONFIRMED NO BLOOD THINNERS
Allergien
NO KNOWN ALLERGIES
Vorherige Impfungen
-

VAERS 2712483

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge u8084ab

gering
Staat
MD
Alter
77,0
Geschlecht
F
Eingang
10.11.2023
Impfdatum
08.11.2023
Beginn
08.11.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Patient requested adjuvanted flu shot and was given non-adjuvanted

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
hypothyroidism
Andere Medikamente
cyclosporin eye drops, flovent inhaler 44mcg, albuterol inhaler, famotidine 40mg, levothyroxine 25mcg, armour thyroid 60mg
Allergien
none known
Vorherige Impfungen
-

VAERS 2710318

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

gering
Staat
WI
Alter
66,0
Geschlecht
F
Eingang
06.11.2023
Impfdatum
27.10.2023
Beginn
27.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blister Skin lesion

Symptomtext

Pt had bulla appear on L wrist hours after having vaccines. These have multiplied in teh course of week to 2 lesions (L wrist and hand).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Blister
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
NA
Vorgeschichte
Vitamin D Deficiency, Osteopenia, Dyslipidemia, Asthma, Allergies
Andere Medikamente
Montelukast, Symbicort, Duoneb/Albuterol prn, Ascorbic Acid, Vitamin D, Magnesium, Vitamin B, Naproxen prn, Ca/Vitamin D
Allergien
Beef
Vorherige Impfungen
-

VAERS 2700120

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

gering
Staat
MA
Alter
63,0
Geschlecht
F
Eingang
23.10.2023
Impfdatum
20.10.2023
Beginn
20.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

High-dose flu shot given to a patient under age 65.

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

VAERS 2700116

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

gering
Staat
MA
Alter
63,0
Geschlecht
M
Eingang
23.10.2023
Impfdatum
20.10.2023
Beginn
23.10.2023
Tage bis Beginn
3,0
Dosis
N/A
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

High-dose flu shot administered to a patient who is under 65 years old,

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

VAERS 2696470

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge u8084ab

gering
Staat
MA
Alter
32,0
Geschlecht
F
Eingang
16.10.2023
Impfdatum
11.10.2023
Beginn
11.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

No adverse effects noted. The incorrect flu shot (Fluzone HD) was removed from the fridge and administered to the patient instead of the correct flu shot (flucelvax)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None disclosed
Vorgeschichte
-
Andere Medikamente
None disclosed
Allergien
None disclosed
Vorherige Impfungen
-

VAERS 2686418

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

gering
Staat
MA
Alter
60,0
Geschlecht
F
Eingang
26.09.2023
Impfdatum
22.09.2023
Beginn
22.09.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

High dose Quadrivalent administered to individual less than 65 years of age. Call placed to individual 3 days following injection to inform of error. She denies any sign or symptoms of concern; no adverse reaction reported as result of error.

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

VAERS 2684543

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

gering
Staat
NJ
Alter
65,0
Geschlecht
F
Eingang
21.09.2023
Impfdatum
19.09.2023
Beginn
20.09.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Lip swelling

Symptomtext

Swollen Right Lip noticed on 9/20 at 5am. Treatment: Medrol dose pack and seen by Occupational Medicine Services 9/20 and follow up 9/21.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Lip swelling
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
None-per her flu consent form
Andere Medikamente
-
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2680531

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8084AB

gering
Staat
DC
Alter
67,0
Geschlecht
F
Eingang
08.09.2023
Impfdatum
08.09.2023
Beginn
08.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient was offered to be vaccinated against the Flu by the technician and she accepted. she also requested to have a covid booster. the FLU shot was processed through her insurance and a paid claim obtained. The pharmacist administered the Flu on the left arm and when trying to administer the covid on the right arm realized that she had a bandage on. The pharmacist then asked why the bandage, it is then that she said she had a flu shot . on verifying from her profile, it was discovered that she had a flu on 09/03/23. when the pharmacist tried to explain that she has been given two shots within a week, she seemed less bothered and left.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
NOT KNOWN
Vorgeschichte
NOT KNOWN
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-