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Reporte zur Charge UJ925AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

18Reporte angezeigt
1Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MN 4 FL 3 CA 2 AZ 2 NH 1 MI 1 AL 1 TX 1 MO 1 OH 1 TN 1

VAERS 2465775

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

kritisch
Staat
NH
Alter
78,0
Geschlecht
F
Eingang
22.10.2022
Impfdatum
27.09.2022
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute myocardial infarction Chest pain Hyperhidrosis Malaise Nausea Asthenia Blood pressure measurement Electrocardiogram Gait disturbance Hypotension Memory impairment Mobility decreased Myocardial infarction Tachycardia Vomiting

Symptomtext

Septal infarction/Patient was very sick/Patient didn't feel well/ Horrible chest pains/ Sweating all over / Very nauseated/ Felt dizzy/ Patient felt terrible / She went in bed; Patient couldn?t even move to the phone to ask for help; Vomited; Patient did not have much memory of those days; Patient had tachycardia, had tachycardia a couple of times; Patient blood pressure went too low; Patient felt super, super weak, not having energy at all; Patient was walking with a walker; This spontaneous case was reported by a patient and describes the occurrence of MYOCARDIAL INFARCTION (Septal infarction/Patient was very sick/Patient didn't feel well/ Horrible chest pains/ Sweating all over / Very nauseated/ Felt dizzy/ Patient felt terrible / She went in bed), MOBILITY DECREASED (Patient couldn?t even move to the phone to ask for help), VOMITING (Vomited), MEMORY IMPAIRMENT (Patient did not have much memory of those days), TACHYCARDIA (Patient had tachycardia, had tachycardia a couple of times), HYPOTENSION (Patient blood pressure went too low), ASTHENIA (Patient felt super, super weak, not having energy at all) and GAIT DISTURBANCE (Patient was walking with a walker) in a 78-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS71Y6B) for COVID-19 prophylaxis. The patient's past medical history included COVID-19. Concurrent medical conditions included Drug hypersensitivity (Codeine allergy), Blood pressure abnormal and Diabetes. Concomitant products included LISINOPRIL for Blood pressure abnormal, METFORMIN for Diabetes, GABAPENTIN for an unknown indication. On 27-Sep-2022, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, the patient experienced MYOCARDIAL INFARCTION (Septal infarction/Patient was very sick/Patient didn't feel well/ Horrible chest pains/ Sweating all over / Very nauseated/ Felt dizzy/ Patient felt terrible / She went in bed) (seriousness criteria hospitalization and medically significant), MOBILITY DECREASED (Patient couldn?t even move to the phone to ask for help) (seriousness criterion hospitalization), VOMITING (Vomited) (seriousness criterion hospitalization), MEMORY IMPAIRMENT (Patient did not have much memory of those days) (seriousness criterion hospitalization), TACHYCARDIA (Patient had tachycardia, had tachycardia a couple of times) (seriousness criterion hospitalization), HYPOTENSION (Patient blood pressure went too low) (seriousness criterion hospitalization), ASTHENIA (Patient felt super, super weak, not having energy at all) (seriousness criterion hospitalization) and GAIT DISTURBANCE (Patient was walking with a walker) (seriousness criterion hospitalization). The patient was treated with Surgery (Cardiac catheterization with IV heparin) for Myocardial infarction. At the time of the report, MYOCARDIAL INFARCTION (Septal infarction/Patient was very sick/Patient didn't feel well/ Horrible chest pains/ Sweating all over / Very nauseated/ Felt dizzy/ Patient felt terrible / She went in bed), MOBILITY DECREASED (Patient couldn?t even move to the phone to ask for help), VOMITING (Vomited), MEMORY IMPAIRMENT (Patient did not have much memory of those days), TACHYCARDIA (Patient had tachycardia, had tachycardia a couple of times), HYPOTENSION (Patient blood pressure went too low), ASTHENIA (Patient felt super, super weak, not having energy at all) and GAIT DISTURBANCE (Patient was walking with a walker) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood pressure measurement: Low. On an unknown date, Electrocardiogram: Septal infarction with T-Wave abnormality. Abnormal ECG.. Patient did not have medical history related to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. Patient did not have other vaccines within 1 month prior to Moderna COVID-19 vaccine. Patient underwent cardiac catheterization with IV heparin as a routine, and she did not needed stents. Patient did not experienced similar event in the past. Company comment: This spontaneous case reported by a patient concerns a 78-year-old female patient, with relevant medical history of diabetes mellitus, hypertension and COVID 19, who experienced the serious (caused hospitalization) unexpected events of Myocardial infarction, Mobility decreased, Vomiting, Memory impairment, Tachycardia, Hypotension, Asthenia, and Gait disturbance which occurred unknown days after fourth dose of mRNA-1273.222 bivalent vaccine administration. Unknown days after vaccination, the patient felt unwell, sick, and experienced nausea, chest pain, sweating, dizziness, vomiting and tachycardia. She was admitted to a hospital. Electrocardiogram was performed and she was diagnosed with septal infarction with T-wave abnormality. Patient underwent cardiac catheterization with IV heparin for treatment. After discharge, she experienced tachycardia, hypotension and needed walker for walking. Mentioned medical history of diabetes mellitus, hypertension and COVID 19 remain confounding for the event myocardial infarction. The benefit -risk relationship of mRNA-1273.222 bivalent vaccine is not affected by this report. This case was linked to MOD-2022-659173, MOD-2022-659178 (Patient Link).; Sender's Comments: This spontaneous case reported by a patient concerns a 78-year-old female patient, with relevant medical history of diabetes mellitus, hypertension and COVID 19, who experienced the serious (caused hospitalization) unexpected events of Myocardial infarction, Mobility decreased, Vomiting, Memory impairment, Tachycardia, Hypotension, Asthenia, and Gait disturbance which occurred unknown days after fourth dose of mRNA-1273.222 bivalent vaccine administration. Unknown days after vaccination, the patient felt unwell, sick, and experienced nausea, chest pain, sweating, dizziness, vomiting and tachycardia. She was admitted to a hospital. Electrocardiogram was performed and she was diagnosed with septal infarction with T-wave abnormality. Patient underwent cardiac catheterization with IV heparin for treatment. After discharge, she experienced tachycardia, hypotension and needed walker for walking. Mentioned medical history of diabetes mellitus, hypertension and COVID 19 remain confounding for the event myocardial infarction. The benefit -risk relationship of mRNA-1273.222 bivalent vaccine is not affected by this report.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
-
Labordaten
Test Name: Blood pressure; Result Unstructured Data: Low; Test Name: ECG; Result Unstructured Data: Septal infarction with T-Wave abnormality. Abnormal ECG.
Aktuelle Erkrankungen
Blood pressure abnormal; Diabetes; Drug hypersensitivity (Codeine allergy)
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19
Andere Medikamente
METFORMIN; LISINOPRIL; GABAPENTIN
Allergien
-
Vorherige Impfungen
-

VAERS 2628527

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

schwer
Staat
MI
Alter
93,0
Geschlecht
F
Eingang
08.05.2023
Impfdatum
07.10.2022
Beginn
22.04.2023
Tage bis Beginn
197,0
Dosis
N/A
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Aortic stenosis Bundle branch block left COVID-19 Cardiac failure acute Cardiac failure congestive Cardiogenic shock Cardiomyopathy Cardiorenal syndrome Carotid artery stenosis Chest pain Condition aggravated Coronary arterial stent insertion Dyslipidaemia General physical health deterioration Hypertension Hypophagia Hypotension Left ventricular failure

Symptomtext

4/22/2023 - 5/3/2023 (11 days) HEART CENTER CAD COVID-19 Severe aortic stenosis Combined cardiomyopathy Acute on chronic combined CHF Normocytic anemia HTN Dyslipidemia LBBB Mitral insufficiency DM type II Carotid stenosis HOSPITAL COURSE: Patient is a 93 year old with known CAD and severe aortic stenosis who had previously undergone work up for TAVR. She had been scheduled for PCI in December however unfortunately her husband passed away and she had to cancel. She was then scheduled for outpt PCI of the LAD 4/26/23 but presented to the local ED with chest pain and was positive for COVID-19. She was transferred to another facility and underwent DES to LAD 4/25/23. Pt developed worsened respiratory status on 4/26/23 requiring bipap and was treated with IV lasix for CHF and also secondary to COVID-19. Pulmonary was consulted and started decadron. Pt had worsening renal function 4/28/23 with early signs of shock with elevated LFTs and borderline lactic acid. BAV was offered but family ultimately preferred comfort approach and did not want any further procedure. Palliative was consulted. Pt continued to decline with worsened renal function, poor oral intake, and hypotension due to cardiogenic shock/severe aortic stenosis and cardiorenal. Hospice was consulted and ultimately decided to transfer to hospice facility.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiogenic shock
Hospital-Tage
11,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Aortic valve stenosis, etiology of cardiac valve disease unspecified Central scotoma, right eye Charles Bonnet syndrome Epiretinal membrane (ERM) of both eyes Intermediate stage dry age-related macular degeneration of both eyes Metamorphopsia Primary open-angle glaucoma, right eye, indeterminate stage CAD in native artery Congestive heart failure (CHF) (HCC)
Andere Medikamente
acetaminophen (TYLENOL) 500 mg tablet acetaminophen (TYLENOL) 650 MG suppository bisacodyl (DULCOLAX) 10 MG suppository haloperidol (HALDOL) 2 MG/ML solution hydrALAZINE (APRESOLINE) 50 MG tablet hydrALAZINE (APRESOLINE) 50 MG tablet hyoscy
Allergien
Penicillins
Vorherige Impfungen
-

VAERS 2597034

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj925aa

moderat
Staat
CA
Alter
78,0
Geschlecht
F
Eingang
15.03.2023
Impfdatum
20.12.2022
Beginn
20.12.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Immediate post-injection reaction Mobility decreased

Symptomtext

PATIENT HAS BEEN EXPERIENCING PAIN IN SHOULDER SINCE THE MOMENT SHE RECEIVED VACCINE 3 MONTHS AGO. SHE STATES THAT SHE COULD BARELY MOVE HER ARM FOR SEVERAL MINUTES POST VACCINE. PAIN IS STILL OCCURING TO THIS DAY, HAS BEEN FOLLOWING UP WITH DOCTORS TO DETERMINE CAUSE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
PATIENT WILL RECEIVE MRI IN MARCH 2023 TO CONFIRM ANY INJURY
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Penicillin
Vorherige Impfungen
PAIN AT INJECTION SITE THAT DID NOT LAST LONGER THAN 2 DAYS

VAERS 2500101

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

mild
Staat
AL
Alter
76,0
Geschlecht
F
Eingang
06.11.2022
Impfdatum
04.11.2022
Beginn
05.11.2022
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site swelling

Symptomtext

Swelling of arm approx 2 inches below administration site to approx 2 inches above elbow; swelling about 2 inches from normal; never had a reaction to flu shot before, no swelling of throat or difficulty swallowing

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

VAERS 2484849

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj925aa

mild
Staat
AZ
Alter
74,0
Geschlecht
F
Eingang
20.10.2022
Impfdatum
18.10.2022
Beginn
20.10.2022
Tage bis Beginn
2,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash

Symptomtext

Rash on arm and body

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

VAERS 2467283

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ925AA

mild
Staat
TX
Alter
70,0
Geschlecht
F
Eingang
03.10.2022
Impfdatum
30.09.2022
Beginn
01.10.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cellulitis Erythema Pruritus

Symptomtext

CELLULITIS TYPE SYMPTOMS; REDNESS, ITCH

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

VAERS 2584491

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) · Charge UJ925AA

gering
Staat
FL
Alter
64,0
Geschlecht
F
Eingang
20.02.2023
Impfdatum
08.02.2023
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age

Symptomtext

N/A

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
Iron deficiency Anemia Hydronephrosis
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2584490

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) · Charge UJ925AA

gering
Staat
FL
Alter
37,0
Geschlecht
M
Eingang
20.02.2023
Impfdatum
04.02.2023
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
-
Andere Medikamente
Fish oils
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2572862

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
MO
Alter
32,0
Geschlecht
M
Eingang
01.02.2023
Impfdatum
27.01.2023
Beginn
27.01.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product use issue

Symptomtext

32-year-old patient a dose of fluzone high dose quadrivalent with no adverse event; Initial information received on 27-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 32-year-old patient who received a dose of Influenza Quadrival A-B high dose HV vaccine [Fluzone high-dose quadrivalent] with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 27-Jan-2023, the patient of 32-year-old received a 0.7 ml dose of suspect Influenza Quadrival A-B high dose HV vaccine with no adverse event (product use issue) (lot UJ925AA, expiry date: 30-Jun-2023 with strength and formulation unknown) via intramuscular route in the left arm as prophylactic vaccination. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event. 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2529044

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
AZ
Alter
56,0
Geschlecht
M
Eingang
12.12.2022
Impfdatum
12.12.2022
Beginn
12.12.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Patient received a high dose flu vaccine instead of the regular dose. Patient was notified of medication error.

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

VAERS 2507990

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
CA
Alter
5,0
Geschlecht
U
Eingang
15.11.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product administered to patient of inappropriate age

Symptomtext

accidentally given a 5 year old child with no adverse event; Initial information received on 05-Nov-2022 regarding an unsolicited valid non-serious case received from a pharmacist via e-mail. This case involves a 5 year old patient of an unknown gender who was accidentally given INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received 0.7 ml of suspect of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot number: UJ925AA, expiry date: 30-June-2023, formulation, and strength not reported) via unknown route in unknown administration site for prophylactic vaccination and accidentally given a 5 year old child with no adverse event (product administered to patient of inappropriate age) (unknown latency). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Unknown for the event. 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2507898

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) · Charge UJ925AA

gering
Staat
MN
Alter
69,0
Geschlecht
M
Eingang
15.11.2022
Impfdatum
07.11.2022
Beginn
07.11.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event Product storage error

Symptomtext

The vial was initially stored in the refrigerator on 6-Oct-2022 and was administered on 7-Nov-2022; No adverse event; Administered expired dose to patient/expired dose was given after the 30 days; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered expired dose to patient/expired dose was given after the 30 days), PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 6-Oct-2022 and was administered on 7-Nov-2022) and NO ADVERSE EVENT (No adverse event) in a 69-year-old male patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 030G22B) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 3V (FLUZONE HIGH DOSE) for an unknown indication. No Medical History information was reported. On 07-Nov-2022, the patient received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE INACT SPLIT 3V (FLUZONE HIGH DOSE) (Intramuscular) 1 dosage form. On 07-Nov-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered expired dose to patient/expired dose was given after the 30 days). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 6-Oct-2022 and was administered on 7-Nov-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered expired dose to patient/expired dose was given after the 30 days), PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 6-Oct-2022 and was administered on 7-Nov-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered EXPIRED PRODUCT ADMINISTERED (Administered expired dose to patient/expired dose was given after the 30 days) and NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 6-Oct-2022 and was administered on 7-Nov-2022). No concomitant medications were provided. The reporter states that vaccine had been punctured and used. It was in their fridge for 32 days. The vial size was 2.5 mL. The vial was initially stored in the refrigerator on 6-Oct-2022 The vial did not undergo any temperature excursion. It was reported that expired dose was given after the 30 days. On 12-feb-2021, patient received 0.5 ml dose 1. On 12-mar-2021, patient received 0.5 ml dose 2 with batch number 032M020A. On 28-oct-2021, patient received 0.25 ml dose 3 with batch number 076C21A in left arm. On 31-mar-2022, patient had dose 4 with batch number 045J21A in left arm. No treatment medication was provided.

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

VAERS 2501941

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
MN
Alter
65,0
Geschlecht
U
Eingang
08.11.2022
Impfdatum
07.11.2022
Beginn
07.11.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered

Symptomtext

BUD of Moderna Vial (in Fridge) was 11/5/22, administered on 11/7/22

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

VAERS 2501932

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
MN
Alter
69,0
Geschlecht
M
Eingang
08.11.2022
Impfdatum
07.11.2022
Beginn
07.11.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered Product storage error

Symptomtext

Fridge BUD for Moderna Bivalent vaccine was 11/5/2022, Given on 11/7/22 (considered expired)

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

VAERS 2487171

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
FL
Alter
57,0
Geschlecht
F
Eingang
24.10.2022
Impfdatum
24.10.2022
Beginn
24.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Wrong Vaccine dose given.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
-
Vorgeschichte
HTN (hypertension) Barrett's esophagus Duodenitis without mention of hemorrhage Hypercholesteremia Insomnia Migraine, other, without mention of intractable migraine GERD Neck Pain
Andere Medikamente
omeprazole 20 mg delayed release capsule 1 cap(s) orally once a day. Motrin 2 tablets Orally Once daily as needed. Valtrex 500 mg tablet 1 tab(s) orally every 12 hours as needed, Notes: TraMADOL Hydrochloride 50 mg tablet 1 t
Allergien
Amoxicillin: Allergy - not specified Topamax: Side Effects - tingling in fingers
Vorherige Impfungen
-

VAERS 2482060

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
OH
Alter
76,0
Geschlecht
M
Eingang
18.10.2022
Impfdatum
18.10.2022
Beginn
18.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect product formulation administered

Symptomtext

Patient received instead of monovalent instead on bivalent Pfizer as booster

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect product formulation administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Metformin 500 ER BID
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2477156

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj925aa

gering
Staat
MN
Alter
91,0
Geschlecht
F
Eingang
13.10.2022
Impfdatum
12.10.2022
Beginn
12.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

I was unaware nursing staff already gave her the flu vaccine. They brought her to me and asked for both flu and covid vaccines. After the fact when reconciling records we noticed that nursing staff also gave the flu vaccine. She received a duplicate flu vaccine. Nursing staff were going to monitor for adverse effects and let me know if she developed side effects.

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

VAERS 2472307

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ925AA

gering
Staat
TN
Alter
68,0
Geschlecht
F
Eingang
07.10.2022
Impfdatum
03.10.2022
Beginn
05.10.2022
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood pressure increased

Symptomtext

Patient reporting have a high BP with systolic values around 170. She went to the doctor where the doctor checked her out and sent her home. This happened 2 days after the vaccination. Patient called and wanted me to report this.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Blood pressure increased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
not known
Vorgeschichte
not known
Andere Medikamente
losartan, hctz
Allergien
not known
Vorherige Impfungen
-