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Reporte zur Charge UT7716MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 2 CT 1 IN 1 NY 1 PA 1

VAERS 2496633

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7716MA

moderat
Staat
OH
Alter
44,0
Geschlecht
M
Eingang
02.11.2022
Impfdatum
02.11.2022
Beginn
02.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injected limb mobility decreased Injection site pain

Symptomtext

From day of vaccination, left shoulder pain. Unable to lift arm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2559516

SEQIRUS, INC. · INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) · Charge UT7716MA

mild
Staat
CT
Alter
32,0
Geschlecht
M
Eingang
13.01.2023
Impfdatum
13.10.2022
Beginn
09.01.2023
Tage bis Beginn
88,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Cough Fatigue Headache Myalgia Restlessness Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On Monday I started having runny nose and a cough not really tired just restless. I also had sore muscles and I tested the next day in which I was positive for COVID-19. I started having a headache Aleve and it did eliminate the pain. I called the doctor, and they did prescribe Paxlovid, and I haven't taken because everything is kind of going away on their own. Its really strange how I got it I have been wiping everything down and staying away from people.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
COVID-19 Test
Aktuelle Erkrankungen
N/A
Vorgeschichte
Underdeveloped Lungs
Andere Medikamente
Albuterol Sulfate; Fluticasone; Robitussin; Mucinex
Allergien
N/A
Vorherige Impfungen
-

VAERS 2545694

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7716MA

mild
Staat
IN
Alter
41,0
Geschlecht
F
Eingang
29.12.2022
Impfdatum
05.10.2022
Beginn
05.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Product administered at inappropriate site

Symptomtext

There was more pain with injection of the vaccine than normal, as I receive flu vaccines annually. I also noted that the injection site was higher than it should be. The pain in my shoulder/muscle has continued since the injection. I haven?t sought medical treatment yet, as I?m assuming this is tendinitis and I am waiting for it to resolve on its own (as I had happen about 8-10years ago as well).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
Same issue in R arm 8-10 years ago with flu vaccine

VAERS 2497716

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7716MA

mild
Staat
-
Alter
35,0
Geschlecht
F
Eingang
03.11.2022
Impfdatum
23.10.2022
Beginn
23.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Circumstance or information capable of leading to medication error Pain in extremity Poor quality product administered Product storage error

Symptomtext

Respiratory therapist received flu vaccine as part of our hospital's flu program where we give flu shots to staff on our unit. I am the administer for our unit and my assistant administered with a non-refrigerated dose. I had accidentally left a box of three doses out for a few days in my box of supplies (because it looks very similar to our band aid box), and was unsure what to do with it. I didn't hear back until several days later from the coordinator, so I left them with the supplies. I was giving them out that day, so I was aware that they were not to be used until I heard back from clinic. However, my assistant, jumped in and gave the doses to the respiratory therapist. I should have labeled the box as "do not use" and so I take responsibility for the error. I reported the incident immediately and we offered to revaccinate. This individual chose not to revaccinate since she is breastfeeding her child and was worried about receiving another dose. We did provide full education from the pharmacist recommending re-vaccination since the former dose was out of the refrigerator for > 72 hours and was considered ineffective. However, she still chose not to be revaccinated. I spoke with her following the injection and the only symptom she described was a sore arm following her injection.

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

VAERS 2480430

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge Ut7716ma

mild
Staat
OH
Alter
31,0
Geschlecht
F
Eingang
17.10.2022
Impfdatum
14.10.2022
Beginn
14.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Asthenia Immediate post-injection reaction Pain Pain in extremity Product administered at inappropriate site Urticaria

Symptomtext

The person who administered the vaccine went to high. Instead of injecting the medicine into my deltoid, she went much high in my shoulder. This immediately cause pain to shoot down my arm to my hand, index and thumb. This was done in my left shoulder. Unrelated to the location and about 36 hours later I developed hives on my back, face, neck, legs and chest. Treatment for the pain and weakness included steroids and this dose didn't seem to help much with the hives. Maybe the hives would have been worse without the steroids. It's hard to say. I'm still experiencing the hives, pain and weakness 3 days after the flu shot was administered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
Physical exam by primary care DR to evaluate pain and strength in left arm and hand.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Zyrtek, Sudafed
Allergien
Bactrim
Vorherige Impfungen
Flu vaccine (hives) chicken pox (rash, pain, fever, hives, swelling in entire arm that received the vaccine)

VAERS 2466842

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge UT7716MA

mild
Staat
NY
Alter
58,0
Geschlecht
F
Eingang
02.10.2022
Impfdatum
19.09.2022
Beginn
22.09.2022
Tage bis Beginn
3,0
Dosis
1
Route/Site
ID / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Urticaria

Symptomtext

Hives occurring after 3 days lasting 4 days and counting

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None, was taking omeprazol due to Barrett?s esophagus for a year. Discontinued a month ago
Vorgeschichte
Reynauds
Andere Medikamente
Daily multivitamin, salmon oil, turmeric/ cur cumin,CoQ10, beet juice. Stopped taking omeprazol a month ago
Allergien
Slight allergy to egg discovered 30 yrs ago but I can eat eggs
Vorherige Impfungen
Unable to provide data, 3 times less sever hives over past 15 years

VAERS 2715885

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7716MA

gering
Staat
PA
Alter
-
Geschlecht
F
Eingang
20.11.2023
Impfdatum
09.11.2023
Beginn
09.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

administered an expired Fluzone qiv pfs (expired on 30-Jun-2023) with no reported adverse event; Initial information was received on10-Nov-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age female patient who was administered influenza quadrival a-b vaccine [Fluzone Quadrivalent] (expired on 30-jun-2023) with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 09-Nov-2023, the patient received a dose of 0.5 ml of suspect Influenza Quadrival A-B Vaccine (lot number: UT7716MA and Expiry date:30-Jun-2023)(Unknown Formulation and strength) via intramuscular route in in the right arm for immunization. On 09-Nov-2023 the patient was administered an expired influenza quadrival a-b vaccine (expired on 30-jun-2023) with no reported adverse event (expired product administered) (Latency: same day). 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2497722

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7716MA

gering
Staat
-
Alter
29,0
Geschlecht
F
Eingang
03.11.2022
Impfdatum
23.10.2022
Beginn
23.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Circumstance or information capable of leading to medication error Drug ineffective No adverse event Product storage error

Symptomtext

Respiratory therapist received flu vaccine as part of our hospital's flu program where we give flu shots to staff on our unit. I am the representative for our unit and my assistant administered employee with a non-refrigerated dose. Earlier that week on Tuesday, Oct 18, I accidentally left a box of three doses out for a few days in my box of supplies (because it looks very similar to our band aid box), and was unsure what to do with it. I didn't hear back until several days later from the coordinator, so I left them with the supplies. I was giving them out that day on the 23rd and was aware that they were not to be used until I heard back from Occupational Health. However, my assistant, jumped in and gave the doses to the respiratory therapist. I should have labeled the box as "do not use" and so I take responsibility for the error. I reported the incident immediately and we offered to revaccinate. This individual chose not to revaccinate. We did provide full education from the pharmacist recommending re-vaccination since the former dose was out of the refrigerator for > 72 hours and was considered ineffective. However, she still chose not to be revaccinated. I spoke with her following the injection and she did not report any symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Circumstance or information capable of leading to medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-