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Reporte zur Charge UT7315JA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

9Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
1Bleibende Schaeden
TX 5 GA 2 NC 1 AL 1

VAERS 1794322

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7315JA

schwer
Staat
TX
Alter
8,0
Geschlecht
M
Eingang
17.10.2021
Impfdatum
17.10.2021
Beginn
17.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Headache Injection site paraesthesia Presyncope Somnolence Vomiting

Symptomtext

Administered vaccine to patient. After returning to pharmacy mother stated that child needed to throw up. I took trash can to parent and patient threw up twice. He stated that he was sleepy and that his arm was tingly at injection site. I continued to monitor the child but he seemed like he was going to faint. He was complaining about having headache and needing to go to the restroom. I called 911. They came to the store and took all necessary vitals of patient. His blood pressure and pulse oxygen were normal. No reaction at injection site. No rash developed. No swelling of the tongue. The EMS stated possible hyperventilation and nerves. After they left mother waited in store another 10 minutes then left. When I called later in day, mother stated he ate meal and was fine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2206571

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7315ja

moderat
Staat
TX
Alter
35,0
Geschlecht
M
Eingang
30.03.2022
Impfdatum
23.11.2021
Beginn
14.12.2021
Tage bis Beginn
21,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Anxiety Arthritis Back pain Blood test normal Cardiac function test normal Cardiovascular disorder Chest X-ray normal Chest pain Chillblains Depression Fatigue Feeling abnormal Fibromyalgia Groin pain Immune system disorder Laboratory test normal Loss of personal independence in daily activities Lymphatic disorder

Symptomtext

Long-covid-like symptoms. Started with a very strong lymphatic reaction that I also had with my second shot. I was sick for almost two weeks after my second shot. After this shot, I was not as sick, but my lymphatic/immune reaction and tired feeling in my back lasted several weeks. As it was ending, I experienced an incredibly painful pain in my upper right back. This lasted for several weeks. I also experienced systemic dysfunction across my body. I now suffer from chronic tinnitus. I have experienced arthritis and arthritic reactions after working out or even minor activity. I have experienced chest pains and palpitation. I have experienced brain fog, anxiety, and depression. I have had issues with bladder control. I have been having nerve or fibromyalgia-type pain. I have been having circulation issues. I had a pseudo-chillblain. I had increased sensitivity to cold. I have had eye focus issues. I have had involuntary contracts and muscle spasms in my head and elsewhere. I have had kidney and groin-area pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
My doctors tested me for lupus and diabetes. I also had a physical. All blood tests were normal. I had a chest x-ray that was normal. My physician tested my heart and it was normal. My urologist tested my prostate and it was normal.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Xyzal 1 daily for allergy, Occasional Ibuprofen for headache
Allergien
Some nuts, berries, fruits
Vorherige Impfungen
Allergy shots.

VAERS 2193051

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

moderat
Staat
NC
Alter
62,0
Geschlecht
F
Eingang
22.03.2022
Impfdatum
01.11.2021
Beginn
01.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Discomfort Injected limb mobility decreased Injection site pain Injection site reaction Joint range of motion decreased X-ray abnormal

Symptomtext

Patient reports pain at the injection site that was not abnormal initially. It did not resolve and she does not have full range of motion after four months. She can not reach behind her back. It is very uncomfortable. She was seen by primary care provider. She has tried a Pred Pak and recently picked up a prescription for naproxen. Upon xray the provider saw a thickening in the area of injection that he could not diagnose and has referred her to an orthopedic. Her provider suggested that she may want us to report this

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
Xray, dates to report
Aktuelle Erkrankungen
none reported patient reports having the Pfizer Adult Vaccine two week Before, same arm
Vorgeschichte
none reported
Andere Medikamente
Provera 2.5mg daily Estrace 1mg daily
Allergien
no history of allergy or previous history of vaccine reactions
Vorherige Impfungen
-

VAERS 1804086

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

moderat
Staat
TX
Alter
38,0
Geschlecht
M
Eingang
21.10.2021
Impfdatum
15.10.2021
Beginn
15.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dyspnoea Fatigue Myalgia Pain Paraesthesia Rash Rash pruritic Throat irritation Throat tightness Wheezing

Symptomtext

Within an hour - shortness of breath, wheezing, throat closing up/tight/itching Itchy rash on neck within an hour Received IM steroid, benadryl Tingling /shooting pain feet within 2 hours tingling/shooting pain of hands within 6 hours Muscle aches/ fatigue

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
turmeric
Vorherige Impfungen
-

VAERS 1873801

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

mild
Staat
AL
Alter
4,0
Geschlecht
F
Eingang
16.11.2021
Impfdatum
10.11.2021
Beginn
12.11.2021
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site reaction Injection site swelling Injection site warmth Pallor

Symptomtext

Left anterior thigh with blanching erythema approx. 8 x 10 cm, warm/ slight swelling, non-tender. Right anterior thigh with approx. 1-2 cm area of redness around injection site.

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

VAERS 2150978

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

gering
Staat
TX
Alter
16,0
Geschlecht
F
Eingang
01.03.2022
Impfdatum
28.02.2022
Beginn
28.02.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event

Symptomtext

No adverse event reported. This report is being submitted as a vaccine ERROR

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

VAERS 1824734

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

gering
Staat
GA
Alter
62,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
11.10.2021
Beginn
11.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

Patient excursion case was accidently used on two patients even though they were no longer suitable for use / no AE; Initial information received on 14-Oct-2021 regarding an unsolicited valid non-serious case received from other health professional, physician and nurse via call center via Medical Information (Reference number- 00813237) in a specific country. This case involves a 62-year-old female patient who received INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] that was reported in a past excursion was accidently used (product storage error). The patient medical history, medical treatments, vaccinations, concomitant medication, and family history were not provided. On 11-Oct-2021, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B VACCINE [lot UT7315JA and expiry date: 30-Jun-2022] via an intramuscular route in the left deltoid for prophylactic vaccination. It was an actual medication error due to product storage error due [Latency: on the same day]. It was reported "nurse states the FLUZONE QIV that was reported in a past excursion case was accidently used on two patients even though they were no longer suitable for use. Nurse was looking for information regarding if they need to re-vaccinate the patients and any possible adverse effects." 2 separate patients accidentally received FLUZONE QUADRIVALENT after an excursion that were aware that they were not supposed to use the FLUZONE QUADRIVALENT. At time of reporting, no adverse event reported. 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
-
Allergien
-
Vorherige Impfungen
-

VAERS 1813083

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

gering
Staat
GA
Alter
56,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
11.10.2021
Beginn
11.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

patient accidentally received FLUZONE QUADRIVALENT after an excursion with no adverse event; Initial information was regarding an unsolicited valid non serious case was received from a nurse via Medical Information (Reference number- 00813179) and transmitted to Sanofi on 14-Oct-2021. This case involves a 56-year-old female patient who received INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] that was reported in a past excursion was accidently used (product storage error). The patient's medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. On 11-Oct-2021, the patient received a 0.5 mL dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (once, suspension for injection, lot UT7315JA, expiry date: 30-Jun-2022) via intramuscular route in the left deltoid for prophylactic vaccination. It was an actual medication error due to product storage error (latency: same day). It was reported "FLUZONE QIV that was reported in a past excursion case was accidently used on two patients even though they were no longer suitable for use". At time of reporting, no adverse event reported. 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
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1693490

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7315JA

gering
Staat
TX
Alter
37,0
Geschlecht
F
Eingang
12.09.2021
Impfdatum
08.09.2021
Beginn
08.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Adverse reaction Bacterial infection

Symptomtext

Pt having reaction in left arm, suspected to be bacterial in nature, will treat with abx, has only gotten worse since date of event.

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