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Reporte zur Charge U8200AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

11Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
WA 5 NM 2 MI 1 WI 1 NE 1 IN 1

VAERS 2720096

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

mild
Staat
MI
Alter
45,0
Geschlecht
M
Eingang
01.12.2023
Impfdatum
28.11.2023
Beginn
01.12.2023
Tage bis Beginn
3,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Axillary pain Back pain Flank pain Injection site pain Tenderness

Symptomtext

Normal course, limited to local soreness at injection site for first 24-48 hours. At ~50 hours since injection, noted tenderness at right sub-axillary space. Initially thought this might be an ingrown / infected hair follicle, but did not note visible redness or inflammation in the area. Upon palpating right armpit with left hand to assess, expressed acute pain to touch. At rest, with arms to sides, can feel some tenderness at right axillary space; but not painful. If I flex arms and hug arms against body as if I were cold, tenderness is more pronounced; but not painful. Only acutely painful upon manual palpation...liken to a deep bruise or, again, how an infected hair follicle might feel. Later in day today, I also noted some achiness in the right side, lower back. In context, I also recalled having some joint achiness of the knees last night (prior to morning of axillary pain). These back and knee pain may or may not be related. Reported symptoms to clinic nurse at occupational health clinic this morning. No additional care/interventions are pursued, beyond this report. I have no prior history of events with vaccines, to my memory... Contextually, this may be the first time I have had concurrent vaccine administrations , at least concurrent with COVID vaccine...

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
-
Vorgeschichte
Hypertriglyceridemia / hyperlipidemia -- not medically treated; lifestyle interventions only Cough, suspected related to GERB symptoms Essential tremor - not treated
Andere Medikamente
PRN OTC ibuprofen and vitamin D supplement -- not taken within 24 hours of vaccination, to my memory (I am the patient)
Allergien
Neomycin
Vorherige Impfungen
-

VAERS 2720075

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge U8200AA

mild
Staat
WI
Alter
52,0
Geschlecht
F
Eingang
01.12.2023
Impfdatum
01.12.2023
Beginn
01.12.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Ear pain Erythema Nasal congestion Nausea Neck pain Oropharyngeal pain Pain Pain in jaw Pyrexia Vaccination site pain

Symptomtext

Quick Left jaw neck and ear pain up from vaccination location and lasting for hours after injection. Red face, throat soreness, nasal congestion and nausea within 30 minutes. Fever and chills 2 hrs post injection, Aches and jabbing pains also beginning at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
asthma (well controlled)
Andere Medikamente
none
Allergien
many, pets/animals/environmental
Vorherige Impfungen
covid and influenza and yellow fever vaccinations

VAERS 2716308

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

mild
Staat
NM
Alter
7,0
Geschlecht
M
Eingang
21.11.2023
Impfdatum
17.11.2023
Beginn
01.11.2023
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Induration Mass Peripheral swelling Trismus Urticaria

Symptomtext

Mom called 3 days after vaccine appt, stating client had a rxn to vaccines, unsure which. Mom states client developed hives all over body, LA was swollen, had hard ball, and redness. Mom stated Friday (11/17/23 day of injections) client took a nap and woke up around 6 or 7 p.m. and had a ?lock jaw,? and no further info was given, unsure how long client had ?lockjaw.? Mom did not take client to urgent care or ED, and did not state when rxn started. Mom has not returned calls to follow up on onset and duration, unsure if client is still having s/sx's.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
none reported
Aktuelle Erkrankungen
none reported
Vorgeschichte
none reported
Andere Medikamente
none reported at appt
Allergien
no known drug allergies
Vorherige Impfungen
-

VAERS 2716303

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

mild
Staat
NM
Alter
18,0
Geschlecht
F
Eingang
21.11.2023
Impfdatum
17.11.2023
Beginn
01.11.2023
Tage bis Beginn
-
Dosis
7+
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Skin warm Swelling face Urticaria

Symptomtext

Mom called 3 days after vaccines administered, stating client had a rxn to vaccines. Mom states client developed hives, facial swelling, RA red and warm to touch. Mom did not take client to urgent care or ED, and did not state when rxn started. Mom has not returned calls to follow up on onset time and duration, unsure if client is still having s/sx's.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
none reported
Aktuelle Erkrankungen
none reported
Vorgeschichte
none reported
Andere Medikamente
none reported at appt
Allergien
no known drug allergies
Vorherige Impfungen
-

VAERS 2713444

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

mild
Staat
NE
Alter
8,0
Geschlecht
F
Eingang
13.11.2023
Impfdatum
07.11.2023
Beginn
09.11.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood culture C-reactive protein increased Cellulitis Chest X-ray Full blood count Peripheral swelling Pyrexia Urine analysis White blood cell count increased

Symptomtext

High fever of 106.1 on 11/9/23 morning. Evaluation in the ER. High CRP. Swelling to the Left arm on 11/20/23 Evaluation at office on 11/10/23 with repeat CBC & CRP. Rocephin given. Elevated CRP & WBC. Evaluation at office on 11/11/23 with repeat CBC & CRP. Rocephin given. Keflex started for cellulitis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
CXR, UA, CBC, CRP, Blood Cultures obtained in the ER for evaluation of fever on 11/9/23. Repeat CBC and CRP on 11/10/23 and 11/11/23
Aktuelle Erkrankungen
No illness one month prior.
Vorgeschichte
Chronic Lung Disease, Hypoplasia optic nerve, Obstructive sleep apnea, Microcephaly, GERD, Seizure disorder, Lennox Gastaut Syndrome, Cerebral Palsy, Periventricular Leukomalacia.
Andere Medikamente
Vitamin D, Nayzilam spray, Melatonin, Pro Air, Flovent, Clobazam, Valproic Acid, Baclofen, Fluticasone, Clonazipam
Allergien
None
Vorherige Impfungen
-

VAERS 2708183

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

mild
Staat
IN
Alter
34,0
Geschlecht
F
Eingang
01.11.2023
Impfdatum
31.10.2023
Beginn
31.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Cold sweat Eye irritation Hot flush Influenza Ocular hyperaemia Pyrexia Vaccine positive rechallenge Vomiting

Symptomtext

Every year I get the flu shot within a few hours I start getting red irritated eyes, vomiting, fever, chills/hot flashes, clammy. Basically, I have all the flu symptoms after getting the vaccine. It has happened since I was a kid.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
ADHD and sinus
Andere Medikamente
Adderall 20 mg Adderall 5mg Flonase
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2725381

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

gering
Staat
WA
Alter
11,0
Geschlecht
M
Eingang
19.12.2023
Impfdatum
18.12.2023
Beginn
18.12.2023
Tage bis Beginn
0,0
Dosis
7+
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

Patient was given flu vaccine when it was not indicated at this time. Patient parent notified and parent wanted VAERS report submitted. Otherwise, patient tolerated well and no ill symptoms at this time.

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

VAERS 2717717

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

gering
Staat
WA
Alter
12,0
Geschlecht
U
Eingang
24.11.2023
Impfdatum
14.11.2023
Beginn
14.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

temperature excursion ,box was left out and was not refrigerated duration: 5 days with no reported adverse event; box was left out and was not refrigerated, vaccines were actually delivered on 08NOV2023 and administered to patient on 14NOV2023 with no reported adverse event; Initial information received on 14-Nov-2023 regarding an unsolicited valid non-serious case received from a consumer/non-health care professional. This case involves a 12 years old unknown gender patient who was administered Influenza Quadrival A-B Vaccine [Fluzone Quadrivalent] on 14nov2023 with no reported adverse event and temperature excursion ,box was left out and was not refrigerated duration: 5 days with no reported adverse event and box was left out and was not refrigerated, vaccines were actually delivered on 08nov2023. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 14-Nov-2023, the patient received dose of 0.5 ml suspect INFLUENZA QUADRIVAL A-B VACCINE once (lot U8200AA and expiry date: 30-Jun-2024) (Unknown formulation and strength) via unknown route in unknown administration site for prophylactic vaccination. On an unknown date there was temperature excursion ,box was left out and was not refrigerated duration: 5 day with no reported adverse event (product storage error)(unknown latency), Influenza Quadrival A-B Vaccine were actually delivered on 08nov2023 and administered to patient on 14nov2023 with no reported adverse event (poor quality 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2717716

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

gering
Staat
WA
Alter
2,0
Geschlecht
U
Eingang
24.11.2023
Impfdatum
14.11.2023
Beginn
14.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

box was left out and was not refrigerated for 5 days and vaccines were administered post excursion with no reported adverse event; box was left out and was not refrigerated for 5 days and vaccines were administered post excursion with no reported adverse event; Initial information received on 14-Nov-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves a 2 years old patient of unknown gender and it was reported box was left out and was not refrigerated for 5 days and influenza quadrival A-B vaccine [Fluzone Quadrivalent] vaccine was administered post excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 14-Nov-2023 at 08:15 AM, the patient received a dose of 0.5 ml once of suspect influenza quadrival A-B vaccine (Suspension for injection) (lot: U8200AA; expiry date: 30-Jun-2024) via unknown route in the unknown administration site for Immunization and it was reported that box was left out and was not refrigerated for 5 days and vaccines were administered post excursion with no reported adverse event (product storage error) (unknown latency) (poor quality 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2716478

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

gering
Staat
WA
Alter
14,0
Geschlecht
U
Eingang
21.11.2023
Impfdatum
14.11.2023
Beginn
14.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

box was left out and was not refrigerated, duration: 5 days with no reported adverse event; the product administered to a patient with no reported adverse event; Initial information received on 14-Nov-2023 regarding an unsolicited valid non-serious case received from a consumer/non-health care professional. This case involves a 14 years old unknown gender patient who was administered the vaccine Influenza Quadrival A-B Vaccine [Fluzone Quadrivalent] whose box was left out and was not refrigerated, duration: 5 days with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 14-Nov-2023, the patient received a dose of 0.5 ml suspect Influenza Quadrival A-B Vaccine (lot U8200AA and expiry date: 30-Jun-2024) (strength, formulation, expiry date unknown)via unknown route in unknown administration site for prophylactic vaccination(Immunization) (poor quality product administered) (Latency: same day). On an unknown date the box was left out and was not refrigerated, duration: 5 days with no reported adverse event (product storage error) (unknown latency) following the administration of Influenza Quadrival A-B Vaccine. It was reported that the box was left out and was not refrigerated. No one knew in the facility, it was delivered. Max/low temperature reached: Unknown since it was in the box. Duration: 5 days Human error- Yes If negative advice, was the product administered to a patient? Yes Does extended stability data cover the excursion- No 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 2705746

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8200AA

gering
Staat
WA
Alter
15,0
Geschlecht
M
Eingang
30.10.2023
Impfdatum
26.10.2023
Beginn
26.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered Product administered to patient of inappropriate age

Symptomtext

When seeing this patient, I saw the child profile and saw that it said Meningococcal but didn?t see the year and thought that this was his first, but it wasn?t turns out that it was his second. I did notify parent already and she knows about the incident and Dr. is aware as well. Gave MenQuadfi NDC 4928159058 exp: 02/28/2026 lot:U7938AB. This will not count in System since he needed to be 16 yrs of age.

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