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Reporte zur Charge UT7325LA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

10Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MN 3 ND 2 WI 2 NJ 1 DE 1

VAERS 1765166

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

schwer
Staat
MN
Alter
28,0
Geschlecht
F
Eingang
06.10.2021
Impfdatum
06.10.2021
Beginn
06.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Condition aggravated Dizziness Hyperhidrosis Syncope

Symptomtext

Note Patient came into Covid/Influenza Vaccine clinic today for both the Covid booster and Influenza vaccine. Patient reported that at times she has syncopal episodes with shot administrations, but not every time. Patient was okay with receiving both vaccines today 10/6/21 around 1215. Upon giving the influenza vaccine patient became lightheaded and diaphoretic. Laid on ground by self during that episode. At that time paramedic on scene came to help watch and assist with patient. Patient reported feeling better within a minute or two and sat back up in chair and still wanted to receive the Covid booster. The paramedic and this RN, still felt safe to proceed with Covid booster. While going through screening questions patient became lightheaded and diaphoretic again and laid back down on the floor. Felt better again momentarily and sat back in the chair. At this time Paramedic and RN were going to move patient to observation area and recliner to receive Covid booster there, and at that time patient had syncopal episode in chair and the Paramedic and RN laid patient on ground, and it took a 30 seconds to a minute before patient woke back up. Vital signs were taken and were stable. After waiting a few minutes moved patient back to observation area around 1225, and with permission from the paramedic, patient, and leadership this RN proceeded to give patient their Covid booster, patient stayed for observation until 1240 and was okay to leave per paramedic. Electronically signed by: R.N. 10/06/21 12:41 PM CDT

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Nervous Dysmenorrhea Pain Foot Left Musculoskeletal Dystrophic Nail Foreign Body Foot Superficial Initial Left Other Maintenance Health Adult Depression Major Recurrent Severe Without Psychotic Features (HCC) Anxiety Generalized Disorder Obsessive Compulsive Disorder
Andere Medikamente
acetaminophen (TYLENOL) 325 mg tablet escitalopram (LEXAPRO) 10 mg tablet Estarylla 0.25-35 mg-mcg per tablet multivitamin (multivitamin) tablet prenatal vitamin-Ca-iron-FA (VINATE ONE) 60 mg iron-1 mg per tablet valACYclovir (Valtrex) 1000
Allergien
Weed PollenCough, Itching,
Vorherige Impfungen
Syncope(Pfizer and other previous vaccination per patient)

VAERS 1876127

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

mild
Staat
NJ
Alter
-
Geschlecht
F
Eingang
17.11.2021
Impfdatum
05.10.2021
Beginn
05.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Headache Lymphadenopathy Pain in extremity Tinnitus

Symptomtext

Ringing in her ears; swollen lymph nodes; achy joints, especially her fingers; headache; Initial information received on 29-Oct-2021 regarding an unsolicited valid non-serious case received from non-healthcare professional via Regulatory Authority (RA) (Reference number- 00835123). This case involves a female patient of unknown age who experienced swollen lymph node (lymphadenopathy), headache, ringing in her ears (tinnitus), achy joints especially fingers (arthralgia) when received vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. Patient gets a flu (INFLUENZA VACCINE) shot every year, and usually experiences a headache and achy joints, which resolve quickly. The patient's medical history, concomitant medication and family history were not provided. On 05-Oct-2021, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot number: UT7325LA and expiry date not reported) via an unknown route at an unknown administration site for prophylactic vaccination. On 05-OCT-2021 the patient developed a non-serious swollen lymph node (lymphadenopathy), headache, ringing in her ears (tinnitus) persisted for over three weeks, achy joints especially fingers (arthralgia) same day following the administration of INFLUENZA QUADRIVAL A-B VACCINE. When the event (tinnitus) persisted for a couple of days, she contacted her healthcare professional. It was reported "Caller states that she experienced adverse effects from FLUZONE QUADRIVALENT and she is asking for information on how to treat those symptoms. She declined to provide demographics." Laboratory details were not reported. The patient was treated with ADVIL [IBUPROFEN] for lymphadenopathy, headache, tinnitus and arthralgia. The Advil caused resolution of events, except the tinnitus. On an unknown date, the patient recovered from the events (lymphadenopathy, headache, arthralgia). At the time of this report, outcome of the events (tinnitus) was not resolved.

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

VAERS 1836590

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

mild
Staat
ND
Alter
37,0
Geschlecht
F
Eingang
02.11.2021
Impfdatum
29.10.2021
Beginn
30.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site pruritus Injection site swelling

Symptomtext

Had a red raised area where the shot was given about the size of a golf ball. Very itchy, no warmth. Called 11/1/2021 at 3pm to report this reaction. States area is already much better, no itching today.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
autoimmune disease, low white blood count
Andere Medikamente
unknown
Allergien
latex, aspirin, benadryl, bee stings
Vorherige Impfungen
Client stated similar reaction to previous flu shot years ago in her hip. Same situation. She was unsure of which brand of flu v

VAERS 1762168

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

mild
Staat
ND
Alter
5,0
Geschlecht
F
Eingang
05.10.2021
Impfdatum
04.10.2021
Beginn
04.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site induration Injection site pain Injection site swelling Injection site warmth

Symptomtext

Injection site started to get red, firm and warm to touch the evening of 10/4/2021, mother took pictures, area was about 2 inches by 2 inches morning of 10/5/2021. As of 1540 on 10/5/2021 the area has become more swollen, still warm to the touch and red as well as approximately 6 inches by 6 inches. Pt reports some pain but is able to still play. Instructed mother to apply a cold/ice compress and childrens Benedryl to help with swelling as well as monitor it and if it continues to get worse then see the local clinic.

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

VAERS 1759264

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

mild
Staat
-
Alter
47,0
Geschlecht
F
Eingang
04.10.2021
Impfdatum
30.09.2021
Beginn
30.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Injection site erythema Injection site pruritus Injection site warmth

Symptomtext

L arm got red 4 inches down from injection site up to L side of neck approximately 5minutes after injection. became slightly warm to the touch, very itchy. took a benadryl 10-15minutes after sx started, immediate relief of sx.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
with 2nd COVID vaccine dose(Pfizer)-same exact sx as this report. 47 yrs. old

VAERS 1734565

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

mild
Staat
DE
Alter
51,0
Geschlecht
F
Eingang
25.09.2021
Impfdatum
21.09.2021
Beginn
23.09.2021
Tage bis Beginn
2,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Motion sickness Nausea SARS-CoV-2 test negative Tension headache Vertigo Vomiting

Symptomtext

Received flu shot mid-morning 9/21, woke morning 9/23 with tension-like headache, vertigo/seasick type of feeling, nausea and vomiting which lasted majority of the day. Symptoms resolved by next morning.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nausea
Hospital-Tage
-
Labordaten
Took a rapid COVID-19 nasal swab which was negative.
Aktuelle Erkrankungen
None
Vorgeschichte
Hypertension
Andere Medikamente
Irbesarten 300mg Daily - I take in the evening.
Allergien
None
Vorherige Impfungen
-

VAERS 1757618

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

gering
Staat
WI
Alter
0,2
Geschlecht
M
Eingang
04.10.2021
Impfdatum
27.09.2021
Beginn
27.09.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error Product administered to patient of inappropriate age Wrong product administered

Symptomtext

A two month old patient accidentally received two injections of Fluzone QIV NP that were intended for family members instead of 2 month vaccine, no AE; A two month old patient accidentally received two injections of Fluzone QIV NP that were intended for family members instead of 2 month vaccine, no AE; Initial information regarding an unsolicited valid non-serious case was received from a physician via consumer/non-health care professional via Agency (Reference number- 00786864) and transmitted to Sanofi on 27-Sep-2021. This case involves a 2 month old male patient who accidentally received two injections of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] that were intended for family members instead of 2 month vaccine (Wrong product administered and Product administered to patient of inappropriate age) Medical history, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included ROTAVIRUS VACCINE LIVE REASSORT ORAL 5V (ROTATEQ) for prophylactic vaccination. On 27-Sep-2021, the patient received a 0.5 ml (dose 1 and 2) of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UT7325LA, expiry date: 30-Jun-2022, Solution for injection in pre-filled syringe) via intramuscular route in the left thigh for prophylactic vaccination twice. It was a case of an actual medication error due to Wrong product administered and Inappropriate age at vaccine administration (latency same day). It was reported "Doctor states that a two-month-old patient accidentally received two injections of FLUZONE QIV NP (no preservative) that were intended for his family members instead of his 2 month vaccines that were scheduled on 27SEP2021. Doctor asked if there was any information regarding FLUZONE QIV NP in patients of this age and also asked if she should report this to the Vaccine Adverse Event Reporting System (VAERS) as well. Doctor asked if she should hold off on the patient's intended vaccinations so that it could be determined if the FLUZONE QIV NP were responsible if the patient developed any adverse events. Doctor states that patient is still in her office and has not experienced any adverse events thus far" At the time of report, no adverse event was 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
ROTATEQ
Allergien
-
Vorherige Impfungen
-

VAERS 1745165

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

gering
Staat
MN
Alter
45,0
Geschlecht
M
Eingang
29.09.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IN / NS
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Incorrect route of product administration No adverse event

Symptomtext

STAFF DECIDED TO GIVE EACH OTHER INFLUENZA VACCINATION. CHOSE WRONG DOSAGE FORM AND ADMINISTERED THE IM FORM INTRANASALLY. STATE NO ADVERSE EFFECTS INSTRUCTED TO REPEAT INFLUENZA VACCINATION AS SOON AS FEASIBLE

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

VAERS 1745142

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

gering
Staat
MN
Alter
38,0
Geschlecht
M
Eingang
29.09.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IN / NS
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect product formulation administered Incorrect route of product administration

Symptomtext

TWO NURSING STAFF DECIDED TO GIVE FLU VACCINE TO EACH OTHER. CHOSE THE WRONG FORM OF VACCINE AND ADMINISTERED IT NASALLY INSTEAD OF IM. STATE NO ADVERSE EFFECTS EXPERIENCED TO DATE INSTRUCTED TO REPEAT FLU VACCINE DOSE AS SOON AS FEASIBLE

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect product formulation administered
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
levaquin, sulfa
Vorherige Impfungen
-

VAERS 1737239

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325LA

gering
Staat
WI
Alter
0,2
Geschlecht
M
Eingang
27.09.2021
Impfdatum
27.09.2021
Beginn
27.09.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

Pt given 2 fluzone vaccines (same lot #) by mistake at 2mo well child check. Also given rotateq, but other 2mo vaccines were not given after error was realized. Pt / mom sat for 30 minutes after injections and no reaction observed. Mom will monitor for any AE and call immediately should anything be observed.

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
n/a
Vorherige Impfungen
-