Zurueck zur Suche

Reporte zur Charge UT7347MA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

14Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NM 4 CO 3 WA 2 CA 1 AZ 1 MN 1 KS 1

VAERS 1945333

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge UT7347MA

schwer
Staat
CA
Alter
4,0
Geschlecht
M
Eingang
13.12.2021
Impfdatum
30.11.2021
Beginn
30.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dizziness Loss of consciousness Seizure like phenomena

Symptomtext

Patient felt dizzy, passed out for few seconds and had a seizure likely activity and recovered well in the room, pt is sent to the ER and was discharge home from the ER

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

VAERS 1884943

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

schwer
Staat
AZ
Alter
9,0
Geschlecht
F
Eingang
19.11.2021
Impfdatum
12.11.2021
Beginn
13.11.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Facial paralysis Ophthalmoplegia

Symptomtext

On 11/13/2021, patient went to ER for Left eye not shutting all the way, and for left facial drooping with smiling - per mom, started in the morning when patient woke up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
no chronic health conditions
Andere Medikamente
multivitamin
Allergien
NKA
Vorherige Impfungen
-

VAERS 1870113

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

schwer
Staat
MN
Alter
11,0
Geschlecht
F
Eingang
15.11.2021
Impfdatum
15.11.2021
Beginn
15.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dizziness Fall Syncope

Symptomtext

Patient presented to clinic as walk in for a COVID-19 vaccine and flu vaccine. Patient received both vaccines as indicated above. Patient stood up and proceeded to the door in which she became faint with syncope response. Evaluated by Dr. with monitoring 30+ minutes following episode. Patient left with family to home. Patient did later present to hometown ED for evaluation due to concern of concussion from fall.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Unknown
Andere Medikamente
Adderall CR Melatonin Diphenhydramine
Allergien
NKA
Vorherige Impfungen
-

VAERS 1929397

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

mild
Staat
WA
Alter
17,0
Geschlecht
M
Eingang
07.12.2021
Impfdatum
02.12.2021
Beginn
03.12.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Skin lesion Urticaria

Symptomtext

Developed hives 36 hours after imms. Started on arms bilaterally, then involved legs bilaterally with a few urticarial lesions behind ears as well. No lip or face swelling, no throat tightness, no light headedness, no nausea, no vomiting, no diarrhea. Took benadryl which helped the hives improve somewhat. 3 days after the urticaria began at the time of clinic visit the the lesions were still present but improving, becoming lighter, with one arm entirely resolved. Initially had itching, but this resolved after 36 hours. He had acute gastroenteritis like illness 3 days prior to receiving vaccines, so viral urticaria is possible as well.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
na
Aktuelle Erkrankungen
na
Vorgeschichte
history of ADHD
Andere Medikamente
none
Allergien
nkda
Vorherige Impfungen
-

VAERS 2329106

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

gering
Staat
CO
Alter
1,8
Geschlecht
M
Eingang
23.06.2022
Impfdatum
20.06.2022
Beginn
20.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

MMR vaccine expired on 6/16/2022 and was administered on 6/20/2022. Contacted health department and heard from nurse who advised the following: "when an expired medication is given to patient, the dose needs to be repeated. Since this was a live vaccine, you should wait at least 4 weeks (28 days) after the previous (expired) dose was given before repeating it. Although simply repeating dose is preferred, serological testing to check for immunity may be accepted." Parent of patient has been called and voice mail left requesting they contact clinic to discuss the above information.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
NO MEDICATIONS
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2324074

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

gering
Staat
NM
Alter
0,2
Geschlecht
F
Eingang
20.06.2022
Impfdatum
14.06.2022
Beginn
14.06.2022
Tage bis Beginn
0,0
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

2 month old was inadvertently administered a dose of Fluzone Quadrivalent with no adverse event; Initial information received on 14-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional via call center. This case involves a 2 months old female patient who was inadvertently administered a dose of fluzone quadrivalent with no adverse event while receiving vaccine influenza quadrival a-b vaccine [Fluzone quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine conj (pneumococcal conjugate vaccine) for immunisation; and rotavirus vaccine live reassort oral 5v (rotateq) for Immunisation. On 14-Jun-2022, the patient received 0.5 ml dose of suspect influenza quadrival a-b vaccine (batch lot UT7347MA,Expiry date:30-Jun-2022) prefilled syringe via intramuscular route in Left Vastus Lateralis. On 14-Jun-2022 (latency :same day) the patient developed a non-serious event of 2 month old was inadvertently administered a dose of fluzone quadrivalent with no adverse event (product administered to patient of inappropriate age) following the administration of influenza quadrival a-b vaccine. 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
PNEUMOCOCCAL CONJUGATE VACCINE; ROTATEQ
Allergien
-
Vorherige Impfungen
-

VAERS 2319113

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7347ma

gering
Staat
NM
Alter
0,2
Geschlecht
F
Eingang
14.06.2022
Impfdatum
14.06.2022
Beginn
14.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

I gave the patient a flu shot instead of a vaxelis shot and the patient is only 2 moths

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2241921

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

gering
Staat
CO
Alter
4,0
Geschlecht
M
Eingang
19.04.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

The patient was given an expired vaccine. The expiration date was 1/8/22 He suffered no side effects

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
No
Vorgeschichte
Speech delay Eczema
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2051143

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

gering
Staat
WA
Alter
17,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

MMR II Lot T001213 Expiration date 1/12/2022 was administered on 1/18/2022. There were no adverse effects to patient. I contacted Merck & Company to discuss with representative if a re-vaccination was necessary. Merck stated that as long as there were no temperature excursions and with the vaccine storage, they stand behind their product with in-house data to still be potent beyond the 6 days usage (after expiration date).

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

VAERS 1959198

PROTEIN SCIENCES CORPORATION · INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) · Charge UT7347MA

gering
Staat
NM
Alter
9,0
Geschlecht
F
Eingang
17.12.2021
Impfdatum
17.12.2021
Beginn
17.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect dose administered Product preparation issue

Symptomtext

Pfizer COVID-19 BioNTech 0.2mL administered without reconstitution. Provider/medical director at the facility notified immediately of vaccine error. Patient was kept in office for monitoring. Provider notified mother of vaccine error. All questions answered and mother will contact provider if needed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Fiber gummies, Claritin
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1959184

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) · Charge UT7347MA

gering
Staat
NM
Alter
9,0
Geschlecht
F
Eingang
17.12.2021
Impfdatum
17.12.2021
Beginn
17.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered Product preparation issue

Symptomtext

Pfizer Covid-BioNTech 0.2ml dosage was given without reconstitution

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Claritin 10mg tablet
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1941968

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

gering
Staat
-
Alter
-
Geschlecht
U
Eingang
11.12.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

Temperature excursion of the product reaches to negative 1.3 Celsius for 4 hours 24 minutes with no adverse event; Initial information received on 23-Nov-2021 regarding an unsolicited valid non-serious case from an other health professional via regulatory agency (under the reference 00870840). This case involves 118 patients (unknown demographics). This case involves temperature excursion of the INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] reaches to negative 1.3 celsius for 4 hours 24 minutes (product storage error). The patients medical history, medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. On an unknown date, the patients received a dose of suspect FLUZONE QUADRIVALENT (lot UT7347MA and expiration date not provided) via unknown route in an unknown administration site for prophylactic vaccination. It was a case of potential medication error due to product storage error temperature too low (same day latency). No adverse event reported. It was reported "I have a question about Fluzone. I have a health department which has all new staff from the clerk to the administrator as well as the nurses, and they went to 3 schools and vaccinated a total of 118 school kiddos with flu vaccine that had experienced a TE (unbeknownst to them of course). they noticed when they went to upload their monthly temps that they had a TE, the refrigerator temperature excursion (TE). I know they likely need to revaccinate, but it's breaking my heart to ask them to do it. please advise?" The causality of the suspect with the event not 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 guidelines. 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 1880698

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) · Charge UT7347MA

gering
Staat
CO
Alter
7,0
Geschlecht
F
Eingang
18.11.2021
Impfdatum
14.10.2021
Beginn
14.10.2021
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Underdose

Symptomtext

Was administering a flu vaccine on 7 yr old. Took about 10 minute for patient stay still for vaccine. After I already had needle in patients L arm, She moved away from me across the room. I pulled out neddle and notice that I had only injected half of flu doses into the patients arm. I directly went to my supervisor and made her aware of the situation

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

VAERS 1857773

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7347MA

gering
Staat
KS
Alter
7,0
Geschlecht
F
Eingang
10.11.2021
Impfdatum
09.11.2021
Beginn
09.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Circumstance or information capable of leading to medication error Extra dose administered

Symptomtext

Flu clinic was performed in school 11/2/2021 and student was given vaccine along with schoolmates. On 11/9 this facility returned to do a second flu clinic for the students who were out on 11/2. This student was brought back in with a second signed permission form and given a second shot. The parent reported the error this AM to the school. The student was assessed by the school nurse who reported, "she shows no signs or symptoms of any issues but will continue to monitor."

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
-