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Reporte zur Charge UJ559AC

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 2 WA 2 NJ 1

VAERS 1450954

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge UJ559AC

schwer
Staat
CA
Alter
14,0
Geschlecht
F
Eingang
06.07.2021
Impfdatum
27.04.2021
Beginn
27.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Bacterial test negative COVID-19 immunisation Chlamydia test negative Fall Full blood count normal Glycosylated haemoglobin normal Head injury Heart rate decreased Human chorionic gonadotropin normal Hypoaesthesia Hypotension Lipids normal Metabolic function test Seizure Syncope Urine analysis normal

Symptomtext

I gave vaccines to this patient i began on the right arm and administered a Flu vaccine, then i moved to the patients left arm and administered HPV#2 vaccine. I then told the mother that we usually have patients wait 15 minuets in the room but because we were so busy i was going to have them wait in the lobby. Mother said that was fine and was about to walk out when her daughter just suddenly fell to the ground in a sitting position, I reached for her arm but she still fell to her left side and hit her head on the ground. I quickly pulled her and held her in my arms blowing air to her face, mother stepped out and got help. An MA walked in the room and saw what happened and went to get the provider. Water was given to the patient and then mother and I carried patient onto the bed. Blood pressure and oxygen were then taken, provider then told us she had it all under control and we stepped out. CARDIAC REFERRAL FOR WITNESSED SYNCOPE IN CLINIC after HPV vaccination, likely vasovagal Patient already saw neurology and cardiology. She is pending a brain MRI with neurology.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
Cbc, Ua, Chlamydia Ua, Gonorrhea Ua, CMP, lipid panel, bHCG, HgA1c ALL CAME BACK NORMAL Cardiology mentioned that they suspected vasovagal syncope and seizure
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
Mom reports 14 year old patient fainted after getting the COVID vaccine on 5/28/2021. Patient reports that she felt it coming pr

VAERS 1393222

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ559AC

mild
Staat
CA
Alter
0,5
Geschlecht
F
Eingang
11.06.2021
Impfdatum
07.06.2021
Beginn
08.06.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site rash Injection site reaction Rash papular

Symptomtext

non-pruritic rash to B/L lower extremities developed the day of after receiving vaccines. Vaccines admin on 6/7/2021, sx reported to have started on 6/8/2021. On 6/11/2021, mom made initial contact w/ our office regarding the rash, at which point, it was mostly resolved per her account. Baby did not develop fever or rash to other parts of her body. Rash per photos emailed on 6/11/2021 was flesh color papules localized to the lower extremities only.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site rash
Hospital-Tage
-
Labordaten
None ordered. Instructed to monitor + provide supportive care.
Aktuelle Erkrankungen
Viral GE 4/23/2021.
Vorgeschichte
No
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1082072

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ559AC

mild
Staat
WA
Alter
11,0
Geschlecht
F
Eingang
08.03.2021
Impfdatum
01.03.2021
Beginn
01.03.2021
Tage bis Beginn
0,0
Dosis
7+
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Lip swelling Nausea

Symptomtext

General fatigue, nausea and lip swelling started about 1-2 hours after injections. Given Benadryl per advice of on -call physician. Symptoms improved but not resolved until following day

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
No known drug allergies
Vorherige Impfungen
-

VAERS 1326278

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ559AC

gering
Staat
NJ
Alter
0,3
Geschlecht
M
Eingang
18.05.2021
Impfdatum
05.05.2021
Beginn
05.05.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age

Symptomtext

A 3-month old male received a dose of the Fluzone Quadrivalent, with no reported adverse event; Initial information received on 05-May-2021 regarding an unsolicited valid non-serious case received from a physician via Other Health Care Professional. This case involves a three month old male patient who received INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (Product administered to patient of inappropriate age). Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On 05-May-2021, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UJ559AC and expiry date: 30-Jun-2021) (Frequency once) via an intramuscular route at an unknown administration site for prophylactic vaccination. It was a case of actual medication error due to inappropriate age at vaccine administration (same day latency). It was also reported that nurse Manager states that they administered FLUZONE QUAD (Prefilled) to a 3 month old. Is there anything that they should do next other than report it. Reporter relationship: health care professional (HCP); Product used: used First time product used: yes still using product: no. 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. 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 administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1272211

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ559AC

gering
Staat
WA
Alter
0,3
Geschlecht
M
Eingang
29.04.2021
Impfdatum
13.04.2021
Beginn
-
Tage bis Beginn
-
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

4 month-old patient was given the FLUZONE QUAD (prefilled) by mistake with no reported adverse event; Initial information was received on 13-Apr-2021 regarding an unsolicited valid non-serious case received from other health professional (Inquiry number: 00560052). It was reported that INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (lot number: UJ559AC, expiry date not reported) (Suspension For Injection) was administered to a four month old female patient via an unknown route for prophylactic vaccination (product administered to patient of inappropriate age). It was a case of actual medication error due to inappropriate age at vaccine administration. At the time of report, 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. 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. There will be no information available on batch number for this case.

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