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Reporte zur Charge UJ937AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IA 2 MO 1 PR 1 TX 1 KS 1 IL 1 NJ 1

VAERS 2508457

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ937AB

mild
Staat
MO
Alter
66,0
Geschlecht
M
Eingang
15.11.2022
Impfdatum
09.11.2022
Beginn
10.11.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity Pyrexia Rash pustular

Symptomtext

Client complained of developing a pustule type rash across his chest around to his back, fever and sore arm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
COPD
Andere Medikamente
Advair Inhaler, OTC allergy med, atorvastatin, montelukast,
Allergien
no know allergies
Vorherige Impfungen
-

VAERS 2501925

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ937AB

mild
Staat
PR
Alter
71,0
Geschlecht
F
Eingang
08.11.2022
Impfdatum
07.11.2022
Beginn
07.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness

Symptomtext

Patient reported feeling dizzy after getting out of the vaccination room while consulting Pharmacist with an OTC medication

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
BP meassured at 07:14 pm - 128/94 pulse 89
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Sulfa
Vorherige Impfungen
-

VAERS 2529004

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ937AB

gering
Staat
TX
Alter
64,0
Geschlecht
F
Eingang
12.12.2022
Impfdatum
10.12.2022
Beginn
10.12.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

I gave the patient a HD flu shot and she was not yet 65

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 2513728

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ937AB

gering
Staat
KS
Alter
-
Geschlecht
U
Eingang
21.11.2022
Impfdatum
07.11.2022
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered

Symptomtext

Recd High Dose Flu 10/18/22 then 11/7/2 - Notified 0 adverse effects - Asked for Flu shot

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2510397

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ937AB

gering
Staat
IA
Alter
62,0
Geschlecht
M
Eingang
17.11.2022
Impfdatum
13.10.2022
Beginn
13.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

patient who is 62 years old and was given fluzone high dose quadrivalent with no reported adverse event; Initial information received on 08-Nov-2022 regarding an unsolicited valid non-serious case received from a consumer/non-hcp (healthcare professional). This case involves a 62 years old male patient who was given Influenza quadrival A-B high dose hv vaccine [Fluzone high-dose quadrivalent] with no reported adverse event . The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 13-Oct-2022, the patient who was 62 received 0.5 ml dose (once) of suspect Influenza quadrival A-B high dose hv vaccine (lot UJ937AB, exp date: 30-Jun-2023) via intramuscular route in the right deltoid for immunistion with no reported adverse event (product administered to patient of inappropriate age) (latency: same day). 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2504581

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ937AB

gering
Staat
IL
Alter
59,0
Geschlecht
F
Eingang
10.11.2022
Impfdatum
07.11.2022
Beginn
07.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

Pt should have been given the regular dose of the flu vaccine, because she is under the age of 65. Pt was given high dose flu vaccine.

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

VAERS 2481906

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge UJ937AB

gering
Staat
IA
Alter
25,0
Geschlecht
F
Eingang
18.10.2022
Impfdatum
17.10.2022
Beginn
01.10.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy Incorrect product formulation administered No adverse event

Symptomtext

Provider ordered initial covid vaccine and patient received Bivalent Pfizer booster dose instead. Employee notified manager. Manager notified provider and pharmacist. Information received from both Department of Public Health and Manufacture - "If a bivalent Pfizer-BioNtech vaccine is administered for primary series dose: Do not repeat the dose. The primary and booster dosages are the same; the bivalent dose can be counted as a primary series dose. Continue with the recommended vaccination schedule: (iel, complete the primary series with a monovalent Pfizer-BioNTech vaccine, then administer a bivalent booster dose at least 2 months after completion of the primary series." All information provided. No adverse reactions noted. No adverse reactions at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Exposure during pregnancy
Hospital-Tage
-
Labordaten
Pt to follow up as scheduled in 3 weeks for second covid vaccine - as noted by Pfizer - the second dose should be a Monovalent vaccine.
Aktuelle Erkrankungen
Pregnancy, headache
Vorgeschichte
Asthma, multiple environmental allergies.
Andere Medikamente
Ferrous Sulfate, Ibuprofen, Fluticasone, Lansoprazole, Loratadine, Albuterol, Benralizumab, Budesonide formoterol and epinephrine
Allergien
NKMA
Vorherige Impfungen
-

VAERS 2481738

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj937ab

gering
Staat
NJ
Alter
56,0
Geschlecht
M
Eingang
18.10.2022
Impfdatum
18.10.2022
Beginn
18.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient given high dose flu rather the regular flu block- no symptoms or signs of issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
none
Vorgeschichte
Anxiety 1/23/2020 Depression 1/23/2020 Gastroesophageal reflux disease 1/23/2020 Hyperlipidemia 1/23/2020
Andere Medikamente
acetaminophen (TYLENOL) 500 mg tablet Sig - Route: Take 1 tablet by mouth as needed. - oral Class: Historical Med atorvastatin (LIPITOR) 20 mg tablet 90 tablet 0 6/28/2022 Sig: TAKE 1 TABLET BY MOUTH EVERY DAY Number of times this orde
Allergien
Severity Noted Reaction Type Reactions Compazine [prochlorperazine] Not Specified 03/13/2020 Ibuprofen Not Specified 03/13/2020 GI intolerance Penicillins Not Specified 01/18/2012 Intolerance
Vorherige Impfungen
-