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Reporte zur Charge UJ772AC

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 2 AZ 2 MN 1 MD 1 MT 1 CA 1 LA 1 OR 1 TN 1

VAERS 1801550

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

schwer
Staat
MN
Alter
80,0
Geschlecht
M
Eingang
20.10.2021
Impfdatum
18.10.2021
Beginn
18.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Facial paralysis Transient ischaemic attack

Symptomtext

Patient was on a conference call and the other participants noticed some facial drooping. Patient felt better following the call and did not seek care until the following morning (10/19/21). Patient was evaluated by primary care provider and determined that he had experienced a TIA (mini stroke). Patient is currently back at home and will be following up with cardiology and neurology to look at long-term issues/damage.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
unknown
Aktuelle Erkrankungen
No specific illnesses at time of vaccination or during the month before
Vorgeschichte
Acid reflux (increased recently); diabetic; CAD; has stent put in June 2021; BPH; fluid retention due to congestion heart failure
Andere Medikamente
alfuzosin 10mg; aspirin EC 81mg; carvedilol 6.25mg (1 tablet with breakfast and 2 tablets with dinner); clopidogrel 75mg; Welchol 667 tablets (total daily dose 3750mg); famotidine 40mg tablets (1 tablet twice daily); finasteride 5mg; furose
Allergien
none known
Vorherige Impfungen
-

VAERS 2216025

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

mild
Staat
-
Alter
67,0
Geschlecht
F
Eingang
05.04.2022
Impfdatum
19.11.2021
Beginn
19.12.2021
Tage bis Beginn
30,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Abscess drainage Pain in extremity Pelvic abscess Pelvic mass Peripheral swelling

Symptomtext

ED visit for left leg pain and swelling - treated and released. Admission to the hospital with a left hemipelvic mass. She underwent CT-guided drainage and fortunately the mass was found to be an abscess rather than a malignancy as we were originally concerned. Drainage was uneventful and patient was placed on vancomycin and Zosyn. Treated and discharged. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
7,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1840733

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj772ac

mild
Staat
MD
Alter
67,0
Geschlecht
F
Eingang
03.11.2021
Impfdatum
01.11.2021
Beginn
01.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash Skin warm

Symptomtext

Patient presented with a rash on the underside of the left arm. It was warm to touch but not itchy. I advised patient to followup with doctor. She was prescribed an antibiotic.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
-
Andere Medikamente
Atorvastatin, Citalopram, Famotidine
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1813368

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772ac

mild
Staat
TX
Alter
83,0
Geschlecht
M
Eingang
23.10.2021
Impfdatum
20.10.2021
Beginn
20.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dizziness

Symptomtext

Learned that Moderna had been approved, believed it to be from CDC when i was from a committee however. Patient did reported temporary dizziness. We've called to check on him a few times that day and the day after. Patient said it was temporary , he felt better as the day went on.

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

VAERS 2231161

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

gering
Staat
MT
Alter
-
Geschlecht
F
Eingang
29.09.2022
Impfdatum
12.04.2022
Beginn
12.04.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

1 year old child was given High Dose influenza injection rather than the regular dose; This non-serious case was received during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-Jul-2022 with the following VAERS Primary ID 2231161-1. The original narrative from the sender is the following: 1 year old child was given High Dose influenza injection rather than the regular dose The reporter did not provide an assessment of causal relationship between Vaxelis and the reported event "1 year old child was given High Dose influenza injection rather than the regular dose". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Upper respiratory infection (1 week prior to immunization)
Andere Medikamente
ALBUTEROL [SALBUTAMOL]; PROVENTIL [SALBUTAMOL]
Allergien
-
Vorherige Impfungen
-

VAERS 1959942

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

gering
Staat
AZ
Alter
64,0
Geschlecht
F
Eingang
17.12.2021
Impfdatum
03.12.2021
Beginn
03.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age

Symptomtext

Patient is a 64 year old woman but was given a Fluzone HD that is indicated for 65+

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

VAERS 1925380

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge uj772ac

gering
Staat
CA
Alter
52,0
Geschlecht
M
Eingang
06.12.2021
Impfdatum
06.12.2021
Beginn
06.12.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

high dose fluzone was given to the patient instead of requested pfizer covid booster shot. patient was called and patient came back into pharmacy and received pfizer covid booster

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 1893368

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

gering
Staat
LA
Alter
67,0
Geschlecht
M
Eingang
23.11.2021
Impfdatum
11.11.2021
Beginn
11.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

patient was given double dose of FLUZONE HD with no reported adverse event; Initial information was regarding an unsolicited valid non serious case was received from a pharmacist via Medical Information (Reference number- 00853740) and transmitted to Sanofi on 11-Nov-2021. This case involves a 67-year-old male patient who received double dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (extra dose administered). The patient's medical history, past medical treatment(s), vaccination(s), concomitant medications and family history were not provided. On 11-Nov-2021, the patient received a 0.75 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ772AC, expiry date: 30-Jun-2022) via intramuscular route in the right deltoid for prophylactic vaccination. It was an actual medication error due to extra dose administered. (latency: same day). It was reported "He would like to find out about likely side effects and next steps." At time of reporting, 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 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
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1866165

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

gering
Staat
AZ
Alter
61,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
11.11.2021
Beginn
11.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

no symptoms rec high dose

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

VAERS 1865688

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge uj772ac

gering
Staat
OR
Alter
68,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
12.11.2021
Beginn
12.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient came in for Moderna covid booster appointment; and accidentally received both Flu shot and Moderna covid booster; Patient had received a flu shot previously on 10/11/2021

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
unknown
Allergien
none
Vorherige Impfungen
-

VAERS 1843647

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ772AC

gering
Staat
TN
Alter
62,0
Geschlecht
F
Eingang
04.11.2021
Impfdatum
04.11.2021
Beginn
04.11.2021
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 is not the correct age to get a high dose flu shot. Nurse gave the medication.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1813420

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj772ac

gering
Staat
TX
Alter
85,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
19.10.2021
Beginn
19.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event

Symptomtext

No Adverse reactions occurred. Learned that moderna had been approved , believed it to of been from the CDC. It was however the Advisory Committee.

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