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Reporte zur Charge UT7325KA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 4 MO 2 SC 2

VAERS 1713455

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7325ka

schwer
Staat
TX
Alter
9,0
Geschlecht
M
Eingang
18.09.2021
Impfdatum
18.09.2021
Beginn
18.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anxiety Asthenia Blood glucose normal Dizziness Dreamy state Heart rate increased Syncope

Symptomtext

Patient received his annual flu vaccine, shortly afterwards (about 15 minutes), mom reported patient had fainted outside on way to their vehicle. Emergency action initiated, 911/ems called, RPh (myself) arrived on scene outside with emergency kit (children epipen, bp meter), pt found awake and responsive and sitting, patient reported feeling weak/dizzy (like in a dream), Pulse found elevated, no signs of rash/swelling/trouble breathing, EMS/Firefighters arrived at this point (post 20 minutes from time of vaccination), found everything WNL except BP showed being low (upper 80s/60s), Ambulance arrived 5 min later, found everything WNL (Blood sugar 95, oxygen 96), determined episode due to anxiousness, child okayed to release/parents denied visit to hospital, said they would follow-up with pediatrician.

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

VAERS 1901906

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325KA

mild
Staat
MO
Alter
37,0
Geschlecht
M
Eingang
26.11.2021
Impfdatum
20.09.2021
Beginn
03.10.2021
Tage bis Beginn
13,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Adverse reaction Chills Cough Erythema Nasopharyngitis Pain Pruritus Rash macular Rash pruritic Rash vesicular Swelling

Symptomtext

Patient called 10/4/21 in the morning about 9:20am stating he had adverse reaction to Varivax shot (indicated the shot in the back of the Right arm) that he had received 9/20/21--stated that he had itchiness, swelling, and red spots start to develop just yesterday 10/3/21 and that it had spread to more spots across his body in at least 3 different locations. Described them as itchy red blisters/bumps. Also said that he has cold/cough symptoms, body aches, and has experienced shivering at night. I called and talked to Merck who sent me clinical trials stating that it is an adverse reaction, indeed.

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

VAERS 1821670

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325KA

mild
Staat
TX
Alter
49,0
Geschlecht
F
Eingang
27.10.2021
Impfdatum
17.09.2021
Beginn
18.09.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Pain in extremity

Symptomtext

Employee reports pain when raising arm above head and laterally above shoulder height. It was recommended that the employee see their primary care provider. Employee has not yet seen provider. For treatment, the employee tried Ibuprofen 3 pills two times a day for a week. She now takes it as needed for pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Seizures
Vorgeschichte
Seizures, Hypertension
Andere Medikamente
Zonisamide Lisinopril Clonazepam Docusate
Allergien
Ciprofloxacin
Vorherige Impfungen
-

VAERS 1818720

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325KA

mild
Staat
TX
Alter
25,0
Geschlecht
M
Eingang
26.10.2021
Impfdatum
22.09.2021
Beginn
24.10.2021
Tage bis Beginn
32,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Pain in extremity

Symptomtext

On 10/21/21 the employee reported that after the vaccine he has been having a stinging pain in his arm when he raises his arm above shoulder height. The employee stated that his arm was sore for the first 24 hours after the vaccine, then he stated the pain went away for the next 24 hours, and then the stinging started when he raises his arm out in front of him, above shoulder height. It was recommended that the employee see his primary care provider. The employee stated that he has tried to stretch his arm, but has not tried any other treatments for the pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1815008

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325KA

mild
Staat
SC
Alter
39,0
Geschlecht
F
Eingang
25.10.2021
Impfdatum
11.10.2021
Beginn
13.10.2021
Tage bis Beginn
2,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Arthralgia Joint range of motion decreased Pain in extremity Vaccination site joint inflammation

Symptomtext

Had vaccine on 9/22/21- just reported this on 10/25/2021. Stated her arm was sore after injection, but not anything unusual. @ days after injection she had a "pinching ache"' in her left arm shoulder joint. Range of motion in the arm was decreased. Motrin and Tramadol were used, but did not relieve the pain. Several days later she did go to an Urgent Care and was diagnosed with "post Vaccination Inflammatory Joint Response". She received Decadron 10mg IM and Toradol 60mg IM, which did give her relief. She continued with a Prednisone dosepak. There is still a dull constant pain, but Motrin 800mg does help relieve this pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Genetic clotting disorder
Andere Medikamente
Aspirin 81 mg daily; Multivitamin 1 daily, Cetirizine 10mg PRN for allergies
Allergien
Penicillin, Latex, IVP dye; No food allergies; No environmental allergies
Vorherige Impfungen
-

VAERS 1797761

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325KA

mild
Staat
SC
Alter
42,0
Geschlecht
F
Eingang
19.10.2021
Impfdatum
15.10.2021
Beginn
15.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Ear pruritus Erythema Pruritus Skin warm Urticaria

Symptomtext

Employee reports that about 10 minutes after receiving the flu vaccine her ears got hot and she started itching behind her left ear on the left side of her neck. Whelps and redness appeared near the left ear and her left wrist. She took Benadryl 25mg and the redness, whelps, itching and heat went away.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Ear pruritus
Hospital-Tage
-
Labordaten
None- she did not visit the ED, Urgent Care of her PCP.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Oregano Oil 175mg - 1 tab twice weekly; Advance Anxiety Stress Release (OTC multi vitamins and Herbs) - 1 daily; Ibuprofen 800 mg PRN (last dose prior to flu vaccine 10/14/21); Tylenol 650mg PRN (last dose prior to flu vaccine 10/14/21)
Allergien
No allergies known to medications, vaccines, food or environmental.
Vorherige Impfungen
-

VAERS 1683254

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT7325KA

mild
Staat
TX
Alter
6,0
Geschlecht
M
Eingang
08.09.2021
Impfdatum
01.09.2021
Beginn
02.09.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Computerised tomogram Pyrexia Swelling face

Symptomtext

Fever and right cheek swollen

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
2,0
Labordaten
Admitted to Hospital on morning of 9/3/2021. CT scan was performed and was administered IV antibiotics for 48hrs.
Aktuelle Erkrankungen
-
Vorgeschichte
vascular malformation in right cheek
Andere Medikamente
-
Allergien
peanuts cephalosporin neomyacin clindamycin
Vorherige Impfungen
-

VAERS 1931708

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7325KA

gering
Staat
MO
Alter
-
Geschlecht
U
Eingang
08.12.2021
Impfdatum
22.11.2021
Beginn
24.11.2021
Tage bis Beginn
2,0
Dosis
3
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

several doses of FLUZONE QIV PFS and FLUZONE HD QIV were activated on 20Nov2021 and then administered on 22Nov2021, 23Nov2021, and 24Nov2021; Initial information received on 24-Nov-2021 regarding an unsolicited valid non-serious case from other healthcare professional via Agency (under the reference 00872588). This case involves 22 patients who received a dose each of vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (Wrong technique in product usage process) on 22-Nov-2021, 23-Nov-2021 or 24-Nov-2021 after the vaccine was activated on 20-Nov-2021. The patients' medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. On 22-Nov-2021, 23-Nov-2021 or on 24-Nov-2021 each of the patients received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot number: UT7325KA, UT7384NA and expiry date: 30-JUN-2022) which was activated on 20-Nov-2021 via an unknown route at an unknown administration site for prophylactic vaccination. It was an actual medication error due to Wrong technique in product usage process (latency : same day). It was reported "Caller states several doses of FLUZONE QIV PFS and FLUZONE HD QIV were activated on 20Nov2021 and then administered on 22Nov2021, 23Nov2021, and 24Nov2021. Caller is looking for information on if they need to revaccinate and if there are any other issues that may arise from administering on a later date after activation." Reporter stated that the syringe cap was removed from the Fluzone Quadrivalent syringes and the needles were attached on 20 Nov 2021, and then the activated syringes were not administered to the patients by the end of the business day. At the 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-