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Reporte zur Charge UJ775AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

9Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 2 KS 1 CA 1 NC 1 TX 1 MI 1 WV 1

VAERS 2228531

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

mild
Staat
KS
Alter
61,0
Geschlecht
F
Eingang
12.04.2022
Impfdatum
08.04.2022
Beginn
09.04.2022
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Fatigue Injection site erythema Injection site induration Injection site mass Injection site pain Injection site swelling Injection site warmth Malaise

Symptomtext

Redness, swelling, and tender/hard lump on L deltoid/upper arm. Area around injection site warm to touch. Red/swollen area reached approximately 4.5" x 3" in diameter. Patient also experienced significant fatigue/malaise.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
unknown - pneumonia in January 2022
Vorgeschichte
Asthma, restless leg syndrome
Andere Medikamente
Cymbalta, Astmacort inhaler, Requip
Allergien
Penicillin, all cephalosporin antibiotics
Vorherige Impfungen
-

VAERS 1971277

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

mild
Staat
OH
Alter
13,0
Geschlecht
F
Eingang
22.12.2021
Impfdatum
22.12.2021
Beginn
22.12.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Injection site erythema

Symptomtext

Patient received influenza vaccine in the Left Deltoid muscle. Patient tolerated the vaccine well. Vaccine administrator walked out of exam room to make a copy of a form. She returned 3-4 minutes later, where mom proceeded to show the vaccinator the area. The injection site area was red. The redness was the size of a tennis ball. Vaccinator retrieved Provider from a different exam room. Provider assessed the area and advised the family to give the patient Benadryl. No other reactions noted at time of assessment. Family left a few minutes after the Provider assessed the patient and the injection site area.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 1910012

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

mild
Staat
-
Alter
45,0
Geschlecht
F
Eingang
30.11.2021
Impfdatum
22.11.2021
Beginn
22.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dizziness

Symptomtext

50 mins post vaccination pt reported light headedness Vitals: 157/94, 66, 16 Pt stable and released from the vaccination site

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
PMH: Asthma, Hypothyroidism, DDD (lumbar), hysterectomy, cervical stenosis of spinal canal, depression, chronic pain, anxiety, panic attacks
Andere Medikamente
Medications: albuterol sulfate (PROVENTIL HFA;VENTOLIN HFA) 90 mcg/actuation HFA inhaler Inhale by mouth. citalopram (CELEXA) 10 MG tablet Take 10 mg by mouth daily. DULoxetine (CYMBALTA) 20 MG capsule Take 20 mg by mouth daily. escitalopra
Allergien
Allergies: Septra (itching, hives, anaphylaxis), Nuts - peanuts, almonds, pecans
Vorherige Impfungen
-

VAERS 1898007

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

mild
Staat
CA
Alter
68,0
Geschlecht
F
Eingang
24.11.2021
Impfdatum
19.11.2021
Beginn
19.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Anxiety Nausea Pallor Throat tightness

Symptomtext

booster given and pt also received flu vaccine . During observation, pt complained to RN of nausea and "throat was feeling tight. Patient looked pale and anxious. Pt was evaluated by provider. Pr received EpiPen 0.3 mg x1. 911 was called for pt. paramedics provide pt Benadryl 50mg IV.

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

VAERS 2492493

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge uj775aa

gering
Staat
NC
Alter
81,0
Geschlecht
F
Eingang
28.10.2022
Impfdatum
20.10.2022
Beginn
20.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

The patient was given an expired dose of flu vaccine; which expired on 6/2022.; Patient contacted and explain what had happened and offered another dose of flu shot; she declined at this time;

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

VAERS 1923108

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

gering
Staat
TX
Alter
-
Geschlecht
M
Eingang
04.12.2021
Impfdatum
19.11.2021
Beginn
20.11.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Hypersensitivity Mouth swelling Swelling face

Symptomtext

allergic reactions; mouth swelling; jaw swelling; Initial information received on 23-Nov-2021 regarding an unsolicited valid non-serious case from another health professional via (under reference 00870031). This case involves a 67 years old male patient who had allergic reactions (hypersensitivity), which includes mouth swelling and jaw swelling (swelling face), after receiving INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. The patient's past medical history included Tracheostomy. Medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. On 19-Nov-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UJ775AA and expiration date: 30-Jun-2022) via unknown route in an unknown administration site for prophylactic vaccination. On 20-Nov-2021, the patient developed non-serious allergic reactions (hypersensitivity), which includes mouth swelling and jaw swelling (swelling face), one day following the administration of INFLUENZA QUADRIVAL A-B VACCINE. It was reported "The caller is requesting the ingredients of FULZONE QUAD." No laboratory data were reported. He went to the Emergency Room (ER) and was treated with oral medication, he did not know what the medication was. He still had some swelling. It had not resolved completely (he did not recover from the reported events).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypersensitivity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Tracheostomy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1908658

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

gering
Staat
MI
Alter
14,0
Geschlecht
M
Eingang
30.11.2021
Impfdatum
13.11.2021
Beginn
13.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Syringe issue Underdose

Symptomtext

The patient received partial dose of vaccine with no adverse event; some if not all of the vaccine came out of the side of the syringe with no adverse event; Initial information received on 16-Nov-2021 regarding an unsolicited valid non-serious case from other health professional, consumer/ non health care professional and physician (under reference 00860005). This case involves a 14 years old male patient who received partial dose of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (underdose), due to the needle was not tightly secured to the prefilled syringe and when they went to administer the vaccine, some if not all of the vaccine came out of the side of the syringe (syringe issue). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had no other concomitant vaccines. On 13-Nov-2021, the patient received a partial dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (Total, lot UJ775AA and expiration date: 30-Jun-2022) via intramuscular route in the left deltoid for prophylactic vaccination. It was a case of an actual medication error due to vaccine underdose and syringe leak (same day latency). It was reported "Caller stated that they believe the needle was not tightly secured to the prefilled syringe and when they went to administer the vaccine, some if not all of the vaccine came out of the side of the syringe. Caller asking if patient should receive another dose and if so, what time frame would they need to give dose in. A clinic reporting a medication error for FLUZONE QUADRIVALENT 0.5 mL prefilled syringe described as the vaccine squirting out the side between the needle attachment and the syringe tipe. The caller reported that it was hard to tell if the consumer received any of the dose and that the needle attached was a 25G X 1 inch needle." The clear location of the leakage was under the Luer-Lok adaptor, out of the vial stopper puncture mark. There were no signs of damage or tampering with the vial, stopper, flip seal and carton. At time of reporting, no adverse event reported.

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

VAERS 1908657

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ775AA

gering
Staat
OH
Alter
0,2
Geschlecht
M
Eingang
30.11.2021
Impfdatum
15.11.2021
Beginn
15.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age Wrong patient received product

Symptomtext

FLUZONE QUADRIVALENT was given to 2 months old patient/ no adverse event; Initial information received on 16-Nov-2021 regarding an unsolicited valid non-serious case from other healthcare professional and non-healthcare professional via Media information (under the reference 00859792). This case involves a 2 months old male patient (date of birth: 15-SEP-2021) who received INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (product administered to patient of inappropriate age). The patient's medical history, past medical treatment, vaccination and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ 7V (CRM197) (PREVNAR), DIPHTHERIA VACCINE TOXOID, HIB VACCINE CONJ (TET TOX), PERTUSSIS VACCINE ACELLULAR 5-COMPONENT, POLIO VACCINE INACT 3V (MRC 5), TETANUS VACCINE TOXOID (PENTACEL) and ROTAVIRUS VACCINE for prophylactic vaccination. On 15-Nov-2021, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (total, solution for injection in pre-filled syringe, lot number: UJ775AA and expiry date: 30-JUN-2022) via an intramuscular route in the left thigh for prophylactic vaccination. It was an actual medication error due to inappropriate age at vaccine administration (same day). It was reported "The Fluzone Quadrivalent was given to the wrong patient, it was supposed to be given to his sibling." At time of reporting, it was unknown whether the patient had any adverse event or not and the outcome was unknown for the reported 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
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PREVNAR; PENTACEL; ROTAVIRUS VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2602074

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ775AA

gering
Staat
WV
Alter
90,0
Geschlecht
F
Eingang
26.10.2021
Impfdatum
26.10.2021
Beginn
26.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation issue

Symptomtext

Dose was given as undiluted by mistake. Family contacted and asked to monitor patient and report any issues that might come up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation issue
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
unknown
Vorgeschichte
-
Andere Medikamente
unknown
Allergien
none
Vorherige Impfungen
-