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Reporte zur Charge UJ694AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

19Reporte angezeigt
1Todesfaelle
1Hospitalisiert
1Lebensbedrohlich
0Bleibende Schaeden
IN 4 TX 3 MI 2 OH 2 CO 2 HI 1 WA 1 ND 1 GU 1 MD 1 UT 1

VAERS 1779214

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

kritisch
Staat
MI
Alter
63,0
Geschlecht
M
Eingang
12.10.2021
Impfdatum
10.09.2021
Beginn
08.10.2021
Tage bis Beginn
28,0
Dosis
1
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

Notified by medical examiner that patient was found deceased at home 10/08/2021, no report of symptoms in interim

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
anemia, ileostomy, type 2 Diabetes mellitus, Wolff-Parkinson-White, chronic pancreatitis, nicotine dependence, adrenal insufficiency, GERD, Crohns, hypertension, mild intermittent asthma, sleep apnea, hypokalemia
Vorgeschichte
anemia, ileostomy, type 2 Diabetes mellitus, Wolff-Parkinson-White, chronic pancreatitis, nicotine dependence, adrenal insufficiency, GERD, Crohns, hypertension, mild intermittent asthma, sleep apnea, hypokalemia
Andere Medikamente
loratadine, fluticasone, omeprazole, lisinopril, tizanidine, carvedilol, hydrocortisone tablet, amlodipine, advair, magnesium oxide, potassium chloride liquid, imodium, prochlorperazine, gabapentin, ferrous sulfate, nortriptyline
Allergien
cephalexin
Vorherige Impfungen
-

VAERS 1754522

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

kritisch
Staat
OH
Alter
6,0
Geschlecht
M
Eingang
01.10.2021
Impfdatum
01.10.2021
Beginn
01.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Circulatory collapse Fall Loss of consciousness

Symptomtext

Syncopal collapse 5 minutes after administration of vaccine which was well tolerated; patient was energetic in clinic room, was jumping, then fell and struck chin / right cheek on ground; spontaneously regained consciousness within 30 seconds; became alert and responsive to previous exam level

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

VAERS 1958092

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UJ694AA

schwer
Staat
IN
Alter
-
Geschlecht
F
Eingang
17.12.2021
Impfdatum
11.10.2021
Beginn
11.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anaphylactic reaction Chest discomfort Choking Dysphagia Pruritus Saliva altered Scar Skin discolouration Swollen tongue Urticaria

Symptomtext

she began choking; condition worsened; She awoke very early in the morning, when her tongue was too swollen to fit in her mouth; having trouble with secretions; couldn't swallow; tightness in her chest; leaving small "pockmarks" in the areas where her hives had been; anaphalactic reaction; within the hour, she began itching; develop hives after getting home from work; Initial information was received on 06-Dec-2021 regarding an unsolicited valid serious case from a nurse (under Medical Information (MI) Inquiry Number: 00886277). This case involves a 58 years old female patient who began choking, anaphalactic reaction (anaphylactic reaction), within the hour, she began itching (pruritus), develop hives after getting home from work (urticaria) condition worsened (condition aggravated), she awoke very early in the morning, when her tongue was too swollen to fit in her mouth (swollen tongue), having trouble with secretions (Saliva altered), couldn't swallow (dysphagia), tightness in her chest (chest discomfort)and leaving small "pockmarks" in the areas where her hives had been (skin discolouration) after receiving vaccine INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE]. The patient's past vaccinations included INFLUENZA VACCINE. The patient's medical history, medical treatments, concomitant medications, and family history were not provided. On 11-Oct-2021, the patient received a 0.5 ml dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED (lot number: UJ694AA and expiry date: 30-Jun-2022) via intramuscular route in unknown administration site for prophylactic vaccination. On 11-Oct-2021 the patient developed a serious anaphalactic reaction (anaphylactic reaction), within the hour, she began itching (pruritus) and develop hives after getting home from work (urticaria) same day following the administration of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED. These events were assessed as medically significant. The patient always took a flu shot, so she did not associate the itching with the vaccine, she thought maybe she had used a different laundry detergent or something. She took DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL) orally and went to bed. On an unknown date she awoke very early in the morning, when her tongue was too swollen to fit in her mouth (swollen tongue), She went to a nearby urgent care, as she was having trouble with secretions (saliva altered), couldn't swallow (dysphagia) (unknown latency). At the urgent care, her condition worsened (condition aggravated) she began choking (choking) This event was assessed as medically significant and experiencing tightness in her chest (chest discomfort). Within 30 minutes of awakening, she was transported to the emergency department following the administration of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED. In emergency department (ED) she received METHYLPREDNISOLONE SODIUM SUCCINATE (SOLUMEDROL), EPINEPHRINE and DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL) via intravenous not otherwise specified (IV NOS). She stated that as soon as she received the intravenous (IV) epinephrine, her symptoms began to subside. She remained in emergency department (ED) for six more hours, for observation. Patient stated that she required medication with these, and oral BENADRYL every 6 hours for about a week. Her symptoms gradually went away, leaving small pockmarks in the areas where her hives had been (skin discolouration). The patient was discharged with oral steroids and topical MOMETASONE. She wanted allergy testing, to determine sensitivity, so she was requesting list of all ingredients. At the time of reporting, the patient recovered from anaphylactic reaction, pruritus, urticaria, condition aggravated, swollen tongue, saliva altered, dysphagia, choking, chest discomfort and was recovering from skin discolouration.

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

VAERS 2396520

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

moderat
Staat
MI
Alter
49,0
Geschlecht
F
Eingang
29.07.2022
Impfdatum
22.10.2021
Beginn
26.07.2022
Tage bis Beginn
277,0
Dosis
N/A
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Chest pain Condition aggravated Dyspnoea Immunodeficiency Malaise Pyrexia Respiratory failure Sinus bradycardia

Symptomtext

Discharge Provider: Primary Care Provider: Admission Date: 7/26/2022 Discharge Date: Jul 28, 2022 PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: Pt. is 50 y.o. with Crohn's disease on infliximab, hypothyroidism, OSA on CPAP, non-insulin-dependent type 2 diabetes mellitus, for evaluation of dyspnea, chest pain, fever, malaise which started on 07/25 and was found to have COVID-19 and hypoxic respiratory failure. She completed 3 days of remdesivir as an inpatient due to her immunocompromised state. She also was given a 10 day course of decadron. After 3 days in the hospital, she improved and was able to be weaned off oxygen. She was noted to have asymptomatic sinus bradycardia but was otherwise well and eager to discharge home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Abdominal pain Irritable bowel syndrome with constipation Tobacco abuse Obesity due to excess calories Ileitis Small bowel obstruction Altered bowel habits Arthritis Depression Dyspnea on exertion Hidradenitis suppurativa History of small bowel obstruction Incisional hernia, without obstruction or gangrene Internal hemorrhoids Lesion of female perineum Medical non-compliance MRSA (methicillin resistant staph aureus) culture positive OSA (obstructive sleep apnea) Prediabetes Ventral hernia, recurrent Morbid obesity Arthritis of right knee Crohn's disease of small intestine without complication COVID-19 Sinus bradycardia
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler benzonatate (TESSALON) 100 MG capsule cyclobenzaprine (FLEXERIL) 10 MG tablet dexamethasone (DECADRON) 6 MG tabl
Allergien
CodeineHives, Nausea and Vomiting
Vorherige Impfungen
-

VAERS 2113206

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

moderat
Staat
CO
Alter
37,0
Geschlecht
F
Eingang
15.02.2022
Impfdatum
15.02.2022
Beginn
15.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Feeling hot Hypoaesthesia Paraesthesia Paraesthesia oral Pruritus

Symptomtext

Numbness and tingling in fingers and toes, tingling in mouth and mouth feeling hot, itching on trunk

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
PPD TUBERSOL
Allergien
History of reaction to pertussis vaccine in the past but requesting TDAP today anyways.
Vorherige Impfungen
-

VAERS 1925370

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

moderat
Staat
IN
Alter
58,0
Geschlecht
F
Eingang
06.12.2021
Impfdatum
11.10.2021
Beginn
11.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood blister Dysphagia Dyspnoea Feeling abnormal Oxygen saturation decreased Pain of skin Pruritus Rash Scar Skin indentation Skin irritation Swollen tongue Urticaria

Symptomtext

Itching started within an hour all over, hives started about 3 PM across abdomen and spread from there, took Benadryl at 7 PM. Bed at 7:30 PM woke up at 5:00 and felt funny and went back to sleep and woke up 7 AM and tongue really swollen, difficulty swallowing and drove self to ER and after arrival, difficulty breathing, O2 sat down to 89%. at 10 minutes later gave IV Benadryl, Solumedrol and IV EPI. Within 1 minute of EPI all symptoms gone except tongues swelling. Stated in ER for 5 hours. Everything normal and discharged. Hives returned 12 hours later and topical cream Mometasone used. Still on Oral Steroids and Oral Benadryl for 10 days. Hives continued for 2 weeks. Developed irritated and painful skin eruptions that looked like blood blister and as disappeared left behind a pit and a scar. Just now resolving in the last week.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
None done yet. Called Sanofi Pasteur and recommend see allergist with attention to item 11 - components of vaccine.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
EFFEXOR 37.5 ONCE DAILY (Hot flashed)
Allergien
NKDA; Wool clothes - rash
Vorherige Impfungen
-

VAERS 1839542

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

moderat
Staat
HI
Alter
46,0
Geschlecht
M
Eingang
03.11.2021
Impfdatum
07.10.2021
Beginn
07.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Mobility decreased

Symptomtext

persistent left shoulder pain. Pain noted the day of the shot and has persisted 3 weeks after the shot. No swelling or lump. He has trouble raising his arm up. Not improving. He has been referred to physical therapy and orthopedics. Unclear at this time if related to vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
hypertension, hyperlipidemia, impaired fasting glucose, asthma, allergic rhinitis, sleep apnea
Andere Medikamente
amlodipine
Allergien
lactose
Vorherige Impfungen
-

VAERS 1894919

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

mild
Staat
WA
Alter
50,0
Geschlecht
F
Eingang
23.11.2021
Impfdatum
22.11.2021
Beginn
23.11.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood glucose increased Laboratory test Nausea Vomiting

Symptomtext

Patient had monoclonal antibodies on November 13, 2021. She then received both a flu shot and her COVID booster yesterday (9 days after monoclonal antibodies). Approx 24 hours after receiving the 2 shots she has having nausea and vomiting and her blood sugar was running high. Triage nurse asked that patient go to the ER to be evaluated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nausea
Hospital-Tage
-
Labordaten
Currently in the ER at the time of this report. Has had a battery of labs done, IV of LR going, has been given Metoclopramide and Ondansetron.
Aktuelle Erkrankungen
Unknown
Vorgeschichte
DM, HTN
Andere Medikamente
Unknown
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1866179

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

mild
Staat
ND
Alter
9,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
24.09.2021
Beginn
24.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Injection site pain No adverse event

Symptomtext

There was no adverse reaction. There was an error in administration, as the nurse gave a full 5 mL dose (from the multi dose vial) to the patient. Follow-up with mother several days later indicated no adverse reaction except soreness at the injection site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
None. Under item 20 below, there was no adverse event, but I put "No" just to complete the form.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1837440

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

mild
Staat
GU
Alter
8,0
Geschlecht
F
Eingang
02.11.2021
Impfdatum
09.10.2021
Beginn
21.10.2021
Tage bis Beginn
12,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Papule Rash

Symptomtext

Patient in for itchy red mostly papules and some vesicles on the face, trunk, upper and lower extremities for 2 days. Rashes are coming out not at the same time. She had her first Varicella vaccine on 10/09/2021 here at the clinic. No exposure to Varicella disease. The mother denies fever, cough, runny nose, fast or labored breathing, vomiting, diarrhea. No sick contacts. She saw Dr. yesterday because she was worried, but Dr. is not sure if it is chickenpox or a side effect of the Varicella vaccine. With 1 red papule on the forehead, 6 on the back, one on the right knee, one on the right leg; one vesicle on the right forearm and right cheek

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
If rashes open up and are noted not drying up with clear fluid or pus, apply Mupirocin Ointment.
Aktuelle Erkrankungen
She still has on and off whitish scales on her scalp. She was using Nizoral 2% Shampoo. Mother did not refill it yet but she has no more at home. She scratches her scalp on and off. Mother denies any cough, colds, fever, decrease of appetite, or decrease of activity.
Vorgeschichte
Mother was advised she has seborrhea capitis. Advised may give Ketoconazole 2% Shampoo every 3 to 4 days for up to 8 weeks alternate with regular shampoo.
Andere Medikamente
NONE
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 1793913

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

mild
Staat
MD
Alter
3,0
Geschlecht
F
Eingang
16.10.2021
Impfdatum
14.10.2021
Beginn
16.10.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Rash Rash maculo-papular Rash pruritic

Symptomtext

Daughter developed diffuse pruritic maculopapular rash on face, with isolated red patches on right arm and right leg as well. The index patch was on right leg; it developed within 24 hours of the flu shot administration. The next patch was on her right arm (within 36 hours). 48 hours after the shot, I discovered she had the facial rash when I woke her up that morning. She is currently being treated with oral antihistamines and Rx-strength topical corticosteroids. I recall that she had a similar reaction to another vaccine at approximately 1 year of age, though I cannot remember which vaccine precipitated the reaction. I submitted a VAERS report then as well, temporary ID was 167498.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Moderate poison ivy rash one month prior, treated with oral antihistamines and prescription strength topical steroids
Vorgeschichte
None
Andere Medikamente
None
Allergien
Poison ivy
Vorherige Impfungen
Cannot recall which vaccine, but I submitted a VAERS report in June 2019 - temporary ID was 167498

VAERS 1788044

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

mild
Staat
UT
Alter
63,0
Geschlecht
F
Eingang
15.10.2021
Impfdatum
13.10.2021
Beginn
14.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Body temperature increased Bone pain Gait disturbance Head discomfort Headache Myalgia Pain Sinusitis

Symptomtext

Had a slight headache the night of vaccination, but about an hour after getting up the next morning, extreme body aches made it difficult to even walk. Every bone, joint, and muscle was sore all day (despite alternating doses of Tylenol and Aleve) until about 8:00 pm when it started to subside. My temperature was also elevated, but no in fever range. I didn't have a true headache, but it felt like my head was going to explode, kind of like a bad sinus infection, but throughout my whole head. Slight headache this morning, but the body aches have gone away.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None
Vorgeschichte
Arthritis
Andere Medikamente
LOSARTAN HCTZ; FLUOXETINE; LEVOTHYROXINE; ROPINIROLE; MELOXICAML CALCIIUM; VITAMIN D, MULTIVITAMIN; PROBIOTIC
Allergien
PO Benzocaine, shrimp, copper, cobalt, & nickel
Vorherige Impfungen
-

VAERS 1784920

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge uj694aa

mild
Staat
IN
Alter
6,0
Geschlecht
M
Eingang
14.10.2021
Impfdatum
13.10.2021
Beginn
13.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site warmth

Symptomtext

Upper arm under flu shot site is red and warm to the touch. Spot is large, roughly 4-5inches in length, and spans the width of arm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Daily Singulair tablet 10 mg
Allergien
-
Vorherige Impfungen
-

VAERS 1769013

SEQIRUS, INC. · INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) · Charge UJ694AA

mild
Staat
IN
Alter
57,0
Geschlecht
F
Eingang
07.10.2021
Impfdatum
07.10.2021
Beginn
07.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Injection site swelling

Symptomtext

injection site pain and swelling

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
penicillin, biaxin, clendomiosin, factiv, septra, sudafed
Vorherige Impfungen
-

VAERS 2123196

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge UJ694AA

gering
Staat
TX
Alter
43,0
Geschlecht
F
Eingang
18.02.2022
Impfdatum
31.01.2022
Beginn
31.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

Patient was given refrigerated Moderna that was expired beyond it's 'Beyond Use Label' date of 01/27/2022. Vial was placed into fridge on 12/28/2021. Vial was not removed from fridge in time for 'Beyond Use' expiry date and inadvertently administered. Manufacturer's expiry date is March 25, 2022. Provider informed. Moderna informed and stated that 'the vaccine administered on January 28 to February 7, 2022 from lot number 033H21A maintained the activity necessary to protect against the SARS-CoV-2 (Covid-19) virus at time of administration'. Unable to get ahold of patient to assess for adverse effects.

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

VAERS 1824743

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

gering
Staat
TX
Alter
48,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
24.09.2021
Beginn
18.10.2021
Tage bis Beginn
24,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

patient receiving an extra dose of Fluzone Quadrivalent with no reported adverse event; Initial information received on 18-Oct-2021 regarding an unsolicited valid non-serious case from a other health professional via Global Medical Information (GMI) (Reference number- 00817290). This case involves a 48-year-old female patient who received vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT], which was double dose of the vaccine (extra dose administered). Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On 18-Oct-2021, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UJ705AB and expiry date: not reported) (Frequency twice) via intramuscular route in the left deltoid for prophylactic vaccination. On 24-Sep-2021, the patient received another dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot UJ694AA and expiry date: not reported) (Frequency twice) via intramuscular route in the left arm for prophylactic vaccination. It was a case of actual medication error due to extra dose administered (latency on same day). It was reported "he nurse was looking for any potential AE information in regards to a patient receiving an extra dose of Fluzone Quadrivalent." 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 set out in the Directive 2001/83/EC and Module VI of the Good 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 1808538

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

gering
Staat
CO
Alter
61,0
Geschlecht
M
Eingang
22.10.2021
Impfdatum
22.10.2021
Beginn
22.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Intended to give Influenza and Moderna Booster. Gave two doses of Influenza vaccine instead. Discussed with patient and provider and booster Moderna dose administered. Patient observed with no reaction.

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

VAERS 1788079

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ694AA

gering
Staat
OH
Alter
22,0
Geschlecht
F
Eingang
15.10.2021
Impfdatum
15.10.2021
Beginn
15.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Needle issue No adverse event Syringe issue Underdose

Symptomtext

Partial administration of fluzone quad vaccine due to leak around needle and syringe when this provider went to administer vaccine. No apparent injury, patient denies discomfort/pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Needle issue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
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VAERS 1741188

UNKNOWN MANUFACTURER · INFLUENZA (SEASONAL) (NO BRAND NAME) · Charge UJ694AA

gering
Staat
TX
Alter
52,0
Geschlecht
F
Eingang
28.09.2021
Impfdatum
27.09.2021
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Unevaluable event

Symptomtext

n/a

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
nka
Vorherige Impfungen
-