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Reporte zur Charge U8049AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

16Reporte angezeigt
0Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
1Bleibende Schaeden
CO 3 TX 3 IL 2 OK 1 OH 1 PA 1 NM 1 NC 1 AL 1 OR 1

VAERS 2708273

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge u8049aa

schwer
Staat
OK
Alter
9,0
Geschlecht
F
Eingang
01.11.2023
Impfdatum
10.10.2023
Beginn
11.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Arthralgia Blood creatine phosphokinase normal Blood test normal C-reactive protein normal Full blood count normal Gait inability Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Influenza virus test negative Lumbar puncture normal Magnetic resonance imaging spinal abnormal Metabolic function test normal Red blood cell sedimentation rate normal SARS-CoV-2 test negative Walking aid user Wheelchair user

Symptomtext

Guillian Barre Syndrome was diagnosed by MRI on 10/16/23 by MRI. Patient had knee pain, numbness, and unable to walk 24 hours after vaccination and has not been previously sick or have a chronic illness. Patient was treated with IVIG once daily for 5 days, patient is still currently having numbness, but has been able to bear weight with walker, but is mainly in wheelchair at this current time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
7,0
Labordaten
10/12/23: CBC, CMP,CK, CRP, Sed rate : all normal 10/13/23: blood work, covid/flu swab, spinal tap: all normal 10/16/23: MRI : mild Guillian Barre Syndrome in the cauda equina
Aktuelle Erkrankungen
None
Vorgeschichte
none
Andere Medikamente
None
Allergien
azithromycin
Vorherige Impfungen
-

VAERS 2708192

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

schwer
Staat
OH
Alter
59,0
Geschlecht
F
Eingang
01.11.2023
Impfdatum
12.10.2023
Beginn
29.10.2023
Tage bis Beginn
17,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Computerised tomogram Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Lumbar puncture Magnetic resonance imaging

Symptomtext

Per Workers Comp email-Caregiver stated she received her annual flu vaccine on 10/12/23 at the Medical Office Bldg. She said approximately 1 week later she began to develop numbness in bilateral feet and it slowly crept up her body. It is now numb from the chest down and bilateral hands. She came to ED on 10/29/23 and was subsequently admitted into the hospital. They ran CT, MRI & lumbar puncture ? she was awaiting the results but said the provider said with the symptoms, they were leaning towards it being Guillain-Barre? syndrome. They are treating her with 5 days of IVIG and she will be admitted the entire time.

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

VAERS 2698220

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge U8049AA

moderat
Staat
CO
Alter
39,0
Geschlecht
F
Eingang
18.10.2023
Impfdatum
14.09.2023
Beginn
14.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Impaired driving ability Joint range of motion decreased Loss of personal independence in daily activities Mobility decreased Musculoskeletal stiffness Pain Pain in extremity Periarthritis Product administered at inappropriate site Wrong technique in product usage process X-ray limb

Symptomtext

I was ordered by my employer to receive a flu shot. At the time off injection, I noticed that my injection was higher than where I've normally received them in the past- about two fingers width below the riding of my shoulder. Within hours of administration I began to experience severe pain and stiffness is my arm. Several days passed and the pain and lack of mobility remained. The intensity eventually subsidized, but I still experienced pain with motion. As time progressed, The pain began to increase. I started experiencing pain when dressing/undressing, turning my wheel while driving, and other basic tasks. Nsaids and Tylenol had no effect when taken. On October 7th, I was in so much pain and experienced a decreased range of motion to the point I was unable to sweep my floor or open a jar. I went to urgent care that afternoon as I suspected that this was no longer within the realm of being a normal side effect. I was advised that this may be a result of an improperly administered vaccine. I was also advised that this may be exacerbated by my Fibromyalgia. I was prescribed Baclofen, given instructions to rotate with ice/heat, but to continue movement and do "spidercrawls" with my fingers. I did as instructed, but my condition not improve over the next week. Today, October 18th, I saw PCP who acknowledged a likely improper administration and diagnosed me with a frozen shoulder. She has prescribed Meloxicam and referred me to physical therapy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
Xray- October 28th. No finding
Aktuelle Erkrankungen
None
Vorgeschichte
PTSD with panic disorder/anxiety/depression, fibromyalgia, headaches
Andere Medikamente
Lyrica, Clonazepam, low dose Naltrexone, dicyclomine
Allergien
Penicillin, tramadol, hydrocodone, oxycodone
Vorherige Impfungen
-

VAERS 2723141

PROTEIN SCIENCES CORPORATION · INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) · Charge U8049AA

mild
Staat
CO
Alter
13,0
Geschlecht
F
Eingang
12.12.2023
Impfdatum
11.12.2023
Beginn
11.12.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness

Symptomtext

Patient walked away from clinic with family. Within 20 feet of clinic patient became lightheaded. Her mother was able to sit her to the ground. After a 1 minute she abmulated with supported assist to the clinic chairs where she was monitored for 10 minutes. PERRLA, NML bp, awake and talking. drinking water and eating lollipop. Once she left, she denied lightheadedness, dizziness, ambulating without issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
2 weeks prior, feeling well presently
Vorgeschichte
none
Andere Medikamente
zyrtec
Allergien
amoxicillin
Vorherige Impfungen
-

VAERS 2719487

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

mild
Staat
PA
Alter
4,0
Geschlecht
F
Eingang
30.11.2023
Impfdatum
29.11.2023
Beginn
29.11.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Injection site pruritus Urticaria

Symptomtext

Patient developed hives on body about 1.5 hours after receiving flu vaccine in clinic. Called in @ 11:46 am & spoke with triage nurse, reported "neck is welted & red". At the time of call mother reported that she was itching site but her breathing was okay. Was advised to take pt to ER if any breathing difficulties developed & to start children's Benadryl. Patient was scheduled for evaluation in office on 11/30/23 @ 10 am. Patient presented in office at this time with hives present on face, torso, arms, & legs. Physician recommending 2nd gen Antihistamine use (cetirizine) daily with continued benadryl as needed. If no resolution with these options, would do a short steroid course in the form of prednisolone x 5-7 days with taper. Continue monitoring for concerning features including mouth/lip/tongue swelling or tingling, throat swelling, difficulty breathing. Should have skin allergy testing for common causes of reactions to flu vaccination. Allergist appt scheduled for 11/30/23 @ 1:30 pm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Enlarged tonsils, dehydration (hospitalized 11/11/23-11/15/23)
Vorgeschichte
Hemoglobin C trait, Seizures, Benign heart murmur, anemia
Andere Medikamente
acetaminophen 160 mg/ 5 ml (PRN), cetirizine 1 mg/ml (Daily), diazepam (PRN), ferrous Sulfate 15 mg (Daily), miralax (PRN)
Allergien
No allergies listed at time of vaccine
Vorherige Impfungen
-

VAERS 2701594

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

mild
Staat
CO
Alter
25,0
Geschlecht
F
Eingang
25.10.2023
Impfdatum
24.10.2023
Beginn
24.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Disorientation Nausea Visual impairment

Symptomtext

Approximately 15 min after vaccine was administered, patient experienced "disorientation and vision issues," no syncope occurred. She laid down and symptoms resolved. Patient unsure if related to actual vaccine or needle. Reports one previous episode of syncope with blood draw. The next day, the patient indicates feeling nauseated, unsure if related to vaccine.

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

VAERS 2691313

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

mild
Staat
TX
Alter
61,0
Geschlecht
F
Eingang
05.10.2023
Impfdatum
03.10.2023
Beginn
04.10.2023
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Joint swelling Peripheral swelling

Symptomtext

24 hr after shot lower legs swollen and ankles swollen and painful as of today day 2 after immunization legs still swollen and will follow up with pcp if no improvement by Friday.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
Hyertension controlled on low does lisinopril
Andere Medikamente
lisinopril synthroid protonix bentyl prn
Allergien
MMR pertussis tetracycline morphine
Vorherige Impfungen
MMR Pertussis 3 mo Steven Johnson syndrome

VAERS 2689345

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

mild
Staat
TX
Alter
38,0
Geschlecht
F
Eingang
02.10.2023
Impfdatum
22.09.2023
Beginn
22.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Flushing Lip swelling Pruritus Rash

Symptomtext

flushing, rash, itching to face and neck, swelling of lips treated with PO Benadryl when event reported, continued to use Benadryl until 9/24 when felt recovered

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
latex, iodine
Vorherige Impfungen
2021 had local "cellulitis" after annual flu vaccination

VAERS 2684493

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

mild
Staat
NM
Alter
24,0
Geschlecht
F
Eingang
21.09.2023
Impfdatum
21.09.2023
Beginn
21.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness

Symptomtext

Patient felt lightheaded and states she felt like she was going to pass out.

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

VAERS 2702648

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

gering
Staat
NC
Alter
21,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
26.10.2023
Beginn
26.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy

Symptomtext

Pt came in to get a flu vaccine. I asked if she had any allergies. I gave fluzone in RD. After giving I noticed pt looked to be possibly pregnant. She did not tell me she was pregnant until I started out of the room and turned and asked if she was pregnant. Then she told me "yes, I am 28 weeks". I immediately called representative at the Imunnization office. I went back to the room and told pt what had been given and advised her to let her OB provider know at next appt. Discussed that there had been no trials with pregnancy and flu vaccine with preservatives. She verbalized understanding and had no further questions.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Exposure during pregnancy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Ant vinum
Vorherige Impfungen
-

VAERS 2700252

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

gering
Staat
IL
Alter
35,0
Geschlecht
M
Eingang
23.10.2023
Impfdatum
06.10.2023
Beginn
06.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

The Vaccination Team was in the Community at a health event. Client reported not having a flu shot in the past year. Client was administered a flu shot on 10/06/2023. When entering vaccination in (medical record) it was determined the client had received a flu vaccine from another provider on 09/22/2023

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

VAERS 2700245

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

gering
Staat
IL
Alter
55,0
Geschlecht
M
Eingang
23.10.2023
Impfdatum
23.10.2023
Beginn
23.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

The Vaccination Team was in the Community at a health event. Client reported not having a flu shot in the past year. Client was administered a flu shot. When entering vaccination in (health medical record) it was determined the client had received a flu vaccine from another provider on 09/29/2023

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

VAERS 2696520

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

gering
Staat
AL
Alter
6,0
Geschlecht
F
Eingang
16.10.2023
Impfdatum
05.10.2023
Beginn
05.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaccination site erythema Vaccination site swelling Vaccination site warmth

Symptomtext

local reaction, redness, swelling and warmth, patient was evaluated at 6 days post vaccination and still had redness, swelling and warmth at vaccination site

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaccination site erythema
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
eczema
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2694466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge U8049AA

gering
Staat
-
Alter
13,0
Geschlecht
M
Eingang
11.10.2023
Impfdatum
07.10.2023
Beginn
07.10.2023
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

Pfizer Covid-19 vaccine (5yrs-11yrs) given to 13 yr old instead of Comirnaty Covid vaccine (12+ yrs). Reported event to Pfizer, was told to repeat vaccination 8 weeks from last dose to ensure full immunity.

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 2694108

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

gering
Staat
OR
Alter
24,0
Geschlecht
F
Eingang
11.10.2023
Impfdatum
05.10.2023
Beginn
06.10.2023
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Swelling

Symptomtext

Area is quite red and she admits to a hard outline of swelling around red area. Pt denies pain, hives, or fever. She only noticed it upon taking off her shirt. Advised pt to use antipyretics, cool compresses, and topical anti-itch ointments. If she develops new or worsening sx, especially >48 hours after vaccination, she should present to UC.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None known
Vorgeschichte
Hx of iron deficiency anemia Menorrhagia with regular cycle Presence of (intrauterine) contraceptive device BMI 33.0-33.9,adult Seasonal allergies
Andere Medikamente
Mirena Montelukast Sodium 10mg
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2685412

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8049AA

gering
Staat
TX
Alter
66,0
Geschlecht
M
Eingang
22.09.2023
Impfdatum
11.09.2023
Beginn
11.09.2023
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 Product storage error

Symptomtext

excursions exceeded 72 hours of went below 0 C with no reported adverse event; patient was given a (Fluzone QIV) vaccine that had undergone a temp excursion with no reported adverse event; Initial information received on 12-Sep-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves a 66 years old male patient who reported excursions exceeded 72 hours of went below 0 c and patient was given a influenza quadrival A-B multidose vaccine preserved [Fluzone Quadrivalent Multidose] that had undergone a temp excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date the patient reported excursions exceeded 72 hours of went below 0 c with no reported adverse event (product storage error) (unknown latency). On 11-Sep-2023, the patient received 0.5ml dose of suspect influenza quadrival A-B multidose vaccine preserved, Suspension for injection (lot U8049AA; strength, expiry date not reported) via intramuscular route in the left deltoid for prophylactic vaccination (Immunization) that had undergone a temp excursion with no reported adverse event (poor quality product administered) (latency: on same day). The situation occurred due Refrigerator malfunction and Human error not involved. Action taken : not applicable. Outcome : Unknown. 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-