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Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

7Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 2 MA 1 VA 1 NC 1 AL 1

VAERS 2696231

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

schwer
Staat
MA
Alter
20,0
Geschlecht
M
Eingang
15.10.2023
Impfdatum
15.10.2023
Beginn
15.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness Posture abnormal Vomiting

Symptomtext

Shortly after flu shot was administered patient slumped down in chair, passed out, and slid down to the floor. A customer called 911. The patient regained consciousness very quickly, seconds after passing out. He stood up, but his father and the pharmacist had him sit down. He threw up shortly after. He was given bottle water. After a few minutes, the ambulance showed up and the patient was evaluated. His blood pressure was taken. It was learned that that patient had passed out after a shot before, and he had not eaten anything since the night before. He left the store with his father, and declined being taken to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
amoxicillin, cefadroxil
Vorherige Impfungen
-

VAERS 2715681

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

moderat
Staat
VA
Alter
49,0
Geschlecht
F
Eingang
20.11.2023
Impfdatum
16.10.2023
Beginn
16.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Discomfort Impaired work ability Inflammation Injected limb mobility decreased Injection site inflammation Injection site pain Loss of personal independence in daily activities Pain Pain in extremity Product administered at inappropriate site Sleep disorder X-ray limb

Symptomtext

Flu Shot received at Workplace Flu Clinic and the shot was given to high in my left arm and the provider missed the muscle and injected the flu shot into my Bursa Sac. Since then, range of motion in left arm is extremely limited and there is a lot of pain and I cannot lift or pull things and it has effected my daily acts of living for example getting dressed and am not able to use that arm without feeling pain down my arm from the shoulder down my left arm, sleep and anything related to using my left arm is effected. My sleep has been very disrupted and am not able to get comfortable and have to prop self up to sleep. There has has been a lot of inflammation, pain down my left arm from the shoulder down my left arm and constant throbbing pain. Saw a healthcare provider through work to report the incident and another provider who I saw that treated me for evaluation and did an Xray and Cortizone Shot. Since the Cortizone Shot, I have had less pain and inflammation, but there is still pain and limited range of motion in that arm. Workplace restrictions are in place and I am not to lift anymore than 10 lbs and have been told not to reach overhead and physical therapy orders have been provided for twice weekly PT. I will be following up with this doctor again at the end of November 2023.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
Saw provider for medical assessment, Xray and Cortisone Shot 11/8/2023
Aktuelle Erkrankungen
N/A
Vorgeschichte
None
Andere Medikamente
Ibuprofen
Allergien
N/A
Vorherige Impfungen
-

VAERS 2716495

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

mild
Staat
TX
Alter
1,0
Geschlecht
M
Eingang
21.11.2023
Impfdatum
20.11.2023
Beginn
21.11.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age Pyrexia

Symptomtext

Pneumovax23 given at 12mo well child appt; mom today reported fever but unsure if due to this vaccine, other vaccines given or if child is sick (attend daycare).

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

VAERS 2715897

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

mild
Staat
NC
Alter
55,0
Geschlecht
F
Eingang
20.11.2023
Impfdatum
29.09.2023
Beginn
29.09.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Alanine aminotransferase normal Albumin globulin ratio normal Anion gap Arthralgia Aspartate aminotransferase normal Basophil count decreased Basophil percentage decreased Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood osmolarity decreased Blood potassium normal Blood sodium normal Blood urea normal Carbon dioxide normal

Symptomtext

Influenza vaccine administered in right arm. Patient presented to Medical Center approx 12 hours later w/ c/o HA, right sided neck & shoulder pain, nausea. CT Brain/Head w/o contrast unremarkable. Treated for HA & released. Provider: 55 yo female presents for evaluation of neck pain. Awoke around 11 pm with pain in right trap extending to right neck and head. Has been trying stretching and warm packs without improvement. Headache is directly caused by pain in trap per patient. Denies any photophobia, throbbing pain, nausea, vomiting, neck stiffness, injury, trauma. Review of Systems General: Denies fever, chills HEENT: Denies headache, change in vision, LAD, sore throat Chest: Denies chest pain, palpitations Lungs: Denies cough, wheezing, sob, doe Abdomen: Denies n/v/d/ab pain Back: Denies flank pain, back pain GU: Denies dysuria, hematuria, polyuria, discharge Skin: denies rash, breakdown Neuro: denies focal deficits/weakness, seizure Physical Exam Vitals & Measurements T: 36.7 ?C (Oral) HR: 60(Peripheral) RR: 17 BP: 159/82 SpO2: 99% WT: 65.90 kg(Dosing) WT: 65.9 kg(Measured) General: awake and alert; no acute distress Head: normocephalic and atraumatic Airway: patent and unobstructed; normal phonation Neck: No JVD; No deformity or swelling Chest: symmetric rise and fall; no deformity Lungs: no tachypnea or IWOB Abdomen: flat, nondistended Ext: moves all extremities; no edema MSK: hypertonic R trapezius with point tenderness over medial aspect extending cephalad along paraspinal musculature, no tenderness around scalp, no overlying skin change. Skin:no rash on examined surfaces Neuro: alert and oriented; no focal deficits, CN 2-12 grossly intact, no cerebellar dysfunction 55 yo female presents for evaluation of neck pain. On initial exam patient is resting comfortably, in no acute pain, non toxic appearing. Given hx and cc initial concern for etiology such as meningitis, fracture, vertebral dissection, zoster, migraine, stroke. Decreased concern for meningitis, fracture, stroke after normal neurologic exam, lack of tenderness of vertebrae. Decreased concern for vertebral dissection given normal neuro exam as well as lack of mechanism for injury. No skin changes to suggest zoster. Meningitis low on differential after examining patient 2/2 lack of neck stiffness, full ROM of neck, no fever, negative jolt test. Muscular point tenderness suggests muscular strain causing tension headache. Plan to treat headache. Lab work and imaging ordered in triage, will evaluate these and address if necessary. Do not feel that imaging was necessary but will follow results. CT imaging not actionable. Lab work reviewed and nonactionable. Trigger point injections as in above procedure note. Reevaluation with mildly improved pain. Denies any worsening symptoms. Plan to discharge home with instruction for RICE and follow up if necessary. Discussed with patient the significance of all tests/lab work/exam findings, diagnosis, treatment plan and follow up recommendations. Patient was in agreement with the plan and all questions/ concerns were addressed. Return precautions were discussed and patient verbalized understanding of these precautions. Patient remained hemodynamically stable while under my care in the emergency department. During all encounters with patient appropriate PPE was warned in the form of goggles, gloves, N95 mask and gown when indicated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
CT W/O CONTRAST 09/30/23 Reason For Exam Headache Report PROCEDURE: CT Brain/Head w/o Contrast REASON: Headache TECHNIQUE: Unenhanced contiguous axial CT sections of the brain were obtained from the skull base to the vertex. FINDINGS: No prior studies available for comparison There is no evidence of intra or extra axial mass, hemorrhage, or fluid collection. There is no evidence of a major vascular distribution infarct. The ventricles and sulci are symmetric and normal in size. There is no midline structural shift. Visualized portions of the orbits and mastoid air cells are unremarkable. Paranasal sinuses clear. The calvarium is intact. IMPRESSION: No acute intracranial abnormality. Report Dictated by Radiologist: WBC 09/30/23 03:54 13.4 High RBC 09/30/23 03:54 4.67 Hemoglobin 09/30/23 03:54 14.1 Hematocrit 09/30/23 03:54 43.0 MCV 09/30/23 03:54 92.1 MCH 09/30/23 03:54 30.2 MCHC 09/30/23 03:54 32.8 Low RDW 09/30/23 03:54 13.7 Platelets 09/30/23 03:54 474 High MPV 09/30/23 03:54 7.9 Neutrophil % Auto 09/30/23 03:54 85.9 High Lymphocyte % Auto 09/30/23 03:54 10.6 Low Monocyte % Auto 09/30/23 03:54 3.3 Low Eosinophil % Auto 09/30/23 03:54 0.0 Low Basophil % Auto 09/30/23 03:54 0.2 Neutro Absolute 09/30/23 03:54 11.5 High Lymph Absolute 09/30/23 03:54 1.4 Mono Absolute 09/30/23 03:54 0.4 Eos Absolute 09/30/23 03:54 0.0 Baso Absolute 09/30/23 03:54 0.0 Routine Chemistry LATEST RESULTS Sodium 09/30/23 03:54 139 Potassium Lvl 09/30/23 03:54 4.3 Chloride 09/30/23 03:54 101 CO2 09/30/23 03:54 28.0 AGAP 09/30/23 03:54 10 Osmo Calc 09/30/23 03:54 280 BUN 09/30/23 03:54 18.0 Creatinine Level 09/30/23 03:54 0.70 eGFR CKD EPI 09/30/23 03:54 102 Glucose Lvl 09/30/23 03:54 115 High Calcium 09/30/23 03:54 10.3 Protein Total 09/30/23 03:54 7.5 Albumin 09/30/23 03:54 4.8 A/G Ratio 09/30/23 03:54 1.8 Bilirubin Total 09/30/23 03:54 0.27 Alk Phos 09/30/23 03:54 79 ALT 09/30/23 03:54 14 AST 09/30/23 03:54 14
Aktuelle Erkrankungen
No illnesses at time of vaccination or during the one month prior
Vorgeschichte
Chronic pain, rhinitis, depression, low back pain, menopause, foot/hip pain, history of combat and operational stress reaction, pes planus, PTSD, presbyopia
Andere Medikamente
albuterol (albuterol 90 mcg/inh aerosol inhaler)2 Puffs Inhalation (breathe in) every 6 hours as needed wheezing. Refills: 2. calcium-vitamin D (calcium (as carbonate)-vitamin D 600 mg-10 mcg (400 intl units) oral tablet)2 tabs Oral (given
Allergien
NKA
Vorherige Impfungen
-

VAERS 2705700

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

mild
Staat
-
Alter
63,0
Geschlecht
F
Eingang
30.10.2023
Impfdatum
06.10.2023
Beginn
07.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Sleep disorder Vaccination site pain

Symptomtext

The following day after the flu vaccine employee reports "shoulder was sore and achey then about 4 days later I started getting shooting pain down my arm and waking me out of a sound sleep. This is still going on and it's been a month. When I raise my arm my entire bicep is tender. I feel the tender area where the vaccine was given and it feels tender at the site like it's black and blue but it is not visibly discolored. I get random shooting throughout the day."

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
heart ablation June 6th 2023
Vorgeschichte
pulmonary embolism and history of numerous blood clots
Andere Medikamente
Warfarin, Sumatriptan, Robinul, Flecainide, Clonazepam PRN evening, Singulair, Potassium
Allergien
Sulfa and erythromycin Rye
Vorherige Impfungen
-

VAERS 2703925

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

mild
Staat
TX
Alter
4,0
Geschlecht
M
Eingang
27.10.2023
Impfdatum
25.10.2023
Beginn
25.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site rash Rash papular Skin warm

Symptomtext

pt in office on 10/25/2023 and received 4 vaccines; by evening on day of office visit MOC noticed right leg with warm raised rash to skin at injection site with approximate size of mini orange (cutie); pt did not have any pain or itch at that time; by next morning sx's were still the same; by Thursday evening (10/26/2023) MOC noticed same sx's to leg leg/thigh with approximate size of a quarter; this morning (Friday 10/27/2023) sx's of rash were lighter in presentation and the rash to right leg appeared to have spread

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site rash
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
no
Vorgeschichte
Allergist seen for further evaluation of possible Asthma
Andere Medikamente
n/a
Allergien
NKA; sensitivity to dairy and mold per Allergist
Vorherige Impfungen
-

VAERS 2717532

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT8144NA

gering
Staat
AL
Alter
30,0
Geschlecht
F
Eingang
24.11.2023
Impfdatum
29.10.2023
Beginn
29.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy No adverse event

Symptomtext

she received Fluzone Quadrivalent and is currently pregnant with no reported adverse event; Initial information was received on 13-Nov-2023 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves a 30 years old female patient who was currently pregnant and exposed to influenza quadrival A-B vaccine [Fluzone quadrivalent]with no reported advesre event. Data regarding this pregnancy were received prospectively, i.e. before pregnancy outcome was known. The date of last menstrual period was not reported. The estimated due date was not reported. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. The patient had unknown previous pregnancy/ies. On 29-Oct-2023, the patient received a 0.5 ml, total (once) dose of suspect influenza quadrival A-B vaccine (Suspension for injection) (lot UT8144NA, expiry date: 30-Jun-2024, strength: standard) via unknown route in unknown administration site for Immunization and she received fluzone quadrivalent and is currently pregnant with no reported advesre event (exposure during pregnancy) (Latency: same day). Action taken: not applicable. At time of reporting, the outcome was Unknown for the event. Additionally, at time of reporting, the outcome of the pregnancy is unknown.

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