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Reporte zur Charge UJ749AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

8Reporte angezeigt
1Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
KS 2 MI 1 TX 1 NC 1 CA 1 PA 1 IL 1

VAERS 2314116

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

kritisch
Staat
MI
Alter
66,0
Geschlecht
F
Eingang
09.06.2022
Impfdatum
27.10.2021
Beginn
07.06.2022
Tage bis Beginn
223,0
Dosis
N/A
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute respiratory failure Angiogram cerebral normal Arteriogram carotid normal Asthenia Asthma COVID-19 Chest X-ray Computerised tomogram head normal Condition aggravated Dyspnoea Fibrin D dimer normal Headache Hypoxia Muscular weakness Neck pain Oxygen saturation decreased Procalcitonin normal Red blood cell sedimentation rate normal

Symptomtext

Admission Date: 6/7/2022 Discharge Date: Jun 8, 2022 PRESENTING PROBLEM: COVID-19 HOSPITAL COURSE: 66-year-old female with a past medical history significant for CML as well as self-reported history of asthma and previous COVID-19 vaccination who presents due to complaints of generalized weakness as well as headache and neck pain. Patient states he has been at her baseline state of health up until the morning of 06/06/2022. She states he has been feeling well has had no complaints that she thought were related to infection. However, after awakening 06/06/2022, she complained of generalized weakness. She states that while she normally ambulates around the house with no assistive devices although she does use a cane and walker outside the house, she felt like her legs at home today were much weaker than usual. She had no numbness or tingling. She did report a headache with some neck pain but she had no visual changes and no photophobia. With her symptoms she was concerned that she may have had a stroke and because of this, she presented to the emergency department. In the emergency department the patient was hemodynamically stable and afebrile. Low suspicion was had for a stroke based on the patient's clinical exam and she did undergo CT angiography of the head and neck as well as CT of the head unenhanced. No acute pathology was seen on imaging. However, the patient did test positive for COVID-19 and with ambulation, her oxygen saturation would drop to the mid 80% range and she would become quite tachycardic. Because of this, she was thought to warrant observation in the hospital and she was started on dexamethasone by the ER provider. in-house: patient presented with generalized weakness as well as headache and neck pain, she was admitted for acute hypoxemic respiratory failure secondary to what was suspected to be a COVID-19 mediated asthma exacerbation. patient was started on prednisone (she was given a dose of dexamethasone in the ED) and nebulizers; micro studies were sent were sent as well. a CXR was obtained and steroids were switched to dexamethasone, procalcitonin and the rest of her 'COVID labs' (d-dimer, ESR, and troponin) were unremarkable. pulmonary rehab saw her and set her up with home oxygen, suspect a component of her hypoxemia (if not all of it) is related to underlying lung disease. patient was arranged to be followed by 'Transition to Home' service. at the time of discharge patient was in good spirits and eager to leave. she said she felt slightly weak (ambulated the halls fine) and head her usual daily morning SOB. all questions and concerns addressed, all meds and follow-ups reviewed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Hypertension Asthma exacerbation attacks Cervical spondylosis with myelopathy Carpal tunnel syndrome Esophageal reflux Iron deficiency anemia Neoplasm of uncertain behavior of other lymphatic and hematopoietic tissues Disease of white blood cells Disturbance of skin sensation Hyperlipidemia Sleep apnea Essential thrombocythemia AVN (avascular necrosis of bone) Tobacco abuse Asthma exacerbation, non-allergic, moderate persistent AVM (arteriovenous malformation) of colon Erythromelalgia Thrombocytosis Myeloproliferative disease Polyp of duodenum Neutrophilic leukocytosis Neoplasm of uncertain behavior of colon Hiatal hernia Angiodysplasia of stomach and duodenum without bleeding Essential hypertension, benign Asthma exacerbation Asthma-COPD overlap syndrome with acute exacerbation Acute upper GI bleed
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet acetaminophen-codeine (TYLENOL #3) 300-30 MG per tablet albuterol (ACCUNEB) 1.25 MG/3ML nebulizer solution albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler (Expir
Allergien
Environmental Seafood SingulairRash Theophylline
Vorherige Impfungen
-

VAERS 1754103

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

kritisch
Staat
TX
Alter
73,0
Geschlecht
M
Eingang
01.10.2021
Impfdatum
30.09.2021
Beginn
01.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

Received call this morning 10/1/2021 from medical examiner that wife found patient deacesed - medical examiner states that he determinded natural causes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none noted
Vorgeschichte
E1165 Type 2 Diabetes Mellitus With Hyperglycemia N183 Chronic Kidney Disease, Stage 3 (moderate) E291 Testicular Hypofunction E782 Mixed Hyperlipidemia M5417 Radiculopathy, Lumbosacral Region Sleep Apnea I714 Abdominal Aortic Aneurysm, Without Rupture
Andere Medikamente
08/04/2021 Jublia 10 % topical solution with applicator 1 application apply to nails daily; cover affected toenail, toenail folds, toenail bed and undersurface of nail x 48 weeks. 07/27/2021 Invokana 100 mg tablet 1 tablet by mouth daily 07
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1795484

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

mild
Staat
KS
Alter
65,0
Geschlecht
F
Eingang
18.10.2021
Impfdatum
06.10.2021
Beginn
06.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Neuralgia Pain in extremity

Symptomtext

On 10/6/21, Patient was administered her flu vaccine at 07:04 am. Patient returned to vaccination site about 4 hours after vaccine stating that her arm was sore. She did not have any swelling or redness, just sore down to the elbow. She returned to employee health today (10/18/21) stating that it was still bothering her. She still did not have any swelling or redness but again stated it has been bothering her since her shot. Patient was given an appointment with the Employee Health physician today (10/18/21). Was told it was likely nerve pain and placed on an oral steroid treatment.

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

VAERS 1753809

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

mild
Staat
NC
Alter
30,0
Geschlecht
F
Eingang
01.10.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age Pruritus Rash Swelling

Symptomtext

Facial Rash-itch and swelling around 5-6pm after being given the vaccine at 2:02pm. Patient reported to the nurse on 09/30/2021 and stated there was no trouble breathing and that Benadryl was helping with the rash and swelling. Patient has allergy to thimersol so a prefilled syringe was needed. High dose was picked up and administered instead of appropriate dose for patient age.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Adderall XR 15mg
Allergien
Thimerosal Cocamidopropyl Betaine
Vorherige Impfungen
Facial rash following Moderna COVID Vaccine x2

VAERS 1746183

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

mild
Staat
CA
Alter
85,0
Geschlecht
F
Eingang
29.09.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abnormal behaviour Confusional state Headache Injection site pain Speech disorder

Symptomtext

Patient became very confused and could not come up with words. She had big behavior changes that were inconsistent with how she normally behaves. She had a bad headache and a lot of pain at the injection site

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
None yet
Aktuelle Erkrankungen
High Blood Pressure (under control with meds) Fibromyalgia Diverticulosis Allergic Rhinitis
Vorgeschichte
See above High Blood Pressure Fibromyalgia
Andere Medikamente
Amlodipine 5mg,Losartan 100mg, Diclofenac 50mg, gabapentin 300mg, multi vitamins, Synthroid 100mcg, zolpidem 10mg,Calcium, Magnesium
Allergien
Crab and Shrimp
Vorherige Impfungen
-

VAERS 1824742

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

gering
Staat
KS
Alter
62,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Contraindicated product prescribed No adverse event Product administered to patient of inappropriate age

Symptomtext

prescription for FLUZONE HIGH DOSE but she is only 62 years old, with no reported AE; prescription for a patient that is immunocompromised (stage 3 kidney disease), with no AE; they did give it to her last year, with no reported AE; Initial information received on 18-Oct-2021 regarding an unsolicited valid non-serious case from a other health professional via Medical Information (Reference number- 00817250).. This case involves a 62-year-old female patient who is immunocompromised for whom the prescription of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] was provided and gave it to her last year (Product prescribing issue, Contraindicated product prescribed and product administered to patient of inappropriate age). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. At the time of the event, the patient had ongoing Renal disorder and Immunodeficiency. It was reported "her doctor has prescribed her to get the Fluzone High Dose which they plan to give her but are calling to get information that it is OK to do so. Caller states they did give it to her last year but they want information this time. States the consumer has Stage 3 kidney disease." It was a case of potential medication error due Product prescribing issue, Contraindicated product prescribed and product administered to patient of inappropriate age. At time of reporting, 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 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
Contraindicated product prescribed
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Immunocompromised; Renal disorder
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1774833

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

gering
Staat
PA
Alter
61,0
Geschlecht
M
Eingang
09.10.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product administered to patient of inappropriate age

Symptomtext

61 year old male patient received dose of FLUZONE HD QIV vaccine with no AE; Initial information received on 29-Sep-2021 regarding an unsolicited valid non-serious case from a other health professional via Agency (Reference number- 00791077). This case involves a 61 year old male patient who was vaccinated with INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT], (product administered to patient of inappropriate age). The patient's past medical history, medical treatment, vaccination, concomitant medication and family history were not provided. On 28-Sep-2021, the patient received a 0.7 ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ749AA and expiry date: 30-Jun-2022) (frequency: Once) via an intramuscular route in the left for prophylactic vaccination. It was an actual medication error case due to inappropriate age at vaccine administration (latency on same day). It was reported "office manager calling about the administration of FLUZONE HD QIV to a patient younger than 65. Caller would like to know how to proceed?" At time of reporting, 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 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1750110

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ749AA

gering
Staat
IL
Alter
88,0
Geschlecht
M
Eingang
30.09.2021
Impfdatum
28.09.2021
Beginn
28.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

Patient received high dose flu vaccine at pharmacy clinic. Following vaccination, I was entering information and identified that patient had already received High Dose Fluzone dose from physician clinic 8 days prior. Patient was notified and stated that he was unaware or did not remember that he had received the flu vaccine already. Stated that he is feeling fine and did not have any adverse side effects following flu vaccine admin.

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