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Reporte zur Charge U8135AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

16Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 4 GA 3 WA 2 MI 2 PA 1 MA 1 CA 1 AZ 1 NY 1

VAERS 2687934

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

moderat
Staat
GA
Alter
81,0
Geschlecht
F
Eingang
28.09.2023
Impfdatum
28.09.2023
Beginn
28.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia Hypoaesthesia oral Paraesthesia

Symptomtext

Patient received high dose flu vaccination on 09/26/2023 at 10 AM in RD. Per patient, she went to pharmacy around 3 PM on 09/26/2023. She states that as she was shopping she started to experience numbness on the L side of her mouth. She states that she then preceded to experience L hand numbness and tingling. She states that the episode lasted less than 5 min. She states that she had never experienced this previously nor has experienced this since the first episode. She states that she has an appt with her PCP today (09/28/2023) to follow up after the episode. She states that no test or procedures have been done at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Controlled Hypertension per patient
Andere Medikamente
unknown
Allergien
none
Vorherige Impfungen
-

VAERS 2687269

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

moderat
Staat
GA
Alter
77,0
Geschlecht
F
Eingang
27.09.2023
Impfdatum
25.09.2023
Beginn
25.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dyspnoea Erythema Feeling abnormal Peripheral swelling Skin warm

Symptomtext

Patient called stating that she was at a rountine Cardiologist appointment and had told her, her symptoms and issues taking place. The Cardiologist told her to call and report her symptoms and reaction to Health Dept. Patient stated that she received her High Dose Flu Vaccine one 09/25/2023 and after receiving waited in the lobby for 20 mins and then left. Patient stated that she felt fine when she left. Then about 2 hours after vaccination she stated she started to feel bad and had a little difficulty breathing but was not concerned enough to go to Emergency Room. Patient also stated that they had sprayed bug spray in house and thought that might have been what contibribute to the breathing issues. However today 09/27/2023 her arm is redden and swollen and warm to touch. Patient was informed that this can be a normal side effect and encouraged to use cool/ warm compressed to help with the reddness and swelling. Patitnet stated that she was not concerned about the reddness or swelling that they has happened in the past when she received her Pneumonia vaccine. But due to her Cardioloist telling her to report she thought she would call and inform health department. Patient was let known that a report would be filled with VAERS.

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

VAERS 2716795

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge u8135aa

mild
Staat
PA
Alter
66,0
Geschlecht
F
Eingang
22.11.2023
Impfdatum
21.11.2023
Beginn
21.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pruritus

Symptomtext

widespread itchiness

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none listed
Allergien
none
Vorherige Impfungen
-

VAERS 2714714

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

mild
Staat
WA
Alter
76,0
Geschlecht
F
Eingang
16.11.2023
Impfdatum
20.10.2023
Beginn
21.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site swelling Injection site warmth

Symptomtext

Redness, warmth and swelling at injection site

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
Received dose of benedryl
Aktuelle Erkrankungen
-
Vorgeschichte
CVA, Depression, Hypothyroidism, pacemaker, CKD Stage III, Anxiety
Andere Medikamente
Aspirin 81 mg, levothyroxine, B-12 vitamin supplement, Paxil, Plavix, Pristiq, Rexulti, Vitamin D, acetaminophen, famotidine, restasis, Diclofenac topical gel, senna, tramadol/APAP, ibuprofen
Allergien
Atorvastatin, Nitrofurantoin, Macrobid, Penicillins, Sulfa Antibiotics
Vorherige Impfungen
-

VAERS 2708122

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

mild
Staat
MA
Alter
86,0
Geschlecht
F
Eingang
01.11.2023
Impfdatum
05.10.2023
Beginn
07.10.2023
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Conjunctivitis Crying Diarrhoea Fatigue Headache Nausea Pruritus Respiratory tract congestion Rhinorrhoea

Symptomtext

10/7/23: Extreme fatigue, chills, headaches 10/16: uncontrollable crying, congestion, nausea, diarrhea, extreme fatigue 10:19- Present: extreme fatigue, bilateral conjunctivitis, runny nose, itching all over

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none
Vorgeschichte
acquired deformity of hand (bilateral) complex regional pain syndrome, type I acute injury of kidney B-cell lymphoma (clinical) bullous pemphigoid cervical spondylosis chronic kidney disease stage 3B chronic obstructive lung disease chronic pain syndrome chronic post-COVID-19 syndrome cobalamin deficiency complex regional pain syndrome type I compression fracture of thoracic spine compression fracture of vertebral column conjunctivitis constipation COVID-19 diverticulitis dry eyes (bilateral) dyspnea edema of lower extremity ex-smoker familial hypercholesterolemia gastroesophageal reflux disease hypercholesterolemia hypertensive renal disease hypothyroidism kyphoscoliosis deformity of spine localized edema lymphoid leukemia malignant tumor of breast mass of neck monoclonal gammopathy of uncertain significance osteoporosis peripheral vascular disease personal history of primary malignant neoplasm of breast Sj?gren's syndrome ulnar deviation of hand (bilateral) underweight
Andere Medikamente
Advair HFA albuterol sulfate aspirin furosemide levothyroxine metoprolol succinate neomycin-polymyxin B-dexameth omeprazole oxycodone prednisone Tylenol Extra Strength
Allergien
amlodipine doxycycline fish derived influenza virus vaccine, specific Levaquin levofloxacin Penicillins propoxyphene tree nut
Vorherige Impfungen
-

VAERS 2699852

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

mild
Staat
OH
Alter
89,0
Geschlecht
F
Eingang
22.10.2023
Impfdatum
08.10.2023
Beginn
08.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Increased bronchial secretion Malaise Throat clearing

Symptomtext

Pt began to not feel well approximately 4 hours after administration. Patient had a lot of mucus in the chest and felt as though she had to continuously clear her throat. Patient called PCP and was given and Azithromycin to prevent infection. Patient is still having symptoms but feels fine. Patient starting flonase and will follow-up with physician if this continues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Malaise
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
NO
Vorgeschichte
HBP, THYROID INSUFFICIENCY, ALLERGIES
Andere Medikamente
GA SHOT FOR MACULAR DEGENERATION IN BOTH EYES (REC'D 9/19/2023), LISINOPRIL, LEVOTHYROXINE, BUSPIRONE, VIT D3, CALCIUM CITRATE + D, OMEGA 3 1000, MULTIVITAMIN SILVER, ALIGN, LORATADINE, FAMOTIDINE,
Allergien
cipro, formaldehyde, gold sodium thiomalate, sulfasalazine
Vorherige Impfungen
-

VAERS 2724186

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
MI
Alter
60,0
Geschlecht
M
Eingang
14.12.2023
Impfdatum
08.12.2023
Beginn
08.12.2023
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 administered to patient of inappropriate age Wrong product administered

Symptomtext

administered with a Fluzone high-dose QIV instead of a standard Fluzone QIV with no reported adverse event; administered with a Fluzone high-dose QIV instead of a standard Fluzone QIV with no reported adverse event; Initial information received on 08-Dec-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 60 years old male patient who was administered with a influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent] instead of a standard influenza quadrival A-B vaccine [Fluzone QIV] with no reported adverse event. The patient's past medical history included Ex-tobacco user. The patient's past medical treatment(s), vaccination(s) and family history were not provided. On 08-Dec-2023, a 60 years old male patient received a dose of 0.7 ml once of suspect influenza quadrival A-B high dose HV vaccine (lot: U8135AA; expiry date: 30-Jun-2024; strength: high dose) via intramuscular route in left deltoid arm instead of influenza quadrival A-B vaccine (Suspension for injection) with no reported adverse event (wrong product administered) (product administered to patient of inappropriate age) (latency: same day) for immunization. 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
Medical History/Concurrent Conditions: Ex-tobacco user
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2722272

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
MI
Alter
60,0
Geschlecht
M
Eingang
08.12.2023
Impfdatum
08.12.2023
Beginn
08.12.2023
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 Wrong product administered

Symptomtext

The patient was given a high dose flu vaccine instead of the regular Flulaval.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Hypertension, hyperlipidemia, glucose intolerance.
Andere Medikamente
Crestor, Multivitamin, Lisinopril, Motrin, Gabapentin and Vit D.
Allergien
None.
Vorherige Impfungen
-

VAERS 2718638

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
OH
Alter
83,0
Geschlecht
F
Eingang
28.11.2023
Impfdatum
19.11.2023
Beginn
19.11.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

Patient was given second dose in error, Patient also received Fluad on 9/23/23

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

VAERS 2705424

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
CA
Alter
70,0
Geschlecht
F
Eingang
29.10.2023
Impfdatum
29.10.2023
Beginn
29.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Underdose

Symptomtext

FULL DOSE WAS NOT ADMINISTERED AS SOME LEAKED OUT ON PATIENT'S ARM AND IMMUNIZER'S GLOVE.

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

VAERS 2702574

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
OH
Alter
89,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
25.10.2023
Beginn
25.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

patient already received a flu vaccine on 9/12/23 per system. This was discovered during billing after vaccine was given on 10/25/23.

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

VAERS 2702553

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
OH
Alter
96,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
25.10.2023
Beginn
25.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

Patient already received a flu vaccine on 10/16/23. This was not discovered until billing was completed (which was after the dose on 10/25/23).

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

VAERS 2699667

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135aa

gering
Staat
WA
Alter
64,0
Geschlecht
M
Eingang
20.10.2023
Impfdatum
20.10.2023
Beginn
20.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

I did a flu clinic and I thought his form said he was 69 but her was actually 64. He did not have a reaction

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

VAERS 2697921

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
AZ
Alter
69,0
Geschlecht
F
Eingang
18.10.2023
Impfdatum
16.10.2023
Beginn
17.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Eye swelling Swelling

Symptomtext

She got the vaccine on Monday and woke up Tuesday morning with some swelling, the worst of which was her eyes. It did resolve itself as the day went on, and was back to normal when I talked to her on Wednesday.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Eye swelling
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
High cholesterol, Hypertension, and Diabetes
Andere Medikamente
Unknown
Allergien
NKA
Vorherige Impfungen
-

VAERS 2690115

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
GA
Alter
30,0
Geschlecht
F
Eingang
03.10.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

patient received FLUZONE-HD QIV however they were under the age of 65 with no reported adverse event; Initial information was received on 25-Sep-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 30 years old female patient who received influenza quadrival a-b high dose hv vaccine [Fluzone HIGH-DOSE QUADRIVALENT] however they were under the age of 65 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 received a dose of 0.7 ml of suspect influenza quadrival a-b high dose hv vaccine (lot U8135AA, Frequency : Total, Expiry date, strength, formulation was unknown) via unknown route in unknown administration site for Immunization. On an unknown date the patient received fluzone-hd qiv however they were under the age of 65 with no reported adverse event (product administered to patient of inappropriate age) (latency : same day). Action taken was not applicable. At time of reporting, the outcome was Unknown for the event patient received fluzone-hd qiv however they were under the age of 65 with no reported adverse 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2687253

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge U8135AA

gering
Staat
NY
Alter
80,0
Geschlecht
F
Eingang
27.09.2023
Impfdatum
25.09.2023
Beginn
27.09.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cellulitis Lymphadenopathy

Symptomtext

Left arm cellulitis, lymph node enlargement left neck/collar bone. Pt scheduled and seen by provider. Prescribed cephalexin 500 mg every 6 hours for 7 days. IF no improvement in next 1-2 days will consider ultrasound.

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