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Reporte zur Charge UJ900AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

21Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 8 PA 4 NJ 3 SC 1 AZ 1 MA 1 IL 1 MO 1 LA 1

VAERS 2454811

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900aa

schwer
Staat
SC
Alter
86,0
Geschlecht
F
Eingang
22.09.2022
Impfdatum
22.09.2022
Beginn
22.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Syncope

Symptomtext

We received a call from pharmacy at 3:03pm alerting us that patient fainted at their store and required transportation to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
HCTZ 25 mg, escitalopram 20 mg, Estratest HS, Famciclovir, omeprazole
Allergien
NKA
Vorherige Impfungen
-

VAERS 2479856

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

moderat
Staat
AZ
Alter
76,0
Geschlecht
M
Eingang
17.10.2022
Impfdatum
29.09.2022
Beginn
29.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal discomfort Chest X-ray Chills Electrocardiogram Fatigue Immobile Mobility decreased Pyrexia SARS-CoV-2 test Vomiting

Symptomtext

have a lingering upset stomach; having a little difficult with mobility,symptoms continued to get worse, was experiencing a complete loss of mobility; fever; vomiting; tiredness; condition aggravated; began to experience chills; Initial information received on 10-Oct-2022 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves a 76 years old male patient who began to experience chills, have a lingering upset stomach, having a little difficult with mobility,symptoms continued to get worse, was experiencing a complete loss of mobility, fever, vomiting and tiredness after receiving vaccine Influenza Quadrival A-B High Dose HV Vaccine [Fluzone High-Dose Quadrivalent]. The patient's past medical history, vaccination(s) and family history were not provided. On 29-Sep-2022 around 10:00 am, the patient received a 0.7 ml (Milliliter) dose of suspect Influenza Quadrival A-B High Dose HV Vaccine (lot- UJ900AA, expiry date- unknown) via intramuscular route in the deltoid nos for immunization. On 29-Sep-2022 the patient began to experience chills (chills), having a little difficult with mobility, was experiencing a complete loss of mobility (mobility decreased) with condition aggravated, fever (pyrexia), vomiting, tiredness (Latency- same day) following the administration of Influenza Quadrival A-B High Dose HV Vaccine. On an unknown date the patient have a lingering upset stomach (abdominal discomfort) (unknown latency) following the administration of Influenza Quadrival A-B High Dose HV Vaccine. It was reported that "the patient was transported via ambulance to the emergency room (ER) of where he was seen and treated by. Patient stated that he was there for around 5 hours, and they "did every test under the sun," including a Covid test, an electrocardiogram, a chest X-ray. They gave him fluids, either glucose or saline, he was not sure which, and they monitored his blood pressure. He was told that if he regained his mobility, they would sign him out, but if he did not, they were going to admit him to the hospital. Around 5 am he had improved and regained his mobility, so he was released from the ER without being admitted to the hospital". Action taken: not applicable. The corrective treatment was unknown for other events and the patient was treated with PARACETAMOL (TYLENOL) for Fever, IBUPROFEN (ADVIL [IBUPROFEN]) for Fever and FAMOTIDINE (PEPCID [FAMOTIDINE]) for Upset stomach. At time of reporting, the outcome was Recovering / Resolving for the events and was Recovered / Resolved on 30-Sep-2022 for the event Mobility decreased.

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

VAERS 2475558

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj900aa

moderat
Staat
MA
Alter
90,0
Geschlecht
F
Eingang
11.10.2022
Impfdatum
05.10.2022
Beginn
06.10.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Housebound Mobility decreased

Symptomtext

the 91yo frail homebound individual received the Moderna bivalent Covid booster (left arm) and High Dose flu vaccine (right arm) at the same time. Approximately 20hrs after the injections she reported not being able to use both arms and both legs. She was monitored by her concerned family members at home during this time. After two days' time, she reports that she was able to again use her arms and legs. She reports recovering completely.

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

VAERS 2467787

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

moderat
Staat
NJ
Alter
69,0
Geschlecht
F
Eingang
03.10.2022
Impfdatum
20.09.2022
Beginn
21.09.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Asthenia Mobility decreased Pain Pyrexia

Symptomtext

Had to go to hospital. Couldn?t get out of bed. Couldn?t move my arms. Very weak. High temperature 102.2. My partner called 911

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None at time of Fluzone High Dose Vaccine Lot UJ900AA Expiration 6/30/2023 Dosage 0.7ml intramuscular Had to go to hospital fever 102.2 couldn?t move my body very very weak and achy
Andere Medikamente
Levothyroxine 88 mcg, Olmesartan 40mg, Ezetimibe 10mg, Tamsulosin 0.4 mg, gabapentin 100mg, Gabapentin cap 400 mg, Pantoprazole 40mg, escitalopram 10 mg Vitam c 1000, coq10 200mg D3 2000
Allergien
None known just grass pollen weeds
Vorherige Impfungen
Moderna

VAERS 2630621

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

mild
Staat
IL
Alter
66,0
Geschlecht
F
Eingang
11.05.2023
Impfdatum
25.10.2022
Beginn
01.10.2022
Tage bis Beginn
-
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Oropharyngeal pain Pain in jaw

Symptomtext

Patient reported that shortly after receiving the vaccine, she encountered a sore throat and jaw pain. The jaw pain was described as "like biting on a needle." Patient reported that symptoms did resolve after a day or two, and she has had no problems since.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Oropharyngeal pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Levothyroxine 50 mcg Triamterene/HCTZ 37.5 mg/25 mg Bupropion XL 300 mg Atorvastatin 10 mg
Allergien
ACE Inhibitors NSAIDs
Vorherige Impfungen
-

VAERS 2509319

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

mild
Staat
PA
Alter
70,0
Geschlecht
F
Eingang
16.11.2022
Impfdatum
14.11.2022
Beginn
14.11.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Peripheral swelling Pruritus Skin warm

Symptomtext

Patient received flu injection yesterday at office. Noticed while she was driving from office that her arm started to swell, become warm, developed itching. She pulled over to the side of the road. Stated that the swelling came to the size of a golf ball. She was able then to drive home. She took Benadryl when she got home which brought the swelling down and relieved some of the itch. She had no respiratory distress or anaphylactic symptoms. Today she slept until 11 am. She has full use of her arm. She spoke with our nurse today who advised her to monitor symptoms and apply ice if needed to the swelling. Physician was advised for further recommendations.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
URI Oct 18th, 2022
Vorgeschichte
Allergic rhinitis Gastrointestinal and Abdominal Chronic hepatitis C without hepatic coma Heartburn Gastroesophageal reflux disease without esophagitis Genitourinary and Reproductive Hot flashes due to menopause Mental Health Anxiety state Moderate major depression Severe anxiety Musculoskelatal and Injuries Wrist pain, chronic, left Arthritis of left shoulder region DJD of right shoulder Chronic pain of both wrists Chronic pain of left knee Fibromyalgia Tendonitis of radial styloid Neuro Carpal tunnel syndrome, bilateral Cognitive impairment Pulmonary and Pneumonias Chronic bronchitis Moderate persistent asthma without complication Skin Thin skin Symptoms and Signs Finger numbness Numbness
Andere Medikamente
albuterol 108 (90 BASE) mcg/act inhaler Angeliq 0.5-1 MG Oral Tablet (Drospirenone-Estradiol) azelastine 0.1 % nasal spray azelastine 0.1 % nasal spray Azelastine HCl 0.05 % Ophthalmic Solution benzonatate 100 MG capsule fluticasone 50 MCG/
Allergien
bupoprion, tramadol, levonorgest-estradiol
Vorherige Impfungen
-

VAERS 2465374

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) · Charge UJ900AA

mild
Staat
TX
Alter
67,0
Geschlecht
F
Eingang
25.09.2022
Impfdatum
17.09.2022
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Flushing Injection site bruising Injection site nodule Injection site swelling Peripheral swelling Pruritus

Symptomtext

Pt develop swelling, knotted area and bruising at site of injection. Swelling and redness and itching spreaded to lower part of the arms worse on the right. Occur on same day of vaccination on 9/17/22 still red/flushed and itchy to today 9/25/22

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site bruising
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
hypothyroidism
Vorgeschichte
hypothyroidism
Andere Medikamente
-
Allergien
Bactrim, Soma Naprosyn, Latexm Penicillin
Vorherige Impfungen
-

VAERS 2549064

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
PA
Alter
68,0
Geschlecht
F
Eingang
03.01.2023
Impfdatum
19.10.2022
Beginn
19.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient given Moderna monovalent booster instead of Moderna bivalent booster. Patient notified.

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

VAERS 2549049

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
PA
Alter
89,0
Geschlecht
F
Eingang
03.01.2023
Impfdatum
18.10.2022
Beginn
18.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient given Moderna monovalent booster instead of Moderna bivalent booster. Patient notified.

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

VAERS 2549018

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
PA
Alter
73,0
Geschlecht
M
Eingang
03.01.2023
Impfdatum
12.10.2022
Beginn
12.10.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect product formulation administered No adverse event

Symptomtext

No adverse reaction. Patient given Moderna monovalent booster instead of Moderna bivalent booster. Patient notified.

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

VAERS 2543220

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
NJ
Alter
67,0
Geschlecht
F
Eingang
26.12.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered No adverse event

Symptomtext

received 0.5 mL but should be 0.7 mL, with no reported adverse event; Initial information received on 13-Oct-2022 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case is linked to case 2022SA426941(CLUSTER). This case involves a 67 years old female patient who received 0.5 ml but should be 0.7 ml, with no reported adverse event after receiving vaccine INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 11-Oct-2022, the patient received 0.5 ml but should be 0.7 ml of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE with no reported adverse event (incorrect dose administered) (lot UJ900AA and expiry date: 30-Jun-2023) via unknown route in unknown administration site for Prophylactic vaccination. 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. Based on information previously received, the following information has been amended by upgraded the case from non-case to valid Agency with no AE with addition of event "wrong dose administered".

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

VAERS 2452139

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj900aa

gering
Staat
MO
Alter
88,0
Geschlecht
F
Eingang
15.11.2022
Impfdatum
19.09.2022
Beginn
19.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event Product dispensing error Product preparation error Product storage error

Symptomtext

No additional adverse events reported.; Pharmacist reports administration of expired PNEUMOVAX 23 syringe.; vaccine expiration was not checked prior to administrating; vaccine expiration was not checked prior to administrating; vaccine expiration was not checked prior to administrating; This spontaneous report was received from a pharmacist and refers to a 88-year-old female patient. The patient's concomitant medications, pertinent medical history, concurrent conditions, drug reactions or allergies were not reported. On 19-SEP-2022, the patient was vaccinated with expired dose of pneumococcal vaccine, polyvalent (23-valent) (PNEUMOVAX23) injection, at a dose of 0.5 milliliters (ml), lot #T031820, expiration date: 10-MAY-2022 (vaccination schedule, and route of administration were not provided) for prophylaxis on left deltoid site (expired product administered); other suspect vaccine included influenza vaccine inact split 4v (FLUZONE QUADRIVALENT), lot # VJ900AA, expiration date: 30-JUN-2023 administrated on left deltoid (strength, formulation, dose, route of administration, and indication were not provided). Additionally, the vaccine provider mentioned that the vaccine expiration date was not checked prior to administrating (product storage error) (product dispensing error) (product preparation error). No additional adverse events were reported.

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

VAERS 2503234

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
54,0
Geschlecht
M
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

Patient is not 65 at time of shot.

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

VAERS 2503229

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
58,0
Geschlecht
F
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
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

Patient is not 65 at time of shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2503225

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
62,0
Geschlecht
F
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
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

Patient was not 65 at time of shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2503219

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
63,0
Geschlecht
M
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
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

Patient was not 65 at time of shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2503214

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
60,0
Geschlecht
M
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

Patient was not 65 at time of shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2503206

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
54,0
Geschlecht
F
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age

Symptomtext

Patient was not 65 at time of shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2503202

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
TX
Alter
53,0
Geschlecht
F
Eingang
09.11.2022
Impfdatum
27.09.2022
Beginn
27.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

Patient was not 65 at time of shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2486155

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
NJ
Alter
71,0
Geschlecht
M
Eingang
22.10.2022
Impfdatum
11.10.2022
Beginn
11.10.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered Medication error No adverse event

Symptomtext

sheet of paper it stated received 0.5 mL but should be 0.7 mL with no reported adverse event; Initial information received on 13-Oct-2022 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves a 71-year-old male patient who reported sheet of paper stated received 0.5 ml but should be 0.7 ml of vaccine INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [Fluzone High-Dose Quadrivalent] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. This case is linked to cases 2022SA425178, 2022SA424555. On 11-Oct-2022, the patient received a dose of suspect Fluzone High-Dose Quadrivalent vaccine received dose 0.5 ml instead should be 0.7ml (lot: UJ900AA, expiry date: 30-Jun-2023) via intramuscular route in unknown administration site for immunization with no reported adverse event (incorrect dose administered) same day latency. Patient stated that the prefilled syringes appeared orange, when the consumer asked about the color, the pharmacist stated that it was just the needle cover on the syringes. Consumer asked if they should receive another influenza vaccine this year. The consumer states that he would like to be contacted regarding this event. When the consumer asked the pharmacist about the volume being incorrect the pharmacist replied, I made an error. Action taken: Not applicable. At time of reporting, the outcome was Unknown for the 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
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2462861

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ900AA

gering
Staat
LA
Alter
73,0
Geschlecht
F
Eingang
28.09.2022
Impfdatum
19.09.2022
Beginn
19.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Syringe issue Underdose

Symptomtext

patient not receiving the full dose of FLUZONE HIGH DOSE QIV due to the vaccine leaking out with no reported adverse event; Initial information received on 19-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 73 years old female patient who did not received the full dose of influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent] due to the vaccine leaking out with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 19-Sep-2022, the patient received 0.5 ml dose of suspect influenza quadrival A-B high dose HV vaccine (strength and formulation not reported) (lot UJ900AA; Expiry Date 30-Jun-2023) via intramuscular route in Right deltoid administration site for prophylactic vaccination. On 19-Sep-2022 the patient did not received the full dose of influenza quadrival A-B high dose HV vaccine due to the vaccine leaking out with no reported adverse event (incorrect dose administered). It was stated that she attached the needle to the pre-filled syringe and when she went to immunize the patient the vaccine started leaking out of the prefilled syringe and she does not know how much of the vaccine actually went into the patient. It was asked if patient needs to be revaccinated or if she can give the rest of the vaccine left in the pre-filled syringe. Patient was still in the office and was able to get a full dose of the vaccine and she doesn't see any damage to the syringe and states the needle was attached properly, the syringe itself was leaking out the vaccine. 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
-