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Reporte zur Charge UJ93788

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 1

VAERS 2503942

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ93788

gering
Staat
CA
Alter
14,0
Geschlecht
M
Eingang
10.11.2022
Impfdatum
31.10.2022
Beginn
31.10.2022
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 Wrong product administered

Symptomtext

14 year old male fluzone high-dose quadrivalent administered instead of Flucelvax Quadrivalent with no reported adverse event; 14 year old male fluzone high-dose quadrivalent administered instead of Flucelvax Quadrivalent with no reported adverse event; Initial information received on 01-Nov-2022 processed along with 2 live follow-ups regarding an unsolicited valid non-serious case received from a pharmacist. GMI case: 01347406 This case involves a 14-year-old male patient to whom INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] administered instead of Flucelvax 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 2022SA455035 and 2022SA456571(same reporter). On 31-Oct-2022, the 14-year-old male patient received an unknown dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot: UJ93788, expiry date: 30-Jun-2022) via intramuscular route in unknown administration site for immunization with no reported adverse event instead of Flucelvax Quadrivalent (Wrong product administered, Product administered to patient of inappropriate age) at same day latency. It was reported that "Pharmacist is checking the safety of FLUZONE HIGH-DOSE QUADRIVALENT when administered to people younger than 65. She states that she is not yet sure if the HIGH-DOSE was administered to a younger patient but wants to have the information. Pharmacist states that last night, an elderly patient came in, and they prepared a FLUZONE HIGH-DOSE vaccine for her, but then she said she thought she might have already gotten it, so they did not administer. Prepared syringe was placed back in the refrigerator. Two other patients came in later; a 45-year-old woman and a 14-year-old boy, who both received flu shots. Pharmacist then noticed that the FLUZONE HIGH-DOSE syringe was no longer in the refrigerator. She states that the intern was supposed to be giving Flucelvax Quadrivalent to the patients < 65, and at first the intern was sure that she had given that to both patients. But they can't find the HIGH-DOSE QUADRIVALENT, so the intern may have gotten the vaccines mixed up. She wanted to check the safety of the FLUZONE HIGH-DOSE QUADRIVALENT being given to younger people." Action taken: Not applicable for both suspects. At time of reporting, the outcome was Unknown for both events. 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 guidelines. 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 2502856

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ93788

gering
Staat
-
Alter
-
Geschlecht
F
Eingang
09.11.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
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 Product storage error

Symptomtext

pharmacist says that fluzone hd qiv may have been given to a 45 year old with no reported ae; a fluzone high-dose vaccine for her, but then she said she thought she might have already gotten it, so they did not administer. prepared syringe was placed back in the refrigerator with no reported ae; Initial information received on 01-Nov-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case is linked to cases 2022SA454572(CLUSTER), 2022SA455035(CLUSTER) and 2022SA455035(CLUSTER). This case involves a 45 years old female patient and pharmacist says that INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] may have been given with no reported ae(adverse event) and a fluzone high-dose vaccine for her, but then she said she thought she might have already gotten it, so they did not administer. prepared syringe was placed back in the refrigerator with no reported ae. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (strength, formulation was unknown, lot UJ93788 and expiry date was unknown) via unknown route in unknown administration site for immunization. On an unknown date the patient developed a non-serious event of pharmacist says that fluzone hd qiv may have been given to a 45 year old with no reported ae (product administered to patient of inappropriate age) (latency: same day) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. On an unknown date the patient developed a non-serious event of a fluzone high-dose vaccine for her, but then she said she thought she might have already gotten it, so they did not administer. prepared syringe was placed back in the refrigerator with no reported ae (product storage error) (latency: unknown) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV 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.; Sender's Comments: SanofiPVPortal20221103000136:

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