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Reporte zur Charge LU7189AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 2

VAERS 2614103

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge LU7189AA

gering
Staat
OH
Alter
23,0
Geschlecht
F
Eingang
12.04.2023
Impfdatum
22.02.2023
Beginn
22.02.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Poor quality product administered Product storage error

Symptomtext

TENIVAC had an excursion at temperature -1.07C for 2 days and 13 hours with no adverse event; TENIVAC administered after an excursion with no adverse event; Initial information received on 07-Apr-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case is linked to case 2023SA111504. This case involves a 23 years old female patient to whom diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult [Tenivac] was administered after an excursion at temperature -1.07c for 2 days and 13 hours with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. It was reported that on an unknown date the tenivac had an excursion at temperature -1.07c for 2 days and 13 hours with no adverse event (product storage error) (unknown latency). The refrigerator door was left open and excursion occurred due to a human error. On 22-Feb-2023, the patient was administered unknown dose of suspect diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult, suspension for injection, (lot LU7189AA; strength and expiry date not reported) via unknown route in unknown administration site for Immunization after an excursion with no adverse event (poor quality product administered) (latency; on same day). 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2614102

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge LU7189AA

gering
Staat
OH
Alter
40,0
Geschlecht
M
Eingang
12.04.2023
Impfdatum
09.02.2023
Beginn
09.02.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Poor quality product administered Product storage error

Symptomtext

TENIVAC had an excursion at temperature -1.07C for 2 days and 13 hours with no adverse event; TENIVAC administered after an excursion with no adverse event.; Initial information received on 07-Apr-2023 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case is linked to case 2023SA111249. This case involves a 40 years old male patient to whom diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult [Tenivac] was administered after an excursion at temperature -1.07c for 2 days and 13 hours with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. It was reported that on an unknown date the tenivac had an excursion at temperature -1.07c for 2 days and 13 hours with no adverse event (product storage error) (unknown latency). The refrigerator door was left open and excursion occurred due to a human error. On 09-Feb-2023, the patient was administered unknown dose of suspect diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult, suspension for injection, (lot LU7189AA; strength and expiry date not reported) via unknown route in unknown administration site for Immunization after an excursion with no adverse event (poor quality product administered) (latency; on same day). 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
-