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Reporte zur Charge U71E9AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

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

VAERS 2322999

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U71E9AA

gering
Staat
NJ
Alter
17,0
Geschlecht
M
Eingang
17.06.2022
Impfdatum
13.06.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Wrong product administered

Symptomtext

administered Tenivac instead of Boostrix with no reported adverse event; Initial information received on 14-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 17 years old male patient who was administered Tenivac instead of Boostrix with no reported adverse event , (suspect vaccine: DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT [TENIVAC]). The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included VARICELLA ZOSTER VACCINE (VARICELLA VACCINE); MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA); HPV VACCINE (HPV VACCINE); and HEPATITIS A VACCINE (HEPATITIS A VACCINE). On 13-Jun-2022, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT, once, ( lot: U71E9AA ; Expiry date: 30-Sep-2023) via intramuscular route in the left deltoid for immunization. The reported stated that they administered Tenivac instead of Boostrix to the patient with no reported adverse event (wrong product administered) (onset: 13-Jun-2022 and latency: 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.; Sender's Comments: 01145385:

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

VAERS 2322998

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U71E9AA

gering
Staat
NJ
Alter
12,0
Geschlecht
M
Eingang
17.06.2022
Impfdatum
13.06.2022
Beginn
13.06.2022
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 Wrong product administered

Symptomtext

administered Tenivac instead of Boostrix with no reported adverse event; Initial information received on 14-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 12 years old male patient who was administered Tenivac instead of Boostrix with no reported adverse event , (suspect vaccine: DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT [TENIVAC]) . Concomitant medications included VARICELLA ZOSTER VACCINE (VARICELLA VACCINE) for Prophylactic vaccination; MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA) for Prophylactic vaccination; HPV VACCINE (HPV VACCINE) for Prophylactic vaccination; HEPATITIS A VACCINE (HEPA [HEPATITIS A VACCINE]) for Prophylactic vaccination; and POLIO VACCINE (POLIO) for Prophylactic vaccination. On 13-Jun-2022, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT, once, ( lot: U71E9AA ; Expiry date: 30-Sep-2023) via intramuscular route in the left deltoid for immunization. The reported stated that they administered Tenivac instead of Boostrix to the patient with no reported adverse event (wrong product administered) (onset and latency: unknown) 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: 01145424:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
VARICELLA VACCINE; MENACTRA; HPV VACCINE; HEPA [HEPATITIS A VACCINE]; POLIO
Allergien
-
Vorherige Impfungen
-