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Reporte zur Charge U6628AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MS 1 OK 1 MI 1 IN 1 OH 1 AZ 1

VAERS 1515465

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6628AA

mild
Staat
MS
Alter
13,0
Geschlecht
M
Eingang
30.07.2021
Impfdatum
30.07.2021
Beginn
30.07.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vomiting

Symptomtext

Client began vomiting around 2 hours after vaccine was administered. Client's parent called the Health Dept and spoke with a nurse. Denies fever, denies sickness, denies any and all other signs and symptoms at this time. Educated on visiting urgent care provider or ER as needed. Educated on side effects and adverse reactions to TDap and when to seek further medical care. Verbalized understanding.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vomiting
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1343498

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6628AA

mild
Staat
OK
Alter
19,0
Geschlecht
F
Eingang
24.05.2021
Impfdatum
07.05.2021
Beginn
07.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Nausea

Symptomtext

Donor returned to center on 5/23/2021 and reported that 2 hours after receiving the tetanus vaccine on 5/7/21 she began to feel nauseous and fatigued donor reported symptoms lasted for approximately 3 days. Donor reported that symptoms resolved on their own without medical treatment.

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

VAERS 1228484

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6628AA

mild
Staat
MI
Alter
38,0
Geschlecht
M
Eingang
19.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cough Erythema Headache Incorrect route of product administration Injection site erythema

Symptomtext

Patient had a pneumococcal and influenza vaccine placed in his left arm, 3 days ago, April 13, 2021. His initial reaction, was pain that developed hours after the injection, with subsequent erythema on left arm. The patient developed erythema around the left injection site, cough and headache. Symptoms are improving, but patient will let us know if his symptoms do not improve or worsen next week.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
Generalized Anxiety disorder, GERD, Migraine without aura, Mild episode of recurrent major depressive disorder, PTSD
Andere Medikamente
prazosin (MINIPRESS) 2 MG capsule, busPIRone (BUSPAR) 10 MG tablet, risperiDONE (RISPERDAL) 0.5 MG tablet, escitalopram (LEXAPRO) 20 MG tablet, naproxen (NAPROSYN) 500 MG tablet,
Allergien
No known Allergies
Vorherige Impfungen
-

VAERS 2322957

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6628AA

gering
Staat
IN
Alter
53,0
Geschlecht
M
Eingang
17.06.2022
Impfdatum
31.05.2022
Beginn
31.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

Pharmacist states that Adacel expired on 04Apr2022 it was accidentally given to a patient with no reported Adverse Event.; Initial information received on 31-May-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 53 years old male patient it was reported by pharmacist states that diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel] expired on 04apr2022 it was accidentally given to a patient with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included VARICELLA ZOSTER VACCINE RGE (CHO) (SHINGRIX) for Immunisation. On 31-May-2022, the patient received a dose of suspect diphtheria-2/tetanus/5 AC pertussis vaccine (lot U6628AA: expiry date 04-Apr-2022) via intramuscular route in the left deltoid for Immunization it was reported by pharmacist adacel expired on 04apr2022 it was accidentally given to a patient with no reported adverse event. (expired product administered). It was asked by reporter that "if the patient needs to be revaccinated and if so, when" Action taken : not applicable. At time of reporting, the outcome was Unknown for the event pharmacist states that adacel expired on 04apr2022 it was accidentally given to a patient 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 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1692826

SANOFI PASTEUR · DTAP (DAPTACEL) · Charge U6628AA

gering
Staat
OH
Alter
12,0
Geschlecht
M
Eingang
11.09.2021
Impfdatum
21.07.2021
Beginn
21.07.2021
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 Wrong product administered

Symptomtext

Patient accidentally received DAPTACEL instead of ADACEL in the office; Initial information was received on 01-Sep-2021 regarding an unsolicited valid non-serious case received from physician and other health care professional via Medical information (under reference number - 00750742). This case involves a 12-year-old male patient who was accidentally vaccinated with DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [DAPTACEL] instead of the DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS VACCINE [ADACEL] with no adverse event (Wrong product administered). The patient's past vaccination(s) included DTAP VACCINE with Patient has already received 4 DTAP vaccinations. The patient's past medical treatments, concomitant therapy and family history were not provided. Concomitant medications included MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA) for prophylactic vaccination. On 21-Jul-2021, the patient received a 0.5ml dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [DAPTACEL] (lot number U6628AA and expiry date 04-Apr-2022) via intramuscular route in the deltoid NOS for prophylactic vaccination (Wrong product administered). There were no laboratory data/results available. It was case of an actual medication error due to Wrong vaccine administered (latency was on same day) At the time of report, no adverse event was reported. 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
MENACTRA
Allergien
-
Vorherige Impfungen
-

VAERS 1316277

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6628AA

gering
Staat
AZ
Alter
-
Geschlecht
U
Eingang
14.05.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration No adverse event

Symptomtext

A patient received Adacel vaccine 2 weeks apart from one another, no AE; Initial information regarding an unsolicited valid non-serious case was received from other healthcare professional via Medical Information (MI) (Reference number- 00581018) and transmitted to Sanofi on 28-Apr-2021. This case involves a patient (unknown demographics) who received two doses of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] (lot U6628AA, expiry date: 04-Apr-2022 and lot U6767AA and expiry date: 31-Jul-2022) via an unknown route in an unknown administration site for prophylactic vaccination 2 weeks apart from one another on an unknown date (inappropriate schedule of product administration). The patient's medical history, past medical treatment(s), vaccination(s), concomitant medications and family history were not provided. This was a case of actual medication error due to drug dose administration interval too short (latency same day). At the time of reporting, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holders compliance with the requirements set out in 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
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-