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Reporte zur Charge U6807BB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 2 NY 1 GA 1 CA 1 AZ 1

VAERS 1303451

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6807BB

schwer
Staat
OH
Alter
14,0
Geschlecht
F
Eingang
10.05.2021
Impfdatum
09.04.2021
Beginn
09.04.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness

Symptomtext

After completion of vaccinations patient passed out momentarily. Mom had patient supported and the RN grabbed the doctor. We laid patient down. Provided crackers and water. Patient began to improve. Patient was able to sit up in the chair after 2-3 minutes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Loratadine 10mg prn
Allergien
soap - rash
Vorherige Impfungen
dizzy after previous vaccine, but mother not sure which

VAERS 1506257

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6807BB

mild
Staat
NY
Alter
60,0
Geschlecht
F
Eingang
27.07.2021
Impfdatum
09.07.2021
Beginn
09.07.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity

Symptomtext

sore arm still 2 weeks after vaccine administered

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
unknown
Aktuelle Erkrankungen
none known
Vorgeschichte
none known
Andere Medikamente
unknown
Allergien
none listed
Vorherige Impfungen
-

VAERS 1185435

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6807BB

mild
Staat
GA
Alter
11,0
Geschlecht
F
Eingang
09.04.2021
Impfdatum
06.04.2021
Beginn
07.04.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site pruritus Injection site swelling

Symptomtext

redness, swelling and itching at site of immunization. on left arm started in the evening on the day of vaccination. on right arm started the following day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
previously unvaccinated
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1118153

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6807BB

mild
Staat
CA
Alter
8,0
Geschlecht
F
Eingang
20.03.2021
Impfdatum
18.03.2021
Beginn
20.03.2021
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site reaction

Symptomtext

localized reaction on the left arm at site of injection.

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

VAERS 2455742

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6807BB

gering
Staat
OH
Alter
14,0
Geschlecht
M
Eingang
23.09.2022
Impfdatum
15.09.2022
Beginn
15.09.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

medical assistant says she gave an expired adacel with no reported adverse event; Initial information received on 15-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 14 years old male patient who reported medical assistant says she gave an expired adacel with no reported adverse event while receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included POLIO VACCINE INACT 3V (VERO) (IPOL [POLIO VACCINE INACT 3V (VERO)]) for Prophylactic vaccination; HEPATITIS A VACCINE (HEPATITIS A) for Prophylactic vaccination; HEPATITIS B VACCINE (HEPATITIS B VACCIN) for Prophylactic vaccination; and HPV VACCINE (HPV VACCINE) for Prophylactic vaccination. On 15-Sep-2022, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE once (lot U6807BB; expiry date: 10-sep-2022) via unknown route in the right arm for prophylactic vaccination. On 15-SEP-2022 the patient developed a non-serious event medical assistant says she gave an expired adacel with no reported adverse event (expired product administered) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event expired product administered. 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
IPOL [POLIO VACCINE INACT 3V (VERO)]; HEPATITIS A; HEPATITIS B VACCIN; HPV VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 1793488

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6807BB

gering
Staat
AZ
Alter
-
Geschlecht
F
Eingang
16.10.2021
Impfdatum
02.04.2021
Beginn
02.04.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

a 71-year-old female was given Adacel as a tetanus booster that was out of the age range, with no reported adverse event; Initial information was received on 11-Oct-2021 regarding an unsolicited valid non-serious case received from a nurse via consumer via physician (under Medical Information (MI) Inquiry Number: 00807107). This case involves a 71- years old female patient who was administered with DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] as a tetanus booster with no reported adverse event (product administered to patient of inappropriate age). The patient's medical history, past medical treatments, vaccinations and family history were not provided. On 02-Apr-2021, the patient received a 0.5 ml booster dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot number: U6807BB and expiry date: 10-Sep-2022 via intramuscular route in the left deltoid for prophylactic vaccination. It was a case of actual medication error due to inappropriate age at vaccine administration (latency: same day). At the time of reporting, no adverse event 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
-
Allergien
-
Vorherige Impfungen
-