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Reporte zur Charge U6638AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 1 MO 1 OR 1 NY 1

VAERS 1433480

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6638AA

mild
Staat
FL
Alter
42,0
Geschlecht
F
Eingang
29.06.2021
Impfdatum
22.06.2021
Beginn
22.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Discomfort Immediate post-injection reaction Pain Shoulder injury related to vaccine administration Sleep disorder

Symptomtext

TDAP vaccine was administered by RN into patient's left deltoid on 6/22. Patient immediately felt discomfort and stated that her arm felt "different" than the discomfort she felt after the COVID vaccination in the same arm 1 month prior. Patient stated that she had issues sleeping and pain with moving her shoulder that increased over the next 3 days. The discomfort then continued, but did not worsen. She was evaluated by a physician on 6/29/21 and diagnosed with SIRVA (shoulder injury resulting from vaccine administration). She was given a course of NSAIDs and asked to follow up in 1 week. She declined steroid injections or any further imaging for now.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
no
Vorgeschichte
migraine with aura
Andere Medikamente
sertraline
Allergien
mahi mahi
Vorherige Impfungen
-

VAERS 961618

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6638AA

mild
Staat
MO
Alter
31,0
Geschlecht
F
Eingang
21.01.2021
Impfdatum
20.01.2021
Beginn
20.01.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Animal bite Inappropriate schedule of product administration Nausea Vomiting

Symptomtext

Tdap was administered within 2 weeks of the client receiving the COVID-19 vaccine (1/15/2021). Tdap was given to client after sustaining an animal bite. Client reported experiencing nausea and vomiting on the afternoon of 1/20/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nausea
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
Recent cat bite to hand - on antibiotics
Vorgeschichte
Asthma
Andere Medikamente
Unknown
Allergien
Vancomycin
Vorherige Impfungen
-

VAERS 928887

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6638AA

mild
Staat
OR
Alter
22,0
Geschlecht
F
Eingang
08.01.2021
Impfdatum
02.01.2021
Beginn
04.01.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Administration site pain Administration site swelling Administration site warmth Haemorrhage Injection site erythema Injection site nodule

Symptomtext

PT REPORTED THAT SHE HAD BLEEDING FOR 6 HOURS AFTER ADMINISTRATION, ON MONDAY THE AREA WAS SWOLLEN, RED, WARM AND PAINFUL. I INSTRUCTED PATIENT THAT SHE COULD BE HAVING AN ALLERGIC REACTION OR SIGNS OF INFECTION. I TOLD HER THAT IF SHE DIDN'T WANT TO GOT TO THE DOCTOR IMMEDIATELY, SHE COULD TRY A COLD COMPRESS AND BENADRYL EVERY 6 HOURS, BUT IF SYMPTOMS GOT WORSE SHE WAS TO SEEK MEDICAL ATTENTION IMMEDIATELY. SHE STATED SHE WOULD NOTIFY ME OF ANY CHANGES. CALLED PATIENT ON 1/8 TO FOLLOW-UP AND SHE STATED THAT THE BENADRYL AND COLD COMPRESS WAS EFFECTIVE. THERE WAS STILL A KNOT AT THE INJECTION SITE BUT ALL OTHER SYMPTOMS SUBSIDED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Administration site pain
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2371888

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6638AA

gering
Staat
NY
Alter
44,0
Geschlecht
M
Eingang
16.07.2022
Impfdatum
05.05.2022
Beginn
05.05.2022
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 Medication error No adverse event

Symptomtext

administered an expired ADACEL to a patient with no reported adverse event; Initial information received on 08-Jul-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 44 years old male patient was administered an expired diphtheria-2/tetanus/5 AC pertussis vaccine [Adacel] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 05-May-2022, the patient was administered an expired 0.5 ml dose of suspect diphtheria-2/tetanus/5 AC pertussis vaccine, suspension for injection, (strength unknown) (lot U6638AA and expiry date: 12-Apr-2022) via intramuscular route in the left arm for Immunization with no reported adverse event (expired product administered). 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-