VAERS Reports 3SN5B

VAERS 2640684

GLAXOSMITHKLINE BIOLOGICALS · TDAP (BOOSTRIX) · Charge 3SN5B

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 22.01.2021
Impfdatum: -
Beginn: 22.01.2020
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chills Tremor

Symptomtext

chills and shaking Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1188617

GLAXOSMITHKLINE BIOLOGICALS · TDAP (BOOSTRIX) · Charge 3SN5B

gering

Staat: KY
Alter: 11,0
Geschlecht: M
Eingang: 10.04.2021
Impfdatum: 07.12.2020
Beginn: 07.12.2020
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

product dispensing error; product administration error; Expired dose of Boostrix; This case was reported by a nurse via call center representative and described the occurrence of expired vaccine used in a 11-year-old male patient who received DTPa (Reduced antigen) (Boostrix) (batch number 3SN5B, expiry date 4th December 2020) for prophylaxis. Concurrent medical conditions included asthma. On 7th December 2020, the patient received Boostrix. On 7th December 2020, unknown after receiving Boostrix, the patient experienced expired vaccine used. On an unknown date, the patient experienced product dispensing error and product administration error. On an unknown date, the outcome of the expired vaccine used, product dispensing error and product administration error were unknown. Follow up information received from a nurse on 2nd April 2021: The patient's demographic details were updated. The patient had current condition of asthma and had NKA (No known Allergies). The patient received Boostrix that expired 3 days prior to the administration of vaccine. As per reporter, error occurred in dispensing and administration, which led to product dispensing error and product administration error. The reporter was unsure why error occurred. There were no adverse effects from this event. As per medical director's recommendations, the patient's parent was advised to consult physician if any injury due to unknown efficacy of the expiration date. The VAERS details updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -