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VAERS Report 2157165

Case Report Section

Détails du rapport Vaer

Âge: N/A

Genre: Male

Région : Outside US

Patient décédé?
Non
Renseignements sur les vaccins

Nom: COVID19 (COVID19 (PFIZER-BIONTECH))

Type : Coronavirus 2019 vaccine

Fabricant: PFIZER

Lot: unknown


Date de réception du rapport
2022-03-04
Date à laquelle le formulaire est complèté
Date de vaccination
2021-12-22
Date d’apparition
0
Nombre de jours (date d’apparition – date de vaccination)
0
Description de l’événement indésirable

pneumonia; severe pericarditis; feel unwell; this is a spontaneous report received from a contactable reporter(s) (physician) from the medicines agency () -web. regulatory number: ie-hpra-2022-093016 (hpra). other case identifier(s): ie-hpra-cvarr2022021225780 (hpra). a 41 year-old male patient received bnt162b2 (comirnaty), administration date 22dec2021 (batch/lot number: unknown) as dose 3 (booster), single for covid-19 immunisation. the patient had no relevant medical history. there were no concomitant medications. vaccination history included: comirnaty (dose 1, single), administration date: jun2021, for covid-19 immunisation; comirnaty (dose 2, single, comirnaty double vaccine in jun2021), administration date: jun2021, for covid-19 immunisation. the following information was reported: pneumonia (hospitalization, medically significant) with onset 15jan2022, outcome "unknown", described as "pneumonia"; pericarditis (hospitalization, medically significant) with onset 15jan2022, outcome "unknown", described as "severe pericarditis"; malaise (hospitalization) with onset dec2021, outcome "unknown", described as "feel unwell". the patient was hospitalized for pneumonia, pericarditis, malaise (start date: 26jan2022, hospitalization duration: 13 day(s)). the events "pneumonia", "severe pericarditis" and "feel unwell" were evaluated at the emergency room visit. therapeutic measures were taken as a result of pneumonia, pericarditis, malaise. clinical course: on 22/dec/2021, the patient was vaccinated with the booster dose of comirnaty (batch details: unknown). in dec/2021, 5-7 days post booster, the patient began to feel unwell. the patient was treated with antibiotics and steroids, however, the symptoms continued to get worse. on 16/jan/2022, the patient attended a&e, where they were told they had pneumonia and was discharged with antibiotics. the symptoms got worse, and the patient again attended a&e on 26/jan/2022, where they were admitted as an inpatient for 13 days. the patient reported that pneumonia got worse, and they were told they had severe pericarditis. at the time of reporting, the outcome was unknown. no follow-up attempts are possible; information about lot/batch number cannot be obtained. no further information is expected.; sender's comments: linked report(s) : ie-hpra-2022-093018

Données de laboratoire
na
Liste des symptômes
malaise pericarditis pneumonia
Patient décédé?
Non
Date de décès
N/A
Anomalie congénitale
false
Vaccin administré par :
Other
Vaccin acheté par :
Inconnu
Visite d’un patient à l’urgence?
Non
Patient hospitalisé?
Oui
Séjour à l’hôpital
Non
Nombre de jours à l’hôpital
Non spécifié
Invalidité permanente?
Non
Allergies:
na
Maladie actuelle
na