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VAERS Report 2095517

Case Report Section

Détails du rapport Vaer

Âge: 72 ans

Genre: Male

Région : Massachusetts

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
2022-02-08
Date à laquelle le formulaire est complèté
Date de vaccination
2022-01-06
Date d’apparition
1
Nombre de jours (date d’apparition – date de vaccination)
1
Description de l’événement indésirable

the patient received his booster of the pfizer covid vaccine on 1/6. beginning the next morning he noted swelling of his arms. he presented to the emergency room on 1/13, and there was concern for compartment syndrome of his arms initially. he underwent a multidisciplinary evaluation and was ultimately found to have bleeding from a new factor viii deficiency. he required icu care and emergent transfusion of factor viii concentrate, as well as pulse dose steroids and cyclophosphamide,. he also developed mediastinal hemorrhage at one point. he had a prolonged hospital course with multiple issues. the hematology consult team investigated for other etiologies and found none so suspected the vaccine to have been the cause

Données de laboratoire
factor viii level 1/14 : <1 factor viii inhibitor 1/20: 13.6
Liste des symptômes
factor viii deficiency anti factor viii antibody positive transfusion haemorrhage peripheral swelling intensive care
Patient décédé?
Non
Date de décès
N/A
Anomalie congénitale
false
Vaccin administré par :
Private
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:
atorvastatin, hydralazine, penicillin (not onfirmed)
Maladie actuelle
na