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: 1f1005a
- Date de réception du rapport
- 2022-03-04
- Date à laquelle le formulaire est complèté
- Date de vaccination
- 2021-11-23
- Date d’apparition
- 5
- Nombre de jours (date d’apparition – date de vaccination)
- 5
- Description de l’événement indésirable
-
cervical myelitis; this is a spontaneous report received from a contactable reporter(s) (physician) from the regulatory authority web. regulatory number: it-minisal02-843014. a 38 year-old male patient received bnt162b2 (comirnaty), administration date 23nov2021 (lot number: 1f1005a) as dose 3 (booster), single for covid-19 immunisation. the patient's relevant medical history and concomitant medications were not reported. vaccination history included: comirnaty (dose 1), for covid-19 immunisation; comirnaty (dose 2), for covid-19 immunisation. the following information was reported: myelitis (hospitalization) with onset 28nov2021, outcome "recovered with sequelae", described as "cervical myelitis". the patient underwent the following laboratory tests and procedures: lumbar puncture: unknown results. actions taken (diagnostic workup, including rachycentesis, high-dose steroid therapy intravenous, neuromotor rehabilitation clinical and radiological follow-up). no follow-up attempts are possible. no further information is expected
- Données de laboratoire
-
test name: rachycentesis; result unstructured data: test result:unknown results
- Liste des symptômes
-
myelitis lumbar puncture
- 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