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VAERS Report 2156569

Case Report Section

Détails du rapport Vaer

Âge: N/A

Genre: Female

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
2022-02-04
Date d’apparition
5
Nombre de jours (date d’apparition – date de vaccination)
5
Description de l’événement indésirable

intermenstrual bleeding; this is a spontaneous report received from a contactable reporter (consumer or other non hcp) from the ra. other case identifier(s): gb-mhra-vac-202202111921080750-0iwcf gb-mhra-adr 26595199. a 38 year-old female patient (not pregnant) received bnt162b2 (comirnaty), administration date 04feb2022 (batch/lot number: unknown) as dose number unknown, single for covid-19 immunisation. the patient's relevant medical history and concomitant medications were not reported. the patient was not pregnant and was not breastfeeding at the time of this report. the last menstrual period was reported as 24jan2022. the following information was reported: intermenstrual bleeding (medically significant) with onset 09feb2022, outcome "not recovered", described as "intermenstrual bleeding". no follow-up attempts are possible; information about lot/batch number cannot be obtained. no further information is expected

Données de laboratoire
na
Liste des symptômes
intermenstrual bleeding
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?
Non
Séjour à l’hôpital
Non
Nombre de jours à l’hôpital
Non spécifié
Invalidité permanente?
Non
Allergies:
na
Maladie actuelle
na