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VAERS Report 2156605

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


Nom: COVID19 (COVID19 (UNKNOWN))

Type : Coronavirus 2019 vaccine

Fabricant: UNKNOWN

Lot: unknown


Date de réception du rapport
2022-03-04
Date à laquelle le formulaire est complèté
Date de vaccination
2021-12-04
Date d’apparition
28
Nombre de jours (date d’apparition – date de vaccination)
28
Description de l’événement indésirable

post menopausal bleeding; contracted covid; contracted covid; this is a spontaneous report received from a contactable reporter(s) (consumer or other non hcp) from the regulatory agency (ra). the reporter is the patient. other case identifier(s): gb-mhra-vac-202202131447339120-2bavn (ra), gb-mhra-adr 26598481 (ra). a 59 year-old female patient received bnt162b2 (comirnaty), administration date 04dec2021 (batch/lot number: unknown) as dose number unknown (booster), single for covid-19 immunisation; covid-19 vaccine (covid-19 vaccine) (batch/lot number: unknown) as dose number unknown, single for covid-19 immunisation. relevant medical history included: "cholesterol high" (unspecified if ongoing); "hypertension" (unspecified if ongoing). concomitant medication(s) included: atorvastatin taken for blood cholesterol increased, start date: mar2021; lisinopril taken for hypertension, start date: 2015. the following information was reported: drug ineffective (medically significant), covid-19 (medically significant) all with onset jan2022, outcome "unknown" and all described as "contracted covid"; postmenopausal haemorrhage (medically significant) with onset 30jan2022, outcome "not recovered", described as "post menopausal bleeding". clinical course: the patient had not had post-menopausal bleeding before. this also started at around the time she contracted covid. the booster vaccine was given on 04dec2021. the reaction/s did not occur as a result of a mistake made in the administration of the vaccine. 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
drug ineffective covid-19 postmenopausal haemorrhage
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