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VAERS Report 2156620

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
Date d’apparition
0
Nombre de jours (date d’apparition – date de vaccination)
0
Description de l’événement indésirable

off label use; interchange of vaccine products; nausea; fatigue; paraesthesia; headache; generalised joint pain; this is a spontaneous report received from a contactable reporter(s) (physician) from the regulatory authority. other case identifier(s): gb-mhra-vac-202202150858459150-jxpgn, gb-mhra-adr 26606329 . a female patient received bnt162b2 (comirnaty) (batch/lot number: unknown) as dose 3 (booster), single for covid-19 immunisation. relevant medical history included: "hypothyroidism" (unspecified if ongoing). concomitant medication(s) included: levothyroxine taken for hypothyroidism. vaccination history included: covid-19 vaccine astrazeneca (dose 1), for covid-19 immunisation; covid-19 vaccine astrazeneca (dose 2), for covid-19 immunisation, reaction(s): "generalised joint pain", "fatigue", "headache", "nausea", "paraesthesia". the following information was reported: off label use (disability, medically significant), outcome "unknown", described as "off label use"; interchange of vaccine products (disability, medically significant), outcome "unknown", described as "interchange of vaccine products"; nausea (disability, medically significant), outcome "not recovered", described as "nausea"; fatigue (disability, medically significant), outcome "not recovered", described as "fatigue"; paraesthesia (disability, medically significant), outcome "not recovered", described as "paraesthesia"; headache (disability, medically significant), outcome "not recovered", described as "headache"; arthralgia (disability, medically significant), outcome "not recovered", described as "generalised joint pain". therapeutic measures were taken as a result of nausea, fatigue, paraesthesia, headache, arthralgia. it was reported that patient had 6 months of symptoms (nausea, fatigue, paraesthesia, headache, generalised joint pain) after initial course of vaccine with astra zeneca had pfizer booster dose as she wanted to travel to australia and all of the above symptoms had returned. very upset that the same thing has happened again and that there doesn't seem to be any support/help with it, medications for symptoms have made no difference. the patient did not think that the reaction occurred 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
paraesthesia fatigue nausea headache arthralgia interchange of vaccine products off label use
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?
Oui
Allergies:
na
Maladie actuelle
na