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VAERS Report 2156961

Case Report Section

Détails du rapport Vaer

Âge: N/A

Genre: Unknown

Région : Outside US

Patient décédé?
Non
Renseignements sur les vaccins

Nom: COVID19 (COVID19 (PFIZER-BIONTECH))

Type : Coronavirus 2019 vaccine

Fabricant: PFIZER

Lot: fe3380


Date de réception du rapport
2022-03-04
Date à laquelle le formulaire est complèté
Date de vaccination
2021-08-23
Date d’apparition
0
Nombre de jours (date d’apparition – date de vaccination)
0
Description de l’événement indésirable

positive covid lateral flow test; positive covid lateral flow test; this is a spontaneous report received from contactable reporter(s) (consumer or other non hcp) from a sales representative. the reporter is the patient. a 22 year-old patient received bnt162b2 (comirnaty), intramuscular, administered in arm, administration date 23aug2021 10:40 (lot number: fe3380) as dose 2, single and intramuscular, administered in arm, administration date 28jun2021 10:30 (lot number: fc8289) as dose 1, single for covid-19 immunisation. the patient had no relevant medical history. there were no concomitant medications. the following information was reported: drug ineffective (medically significant), covid-19 (medically significant), outcome "unknown" and all described as "positive covid lateral flow test". the patient underwent the following laboratory tests and procedures: antibody test: unknown results, notes: antibody test to platelet factor iv; sars-cov-2 test: positive, notes: positive covid lateral flow test. clinical course: positive covid lateral flow test and covid symptoms (cold, headache, fatigue) in patient who has had pfizer covid vaccine. optional information: last pfizer covid vaccine was administered 6 months before positive test and patient has had booster jab from different company in the meantime. the patient took no prior vaccinations (within 4 weeks) and specific relevant test for thromboembolic events with thrombocytopenia was none. follow-up (21feb2022): this is a spontaneous follow-up report from a contactable consumer. this consumer reported in response to the non-hcp letter sent that included: updated information: reporter detail (slider#01) was updated. patient age was added. relevant medical history and concomitant medications details were updated. suspect product details (dose 1 and dose 2) were updated. lab tests were added, and narrative updated accordingly. no follow-up attempts are possible. no further information is expected

Données de laboratoire
test name: antibody test; result unstructured data: test result:unknown results; comments: antibody test to platelet factor iv; test name: lateral flow test; test result: positive ; comments: positive covid lateral flow test
Liste des symptômes
drug ineffective covid-19 sars-cov-2 test antibody test
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