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VAERS Report 2156958

Case Report Section

Détails du rapport Vaer

Âge: 17 ans

Genre: Female

Région : Outside US

Patient décédé?
Renseignements sur les vaccins


Type : Coronavirus 2019 vaccine

Fabricant: PFIZER

Lot: ff331g

Date de réception du rapport
Date à laquelle le formulaire est complèté
Date de vaccination
Date d’apparition
Nombre de jours (date d’apparition – date de vaccination)
Description de l’événement indésirable

drug ineffective; sars-cov-2 infection; muscle pain; this is a solicited report from the uk-mhra yellow card vaccine monitor program from a contactable consumer. this is a report received from the regulatory authority. regulatory authority report number gb-mhra-ycvm-202108151403440960-yder6, safety report unique identifier gb-mhra-adr 25828053. a 17-year-old female patient received bnt162b2 (pfizer-biontech covid-19 vaccine,, solution for injection, lot number: ff331g), via an unspecified route of administration on 19aug2021 (at the age of 17-years-old) as dose 1, single for covid-19 immunization. the patient's medical history and concomitant medications were not reported. on 19aug2021 the patient experienced muscle pain (myalgia). the patient underwent lab tests and procedures which included sars-cov-2 test was negative on 03jul2021 no - negative covid-19 test. patient lmp date: 19jun2021. patient has not had symptoms associated with covid-19 patient was not pregnant, patient was not currently breastfeeding. patient has not tested positive for covid-19 since having the vaccine. patient was not enrolled in clinical trial. on 11feb2022, patient experienced sars-cov-2 infection (suspected -covid-19) and drug ineffective. events sars-cov-2 infection and drug ineffective considered medically significant. no causality was provided for muscle pain, sars-cov-2 infection and drug ineffective. the outcome of event muscle pain was recovered with sequelae. the outcome of event sars-cov-2 infection was recovered on 19feb2022 and outcome of event drug ineffective was unknown. the reporter's assessment of the causal relationship of the events with the suspect product was not provided at the time of this report. since no determination has been received, the case is managed based on the company causality assessment no follow-up attempts are possible. no further information is expected. follow up (25feb2022): this is a solicited follow-up report received from the contactable consumer via regulatory authority card vaccine monitor program. updated information: study information; event sars-cov-2 infection and drug ineffective added.; sender's comments: based on the information in the case report and a plausible temporal relationship, a possible causal association between the events and suspect drug bnt162b2 cannot be excluded

Données de laboratoire
test date: 20210703; test name: covid-19 virus test; test result: negative ; comments: no - negative covid-19 test
Liste des symptômes
drug ineffective myalgia sars-cov-2 test suspected covid-19
Patient décédé?
Date de décès
Anomalie congénitale
Vaccin administré par :
Vaccin acheté par :
Visite d’un patient à l’urgence?
Patient hospitalisé?
Séjour à l’hôpital
Nombre de jours à l’hôpital
Non spécifié
Invalidité permanente?
Maladie actuelle