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VAERS Report 2156775

Case Report Section

Détails du rapport Vaer

Âge: 63 ans

Genre: Female

Région : Outside US

Patient décédé?
Renseignements sur les vaccins


Type : Coronavirus 2019 vaccine

Fabricant: PFIZER

Lot: fl9994

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

pain; arthritis flare up; ra came on; feel unwell; violently sick; this is a spontaneous report received from a contactable reporter(s) (consumer or other non hcp) from the regulatory agency. the reporter is the patient. regulatory number: gb-mhra-webcovid-202202161520510700-vovzv. other case identifier(s): gb-mhra-adr 26610447. a 63 year-old female patient received bnt162b2 (comirnaty), administration date 12feb2022 (lot number: fl9994) at the age of 63 years as dose 4 (booster), single for covid-19 immunisation. relevant medical history included: "rheumatoid arthritis" (unspecified if ongoing), notes: taking regular medicines for rheumatoid arthritis (or other types of arthritis except osteoarthr. concomitant medication(s) included: concomitant medication(s) included: cimzia taken for rheumatoid arthritis, stop date: 12feb2022; prednisolone (ongoing). vaccination history included: covid-19 vaccine (dose 3, manufacturer unknown), for covid-19 immunisation; covid-19 vaccine (dose 2, manufacturer unknown), for covid-19 immunisation; covid-19 vaccine (dose 1, manufacturer unknown), for covid-19 immunisation. the following information was reported: malaise (medically significant) with onset 12feb2022, outcome "unknown", described as "feel unwell"; illness (medically significant) with onset 12feb2022, outcome "unknown", described as "violently sick"; pain (medically significant), outcome "not recovered", described as "pain"; arthritis (medically significant) with onset 13feb2022, outcome "recovering", described as "arthritis flare up"; rheumatoid arthritis (medically significant) with onset 13feb2022, outcome "recovering", described as "ra came on". later on 12feb2022, patient took injection of cimzia (biologic for ra) which was due that date (2 weekly intervals). some hours later patient began to feel unwell and went to bed early (9pm), she was violently sick and a flare of ra came on. she was in absolute agony all night long, she was unable to stand as ankles (both) were far too painful, as were both arms. patient instructed her husband to get the prednisolone and she took 2 x 2.5mg every 2 hours plus one co codamol at the same time. the pain was unbearable but eventually slowly subsided during the course of the following day. it was after lunchtime before she was able to walk with assistance to the bathroom a few steps away. she reported the incident to her ra team at the hospital she attended. gradually she was getting back to normal having been stable on cimzia for years so she can only assume the co administration of the two injections caused a storm in her immune system and presented in the form of a severe flare. the patient underwent the following laboratory tests and procedures: sars-cov-2 test: (15feb2022) no - negative covid-19 test. patient has not tested positive for covid-19 since having the vaccine. therapeutic measures were taken as a result of pain, arthritis, rheumatoid arthritis. patient is not enrolled in clinical trial. no follow-up attempts are possible. no further information is expected

Données de laboratoire
test date: 20220215; test name: covid-19 virus test; result unstructured data: test result:no - negative covid-19 test
Liste des symptômes
malaise arthritis rheumatoid arthritis pain sars-cov-2 test illness
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