depression; this is a spontaneous report received from a contactable reporter(s) (consumer or other non hcp) from the regulatory agency (ra). regulatory number: gb-mhra-webcovid-202202192114293090-elflx (ra). other case identifier(s): gb-mhra-adr 26626079 (ra). a 54 year-old female patient (not pregnant) received bnt162b2 (comirnaty), administration date 15oct2021 (batch/lot number: unknown) as dose 3 (booster), single for covid-19 immunisation. the patient's relevant medical history and concomitant medications were not reported. vaccination history included: bnt162b2 (dose-1, manufacturer unknown), for covid-19 immunisation; bnt162b2 (dose-2, manufacturer unknown), for covid-19 immunisation. the following information was reported: depression (disability), outcome "not recovered", described as "depression". the patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative, notes: no - negative covid-19 test. no follow-up attempts are possible; information about lot/batch number cannot be obtained. no further information is expected

test name: covid-19 virus test; test result: negative ; comments: no - negative covid-19 test

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