continuing pain in base of thumbs; joint pain; inappropriate schedule of vaccine administered; this is a spontaneous report received from a contactable reporter(s) (consumer or other non hcp) from the regulatory agency (ra). the reporter is the patient. a 73 year-old female patient received bnt162b2 (bnt162b2), administration date 10apr2021 (batch/lot number: unknown) as dose 2, single for covid-19 immunisation. relevant medical history included: "anxiety" (unspecified if ongoing); "underactive" (unspecified if ongoing); "cholesterol" (unspecified if ongoing). concomitant medication(s) included: citalopram taken for anxiety; influenza virus, administration date 21oct2021; levothyroxine taken for decreased activity; lipitor taken for blood cholesterol. vaccination history included: bnt162b2 (dose-1), administration date: 07feb2021, for covid-19 immunisation, reaction(s): "shingles in face". the following information was reported: arthralgia (medically significant) with onset 01jun2021, outcome "recovering", described as "joint pain"; pain in extremity (medically significant), outcome "unknown", described as "continuing pain in base of thumbs"; inappropriate schedule of product administration (non-serious) with onset 10apr2021, outcome "unknown", described as "inappropriate schedule of vaccine administered". the patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative, notes: no - negative covid-19 test. patient has not had symptoms associated with covid-19.patient has not tested positive for covid-19 since having the vaccine. patient is not enrolled in clinical trial. no follow-up attempts are possible; information about lot/batch number cannot be obtained. no further information is expected.; sender's comments: linked report(s) : gb-pfizer inc-202200306087 same patient/same product, different dose/events.;gb-pfizer inc-202200290098 same patient/same product, different dose/events

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

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