이상반응 보고
VAERS ID | 2237782 |
---|---|
성별 | 알 수 없음 |
나이 | |
주 코드 | |
제약회사 | PFIZER\BIONTECH |
로트 번호 | |
예방접종 횟수 | |
접종일 | 2022-04-06 |
발병일 | 2022-04-07 |
상태 |
증상
- 사지의 통증(Pain in extremity)
- 근육 약화(Muscular weakness)
- 보행 장애(Gait disturbance)
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증상 상세
Upper part of my leg is so sore and weak that I can hard, I am using a cane to walk with as I can barely walk, it's in acute pain; Upper part of my leg is so sore and weak that I can hard, I am using a cane to walk with as I can barely walk, it's in acute pain; Upper part of my leg is so sore and weak that I can hard, I am using a cane to walk with as I can barely walk, it's in acute pain/I can hardly walk; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP).
The reporter is the patient.
A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 06Apr2022 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation.
The patient's relevant medical history and concomitant medications were not reported.
Vaccination history included: Covid-19 vaccine (Previous immunization series complete, MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (Booster, MANUFACTURER UNKNOWN), for COVID-19 Immunization.
The following information was reported: PAIN IN EXTREMITY (non-serious), MUSCULAR WEAKNESS (non-serious) all with onset 07Apr2022, outcome "unknown" and all described as "Upper part of my leg is so sore and weak that I can hard, I am using a cane to walk with as I can barely walk, it's in acute pain"; GAIT DISTURBANCE (non-serious) with onset 07Apr2022, outcome "unknown", described as "Upper part of my leg is so sore and weak that I can hard, I am using a cane to walk with as I can barely walk, it's in acute pain/I can hardly walk".
Additional Information: Consumer stated, "I had my second booster yesterday and I woke this morning and the upper part of my leg is so sore and weak that I can hard, I am using a cane to walk with as I can barely walk, it's in acute pain.
" Comment: Reporter type could not be probed as the consumer was unwilling to share any further information, hence captured by default as consumer or other non-health professional in tab.
No follow-up attempts are possible; information about lot/batch number cannot be obtained.
No further information is expected.