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|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||EX7823 / 2||- / OT|
Administered by: Other Purchased by: ??
Symptoms: Angina pectoris, Fatigue, Headache, Contusion
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Diagnostic Lab Data:
CDC 'Split Type': BGPFIZER INC2021664186
Write-up: heart pain; large bruise at the application site; general fatigue; headaches; This is a spontaneous report from a contactable consumer. This is second case of two cases for same patient, same product, difference adverse events and dose. A 42-years-old female patient received second dose of bnt162b2 (COMIRNATY, Solution for injection, Batch/Lot Number: EX7823, Expiration date was not reported), via intramuscular on 31May2021 as 2nd dose, single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously took (COMIRNATY Solution for injection) for covid-19 immunisation. On 01Jun2021 the patient experienced large bruise at the application site, general fatigue, heart pain, headaches. Three days before the vaccine and 4 days after the patient was taking an antihistamine. Patient did not received any treatment. On an unspecified date in 2021, the outcome of the events was recovered without treatment. Follow-up attempt completed. No expected further information. Amendment: This follow-up report is being submitted to amend previously reported Information: Amended the reported "heart pain" to LLT Cardiac Pain (PT Angina Pectoris) and upgraded the event to serious as this term is included the MedDRA Critical Preferred Terms List.
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