Symptomtext
Strong headache that lasted through the day; slight fever; had chills; Dizziness; lack of appetite; aching all over body, especially the spine; aching all over body, especially the spine; Arm where shot was received was very sore and painul to move; This is a spontaneous report from a contactable consumer. This 23-year-old male consumer reported for himself. A 23-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection, Batch/Lot Number: EW0181), dose 3 via an unspecified route of administration, administered in left arm on 11Oct2021 as DOSE 3, (BOOSTER) SINGLE for COVID-19 immunization; influenza vaccine (FLUZONE [INFLUENZA VACCINE]), via an unspecified route of administration, administered in right arm on 11Oct2021 (Batch/Lot Number: UT7347JA), as single dose for an unspecified indication (both at the age of 23-years-old). The patient's medical history was not reported. There were no concomitant medications. The patient's historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection, Batch/Lot Number: EK9231), dose 1 via an unspecified route of administration, administered in left arm on 26Dec2020, as DOSE 1, SINGLE; and bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection, Batch/Lot Number: EL3247) dose 2, via an unspecified route of administration, administered in left arm on 19Jan2021, as DOSE 2, SINGLE (both at the age of 22-years-old) and both for COVID-19 immunization. The patient had no other vaccine within four weeks, and no other medications in two weeks. The patient had no COVID prior to vaccination and was not tested for COVID post vaccination. On 12Oct2021, the patient experienced strong headache that lasted through the day until pain meds taken in the mid-afternoon. On 12Oct2021, the patient ran a slight fever and had chills, experienced dizziness, lack of appetite, aching all over body, especially the spine. The arm where shot was received was very sore and painful to move. The adverse event did not result in emergency room visit or physician office visit. The patient underwent lab tests and procedures which included slight fever: slight on 12Oct2021. Therapeutic measures were taken as a result of strong headache that lasted through the day (headache). Treatment was not provided for other adverse events. The action taken in response to the events for influenza vaccine was not applicable. The clinical outcome of the events was recovered on an unspecified date in Oct2021. Follow-Up: Follow-up attempts are completed. No further information is expected.