Adverse Event Reporting

VAERS ID	1835173
Gender	Male
Age
StateCode	FR
Pharmaceutical Company	PFIZER\BIONTECH
Lot Number	EX8680
Number of vaccinations	1
Vaccinated	2002-01-02
Onset	2021-06-26
Condition	Permanent Disability

Symptoms

• Arthralgia

Current Illness

Preexisting Conditions

Medical History/Concurrent Conditions: Myocardial infarction

Other Medications

Previous Vaccinations

Allergies

Laboratory Data

Write-up

Joint pain; This is a spontaneous report from a contactable consumer, downloaded from the Regulatory Authority (A)-WEB, RegulatoryR authority number: SE-MPA-2021-088335.
A 59-years-old male patient received bnt162b2 (COMIRNATY), dose 1 via an unspecified route of administration on 18May2021 (Batch/Lot Number: EX8680) as dose 1, single for Covid-19 immunisation; acetylsalicylic acid (TROMBYL), oral from 02Jan2002 (Batch/Lot Number: Unknown) to an unspecified date, at 75 mg, 1x/day for myocardial infarction.
Medical history included myocardial infarction from 2002 to an unknown date.
The patient's concomitant medications were not reported.
The patient experienced joint pain on 26Jun2021.
The event occurred 19 years after the insertion of Trombyl.
It is just over a month and a week after vaccination with dose 1 of Comirnaty that the man experienced joint pain.
He has pain in his thumbs and joints.
Dose 2 was administered on 29Jun2021 (batch/lot number: FD6840).
The event had not resolved.
The case is assessed as serious, permanent disability.
No follow-up attempts are possible.
No further information is expected.