Adverse Event Reporting
VAERS ID | 1978850 |
---|---|
Gender | Unknown |
Age | |
StateCode | |
Pharmaceutical Company | PFIZER\BIONTECH |
Lot Number | |
Number of vaccinations | 2 |
Vaccinated | |
Onset | |
Condition |
Symptoms
- Poor venous access
Current Illness
Preexisting Conditions
Other Medications
Previous Vaccinations
Allergies
Laboratory Data
Write-up
neither one of us ever had issues drawing blood out of our veins till ever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP).
A patient (no qualifiers provided) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection), administered in arm (Batch/Lot number: unknown) as dose 2, single for COVID-19 immunisation.
The patient's relevant medical history and concomitant medications were not reported.
Vaccination history included: Bnt162b2 (1st dose), for COVID-19 immunisation.
The following information was reported: POOR VENOUS ACCESS (non-serious), outcome "unknown", described as "neither one of us ever had issues drawing blood out of our veins till ever".
Additional information: The reporter and the patient received the first and second shot of BNT162B2.
The reporter and the patient have routine blood drawn for a routine check up and neither one of them ever had issues drawing blood out of their veins until they got the vaccine.
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) : US-PFIZER INC-2021264488 Same reporter/product/event, different patient